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EDITORIAL article

Front. Cell. Infect. Microbiol., 18 October 2023
Sec. Clinical Microbiology
This article is part of the Research Topic Vaginal microecological disorder and gynecological diseases View all 16 articles

Editorial: Vaginal microecological disorder and gynecological diseases

  • 1National Engineering Research Center for Bioengineering Drugs and the Technologies, Institute of Translational Medicine, Nanchang University, Nanchang, China
  • 2Biological Science Division, Pacific Northwest National Laboratory, Richland, WA, United States
  • 3Key Laboratory of Development and Application of Rural Renewable Energy, Biogas Institute of Ministry of Agriculture and Rural Affairs, Chengdu, China
  • 4Department of Obstetrics and Gynecology, Beijing Tsinghua Changgung Hospital, School of Clinical Medicine, Tsinghua University, Beijing, China
  • 5Shenzhen Wedge Microbiology Research Co.Ltd, Shenzhen, China

Researchers have been increasingly interested in investigating microbial communities in the lower and upper reproductive tract and their impact on female reproductive health. A healthy vaginal ecosystem is dominated by Lactobacillus spp., which can be infected by various pathogens, including human papillomavirus (HPV) and human immunodeficiency virus, and is susceptible to dysbiosis of its microbiota. Pathogenic overgrowth results in the development of diseases, including aerobic vaginitis, bacterial vaginosis(BV), cytolytic vaginosis, trichomonas vaginitis, vulvovaginal candidiasis (VVC), urinary tract infections, sexually transmitted infections (STIs), and gynecological oncology. Determining the associations between the vaginal microbiota and these diseases can provide valuable insights for detecting diagnosing, and interventing complex female illnesses.

This Research Topic comprises fifteen papers, consisting of three subtopics: vaginal inflammation, HPV, and reproductive health.

The first subtopic on vaginal inflammation, comprises one review, two BV-related research articles, and two VVC-related articles. Gao et al. observed the top five potential common pathogens of vaginal infection, with Haemophilus influenzae having the highest prevalence, followed by Streptococcus pyogenes, Candida albicans, Escherichia coli, and Staphylococcus aureus. Zhou et al. examined the vaginal microbiota of patients with BV before and after antibiotic treatment, compared with healthy controls and identified Lactobacillus iners as a potential predictive indicator of clinical outcomes in patients with BV. Shen et al. showed that a postbiotic gel alleviated BV symptoms by increasing Lactobacillus spp., and reducing the presence of potential vaginal pathogens. Sun et al. summarized the changes in vaginal microbiota during VVC infection and highlighted the potential use of Lactobacillus spp. as probiotics for VVC treatment. Considering the high costs and potential side effects associated with antifungal agents for VVC treatment, Lu et al. found that X33 antimicrobial oligopeptide (X33 AMOP) effectively inhibited the virulence of C.albicans by reducing phospholipase activity and disrupting mycelium formation. Notably, while Lactobacillus spp. has shown promise in preventing and treating vaginal inflammation, clinical data regarding its efficacy remain limited and require further exploration.

Four papers discuss the subtopic of HPV and its relationship with cervical cancer. A et al. discovered a higher prevalence of vaginal infections and cervical STIs in the HPV-positive group than in the HPV-negative group. To explore the impact of probiotics on HPV persistence and clearance, Zeng et al. compared 90 patients with HPV and 45 healthy individuals and found that probiotics, as an interferon adjuvant therapy, effectively enhanced virus clearance in some patients. Patients with HPV clearance had significantly lower alpha diversity, accompanied by a decreased abundance of Fusobacterium, Bacteroides, Neisseria and Helicobacter, than those in the HPV-persistent group. Zhu et al. observed negative correlation between interleukin-2 (IL-2) levels and the risk of cervical intraepithelial neoplasia in Chinese women, regardless of high-risk HPV infection. Furthermore, Li et al. found that vaginal microecological abnormalities might contribute to a higher false-positive diagnosis rate of atypical squamous cells of undetermined significance, which is diagnosed as precancerous lesions. These findings highlight the significant impact of vaginal microbiota on female health, emphasizing the importance of understanding and maintaining a balanced microbiome.

Six papers were included in the last subtopic of reproductive health. Chao et al. collected uterine lavage samples via hysteroscopy from women with endometrial hyperplasia (EH) or endometrial cancer (EC) and found an increased relative abundance of two plastic-degrading bacteria, Bacillus pseudofirmus, and Stenotrophomonas rhizophila, in the endometrial lavage microbiota of women with EC/EH. Liang et al. analyzed the uterine cavity, cervix, and vagina samples of 134 patients with infertility and revealed that endometrial microbiota composed of Staphylococcus, Gardnerella, Atobor, Streptococcus, Peptostreptococcus, Chlamydia, Fusobacterium and Acinetobacter are related to CE and EP. Wang et al. discovered that vaginal bacteria, including Ensifer, Devosia, Bosea, Cellomonas, Helicobacter, and Sphingopyxis, as well as specific endometrial microbiota, including Candidatus Symbiobacter, Odoribacter, Blautia, Nocardioides, and Ileibacterium, exhibited predictive value for embryo arrest. Xie et al. found that vaginal microbiota transfer to newborns could help restore the disturbed microbiome caused by cesarean section delivery, resulting in a microbial composition similar to that of infants born through vaginal delivery. Dong et al. focused on recent advancements in understanding the interactions between microbiota and the cervical mucosal barrier. Furthermore, they found a significant impact of host-microbiota interactions on STIs outcomes. For instance, Chlamydia trachomatis infection, can cause tubal inflammation, fibrosis, and even obstruction, which have adverse effects on pregnancy. Tian et al. found that oral antibiotics can induce gut dysbiosis in DBA2/J mice, contributing to the development of Chlamydia-induced hydrosalpinx in the upper genital tract.

We reviewed recent research efforts that could further guide the discovery of the underlying mechanisms of microbial-mediated vaginal diseases and provide readers with valuable insights into the prediction, prevention, and treatment of gynecological diseases through reproductive tract microorganisms. In the future, more rigorous and clinically focused research is necessary to explore the specific mechanisms by which microorganisms contribute to the occurrence and development of female diseases. A deeper understanding of these mechanisms will provide crucial information for the diagnosis, treatment strategies, and development and optimization of drugs, probiotics, postbiotics, and vaginal microbiota transplantation.

Author contributions

TC: Writing – original draft, Writing – review & editing. RW: Writing – review & editing. LC: Writing – review & editing. QL: Writing – review & editing. ZC: Resources, Writing – original draft, Writing – review & editing.

Funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work is supported by grants from the National Natural Science Foundation of China (Grant No. 81900541).

Acknowledgments

We greatly appreciate the contributions to this Research Topic by all authors and reviewers. We thank all the guest-associated editors of the Research Topic, and the editorial board of the Journal of Frontiers, for their support.

Conflict of interest

ZC is employed by Shenzhen Wedge Microbiology Research Co. Ltd.

The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Keywords: vaginal microbiota, uterine microbiota, human papillomavirus, vulvovaginal candidiasis, bacterial vaginitis

Citation: Chen T, Wu R, Cheng L, Liao Q and Chen Z (2023) Editorial: Vaginal microecological disorder and gynecological diseases. Front. Cell. Infect. Microbiol. 13:1292815. doi: 10.3389/fcimb.2023.1292815

Received: 12 September 2023; Accepted: 11 October 2023;
Published: 18 October 2023.

Edited by:

Nahed Ismail, University of Illinois Chicago, United States

Reviewed by:

Eva Pericolini, University of Modena and Reggio Emilia, Italy

Copyright © 2023 Chen, Wu, Cheng, Liao and Chen. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Zhangran Chen, zhangran22105@163.com; Qinping Liao, qinpingliao@sina.com

These authors have contributed equally to this work

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.