Cargando…
Modeling the temporal dynamics of cervicovaginal microbiota identifies targets that may promote reproductive health
BACKGROUND: Cervicovaginal bacterial communities composed of diverse anaerobes with low Lactobacillus abundance are associated with poor reproductive outcomes such as preterm birth, infertility, cervicitis, and risk of sexually transmitted infections (STIs), including human immunodeficiency virus (H...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8314590/ https://www.ncbi.nlm.nih.gov/pubmed/34311774 http://dx.doi.org/10.1186/s40168-021-01096-9 |
_version_ | 1783729582615035904 |
---|---|
author | Munoz, Alexander Hayward, Matthew R. Bloom, Seth M. Rocafort, Muntsa Ngcapu, Sinaye Mafunda, Nomfuneko A. Xu, Jiawu Xulu, Nondumiso Dong, Mary Dong, Krista L. Ismail, Nasreen Ndung’u, Thumbi Ghebremichael, Musie S. Kwon, Douglas S. |
author_facet | Munoz, Alexander Hayward, Matthew R. Bloom, Seth M. Rocafort, Muntsa Ngcapu, Sinaye Mafunda, Nomfuneko A. Xu, Jiawu Xulu, Nondumiso Dong, Mary Dong, Krista L. Ismail, Nasreen Ndung’u, Thumbi Ghebremichael, Musie S. Kwon, Douglas S. |
author_sort | Munoz, Alexander |
collection | PubMed |
description | BACKGROUND: Cervicovaginal bacterial communities composed of diverse anaerobes with low Lactobacillus abundance are associated with poor reproductive outcomes such as preterm birth, infertility, cervicitis, and risk of sexually transmitted infections (STIs), including human immunodeficiency virus (HIV). Women in sub-Saharan Africa have a higher prevalence of these high-risk bacterial communities when compared to Western populations. However, the transition of cervicovaginal communities between high- and low-risk community states over time is not well described in African populations. RESULTS: We profiled the bacterial composition of 316 cervicovaginal swabs collected at 3-month intervals from 88 healthy young Black South African women with a median follow-up of 9 months per participant and developed a Markov-based model of transition dynamics that accurately predicted bacterial composition within a broader cross-sectional cohort. We found that Lactobacillus iners-dominant, but not Lactobacillus crispatus-dominant, communities have a high probability of transitioning to high-risk states. Simulating clinical interventions by manipulating the underlying transition probabilities, our model predicts that the population prevalence of low-risk microbial communities could most effectively be increased by manipulating the movement between L. iners- and L. crispatus-dominant communities. CONCLUSIONS: The Markov model we present here indicates that L. iners-dominant communities have a high probability of transitioning to higher-risk states. We additionally identify transitions to target to increase the prevalence of L. crispatus-dominant communities. These findings may help guide future intervention strategies targeted at reducing bacteria-associated adverse reproductive outcomes among women living in sub-Saharan Africa. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-021-01096-9. |
format | Online Article Text |
id | pubmed-8314590 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-83145902021-07-28 Modeling the temporal dynamics of cervicovaginal microbiota identifies targets that may promote reproductive health Munoz, Alexander Hayward, Matthew R. Bloom, Seth M. Rocafort, Muntsa Ngcapu, Sinaye Mafunda, Nomfuneko A. Xu, Jiawu Xulu, Nondumiso Dong, Mary Dong, Krista L. Ismail, Nasreen Ndung’u, Thumbi Ghebremichael, Musie S. Kwon, Douglas S. Microbiome Research BACKGROUND: Cervicovaginal bacterial communities composed of diverse anaerobes with low Lactobacillus abundance are associated with poor reproductive outcomes such as preterm birth, infertility, cervicitis, and risk of sexually transmitted infections (STIs), including human immunodeficiency virus (HIV). Women in sub-Saharan Africa have a higher prevalence of these high-risk bacterial communities when compared to Western populations. However, the transition of cervicovaginal communities between high- and low-risk community states over time is not well described in African populations. RESULTS: We profiled the bacterial composition of 316 cervicovaginal swabs collected at 3-month intervals from 88 healthy young Black South African women with a median follow-up of 9 months per participant and developed a Markov-based model of transition dynamics that accurately predicted bacterial composition within a broader cross-sectional cohort. We found that Lactobacillus iners-dominant, but not Lactobacillus crispatus-dominant, communities have a high probability of transitioning to high-risk states. Simulating clinical interventions by manipulating the underlying transition probabilities, our model predicts that the population prevalence of low-risk microbial communities could most effectively be increased by manipulating the movement between L. iners- and L. crispatus-dominant communities. CONCLUSIONS: The Markov model we present here indicates that L. iners-dominant communities have a high probability of transitioning to higher-risk states. We additionally identify transitions to target to increase the prevalence of L. crispatus-dominant communities. These findings may help guide future intervention strategies targeted at reducing bacteria-associated adverse reproductive outcomes among women living in sub-Saharan Africa. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-021-01096-9. BioMed Central 2021-07-26 /pmc/articles/PMC8314590/ /pubmed/34311774 http://dx.doi.org/10.1186/s40168-021-01096-9 Text en © The Author(s) 2021, corrected publication 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Munoz, Alexander Hayward, Matthew R. Bloom, Seth M. Rocafort, Muntsa Ngcapu, Sinaye Mafunda, Nomfuneko A. Xu, Jiawu Xulu, Nondumiso Dong, Mary Dong, Krista L. Ismail, Nasreen Ndung’u, Thumbi Ghebremichael, Musie S. Kwon, Douglas S. Modeling the temporal dynamics of cervicovaginal microbiota identifies targets that may promote reproductive health |
title | Modeling the temporal dynamics of cervicovaginal microbiota identifies targets that may promote reproductive health |
title_full | Modeling the temporal dynamics of cervicovaginal microbiota identifies targets that may promote reproductive health |
title_fullStr | Modeling the temporal dynamics of cervicovaginal microbiota identifies targets that may promote reproductive health |
title_full_unstemmed | Modeling the temporal dynamics of cervicovaginal microbiota identifies targets that may promote reproductive health |
title_short | Modeling the temporal dynamics of cervicovaginal microbiota identifies targets that may promote reproductive health |
title_sort | modeling the temporal dynamics of cervicovaginal microbiota identifies targets that may promote reproductive health |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8314590/ https://www.ncbi.nlm.nih.gov/pubmed/34311774 http://dx.doi.org/10.1186/s40168-021-01096-9 |
work_keys_str_mv | AT munozalexander modelingthetemporaldynamicsofcervicovaginalmicrobiotaidentifiestargetsthatmaypromotereproductivehealth AT haywardmatthewr modelingthetemporaldynamicsofcervicovaginalmicrobiotaidentifiestargetsthatmaypromotereproductivehealth AT bloomsethm modelingthetemporaldynamicsofcervicovaginalmicrobiotaidentifiestargetsthatmaypromotereproductivehealth AT rocafortmuntsa modelingthetemporaldynamicsofcervicovaginalmicrobiotaidentifiestargetsthatmaypromotereproductivehealth AT ngcapusinaye modelingthetemporaldynamicsofcervicovaginalmicrobiotaidentifiestargetsthatmaypromotereproductivehealth AT mafundanomfunekoa modelingthetemporaldynamicsofcervicovaginalmicrobiotaidentifiestargetsthatmaypromotereproductivehealth AT xujiawu modelingthetemporaldynamicsofcervicovaginalmicrobiotaidentifiestargetsthatmaypromotereproductivehealth AT xulunondumiso modelingthetemporaldynamicsofcervicovaginalmicrobiotaidentifiestargetsthatmaypromotereproductivehealth AT dongmary modelingthetemporaldynamicsofcervicovaginalmicrobiotaidentifiestargetsthatmaypromotereproductivehealth AT dongkristal modelingthetemporaldynamicsofcervicovaginalmicrobiotaidentifiestargetsthatmaypromotereproductivehealth AT ismailnasreen modelingthetemporaldynamicsofcervicovaginalmicrobiotaidentifiestargetsthatmaypromotereproductivehealth AT ndunguthumbi modelingthetemporaldynamicsofcervicovaginalmicrobiotaidentifiestargetsthatmaypromotereproductivehealth AT ghebremichaelmusies modelingthetemporaldynamicsofcervicovaginalmicrobiotaidentifiestargetsthatmaypromotereproductivehealth AT kwondouglass modelingthetemporaldynamicsofcervicovaginalmicrobiotaidentifiestargetsthatmaypromotereproductivehealth |