Lactobacilli-dominated cervical microbiota in women with preterm prelabor rupture of membranes
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
31791041
DOI
10.1038/s41390-019-0692-1
PII: 10.1038/s41390-019-0692-1
Knihovny.cz E-resources
- MeSH
- Amniocentesis methods MeSH
- Cervix Uteri microbiology MeSH
- Chlamydia trachomatis MeSH
- Chorioamnionitis microbiology MeSH
- Lactobacillus crispatus * MeSH
- Lactobacillus * MeSH
- Humans MeSH
- Microbiota MeSH
- Mycoplasma hominis MeSH
- Infant, Newborn MeSH
- Amniotic Fluid microbiology MeSH
- Obstetric Labor, Premature MeSH
- Fetal Membranes, Premature Rupture microbiology MeSH
- Retrospective Studies MeSH
- Pregnancy MeSH
- Ureaplasma MeSH
- Check Tag
- Humans MeSH
- Infant, Newborn MeSH
- Pregnancy MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
BACKGROUND: To determine the association between microbial invasion of the amniotic cavity (MIAC) and the presence of Lactobacillus crispatus- or Lactobacillus iners-dominated cervical microbiota in pregnancies with preterm prelabor rupture of membrane. Next, to assess the relationship between the presence of L. crispatus- or L. iners-dominated cervical microbiota and short-term neonatal morbidity. METHOD: A total of 311 women were included. Cervical samples were obtained using a Dacron polyester swab and amniotic fluid samples were obtained by transabdominal amniocentesis. Bacterial DNA, L. crispatus, and L. iners in the cervical samples were assessed by PCR. Cervical microbiota was assigned as L. crispatus- or L. iners-dominated when the relative abundance of L. crispatus or L. iners was ≥50% of the whole cervical microbiota, respectively. RESULTS: Women with MIAC showed a lower rate of L. crispatus-dominated cervical microbiota (21% vs. 39%; p = 0.003) than those without MIAC. Lactobacillus crispatus-dominated cervical microbiota was associated with a lower rate of early-onset sepsis (0% vs. 5%; p = 0.02). CONCLUSIONS: The presence of L. crispatus-dominated cervical microbiota in women with preterm prelabor rupture of membrane was associated with a lower risk of intra-amniotic complications and subsequent development of early-onset sepsis of newborns.
Biomedical Research Center University Hospital Hradec Kralove Hradec Kralove Czech Republic
Department of Obstetrics and Gynecology University Hospital Ostrava Ostrava Czech Republic
See more in PubMed
Mercer, B. M. Preterm premature rupture of the membranes. Obstet. Gynecol. 101, 178–193 (2003). PubMed
Mercer, B. M. Preterm premature rupture of the membranes: current approaches to evaluation and management. Obstet. Gynecol. Clin. North Am. 32, 411–428 (2005). DOI
Mingione, M. J., Pressman, E. K. & Woods, J. R. Prevention of PPROM: current and future strategies. J. Matern. Fetal Neonatal Med. 19, 783–789 (2006). DOI
Musilova, I. et al. Intraamniotic inflammation in women with preterm prelabor rupture of membranes. PLoS ONE 10, e0133929 (2015). DOI
Cobo, T. et al. Intra-amniotic inflammation predicts microbial invasion of the amniotic cavity but not spontaneous preterm delivery in preterm prelabor membrane rupture. Acta Obstet. Gynecol. Scand. 91, 930–935 (2012). DOI
DiGiulio, D. B. et al. Prevalence and diversity of microbes in the amniotic fluid, the fetal inflammatory response, and pregnancy outcome in women with preterm pre-labor rupture of membranes. Am. J. Reprod. Immunol. 64, 38–57 (2010). PubMed PMC
Romero, R. et al. Sterile and microbial-associated intra-amniotic inflammation in preterm prelabor rupture of membranes. J. Matern. Fetal Neonatal Med. 28, 1394–1409 (2015). DOI
Fortner, K. B. et al. Bacteria localization and chorion thinning among preterm premature rupture of membranes. PLoS ONE 9, e83338 (2014). DOI
Anton, L. et al. Common cervicovaginal microbial supernatants alter cervical epithelial function: mechanisms by which Lactobacillus crispatus contributes to cervical health. Front Microbiol 9, 2181 (2018). DOI
Rampersaud, R. et al. Inerolysin, a cholesterol-dependent cytolysin produced by Lactobacillus iners. J. Bacteriol. 193, 1034–1041 (2011). DOI
Ravel, J. et al. Vaginal microbiome of reproductive-age women. Proc. Natl. Acad. Sci. USA 108(Suppl. 1), 4680–4687 (2011). DOI
Romero, R. et al. The composition and stability of the vaginal microbiota of normal pregnant women is different from that of non-pregnant women. Microbiome 2, 4 (2014). DOI
Romero, R. et al. The vaginal microbiota of pregnant women who subsequently have spontaneous preterm labor and delivery and those with a normal delivery at term. Microbiome 2, 18 (2014). DOI
Kacerovsky, M. et al. Cervical microbiota in women with preterm prelabor rupture of membranes. PLoS ONE 10, e0126884 (2015). DOI
Brown, R. G. et al. Vaginal dysbiosis increases risk of preterm fetal membrane rupture, neonatal sepsis and is exacerbated by erythromycin. BMC Med. 16, 9 (2018). DOI
Dols, J. A. et al. Molecular assessment of bacterial vaginosis by Lactobacillus abundance and species diversity. BMC Infect. Dis. 16, 180 (2016). DOI
Petrova, M. I., Reid, G., Vaneechoutte, M. & Lebeer, S. Lactobacillus iners: friend or foe? Trends Microbiol. 25, 182–191 (2017). DOI
Kindinger, L. M. et al. The interaction between vaginal microbiota, cervical length, and vaginal progesterone treatment for preterm birth risk. Microbiome 5, 6 (2017). DOI
Servin, A. L. Antagonistic activities of lactobacilli and bifidobacteria against microbial pathogens. FEMS Microbiol. Rev. 28, 405–440 (2004). DOI
Ghartey, J. P. et al. Lactobacillus crispatus dominant vaginal microbiome is associated with inhibitory activity of female genital tract secretions against Escherichia coli. PLoS ONE 9, e96659 (2014). DOI
Kusters, J. G., Reuland, E. A., Bouter, S., Koenig, P. & Dorigo-Zetsma, J. W. A multiplex real-time PCR assay for routine diagnosis of bacterial vaginosis. Eur. J. Clin. Microbiol. Infect. Dis. 34, 1779–1785 (2015). DOI
Liu, C. M. et al. BactQuant: an enhanced broad-coverage bacterial quantitative real-time PCR assay. BMC Microbiol. 12, 56 (2012). DOI
Fouhy, F. et al. The effects of freezing on faecal microbiota as determined using MiSeq sequencing and culture-based investigations. PLoS ONE 10, e0119355 (2015). DOI
Kacerovsky, M. et al. Bedside assessment of amniotic fluid interleukin-6 in preterm prelabor rupture of membranes. Am. J. Obstet. Gynecol. 211, 385 e381–385 e389 (2014). DOI
Paramel Jayaprakash, T. et al. High diversity and variability in the vaginal microbiome in women following preterm premature rupture of membranes (PPROM): a prospective cohort study. PLoS ONE 11, e0166794 (2016). DOI
Chaemsaithong, P. et al. A rapid interleukin-6 bedside test for the identification of intra-amniotic inflammation in preterm labor with intact membranes. J. Matern. Fetal Neonatal Med. 29, 349–359 (2016). DOI
Chaemsaithong, P. et al. A point of care test for interleukin-6 in amniotic fluid in preterm prelabor rupture of membranes: a step toward the early treatment of acute intra-amniotic inflammation/infection. J. Matern. Fetal Neonatal Med. 29, 360–367 (2016). DOI
Ely, J. W., Rijhsinghani, A., Bowdler, N. C. & Dawson, J. D. The association between manual removal of the placenta and postpartum endometritis following vaginal delivery. Obstet. Gynecol. 86, 1002–1006 (1995). DOI
Papile, L. A., Burstein, J., Burstein, R. & Koffler, H. Incidence and evolution of subependymal and intraventricular hemorrhage: a study of infants with birth weights less than 1,500 gm. J. Pediatr. 92, 529–534 (1978). DOI
Yoon, B. H. et al. Microbial invasion of the amniotic cavity with Ureaplasma urealyticum is associated with a robust host response in fetal, amniotic, and maternal compartments. Am. J. Obstet. Gynecol. 179, 1254–1260 (1998). DOI
Kacerovsky, M. et al. Amniotic fluid protein profiles of intraamniotic inflammatory response to Ureaplasma spp. and other bacteria. PLoS ONE 8, e60399 (2013). DOI
Stray-Pedersen, B., Bruu, A. L. & Molne, K. Infertility and uterine colonization with Ureaplasma urealyticum. Acta Obstet. Gynecol. Scand. 61, 21–24 (1982). DOI
Aaltonen, R., Heikkinen, J., Vahlberg, T., Jensen, J. S. & Alanen, A. Local inflammatory response in choriodecidua induced by Ureaplasma urealyticum. BJOG 114, 1432–1435 (2007). DOI
Dalton, E. & Castillo, E. Post partum infections: a review for the non-OBGYN. Obstet. Med. 7, 98–102 (2014). DOI
Furman, B., Shoham-Vardi, I., Bashiri, A., Erez, O. & Mazor, M. Clinical significance and outcome of preterm prelabor rupture of membranes: population-based study. Eur. J. Obstet. Gynecol. Reprod. Biol. 92, 209–216 (2000). DOI
Kim, J. Y. et al. Novel antibacterial activity of beta(2)-microglobulin in human amniotic fluid. PLoS ONE 7, e47642 (2012). DOI
Oka, K. et al. The effect of transferrin and lysozyme on antibacterial activity of amniotic fluid. Biol. Res. Pregnancy Perinatol. 8(1 1ST Half), 1–6 (1987). PubMed
Michaels, J. E. et al. Comprehensive proteomic analysis of the human amniotic fluid proteome: gestational age-dependent changes. J. Proteome Res. 6, 1277–1285 (2007). DOI
Alcendor, D. J. Evaluation of health disparity in bacterial vaginosis and the implications for HIV-1 acquisition in African American women. Am. J. Reprod. Immunol. 76, 99–107 (2016). DOI
Kramer, M. R. & Hogue, C. R. Place matters: variation in the black/white very preterm birth rate across U.S. metropolitan areas, 2002–2004. Public Health Rep. 123, 576–585 (2008). DOI
Cervical Gardnerella vaginalis in women with preterm prelabor rupture of membranes