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Antibodies to the Novel Human Pegivirus 2 Are Associated with Active and Resolved Infections.
Coller, Kelly E; Berg, Michael G; Frankel, Matthew; Forberg, Kenn; Surani, Rita; Chiu, Charles Y; Hackett, John; Dawson, George J.
Afiliación
  • Coller KE; Abbott Laboratories, Abbott Park, Illinois, USA kelly.coller@abbott.com.
  • Berg MG; Abbott Laboratories, Abbott Park, Illinois, USA.
  • Frankel M; Abbott Laboratories, Abbott Park, Illinois, USA.
  • Forberg K; Abbott Laboratories, Abbott Park, Illinois, USA.
  • Surani R; Abbott Laboratories, Abbott Park, Illinois, USA.
  • Chiu CY; Department of Laboratory Medicine, University of California, San Francisco, California, USA UCSF-Abbott Viral Diagnostics and Discovery Center, San Francisco, California, USA Department of Medicine, Division of Infectious Diseases, University of California, San Francisco, California, USA.
  • Hackett J; Abbott Laboratories, Abbott Park, Illinois, USA.
  • Dawson GJ; Abbott Laboratories, Abbott Park, Illinois, USA.
J Clin Microbiol ; 54(8): 2023-30, 2016 08.
Article en En | MEDLINE | ID: mdl-27225404
A novel blood-borne human pegivirus (HPgV), HPgV-2, was recently identified in hepatitis C virus (HCV)-infected individuals and individuals who had received multiple transfusions. Robust serological assays capable of detecting antibodies in HPgV-2-infected individuals are needed to establish global seroprevalence rates and potential disease associations. The two objectives of this study were to determine the utility of mammalian cell-expressed HPgV-2 E2 glycoprotein or bacterium-expressed nonstructural protein 4AB (NS4AB) in detecting past or present infections and to compare the total prevalence (antibody and RNA positive) of HPgV-2 with that of the other human pegivirus, HPgV-1 (GB virus C [GBV-C]). HPgV-2 E2 antibodies were detected in 13 (92.86%) of 14 HPgV-2-viremic cases, and NS4AB antibodies were detected in 8 (57.14%) of 14 cases. The HPgV-2 seroprevalence was significantly higher (P < 0.0001) among HCV-infected individuals (3.31% [24 of 726 samples]) than among non-HCV-infected individuals (0.30% [4 of 1,348 samples]). Of 31 anti-E2-positive samples, 22 had supplemental supporting data; 12 samples were HPgV-2 RNA positive and 10 nonviremic samples were antibody positive for peptides or NS4AB. The total prevalence of HPgV-1 (35.00%) was significantly higher than that of HPgV-2 (1.33%) in all populations tested (P < 0.0001). For HPgV-1, codetection of antibodies to E2 and RNA was infrequent (5.88%). In contrast, antibodies to E2 were detected in most HPgV-2-viremic individuals (92.86%), as is observed among individuals chronically infected with HCV, most of whom are antibody positive for HCV E2. Our studies indicate that HPgV-2 circulates with HCV and displays a profile similar to the serological profile of HCV-infected persons, although the pathogenicity of this virus has yet to be established.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Infecciones por Flaviviridae / Flaviviridae / Anticuerpos Antivirales Tipo de estudio: Risk_factors_studies Límite: Humans Idioma: En Revista: J Clin Microbiol Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Infecciones por Flaviviridae / Flaviviridae / Anticuerpos Antivirales Tipo de estudio: Risk_factors_studies Límite: Humans Idioma: En Revista: J Clin Microbiol Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos
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