Characterization of pelvic and cervical microbiotas from patients with pelvic inflammatory disease

Yue Wang1, Ye Zhang2,3, Qi Zhang2,3

  • 11​Department of Gynecology, Women's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, PR China.

Abstract

Insights

Pelvic inflammatory disease (PID) involves distinct microbial communities in the pelvis and cervix. Cervical microbiota analysis alone may lead to incorrect antibiotic treatment for PID.

Area of Science:

  • Microbiology
  • Gynecology
  • Infectious Diseases

Background:

  • Pelvic inflammatory disease (PID) is a serious infection of the female reproductive organs.
  • The ascending infection hypothesis suggests vaginal or cervical microbes cause PID by spreading to the upper genital tract.
  • Understanding the microbial communities involved is crucial for effective diagnosis and treatment.

Purpose of the Study:

  • To profile and compare pelvic and cervical microbiota in patients with PID.
  • To evaluate the ascending infection hypothesis in the context of PID etiology.
  • To assess the utility of cervical microbiota profiling for guiding PID treatment decisions.

Main Methods:

  • Enrolled 38 PID patients and 19 controls undergoing salpingectomy or salpingo-oophorectomy.
  • Collected pelvic and cervical samples during surgery.
  • Utilized culture diagnosis and next-generation sequencing (NGS)-based 16S rRNA profiling.

Main Results:

  • NGS revealed half of pelvic samples had single-organism dominance, the other half polymicrobial infections.
  • Pelvic microbiota was dominated by Acinetobacter, Escherichia, Sneathia, and Streptococcus.
  • Cervical microbiota was dominated by Lactobacillus and Gardnerella; pelvic and cervical microbiota were inconsistent.
  • Hydrosalpinx samples showed richer bacterial composition than pyosalpinx samples.

Conclusions:

  • NGS-based 16S rRNA profiling offers a more comprehensive view of pelvic microbiota than traditional culture methods.
  • Significant inconsistencies exist between pelvic and cervical microbiota in PID patients.
  • Relying solely on cervical microbiota for therapeutic decisions in PID risks antimicrobial misuse.

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