Microbiota in the oral cavity of school-age children with HIV who started antiretroviral therapy at young ages in South Africa.


Journal

AIDS (London, England)
ISSN: 1473-5571
Titre abrégé: AIDS
Pays: England
ID NLM: 8710219

Informations de publication

Date de publication:
01 08 2023
Historique:
pmc-release: 01 08 2024
medline: 17 7 2023
pubmed: 18 5 2023
entrez: 18 5 2023
Statut: ppublish

Résumé

Infancy is an important developmental period when the microbiome is shaped. We hypothesized that earlier antiretroviral therapy (ART) initiation would attenuate HIV effects on microbiota in the mouth. Oral swabs were collected from 477 children with HIV (CWH) and 123 children without (controls) at two sites in Johannesburg, South Africa. CWH had started ART less than 3 years of age; 63% less than 6 months of age. Most were well controlled on ART at median age 11 years when the swab was collected. Controls were age-matched and recruited from the same communities. Sequencing of V4 amplicon of 16S rRNA was done. Differences in microbial diversity and relative abundances of taxa were compared between the groups. CWH had lower alpha diversity than controls. Genus-level abundances of Granulicatella, Streptococcus, and Gemella were greater and Neisseria and Haemophilus less abundant among CWH than controls. Associations were stronger among boys. Associations were not attenuated with earlier ART initiation. Shifts in genus-level taxa abundances in CWH relative to controls were most marked in children on lopinavir/ritonavir regimens, with fewer shifts seen if on efavirenz ART regimens. A distinct profile of less diverse oral bacterial taxa was observed in school-aged CWH on ART compared with uninfected controls suggesting modulation of microbiota in the mouth by HIV and/or its treatments. Earlier ART initiation was not associated with microbiota profile. Proximal factors, including current ART regimen, were associated with contemporaneous profile of oral microbiota and may have masked associations with distal factors such as age at ART initiation.

Sections du résumé

BACKGROUND
Infancy is an important developmental period when the microbiome is shaped. We hypothesized that earlier antiretroviral therapy (ART) initiation would attenuate HIV effects on microbiota in the mouth.
METHODS
Oral swabs were collected from 477 children with HIV (CWH) and 123 children without (controls) at two sites in Johannesburg, South Africa. CWH had started ART less than 3 years of age; 63% less than 6 months of age. Most were well controlled on ART at median age 11 years when the swab was collected. Controls were age-matched and recruited from the same communities. Sequencing of V4 amplicon of 16S rRNA was done. Differences in microbial diversity and relative abundances of taxa were compared between the groups.
RESULTS
CWH had lower alpha diversity than controls. Genus-level abundances of Granulicatella, Streptococcus, and Gemella were greater and Neisseria and Haemophilus less abundant among CWH than controls. Associations were stronger among boys. Associations were not attenuated with earlier ART initiation. Shifts in genus-level taxa abundances in CWH relative to controls were most marked in children on lopinavir/ritonavir regimens, with fewer shifts seen if on efavirenz ART regimens.
CONCLUSION
A distinct profile of less diverse oral bacterial taxa was observed in school-aged CWH on ART compared with uninfected controls suggesting modulation of microbiota in the mouth by HIV and/or its treatments. Earlier ART initiation was not associated with microbiota profile. Proximal factors, including current ART regimen, were associated with contemporaneous profile of oral microbiota and may have masked associations with distal factors such as age at ART initiation.

Identifiants

pubmed: 37199568
doi: 10.1097/QAD.0000000000003599
pii: 00002030-202308010-00011
pmc: PMC10524539
mid: NIHMS1899580
doi:

Substances chimiques

RNA, Ribosomal, 16S 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1583-1591

Subventions

Organisme : NICHD NIH HHS
ID : R01 HD061255
Pays : United States
Organisme : NICHD NIH HHS
ID : R01 HD047177
Pays : United States
Organisme : NIDCR NIH HHS
ID : R01 DE028135
Pays : United States
Organisme : NICHD NIH HHS
ID : R01 HD073952
Pays : United States
Organisme : NICHD NIH HHS
ID : R01 HD073977
Pays : United States

Informations de copyright

Copyright © 2023 Wolters Kluwer Health, Inc. All rights reserved.

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Auteurs

Louise Kuhn (L)

Gertrude H. Sergievsky Center, Vagelos College of Physicians and Surgeons, Department of Epidemiology, Mailman School of Public Health.

Tian Wang (T)

Department of Biostatistics, Mailman School of Public Health, Columbia University Irving Medical Center, New York, New York.

Fan Li (F)

Department of Pediatrics, University of California Los Angeles, Los Angeles, California, USA.

Renate Strehlau (R)

VIDA Nkanyezi Research Unit, Rahima Moosa Mother and Child Hospital, Department of Paediatrics and Child Health.

Nicole H Tobin (NH)

Department of Pediatrics, University of California Los Angeles, Los Angeles, California, USA.

Avy Violari (A)

Perinatal HIV Research Unit, Chris Hani Baragwanath Hospital.

Sarah Brooker (S)

Department of Pediatrics, University of California Los Angeles, Los Angeles, California, USA.

Faeezah Patel (F)

Wits RHI, Shandukani Research Centre, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

Afaaf Liberty (A)

Perinatal HIV Research Unit, Chris Hani Baragwanath Hospital.

Stephanie Shiau (S)

Department of Biostatistics and Epidemiology, Rutgers School of Public Health, Piscataway, New Jersey.

Stephen M Arpadi (SM)

Gertrude H. Sergievsky Center, Vagelos College of Physicians and Surgeons, Department of Epidemiology, Mailman School of Public Health.

Sunil Wadhwa (S)

College of Dental Medicine.

Michael T Yin (MT)

Division of Infectious Diseases, Department of Medicine, Vagelos College of Physicians and Surgeons, Columbia University Irving Medical Center, New York, New York.

Shuang Wang (S)

Department of Biostatistics, Mailman School of Public Health, Columbia University Irving Medical Center, New York, New York.

Caroline T Tiemessen (CT)

National Institutes for Communicable Diseases, and Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

Grace M Aldrovandi (GM)

Department of Pediatrics, University of California Los Angeles, Los Angeles, California, USA.

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Classifications MeSH