Search

Mother-to-child transmission (MTCT) of human immunodeficiency virus type 1 (HIV-1) as described for women with an established infection is, in most cases, associated with the transmission of few maternal variants. This study analysed virus variability in four cases of maternal primary infection occurring during pregnancy and/or breastfeeding. Estimated time of seroconversion was at 4 months of pregnancy for one woman (early seroconversion) and during the last months of pregnancy and/or breastfeeding for the remaining three (late seroconversion). The C2V3 envelope region was analysed in samples of mother–child pairs by molecular cloning and sequencing. Comparisons of nucleotide and amino acid sequences as well as phylogenetic analysis were performed. The results showed low variability in the virus population of both mother and child. Maximum-likelihood analysis showed that, in the early pregnancy seroconversion case, a minor viral variant with further evolution in the child was transmitted, which could indicate a selection event in MTCT or a stochastic event, whereas in the late seroconversion cases, the mother's and child's sequences were intermingled, which is compatible with the transmission of multiple viral variants from the mother's major population. These results could be explained by the less pronounced selective pressure exerted by the immune system in the early stages of the mother's infection, which could play a role in MTCT of HIV-1.

HIV-1 infection in children less than 15 years of age is mainly due to mother-to-child transmission. The aim of this work was to investigate molecular evidence to prove father-to-be horizontal transmission in two possible events of transmission. In the first event a boy was identified as HIV infected at 2-3 years of age. At the same time infection was confirmed in the father, while mother and siblings were negative. In the second event a girl was negative for HIV at age 1 and identified as HIV-1 infected at age 6. The father's HIV infection was diagnosed in the same period while the mother was repeatedly negative. No evidence of sexual assault or transfusion was recorded in any case. Peripheral blood mononuclear cells were obtained from both fathers and children. After PCR amplification, the C2V3 region of the envelope gene and the region coding for amino acid 132 of p24 up to amino acid 40 of p7 of the gag gene were sequenced. Genetic distance measurements and phylogenetic tree analysis showed that in both cases the father's and child's viral sequences were closely related. They were distinct when compared to Argentina sequences including sequences from the same geographic region. Epidemiological and molecular data strongly suggest that horizontal transmission had occurred, probably related to the close father-to-child contact.

The presence of recombinant intersubtypes of HIV-1 in Argentina has been reported since the mid-1990s. In this study sequences of a region of the gag pol and vpu genes of HIV-1 were analyzed in samples of 21 injection drug users (IDUs) residing in the suburbs of the city of Buenos Aires. Genomic characterization and identification of recombination sites were made comparing the 3 regions with reference isolation sequences of subtypes B F C A and B/F recombinants: CRF12_BF and non-CRF12_BF sequences. Subtype assignment of the analyzed segments was phylogenetically confirmed. All the samples turned out to be BF recombinants in at least 1 of the 3 studied genes. Twelve samples (57%) had the same pattern as the Argentinean CRF12_BF whereas in the rest the pattern differed in at least 1 of the 3 genes. The relation of these fragments to the CRF12_BF was phylogenetically verified. These results indicate the predominance of BF recombinants and the presence of a high percentage of sequences closely related to the CRF12_BF in the IDU population in Argentina and suggest a possible association between viral variants and the transmission route. (excerpt)

This study determined the risk behaviors and viral subtypes of HIV-1 found in 134 heterosexual HIV-seroprevalent maternity patients, 41 of their sexual partners (men who have sex with women [MSW]), and 95 homosexual men (men who have sex with men [MSM]) from Buenos Aires, Argentina. Peripheral blood mononuclear cells (PBMCs) were purified from blood and used for DNA extraction, amplification, and genotyping by the envelope heteroduplex mobility assay (env HMA). Most of the women had been infected by having sex with an already infected partner (84%), whereas most of the male partners had been infected via drug use (76%). Both the patients and their sexual partners were poorly educated, only 30% having completed secondary school. The MSM study subjects, however, were significantly better educated and had a lower prevalence of injecting drug use.Env HMA subtype F was found in 77% (103 of 134) of the maternity patients, with similar rates in their partners (73%). Most of the remaining samples were env subtype B. All but one of the couples was concordant in subtype. In the MSM risk group, however, only 10% were env HMA subtype F. Ninety percent of the MSM samples were subtype B. There are at least two independent epidemics of HIV-1 infection in Buenos Aires, Argentina. One, in heterosexual men and women, is dominated by env subtype F whereas the other, in homosexual men, is dominated by env subtype B, as determined by env HMA.

Continuous cultivation of murine L cells infected with lymphocytic choriomeningitis virus strain Armstrong leads to production of L(Arm) cells, which produce a predominantly cell-associated attenuated variant, the L(Arm) virus. The relatively few infectious particles that are released have lost the ability to form plaques on L cells and to cause illness in mice even if inoculated intracerebrally. Based on equal protein M(r)s, antigenicity and protein kinase activity, essentially identical results were obtained for the purified Armstrong and L(Arm) viruses. There was also no difference in production and release of particles with the potential to cause homologous interference. Such particles consisted of two types, one of which was highly susceptible to u.v.-irradiation, the other was highly resistant. In the case of the L(Arm) virus interfering particles, it appears that the u.v.-irradiation-susceptible forms represented infectious virus. Purified L(Arm) virus particles contained considerable quantities of subgenomic forms of (small) S- and (large) L-RNA and their complementary counterparts, which all appeared to be replicated autonomously in an unenriched manner.

Background Genetic characterization of HIV-1 in Argentina has shown that BF recombinants predominate among heterosexuals and injecting drug users, while in men who have sex with men the most prevalent form is subtype B. Objectives The aim of this work was to investigate the presence of HIV dual infections in HIV-infected individuals with high probability of reinfection Study design Blood samples were collected from 23 HIV positive patients with the risk of reinfection from Buenos Aires. A fragment of the HIV gene pol was amplified and phylogenetic analyses were performed. Antiretroviral drug resistance patterns of all the sequences were analyzed. Results Five dual infections were detected with four patients coinfected with subtype B and BF recombinants and one patient was coinfected with two BF recombinants presenting different recombination patterns. Prolonged infection with a stable clinical condition was observed in the five individuals. Resistance mutation patterns were different between the predominant and the minority strains. Conclusions Our results show that HIV dual infection can occur with closely related subtypes, and even with different variants of the same recombinant form in certain populations. Clinical observations showed neither aggressive disease progression nor impact on the resistance patterns in the dually-infected patients.

To analyze humoral cross-reactivity to V3 peptides from subtype B and BF recombinant forms, plasma samples from 50 HIV-1-infected patients were characterized by sequencing fragments of the env and pol genes. An in-house EIA was performed using peptides corresponding to the 15 central amino acids of the V3 loop of gp120 from subtypes B (MN, SF2) and F1 and a consensus peptide from Argentinean BF recombinants. No differences were found with respect to the infecting subtype, but significant differences were found among the peptides. Reactivity was higher against the MN and BF peptides in both groups infected with subtype B (n = 28) and BF (n = 22) recombinants than against subtype F1 and SF2 peptides. Fil: Ambrosioni, J.. Universidad de Buenos Aires. Facultad de Medicina. Departamento de Microbiología. Centro Nacional de Referencia para el Sida; Argentina Fil: Andreani, Guadalupe. Universidad de Buenos Aires. Facultad de Medicina. Departamento de Microbiología. Centro Nacional de Referencia para el Sida; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Acuipil, Carolina Vanesa. Universidad de Buenos Aires. Facultad de Medicina. Departamento de Microbiología. Centro Nacional de Referencia para el Sida; Argentina Fil: Barral, R.. Universidad de Buenos Aires. Facultad de Medicina. Departamento de Microbiología. Centro Nacional de Referencia para el Sida; Argentina Fil: Rabinovich, Roberto Daniel. Universidad de Buenos Aires. Facultad de Medicina. Departamento de Microbiología. Centro Nacional de Referencia para el Sida; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Martinez Peralta, Liliana A.. Universidad de Buenos Aires. Facultad de Medicina. Departamento de Microbiología. Centro Nacional de Referencia para el Sida; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina

Conclusion These results correlate with previous studies conducted among IDUs from New York city, Vietnam and Southern Europe where HTLV-IIb was more frequently found. In contrast, IIa is found among IDUs from other regions of the USA, Europe and Brazil. This is the first time in which subtype b is described in Argentina among IDUs. Its presence may be due to migrations of aborigines to big cities and the introduction of drugs in this population. Lately, there was also a high rate of migration and tourism to Argentina, especially from southern Europe and USA, possibly contributing to the spread of HTLV-IIb in our country. Interestingly, the IIa sample described here was found to be related with Brazilian aborigine sequences in contrast to the previous Argentinian IDU which was closer to African isolates. from 2006 International Meeting of The Institute of Human Virology Baltimore, USA. 17–21 November, 2006

Injection drug use is the main mechanism of human immunodeficiency virus (HIV) transmission in Argentina (40% of reported AIDS cases in Argentina). This study was conducted among street-recruited injection drug users (IDUs) from Buenos Aires, with the aim of estimating seroprevalence and coinfection of HIV, hepatitis B virus (HBV), hepatitis C virus (HCV), and human T-lymphotropic viruses (HTLVs). A total of 174 volunteers participated in this study; 137 were men (78.7% of volunteers). The average age of the participants was 30 years. Only 64 of participants (37%) had no viral infection, whereas 110 (63%) were infected with > or =1 viruses. Seroprevalences were 44.3% for HIV, 54.6% for HCV, 42.5% for HBV, 2.3% for HTLV-I, and 14.5% for HTLV-II. Among the 77 HIV-infected persons, only 6.5% (5 persons) were not coinfected with other viruses; 88.3% (68) were coinfected with HCV and 68.8% (53) were coinfected with HBV. We demonstrated the existence of multiple viral infections with a high rate of prevalence in IDUs in Buenos Aires, Argentina.

To investigate GB virus C (GBV-C)/hepatitis G virus (HGV) mother-to-infant transmission when only 5′ noncoding region (NCR) sequences were available, a retrospective study was carried out. Although the 5′ NCR is widely used for GBV-C/HGV detection due to the high degree of sequence conservation among isolates (8), this fact clearly limits its potential use to trace chains of transmission, despite the presence of scattered subregions with higher heterogeneity. Nevertheless, since the 5′ NCR has been reported to be unmodified after 8.4 years of evolution (5), a mother-to-infant chain was expected to show (almost) identical sequences unless specific 5′ NCR variants were involved in selective transmission. Analyzed sequences were obtained from (i) a study group which encompassed plasma samples simultaneously obtained from 34 human immunodeficiency virus (HIV)-infected mothers (13 intravenous-drug users [IVDU] and 21 nonaddict women putatively infected by a heterosexual route [IHSR]) as well as from their respective infants (1 to 7 months old, without history of blood transfusion) born to either HIV-positive and GBV-C/HGV-infected mothers (n = 8) or to HIV-positive but GBV-C/HGV nonviremic mothers (n = 26) and (ii) a control group which comprised 31 5′ NCR sequences derived from contemporary isolates circulating in the city of Buenos Aires and 6 others from the rest of the world. Several precautions (3) as well as appropriate controls were included to minimize the possibility that sequence identity among samples was the mere result of PCR contamination: (i) samples from mothers and infants were analyzed separately (elapsed time, 2 months); (ii) each positive result was confirmed in duplicate; and (iii) one negative control (SDW) was included for every three samples. To estimate the potential influence of Taq-dependent misincorporated nucleotides during PCR amplification (4), three cDNAs from local isolates of GBV-C/HGV whose sequences (325 bp) had been previously established (6) were amplified in duplicate and bidirectionally sequenced. A total of 4 of 13 IVDU and 4 of 21 IHSR mothers (30.8 and 19.0%, respectively; P not significant) proved positive for GBV-C/HGV RNA ascribed to genogroup 2a (n = 4), 2b (n = 2), or 3 (n = 2). Only three of eight infants born from viremic mothers (and none from 26 nonviremic mothers) exhibited GBV-C/HGV RNA (37.5%; one born to an IVDU and two to IHSR GBV-C/HGV-positive mothers); their genogroups, as established by both restriction fragment length polymorphism and cDNA sequencing (8), were the same as those of their respective mothers. The phylogenetic analysis was based on both genetic distance (neighbor joining) (Fig. ​(Fig.1)1) and maximum parsimony (data available upon request) methodologies. Both procedures showed unambiguously a genetic relatedness (i.e., no mutation between them) in each GBV-C/HGV mother-infant pair. In contrast to such a lack of nucleotide differences among the three mother-infant pairs, a mean ± standard deviation of 11.56 ± 6.17 nucleotide (nt) replacements was found among unrelated chosen sequences (n = 155 pairs of sequences analyzed). These control sequences corresponded to simultaneously circulating strains in the city of Buenos Aires which were ascribed to the same genogroups putatively associated with transmission chains in this study (i.e., genogroups 2a [n = 17 isolates] and 3 [n = 9]). None of these 26 sequences were identical. When nucleotide replacements were analyzed separately among all included (sub)group 2a (n = 119) and group 3 (n = 36) pairs of sequences, means ± standard deviations of 10.13 ± 3.16 and 16.77 ± 9.77 changes, respectively, were recorded (P < 0.00001; Student t test [two-sided test]). However, one pair of epidemiologically unrelated sequences (Arg15/Arg25) exhibited only one nucleotide difference (a 1-nt gap), seemingly appearing genetically related by the neighbor-joining analysis (Fig. ​(Fig.1).1). When maximum parsimony was carried out, only the three pairs of mother-infant 5′ NCR sequences remained undoubtedly related, since the lengths of their respective tree segments (in units of expected nucleotide substitutions per site) were equal to 0 and those between the above-mentioned sequences exhibiting a 1-nt gap were equal to 0.1073. Such a discrepancy between the two phylogenetic methodologies might be attributable to the reported (7) known loss of information with neighbor joining compared with maximum parsimony (distance versus discrete methods, respectively). FIG. 1. Phylogenetic analysis of GBV-C/HGV sequences (nt positions 132 to 337) from mother A (MA) and infant A (IA), MB and IB, and MC and IC compared with those obtained from simultaneously circulating strains in Argentina (ARG) and the rest of the world (W). ... The use of one mutation as a cutoff to discriminate related versus unrelated 5′ NCR sequences has the inherent risk of being Taq dependent. However, sequencing of the three control cDNAs (2,150 nt) rendered uniformly conserved (and repeatedly obtained) results. Thus, considering one mutation as the best cutoff value to discriminate between the related and unrelated 5′ NCR sequences analyzed in this study, the Youden's Index (sensitivity + specificity − 1) was equal to 1, the maximum possible value (1). In agreement with this view, the probability that three pairs of 5′ NCR sequences were identical (between members of pairs) due to random events is less than 1/17,576 (1/26 × 1/26 × 1/26), or 0.000056895, since none of the 26 simultaneously circulating local isolates ascribed to the same genomic group or subgroup implicated in putative chains of transmission were identical. Such mathematical support is coincident with the epidemiological data, since the studied babies lacked any risk factor for GBV-C/HGV infection except the corresponding mother's ongoing infection. As a whole, results obtained provided strong support to suggest the occurrence of GBV-C/HGV mother-to-infant transmission. The 5′ NCR was recently studied in transmission chains among hemodialyzed patients (2). To our knowledge, this is the first report to use both mathematical and phylogeneticanalyses to examine the eventual use of 5′ NCR sequences—when they are the only available data—to evaluate putative transmission chains.

The Tacaribe complex of Arenaviridae is comprised of a group of 10 serologically cross-related viruses that are transmitted by rodents living in different geographic locations of the Western hemisphere from Florida to Argentina. So far, members of the Tacaribe group, also referred to as the New World arenaviruses, include Junin (the agent of Argentine hemorrhagic fever), Machupo (the agent of Bolivian hemorrhagic fever), Guanarito (the agent of Venezuelan hemorrhagic fever), and Pichinde, Tacaribe, Tamiami, Latino, Amapari, Flexal, and Parana viruses, none of which are currently known to be naturally infectious or pathogenic for humans (Howard, 1986).

Address: 1National Reference Centre for AIDS, Microbiology Department, School of Medicine, University of Buenos Aires, Buenos Aires, Argentina, 2Laboratory of Parasitology, Microbiology Department, School of Medicine, University of Buenos Aires, Buenos Aires, Argentina and 3Endocrinology Service, Clinic Biochemistry Department, Jose de San Martin Hospital, School of Pharmacy and Biochemistry, University of Buenos Aires, Buenos Aires, Argentina * Corresponding author

Analysis of radioactively labelled and highly purified infectious lymphocytic choriomeningitis (LCM) virus by polyacrylamide gel electrophoresis (PAGE) revealed 12 components which, according to their apparent molecular weight and glycosylation status, were designated as p19, p25, p26, gp35, p38, gp44, gp60, p63, p77, gp85, gp130, and p200. As shown by immunoprecipitation, they all bound to rabbit anti-LCM virus antibodies. Three proteins, namely gp35 (= 'GP-2'), gp44 (= 'GP-1') and p63 (= 'NP'), had previously been described by others as major constituents of the virion. Our results confirm this and suggest that gp60, p77, gp85, and p200 are further distinct structural proteins. In contrast, p25 and p38 appear to be cleavage or degradation products of p63; p19 and p26 seem to belong to gp60, which could be the monomeric form of a dimer, gp130. Peptide mapping by limited proteolysis revealed considerable overlapping of amino acid sequences among the major glycoproteins with one peptide being common to all. From the results of PAGE performed after external labelling of intact virions, we conclude that gp44, gp60, and gp85 (but not gp35) form the surface of the virus envelope. Analytical isoelectric focusing under non-reducing conditions has shown that the major glycoproteins appeared to consist of several components with different isoelectric points.

Summary Lymphocytic choriomeningitis (LCM) virus interfering particles were enriched relative to infectious virions by ultracentrifugation in a shallow gradient made of Urografin. Electrophoretic analysis revealed that they lacked the small (‘S’) 23S RNA as well as GP-1 and GP-2 of the infectious virion and also lacked a newly characterized glycoprotein of apparent mol. wt. 85 × 103; instead, they contained a novel glycoprotein with mol. wt. 65 × 103.

In this article we describe two lethal cases of MTCT of HIV and T.cruzi in the province of Buenos Aires, Argentina. Child 1 was admitted to the hospital being 1 month old with respiratory difficulty and diarrhoea. Being six months old he was released but being 22 months old he presented sepsis and died. The mother was not treated during pregnancy, while the child was treated with combined HAART and benznidazol. Child 2 was admitted to a provincial Hospital being 20 days old, and referred to the Children´s Hospital. After 39 days at the ICU the child died with sepsis. His mother received ZDV late in her pregnancy. The child received was treated with HAART, interrupted at 3 months due to severe organic failure. The lack of diagnosis of T. cruzi in both mothers worsened the prognosis of these two children, since treatment with antiparasitic drugs is used since birth. Fil: Agosti, Maria Rosa. Hospital de Niños Sor María Ludovica, la Plata; Argentina Fil: Ercoli, Pablo. Universidad de Buenos Aires. Facultad de Medicina. Departamento de Microbiología. Centro Nacional de Referencia para el Sida; Argentina Fil: Dolcini, Guillermina Laura. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Medicina. Departamento de Microbiología. Centro Nacional de Referencia para el Sida; Argentina Fil: Andreani, Guadalupe. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Medicina. Departamento de Microbiología. Centro Nacional de Referencia para el Sida; Argentina Fil: Martinez Peralta, Liliana A.. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Medicina. Departamento de Microbiología; Argentina Fil: Gonzalez Ayala, Silvia Elena. Hospital de Niños Sor María Ludovica, la Plata; Argentina

Background HIV triggers the decline of CD4+ T cells and leads to progressive dysfunction of cell-mediated immunity. Although an increased susceptibility to cell death occurs during the acute phase of HIV infection, persistently-infected macrophages and quiescent T-cells seem to be resistant to cell death, representing a potential reservoir for virus production. Results Lymphoid (H9/HTLVIIIB and J1.1) and pro-monocytic (U1) HIV-1 persistently-infected cell lines were treated with hydrogen peroxide (H2O2) and staurosporine (STS) for 24 h, and susceptibility to apoptosis was evaluated and compared with uninfected counterparts (H9, Jurkat and U937 respectively). When exposed to different pro-apoptotic stimuli, all persistently-infected cell lines showed a dramatic reduction in the frequency of apoptotic cells in comparison with uninfected cells. This effect was independent of the magnitude of viral replication, since the induction of viral production in lymphoid or pro-monocytic cells by exposure to TNF-α or PMA did not significantly change their susceptibility to H2O2- or STS-induced cell death. A mechanistic analysis revealed significant diferences in mitochondrial membrane potential (MMP) and caspase-3 activation between uninfected and persistently-infected cells. In addition, Western blot assays showed a dramatic reduction of the levels of pro-apototic Bax in mitochondria of persistently-infected cells treated with H2O2 or STS, but not in uninfected cells. Conclusion This study represents the first evidence showing that resistance to apoptosis in persistently-infected lymphoid and monocytic cells is independent of active viral production and involves modulation of the mitochondrial pathway. Understanding this effect is critical to specifically target the persistence of viral reservoirs, and provide insights for future therapeutic strategies in order to promote complete viral eradication.

Background Several factors determine the risk of HIV mother-to-child transmission (MTCT), such as coinfections in placentas from HIV-1 positive mothers with other pathogens. Chagas' disease is one of the most endemic zoonoses in Latin America, caused by the protozoan Trypanosoma cruzi. The purpose of the study was to determine whether T. cruzi modifies HIV infection of the placenta at the tissue or cellular level. Results Simple and double infections were carried out on a placental histoculture system (chorionic villi isolated from term placentas from HIV and Chagas negative mothers) and on the choriocarcinoma BeWo cell line. Trypomastigotes of T. cruzi (VD lethal strain), either purified from mouse blood or from Vero cell cultures, 24 h-supernatants of blood and cellular trypomastigotes, and the VSV-G pseudotyped HIV-1 reporter virus were used for the coinfections. Viral transduction was evaluated by quantification of luciferase activity. Coinfection with whole trypomastigotes, either from mouse blood or from cell cultures, decreased viral pseudotype luciferase activity in placental histocultures. Similar results were obtained from BeWo cells. Supernatants of stimulated histocultures were used for the simultaneous determination of 29 cytokines and chemokines with the Luminex technology. In histocultures infected with trypomastigotes, as well as in coinfected tissues, IL-6, IL-8, IP-10 and MCP-1 production was significantly lower than in controls or HIV-1 transducted tissue. A similar decrease was observed in histocultures treated with 24 h-supernatants of blood trypomastigotes, but not in coinfected tissues. Conclusion Our results demonstrated that the presence of an intracellular pathogen, such as T. cruzi, is able to impair HIV-1 transduction in an in vitro system of human placental histoculture. Direct effects of the parasite on cellular structures as well as on cellular/viral proteins essential for HIV-1 replication might influence viral transduction in this model. Nonetheless, additional mechanisms including modulation of cytokines/chemokines at placental level could not be excluded in the inhibition observed. Further experiments need to be conducted in order to elucidate the mechanism(s) involved in this phenomenon. Therefore, coinfection with T. cruzi may have a deleterious effect on HIV-1 transduction and thus could play an important role in viral outcome at the placental level.