Phyloanatomic characterization of the distinct T cell and monocyte contributions to the peripheral blood HIV population within the host

Author:

RifeMagalis Brittany1ORCID,Strickland Samantha L1,Shank Stephen D2,Autissier Patrick3,Schuetz Alexandra45,Sithinamsuwan Pasiri6,Lerdlum Sukalaya7,Fletcher James L K8,de Souza Mark8,Ananworanich Jintanat458,Valcour Victor9,Williams Kenneth C3,Kosakovsky Pond Sergei L2,RattoKim Silvia45,Salemi Marco1,

Affiliation:

1. Department of Pathology, Immunology, and Laboratory Medicine, Emerging Pathogens Institute, University of Florida, Gainesville, FL 32601, USA

2. Department of Biology, Temple University, Philadelphia, PA 19122, USA

3. Department of Biology, Boston College, Chestnut Hill, MA 02467, USA

4. Department of Retrovirology, Armed Forces Research Institute of Medical Sciences - United States Component, Bangkok 10400, Thailand

5. SEARCH, Thai Red Cross AIDS Research Center, Bangkok 10330, Thailand

6. U.S. Military HIV Research Program, Walter Reed Army Institute of Research, Rockville, MD 20850, USA

7. Division of Neurology, Department of Medicine, Phramongkutklao Hospital, Bangkok 10400, Thailand

8. Faculty of Medicine, Department of Radiology, Chulalongkorn University, Bangkok 10330, Thailand

9. Department of Neurology, University of California San Francisco, San Francisco, CA 94143, USA

Abstract

AbstractHuman immunodeficiency virus (HIV) is a rapidly evolving virus, allowing its genetic sequence to act as a fingerprint for epidemiological processes among, as well as within, individual infected hosts. Though primarily infecting the CD4+ T-cell population, HIV can also be found in monocytes, an immune cell population that differs in several aspects from the canonical T-cell viral target. Using single genome viral sequencing and statistical phylogenetic inference, we investigated the viral RNA diversity and relative contribution of each of these immune cell types to the viral population within the peripheral blood. Results provide evidence of an increased prevalence of circulating monocytes harboring virus in individuals with high viral load in the absence of suppressive antiretroviral therapy. Bayesian phyloanatomic analysis of three of these individuals demonstrated a measurable role for these cells, but not the circulating T-cell population, as a source of cell-free virus in the plasma, supporting the hypothesis that these cells can act as an additional conduit of virus spread.

Funder

National Institute of Neurological Disease and Stroke at the National Institutes of Health

National Institute of General Medical Sciences

Publisher

Oxford University Press (OUP)

Subject

Virology,Microbiology

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