INVESTIGADORES
LAUFER Natalia Lorna
congresos y reuniones científicas
Título:
Evidence of HIV impact on HBV genotypic dominance in coinfected patients
Autor/es:
FRANCO MORETTI; NATALIA LAUFER; LUCILA CASSINO; MARÍA BELÉN BOUZAS; SILVINA FERNÁNDEZ GIULIANO; HÉCTOR PÉREZ; PEDRO CAHN; HORACIO SALOMÓN; JORGE QUARLERI
Lugar:
Sydney, Australia
Reunión:
Conferencia; 4th IAS Conference on HIV Pathogenesis, Treatment and Prevention; 2007
Institución organizadora:
IAS
Resumen:
Objectives: Coinfection with hepatitis B virus (HBV) and HIV is one of the leading causes of morbidity and mortality in PLWHA. Different HBV genotypes have distinct geographical distribution associated with severity of liver disease. The present study aims to investigate the epidemiology of HBV genotypes among Argentinean patients coinfected with HIV-1. In Argentina the HBV-F genotype is predominant among HIV-1 non-infected patients.Coinfection with hepatitis B virus (HBV) and HIV is one of the leading causes of morbidity and mortality in PLWHA. Different HBV genotypes have distinct geographical distribution associated with severity of liver disease. The present study aims to investigate the epidemiology of HBV genotypes among Argentinean patients coinfected with HIV-1. In Argentina the HBV-F genotype is predominant among HIV-1 non-infected patients. Methods: A cross-sectional analysis examined HBV-related characteristics in a cohort of 246 HIV-1 patients who exhibited HBsAg and/or anti-HBc serological reactivity. HBV DNA detection and genotyping were carried out by PCR and by phylogenetic analyses of the surface (S) partial gene, respectively. Molecular cloning was performed in samples with unclear phylogenetic clustering. Recombinant analysis at the S gene was carried out by bootscanning.A cross-sectional analysis examined HBV-related characteristics in a cohort of 246 HIV-1 patients who exhibited HBsAg and/or anti-HBc serological reactivity. HBV DNA detection and genotyping were carried out by PCR and by phylogenetic analyses of the surface (S) partial gene, respectively. Molecular cloning was performed in samples with unclear phylogenetic clustering. Recombinant analysis at the S gene was carried out by bootscanning. Results: HBV DNA was found in 24 out of 246 patients (9.8%); 4 of them with occult infection. The HBV genotype distribution was A: 83.3% (20/24); D: 8.3% (2/24); F: 4.2% (1/24). One sample exhibited an heterogeneous viral population involving genotypes A and D and also 3 intergenotypic recombinants forms with different mosaic S-gene patterns at first; in a subsequent sample 18 months after, the HBV population was homogeneous and exclusively ascribed to genotype A. HBV occult infection was only related to genotype A. Genotype distribution was unrelated to a particular risk transmission group.HBV DNA was found in 24 out of 246 patients (9.8%); 4 of them with occult infection. The HBV genotype distribution was A: 83.3% (20/24); D: 8.3% (2/24); F: 4.2% (1/24). One sample exhibited an heterogeneous viral population involving genotypes A and D and also 3 intergenotypic recombinants forms with different mosaic S-gene patterns at first; in a subsequent sample 18 months after, the HBV population was homogeneous and exclusively ascribed to genotype A. HBV occult infection was only related to genotype A. Genotype distribution was unrelated to a particular risk transmission group. Conclusions: We report data of HIV impact on HBV genotypic dominance in coinfected patients showing a switch toward a wide prevalence of HBV-A. Preliminary, this genotype appears to prevail against genotypes D and F when HIV is also present by unidentified reasons. Previously unknown HBV A-D intergenotypic recombinant strains with 3 different motifs were characterized by first time in South America. The modification of the HBV genotype pattern in HIV-coinfected patients may require new therapeutic strategies, and further survey studies.We report data of HIV impact on HBV genotypic dominance in coinfected patients showing a switch toward a wide prevalence of HBV-A. Preliminary, this genotype appears to prevail against genotypes D and F when HIV is also present by unidentified reasons. Previously unknown HBV A-D intergenotypic recombinant strains with 3 different motifs were characterized by first time in South America. The modification of the HBV genotype pattern in HIV-coinfected patients may require new therapeutic strategies, and further survey studies.