Cervical microbiota in women with preterm prelabor rupture of membranes

PLoS One. 2015 May 20;10(5):e0126884. doi: 10.1371/journal.pone.0126884. eCollection 2015.

Abstract

Objective: To analyze the cervical microbiota in women with preterm prelabor rupture of membranes (PPROM) by pyrosequencing and to document associations between cervical microbiota, cervical inflammatory response, microbial invasion of the amniotic cavity (MIAC), histological chorioamnionitis, and intraamniotic infection (IAI).

Study design: Sixty-one women with singleton pregnancies complicated by PPROM were included in the study. Specimens of cervical and amniotic fluid were collected on admission. The cervical microbiota was assessed by 16S rRNA gene sequencing by pyrosequencing. Interleukin (IL)-6 concentration in the cervical fluid and amniotic fluid was measured by ELISA and lateral flow immunoassay, respectively.

Results: Four bacterial community state types [CST I (Lactobacillus crispatus dominated), CST III (Lactobacillus iners dominated), CST IV-A (non-Lactobacillus bacteria dominated), and CST IV-B (Gardnerella vaginalis and Sneathia sanguinegens dominated)] were observed in the cervical microbiota of women with PPROM. Cervical fluid IL-6 concentrations differed between CSTs (CST I = 145 pg/mL, CST III = 166 pg/mL, CST IV-A = 420 pg/mL, and CST IV-B = 322 pg/mL; p = 0.004). There were also differences in the rates of MIAC, of both MIAC and histological chorioamnionitis, and of IAI among CSTs. No difference in the rate of histological chorioamnionitis was found among CSTs.

Conclusions: The cervical microbiota in PPROM women in this study was characterized by four CSTs. The presence of non-Lactobacillus CSTs was associated with a strong cervical inflammatory response and higher rates of MIAC, both MIAC and histological chorioamnionitis, and IAI representing a PPROM subtype with pronounced inflammation. CST I represents the dominant type of PPROM with a low rate of MIAC, IAI, and the combination of MIAC and histological chorioamnionitis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Amnion / microbiology
  • Amniotic Fluid / metabolism
  • Body Fluids / microbiology
  • Cervix Uteri / microbiology*
  • Cervix Uteri / pathology
  • Chorioamnionitis / microbiology
  • Demography
  • Female
  • Fetal Membranes, Premature Rupture / microbiology*
  • Humans
  • Infant, Newborn
  • Interleukin-6 / metabolism
  • Microbiota*
  • Obstetric Labor, Premature / microbiology*
  • Pregnancy
  • Species Specificity
  • Young Adult

Substances

  • IL6 protein, human
  • Interleukin-6

Grants and funding

This work was supported by Institutional Resources for Supporting the Research Organization provided by the Ministry of Health of the Czech Republic DRO (UHHK, 00179906), by a grant from the Ministry of Health of the Czech Republic (NT13461-4/2012) and by Charles University in Prague, the Faculty of Medicine in Hradec Kralove, Czech Republic, project “PRVOUK” P37/10. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.