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The heat transfer from the low latitudes to high latitudes is responsible for maintaining the earth's climate dynamics. Thus, deciphering the possible mechanism driving the variability of the Indian summer monsoon (ISM) during the Holocene Epoch has been critical to understand the hydroclimatic changes of the low latitudes. Despite several efforts, the teleconnection of ISM with the global climate dynamics remains under-represented and poorly understood. The present study aims to delineate the ISM variability and its possible forcing mechanism from western India (Gujarat). In this study, a sediment core (~65 cm long) was raised from the Jaffrabad mudflat (MIT) in western Gujarat. The sediment samples were subjected to geochemical analysis to investigate paleomonsoon, paleo-sediment source and paleoweathering changes. The results show that, with the addition of intermediate sources, the sediments were principally derived from the hinterland's Deccan basalts. Further, the study suggested a warm and wet climate due to strong ISM during 10,650−5500 cal yr BP associated with the solar as well as orbital forcings. The weak monsoon during 5500−2700 cal yr BP has been linked with southward migration of the Intertropical Convergence Zone (ITCZ) along with the increased El Niño-like conditions. Further, the wavelet analysis revealed that a combined influence of solar, orbital and North Atlantic forcings led to monsoon variability along western India, during the Holocene Epoch. By reconciling the geochemical proxies, the present study has implications in the reconstruction of paleomonsoon and establishing the possible teleconnection with the global climate system. [ABSTRACT FROM AUTHOR]

Continuous injection-based islanding detection of Inverter-Interfaced Distributed Generator (IIDG) has been a general trend. The major issues in previous islanding detection methods are large Non-Detection Zone (NDZ), poor Power Quality (PQ), high implementation cost, and lack of real-time validation. Further, the threshold in most methods is not generic and depends on the system’s rating. Hence, this paper proposes a local voltage and current measurement-based islanding detection method for IIDGs. It utilizes parameters estimated from the fundamental phasors of voltage and current at the Point of Common Coupling (PCC) of IIDG using Space Vector Rotation (SVR) and a controlled self-decaying current injection. The proposed disturbance is injected only after disturbance detection by SVR parameters to mitigate the impact on PQ. Disturbance identification is easy due to the combined PCC voltage and current effects on parameter estimation. Real-Time Digital Simulator (RTDS) and Controller Hardware In the Loop (CHIL) setup-based results from the proposed method have been obtained and compared with previous methods. These results indicate the proposed method’s real-time efficacy (low islanding detection time) with no NDZ and negligible impact on PQ for different islanding events. Also, the proposed method is independent of the microgrid’s rating and reliable for non-islanding events. [ABSTRACT FROM AUTHOR]

Background: In India, multi-drug resistance in Salmonella enterica serovar Typhimurium poses a significant health threat. Indeed, S. Typhimurium has remained unknown for a large portion of its genome associated with various physiological functions including mechanism of drug resistance and virulence. The whole-genome sequence of a Salmonella strain obtained from feces of a patient with gastroenteritis in Odisha, India, was analyzed for understanding the disease association and underlying virulence mechanisms. Results: The de novo assembly yielded 17 contigs and showed 99.9% similarity to S. enterica sub sp enterica strain LT2 and S. enteric subsp salamae strain DSM 9220. S. Typhimurium ms202 strain constitutes six known Salmonella pathogenicity islands and nine different phages. The comparative interpretation of pathogenic islands displayed the genes contained in SPI-1 and SPI-2 to be highly conserved. We identified sit ABCD cluster regulatory cascade in SPI-1. Multiple antimicrobial resistance genes were identified that directly implies antibiotic-resistant phenotype. Notably, seven unique genes were identified as "acquired antibiotic resistance". These data suggest that virulence in S. enterica Typhimurium ms202 is associated with SPI-1 and SPI-2. Further, we found several virulent genes encoding SPI regions belonging to type III secretion systems (T3SS) of bacteria were significantly upregulated in ms202 compared to control LT2. Moreover, all these genes were significantly downregulated in S. enterica Typhimurium ms202 as compared to control LT2 on adding Mn2+ exogenously. Conclusions: Our study raises a vital concern about the potential diffusion of a novel multi-drug resistant S. enterica Typhimurium ms202. It justifies this clinical pathogen to demonstrate a higher degree survival due to higher expression of virulent genes and enhanced ability of metallic ion acquisition. [ABSTRACT FROM AUTHOR]

Pseudomonas aeruginosa, an ESKAPE pathogen causes many fatal clinical diseases in humans across the globe. Despite an increase in clinical instances of Pseudomonas infection, there is currently no effective vaccine or treatment available. The major membrane protein candidate of the P. aeruginosa bacterial cell is known to be a critical component for cellular bacterial susceptibility to antimicrobial peptides and survival inside the host organisms. Therefore, the current computational study aims to examine P. aeruginosa's major membrane protein, OprF, and OprI, in order to design linear B-cell, cytotoxic T-cell, and helper T-cell peptide-based vaccine constructs. Utilizing various immune-informatics tools and databases, a total of two B-cells and twelve T-cells peptides were predicted. The final vaccine design was simulated to generate a high-quality three-dimensional structure, which included epitopes, adjuvant, and linkers. The vaccine was shown to be nonallergenic, antigenic, soluble, and had the best biophysical properties. The vaccine and Toll-like receptor 4 have a strong and stable interaction, according to protein-protein docking and molecular dynamics simulations. Additionally, in silico cloning was employed to see how the developed vaccine expressed in the pET28a (+) vector. Ultimately, an immune simulation was performed to see the vaccine efficacy. In conclusion, the newly developed vaccine appears to be a promising option for a vaccine against P. aeruginosa infection. [ABSTRACT FROM AUTHOR]

Acute/chronic gastroenteritis is caused by a few serovars of Salmonella enterica. Among different serovars, S. enterica Typhimurium is a potent pathogen that contributes significantly to self-limiting diarrhea related mortality worldwide. With no successful vaccine in hand against this pathogen, antibiotics are used as for gold standard for treatment against Salmonella induced gastroenteritis. Indispensably, rise in multi drug resistance against Salmonella Typhimurium poses challenge to treatment options. South East Asia, with 11 different countries, stands 3rd as super region for global burden of Salmonella induced gastroenteritis. In this review, we made an attempt to discuss on prevalence and multidrug resistance in Salmonella Typhimurium in 11 countries of South East Asia—the issue that has not been seriously addressed so far. By thorough analysis of reported data, we found varying frequencies for prevalence of Salmonella Typhimurium as well as subtle evidences on resistance of this pathogen to multiple antibiotics in different countries. Vietnam ranked top in terms of reports for prevalence and antimicrobial resistance. However, in countries such as Brunei and Timor Leste, no study has been performed so far to track the frequency of incidence and drug resistance of this pathogen. Our review, the first of its kind, emphasizes that, although the pathogen was not found as dominant serovar in South East Asia in last 20 years unlike sub-Saharan Africa, it may be still considered as a major threat in this region due to available evidences for infection in humans as well as contamination in several animal and food sources. More importantly, the importance as a public threat in this subregion of Asia is also due to resistance of this pathogen to multiple antibiotics. South East Asian countries showing incidence and multi drug resistance of Salmonella enterica Typhimurium in human and non-human sources (1969–2020). —Drug resistant S. enterica Typhimurium. [ABSTRACT FROM AUTHOR]

System inertia plays a vital role in controlling the angular stability of the system during a disturbance. Due to increased penetration of power electronic interfaced sources, such as Solar Photovoltaic (SPV) source, the overall system inertia reduces and varies depending on their operating conditions. In this paper, an approach for online inertia estimation in the power system network with SPV sources is proposed, using the synchronized measurements from Phasor Measurement Units (PMUs). An equivalent swing equation is used to emulate the network dynamics. A relationship between the inertia constant and the roots of this equation is determined. In order to numerically obtain the roots, the Estimation of Signal Parameter via Rotational Invariance Techniques (ESPRIT) method is first used to find the modes present in the frequency signal. A new formulation is proposed to extract an equivalent mode from all the obtained modes. Also, to avoid phase step error, Rate Of Change Of Frequency (ROCOF) is estimated from the equivalent mode of the frequency signal. Results obtained for the 39 bus New England system for various test cases, using Real-Time Digital Simulator (RTDS), prove the efficacy and superiority of the proposed approach over the existing approaches in the literature. [ABSTRACT FROM AUTHOR]

Synchronous reference frame (SRF) control strategy for solar photovoltaic (SPV) sources is widely used to deliver maximum power to the grid. However, poor inertia support just after a disturbance and improper phase angle tracking in presence of the harmonics and system unbalance are noticed when the conventional phase‐locked loop (PLL) based SRF control structure is used. In this study, an inertia enhancement method for inverter interfaced SPV sources is proposed, which adjusts only the PLL parameters with a notch filter (NF) in the SRF controller. NF in PLL is used due to its disturbance rejection potential and accurate phase angle tracking, even during system unbalance. The dynamic equation of pseudo induced voltage (PIV) vector with respect to the point of common coupling is derived. The kinematic equation of the PIV angle vector correlates inertia contribution and inverter terminal voltage. The impact of the change in PLL parameters on inertia enhancement is analyzed by validating the proposed technique on a test system in the real‐time digital simulator. The frequency response by the proposed method has been compared with two state‐of‐art methods to prove the superiority of the proposed approach in enhancing the inertia of the SPV source in a microgrid. [ABSTRACT FROM AUTHOR]

Introduction: Bloodstream infections (BSIs) are associated with a high mortality rate of 20%-50%. Blood culture is paramount to identify causative agents of BSIs to choose an appropriate antimicrobial therapy. Objectives: The present study was undertaken to analyze the various microorganisms causing BSIs and study their antimicrobial resistance patterns in a tertiary care hospital, Eastern India. Materials and Methods: A total of 239 blood specimens from clinically suspected cases of BSIs were studied for 6 months from July 2015 to December 2015. Blood specimens were incubated in BacT/ALERT ® 3D system (bioMerieux, Durham, NC, USA) a fully automated blood culture system for detection of aerobic growth. Identification and antimicrobial susceptibility testing were conducted on VITEK ® 2 (bioMerieux, Durham, NC, USA) as per Clinical Laboratory Standards Institute guidelines. Results: Out of 239 specimens, 41 (17.2%) yielded growth of different microorganisms. From these isolates, 20 (48.8%) were Gram-negative bacilli, 18 (43.9%) were Gram-positive cocci and rest 3 (7.3%) were yeasts. Among Gram-negative bacilli, Klebsiella pneumoniae sub spp. pneumoniae (70%) was most commonly isolated. Coagulase-negative staphylococci (88.9%) were the most common isolate among Gram-positive cocci. All three Candida spp. isolated were nonalbicans Candida (two Candida tropicalis and one Candida krusei). Gram-negative isolates were least resistant to tigecycline and colistin. All Gram-positive cocci were sensitive to linezolid. Conclusion: Monitoring of data regarding the prevalence of microorganisms and its resistance patterns would help in currently prescribing antimicrobial regimens and improving the infection control practices by formulating policies for empirical antimicrobial therapy. [ABSTRACT FROM AUTHOR]

Introduction: Methicillin resistant Staphylococcus aureus has emerged as an important pathogen in nosocomial and community acquired infections. Accurate and rapid identification of MRSA in clinical specimens is essential for timely decision of effective antimicrobial chemotherapy. Aim: The present study was conducted to compare efficacy of four conventional phenotypic methods, with mec- A based polymerase chain reaction (PCR) for MRSA identification. materials and methods: Methicillin resistance was determined in 200 S.aureus isolates by oxacillin disc diffusion, cefoxitin disc diffusion, Oxacillin Resistance Screening Agar and E-test. The results were compared with mec-A based PCR. Results: Among 200 S.aureus isolates 62 (31%) were positive for mec-A gene by PCR. Cefoxitin disc diffusion, Oxacillin Resistance Screening Agar and E-test showed 100% specificity. Oxacillin disc diffusion had lowest sensitivity (82.5%) and specificity (98.5%) among all. The conventional methods take more time than PCR for diagnosing MRSA. Linezolid, Vancomycin & Dalfopristin were the highly sensitive drugs against MRSA isolates. Conclusion: Cefoxitin disc diffusion, is rapid, simple and cheaper, hence can be used routinely as an alternative to PCR for detection of MRSA in resource constraint laboratories. [ABSTRACT FROM AUTHOR]