Dynamics of the species composition of vaginal microorganisms in women before delivery and at different times of the postpartum period

Anna A. Siniakova , Olga V. Budilovskaya , Tatiana A. Khusnutdinova , Anna A. Krysanova , Kira V. Shalepo , Olesya N. Bespalova , Alevtina M. Savicheva , Igor Yu. Kogan

Journal of obstetrics and women's diseases ›› 2024, Vol. 73 ›› Issue (6) : 162 -171.

PDF
Journal of obstetrics and women's diseases ›› 2024, Vol. 73 ›› Issue (6) : 162 -171. DOI: 10.17816/JOWD635626
Original study articles
research-article

Dynamics of the species composition of vaginal microorganisms in women before delivery and at different times of the postpartum period

Author information +
History +
PDF

Abstract

Background: Vaginal microbiota is a factor that determines a woman’s health. Infectious complications of pregnant women, women in labor and newborns are often associated with a significant change in its composition. Analysis of the species diversity of vaginal microbiota during pregnancy and the postpartum period primarily contributes to the study of physiological processes and the concept of a “healthy” vaginal environment during these significant periods of a woman’s life.

Aim: The aim of this study was to evaluate the dynamic change in the species composition of vaginal microorganisms before delivery and at different times of the postpartum period in women with natural labor.

Materials and methods: This study involved 24 pregnant women who delivered vaginally. Each patient was examined at three time points: 37–40 weeks of pregnancy (visit 1), 4–5 days of the postpartum period (visit 2), and 6–8 weeks after delivery (visit 3). The species composition of the vaginal microbiota was studied using a comprehensive test based on real-time quantitative polymerase chain reaction.

Results: We found a decrease in the total bacterial mass in the vaginal biotope of women in labor after 4–5 days of the postpartum period and 6–8 weeks after delivery in comparison with the examination before delivery (p < 0.0005). Similar changes were noted in the composition of the lactobacillary microbiota: the concentration of lactobacilli decreased in the postpartum period in comparison with that before delivery (p < 0.05). Compared to the examination before delivery, 6–8 weeks after delivery in women, we observed a decrease in the frequency of Lactobacillus crispatus dominance (p < 0.05), while the frequency of Lactobacillus iners dominance in the postpartum period increased (p < 0.05). Among the representatives of the opportunistic vaginal microflora, the most frequently prevalent species were Gardnerella vaginalis, Prevotella bivia, Porphyromonas spp., Fannyhessea vaginae, Staphylococcus spp., Streptococcus spp., and Ureaplasma spp. In all women with severe vaginal microbiota disruption before delivery, an ascending bacterial infection was established according to the histological examination of the placenta after delivery (p < 0.05).

Conclusions: In most cases, the observed changes in the qualitative and quantitative composition of the vaginal microbiota in pregnant women and women in labor are physiological. At the same time, a consistent study of the vaginal microbiota during pregnancy and at different times of the postpartum period will allow for identifying possible risk factors for the development of infectious diseases in the mother and newborn and expand the possibilities for timely diagnosis and treatment of the identified disorders.

Keywords

vaginal microbiota / postpartum period / pregnancy

Cite this article

Download citation ▾
Anna A. Siniakova, Olga V. Budilovskaya, Tatiana A. Khusnutdinova, Anna A. Krysanova, Kira V. Shalepo, Olesya N. Bespalova, Alevtina M. Savicheva, Igor Yu. Kogan. Dynamics of the species composition of vaginal microorganisms in women before delivery and at different times of the postpartum period. Journal of obstetrics and women's diseases, 2024, 73(6): 162-171 DOI:10.17816/JOWD635626

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Ravel J, Gajer P, Abdo Z, et al. Vaginal microbiome of reproductive-age women. Proc Natl Acad Sci USA. 2011;108(Suppl 1):4680–4687. doi: 10.1073/pnas.10026111072

[2]

Ravel J., Gajer P., Abdo Z., et al. Vaginal microbiome of reproductive-age women // Proc Natl Acad Sci USA. 2011. Vol. 108, Suppl 1. P. 4680–4687. doi: 10.1073/pnas.10026111072

[3]

Dixon M, Dunlop AL, Corwin EJ, et al. Joint effects of individual socioeconomic status and residential neighborhood context on vaginal microbiome composition. Front Public Health. 2023;11:1029741. doi: 10.3389/fpubh.2023.10297413.

[4]

Dixon M., Dunlop A.L., Corwin E.J., et al. Joint effects of individual socioeconomic status and residential neighborhood context on vaginal microbiome composition // Front Public Health. 2023. Vol. 11. ID: 1029741. doi: 10.3389/fpubh.2023.10297413.

[5]

Ceccarani C, Foschi C, Parolin C, et al. Diversity of vaginal microbiome and metabolome during genital infections. Sci Rep. 2019;9(1):14095. doi: 10.1038/s41598-019-50410-x

[6]

Ceccarani C., Foschi C., Parolin C., et al. Diversity of vaginal microbiome and metabolome during genital infections // Sci Rep. 2019. Vol. 9, N 1. P. 14095. doi: 10.1038/s41598-019-50410-x

[7]

Anahtar MN, Gootenberg DB, Mitchell CM, et al. Cervicovaginal microbiota and reproductive health: the virtue of simplicity. Cell Host Microbe. 2018;23(2):159–168. doi: 10.1016/j.chom.2018.01.013

[8]

Anahtar M.N., Gootenberg D.B., Mitchell C.M., et al. Cervicovaginal microbiota and reproductive health: the virtue of simplicity // Cell Host Microbe. 2018. Vol. 23, N 2. P. 159–168. doi: 10.1016/j.chom.2018.01.013

[9]

Fettweis JM, Serrano MG, Brooks JP, et al. The vaginal microbiome and preterm birth. Nat Med. 2019;25(6):1012–1021. doi: 10.1038/s41591-019-0450-2

[10]

Fettweis J.M., Serrano M.G., Brooks J.P., et al. The vaginal microbiome and preterm birth // Nat Med. 2019. Vol. 25, N 6. P. 1012–1021. doi: 10.1038/s41591-019-0450-2

[11]

Dos Anjos Borges LG, Pastuschek J, Heimann Y, et al. Vaginal and neonatal microbiota in pregnant women with preterm premature rupture of membranes and consecutive early onset neonatal sepsis. BMC Med. 2023;21(1):92. doi: 10.1186/s12916-023-02805-x

[12]

Dos Anjos Borges L.G., Pastuschek J., Heimann Y., et al. Vaginal and neonatal microbiota in pregnant women with preterm premature rupture of membranes and consecutive early onset neonatal sepsis // BMC Med. 2023. Vol. 21, N 1. P. 92. doi: 10.1186/s12916-023-02805-x

[13]

Marangoni A, Laghi L, Zagonari S, et al. New insights into vaginal environment during pregnancy. Front Mol Biosci. 2021;8:656844. doi: 10.3389/fmolb.2021.656844

[14]

Marangoni A., Laghi L., Zagonari S., et al. New insights into vaginal environment during pregnancy // Front Mol Biosci. 2021. Vol. 8. ID: 656844. doi: 10.3389/fmolb.2021.656844

[15]

Di Simone N, Santamaria Ortiz A, Specchia M, et al. Recent insights on the maternal microbiota: impact on pregnancy outcomes. Front Immunol. 2020;11:528202. doi: 10.3389/fimmu.2020.528202

[16]

Di Simone N., Santamaria Ortiz A., Specchia M., et al. Recent insights on the maternal microbiota: impact on pregnancy outcomes // Front Immunol. 2020. Vol. 11. ID: 528202. doi: 10.3389/fimmu.2020.528202

[17]

Doyle R, Gondwe A, Fan YM, et al. A Lactobacillus-deficient vaginal microbiota dominates postpartum women in rural malawi. Appl Environ Microbiol. 2018;84(6):e02150–17. doi: 10.1128/AEM.02150-17

[18]

Doyle R., Gondwe A., Fan Y.M., et al. A Lactobacillus-deficient vaginal microbiota dominates postpartum women in rural malawi // Appl Environ Microbiol. 2018. Vol. 84, N 6. ID: e02150–17. doi: 10.1128/AEM.02150-17

[19]

MacIntyre DA, Chandiramani M, Lee YS, et al. The vaginal microbiome during pregnancy and the postpartum period in a European population. Sci Rep. 2015;5:8988. doi: 10.1038/srep08988

[20]

MacIntyre D.A., Chandiramani M., Lee Y.S., et al. The vaginal microbiome during pregnancy and the postpartum period in a European population // Sci Rep. 2015. Vol. 5. P. 8988. doi: 10.1038/srep08988

[21]

Aagaard K, Riehle K, Ma J, et al. A metagenomic approach to characterization of the vaginal microbiome signature in pregnancy. PLoS One. 2012;7(6):e36466. doi: 10.1371/journal.pone.0036466

[22]

Aagaard K., Riehle K., Ma J., et al. A metagenomic approach to characterization of the vaginal microbiome signature in pregnancy // PLoS One. 2012. Vol. 7, N 6. ID: e36466. doi: 10.1371/journal.pone.0036466

[23]

Kira E.F. Bacterial vaginosis. Moscow: Medical Information Agency; 2012. (In Russ.) EDN: SZPGYL

[24]

Кира Е.Ф. Бактериальный вагиноз. Москва: Медицинское информационное агентство, 2012. EDN: SZPGYL

[25]

Romero R, Hassan SS, Gajer P, et al. The composition and stability of the vaginal microbiota of normal pregnant women is different from that of non-pregnant women. Microbiome. 2014;2(1):4. doi: 10.1186/2049-2618-2-4

[26]

Romero R., Hassan S.S., Gajer P., et al. The composition and stability of the vaginal microbiota of normal pregnant women is different from that of non-pregnant women // Microbiome. 2014 Vol. 2, N 1. P. 4. doi: 10.1186/2049-2618-2-4

[27]

Serrano MG, Parikh HI, Brooks JP, et al. Racioethnic diversity in the dynamics of the vaginal microbiome during pregnancy. Nat Med. 2019;25(6):1001–1011. doi: 10.1038/s41591-019-0465-8

[28]

1Serrano M.G., Parikh H.I., Brooks J.P., et al. Racioethnic diversity in the dynamics of the vaginal microbiome during pregnancy // Nat Med. 2019. Vol. 25, N 6. P. 1001–1011. doi: 10.1038/s41591-019-0465-8

[29]

Rasmussen MA, Thorsen J, Dominguez-Bello MG, et al. Ecological succession in the vaginal microbiota during pregnancy and birth. ISME J. 2020;14(9):2325–2335. doi: 10.1038/s41396-020-0686-3

[30]

Rasmussen M.A., Thorsen J., Dominguez-Bello M.G., et al. Ecological succession in the vaginal microbiota during pregnancy and birth // ISME J. 2020. Vol. 14, N 9. P. 2325–2335. doi: 10.1038/s41396-020-0686-3

[31]

You YA, Park S, Kim K, et al. Transition in vaginal Lactobacillus species during pregnancy and prediction of preterm birth in Korean women. Sci Rep. 2022;12(1):22303. doi: 10.1038/s41598-022-26058-5

[32]

You Y.A., Park S., Kim K., et al. Transition in vaginal Lactobacillus species during pregnancy and prediction of preterm birth in Korean women // Sci Rep. 2022. Vol. 12, N 1. P. 22303. doi: 10.1038/s41598-022-26058-5

[33]

MacIntyre DA, Chandiramani M, Lee YS, et al. The vaginal microbiome during pregnancy and the postpartum period in a European population. Sci Rep. 2015;5:8988. doi: 10.1038/srep08988

[34]

MacIntyre D.A., Chandiramani M., Lee Y.S., et al. The vaginal microbiome during pregnancy and the postpartum period in a European population // Sci Rep. 2015. Vol. 5. P. 8988. doi: 10.1038/srep08988

[35]

Nunn KL, Witkin SS, Schneider GM, et al. Changes in the vaginal microbiome during the pregnancy to postpartum transition. Reprod Sci. 2021;28(7):1996–2005. doi: 10.1007/s43032-020-00438-6

[36]

Nunn K.L., Witkin S.S., Schneider G.M., et al. Changes in the vaginal microbiome during the pregnancy to postpartum transition // Reprod Sci. 2021. Vol. 28, N. 7. P. 1996–2005. doi: 10.1007/s43032-020-00438-6

[37]

Tortelli BA, Lewis WG, Allsworth JE, et al. Associations between the vaginal microbiome and Candida colonization in women of reproductive age. Am J Obstet Gynecol. 2020;222(5):471.e1–471.e9. doi: 10.1016/j.ajog.2019.10.008

[38]

Tortelli B.A., Lewis W.G., Allsworth J.E., et al. Associations between the vaginal microbiome and Candida colonization in women of reproductive age // Am J Obstet Gynecol. 2020. Vol. 222, N 5. P. 471.e1–471.e9. doi: 10.1016/j.ajog.2019.10.008

[39]

Sarmento SGP, Moron AF, Forney LJ, et al. An exploratory study of associations with spontaneous preterm birth in primigravid pregnant women with a normal cervical length. J Matern Fetal Neonatal Med. 2022;35(25):5383–5388. doi: 10.1080/14767058.2021.1879786

[40]

Sarmento S.G.P., Moron A.F., Forney L.J., et al. An exploratory study of associations with spontaneous preterm birth in primigravid pregnant women with a normal cervical length // J Matern Fetal Neonatal Med. 2022. Vol. 35, N 205. P. 5383–5388. doi: 10.1080/14767058.2021.1879786

[41]

Sprong KE, Mabenge M, Wright CA, et al. Ureaplasma species and preterm birth: current perspectives. Crit Rev Microbiol. 2020;46(2):169–181. doi: 10.1080/1040841X.2020.1736986

[42]

Sprong K.E., Mabenge M., Wright C.A., et al. Ureaplasma species and preterm birth: current perspectives // Crit Rev Microbiol. 2020. Vol. 46, N 2. P. 169–181. doi: 10.1080/1040841X.2020.1736986

[43]

Zhan C, Chen L, Hu L. Neonatal Ureaplasma parvum meningitis complicated with subdural hematoma: a case report and literature review. BMC Infect Dis. 2021;21(1):268. doi: 10.1186/s12879-021-05968-1

[44]

Zhan C., Chen L., Hu L. Neonatal Ureaplasma parvum meningitis complicated with subdural hematoma: a case report and literature review // BMC Infect Dis. 2021. Vol. 21, N 1. P. 268. doi: 10.1186/s12879-021-05968-1

[45]

Jonduo ME, Vallely LM, Wand H, et al. Adverse pregnancy and birth outcomes associated with Mycoplasma hominis, Ureaplasma urealyticum and Ureaplasma parvum: a systematic review and meta-analysis. BMJ Open. 2022;12(8):e062990. doi: 10.1136/bmjopen-2022-062990

[46]

Jonduo M.E., Vallely L.M., Wand H., et al. Adverse pregnancy and birth outcomes associated with Mycoplasma hominis, Ureaplasma urealyticum and Ureaplasma parvum: a systematic review and meta-analysis // BMJ Open. 2022. Vol. 12, N 8. ID: e062990. doi: 10.1136/bmjopen-2022-062990

RIGHTS & PERMISSIONS

Eсо-Vector

AI Summary AI Mindmap
PDF

46

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/