The Impact of Human Pegivirus on CD4 Cell Count in HIV-Positive Persons in Botswana

Author:

N’Guessan Kombo F1,Anderson Motswedi23,Phinius Bonolo2,Moyo Sikhulile24,Malick Alyyah25,Mbangiwa Tshepiso26,Choga Wonderful T2,Makhema Joseph24,Marlink Richard24,Essex Max24,Musonda Rosemary24,Gaseitsiwe Simani24,Blackard Jason T1

Affiliation:

1. University of Cincinnati College of Medicine, Cincinnati, Ohio

2. Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana

3. Department of Biological Sciences, Gaborone, Botswana

4. Department of Immunology and Infectious Diseases, Harvard T. H. Chan School of Public Health, Boston, Massachusetts

5. Harvard College, Cambridge, Massachusetts

6. School of Allied Health Professions, University of Botswana, Gaborone, Botswana

Abstract

Abstract Background Human pegiviruses (HPgV)—formerly known as hepatitis G virus or GB virus C (GBV-C)—are common single-stranded RNA viruses that may have a beneficial impact on slowing HIV disease progression. The data on HPgV in resource-limited regions such as Sub-Saharan Africa are scarce. Thus, we conducted the first study of HPgV in Botswana as part of a natural history study of HIV subtype C disease progression. Methods Plasma samples from 133 HIV-positive adults were evaluated for HPgV RNA, and the 5’UTR was sequenced to determine the HPgV genotype. Results HPgV RNA was detected in 41 (30.8%) individuals. While the presence of HPgV RNA had no impact on baseline HIV viral load, a significant difference in baseline CD4 cell count was observed. HPgV genotypes were determined for 27 individuals and included 5 individuals (18.5%) with genotype 1 and 22 (81.5%) with genotype 5. Baseline CD4 cell counts were significantly higher for persons infected with HPgV genotype 5 compared with genotype 1. Conclusions These data suggest that HPgV infection is common among HIV-positive individuals in Botswana and has a significant impact on CD4 cell count. This difference in CD4 cell count based on HPgV genotype suggests that HPgV genotype should be evaluated as a possible predictor of HIV disease progression and highlights the need for additional studies of this virus in resource-limited settings.

Funder

Sub-Saharan Africa Network for TB/HIV Research Excellence

NIH Fogarty International Center

Oak Foundation

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Oncology

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