Genomic composition of the vaginal microbiota in the first trimester and pregnancy outcomes
AbstractThe role of the vaginal microbiota during pregnancy acquires additional importance, acting as an anti-infective barrier for both mother and fetus. The change in the composition of the vaginal microbiota begins already from the first weeks of pregnancy. However, to date, the details of how changes in the composition and diversity of the vaginal microflora can affect pregnancy outcomes have not been sufficiently studied.
The aim of the study was to determine the genomic composition of the vaginal microbiota in the first trimester of pregnancy and to track pregnancy outcomes in different types of microbiocenosis.
Material and methods. 123 pregnant women who were registered in a women’s clinic for up to 12 weeks were examined. According to the outcome of pregnancy, all women were divided into 3 groups: group 1 – women who gave birth on time (n=91); group 2 – women who had premature birth (n=13); group 3 – women whose pregnancy was terminated before 22 weeks (n=19). At registration, a vaginal discharge was obtained in all pregnant women for microscopic and molecular biological assessment of microbiocenosis.
Results. The study of the genomic composition of the vaginal microbiota in the first trimester of pregnancy showed the presence of lactobacilli in all samples with the predominance of L. iners and L. crispatus species, while the L. iners species was more often found in pregnant women who gave birth prematurely. The dominance of the L. crispatus species was noted much more often in women who gave birth on time. Bacterial vaginosis was diagnosed in 11% of pregnant women, was asymptomatic and in no case was associated with premature birth. The detection of any conditionally pathogenic microorganisms, including mycoplasmas or ureaplasmas in early pregnancy, was also not associated with adverse pregnancy outcomes.
Conclusion. The dominance of lactobacilli, especially the L. crispatus species, is a favorable prognostic criterion for pregnancy, since it suppresses the diversity of the vaginal microbiota, reduces the risk of colonization by facultative and obligate anaerobes and potential pathogens, and also reduces the corresponding risk of premature birth.
Keywords: vaginal microbiota; vaginal lactobacilli; pregnancy outcomes; emergency delivery; premature birth; miscarriages
Funding. The study was conducted within the framework of the ESR: “Development of a diagnostic and prognostic panel of adverse pregnancy outcomes based on genomic analysis of the vaginal microbiota” 1022040700832-9-3.2.2.
Conflict of interest. The authors declare no conflict of interest.
Ethics. The protocol of the study was approved by the local Ethics Committee of the Research Institute of Obstetrics, Gynecology and Reproductology named after D.O. Ott (No. 125 of 12.05.2023).
Contribution. All authors made significant contributions to the conception, conduct of the study and preparation of the article, and read and approved the final version before publication. Literature review, processing of materials, analysis of the obtained data, writing the text – Budilovskaya O.V.; collection of clinical material, analysis of the obtained data, description of the results – Beliaeva N.R.; analysis of the obtained data, literature review – Shalepo K.V.; laboratory studies, analysis of the obtained data – Khusnutdinova T.A., Krysanova A.A.; concept and design of the study, making final edits – Tapilskaya N.I., Kogan I.Yu.; analysis of the obtained data, concept and design of the study, making final edits – Savicheva A.M.
For citation: Budilovskaya O.V., Belyaeva N.R., Khusnutdinova T.A., Shalepo K.V., Krysanova A.A., Tapilskaya N.I., Savicheva A.M., Kogan I.Yu. Genomic composition of the vaginal microbiota in the first trimester and pregnancy outcomes. Akusherstvo i ginekologiya: novosti, mneniya, obuchenie [Obstetrics and Gynecology: News, Opinions, Training]. 2025; 13 (1): 17–25. DOI: https://doi.org/10.33029/2303-9698-2025-13-1-17-25 (in Russian)
References
- Dominguez-Bello M.G. Gestational shaping of the maternal vaginal microbiome. Nat Med. 2019; 25 (6): 882–3. DOI: https://doi.org/10.1038/s41591-019-0483-6
- Giannella L., Grelloni C., Quintili D., et al. Microbiome changes in pregnancy disorders. Antioxidants (Basel). 2023; 12 (2): 463. DOI: https://doi.org/10.3390/antiox12020463
- Zierden H.C., DeLong K., Zulfiqar F., et al. Cervicovaginal mucus barrier properties during pregnancy are impacted by the vaginal microbiome. Front Cell Infect Microbiol. 2023; 13. Article ID 1015625. DOI: https://doi.org/10.3389/fcimb.2023.1015625
- Abou Chacra L., Fenollar F., Diop K. Bacterial vaginosis: what do we currently know? Front Cell Infect Microbiol. 2022; 11: 672429. DOI: https://doi.org/10.3389/fcimb.2021.672429
- Anahtar M.N., Gootenberg D.B., Mitchell C.M., Kwon D.S. Cervicovaginal microbiota and reproductive health: the virtue of simplicity. Cell Host Microbe. 2018; 23 (2): 159–68. DOI: https://doi.org/10.1016/J.CHOM.2018.01.013
- Cohain J.S., Buxbaum R.E., Mankuta D. Spontaneous first trimester miscarriage rates per woman among parous women with 1 or more pregnancies of 24 weeks or more. BMC Pregnancy Childbirth. 2017; 17 (1): 437. DOI: https://doi.org/10.1186/s12884-017-1620-1
- Zierden H.C., Ortiz Ortiz J.I., Dimitrion P., et al. Characterization of an adapted murine model of intrauterine inflammation-induced preterm birth. Am J Pathol. 2020; 190 (2): 295–305. DOI: https://doi.org/10.1016/j.ajpath.2019.10.013
- Savicheva A.M. Modern concepts of laboratory diagnostics of reproductively significant infections in women of reproductive age. Expert opinion. Voprosy prakticheskoy kol’poskopii. Genital’nye infektsii [Problems of Practical Colposcopy. Genital Infections]. 2022; (3): 34–9. DOI: https://doi.org/10.46393/27826392_2022_3_34 (in Russian)
- Marschalkó M., Ambrus L. A nöialsó genitalis traktus mikrobiom tulajdonságaiésszerepe [Characteristics and physiologic role of female lower genital microbiome]. Orv Hetil. 2023; 164 (24): 923–30. DOI: https://doi.org/10.1556/650.2023.32791 [in Hungarian]
- Serrano M.G., Parikh H.I., Brooks J.P., et al. Racioethnic diversity in the dynamics of the vaginal microbiome during pregnancy. Nat Med. 2019; 25 (6): 1001–11. DOI: https://doi.org/10.1038/s41591-019-0465-8
- Baud A., Hillion K.H., Plainvert C., et al. Microbial diversity in the vaginal microbiota and its link to pregnancy outcomes. Sci Rep. 2023; 13 (1): 9061. DOI: https://doi.org/10.1038/s41598-023-36126-z
- Sinyakova A.A., Shipitsyna E.V., Budilovskaya O.V., et al. Features of the vaginal microflora in the first trimester in women with a history of miscarriage. Zhurnal akusherstva i zhenskikh bolezney [Journal of Obstetrics and Women’s Diseases]. 2018; 67 (5): 32–41. DOI: https://doi.org/10.17816/JOWD67532-41 (in Russian)
- Zheng N., Guo R., Wang J., et al. Contribution of Lactobacillus iners to vaginal health and diseases: a systematic review. Front Cell Infect Microbiol. 2021; 11: 792787. DOI: https://doi.org/10.3389/fcimb.2021.792787
- Edwards V.L., Smith S.B., McComb E.J., et al. The cervicovaginal microbiota-host interaction modulates Chlamydia trachomatis infection. mBio. 2019; 10 (4): e01548-19. DOI: https://doi.org/10.1128/mBio.01548-19
- Hoang T., Toler E., DeLong K., et al. The cervicovaginal mucus barrier to HIV-1 is diminished in bacterial vaginosis. PLoS Pathog. 2020; 16 (1): e1008236. DOI: https://doi.org/10.1371/journal.ppat.1008236
- Norenhag J., Du J., Olovsson M., Verstraelen H., et al. The vaginal microbiota, human papillomavirus and cervical dysplasia: a systematic review and network meta-analysis. BJOG. 2020; 127 (2): 171–80. DOI: https://doi.org/10.1111/1471-0528.15854
- Walther-António M.R., Jeraldo P., Berg Miller M.E., et al. Pregnancy’s stronghold on the vaginal microbiome. PLoS One. 2014; 9 (6): e98514. DOI: https://doi.org/10.1371/journal.pone.0098514
- Chen P., Hu T., Zheng Z., et al. Characteristics of cervicovaginal microflora at different cervical maturity during late pregnancy: a nested case-control study. PLoS One. 2024; 19 (3): e0300510. DOI: https://doi.org/10.1371/journal.pone.0300510
- Horner P., Donders G., Cusini M., et al. Should we be testing for urogenital Mycoplasma hominis, Ureaplasma parvum and Ureaplasma urealyticum in men and women? – a position statement from the European STI Guidelines Editorial Board. J Eur Acad Dermatol Venereol. 2018; 32 (11): 1845–51. DOI: https://doi.org/10.1111/jdv.15146
- Noda-Nicolau N.M., Tantengco O.A.G., Polettini J., et al. Genital Mycoplasmas and biomarkers of inflammation and their association with spontaneous preterm birth and preterm prelabor rupture of membranes: a systematic review and meta-analysis. Front Microbiol. 2022; 13: 859732. DOI: https://doi.org/10.3389/fmicb.2022.859732
- Plummer E.L., Vodstrcil L.A., Bodiyabadu K., et al. Are Mycoplasma hominis, Ureaplasma urealyticum and Ureaplasma parvum associated with specific genital symptoms and clinical signs in nonpregnant women? Clin Infect Dis. 2021; 73: 659–68. DOI: https://doi.org/10.1093/CID/CIAB061
- Rittenschober-Böhm J., Waldhoer T., Schulz S.M., et al. First trimester vaginal ureaplasma biovar colonization and preterm birth: results of a prospective multicenter study. Neonatology. 2018; 113: 1–6. DOI: https://doi.org/10.1159/000480065
- Rumyantseva T., Khayrullina G., Guschin A., Donders G. Prevalence of Ureaplasma spp. and Mycoplasma hominis in healthy women and patients with flora alterations. Diagn Microbiol Infect Dis. 2019; 93 (3): 227–31. DOI: https://doi.org/10.1016/j.diagmicrobio.2018.10.001
- Sherrard J., Wilson J., Donders G., Mendling W., Jensen J.S. 2018 European (IUSTI/WHO) International Union against sexually transmitted infections (IUSTI) World Health Organisation (WHO) guideline on the management of vaginal discharge. Int J STD AIDS. 2018; 29 (13): 1258–72. DOI: https://doi.org/10.1177/0956462418785451