The association between ethnicity and vaginal microbiota composition in Amsterdam, the Netherlands
To evaluate whether ethnicity is independently associated with vaginal microbiota (VMB) composition in women living in Amsterdam, the Netherlands, as has been shown for American women. Women (18-34 years, non-pregnant, N = 610) representing the six largest ethnic groups (Dutch, African Surinamese, S...
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Published in | PloS one Vol. 12; no. 7; p. e0181135 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
Public Library of Science
11.07.2017
Public Library of Science (PLoS) |
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Abstract | To evaluate whether ethnicity is independently associated with vaginal microbiota (VMB) composition in women living in Amsterdam, the Netherlands, as has been shown for American women.
Women (18-34 years, non-pregnant, N = 610) representing the six largest ethnic groups (Dutch, African Surinamese, South-Asian Surinamese, Turkish, Moroccan, and Ghanaian) were sampled from the population-based HELIUS study. Sampling was performed irrespective of health status or healthcare seeking behavior. DNA was extracted from self-sampled vaginal swabs and sequenced by Illumina MiSeq (16S rRNA gene V3-V4 region).
The overall prevalence of VMBs not dominated by lactobacilli was 38.5%: 32.2% had a VMB resembling bacterial vaginosis and another 6.2% had a VMB dominated by Bifidobacteriaceae (not including Gardnerella vaginalis), Corynebacterium, or pathobionts (streptococci, staphylococci, Proteus or Enterobacteriaceae). The most prevalent VMB in ethnically Dutch women was a Lactobacillus crispatus-dominated VMB, in African Surinamese and Ghanaian women a polybacterial G. vaginalis-containing VMB, and in the other ethnic groups a L. iners-dominated VMB. After adjustment for sociodemographic, behavioral and clinical factors, African Surinamese ethnicity (adjusted odds ratio (aOR) 5.1, 95% confidence interval (CI) 2.1-12.0) and Ghanaian ethnicity (aOR 4.8, 95% CI 1.8-12.6) were associated with having a polybacterial G. vaginalis-containing VMB, and African Surinamese ethnicity with a L. iners-dominated VMB (aOR 2.8, 95% CI 1.2-6.2). Shorter steady relationship duration, inconsistent condom use with casual partners, and not using hormonal contraception were also associated with having a polybacterial G. vaginalis-containing VMB, but human papillomavirus infection was not. Other sexually transmitted infections were uncommon.
The overall prevalence of having a VMB not dominated by lactobacilli in this population-based cohort of women aged 18-34 years in Amsterdam was high (38.5%), and women of sub-Saharan African descent were significantly more likely to have a polybacterial G. vaginalis-containing VMB than Dutch women independent of modifiable behaviors. |
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AbstractList | To evaluate whether ethnicity is independently associated with vaginal microbiota (VMB) composition in women living in Amsterdam, the Netherlands, as has been shown for American women. Women (18-34 years, non-pregnant, N = 610) representing the six largest ethnic groups (Dutch, African Surinamese, South-Asian Surinamese, Turkish, Moroccan, and Ghanaian) were sampled from the population-based HELIUS study. Sampling was performed irrespective of health status or healthcare seeking behavior. DNA was extracted from self-sampled vaginal swabs and sequenced by Illumina MiSeq (16S rRNA gene V3-V4 region). The overall prevalence of VMBs not dominated by lactobacilli was 38.5%: 32.2% had a VMB resembling bacterial vaginosis and another 6.2% had a VMB dominated by Bifidobacteriaceae (not including Gardnerella vaginalis), Corynebacterium, or pathobionts (streptococci, staphylococci, Proteus or Enterobacteriaceae). The most prevalent VMB in ethnically Dutch women was a Lactobacillus crispatus-dominated VMB, in African Surinamese and Ghanaian women a polybacterial G. vaginalis-containing VMB, and in the other ethnic groups a L. iners-dominated VMB. After adjustment for sociodemographic, behavioral and clinical factors, African Surinamese ethnicity (adjusted odds ratio (aOR) 5.1, 95% confidence interval (CI) 2.1-12.0) and Ghanaian ethnicity (aOR 4.8, 95% CI 1.8-12.6) were associated with having a polybacterial G. vaginalis-containing VMB, and African Surinamese ethnicity with a L. iners-dominated VMB (aOR 2.8, 95% CI 1.2-6.2). Shorter steady relationship duration, inconsistent condom use with casual partners, and not using hormonal contraception were also associated with having a polybacterial G. vaginalis-containing VMB, but human papillomavirus infection was not. Other sexually transmitted infections were uncommon. The overall prevalence of having a VMB not dominated by lactobacilli in this population-based cohort of women aged 18-34 years in Amsterdam was high (38.5%), and women of sub-Saharan African descent were significantly more likely to have a polybacterial G. vaginalis-containing VMB than Dutch women independent of modifiable behaviors. Objective To evaluate whether ethnicity is independently associated with vaginal microbiota (VMB) composition in women living in Amsterdam, the Netherlands, as has been shown for American women. Methods Women (18–34 years, non-pregnant, N = 610) representing the six largest ethnic groups (Dutch, African Surinamese, South-Asian Surinamese, Turkish, Moroccan, and Ghanaian) were sampled from the population-based HELIUS study. Sampling was performed irrespective of health status or healthcare seeking behavior. DNA was extracted from self-sampled vaginal swabs and sequenced by Illumina MiSeq (16S rRNA gene V3-V4 region). Results The overall prevalence of VMBs not dominated by lactobacilli was 38.5%: 32.2% had a VMB resembling bacterial vaginosis and another 6.2% had a VMB dominated by Bifidobacteriaceae (not including Gardnerella vaginalis), Corynebacterium, or pathobionts (streptococci, staphylococci, Proteus or Enterobacteriaceae). The most prevalent VMB in ethnically Dutch women was a Lactobacillus crispatus-dominated VMB, in African Surinamese and Ghanaian women a polybacterial G. vaginalis-containing VMB, and in the other ethnic groups a L. iners-dominated VMB. After adjustment for sociodemographic, behavioral and clinical factors, African Surinamese ethnicity (adjusted odds ratio (aOR) 5.1, 95% confidence interval (CI) 2.1–12.0) and Ghanaian ethnicity (aOR 4.8, 95% CI 1.8–12.6) were associated with having a polybacterial G. vaginalis-containing VMB, and African Surinamese ethnicity with a L. iners-dominated VMB (aOR 2.8, 95% CI 1.2–6.2). Shorter steady relationship duration, inconsistent condom use with casual partners, and not using hormonal contraception were also associated with having a polybacterial G. vaginalis-containing VMB, but human papillomavirus infection was not. Other sexually transmitted infections were uncommon. Conclusions The overall prevalence of having a VMB not dominated by lactobacilli in this population-based cohort of women aged 18–34 years in Amsterdam was high (38.5%), and women of sub-Saharan African descent were significantly more likely to have a polybacterial G. vaginalis-containing VMB than Dutch women independent of modifiable behaviors. Objective To evaluate whether ethnicity is independently associated with vaginal microbiota (VMB) composition in women living in Amsterdam, the Netherlands, as has been shown for American women. Methods Women (18–34 years, non-pregnant, N = 610) representing the six largest ethnic groups (Dutch, African Surinamese, South-Asian Surinamese, Turkish, Moroccan, and Ghanaian) were sampled from the population-based HELIUS study. Sampling was performed irrespective of health status or healthcare seeking behavior. DNA was extracted from self-sampled vaginal swabs and sequenced by Illumina MiSeq (16S rRNA gene V3-V4 region). Results The overall prevalence of VMBs not dominated by lactobacilli was 38.5%: 32.2% had a VMB resembling bacterial vaginosis and another 6.2% had a VMB dominated by Bifidobacteriaceae (not including Gardnerella vaginalis ), Corynebacterium , or pathobionts (streptococci, staphylococci, Proteus or Enterobacteriaceae ). The most prevalent VMB in ethnically Dutch women was a Lactobacillus crispatus -dominated VMB, in African Surinamese and Ghanaian women a polybacterial G . vaginalis -containing VMB, and in the other ethnic groups a L . iners -dominated VMB. After adjustment for sociodemographic, behavioral and clinical factors, African Surinamese ethnicity (adjusted odds ratio (aOR) 5.1, 95% confidence interval (CI) 2.1–12.0) and Ghanaian ethnicity (aOR 4.8, 95% CI 1.8–12.6) were associated with having a polybacterial G . vaginalis -containing VMB, and African Surinamese ethnicity with a L . iners -dominated VMB (aOR 2.8, 95% CI 1.2–6.2). Shorter steady relationship duration, inconsistent condom use with casual partners, and not using hormonal contraception were also associated with having a polybacterial G . vaginalis -containing VMB, but human papillomavirus infection was not. Other sexually transmitted infections were uncommon. Conclusions The overall prevalence of having a VMB not dominated by lactobacilli in this population-based cohort of women aged 18–34 years in Amsterdam was high (38.5%), and women of sub-Saharan African descent were significantly more likely to have a polybacterial G . vaginalis -containing VMB than Dutch women independent of modifiable behaviors. OBJECTIVETo evaluate whether ethnicity is independently associated with vaginal microbiota (VMB) composition in women living in Amsterdam, the Netherlands, as has been shown for American women.METHODSWomen (18-34 years, non-pregnant, N = 610) representing the six largest ethnic groups (Dutch, African Surinamese, South-Asian Surinamese, Turkish, Moroccan, and Ghanaian) were sampled from the population-based HELIUS study. Sampling was performed irrespective of health status or healthcare seeking behavior. DNA was extracted from self-sampled vaginal swabs and sequenced by Illumina MiSeq (16S rRNA gene V3-V4 region).RESULTSThe overall prevalence of VMBs not dominated by lactobacilli was 38.5%: 32.2% had a VMB resembling bacterial vaginosis and another 6.2% had a VMB dominated by Bifidobacteriaceae (not including Gardnerella vaginalis), Corynebacterium, or pathobionts (streptococci, staphylococci, Proteus or Enterobacteriaceae). The most prevalent VMB in ethnically Dutch women was a Lactobacillus crispatus-dominated VMB, in African Surinamese and Ghanaian women a polybacterial G. vaginalis-containing VMB, and in the other ethnic groups a L. iners-dominated VMB. After adjustment for sociodemographic, behavioral and clinical factors, African Surinamese ethnicity (adjusted odds ratio (aOR) 5.1, 95% confidence interval (CI) 2.1-12.0) and Ghanaian ethnicity (aOR 4.8, 95% CI 1.8-12.6) were associated with having a polybacterial G. vaginalis-containing VMB, and African Surinamese ethnicity with a L. iners-dominated VMB (aOR 2.8, 95% CI 1.2-6.2). Shorter steady relationship duration, inconsistent condom use with casual partners, and not using hormonal contraception were also associated with having a polybacterial G. vaginalis-containing VMB, but human papillomavirus infection was not. Other sexually transmitted infections were uncommon.CONCLUSIONSThe overall prevalence of having a VMB not dominated by lactobacilli in this population-based cohort of women aged 18-34 years in Amsterdam was high (38.5%), and women of sub-Saharan African descent were significantly more likely to have a polybacterial G. vaginalis-containing VMB than Dutch women independent of modifiable behaviors. To evaluate whether ethnicity is independently associated with vaginal microbiota (VMB) composition in women living in Amsterdam, the Netherlands, as has been shown for American women. Women (18-34 years, non-pregnant, N = 610) representing the six largest ethnic groups (Dutch, African Surinamese, South-Asian Surinamese, Turkish, Moroccan, and Ghanaian) were sampled from the population-based HELIUS study. Sampling was performed irrespective of health status or healthcare seeking behavior. DNA was extracted from self-sampled vaginal swabs and sequenced by Illumina MiSeq (16S rRNA gene V3-V4 region). The overall prevalence of VMBs not dominated by lactobacilli was 38.5%: 32.2% had a VMB resembling bacterial vaginosis and another 6.2% had a VMB dominated by Bifidobacteriaceae (not including Gardnerella vaginalis), Corynebacterium, or pathobionts (streptococci, staphylococci, Proteus or Enterobacteriaceae). The most prevalent VMB in ethnically Dutch women was a Lactobacillus crispatus-dominated VMB, in African Surinamese and Ghanaian women a polybacterial G. vaginalis-containing VMB, and in the other ethnic groups a L. iners-dominated VMB. After adjustment for sociodemographic, behavioral and clinical factors, African Surinamese ethnicity (adjusted odds ratio (aOR) 5.1, 95% confidence interval (CI) 2.1-12.0) and Ghanaian ethnicity (aOR 4.8, 95% CI 1.8-12.6) were associated with having a polybacterial G. vaginalis-containing VMB, and African Surinamese ethnicity with a L. iners-dominated VMB (aOR 2.8, 95% CI 1.2-6.2). Shorter steady relationship duration, inconsistent condom use with casual partners, and not using hormonal contraception were also associated with having a polybacterial G. vaginalis-containing VMB, but human papillomavirus infection was not. Other sexually transmitted infections were uncommon. The overall prevalence of having a VMB not dominated by lactobacilli in this population-based cohort of women aged 18-34 years in Amsterdam was high (38.5%), and women of sub-Saharan African descent were significantly more likely to have a polybacterial G. vaginalis-containing VMB than Dutch women independent of modifiable behaviors. |
Audience | Academic |
Author | Alberts, Catharina J van Houdt, Robin Geerlings, Suzanne E Bruisten, Sylvia M Prins, Maria van der Veer, Charlotte de Vries, Henry J Schim van der Loeff, Maarten F Borgdorff, Hanneke Snijder, Marieke B van de Wijgert, Janneke H H M |
AuthorAffiliation | 8 Department of Clinical Epidemiology, Biostatistics and Bioinformatics, Academic Medical Center, Amsterdam, The Netherlands 9 Department of Internal Medicine, Division of Infectious Diseases, Academic Medical Center, Amsterdam, The Netherlands 1 Amsterdam Institute for Global Health and Development, Amsterdam, The Netherlands 4 Department of Medical Microbiology and Infection Control, VU University Medical Center, Amsterdam, The Netherlands 7 Department of Public Health, Academic Medical Center, Amsterdam, The Netherlands 2 Center for Infection and Immunity Amsterdam, Academic Medical Center, Amsterdam, The Netherlands 6 Department of Dermatology, Academic Medical Center, Amsterdam, The Netherlands Fred Hutchinson Cancer Research Center, UNITED STATES 3 Public Health Laboratory, Public Health Service of Amsterdam (GGD), Amsterdam, The Netherlands 5 Department of Infectious Diseases, Public Health Service of Amsterdam (GGD), Amsterdam, the Netherlands 10 Department of Clinical Infection, Microbi |
AuthorAffiliation_xml | – name: 4 Department of Medical Microbiology and Infection Control, VU University Medical Center, Amsterdam, The Netherlands – name: 8 Department of Clinical Epidemiology, Biostatistics and Bioinformatics, Academic Medical Center, Amsterdam, The Netherlands – name: Fred Hutchinson Cancer Research Center, UNITED STATES – name: 10 Department of Clinical Infection, Microbiology and Immunology, Institute of Infection and Global Health, University of Liverpool, Liverpool, United Kingdom – name: 5 Department of Infectious Diseases, Public Health Service of Amsterdam (GGD), Amsterdam, the Netherlands – name: 6 Department of Dermatology, Academic Medical Center, Amsterdam, The Netherlands – name: 2 Center for Infection and Immunity Amsterdam, Academic Medical Center, Amsterdam, The Netherlands – name: 7 Department of Public Health, Academic Medical Center, Amsterdam, The Netherlands – name: 9 Department of Internal Medicine, Division of Infectious Diseases, Academic Medical Center, Amsterdam, The Netherlands – name: 1 Amsterdam Institute for Global Health and Development, Amsterdam, The Netherlands – name: 3 Public Health Laboratory, Public Health Service of Amsterdam (GGD), Amsterdam, The Netherlands |
Author_xml | – sequence: 1 givenname: Hanneke surname: Borgdorff fullname: Borgdorff, Hanneke organization: Center for Infection and Immunity Amsterdam, Academic Medical Center, Amsterdam, The Netherlands – sequence: 2 givenname: Charlotte surname: van der Veer fullname: van der Veer, Charlotte organization: Department of Medical Microbiology and Infection Control, VU University Medical Center, Amsterdam, The Netherlands – sequence: 3 givenname: Robin surname: van Houdt fullname: van Houdt, Robin organization: Department of Medical Microbiology and Infection Control, VU University Medical Center, Amsterdam, The Netherlands – sequence: 4 givenname: Catharina J surname: Alberts fullname: Alberts, Catharina J organization: Department of Infectious Diseases, Public Health Service of Amsterdam (GGD), Amsterdam, the Netherlands – sequence: 5 givenname: Henry J surname: de Vries fullname: de Vries, Henry J organization: Department of Dermatology, Academic Medical Center, Amsterdam, The Netherlands – sequence: 6 givenname: Sylvia M surname: Bruisten fullname: Bruisten, Sylvia M organization: Public Health Laboratory, Public Health Service of Amsterdam (GGD), Amsterdam, The Netherlands – sequence: 7 givenname: Marieke B surname: Snijder fullname: Snijder, Marieke B organization: Department of Clinical Epidemiology, Biostatistics and Bioinformatics, Academic Medical Center, Amsterdam, The Netherlands – sequence: 8 givenname: Maria surname: Prins fullname: Prins, Maria organization: Department of Internal Medicine, Division of Infectious Diseases, Academic Medical Center, Amsterdam, The Netherlands – sequence: 9 givenname: Suzanne E surname: Geerlings fullname: Geerlings, Suzanne E organization: Department of Internal Medicine, Division of Infectious Diseases, Academic Medical Center, Amsterdam, The Netherlands – sequence: 10 givenname: Maarten F surname: Schim van der Loeff fullname: Schim van der Loeff, Maarten F organization: Department of Internal Medicine, Division of Infectious Diseases, Academic Medical Center, Amsterdam, The Netherlands – sequence: 11 givenname: Janneke H H M orcidid: 0000-0003-2728-4560 surname: van de Wijgert fullname: van de Wijgert, Janneke H H M organization: Department of Clinical Infection, Microbiology and Immunology, Institute of Infection and Global Health, University of Liverpool, Liverpool, United Kingdom |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28700747$$D View this record in MEDLINE/PubMed |
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ContentType | Journal Article |
Copyright | COPYRIGHT 2017 Public Library of Science 2017 Borgdorff et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. 2017 Borgdorff et al 2017 Borgdorff et al |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Competing Interests: M. F. Schim van der Loeff received HPV research funding from Sanofi Pasteur MSD; he is a co-investigator in a Merck-funded investigator-initiated study on Gardasil; he is an investigator on a Sanofi Pasteur MSD sponsored HPV vaccine trial; he served on a HPV vaccine advisory board of GSK; he received in-kind contribution for another HPV study from Stichting Pathologie Onderzoek en Ontwikkeling (SPOO); and his institution receives HPV research funding from Janssen Infectious Diseases and Vaccines. This does not alter our adherence to PLOS ONE policies on sharing data and materials. The other authors report no competing interests. |
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Snippet | To evaluate whether ethnicity is independently associated with vaginal microbiota (VMB) composition in women living in Amsterdam, the Netherlands, as has been... Objective To evaluate whether ethnicity is independently associated with vaginal microbiota (VMB) composition in women living in Amsterdam, the Netherlands, as... OBJECTIVETo evaluate whether ethnicity is independently associated with vaginal microbiota (VMB) composition in women living in Amsterdam, the Netherlands, as... Objective To evaluate whether ethnicity is independently associated with vaginal microbiota (VMB) composition in women living in Amsterdam, the Netherlands, as... |
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SubjectTerms | Adolescent Adult Bacteria Bifidobacterium - genetics Bifidobacterium - physiology Bioinformatics Biology and Life Sciences Composition Confidence intervals Contraception Corynebacterium - genetics Corynebacterium - physiology Cytokines Deoxyribonucleic acid Disease control DNA Enterobacteriaceae - genetics Enterobacteriaceae - physiology Ethnicity Female Health aspects Health care Health services Human papillomavirus Humans Infections Infectious diseases Internal medicine Laboratories Lactobacilli Lactobacillus - genetics Lactobacillus - physiology Medicine and Health Sciences Microbiota (Symbiotic organisms) Microbiota - genetics Microbiota - physiology Minority & ethnic groups Netherlands Nucleotide sequence People and Places Phylogenetics Population studies Pregnancy Proteus - genetics Proteus - physiology Public health RNA, Ribosomal, 16S - genetics rRNA 16S Sociodemographics Staphylococcus - genetics Staphylococcus - physiology Streptococcus - genetics Streptococcus - physiology Studies Teaching hospitals Vagina Vagina - microbiology Vaginosis Women's health Womens health Young Adult |
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Title | The association between ethnicity and vaginal microbiota composition in Amsterdam, the Netherlands |
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