Detection and molecular characterization of urinary tract HIV-1 populations.


Journal

Annals of clinical microbiology and antimicrobials
ISSN: 1476-0711
Titre abrégé: Ann Clin Microbiol Antimicrob
Pays: England
ID NLM: 101152152

Informations de publication

Date de publication:
24 Sep 2019
Historique:
received: 06 09 2018
accepted: 16 09 2019
entrez: 26 9 2019
pubmed: 26 9 2019
medline: 6 2 2020
Statut: epublish

Résumé

Identification of all possible HIV reservoirs is an important aspect in HIV eradication efforts. The urinary tract has however not been well studied as a potential HIV reservoir. In this pilot study we molecularly characterized HIV-1 viruses in urine and plasma samples to investigate HIV-1 replication, compartmentalization and persistence in the urinary tract. Prospectively collected urine and blood samples collected over 12-36 months from 20 HIV-1 infected individuals were analysed including sampling points from prior to and after ART initiation. HIV-1 pol gene RNA and DNA from urine supernatant and urine pellets respectively were analysed and compared to plasma RNA viruses from the same individual. HIV-1 nucleic acid was detected in urine samples from at least one time point in 8/20 (40%) treatment-naïve subjects compared to 1/13 (7.7%) individuals on antiretroviral treatment (ART) during periods of plasma viral suppression and 1/7 (14.3%) individuals with virological failure. HIV-1 RNA was undetectable in urine samples after ART initiation but HIV-1 DNA was detectable in one patient more than 6 months after treatment initiation. There was co-clustering of urine-derived pol sequences but some urine-derived sequences were interspersed among the plasma-derived sequences. Suppressive ART reduces HIV-1 replication in the urinary tract but HIV-1 DNA may persist in these cells despite treatment. A larger number of sequences would be required to confirm HIV compartmentalization in the urinary tract.

Sections du résumé

BACKGROUND BACKGROUND
Identification of all possible HIV reservoirs is an important aspect in HIV eradication efforts. The urinary tract has however not been well studied as a potential HIV reservoir. In this pilot study we molecularly characterized HIV-1 viruses in urine and plasma samples to investigate HIV-1 replication, compartmentalization and persistence in the urinary tract.
METHODS METHODS
Prospectively collected urine and blood samples collected over 12-36 months from 20 HIV-1 infected individuals were analysed including sampling points from prior to and after ART initiation. HIV-1 pol gene RNA and DNA from urine supernatant and urine pellets respectively were analysed and compared to plasma RNA viruses from the same individual.
RESULTS RESULTS
HIV-1 nucleic acid was detected in urine samples from at least one time point in 8/20 (40%) treatment-naïve subjects compared to 1/13 (7.7%) individuals on antiretroviral treatment (ART) during periods of plasma viral suppression and 1/7 (14.3%) individuals with virological failure. HIV-1 RNA was undetectable in urine samples after ART initiation but HIV-1 DNA was detectable in one patient more than 6 months after treatment initiation. There was co-clustering of urine-derived pol sequences but some urine-derived sequences were interspersed among the plasma-derived sequences.
CONCLUSIONS CONCLUSIONS
Suppressive ART reduces HIV-1 replication in the urinary tract but HIV-1 DNA may persist in these cells despite treatment. A larger number of sequences would be required to confirm HIV compartmentalization in the urinary tract.

Identifiants

pubmed: 31551072
doi: 10.1186/s12941-019-0326-9
pii: 10.1186/s12941-019-0326-9
pmc: PMC6760049
doi:

Substances chimiques

Anti-Retroviral Agents 0
DNA, Viral 0
RNA, Viral 0
pol Gene Products, Human Immunodeficiency Virus 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

27

Subventions

Organisme : National Institutes of Health, USA
ID : R01HL090312
Organisme : National Institutes of Health, USA
ID : P30AI094189

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Auteurs

M L Mzingwane (ML)

Department of Pathology, Faculty of Medicine, National University of Science & Technology, Ascot, P. O Box AC 939, Bulawayo, Zimbabwe. mayibongwe.mzingwane@nust.ac.zw.
Department of Medical Virology, University of Pretoria, Pretoria, South Africa. mayibongwe.mzingwane@nust.ac.zw.

G Hunt (G)

Centre for HIV and Sexually Transmitted Infections, National Institute for Communicable Diseases, Johannesburg, South Africa.
Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

R Lassauniere (R)

Centre for HIV and Sexually Transmitted Infections, National Institute for Communicable Diseases, Johannesburg, South Africa.
Virus Research and Development Laboratory, Department of Virus and Microbiological Special Diagnostics, Statens Serum Institut, Copenhagen, Denmark.

M Kalimashe (M)

Centre for HIV and Sexually Transmitted Infections, National Institute for Communicable Diseases, Johannesburg, South Africa.

A Bongwe (A)

Centre for HIV and Sexually Transmitted Infections, National Institute for Communicable Diseases, Johannesburg, South Africa.

J Ledwaba (J)

Centre for HIV and Sexually Transmitted Infections, National Institute for Communicable Diseases, Johannesburg, South Africa.

R E Chaisson (RE)

Johns Hopkins University Center for AIDS Research, Baltimore, MD, USA.

N Martinson (N)

Perinatal HIV Research Unit (PHRU), SA MRC Soweto Matlosana Collaborating Centre for HIV/AIDS and TB, University of the Witwatersrand, Johannesburg, South Africa.

K Richter (K)

Department of Medical Virology, University of Pretoria, Pretoria, South Africa.
National Health Laboratory Services Tshwane Academic Division, Pretoria, South Africa.

S M Bowyer (SM)

Department of Medical Virology, University of Pretoria, Pretoria, South Africa.

C T Tiemessen (CT)

Centre for HIV and Sexually Transmitted Infections, National Institute for Communicable Diseases, Johannesburg, South Africa.
Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

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Classifications MeSH