Vaginal microbiota of American Indian women and associations with measures of psychosocial stress.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2021
Historique:
received: 05 02 2021
accepted: 17 11 2021
entrez: 10 12 2021
pubmed: 11 12 2021
medline: 8 1 2022
Statut: epublish

Résumé

Molecular-bacterial vaginosis (BV) is characterized by low levels of vaginal Lactobacillus species and is associated with higher risk of sexually transmitted infections (STI). Perceived psychosocial stress is associated with increased severity and persistence of infections, including STIs. American Indians have the highest rates of stress and high rates of STIs. The prevalence of molecular-BV among American Indian women is unknown. We sought to evaluate measures of psychosocial stress, such as historic loss (a multigenerational factor involving slavery, forced removal from one's land, legally ratified race-based segregation, and contemporary discrimination) and their association with the vaginal microbiota and specific metabolites associated with BV, in 70 Northwestern Plains American Indian women. Demographics, perceived psychosocial stressors, sexual practices, and known BV risk factors were assessed using a modified version of the American Indian Service Utilization, Psychiatric Epidemiology, Risk and Protective Factors Project survey. Self-collected mid-vaginal swabs were profiled for bacterial composition by 16S rRNA gene amplicon sequencing and metabolites quantified by targeted liquid-chromatography mass spectrometry. Sixty-six percent of the participants were classified as having molecular-BV, with the rest being either dominated by L. crispatus (10%) or L. iners (24%). High levels of lifetime trauma were associated with higher odds of having molecular-BV (adjusted Odds Ratio (aOR): 2.5, 95% Credible Interval (CrI): 1.1-5.3). Measures of psychosocial stress, including historic loss and historic loss associated symptoms, were significantly associated with lifestyle and behavioral practices. Higher scores of lifetime trauma were associated with increased concentrations of spermine (aFC: 3.3, 95% CrI: 1.2-9.2). Historic loss associated symptoms and biogenic amines were the major correlates of molecular-BV. Historical loss associated symptoms and lifetime trauma are potentially important underlying factors associated with BV.

Identifiants

pubmed: 34890405
doi: 10.1371/journal.pone.0260813
pii: PONE-D-21-03745
pmc: PMC8664215
doi:

Substances chimiques

DNA, Bacterial 0
DNA, Ribosomal 0
RNA, Ribosomal, 16S 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0260813

Subventions

Organisme : NIGMS NIH HHS
ID : P20 GM103474
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI116799
Pays : United States
Organisme : NIAID NIH HHS
ID : R21 AI111145
Pays : United States
Organisme : NIGMS NIH HHS
ID : U54 GM115371
Pays : United States

Déclaration de conflit d'intérêts

JR is the co‐ founder of LUCA Biologics, a biotechnology company focusing on translating microbiome research into live biotherapeutic drugs for women’s health. All other authors have declared that no competing interests exist.

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Auteurs

Joanna-Lynn C Borgogna (JC)

Department of Microbiology and Immunology, Montana State University, Bozeman, Montana, United States of America.
Department of Animal and Range Sciences, Montana State University, Bozeman, Montana, United States of America.

Michael Anastario (M)

Department of Health Promotion and Disease Prevention, Florida International University, Miami, Florida, United States of America.

Paula Firemoon (P)

Fort Peck Community College, Poplar, Montana, United States of America.

Elizabeth Rink (E)

Department of Health and Human Development, Montana State University, Bozeman, Montana, United States of America.

Adriann Ricker (A)

School of Public Health-Center for American Indian Health and School of Nursing, John Hopkins University, Baltimore, Maryland, United States of America.

Jacques Ravel (J)

Institute for Genome Sciences, University of Maryland School of Medicine, Baltimore, Maryland, United States of America.
Department of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, Maryland, United States of America.

Rebecca M Brotman (RM)

Institute for Genome Sciences, University of Maryland School of Medicine, Baltimore, Maryland, United States of America.
Department of Epidemiology and Public Health, University of Maryland School of Medicine, Baltimore, Maryland, United States of America.

Carl J Yeoman (CJ)

Department of Microbiology and Immunology, Montana State University, Bozeman, Montana, United States of America.
Department of Animal and Range Sciences, Montana State University, Bozeman, Montana, United States of America.

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