Микробиом влагалища у беременных с преждевременным разрывом плодных оболочек в сроке от 22 до 28 недель беременности

1. Proctor L., Lo Tempio J., Marquitz A., Daschner P., Xi D., Flores R. et al. NIH Human Microbiome Portfolio Analysis Team. A review of 10 years of human microbiome research activities at the US National Institutes of Health, Fiscal Years 2007-2016. Microbiome. 2019; 7(1): 31. https://dx.doi.org/10.1186/s40168-019-0620-y.
2. Paramel Jayaprakash T., Wagner E.C., van Schalkwyk J., Albert A.Y., Hill J.E., Money D.M.; PPROM Study Group. High diversity and variability in the vaginal microbiome in women following preterm premature rupture of membranes (PPROM): a prospective cohort study. PLoS One. 2016; 11(11): e0166794. https://dx.doi.org/10.1371/journal.pone.0166794.
3. Petricevic L., Domig K.J., Nierscher F.J., Sandhofer M.J., Fidesser M., Kron-dorfer I. et al. Characterisation of the vaginal Lactobacillus microbiota associated with preterm delivery. Sci. Rep. 2014; 4: 5136. https://dx.doi.org/10.1038/srep05136.
4. Romero R., Hassan S.S., Gajer P., Tarca A.L., Fadrosh D.W., Bieda J. et al. The vaginal microbiota of pregnant women who subsequently have spontaneous preterm labor and delivery and those with a normal delivery at term. Microbiome. 2014; 2: 18. https://dx.doi.org/10.1186/2049-2618-2-18.
5. DiGiulio D.B., Callahan B.J., McMurdie P.J., Costello E.K., Lyell D.J., Robaczewska A. et al. Temporal and spatial variation of the human microbiota during pregnancy. Proc. Natl. Acad. Sci. USA. 2015; 112(35): 11060-5. https://dx.doi.org/10.1073/pnas.1502875112.
6. R Core Team. R: a language and environment for statistical computing. R Foundation for Statistical Computing. Vienna, Austria; 2018. Available at: https://www.gbif.org/ru/tool/81287/r-a-language-and-environment-for-statistical-computing
7. Callahan B.J., McMurdie P.J., Rosen M.J., Han A.W., Johnson A.J., Holmes S.P. DADA2: High-resolution sample inference from Illumina amplicon data. Nat. Methods. 2016; 13(7): 581-3. https://dx.doi.org/10.1038/nmeth.3869.
8. Quast C., Pruesse E., Yilmaz P., Gerken J., Schweer T., Yarza P. et al. The SILVA ribosomal RNA gene database project: improved data processing and web-based tools. Nucleic Acids Res. 2013; 41(Database issue): D590-6. https://dx.doi.org/10.1093/nar/gks1219.
9. Ходжаева З.С., Припутневич Т.В., Муравьева В.В., Гусейнова Г.Э., Горина К.А., Мишина Н.Д. Оценка состава и стабильности микробиоты влагалища у беременных в процессе динамического наблюдения. Акушерство и гинекология. 2019; 7: 30-8.
10. Ragaliauskas T., Plečkaitytė M., Jankunec M., Labanauskas L., Baranauskiene L., Valincius G. Inerolysin and vaginolysin, the cytolysins implicated in vaginal dysbiosis, differently impair molecular integrity of phospholipid membranes. Sci. Rep. 2019; 9(1): 10606. https://dx.doi.org/10.1038/s41598-019-47043-5.
11. Mehta R., Arya R., Goyal K., Singh M., Sharma A.K. Bio-preservative and therapeutic potential of pediocin: recent trends and future perspectives. Recent Pat. Biotechnol. 2013; 7(3): 172-8. https://dx.doi.org/10.2174/18722083113076660008.
12. Kaur B., Garg N., Sachdev A., Kumar B. Effect of the oral intake of probi-otic Pediococcus acidilactici BA28 on Helicobacter pylori causing peptic ulcer in C57BL/6 mice models. Appl. Bochem. Biotechnol. 2014; 172(2): 973-83. https://dx.doi.org/10.1007/s12010-013-0585-4.
13. Ходжаева З.С., Гусейнова Г.Э., Муравьева В.В., Донников А.Е., Мишина Н.Д., Припутневич Т.В. Характеристика микробиоты влагалища у беременных с досрочным преждевременным разрывом плодных оболочек. Акушерство и гинекология. 2019; 12: 66-74.
14. Henderson G., Yilmaz P., Kumar S., Forster R.J., Kelly W.J, Leahy S.C. et al. Improved taxonomic assignment of rumen bacterial 16S rRNA sequences using a revised SILVA taxonomic framework. PeerJ. 2019; 7: e6496. https://dx.doi.org/ 10.7717/peerj.6496.
15. Doyle R.M., Harris K., Kamiza S., Harjunmaa U., Ashorn U., Nkhoma M. et al. Bacterial communities found in placental tissues are associated with severe chorioamnionitis and adverse birth outcomes. PLoS One. 2017; 12(7): e0180167. https://dx.doi.org/10.1371/journal.pone.0180167.
16. Doyle R.M., Alber D.G., Jones H.E., Harris K., Fitzgerald F., Peebles D. et al. Term and preterm labour are associated with distinct microbial community structures in placental membranes which are independent of mode of delivery. Placenta. 2014; 35(12): 1099-101. https://dx.doi.org/10.1016/j.placenta.2014.10.007.
17. Wang X., Buhimschi C.S., Temoin S., Bhandari V., Han Y.W., Buhimschi I.A. Comparative microbial analysis of paired amniotic fluid and cord blood from pregnancies complicated by preterm birth and early-onset neonatal sep-sis. PLoS One. 2013; 8(2): e56131. https://dx.doi.org/10.1371/journal.pone.0056131.
18. Gonzales-Marin C., Spratt D.A., Allaker R.P. Maternal oral origin of Fuso-bacterium nucleatum in adverse pregnancy outcomes as determined using the 16S-23S rRNA gene intergenic transcribed spacer region. J. Med. Microbiol. 2013; 62(Pt. 1): 133-44. https://dx.doi.org/10.1099/jmm.0.049452-0.
19. Vander Haar E.L., So J., Gyamfi-Bannerman C., Han Y.W. Fusobacterium nucleatum and adverse pregnancy outcomes: epidemiological and mechanistic evidence. Anaerobe. 2018; 50: 55-9. https://dx.doi.org/10.1016/j.anaerobe.2018.01.008.
20. Romero R., Hassan S.S., Gajer P., Tarca A.L, Fadrosh D.W., Nikita L. 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. https://dx.doi.org/10.1186/2049-2618-2-4.
21. Carlstein C., Søes L.M., Christensen J.J. Aerococcus christensenii as part of severe polymicrobial chorioamnionitis in a pregnant woman. Open Microbiol. J. 2016; 10: 27-31. https://dx.doi.org/10.2174/1874285801610010027.
22. Nicholson A.C., Bell M., Humrighouse B.W., McQuiston J.R. Complete genome sequences for two strains of a novel fastidious, partially acid-fast, gram-positive Corynebacterineae bacterium, derived from human clinical samples. Genome Announc. 2015; 3(6): e01462-15. https://dx.doi.org/10.1128/ genomeA.01462-15.
23. Bell M.E., Bernard K.A., Harrington S.M., Patel N.B., Tucker T.A., Metcalfe M.G. et al. Lawsonella clevelandensis gen. nov., sp. nov., a new member of the suborder Corynebacterineae isolated from human abscesses. Int. J. Syst. Evol. Microbiol. 2016; 66(8): 2929-35. https://dx.doi.org/10.1099 / ijsem.0.001122.
24. Hiippala K., Kainulainen V., Kalliomäki M., Arkkila P., Satokari R. Mucosal prevalence and interactions with the epithelium indicate commensalism of Sutterella spp. Front. Microbiol. 2016; 7: 1706. https://dx.doi.org/10.3389/ fmicb.2016.01706.
25. Balle C., Lennard K., Dabee S., Barnabas S.L., Jaumdally S.Z., Gasper M.A. et al. Endocervical and vaginal microbiota in South African adolescents with asymptomatic Chlamydia trachomatis infection. Sci. Rep. 2018; 8(1): 11109. https://dx.doi.org/10.1038/s41598-018-29320-x.
26. Подгорная А.В., Maхмутходжаев А.Ш., Михеенко Г.А. Микрофлора влагалища при бактериальном вагинозе у беременных женщин. Современные проблемы науки и образования. 2015; 6; 212.
27. Amabebe E., Chapman D.R., Stern V.L., Stafford G., Anumba D.O.C. Mid-gestational changes in cervicovaginal fluid cytokine levels in asymptomatic pregnant women are predictive markers of inflammation-associated spontaneous preterm birth. J. Reprod. Immunol. 2018; 126: 1-10. https://dx.doi.org/10.1016/j.jri.2018.01.001.
28. Zhu L., Luo F., Hu W., Han Y., Wang Y., Zheng H. et al. Bacterial communities in the womb during healthy pregnancy. Front. Microbiol. 2018; 9: 2163. https://dx.doi.org/10.3389/fmicb.2018.02163.

Поступила 25.08.2020

Принята в печать 09.11.2020