Vaginal Microbiota, Genital Inflammation and Extracellular Matrix Remodelling Collagenase: MMP-9 in Pregnant Women With HIV, a Potential Preterm Birth Mechanism Warranting Further Exploration

BackgroundPregnant women living with HIV infection (PWLWH) have elevated rates of preterm birth (PTB) in which HIV and cART are implicated. PWLWH also have a high prevalence of adverse vaginal microbiota, which associate with genital tract inflammation. The mechanism underlying PTB in PWLWH is unkno...

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Autores principales: Charlotte-Eve S. Short, Rachael A. Quinlan, Xuan Wang, Veronica Georgiana Preda, Ann Smith, Julian R. Marchesi, Yooni S. Lee, David A. MacIntyre, Phillip R. Bennett, Graham P. Taylor
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spelling oai:doaj.org-article:eec88b2ac81143078ce53c90bba81e6d2021-12-01T14:29:09ZVaginal Microbiota, Genital Inflammation and Extracellular Matrix Remodelling Collagenase: MMP-9 in Pregnant Women With HIV, a Potential Preterm Birth Mechanism Warranting Further Exploration2235-298810.3389/fcimb.2021.750103https://doaj.org/article/eec88b2ac81143078ce53c90bba81e6d2021-11-01T00:00:00Zhttps://www.frontiersin.org/articles/10.3389/fcimb.2021.750103/fullhttps://doaj.org/toc/2235-2988BackgroundPregnant women living with HIV infection (PWLWH) have elevated rates of preterm birth (PTB) in which HIV and cART are implicated. PWLWH also have a high prevalence of adverse vaginal microbiota, which associate with genital tract inflammation. The mechanism underlying PTB in PWLWH is unknown. We present the first data in PWLWH on genital-tract matrix-metalloproteinase-9(MMP-9), an important collagenase implicated in labour onset, and tissue inhibitor of metalloproteinases-1(TIMP-1) and explore correlations with local inflammation and vaginal bacteria.Material and MethodsCervical vaginal fluid (CVF) collected by a soft cup and high vaginal swabs (HVS) were obtained from PWLWH and HIV uninfected pregnant women (HUPW) at three antenatal time points. Maternal characteristics, combination antiretroviral therapy (cART) exposure, and pregnancy outcome were recorded. Concentrations of MMP-9, TIMP-1 and ten cytokines were measured by immunoassays. Vaginal microbiota composition was determined through 16S rRNA amplicon sequencing. MMP-9, TIMP-1 and cytokine concentrations were compared by HIV status, cART, and prematurity and in PWLWH correlations with polymorphonuclear leucocytes, cytokines and bacterial genera were explored.ResultsCVF was available for 50 PWLWH (108 samples) and 12 HUPW (20 samples) between gestation weeks 14-38. Thirty-six PWLWH conceived on cART and 14 initiated post-conception. There were five and one PTB outcomes in PWLWH and HUPW respectively. PWLWH had higher mean CVF concentrations of MMP-9 (p<0.001) and TIMP-1 (p=0.035) in the second trimester compared with HUPW with a similar trend in the third trimester. PWLWH also had higher CVF values of cytokines: IL-1β, IL-8, IL-12 and TNF-α in both trimesters compared to HUPW (p ≤ 0.003). In PWLWH, MMP-9 positively correlated with TIMP-1 (r=0.31, p=0.002) and CVF polymorphonuclear leucocytes (r=0.57, p=0.02). Correlations were observed between MMP-9 and three cytokines: IL-1β (r=0.61), IL-8 (r=0.57) and TNF-α (r=0.64), p<0.001, similarly for TIMP-1. Abundance of anaerobic pathobionts correlated with MMP-9: Gardnerella (r=0.44, p<0.001), Atopobium (r=0.33, p=0.005), and Prevotella genera (r=0.39, p<0.001). Conversely proportion of Lactobacillus genera negatively correlated with MMP-9 (rho=-0.46, p<0.001). MMP-9/TIMP-1 ratio increased with gestational age at sampling in PWLWH, but this was no longer significant after adjusting for confounders and no difference by prematurity was observed in this sub-study.ConclusionsHere we show strong correlations of MMP-9 to genital tract inflammation and sub-optimal bacterial genera in PWLWH indicating the ascending genital tract infection pathway may be a contributory mechanism to the high risk of PTB.Charlotte-Eve S. ShortCharlotte-Eve S. ShortRachael A. QuinlanRachael A. QuinlanXuan WangVeronica Georgiana PredaVeronica Georgiana PredaAnn SmithAnn SmithJulian R. MarchesiJulian R. MarchesiYooni S. LeeYooni S. LeeDavid A. MacIntyreDavid A. MacIntyrePhillip R. BennettPhillip R. BennettGraham P. TaylorGraham P. TaylorFrontiers Media S.A.articleHIV - human immunodeficiency viruspreterm (birth)metalloproteinasemicrobiome and dysbiosisGardnerella speciesMicrobiologyQR1-502ENFrontiers in Cellular and Infection Microbiology, Vol 11 (2021)
institution DOAJ
collection DOAJ
language EN
topic HIV - human immunodeficiency virus
preterm (birth)
metalloproteinase
microbiome and dysbiosis
Gardnerella species
Microbiology
QR1-502
spellingShingle HIV - human immunodeficiency virus
preterm (birth)
metalloproteinase
microbiome and dysbiosis
Gardnerella species
Microbiology
QR1-502
Charlotte-Eve S. Short
Charlotte-Eve S. Short
Rachael A. Quinlan
Rachael A. Quinlan
Xuan Wang
Veronica Georgiana Preda
Veronica Georgiana Preda
Ann Smith
Ann Smith
Julian R. Marchesi
Julian R. Marchesi
Yooni S. Lee
Yooni S. Lee
David A. MacIntyre
David A. MacIntyre
Phillip R. Bennett
Phillip R. Bennett
Graham P. Taylor
Graham P. Taylor
Vaginal Microbiota, Genital Inflammation and Extracellular Matrix Remodelling Collagenase: MMP-9 in Pregnant Women With HIV, a Potential Preterm Birth Mechanism Warranting Further Exploration
description BackgroundPregnant women living with HIV infection (PWLWH) have elevated rates of preterm birth (PTB) in which HIV and cART are implicated. PWLWH also have a high prevalence of adverse vaginal microbiota, which associate with genital tract inflammation. The mechanism underlying PTB in PWLWH is unknown. We present the first data in PWLWH on genital-tract matrix-metalloproteinase-9(MMP-9), an important collagenase implicated in labour onset, and tissue inhibitor of metalloproteinases-1(TIMP-1) and explore correlations with local inflammation and vaginal bacteria.Material and MethodsCervical vaginal fluid (CVF) collected by a soft cup and high vaginal swabs (HVS) were obtained from PWLWH and HIV uninfected pregnant women (HUPW) at three antenatal time points. Maternal characteristics, combination antiretroviral therapy (cART) exposure, and pregnancy outcome were recorded. Concentrations of MMP-9, TIMP-1 and ten cytokines were measured by immunoassays. Vaginal microbiota composition was determined through 16S rRNA amplicon sequencing. MMP-9, TIMP-1 and cytokine concentrations were compared by HIV status, cART, and prematurity and in PWLWH correlations with polymorphonuclear leucocytes, cytokines and bacterial genera were explored.ResultsCVF was available for 50 PWLWH (108 samples) and 12 HUPW (20 samples) between gestation weeks 14-38. Thirty-six PWLWH conceived on cART and 14 initiated post-conception. There were five and one PTB outcomes in PWLWH and HUPW respectively. PWLWH had higher mean CVF concentrations of MMP-9 (p<0.001) and TIMP-1 (p=0.035) in the second trimester compared with HUPW with a similar trend in the third trimester. PWLWH also had higher CVF values of cytokines: IL-1β, IL-8, IL-12 and TNF-α in both trimesters compared to HUPW (p ≤ 0.003). In PWLWH, MMP-9 positively correlated with TIMP-1 (r=0.31, p=0.002) and CVF polymorphonuclear leucocytes (r=0.57, p=0.02). Correlations were observed between MMP-9 and three cytokines: IL-1β (r=0.61), IL-8 (r=0.57) and TNF-α (r=0.64), p<0.001, similarly for TIMP-1. Abundance of anaerobic pathobionts correlated with MMP-9: Gardnerella (r=0.44, p<0.001), Atopobium (r=0.33, p=0.005), and Prevotella genera (r=0.39, p<0.001). Conversely proportion of Lactobacillus genera negatively correlated with MMP-9 (rho=-0.46, p<0.001). MMP-9/TIMP-1 ratio increased with gestational age at sampling in PWLWH, but this was no longer significant after adjusting for confounders and no difference by prematurity was observed in this sub-study.ConclusionsHere we show strong correlations of MMP-9 to genital tract inflammation and sub-optimal bacterial genera in PWLWH indicating the ascending genital tract infection pathway may be a contributory mechanism to the high risk of PTB.
format article
author Charlotte-Eve S. Short
Charlotte-Eve S. Short
Rachael A. Quinlan
Rachael A. Quinlan
Xuan Wang
Veronica Georgiana Preda
Veronica Georgiana Preda
Ann Smith
Ann Smith
Julian R. Marchesi
Julian R. Marchesi
Yooni S. Lee
Yooni S. Lee
David A. MacIntyre
David A. MacIntyre
Phillip R. Bennett
Phillip R. Bennett
Graham P. Taylor
Graham P. Taylor
author_facet Charlotte-Eve S. Short
Charlotte-Eve S. Short
Rachael A. Quinlan
Rachael A. Quinlan
Xuan Wang
Veronica Georgiana Preda
Veronica Georgiana Preda
Ann Smith
Ann Smith
Julian R. Marchesi
Julian R. Marchesi
Yooni S. Lee
Yooni S. Lee
David A. MacIntyre
David A. MacIntyre
Phillip R. Bennett
Phillip R. Bennett
Graham P. Taylor
Graham P. Taylor
author_sort Charlotte-Eve S. Short
title Vaginal Microbiota, Genital Inflammation and Extracellular Matrix Remodelling Collagenase: MMP-9 in Pregnant Women With HIV, a Potential Preterm Birth Mechanism Warranting Further Exploration
title_short Vaginal Microbiota, Genital Inflammation and Extracellular Matrix Remodelling Collagenase: MMP-9 in Pregnant Women With HIV, a Potential Preterm Birth Mechanism Warranting Further Exploration
title_full Vaginal Microbiota, Genital Inflammation and Extracellular Matrix Remodelling Collagenase: MMP-9 in Pregnant Women With HIV, a Potential Preterm Birth Mechanism Warranting Further Exploration
title_fullStr Vaginal Microbiota, Genital Inflammation and Extracellular Matrix Remodelling Collagenase: MMP-9 in Pregnant Women With HIV, a Potential Preterm Birth Mechanism Warranting Further Exploration
title_full_unstemmed Vaginal Microbiota, Genital Inflammation and Extracellular Matrix Remodelling Collagenase: MMP-9 in Pregnant Women With HIV, a Potential Preterm Birth Mechanism Warranting Further Exploration
title_sort vaginal microbiota, genital inflammation and extracellular matrix remodelling collagenase: mmp-9 in pregnant women with hiv, a potential preterm birth mechanism warranting further exploration
publisher Frontiers Media S.A.
publishDate 2021
url https://doaj.org/article/eec88b2ac81143078ce53c90bba81e6d
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