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Characteristics of Vaginal Microbiome in Women with Pelvic Inflammatory Disease in Koreaopen access

Authors
Kim, SukyungSeo, HoonheeRahim, Md AbdurTajdozian, HaniehKim, Yun-SookSong, Ho-Yeon
Issue Date
Sep-2021
Publisher
Polskie Towarzystwo Mikrobiologow/Polish Society of Microbiologists
Keywords
vaginal microflora; pelvic inflammatory disease; 16S rRNA amplicon sequencing; premenopausal; Korean
Citation
Polish Journal of Microbiology, v.70, no.3, pp 345 - 357
Pages
13
Journal Title
Polish Journal of Microbiology
Volume
70
Number
3
Start Page
345
End Page
357
URI
https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/20004
DOI
10.33073/pjm-2021-033
ISSN
1733-1331
2544-4646
Abstract
Human vaginal microorganisms play an important role in maintaining good health throughout the human life cycle. An imbalance in the vaginal microbiota is associated with an increased risk of pelvic inflammatory disease (PID). This study aimed to characterize and compare vaginal microbial profiles of premenopausal Korean women with and without PID. 74 Korean premenopausal female vaginal samples were obtained; 33 were from healthy women (a control group) and 41 from PID patients. Vaginal fluid samples were collected from the vaginal wall and posterior cervix and then analyzed by 16S ribosomal ribonucleic acid (rRNA) gene-based amplicon sequencing. Results showed a significant difference between the vaginal microbial communities of the two groups (Jensen-Shannon, p = 0.014; Bray-Curtis, p = 0.009; Generalized UniFrac, p = 0.007; UniFrac, p = 0.008). Lactobacillus accounted for the highest percentage (61.0%) of the control group but was significantly decreased (34.9%) in PID patients; this was the most significant difference among all bacterial communities (p = 0.028, LDA effect size = 5.129). In addition, in the PID patient group, species diversity significantly increased (Simpson, p = 0.07) as the proportion of various pathogens increased evenly, resulting in a polymicrobial infection. Similarly, lactate, which constituted the highest percentage of the organic acids in the control group, was significantly decreased in the PID patient group (p = 0.04). The present study's findings will help understand PID from the microbiome perspective and are expected to contribute to the development of more efficient PID diagnosis and treatment modalities.
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