119 results on '"Giovanetti, Marta"'
Search Results
2. Suitable Mouse Model to Study Dynamics of West Nile Virus Infection in Culex quinquefasciatus Mosquitoes.
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Baldon, Lívia, de Mendonça, Silvana, Santos, Ellen, Marçal, Bruno, de Freitas, Amanda Cupertino, Rezende, Fernanda, Moreira, Rafaela, Sousa, Viviane, Comini, Sara, Lima, Mariana, Ferreira, Flávia, de Almeida, João Paulo, Silva, Emanuele, Amadou, Siad, Rocha, Marcele, Leite, Thiago, Todjro, Yaovi, de Carvalho, Camila, Santos, Viviane, and Giovanetti, Marta
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- 2024
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3. Viral Hepatitis: Host Immune Interaction, Pathogenesis and New Therapeutic Strategies.
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Quirino, Angela, Marascio, Nadia, Branda, Francesco, Ciccozzi, Alessandra, Romano, Chiara, Locci, Chiara, Azzena, Ilenia, Pascale, Noemi, Pavia, Grazia, Matera, Giovanni, Casu, Marco, Sanna, Daria, Giovanetti, Marta, Ceccarelli, Giancarlo, Alaimo di Loro, Pierfrancesco, Ciccozzi, Massimo, Scarpa, Fabio, and Maruotti, Antonello
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Viral hepatitis is a major cause of liver illness worldwide. Despite advances in the understanding of these infections, the pathogenesis of hepatitis remains a complex process driven by intricate interactions between hepatitis viruses and host cells at the molecular level. This paper will examine in detail the dynamics of these host–pathogen interactions, highlighting the key mechanisms that regulate virus entry into the hepatocyte, their replication, evasion of immune responses, and induction of hepatocellular damage. The unique strategies employed by different hepatitis viruses, such as hepatitis B, C, D, and E viruses, to exploit metabolic and cell signaling pathways to their advantage will be discussed. At the same time, the innate and adaptive immune responses put in place by the host to counter viral infection will be analyzed. Special attention will be paid to genetic, epigenetic, and environmental factors that modulate individual susceptibility to different forms of viral hepatitis. In addition, this work will highlight the latest findings on the mechanisms of viral persistence leading to the chronic hepatitis state and the potential implications for the development of new therapeutic strategies. Fully understanding the complex host–pathogen interactions in viral hepatitis is crucial to identifying new therapeutic targets, developing more effective approaches for treatment, and shedding light on the mechanisms underlying progression to more advanced stages of liver damage. [ABSTRACT FROM AUTHOR]
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- 2024
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4. Reassessing the Risk of Severe Parvovirus B19 Infection in the Immunocompetent Population: A Call for Vigilance in the Wake of Resurgence.
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Ceccarelli, Giancarlo, Branda, Francesco, Ciccozzi, Alessandra, Romano, Chiara, Sanna, Daria, Casu, Marco, Albanese, Mattia, Alessandri, Francesco, d'Ettorre, Gabriella, Ciccozzi, Massimo, Scarpa, Fabio, and Giovanetti, Marta
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PUBLIC health surveillance ,YOUNG adults ,PREGNANT women ,PARVOVIRUS B19 ,PARVOVIRUS diseases - Abstract
Despite Parvovirus B19 (B19V) generally causing mild or asymptomatic infections, and only certain high-risk groups such as hematological or immunocompromised patients and pregnant women tending to develop complications, several factors challenge the assumption of a "benign" clinical course in immunocompetent adults and adolescents. A significant proportion of the population may harbor undiagnosed health conditions or genetic predispositions that could render them more susceptible to severe B19V complications. These could include mild hematological disorders, immune dysregulation not resulting in overt immunodeficiency, or underlying cardiac conditions. Concurrent infections with other pathogens, even seemingly minor ones, could synergistically increase the severity of B19V infection, leading to more pronounced clinical manifestations. While not definitively proven, the possibility of emerging B19V strains with increased virulence or altered tissue tropism cannot be entirely discounted. Additionally, the period of pandemic-related restrictions likely led to reduced B19V circulation, potentially resulting in a cohort of young adults with limited natural immunity, making them more vulnerable to infection. Potential clinical consequences include atypical and severe presentations, even in individuals without known risk factors. The traditional focus on B19V primarily as a pediatric concern might lead to underdiagnosis or delayed diagnosis in adults, potentially hindering timely intervention and management. A surge in B19V-related complications, even if individually mild, could collectively strain healthcare resources, particularly in settings with limited capacity or pre-existing pressures. Possible recommendations are to heighten clinical awareness with a high index of suspicion for B19V infection in adults and adolescents presenting with compatible symptoms, even in the absence of classic risk factors. Additionally, expanding testing criteria and enhancing public health surveillance efforts would be prudent. [ABSTRACT FROM AUTHOR]
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- 2024
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5. Integrating Digital Health Solutions with Immunization Strategies: Improving Immunization Coverage and Monitoring in the Post-COVID-19 Era.
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Pavia, Grazia, Branda, Francesco, Ciccozzi, Alessandra, Romano, Chiara, Locci, Chiara, Azzena, Ilenia, Pascale, Noemi, Marascio, Nadia, Quirino, Angela, Matera, Giovanni, Giovanetti, Marta, Casu, Marco, Sanna, Daria, Ceccarelli, Giancarlo, Ciccozzi, Massimo, and Scarpa, Fabio
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DIGITAL health ,VACCINATION complications ,MEDICAL personnel ,DATA privacy ,VACCINATION coverage - Abstract
The COVID-19 pandemic underscored the critical importance of vaccination to global health security and highlighted the potential of digital health solutions to improve immunization strategies. This article explores integrating digital health technologies with immunization programs to improve coverage, monitoring, and public health outcomes. It examines the current landscape of digital tools used in immunization initiatives, such as mobile health apps, electronic health records, and data analytics platforms. Case studies from different regions demonstrate the effectiveness of these technologies in addressing challenges such as vaccine hesitancy, logistics, and real-time monitoring of vaccine distribution and adverse events. The paper also examines ethical considerations, data privacy issues, and the need for a robust digital infrastructure to support these innovations. By analyzing the successes and limitations of digital health interventions in immunization campaigns during and after the COVID-19 pandemic, we provide recommendations for future integration strategies to ensure resilient and responsive immunization systems. This research aims to guide policymakers, health professionals, and technologists in leveraging digital health to strengthen immunization efforts and prepare for future public health emergencies. [ABSTRACT FROM AUTHOR]
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- 2024
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6. The Prevention of Viral Infections: The Role of Intestinal Microbiota and Nutritional Factors.
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Altomare, Annamaria, Giovanetti, Marta, Baldaro, Francesca, Ciccozzi, Massimo, Cicala, Michele, and Guarino, Michele Pier Luca
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Viral infections pose significant global challenges due to their rapid transmissibility. Therefore, preventing and treating these infections promptly is crucial to curbing their spread. This review focuses on the vital link between nutrition and viral infections, underscoring how dietary factors influence immune system modulation. Malnutrition, characterized by deficiencies in essential nutrients such as vitamins A, C, D, E, and zinc, can impair the immune system, thereby increasing vulnerability to viral infections and potentially leading to more severe health outcomes that complicate recovery. Additionally, emerging evidence highlights the role of commensal microbiota in immune regulation, which can affect hosts' susceptibility to infections. Specific dietary components, including bioactive compounds, vitamins, and probiotics, can beneficially modify gut microbiota, thus enhancing immune response and offering protection against viral infections. This review aims to elucidate the mechanisms by which dietary adjustments and gut microbiota impact the pathogenesis of viral infections, with a particular focus on strengthening the immune system. [ABSTRACT FROM AUTHOR]
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- 2024
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7. Exploring Microorganisms Associated to Acute Febrile Illness and Severe Neurological Disorders of Unknown Origin: A Nanopore Metagenomics Approach.
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Moreno, Keldenn Melo Farias, de Andrade, Virgínia Antunes, de Melo Iani, Felipe Campos, Fonseca, Vagner, Lima, Maurício Teixeira, de Castro Barbosa, Emerson, Tomé, Luiz Marcelo Ribeiro, Guimarães, Natália Rocha, Fritsch, Hegger Machado, Adelino, Talita, Oliveira Fereguetti, Tatiana, Aspahan, Maíra Cardoso, Gamarano Barros, Tereza, Alcantara, Luiz Carlos Junior, and Giovanetti, Marta
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GENOMICS ,HIV ,NEUROLOGICAL disorders ,ACUTE diseases ,METAGENOMICS - Abstract
Acute febrile illness (AFI) and severe neurological disorders (SNDs) often present diagnostic challenges due to their potential origins from a wide range of infectious agents. Nanopore metagenomics is emerging as a powerful tool for identifying the microorganisms potentially responsible for these undiagnosed clinical cases. In this study, we aim to shed light on the etiological agents underlying AFI and SND cases that conventional diagnostic methods have not been able to fully elucidate. Our approach involved analyzing samples from fourteen hospitalized patients using a comprehensive nanopore metagenomic approach. This process included RNA extraction and enrichment using the SMART-9N protocol, followed by nanopore sequencing. Subsequent steps involved quality control, host DNA/cDNA removal, de novo genome assembly, and taxonomic classification. Our findings in AFI cases revealed a spectrum of disease-associated microbes, including Escherichia coli, Streptococcus sp., Human Immunodeficiency Virus 1 (Subtype B), and Human Pegivirus. Similarly, SND cases revealed the presence of pathogens such as Escherichia coli, Clostridium sp., and Dengue virus type 2 (Genotype-II lineage). This study employed a metagenomic analysis method, demonstrating its efficiency and adaptability in pathogen identification. Our investigation successfully identified pathogens likely associated with AFI and SNDs, underscoring the feasibility of retrieving near-complete genomes from RNA viruses. These findings offer promising prospects for advancing our understanding and control of infectious diseases, by facilitating detailed genomic analysis which is critical for developing targeted interventions and therapeutic strategies. [ABSTRACT FROM AUTHOR]
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- 2024
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8. Detection of Multiple Human Viruses, including Mpox, Using a Wastewater Surveillance Approach in Brazil.
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Calabria de Araujo, Juliana, Carvalho, Ana Paula Assad, Leal, Cintia D., Natividade, Manuelle, Borin, Marcus, Guerra, Augusto, Carobin, Natália, Sabino, Adriano, Almada, Mariana, Costa, Maria Cristina M., Saia, Flavia, Frutuoso, Livia V., Iani, Felipe C. M., Adelino, Talita, Fonseca, Vagner, Giovanetti, Marta, and Alcantara, Luiz Carlos Junior
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WHOLE genome sequencing ,SEWAGE disposal plants ,PUBLIC health surveillance ,MONKEYPOX ,SEWAGE - Abstract
Sewage surveillance can be used as an effective complementary tool for detecting pathogens in local communities, providing insights into emerging threats and aiding in the monitoring of outbreaks. In this study using qPCR and whole genomic sewage surveillance, we detected the Mpox virus along with other viruses, in municipal and hospital wastewaters in Belo Horizonte, Brazil over a 9-month period (from July 2022 until March 2023). MPXV DNA detection rates varied in our study, with 19.6% (11 out of 56 samples) detected through the hybrid capture method of whole-genome sequencing and 20% (12 out of 60 samples) through qPCR. In hospital wastewaters, the detection rate was higher, at 40% (12 out of 30 samples) compared to 13.3% (4 out of 30 samples) in municipal wastewaters. This variation could be attributed to the relatively low number of MPXV cases reported in the city, which ranged from 106 to 341 cases during the study period, and the dilution effects, given that each of the two wastewater treatment plants (WWTP) investigated serves approximately 1.1 million inhabitants. Additionally, nine other virus families were identified in both hospitals and municipal wastewaters, including Adenoviridade, Astroviridae, Caliciviridae, Picornaviridade, Polyomaviridae, Coronaviridae (which includes SARS-CoV-2), Herspesviridae, Papillomaviridae and Flaviviridae (notably including Dengue). These findings underscore the potential of genomic sewage surveillance as a robust public health tool for monitoring a wide range of viruses circulating in both community and hospitals environments, including MPXV. [ABSTRACT FROM AUTHOR]
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- 2024
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9. Mpox: An Overview of Pathogenesis, Diagnosis, and Public Health Implications.
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Branda, Francesco, Romano, Chiara, Ciccozzi, Massimo, Giovanetti, Marta, Scarpa, Fabio, Ciccozzi, Alessandra, and Maruotti, Antonello
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MONKEYPOX ,ANIMAL communities ,PUBLIC health ,DIAGNOSIS ,INFECTIOUS disease transmission - Abstract
Mpox, caused by viruses of the genus Orthopoxvirus, is an emerging threat to human and animal health. With increasing urbanization and more frequent interaction between humans and wild animals, the risk of Mpox transmission to humans has increased significantly. This review aims to examine in depth the epidemiology, pathogenesis, and diagnosis of Mpox, with a special focus on recent discoveries and advances in understanding the disease. Molecular mechanisms involved in viral replication will be examined, as well as risk factors associated with interspecific transmission and spread of the disease in human populations. Currently available diagnostic methods will also be discussed, with a critical analysis of their limitations and possible future directions for improving the accuracy and timeliness of diagnosis. Finally, this review will explore the public health implications associated with Mpox, emphasizing the importance of epidemiological surveillance, vaccination, and emergency preparedness to prevent and manage possible outbreaks. Understanding the epidemiology and control strategies for Mpox is critical to protecting the health of human and animal communities and mitigating the risk of interspecific transmission and spread of the disease. [ABSTRACT FROM AUTHOR]
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- 2024
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10. Global Measles Surveillance: Trends, Challenges, and Implications for Public Health Interventions.
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Branda, Francesco, Giovanetti, Marta, Romano, Chiara, Benvenuto, Domenico, Ciccozzi, Alessandra, Sanna, Daria, Ciccozzi, Massimo, and Scarpa, Fabio
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MEASLES , *COMMUNICABLE diseases , *PUBLIC health , *SIGNAL detection , *IMMUNIZATION , *RUBELLA - Abstract
Measles, a highly contagious disease primarily affecting children, carries serious health risks, including complications and mortality. Vaccination remains the most effective preventive measure against measles transmission. The COVID-19 pandemic has exacerbated challenges in surveillance and immunization efforts, leaving millions of people exposed to preventable diseases such as measles. Globally accelerated immunization campaigns are critical for achieving regional elimination goals and mitigating the risk of outbreaks. Our team has developed an open-access database for global measles monitoring, facilitating standardized data collection and analysis. The analysis of measles cases from 2011 to 2023 reveals fluctuating trends, with notable increases in Africa in 2019 and 2023, indicating potential gaps in control strategies. Using an automated signal detection tool developed by the European Centre for Disease Prevention and Control (ECDC) team, we identified significant variations between World Health Organization (WHO) regions, underscoring the importance of continuous monitoring to detect epidemiological changes early. These results underscore the need for robust surveillance systems and accelerated vaccination efforts to safeguard public health. [ABSTRACT FROM AUTHOR]
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- 2024
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11. The High Capacity of Brazilian Aedes aegypti Populations to Transmit a Locally Circulating Lineage of Chikungunya Virus.
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de Freitas, Amanda, Rezende, Fernanda, de Mendonça, Silvana, Baldon, Lívia, Silva, Emanuel, Ferreira, Flávia, Almeida, João, Amadou, Siad, Marçal, Bruno, Comini, Sara, Rocha, Marcele, Fritsch, Hegger, Santos, Ellen, Leite, Thiago, Giovanetti, Marta, Alcantara, Luiz Carlos Junior, Moreira, Luciano, and Ferreira, Alvaro
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AEDES aegypti ,CHIKUNGUNYA virus ,MOSQUITO vectors ,CHIKUNGUNYA ,MOSQUITOES - Abstract
The incidence of chikungunya has dramatically surged worldwide in recent decades, imposing an expanding burden on public health. In recent years, South America, particularly Brazil, has experienced outbreaks that have ravaged populations following the rapid dissemination of the chikungunya virus (CHIKV), which was first detected in 2014. The primary vector for CHIKV transmission is the urban mosquito species Aedes aegypti, which is highly prevalent throughout Brazil. However, the impact of the locally circulating CHIKV genotypes and specific combinations of local mosquito populations on vector competence remains unexplored. Here, we experimentally analyzed and compared the infectivity and transmissibility of the CHIKV-ECSA lineage recently isolated in Brazil among four Ae. aegypti populations collected from different regions of the country. When exposed to CHIKV-infected AG129 mice for blood feeding, all the mosquito populations displayed high infection rates and dissemination efficiency. Furthermore, we observed that all the populations were highly efficient in transmitting CHIKV to a vertebrate host (naïve AG129 mice) as early as eight days post-infection. These results demonstrate the high capacity of Brazilian Ae. aegypti populations to transmit the locally circulating CHIKV-ECSA lineage. This observation could help to explain the high prevalence of the CHIKV-ECSA lineage over the Asian lineage, which was also detected in Brazil in 2014. However, further studies comparing both lineages are necessary to gain a better understanding of the vector's importance in the epidemiology of CHIKV in the Americas. [ABSTRACT FROM AUTHOR]
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- 2024
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12. Phylodynamic and Evolution of the Hemagglutinin (HA) and Neuraminidase (NA) Genes of Influenza A(H1N1) pdm09 Viruses Circulating in the 2009 and 2023 Seasons in Italy.
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Scarpa, Fabio, Sernicola, Leonardo, Farcomeni, Stefania, Ciccozzi, Alessandra, Sanna, Daria, Casu, Marco, Vitale, Marco, Cicenia, Alessia, Giovanetti, Marta, Romano, Chiara, Branda, Francesco, Ciccozzi, Massimo, and Borsetti, Alessandra
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NEURAMINIDASE ,HEMAGGLUTININ ,INFLUENZA ,GENETIC drift ,H7N9 Influenza ,VIRAL transmission ,FLU vaccine efficacy - Abstract
The influenza A(H1N1) pdm09 virus, which emerged in 2009, has been circulating seasonally since then. In this study, we conducted a comprehensive genome-based investigation to gain a detailed understanding of the genetic and evolutionary characteristics of the hemagglutinin (HA) and neuraminidase (NA) surface proteins of A/H1N1pdm09 strains circulating in Italy over a fourteen-year period from 2009 to 2023 in relation to global strains. Phylogenetic analysis revealed rapid transmission and diversification of viral variants during the early pandemic that clustered in clade 6B.1. In contrast, limited genetic diversity was observed during the 2023 season, probably due to the genetic drift, which provides the virus with a constant adaptability to the host; furthermore, all isolates were split into two main groups representing two clades, i.e., 6B.1A.5a.2a and its descendant 6B.1A.5a.2a.1. The HA gene showed a faster rate of evolution compared to the NA gene. Using FUBAR, we identified positively selected sites 41 and 177 for HA and 248, 286, and 455 for NA in 2009, as well as sites 22, 123, and 513 for HA and 339 for NA in 2023, all of which may be important sites related to the host immune response. Changes in glycosylation acquisition/loss at prominent sites, i.e., 177 in HA and 248 in NA, should be considered as a predictive tool for early warning signs of emerging pandemics, and for vaccine and drug development. [ABSTRACT FROM AUTHOR]
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- 2024
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13. Metagenomic Analysis for Diagnosis of Hemorrhagic Fever in Minas Gerais, Brazil.
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Iani, Felipe Campos de Melo, de Campos, Gabriel Montenegro, Adelino, Talita Emile Ribeiro, da Silva, Anielly Sarana, Kashima, Simone, Alcantara, Luiz Carlos Junior, Sampaio, Sandra Coccuzzo, Giovanetti, Marta, Elias, Maria Carolina, and Slavov, Svetoslav Nanev
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HEMORRHAGIC fever ,METAGENOMICS ,HEMORRHAGIC diseases ,LEPTOSPIRA interrogans ,YELLOW fever - Abstract
Viral hemorrhagic fever poses a significant public health challenge due to its severe clinical presentation and high mortality rate. The diagnostic process is hindered by similarity of symptoms across different diseases and the broad spectrum of pathogens that can cause hemorrhagic fever. In this study, we applied viral metagenomic analysis to 43 serum samples collected by the Public Health Laboratory (Fundação Ezequiel Dias, FUNED) in Minas Gerais State, Brazil, from patients diagnosed with hemorrhagic fever who had tested negative for the standard local hemorrhagic disease testing panel. This panel includes tests for Dengue virus (DENV) IgM, Zika virus IgM, Chikungunya virus IgM, yellow fever IgM, Hantavirus IgM, Rickettsia rickettsii IgM/IgG, and Leptospira interrogans IgM, in addition to respective molecular tests for these infectious agents. The samples were grouped into 18 pools according to geographic origin and analyzed through next-generation sequencing on the NextSeq 2000 platform. Bioinformatic analysis revealed a prevalent occurrence of commensal viruses across all pools, but, notably, a significant number of reads corresponding to the DENV serotype 2 were identified in one specific pool. Further verification via real-time PCR confirmed the presence of DENV-2 RNA in an index case involving an oncology patient with hemorrhagic fever who had initially tested negative for anti-DENV IgM antibodies, thereby excluding this sample from initial molecular testing. The complete DENV-2 genome isolated from this patient was taxonomically classified within the cosmopolitan genotype that was recently introduced into Brazil. These findings highlight the critical role of considering the patient's clinical condition when deciding upon the most appropriate testing procedures. Additionally, this study showcases the potential of viral metagenomics in pinpointing the viral agents behind hemorrhagic diseases. Future research is needed to assess the practicality of incorporating metagenomics into standard viral diagnostic protocols. [ABSTRACT FROM AUTHOR]
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- 2024
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14. Exploring the Interplay between COVID-19 and Gut Health: The Potential Role of Prebiotics and Probiotics in Immune Support.
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Giovanetti, Marta, Pannella, Gianfranco, Altomare, Annamaria, Rocchi, Giulia, Guarino, Michele, Ciccozzi, Massimo, Riva, Elisabetta, and Gherardi, Giovanni
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PREBIOTICS , *PROBIOTICS , *POST-acute COVID-19 syndrome , *GUT microbiome , *COVID-19 , *COVID-19 pandemic , *VIRUS diseases - Abstract
The COVID-19 pandemic has profoundly impacted global health, leading to extensive research focused on developing strategies to enhance outbreak response and mitigate the disease's severity. In the aftermath of the pandemic, attention has shifted towards understanding and addressing long-term health implications, particularly in individuals experiencing persistent symptoms, known as long COVID. Research into potential interventions to alleviate long COVID symptoms has intensified, with a focus on strategies to support immune function and mitigate inflammation. One area of interest is the gut microbiota, which plays a crucial role in regulating immune responses and maintaining overall health. Prebiotics and probiotics, known for their ability to modulate the gut microbiota, have emerged as potential therapeutic agents in bolstering immune function and reducing inflammation. This review delves into the intricate relationship between long COVID, the gut microbiota, and immune function, with a specific focus on the role of prebiotics and probiotics. We examine the immune response to long COVID, emphasizing the importance of inflammation and immune regulation in the persistence of symptoms. The potential of probiotics in modulating immune responses, including their mechanisms in combating viral infections such as COVID-19, is discussed in detail. Clinical evidence supporting the use of probiotics in managing long COVID symptoms is summarized, highlighting their role as adjunctive therapy in addressing various aspects of SARS-CoV-2 infection and its aftermath. [ABSTRACT FROM AUTHOR]
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- 2024
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15. Resurgence of Dengue Virus Serotype 3 in Minas Gerais, Brazil: A Case Report.
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Adelino, Talita, Lima, Maurício, Guimarães, Natália R., Xavier, Joilson, Fonseca, Vagner, Tomé, Luiz Marcelo R., Pereira, Maira Alves, Machado, Vanessa Ferreira, Alcantara, Luiz Carlos Junior, Iani, Felipe C. de Melo, and Giovanetti, Marta
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DENGUE ,DENGUE viruses ,MOSQUITO-borne diseases ,MOSQUITO control - Abstract
This report provides a detailed overview of the resurgence of DENV-3 in the state of Minas Gerais, Brazil, which is a concerning scenario in the context of dengue, a mosquito-borne viral disease. Historically, Brazil has grappled with dengue epidemics caused primarily by the DENV-1 and DENV-2 serotypes. However, in 2023, a significant shift in this pattern was observed as DENV-3 made a notable resurgence. This resurgence was characterized by the increase in DENV-3 cases within the country and the region of the Americas. Given the absence of sustained DENV-3 circulation in Brazil in previous years, this situation poses a significant risk, making the population highly susceptible to a potential novel epidemic. In November 2023, a 31-year-old male patient in Belo Horizonte exhibited symptoms of acute febrile syndrome. Multiplex RT-qPCR using the Kit Molecular ZC D-Tipagem confirmed DENV-3 infection, suggesting a likely autochthonous case, as the patient reported no travel history. To promptly assess this resurgence, we applied the nanopore sequencing technology. This allowed for the rapid characterization of the initial DENV-3 case isolated in Minas Gerais in 2023, representing a 13-year interval since the serotype's previous documented circulation in that state. This case report underscores the critical importance of proactive monitoring and the swift implementation of targeted control strategies to address the evolving dynamics of dengue, with a specific emphasis on the resurgence of DENV-3 in the state. [ABSTRACT FROM AUTHOR]
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- 2024
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16. Updated Insights into the Phylogenetics, Phylodynamics, and Genetic Diversity of Nipah Virus (NiV).
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de Campos, Gabriel Montenegro, Cella, Eleonora, Kashima, Simone, Alcântara, Luiz Carlos Júnior, Sampaio, Sandra Coccuzzo, Elias, Maria Carolina, Giovanetti, Marta, and Slavov, Svetoslav Nanev
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NIPAH virus ,GENETIC variation ,VIRUS diversity ,NONINVASIVE ventilation ,PHYLOGENY ,GENETIC vectors - Abstract
Nipah virus (NiV), a biosafety level 4 agent, was first identified in human clinical cases during an outbreak in 1998 in Malaysia and Singapore. While flying foxes are the primary host and viral vector, the infection is associated with a severe clinical presentation in humans, resulting in a high mortality rate. Therefore, NiV is considered a virus with an elevated epidemic potential which is further underscored by its recent emergence (September 2023) as an outbreak in India. Given the situation, it is paramount to understand the molecular dynamics of the virus to shed more light on its evolution and prevent potential future outbreaks. In this study, we conducted Bayesian phylogenetic analysis on all available NiV complete genomes, including partial N-gene NiV sequences (≥1000 bp) in public databases since the first human case, registered in 1998. We observed the distribution of genomes into three main clades corresponding to the genotypes Malaysia, Bangladesh and India, with the Malaysian clade being the oldest in evolutionary terms. The Bayesian skyline plot showed a recent increase in the viral population size since 2019. Protein analysis showed the presence of specific protein families (Hendra_C) in bats that might keep the infection in an asymptomatic state in bats, which also serve as viral vectors. Our results further indicate a shortage of complete NiV genomes, which would be instrumental in gaining a better understanding of NiV's molecular evolution and preventing future outbreaks. Our investigation also underscores the critical need to strengthen genomic surveillance based on complete NiV genomes that will aid thorough genetic characterization of the circulating NiV strains and the phylogenetic relationships between the henipaviruses. This approach will better prepare us to tackle the challenges posed by the NiV virus and other emerging viruses. [ABSTRACT FROM AUTHOR]
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- 2024
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17. Comprehensive Analysis of HIV-1 Integrase Resistance-Related Mutations in African Countries.
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Branda, Francesco, Giovanetti, Marta, Sernicola, Leonardo, Farcomeni, Stefania, Ciccozzi, Massimo, and Borsetti, Alessandra
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NON-nucleoside reverse transcriptase inhibitors ,HIV ,DRUG resistance ,ANTI-HIV agents ,MOLECULAR epidemiology - Abstract
The growing emergence of non-nucleoside reverse transcriptase inhibitor (NNRTI) HIV drug resistance in sub-Saharan Africa (SSA) led to the World Health Organization (WHO) recommending, in 2018, a transition to dolutegravir (DTG) as a first-line antiretroviral therapy (ART) in SSA. The broad HIV-1 genetic diversity in SSA could shape DTG effectiveness and the pattern of drug resistance mutations (DRMs) in this region. This study evaluated HIV-1 integrase (IN) DRMs and conserved regions among published groups M, N, O, and P HIV-1 sequences spanning forty years of the HIV epidemic during the transition of DTG-based ART. Overall, we found low levels of integrase strand transfer inhibitor (INSTI)-DRMs (<1%) across HIV groups between the years 1983 and 2023; however, it was unexpected to detect DRMs at statistically significantly higher frequencies in pre-INSTI (1983–2007) than in the INSTI (2008–2023) era. The variability of accessory INSTI-DRMs depended on the HIV subtypes, with implications for susceptibility to DTG. Our findings provide new perspectives on the molecular epidemiology and drug resistance profiles of INSTIs in SSA, emphasizing the need for ongoing surveillance and customized treatment approaches to address the continent's varied HIV subtypes and changing resistance patterns. [ABSTRACT FROM AUTHOR]
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- 2024
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18. Epidemiological and Genomic Analysis of Asymptomatic SARS-CoV-2 Infections during the Delta and Omicron Epidemic Waves in São Paulo City, Brazil.
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Slavov, Svetoslav N., Lima, Alex R. J., Ribeiro, Gabriela, de Lima, Loyze P. O., Barros, Claudia R. dos S., Marqueze, Elaine C., Martins, Antonio J., Martininghi, Maiara, Palmieri, Melissa, Caldeira, Luiz A. V., da Silva, Fabiana E. V., Cacherik, Giselle, Nicolodelli, Aline L., Kashima, Simone, Giovanetti, Marta, Alcantara, Luiz Carlos Junior, Sampaio, Sandra C., and Elias, Maria C.
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SARS-CoV-2 Omicron variant ,GENOMICS ,SARS-CoV-2 ,BUS terminals ,EPIDEMICS - Abstract
We examined the asymptomatic rates of SARS-CoV-2 infection during the Delta and Omicron waves in the city of São Paulo. Nasopharyngeal swabs were collected at strategic points of the city (open-air markets, bus terminals, airports) for SARS-CoV-2 RNA testing. Applying the questionnaire, the symptomatic individuals were excluded, and only asymptomatic cases were analyzed. During the Delta wave, a total of 4315 samples were collected, whereas 2372 samples were collected during the first Omicron wave. The incidence of the asymptomatic SARS-CoV-2 infection was 0.6% during the Delta wave and 0.8% during the Omicron wave. No statistical differences were found in the threshold amplification cycle. However, there was a statistical difference observed in the sublineage distribution between asymptomatic and symptomatic individuals. Our study determined the incidence of asymptomatic infection by monitoring individuals who remained symptom-free, thereby providing a reliable evaluation of asymptomatic SARS-CoV-2 carriage. Our findings reveal a relatively low proportion of asymptomatic cases, which could be attributed to our rigorous monitoring protocol for the presence of clinical symptoms. Investigating asymptomatic infection rates is crucial to develop and implement effective disease control strategies. [ABSTRACT FROM AUTHOR]
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- 2023
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19. Exploring Viral Metagenomics in Pediatric Patients with Acute Respiratory Infections: Unveiling Pathogens beyond SARS-CoV-2.
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de Campos, Gabriel Montenegro, de La-Roque, Debora Glenda Lima, Lima, Alex Ranieri Jerônimo, Zucherato, Victória Simionatto, de Carvalho, Eneas, de Lima, Loyze Paola Oliveira, de Queiroz Cattony Neto, Pedro, dos Santos, Murilo Marconi, Ciccozzi, Massimo, Giovanetti, Marta, Haddad, Rodrigo, Alcantara, Luiz Carlos Júnior, Elias, Maria Carolina, Sampaio, Sandra Coccuzzo, Covas, Dimas Tadeu, Kashima, Simone, and Slavov, Svetoslav Nanev
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METAGENOMICS ,CHILD patients ,COVID-19 ,RESPIRATORY infections ,RESPIRATORY syncytial virus ,PEDIATRIC respiratory diseases ,SARS-CoV-2 - Abstract
The emergence of SARS-CoV-2 and the subsequent pandemic have prompted extensive diagnostic and clinical efforts to mitigate viral spread. However, these strategies have largely overlooked the presence of other respiratory viruses. Acute respiratory diseases in pediatric patients can be caused by a diverse range of viral agents, and metagenomics represents a powerful tool for their characterization. This study aimed to investigate the viral abundance in pediatric patients with acute respiratory symptoms who tested negative for SARS-CoV-2 during the Omicron pandemic wave. To achieve this, viral metagenomics and next-generation sequencing were employed on 96 nasopharyngeal swab samples, which were organized into 12 pools, with each pool consisting of eight individual samples. Metagenomic analysis revealed that the most prevalent viruses associated with acute disease in pediatric patients were respiratory syncytial virus (detected in all pools) and enteroviruses, which are known to cause significant morbidity and mortality in children. Additionally, clinically significant viruses such as mumps orthorubulavirus, human metapneumovirus, influenza A, and a wide array of human herpesviruses (1, 3–7) were identified. These findings highlight the extensive potential of viral metagenomics in identifying viruses other than SARS-CoV-2 that contribute to acute infections in children. Consequently, this methodology should garner clinical attention in terms of differential diagnosis and the development of public policies to address such conditions in the global pediatric population. [ABSTRACT FROM AUTHOR]
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- 2023
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20. Genomic Epidemiology and Lineage Dynamics of SARS-CoV-2 in Bulgaria: Insights from a Three-Year Pandemic Analysis.
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Giovanetti, Marta, Cella, Eleonora, Ivanov, Ivan, Grigorova, Lyubomira, Stoikov, Ivan, Donchev, Deyan, Dimitrova, Reneta, Slavov, Svetoslav Nanev, Mavian, Carla, Fonseca, Vagner, Scarpa, Fabio, Borsetti, Alessandra, Korsun, Neli, Trifonova, Ivelina, Dobrinov, Veselin, Kantardjiev, Todor, Christova, Iva, Ciccozzi, Massimo, and Alexiev, Ivailo
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COVID-19 , *SARS-CoV-2 , *VIRAL transmission - Abstract
The COVID-19 pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has brought about significant challenges worldwide. In this study, we present a comprehensive analysis of the genomic epidemiology and lineage dynamics of SARS-CoV-2 in Bulgaria over a three-year period. Through extensive genomic sequencing and data analysis, we investigated the evolution of the virus, the emergence of variants of concern (VOCs), and their impact on the country's pandemic trajectory. We also assessed the relationship between viral diversity and COVID-19 morbidity and mortality in Bulgaria. Our findings shed light on the temporal and spatial distribution of SARS-CoV-2 lineages and provide crucial insights into the dynamics of the pandemic in the country. The interplay between international travel and viral transmission plays a significant role in the emergence and dissemination of different SARS-CoV-2 variants. The observed proportions of exportation to various continents provide insights into the potential pathways through which these lineages spread globally. Understanding the genomic epidemiology of SARS-CoV-2 in Bulgaria is essential for formulating targeted public health strategies, enhancing vaccination efforts, and effectively managing future outbreaks. [ABSTRACT FROM AUTHOR]
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- 2023
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21. Dengue Fever Surveillance in Mato Grosso do Sul: Insights from Genomic Analysis and Implications for Public Health Strategies.
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Castilho de Arruda, Larissa Domingues, Giovanetti, Marta, Fonseca, Vagner, Zardin, Marina Castilhos Souza Umaki, Lichs, Gislene Garcia de Castro, Asato, Silvia, Esposito, Ana Olivia Pascoto, Tokeshi Müller, Miriam, Xavier, Joilson, Fritsch, Hegger, Lima, Mauricio, de Oliveira, Carla, Santos, Elaine Vieira, Maziero, Livia de Mello Almeida, Frias, Danila Fernanda Rodrigues, Ahad das Neves, Danielle, Ferreira da Silva, Liliane, Rodrigues Barretos, Ellen Caroline, Tsuha Oshiro, Paulo Eduardo, and Modafari Goday, Bianca
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DENGUE , *GENOMICS , *DENGUE viruses , *VIRAL transmission , *ARBOVIRUS diseases , *PUBLIC health , *PUBLIC health surveillance - Abstract
Since its discovery in early 1916, dengue fever, a common vector-borne illness in Brazil, has resulted in extensive urban outbreaks and poses a serious threat to the public's health. Understanding the dynamics of Dengue Virus (DENV) serotypes circulating in different regions of Brazil is essential for implementing effective disease control and prevention measures. In response to this urgent need, we conducted an on-site training program in genomic surveillance in collaboration with the Central Laboratory of Health and the Secretary of Health of the Mato Grosso do Sul state. This initiative resulted in the generation of 177 DENV genome sequences collected between May 2021 and May 2022, a period during which over 11,391 dengue fever cases were reported in the state. Through this approach, we were able to identify the co-circulation of two different dengue serotypes (DENV1 and DENV2) as well as the existence of diverse viral lineages within each genotype, suggesting that multiple introduction events of different viral strains occurred in the region. By integrating epidemiological data, our findings unveiled temporal fluctuations in the relative abundance of different serotypes throughout various epidemic seasons, highlighting the complex and changing dynamics of DENV transmission throughout time. These findings demonstrate the value of ongoing surveillance activities in tracking viral transmission patterns, monitoring viral evolution, and informing public health actions. [ABSTRACT FROM AUTHOR]
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- 2023
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22. Integrative Genome-Based Survey of the SARS-CoV-2 Omicron XBB.1.16 Variant.
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Scarpa, Fabio, Azzena, Ilenia, Ciccozzi, Alessandra, Giovanetti, Marta, Locci, Chiara, Casu, Marco, Fiori, Pier Luigi, Borsetti, Alessandra, Cella, Eleonora, Quaranta, Miriana, Pascarella, Stefano, Sanna, Daria, and Ciccozzi, Massimo
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SARS-CoV-2 Omicron variant ,SARS-CoV-2 ,GENETIC drift ,GENETIC variation - Abstract
The XBB.1.16 SARS-CoV-2 variant, also known as Arcturus, is a recent descendant lineage of the recombinant XBB (nicknamed Gryphon). Compared to its direct progenitor, XBB.1, XBB.1.16 carries additional spike mutations in key antigenic sites, potentially conferring an ability to evade the immune response compared to other circulating lineages. In this context, we conducted a comprehensive genome-based survey to gain a detailed understanding of the evolution and potential dangers of the XBB.1.16 variant, which became dominant in late June. Genetic data indicates that the XBB.1.16 variant exhibits an evolutionary background with limited diversification, unlike dangerous lineages known for rapid changes. The evolutionary rate of XBB.1.16, which amounts to 3.95 × 10
−4 subs/site/year, is slightly slower than that of its direct progenitors, XBB and XBB.1.5, which have been circulating for several months. A Bayesian Skyline Plot reconstruction suggests that the peak of genetic variability was reached in early May 2023, and currently, it is in a plateau phase with a viral population size similar to the levels observed in early March. Structural analyses indicate that, overall, the XBB.1.16 variant does not possess structural characteristics markedly different from those of the parent lineages, and the theoretical affinity for ACE2 does not seem to change among the compared variants. In conclusion, the genetic and structural analyses of SARS-CoV-2 XBB.1.16 do not provide evidence of its exceptional danger or high expansion capability. Detected differences with previous lineages are probably due to genetic drift, which allows the virus constant adaptability to the host, but they are not necessarily connected to a greater danger. Nevertheless, continuous genome-based monitoring is essential for a better understanding of its descendants and other lineages. [ABSTRACT FROM AUTHOR]- Published
- 2023
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23. Monitoring Monkeypox: Safeguarding Global Health through Rapid Response and Global Surveillance.
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Giovanetti, Marta, Cella, Eleonora, Moretti, Sonia, Scarpa, Fabio, Ciccozzi, Alessandra, Slavov, Svetoslav Nanev, Benedetti, Francesca, Zella, Davide, Ceccarelli, Giancarlo, Ciccozzi, Massimo, and Borsetti, Alessandra
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MONKEYPOX ,ZOONOSES ,WORLD health ,VIRUS diseases ,INFORMATION sharing ,VIDEO surveillance - Abstract
Monkeypox, a viral zoonotic disease, has emerged as a significant global threat in recent years. This review focuses on the importance of global monitoring and rapid response to monkeypox outbreaks. The unpredictable nature of monkeypox transmissions, its potential for human-to-human spread, and its high morbidity rate underscore the necessity for proactive surveillance systems. By analyzing the existing literature, including recent outbreaks, this review highlights the critical role of global surveillance in detecting, containing, and preventing the further spread of monkeypox. It also emphasizes the need for enhanced international collaboration, data sharing, and real-time information exchange to effectively respond to monkeypox outbreaks as a global health concern. Furthermore, this review discusses the challenges and opportunities of implementing robust surveillance strategies, including the use of advanced diagnostic tools and technologies. Ultimately, these findings underscore the urgency of establishing a comprehensive global monitoring framework for monkeypox, enabling early detection, prompt response, and effective control measures to protect public health worldwide. [ABSTRACT FROM AUTHOR]
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- 2023
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24. Human Pegivirus-1 Detection and Genotyping in Brazilian Patients with Fulminant Hepatitis.
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da Silva, Anielly Sarana, de Campos, Gabriel Montenegro, Villanova, Marcia Guimarães, Bezerra, Rafael dos Santos, Santiago, Luciana Maria Mendes, Haddad, Rodrigo, Covas, Dimas Tadeu, Giovanetti, Marta, Alcantara, Luiz Carlos Junior, Elias, Maria Carolina, Sampaio, Sandra Coccuzzo, Kashima, Simone, and Slavov, Svetoslav Nanev
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HEPATITIS ,COMMUNICABLE diseases ,METAGENOMICS ,GENOTYPES - Abstract
Fulminant hepatitis is a severe clinical disease characterized by a marked decline in liver function and encephalopathy. In a previous survey, using metagenomics in a group of 27 patients with this clinical condition, we observed an expressive quantity of reads of the Human pegivirus-1 (HPgV-1). Therefore, the objective of this study was to evaluate the frequency, molecular features, and HPgV-1 circulating genotypes in patients with fulminant hepatitis. After testing the collected plasma samples, we discovered twelve samples (44.4%) that were positive for HPgV-1 RNA (using both real-time and nested PCR). The positive samples presented a mean cycle threshold (Ct) of 28.5 (±7.3). Genotyping assignments revealed that all HPgV-1 positive samples belonged to the HPgV-1 genotype 2 (both subgenotypes 2A and 2B were identified). Although HPgV-1 is considered a commensal virus, little is known regarding its prevalence and genotypes in cases of fulminant hepatitis. More research is needed to understand whether HPgV-1 can be implicated in clinical disorders and infectious diseases. [ABSTRACT FROM AUTHOR]
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- 2023
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25. Joining Forces against Antibiotic Resistance: The One Health Solution.
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Cella, Eleonora, Giovanetti, Marta, Benedetti, Francesca, Scarpa, Fabio, Johnston, Catherine, Borsetti, Alessandra, Ceccarelli, Giancarlo, Azarian, Taj, Zella, Davide, and Ciccozzi, Massimo
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DRUG resistance in bacteria ,MEDICAL personnel ,LIVESTOCK growth ,ANTIBIOTIC overuse ,ANIMAL populations ,HUMAN-animal relationships ,BIOFILMS - Abstract
Antibiotic resistance is a significant global health concern that affects both human and animal populations. The One Health approach acknowledges the interconnectedness of human health, animal health, and the environment. It emphasizes the importance of collaboration and coordination across these sectors to tackle complex health challenges such as antibiotic resistance. In the context of One Health, antibiotic resistance refers to the ability of bacteria to withstand the efficacy of antibiotics, rendering them less effective or completely ineffective in treating infections. The emergence and spread of antibiotic-resistant bacteria pose a threat to human and animal health, as well as to the effectiveness of medical treatments and veterinary interventions. In particular, One Health recognizes that antibiotic use in human medicine, animal agriculture, and the environment are interconnected factors contributing to the development and spread of antibiotic resistance. For example, the misuse and overuse of antibiotics in human healthcare, including inappropriate prescribing and patient non-compliance, can contribute to the selection and spread of resistant bacteria. Similarly, the use of antibiotics in livestock production for growth promotion and disease prevention can contribute to the development of antibiotic resistance in animals and subsequent transmission to humans through the food chain. Addressing antibiotic resistance requires a collaborative One Health approach that involves multiple participants, including healthcare professionals, veterinarians, researchers, and policymakers. [ABSTRACT FROM AUTHOR]
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- 2023
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26. HIV-1–Host Interaction in Gut-Associated Lymphoid Tissue (GALT): Effects on Local Environment and Comorbidities.
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Moretti, Sonia, Schietroma, Ivan, Sberna, Giuseppe, Maggiorella, Maria Teresa, Sernicola, Leonardo, Farcomeni, Stefania, Giovanetti, Marta, Ciccozzi, Massimo, and Borsetti, Alessandra
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LYMPHOID tissue ,HIV infections ,INTESTINAL mucosa ,HIV-positive persons ,GUT microbiome - Abstract
HIV-1 replication in the gastrointestinal (GI) tract causes severe CD4+ T-cell depletion and disruption of the protective epithelial barrier in the intestinal mucosa, causing microbial translocation, the main driver of inflammation and immune activation, even in people living with HIV (PLWH) taking antiretroviral drug therapy. The higher levels of HIV DNA in the gut compared to the blood highlight the importance of the gut as a viral reservoir. CD4+ T-cell subsets in the gut differ in phenotypic characteristics and differentiation status from the ones in other tissues or in peripheral blood, and little is still known about the mechanisms by which the persistence of HIV is maintained at this anatomical site. This review aims to describe the interaction with key subsets of CD4+ T cells in the intestinal mucosa targeted by HIV-1 and the role of gut microbiome and its metabolites in HIV-associated systemic inflammation and immune activation that are crucial in the pathogenesis of HIV infection and related comorbidities. [ABSTRACT FROM AUTHOR]
- Published
- 2023
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27. Update on the Phylodynamic and Genetic Variability of Marburg Virus.
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Scarpa, Fabio, Bazzani, Liliana, Giovanetti, Marta, Ciccozzi, Alessandra, Benedetti, Francesca, Zella, Davide, Sanna, Daria, Casu, Marco, Borsetti, Alessandra, Cella, Eleonora, Pascarella, Stefano, Maruotti, Antonello, and Ciccozzi, Massimo
- Subjects
MARBURG virus ,GENETIC variation ,VIRAL variation ,COVID-19 pandemic ,WHOLE genome sequencing - Abstract
The COVID-19 pandemic has not only strained healthcare systems in Africa but has also intensified the impact of emerging and re-emerging diseases. Specifically in Equatorial Guinea, mirroring the situation in other African countries, unique zoonotic outbreaks have occurred during this challenging period. One notable resurgence is Marburg virus disease (MVD), which has further burdened the already fragile healthcare system. The re-emergence of the Marburg virus amid the COVID-19 pandemic is believed to stem from a probable zoonotic spill-over, although the precise transmission routes remain uncertain. Given the gravity of the situation, addressing the existing challenges is paramount. Though the genome sequences from the current outbreak were not available for this study, we analyzed all the available whole genome sequences of this re-emerging pathogen to advocate for a shift towards active surveillance. This is essential to ensure the successful containment of any potential Marburg virus outbreak in Equatorial Guinea and the wider African context. This study, which presents an update on the phylodynamics and the genetic variability of MARV, further confirmed the existence of at least two distinct patterns of viral spread. One pattern demonstrates a slower but continuous and recurring virus circulation, while the other exhibits a faster yet limited and episodic spread. These results highlight the critical need to strengthen genomic surveillance in the region to effectively curb the pathogen's dissemination. Moreover, the study emphasizes the importance of prompt alert management, comprehensive case investigation and analysis, contact tracing, and active case searching. These steps are vital to support the healthcare system's response to this emerging health crisis. By implementing these strategies, we can better arm ourselves against the challenges posed by the resurgence of the Marburg virus and other infectious diseases. [ABSTRACT FROM AUTHOR]
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- 2023
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28. Genomic Detection of the Emerging, Highly Pathogenic HIV-1 Subtype D in Bahia, Northeast Brazil.
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de Almeida Rego, Filipe Ferreira, de Moraes, Laise, Giovanetti, Marta, Silva, José Adriano Góes, Torres, Felipe Guimarães, de Oliveira Silva, Marcio, da Purificação Pereira da Silva, Maria, Van Weyenbergh, Johan, Santos, Luciane Amorim, and Khouri, Ricardo
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HIV ,VIRAL load ,HIV infection transmission ,INFECTIOUS disease transmission ,WATCHFUL waiting ,AVIAN influenza - Abstract
(1) Background: The HIV subtype D is generally associated with a faster decline in CD4
+ T cell counts, a higher viral load, and a faster progression to AIDS. However, it is still poorly characterized in Brazil. In this study, we used genomics and epidemiological data to investigate the transmission dynamics of HIV subtype D in the state of Bahia, Northeast Brazil. (2) Methods: To achieve this goal, we obtained four novel HIV-1 subtype D partial pol genome sequences using the Sanger method. To understand the emergence of this novel subtype in the state of Bahia, we used phylodynamic analysis on a dataset comprising 3704 pol genome sequences downloaded from the Los Alamos database. (3) Results: Our analysis revealed three branching patterns, indicating multiple introductions of the HIV-1 subtype D in Brazil from the late 1980s to the late 2000s and a single introduction event in the state of Bahia. Our data further suggest that these introductions most likely originated from European, Eastern African, Western African, and Southern African countries. (4) Conclusion: Understanding the distribution of HIV-1 viral strains and their temporal dynamics is crucial for monitoring the real-time evolution of circulating subtypes and recombinant forms, as well as for designing novel diagnostic and vaccination strategies. We advocate for a shift to active surveillance, to ensure adequate preparedness for future epidemics mediated by emerging viral strains. [ABSTRACT FROM AUTHOR]- Published
- 2023
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29. Early Detection of the Recombinant SARS-CoV-2 XAN Variant in Bulgaria: Initial Genomic Insights into Yet Another Piece of the Growing Puzzle of Recombinant Clades.
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Alexiev, Ivailo, Ivanov, Ivan, Giovanetti, Marta, Cella, Eleonora, Stoikov, Ivan, Donchev, Deyan, Grigorova, Lyubomira, Gancheva, Anna, Dimitrova, Reneta, Scarpa, Fabio, Korsun, Neli, Trifonova, Ivelina, Dobrinov, Veselin, Kantardjiev, Todor, Christova, Iva, and Ciccozzi, Massimo
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SARS-CoV-2 ,SARS-CoV-2 Omicron variant ,PUBLIC health - Abstract
The first recombinant SARS-CoV-2 variants were identified in 2022, causing public health concerns. The importance of recombinant variants has increased especially since the WHO designated the recombinant variant XBB and its lineages as subvariants that require monitoring on 20 November 2022. In this study, we provide the first insights into the new SARS-CoV-2 variant named XAN, a recombinant composed of Omicron sub-lineages BA.2 and BA.5. To our knowledge, this is the first report on the recombinant SARS-CoV-2 XAN variant identified in Bulgaria. [ABSTRACT FROM AUTHOR]
- Published
- 2023
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30. Unveiling the Impact of the Omicron Variant: Insights from Genomic Surveillance in Mato Grosso do Sul, Midwest Brazil.
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de Mello Almeida Maziero, Lívia, Giovanetti, Marta, Fonseca, Vagner, Zardin, Marina Castilhos Souza Umaki, de Castro Lichs, Gislene Garcia, de Rezende Romera, Grazielli Rocha, Tsuha, Daniel Henrique, Frias, Danila Fernanda Rodrigues, Escandolhero, Valdir Castanho, Demarchi, Luiz Henrique, Domingues Castilho, Larissa, Barbosa, Karine Ferreira, Tebet, Danielle Galindo Martins, Xavier, Joilson, Fritsch, Hegger, Lima, Mauricio, de Oliveira, Carla, Santos, Elaine Vieira, Kashima, Simone, and Said, Rodrigo Fabiano do Carmo
- Subjects
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SARS-CoV-2 Omicron variant , *COVID-19 pandemic , *SARS-CoV-2 , *SEQUENCE analysis , *INFORMATION sharing , *EXOMES - Abstract
Genomic surveillance has emerged as a crucial tool in monitoring and understanding the dynamics of viral variants during the COVID-19 pandemic. In the Midwest region of Brazil, Mato Grosso do Sul has faced a significant burden from the SARS-CoV-2 epidemic, with a total of 613,000 confirmed cases as of June 2023. In collaboration with the Central Public Health Laboratory in the capital city of Campo Grande, we conducted a portable whole-genome sequencing and phylodynamic analysis to investigate the circulation of the Omicron variant in the region. The study aimed to uncover the genomic landscape and provide valuable insights into the prevalence and transmission patterns of this highly transmissible variant. Our findings revealed an increase in the number of cases within the region during 2022, followed by a gradual decline as a result of the successful impact of the vaccination program together with the capacity of this unpredictable and very transmissible variant to quickly affect the proportion of susceptible population. Genomic data indicated multiple introduction events, suggesting that human mobility played a differential role in the variant's dispersion dynamics throughout the state. These findings emphasize the significance of implementing public health interventions to mitigate further spread and highlight the powerful role of genomic monitoring in promptly tracking and uncovering the circulation of viral strains. Together those results underscore the importance of proactive surveillance, rapid genomic sequencing, and data sharing to facilitate timely public health responses. [ABSTRACT FROM AUTHOR]
- Published
- 2023
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31. SARS-CoV-2 Recombinants: Genomic Comparison between XBF and Its Parental Lineages.
- Author
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Scarpa, Fabio, Locci, Chiara, Azzena, Ilenia, Casu, Marco, Fiori, Pier Luigi, Ciccozzi, Alessandra, Giovanetti, Marta, Quaranta, Miriana, Ceccarelli, Giancarlo, Pascarella, Stefano, Ciccozzi, Massimo, and Sanna, Daria
- Subjects
COVID-19 pandemic ,SARS-CoV-2 ,VIRAL genomes ,GENETIC variation ,RNA viruses - Abstract
Recombination events are very common and represent one of the primary drivers of RNA virus evolution. The XBF SARS-CoV-2 lineage is one of the most recently generated recombinants during the COVID-19 pandemic. It is a recombinant of BA.5.2.3 and BA.2.75.3, both descendants of lineages that caused many concerns (BA.5 and BA.2.75, respectively). Here, we performed a genomic survey focused on comparing the recombinant XBF with its parental lineages to provide a comprehensive assessment of the evolutionary potential, epidemiological trajectory, and potential risks. Genetic analyses indicated that although XBF initially showed the typical expansion depicted by a steep curve, causing several concerns, currently there is no indication of significant expansion potential or a contagion rate surpassing that of other currently active or previously prevalent lineages. BSP indicated that the peak has been reached around 19 October 2022 and then the genetic variability suffered slight oscillations until early 5 March 2023 when the population size reduced for the last time starting its last plateau that is still lasting. Structural analyses confirmed its reduced potential, also indicating that properties of NTDs and RBDs of XBF and its parental lineages present no significant difference. Of course, cautionary measures must still be taken and genome-based monitoring remains the best tool for detecting any important changes in viral genome composition. [ABSTRACT FROM AUTHOR]
- Published
- 2023
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32. Avian Influenza: Could the H5N1 Virus Be a Potential Next Threat?
- Author
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Imperia, Elena, Bazzani, Liliana, Scarpa, Fabio, Borsetti, Alessandra, Petrosillo, Nicola, Giovanetti, Marta, and Ciccozzi, Massimo
- Subjects
AVIAN influenza ,INFLUENZA A virus, H5N1 subtype ,AVIAN influenza A virus ,COVID-19 pandemic ,PLANT viruses ,INFLUENZA A virus ,INFLUENZA viruses - Abstract
Avian influenza virus (AIV) poses a significant challenge to poultry production, with negative repercussions for both the economy and public health worldwide. Since January 2003, a total of 868 human cases of AIV H5N1 have been reported from four countries in the Western Pacific Region, as of 9 March 2023. When AIVs are circulating in poultry, there is a risk of sporadic infections and small clusters of human cases due to exposure to infected poultry or contaminated environments. The increase in reported A(H5N1) infections may reflect continued virus circulation in birds, as well as enhanced surveillance and diagnostic capacity resulting from the response to the COVID-19 pandemic. Numerous countermeasures, including vaccines and antiviral treatments, are available for influenza infection. However, their effectiveness is often debated due to the ongoing resistance to antivirals and the relatively low and unpredictable efficiency of influenza vaccines compared to other vaccines. Vaccination remains the primary method for preventing influenza acquisition or avoiding serious complications related to the disease. In this review, we summarize the global landscape of the Influenza A virus and provide insights into human clinical symptomatology. We call for urgent investment in genomic surveillance strategies to timely detect and shape the emergence of any potential viral pathogen, which is essential for epidemic/pandemic preparedness. [ABSTRACT FROM AUTHOR]
- Published
- 2023
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33. Khosta: A Genetic and Structural Point of View of the Forgotten Virus.
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Scarpa, Fabio, Imperia, Elena, Ciccozzi, Alessandra, Pascarella, Stefano, Quaranta, Miriana, Giovanetti, Marta, Borsetti, Alessandra, Petrosillo, Nicola, and Ciccozzi, Massimo
- Subjects
SARS Epidemic, 2002-2003 ,HORSESHOE bats - Abstract
Bats are well-known to be natural reservoirs of various zoonotic coronaviruses, which have caused outbreaks of severe acute respiratory syndrome (SARS) and the COVID-19 pandemic in 2002 and 2019, respectively. In late 2020, two new Sarbecoviruses were found in Russia, isolated in Rhinolophus bats, i.e., Khosta-1 in R. ferrumequinum and Khosta-2 in R. hipposideros. The potential danger associated with these new species of Sarbecovirus is that Khosta-2 has been found to interact with the same entry receptor as SARS-CoV-2. Our multidisciplinary approach in this study demonstrates that Khosta-1 and -2 currently appear to be not dangerous with low risk of spillover, as confirmed by prevalence data and by phylogenomic reconstruction. In addition, the interaction between Khosta-1 and -2 with ACE2 appears weak, and furin cleavage sites are absent. While the possibility of a spillover event cannot be entirely excluded, it is currently highly unlikely. This research further emphasizes the importance of assessing the zoonotic potential of widely distributed batborne CoV in order to monitor changes in genomic composition of viruses and prevent spillover events (if any). [ABSTRACT FROM AUTHOR]
- Published
- 2023
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- View/download PDF
34. SARS-CoV CH.1.1 Variant: Genomic and Structural Insight.
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Bazzani, Liliana, Imperia, Elena, Scarpa, Fabio, Sanna, Daria, Casu, Marco, Borsetti, Alessandra, Pascarella, Stefano, Petrosillo, Nicola, Cella, Eleonora, Giovanetti, Marta, and Ciccozzi, Massimo
- Subjects
SARS virus ,SARS-CoV-2 ,SARS-CoV-2 Omicron variant ,WHOLE genome sequencing ,ELECTRIC potential - Abstract
In early February 2023, the Omicron subvariant XBB.1.5, also known as "Kraken", accounted for more than 44% of new COVID-19 cases worldwide, whereas a relatively new Omicron subvariant named CH.1.1, deemed "Orthrus", accounted for less than 6% of new COVID-19 cases during the subsequent weeks. This emerging variant carries a mutation, L452R, previously observed in the highly pathogenic Delta and the highly transmissible BA.4 and BA.5 variants, necessitating a shift to active surveillance to assure adequate preparedness for likely future epidemic peaks. We provide a preliminary understanding of the global distribution of this emerging SARS-CoV-2 variant by combining genomic data with structural molecular modeling. In addition, we shield light on the number of specific point mutations in this lineage that may have functional significance, thereby increasing the risk of disease severity, vaccine resistance, and increased transmission. This variant shared about 73% of the mutations with Omicron-like strains. Our homology modeling analysis revealed that CH.1.1 may have a weakened interaction with ACE2 and that its electrostatic potential surface appears to be more positive than that of the reference ancestral virus. Finally, our phylogenetic analysis revealed that this likely-emerging variant was already cryptically circulating in European countries prior to its first detection, highlighting the importance of having access to whole genome sequences for detecting and controlling emerging viral strains. [ABSTRACT FROM AUTHOR]
- Published
- 2023
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35. The Importance of Entomo-Virological Investigation of Yellow Fever Virus to Strengthen Surveillance in Brazil.
- Author
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Cruz, Ana Cecília Ribeiro, Hernández, Leonardo Henrique Almeida, Aragão, Carine Fortes, da Paz, Thito Yan Bezerra, da Silva, Sandro Patroca, da Silva, Fábio Silva, de Aquino, Ana Alice, Cereja, Glennda Juscely Galvão Pereira, Nascimento, Bruna Lais Sena do, Rosa Junior, José Wilson, Elias, Carmeci Natalina, Nogueira, Cristiano Gomes, Ramos, Daniel Garkauskas, Fonseca, Vagner, Giovanetti, Marta, Alcantara, Luiz Carlos Junior, Nunes, Bruno Tardelli Diniz, Vasconcelos, Pedro F. da Costa, Martins, Livia Carício, and Nunes-Neto, Joaquim Pinto
- Published
- 2023
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36. Phylogenetic Reconstructions Reveal the Circulation of a Novel Dengue Virus-1V Clade and the Persistence of a Dengue Virus-2 III Genotype in Northeast Brazil.
- Author
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Fritsch, Hegger, Moreno, Keldenn, Lima, Italo Andrade Barbosa, Santos, Cleiton Silva, Costa, Bernardo Gratival Gouvea, de Almeida, Breno Lima, dos Santos, Ronald Alves, Francisco, Marcos Vinicius Lima de Oliveira, Sampaio, Maria Paula Souza, de Lima, Maricelia Maia, Pereira, Felicidade Mota, Fonseca, Vagner, Tosta, Stephane, Xavier, Joilson, de Oliveira, Carla, Adelino, Talita, de Mello, Arabela Leal e Silva, Gräf, Tiago, Alcantara, Luiz Carlos Junior, and Giovanetti, Marta
- Subjects
DENGUE ,GENOTYPES ,NUCLEOTIDE sequencing ,MEMBRANE proteins ,PUBLIC health ,ARBOVIRUS diseases - Abstract
Dengue fever is among the most significant public health concerns in Brazil. To date, the highest number of Dengue notifications in the Americas has been reported in Brazil, with cases accounting for a total number of 3,418,796 reported cases as of mid-December 2022. Furthermore, the northeastern region of Brazil registered the second-highest incidence of Dengue fever in 2022. Due to the alarming epidemiological scenario, in this study, we used a combination of portable whole-genome sequencing, phylodynamic, and epidemiological analyses to reveal a novel DENV-1 genotype V clade and the persistence of DENV-2 genotype III in the region. We further report the presence of non-synonymous mutations associated with non-structural domains, especially the NS2A (non-structural protein 2A), as well as describe synonymous mutations in envelope and membrane proteins, distributed differently between clades. However, the absence of clinical data at the time of collection and notification, as well as the impossibility of monitoring patients in order to observe worsening or death, restricts our possibility of correlating mutational findings with possible clinical prognoses. Together, these results reinforce the crucial role of genomic surveillance to follow the evolution of circulating DENV strains and understand their spread across the region through inter-regional importation events, likely mediated by human mobility, and also the possible impacts on public health and outbreak management. [ABSTRACT FROM AUTHOR]
- Published
- 2023
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37. Genetic and Structural Data on the SARS-CoV-2 Omicron BQ.1 Variant Reveal Its Low Potential for Epidemiological Expansion
- Author
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Scarpa, Fabio, Sanna, Daria, Benvenuto, Domenico, Borsetti, Alessandra, Azzena, Ilenia, Casu, Marco, Fiori, Pier Luigi, Giovanetti, Marta, Maruotti, Antonello, Ceccarelli, Giancarlo, Caruso, Arnaldo, Caccuri, Francesca, Cauda, Roberto, Cassone, Antonio, Pascarella, Stefano, Ciccozzi, Massimo, Cauda, Roberto (ORCID:0000-0002-1498-4229), Scarpa, Fabio, Sanna, Daria, Benvenuto, Domenico, Borsetti, Alessandra, Azzena, Ilenia, Casu, Marco, Fiori, Pier Luigi, Giovanetti, Marta, Maruotti, Antonello, Ceccarelli, Giancarlo, Caruso, Arnaldo, Caccuri, Francesca, Cauda, Roberto, Cassone, Antonio, Pascarella, Stefano, Ciccozzi, Massimo, and Cauda, Roberto (ORCID:0000-0002-1498-4229)
- Abstract
The BQ.1 SARS-CoV-2 variant, also known as Cerberus, is one of the most recent Omicron descendant lineages. Compared to its direct progenitor BA.5, BQ.1 has some additional spike mutations in some key antigenic sites, which confer further immune escape ability over other circulating lineages. In such a context, here, we perform a genome-based survey aimed at obtaining a complete-as-possible nuance of this rapidly evolving Omicron subvariant. Genetic data suggest that BQ.1 represents an evolutionary blind background, lacking the rapid diversification that is typical of a dangerous lineage. Indeed, the evolutionary rate of BQ.1 is very similar to that of BA.5 (7.6 x 10(-4) and 7 x 10(-4) subs/site/year, respectively), which has been circulating for several months. The Bayesian Skyline Plot reconstruction indicates a low level of genetic variability, suggesting that the peak was reached around 3 September 2022. Concerning the affinity for ACE2, structure analyses (also performed by comparing the properties of BQ.1 and BA.5 RBD) indicate that the impact of the BQ.1 mutations may be modest. Likewise, immunoinformatic analyses showed moderate differences between the BQ.1 and BA5 potential B-cell epitopes. In conclusion, genetic and structural analyses on SARS-CoV-2 BQ.1 suggest no evidence of a particularly dangerous or high expansion capability. Genome-based monitoring must continue uninterrupted for a better understanding of its descendants and all other lineages.
- Published
- 2022
38. Molecular In-Depth on the Epidemiological Expansion of SARS-CoV-2 XBB.1.5.
- Author
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Scarpa, Fabio, Azzena, Ilenia, Locci, Chiara, Casu, Marco, Fiori, Pier Luigi, Ciccozzi, Alessandra, Angeletti, Silvia, Imperia, Elena, Giovanetti, Marta, Maruotti, Antonello, Borsetti, Alessandra, Cauda, Roberto, Cassone, Antonio, Via, Allegra, Pascarella, Stefano, Sanna, Daria, and Ciccozzi, Massimo
- Subjects
SARS-CoV-2 Omicron variant ,SARS-CoV-2 ,GENETIC variation ,MOLECULAR epidemiology - Abstract
Since the beginning of the pandemic, the generation of new variants periodically recurs. The XBB.1.5 SARS-CoV-2 variant is one of the most recent. This research was aimed at verifying the potential hazard of this new subvariant. To achieve this objective, we performed a genome-based integrative approach, integrating results from genetic variability/phylodynamics with structural and immunoinformatic analyses to obtain as comprehensive a viewpoint as possible. The Bayesian Skyline Plot (BSP) shows that the viral population size reached the plateau phase on 24 November 2022, and the number of lineages peaked at the same time. The evolutionary rate is relatively low, amounting to 6.9 × 10
−4 subs/sites/years. The NTD domain is identical for XBB.1 and XBB.1.5 whereas their RBDs only differ for the mutations at position 486, where the Phe (in the original Wuhan) is replaced by a Ser in XBB and XBB.1, and by a Pro in XBB.1.5. The variant XBB.1.5 seems to spread more slowly than sub-variants that have caused concerns in 2022. The multidisciplinary molecular in-depth analyses on XBB.1.5 performed here does not provide evidence for a particularly high risk of viral expansion. Results indicate that XBB.1.5 does not possess features to become a new, global, public health threat. As of now, in its current molecular make-up, XBB.1.5 does not represent the most dangerous variant. [ABSTRACT FROM AUTHOR]- Published
- 2023
- Full Text
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39. The D405N Mutation in the Spike Protein of SARS-CoV-2 Omicron BA.5 Inhibits Spike/Integrins Interaction and Viral Infection of Human Lung Microvascular Endothelial Cells.
- Author
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Bugatti, Antonella, Filippini, Federica, Messali, Serena, Giovanetti, Marta, Ravelli, Cosetta, Zani, Alberto, Ciccozzi, Massimo, Caruso, Arnaldo, and Caccuri, Francesca
- Subjects
SARS-CoV-2 Omicron variant ,VIRUS diseases ,LUNGS ,ENDOTHELIAL cells ,SARS-CoV-2 ,INTEGRINS - Abstract
Severe COVID-19 is characterized by angiogenic features, such as intussusceptive angiogenesis, endothelialitis, and activation of procoagulant pathways. This pathological state can be ascribed to a direct SARS-CoV-2 infection of human lung ECs. Recently, we showed the capability of SARS-CoV-2 to infect ACE2-negative primary human lung microvascular endothelial cells (HL-mECs). This occurred through the interaction of an Arg-Gly-Asp (RGD) motif, endowed on the Spike protein at position 403–405, with α
v β3 integrin expressed on HL-mECs. HL-mEC infection promoted the remodeling of cells toward a pro-inflammatory and pro-angiogenic phenotype. The RGD motif is distinctive of SARS-CoV-2 Spike proteins up to the Omicron BA.1 subvariant. Suddenly, a dominant D405N mutation was expressed on the Spike of the most recently emerged Omicron BA.2, BA.4, and BA.5 subvariants. Here we demonstrate that the D405N mutation inhibits Omicron BA.5 infection of HL-mECs and their dysfunction because of the lack of Spike/integrins interaction. The key role of ECs in SARS-CoV-2 pathogenesis has been definitively proven. Evidence of mutations retrieving the capability of SARS-CoV-2 to infect HL-mECs highlights a new scenario for patients infected with the newly emerged SARS-CoV-2 Omicron subvariants, suggesting that they may display less severe disease manifestations than those observed with previous variants. [ABSTRACT FROM AUTHOR]- Published
- 2023
- Full Text
- View/download PDF
40. Retrospective Insights of the COVID-19 Epidemic in the Major Latin American City, São Paulo, Southeastern Brazil.
- Author
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Assato, Patricia Akemi, Clemente, Luan Gaspar, Giovanetti, Marta, Ribeiro, Gabriela, Lima, Alex Ranieri Jeronimo, Palmieri, Melissa, de Moraes, Leonardo Nazario, Kashima, Simone, Fukumasu, Heidge, Nogueira, Maurício Lacerda, Alcantara, Luiz Carlos Junior, Nicolodelli, Aline Lais, Martins, Antonio Jorge, Petry, Bruna, Banho, Cecilia Artico, Dos Santos Barros, Claudia Renata, Moncau-Gadbem, Cristina Tschorny, Moretti, Debora Botequio, De La Roque, Debora Glenda Lima, and Marqueze, Elaine Cristina
- Subjects
COVID-19 pandemic ,SARS-CoV-2 Omicron variant ,INFECTIOUS disease transmission ,SARS-CoV-2 ,BUSINESS tourism ,COVID-19 - Abstract
São Paulo is the financial center of Brazil, with a population of over 12 million, that receives travelers from all over the world for business and tourism. It was the first city in Brazil to report a case of COVID-19 that rapidly spread across the city despite the implementation of the restriction measures. Despite many reports, much is still unknown regarding the genomic diversity and transmission dynamics of this virus in the city of São Paulo. Thus, in this study, we provide a retrospective overview of the COVID-19 epidemic in São Paulo City, Southeastern, Brazil, by generating a total of 9995 near-complete genome sequences from all the city's different macro-regions (North, West, Central, East, South, and Southeast). Our analysis revealed that multiple independent introduction events of different variants (mainly Gamma, Delta, and Omicron) occurred throughout time. Additionally, our estimates of viral movement within the different macro-regions further suggested that the East and the Southeast regions were the largest contributors to the Gamma and Delta viral exchanges to other regions. Meanwhile, the North region had a higher contribution to the dispersion of the Omicron variant. Together, our results reinforce the importance of increasing SARS-CoV-2 genomic monitoring within the city and the country to track the real-time evolution of the virus and to detect earlier any eventual emergency of new variants of concern that could undermine the fight against COVID-19 in Brazil and worldwide. [ABSTRACT FROM AUTHOR]
- Published
- 2023
- Full Text
- View/download PDF
41. SARS-CoV-2 Lineage P.4 Detection in Southeast Brazil: A Retrospective Genomic and Clinical Overview.
- Author
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Poleti, Mirele Daiana, Lesbon, Jéssika Cristina Chagas, de Mattos Oliveira, Elisângela Chicaroni, Patané, José Salvatore Leister, Clemente, Luan Gaspar, Viala, Vincent Louis, Ribeiro, Gabriela, Pinheiro, Jéssica Fernanda Perissato, Giovanetti, Marta, Alcantara, Luiz Carlos Junior, de Lima, Loyze Paola Oliveira, Martins, Antonio Jorge, dos Santos Barros, Claudia Renata, Marqueze, Elaine Cristina, de Souza Todão Bernardino, Jardelina, Moretti, Debora Botequio, Brassaloti, Ricardo Augusto, de Lello Rocha Campos Cassano, Raquel, Mariani, Pilar Drummond Sampaio Corrêa, and Slavov, Svetoslav Nanev
- Subjects
SARS-CoV-2 ,DNA sequencing ,PUBLIC health ,GENETIC mutation ,DISEASE prevalence - Abstract
São Paulo state has been the epicenter of the Coronavirus Disease 2019 (COVID-19) in Brazil, ranking first by state with over six million reported cases. In February 2021, the P.4 lineage was reported in 21 cities across the state by public health authorities due to the L452R mutation. Here, by analyzing 17,304 genome sequences of SARS-CoV-2 sampled between February and August of 2021 in 476 distinct cities in São Paulo, we assess the transmission dynamics of the P.4 lineage and other SARS-CoV-2 variants that were, at the time of the study, co-circulating in the state. Additionally, clinical parameters from the city of Araras, São Paulo (N = 251) were considered to estimate the potential risk and mortality rate associated with the P.4 lineage since its higher prevalence was observed in that city. Our data suggest a low frequency (0.55%) of the P.4 lineage across the state, with the gamma variant being the dominant form in all regions (90%) at that time. Furthermore, no evidence of increased transmissibility and disease severity related to the P.4 lineage was observed. The displacement through the time of different lineages in São Paulo highlights how challenging genomic surveillance appears to track the emergence of new SARS-CoV-2 lineages, which could better guide the implementation of control measures. [ABSTRACT FROM AUTHOR]
- Published
- 2022
- Full Text
- View/download PDF
42. SARS-CoV-2 Variants in COVID-19 Disease: A Focus on Disease Severity and Vaccine Immunity in Patients Admitted to the Emergency Department.
- Author
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Fogolari, Marta, Francesconi, Maria, De Florio, Lucia, Giovanetti, Marta, Veralli, Roberta, De Flora, Cecilia, Maruotti, Antonello, Scarpa, Fabio, Spoto, Silvia, Sambuco, Federica, Riva, Elisabetta, Ciccozzi, Massimo, and Angeletti, Silvia
- Subjects
COVID-19 ,SARS-CoV-2 ,HOSPITAL emergency services ,VACCINATION ,PREVENTIVE medicine - Abstract
Tracking SARS-CoV-2 variants along with vaccinations are fundamental for severe COVID-19 disease prevention. A study was performed that focused on 43 patients with the SARS-CoV-2 infection who were admitted to the Emergency Department. RT-PCR–positive nasopharyngeal samples were sequenced using the MiSeq II system for variant detection. The main reason for Emergency Department admission was COVID-19 (67%), followed by other causes (33%); 51% patients were unvaccinated or vaccinated with a single dose and 49% had completed the vaccination course with two or three doses. Among the vaccinated group, 38% were admitted for COVID-19, versus 94.5% of the unvaccinated group. After admission, 50% of the vaccinated group and 36% of the unvaccinated group were discharged and allowed to go home, and 80% of the unvaccinated had no major comorbidities; 63% needed hospital admission and 5% required a stay in the Intensive Care Unit. Of these, 37% were vaccinated with 3 doses, 11% with two doses, 4% with a single dose, and 48% were unvaccinated. The 70% of the vaccinated patients who were admitted to hospital presented major comorbidities versus 38% of the unvaccinated group. Two unvaccinated patients that needed intensive care had relevant comorbidities and died. Genome sequencing showed the circulation of three omicron and two pure sub-lineages of omicron, including 22 BA.1, 12 BA.1.1, and 7 BA.2. Data showed the SARS-CoV-2 national and international migration patterns and how vaccination was useful for severe COVID-19 disease prevention. [ABSTRACT FROM AUTHOR]
- Published
- 2022
- Full Text
- View/download PDF
43. Genomic Epidemiology Reveals the Circulation of the Chikungunya Virus East/Central/South African Lineage in Tocantins State, North Brazil.
- Author
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Souza, Ueric José Borges de, Santos, Raíssa Nunes dos, Giovanetti, Marta, Alcantara, Luiz Carlos Junior, Galvão, Jucimária Dantas, Cardoso, Franciano Dias Pereira, Brito, Feliph Cássio Sobrinho, Franco, Ana Cláudia, Roehe, Paulo Michel, Ribeiro, Bergmann Morais, Spilki, Fernando Rosado, and Campos, Fabrício Souza
- Subjects
CHIKUNGUNYA virus ,PLANT viruses ,VIRAL genomes ,CYTOSKELETAL proteins ,VIRAL transmission ,EPIDEMIOLOGY ,VIRAL mutation - Abstract
The chikungunya virus (CHIKV) is a mosquito-borne virus of the family Togaviridae transmitted to humans by Aedes spp. mosquitoes. In Brazil, imported cases have been reported since June 2014 through two independent introductions, one caused by Asian Lineage in Oiapoque, Amapá state, North Region, and another caused by East/Central/South African (ECSA) in Feira de Santana, Bahia state, Northeast Region. Moreover, there is still limited information about the genomic epidemiology of the CHIKV from surveillance studies. The Tocantins state, located in Northern Brazil, reported an increase in the number of CHIKV cases at the end of 2021 and the beginning of 2022. Thus, to better understand the dispersion dynamics of this viral pathogen in the state, we generated 27 near-complete CHIKV genome sequences from four cities, obtained from clinical samples. Our results showed that the newly CHIKV genomes from Tocantins belonged to the ECSA lineage. Phylogenetic reconstruction revealed that Tocantins' strains formed a single well-supported clade, which appear to be closely related to isolates from the Rio Grande do Norte state (Northeast Brazil) and the Rio de Janeiro state (Southeast Brazil), that experienced an explosive ECSA epidemic between 2016–2019. Mutation analyses showed eleven frequent non-synonymous mutations in the structural and non-structural proteins, indicating the autochthonous transmission of the CHIKV in the state. None of the genomes recovered within the Tocantins samples carry the A226V mutation in the E1 protein associated with increased transmission in A. albopictus. The study presented here highlights the importance of continued genomic surveillance to provide information not only on recording mutations along the viral genome but as a molecular surveillance tool to trace virus spread within the country, to predict events of likely occurrence of new infections, and, as such, contribute to an improved public health service. [ABSTRACT FROM AUTHOR]
- Published
- 2022
- Full Text
- View/download PDF
44. Viral Metagenomics for the Identification of Emerging Infections in Clinical Samples with Inconclusive Dengue, Zika, and Chikungunya Viral Amplification.
- Author
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Souza, Juliana Vanessa Cavalcante, Santos, Hazerral de Oliveira, Leite, Anderson Brandão, Giovanetti, Marta, Bezerra, Rafael dos Santos, Carvalho, Eneas de, Bernardino, Jardelina de Souza Todão, Viala, Vincent Louis, Haddad, Rodrigo, Ciccozzi, Massimo, Alcantara, Luiz Carlos Junior, Sampaio, Sandra Coccuzzo, Covas, Dimas Tadeu, Kashima, Simone, Elias, Maria Carolina, and Slavov, Svetoslav Nanev
- Subjects
EMERGING infectious diseases ,METAGENOMICS ,CHIKUNGUNYA ,ARBOVIRUS diseases ,DENGUE ,NUCLEOTIDE sequencing ,ARBOVIRUSES - Abstract
Viral metagenomics is increasingly being used for the identification of emerging and re-emerging viral pathogens in clinical samples with unknown etiology. The objective of this study was to shield light on the metavirome composition in clinical samples obtained from patients with clinical history compatible with an arboviral infection, but that presented inconclusive results when tested using RT-qPCR. The inconclusive amplification results might be an indication of the presence of an emerging arboviral agent that is inefficiently amplified by conventional PCR techniques. A total of eight serum samples with inconclusive amplification results for the routinely tested arboviruses—dengue (DENV), Zika (ZIKV), and Chikungunya (CHIKV) obtained during DENV and CHIKV outbreaks registered in the state of Alagoas, Northeast Brazil between July and August 2021—were submitted to metagenomic next-generation sequencing assay using NextSeq 2000 and bioinformatic pipeline for viral discovery. The performed bioinformatic analysis revealed the presence of two arboviruses: DENV type 2 (DENV-2) and CHIKV with a high genome coverage. Further, the metavirome of those samples revealed the presence of multiple commensal viruses apparently without clinical significance. The phylogenetic analysis demonstrated that the DENV-2 genome belonged to the Asian/American genotype and clustered with other Brazilian strains. The identified CHIKV genome was taxonomically assigned as ECSA genotype, which is circulating in Brazil. Together, our results reinforce the utility of metagenomics as a valuable tool for viral identification in samples with inconclusive arboviral amplification. Viral metagenomics is one of the most potent methods for the identification of emerging arboviruses. [ABSTRACT FROM AUTHOR]
- Published
- 2022
- Full Text
- View/download PDF
45. Gut Microbiota and COVID-19: Potential Implications for Disease Severity.
- Author
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Rocchi, Giulia, Giovanetti, Marta, Benedetti, Francesca, Borsetti, Alessandra, Ceccarelli, Giancarlo, Zella, Davide, Altomare, Annamaria, Ciccozzi, Massimo, and Guarino, Michele Pier Luca
- Abstract
The SARS-CoV-2 pandemic resulted in an unprecedented global crisis. SARS-CoV-2 primarily causes lung infection trough the binding of the virus with the ACE-2 cell receptor located on the surface of the alveolar epithelial cells. Notably, ACE-2 cell receptors are also expressed in the epithelial cells of the intestinal tract (GI). Recent data showed that the microbial communities of the GI might act as local and systematic inflammatory modulators. Gastrointestinal symptoms, including diarrhea, are frequently observed in infected individuals, and recent released data indicate that SARS-CoV-2 may also spread by fecal–oral transmission. Moreover, the gut microbiota's ecosystem can regulate and be regulated by invading pathogens, including viruses, facilitating an effective immune response, which in turn results in less severe diseases. In this regard, increased SARS-CoV-2 mortality and morbidities appear to be frequently observed in elderly immunocompromised patients and in people with essential health problems, such as diabetes, who, indeed, tend to have a less diverse gut microbiota (dysbiosis). Therefore, it is important to understand how the interaction between the gut microbiota and SARS-CoV-2 might shape the intensity of the infection and different clinical outcomes. Here, we provide insights into the current knowledge of dysbiosis during SARS-CoV-2 infection and methods that may be used to re-establish a more correct microbiota composition. [ABSTRACT FROM AUTHOR]
- Published
- 2022
- Full Text
- View/download PDF
46. Genomic Epidemiology Unveil the Omicron Transmission Dynamics in Rome, Italy.
- Author
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Francesconi, Maria, Giovanetti, Marta, De Florio, Lucia, Fogolari, Marta, Veralli, Roberta, De Flora, Cecilia, Spoto, Silvia, Maruotti, Antonello, Riva, Elisabetta, Angeletti, Silvia, and Ciccozzi, Massimo
- Abstract
Since 2020, the COVID-19 pandemic represented an important worldwide burden. Well-structured surveillance by reliable and timely genomic data collection is crucial. In this study, a genomic monitoring analysis of all SARS-CoV-2 positive samples retrieved at the Fondazione Policlinico Universitario Campus Bio-Medico, in Rome, Italy, between December 2021 and June 2022, was performed. Two hundred and seventy-four SARS-CoV-2-positive samples were submitted to viral genomic sequencing by Illumina MiSeqII. Consensus sequences were generated by de novo assembling using the iVar tool and deposited on the GISAID database. Lineage assignment was performed using the Pangolin lineage classification. Sequences were aligned using ViralMSA and maximum-likelihood phylogenetic analysis was performed by IQ-TREE2. TreeTime tool was used to obtain dated trees. Our genomic monitoring revealed that starting from December 2021, all Omicron sub-lineages (BA.1, BA.2, BA.3, BA.4, and BA.5) were circulating, although BA.1 was still the one with the highest prevalence thought time in this early period. Phylogeny revealed that Omicron isolates were scattered throughout the trees, suggesting multiple independent viral introductions following national and international human mobility. This data represents a sort of thermometer of what happened from July 2021 to June 2022 in Italy. Genomic monitoring of the circulating variants should be encouraged considering that SARS-CoV-2 variants or sub-variants emerged stochastically and unexpectedly. [ABSTRACT FROM AUTHOR]
- Published
- 2022
- Full Text
- View/download PDF
47. The Biological Properties of the SARS-CoV-2 Cameroon Variant Spike: An Intermediate between the Alpha and Delta Variants.
- Author
-
Pascarella, Stefano, Bianchi, Martina, Giovanetti, Marta, Benvenuto, Domenico, Borsetti, Alessandra, Cauda, Roberto, Cassone, Antonio, and Ciccozzi, Massimo
- Subjects
SARS-CoV-2 Delta variant ,SARS-CoV-2 ,CELL receptors ,SARS-CoV-2 Omicron variant ,SURFACE potential - Abstract
An analysis of the structural effect of the mutations of the B.1.640.2 (IHU) Spike Receptor Binding Domain (RBD) and N-terminal Domain (NTD) is reported along with a comparison with the sister lineage B.1.640.1. and a selection of variants of concern. The effect of the mutations on the RBD–ACE2 interaction was also assessed. The structural analysis applied computational methods that are able to carry out in silico mutagenesis to calculate energy minimization and the folding energy variation consequent to residue mutations. Tools for electrostatic calculation were applied to quantify and display the protein surface electrostatic potential. Interactions at the RBD–ACE2 interface were scrutinized using computational tools that identify the interactions and predict the contribution of each interface residue to the stability of the complex. The comparison among the RBDs shows that the most evident differences between the variants is in the distribution of the surface electrostatic potential: that of B.1.640.1 is as that of the Alpha RBD, while B.1.640.2 appears to have an intermediate surface potential pattern with characteristics between those of the Alpha and Delta variants. Moreover, the B.1.640.2 Spike includes the mutation E484K that in other variants has been suggested to be involved in immune evasion. These properties may hint at the possibility that B.1.640.2 emerged with a potentially increased infectivity with respect to the sister B.1.640.1 variant, but significantly lower than that of the Delta and Omicron variants. However, the analysis of their NTD domains highlights deletions, destabilizing mutations and charge alterations that can limit the ability of the B.1.640.1 and B.1.640.2 variants to interact with cellular components, such as cell surface receptors. [ABSTRACT FROM AUTHOR]
- Published
- 2022
- Full Text
- View/download PDF
48. Molecular Identification and Ecology of Portuguese Wild-Caught Phlebotomine Sandfly Specimens.
- Author
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Zé-Zé, Líbia, Amaro, Fátima, Costa Osório, Hugo, Giovanetti, Marta, Lourenço, José, and Alves, Maria João
- Subjects
PHLEBOTOMUS fever ,MOSQUITOES ,GENETIC variation ,SPATIAL distribution (Quantum optics) ,SPECIES diversity - Abstract
Phlebotomine sandflies are important vectors of Leishmania spp. and phleboviruses causing disease in animals and humans. Morphological identification of phlebotomine sandflies to the species level is challenging, requiring microscopical examination of the genitalia, which is demanding and time consuming. Molecular sandfly species identification can be a practical solution to save resources since it enables further molecular studies capable of generating data, such as biting preferences by blood meal analysis. In this study, resorting to a sandfly dataset collected between 2014 and 2018 across Portuguese territory under active mosquito surveillance and sandfly specific surveys, we used molecular methods to explore the genetic diversity and spatial distribution, further exploring ecological co-variants of four sandfly species-Phlebotomus ariasi, P. perniciosus, P. sergenti, and Sergentomyia minuta-all of which are of public health importance. Sandflies were collected from Spring to Autumn (May-November) following local temperature patterns. P. perniciosus was the most widespread detected species, with a nationwide distribution. All studied species clustered together with known samples from the Iberian Peninsula. Further monitoring studies of sandfly species diversity, distribution, and seasonality are essential for surveillance and control of sandfly-borne pathogens both nationally and globally. [ABSTRACT FROM AUTHOR]
- Published
- 2022
- Full Text
- View/download PDF
49. Correction: Lesbon et al. Nucleocapsid (N) Gene Mutations of SARS-CoV-2 Can Affect Real-Time RT-PCR Diagnostic and Impact False-Negative Results. Viruses 2021, 13 , 2474.
- Author
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Lesbon, Jéssika Cristina Chagas, Poleti, Mirele Daiana, de Mattos Oliveira, Elisângela Chicaroni, Patané, José Salvatore Leister, Clemente, Luan Gaspar, Viala, Vincent Louis, Ribeiro, Gabriela, Giovanetti, Marta, de Alcantara, Luiz Carlos Junior, Teixeira, Olivia, Nonato, Maria Cristina, de Lima, Loyze Paola Oliveira, Martins, Antonio Jorge, dos Santos Barros, Claudia Renata, Marqueze, Elaine Cristina, de Souza Todão Bernardino, Jardelina, Moretti, Debora Botequio, Brassaloti, Ricardo Augusto, de Lello Rocha Campos Cassano, Raquel, and Mariani, Pilar Drummond Sampaio Correa
- Subjects
SARS-CoV-2 ,REVERSE transcriptase polymerase chain reaction ,PROTEIN crystallography ,PROTEIN structure ,GENETIC mutation - Abstract
Nucleocapsid (N) Gene Mutations of SARS-CoV-2 Can Affect Real-Time RT-PCR Diagnostic and Impact False-Negative Results. The authors hereby request the inclusion of two authors (Olivia Teixeira and Maria Cristina Nonato) in the recently published article in I Viruses i entitled "Nucleocapsid (N) gene mutations of SARS-CoV-2 can affect real-time RT-PCR diagnostic and impact false-negative results" [[1]]. Insert New Author Contributions Statement The contributions of Olivia Teixeira and Maria Cristina Nonato were not included in the original publication. [Extracted from the article]
- Published
- 2022
- Full Text
- View/download PDF
50. Role of Q675H Mutation in Improving SARS-CoV-2 Spike Interaction with the Furin Binding Pocket.
- Author
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Bertelli, Anna, D'Ursi, Pasqualina, Campisi, Giovanni, Messali, Serena, Milanesi, Maria, Giovanetti, Marta, Ciccozzi, Massimo, Caccuri, Francesca, and Caruso, Arnaldo
- Subjects
SARS-CoV-2 ,GENETIC mutation ,VIRAL proteins - Abstract
Genotype screening was implemented in Italy and showed a significant prevalence of new SARS-CoV-2 mutants carrying Q675H mutation, near the furin cleavage site of spike protein. Currently, this mutation, which is expressed on different SARS-CoV-2 lineages circulating worldwide, has not been thoughtfully investigated. Therefore, we performed phylogenetic and biocomputational analysis to better understand SARS-CoV-2 Q675H mutants' evolutionary relationships with other circulating lineages and Q675H function in its molecular context. Our studies reveal that Q675H spike mutation is the result of parallel evolution because it arose independently in separate evolutionary clades. In silico data show that the Q675H mutation gives rise to a hydrogen-bonds network in the spike polar region. This results in an optimized directionality of arginine residues involved in interaction of spike with the furin binding pocket, thus improving proteolytic exposure of the viral protein. Furin was predicted to have a greater affinity for Q675H than Q675 substrate conformations. As a consequence, Q675H mutation could confer a fitness advantage to SARS-CoV-2 by promoting a more efficient viral entry. Interestingly, here we have shown that Q675H spike mutation is documented in all the VOCs. This finding highlights that VOCs are still evolving to enhance viral fitness and to adapt to the human host. At the same time, it may suggest Q675H spike mutation involvement in SARS-CoV-2 evolution. [ABSTRACT FROM AUTHOR]
- Published
- 2021
- Full Text
- View/download PDF
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