Characterization of Amniotic Fluid Ureaplasma Species from Pregnancies Complicated by Preterm Prelabor Rupture of Membranes
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články
Grantová podpora
a long-term developmental plan
Fakultní nemocnice Hradec Králové
PubMed
39317888
DOI
10.1007/s43032-024-01697-3
PII: 10.1007/s43032-024-01697-3
Knihovny.cz E-zdroje
- Klíčová slova
- Genital mycoplasma, Microbial invasion of the amniotic cavity, Molecular biology, Mollicutes, Morbidity, Neonates, Preterm delivery, Sequencing,
- MeSH
- DNA bakterií analýza genetika MeSH
- dospělí MeSH
- fylogeneze MeSH
- gestační stáří MeSH
- infekční komplikace v těhotenství mikrobiologie MeSH
- lidé MeSH
- multilokusová sekvenční typizace * MeSH
- plodová voda * mikrobiologie MeSH
- předčasný odtok plodové vody * mikrobiologie MeSH
- retrospektivní studie MeSH
- těhotenství MeSH
- Ureaplasma * genetika izolace a purifikace MeSH
- ureaplasmatické infekce * mikrobiologie MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- těhotenství MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- DNA bakterií MeSH
The main aim of this study was to determine expanded sequence types (eSTs) of Ureaplasma species (U. spp.). DNA isolated from the amniotic fluid of pregnancies complicated by preterm prelabor rupture of membranes (PPROM) using an expanded multilocus sequence typing scheme. Additionally, the study sought to examine whether phylogenetic subgroups of U. spp. DNA differ with respect to maternal demographic and clinical parameters and selected aspects of short-term neonatal morbidity. This retrospective cohort study was focused on singleton pregnancies complicated by PPROM occurring between the gestational ages of 24+0 and 36+6 weeks, where amniocentesis was conducted to assess the intra-amniotic environment and the presence of U. spp. DNA in the amniotic fluid samples was confirmed. The stored aliquots of U. spp. DNA were used to assess differences in nucleotide sequences in six U. spp. genes (ftsH, rpL22, valS, thrS,ureG, and mba-np1) using the eMLST scheme. The expanded multilocus sequence typing scheme was performed in 73 samples of U. spp. DNA isolated from pregnancies complicated by PPROM. In total, 33 different U. spp. DNA eSTs were revealed, 21 (#20, 233-244, 248-251, 253, 255, 259, and 262) of which were novel. The most frequently identified eST was #41, identified in 18% (13/73) of the aliquots. Based on their genetic relationships, the U. spp. DNA was divided into two clusters and four subgroups [cluster I (U. parvum): A, 43% (n = 31); B, 15% (n = 11); and C, 26% (n = 19); cluster II (U. urealyticum): 1; 16% (n = 12)]. Cluster II had a higher rate of polymicrobial findings than cluster I (58% vs 16%; p = 0.005), while subgroup A had the highest rate of concomitant Mycoplasma hominis in the amniotic fluid samples (66%; p = 0.04). In conclusion, Ureaplasma spp. DNA obtained from PPROM consisted of 33 different eSTs of U. spp. DNA. No differences in maternal and neonatal characteristics were found among the phylogenetical subgroups of U. spp. DNA, except for a higher rate of polymicrobial amniotic fluid findings in those with U. urealyticumand the concomitant presence of M. hominis in the amniotic fluid in those with the presence of U. parvum.
Department of Obstetrics and Gynecology Hospital Most Krajska Zdravotni a s Most Czech Republic
Generi Biotech Hradec Kralove Czech Republic
Institute of Clinical Microbiology University Hospital Hradec Kralove Czech Republic
Zobrazit více v PubMed
Mercer BM. Preterm premature rupture of the membranes. Obstet Gynecol. 2003;101(1):178–93. PubMed
Mercer BM. Preterm premature rupture of the membranes: current approaches to evaluation and management. Obstet Gynecol Clin North Am. 2005;32(3):411–28. PubMed DOI
Johanzon M, et al. Extreme preterm birth: onset of delivery and its effect on infant survival and morbidity. Obstet Gynecol. 2008;111(1):42–50. PubMed DOI
Menon R, et al. Novel pathways of inflammation in human fetal membranes associated with preterm birth and preterm pre-labor rupture of the membranes. Semin Immunopathol. 2020;42(4):431–50. PubMed DOI PMC
DiGiulio DB, et al. Prevalence and diversity of microbes in the amniotic fluid, the fetal inflammatory response, and pregnancy outcome in women with preterm pre-labor rupture of membranes. Am J Reprod Immunol. 2010;64(1):38–57. PubMed DOI PMC
Kacerovsky M, et al. Clinical characteristics of colonization of the amniotic cavity in women with preterm prelabor rupture of membranes, a retrospective study. Sci Rep. 2022;12(1):5062. PubMed DOI PMC
Kacerovsky M, et al. Amniotic fluid protein profiles of intraamniotic inflammatory response to Ureaplasma spp. and other bacteria. PLoS ONE. 2013;8(3):e60399. PubMed DOI
Noda-Nicolau NM, 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. PubMed DOI PMC
Sprong KE, et al. Ureaplasma species and preterm birth: current perspectives. Crit Rev Microbiol. 2020;46(2):169–81. PubMed DOI
Schelonka RL, Waites KB. Ureaplasma infection and neonatal lung disease. Semin Perinatol. 2007;31(1):2–9. PubMed DOI
Zhang J, et al. Development of a multilocus sequence typing scheme for Ureaplasma. Eur J Clin Microbiol Infect Dis. 2014;33(4):537–44. PubMed DOI
Zhang J, et al. Correlation between Ureaplasma subgroup 2 and genitourinary tract disease outcomes revealed by an expanded multilocus sequence typing (eMLST) scheme. PLoS ONE. 2014;9(8):e104347. PubMed DOI PMC
Jacobsson B, et al. Quantification of Ureaplasma urealyticum DNA in the amniotic fluid from patients in PTL and pPROM and its relation to inflammatory cytokine levels. Acta Obstet Gynecol Scand. 2009;88(1):63–70. PubMed DOI
Kasper DC, et al. The bacterial load of Ureaplasma parvum in amniotic fluid is correlated with an increased intrauterine inflammatory response. Diagn Microbiol Infect Dis. 2010;67(2):117–21. PubMed DOI
Kacerovsky M, et al. The microbial load with genital mycoplasmas correlates with the degree of histologic chorioamnionitis in preterm PROM. Am J Obstet Gynecol. 2011;205(3):e2131–7. DOI
Kacerovsky M, et al. The impact of the microbial load of genital mycoplasmas and gestational age on the intensity of intraamniotic inflammation. Am J Obstet Gynecol. 2012;206(4):e3421–8. DOI
Rittenschober-Bohm J, et al. Vaginal Ureaplasma parvum serovars and spontaneous preterm birth. Am J Obstet Gynecol. 2019;220(6):e5941–9. DOI
Kim M, et al. Biovar diversity of Ureaplasma urealyticum in amniotic fluid: distribution, intrauterine inflammatory response and pregnancy outcomes. J Perinat Med. 2003;31(2):146–52. PubMed DOI
Stranik J, et al. IgGFc-binding protein in pregnancies complicated by spontaneous preterm delivery: a retrospective cohort study. Sci Rep. 2021;11(1):6107. PubMed DOI PMC
Kacerovsky M, et al. Prevalence and load of cervical Ureaplasma species with respect to intra-amniotic complications in women with preterm prelabor rupture of membranes before 34 weeks. Front Pharmacol. 2022;13:860498. PubMed DOI PMC
Kacerovsky M, et al. Intra-amniotic infection and sterile intra-amniotic inflammation in women with preterm labor with intact membranes are associated with a higher rate of Ureaplasma species DNA presence in the cervical fluid. J Matern Fetal Neonatal Med. 2022;35(25):7344–52. PubMed DOI
Jolley KA, Bray JE, Maiden MCJ. Open-access bacterial population genomics: BIGSdb software, the PubMLST.org website and their applications. Wellcome Open Res. 2018;3:124. PubMed DOI
Team RC. R: a language and environment for statistical computing. 2023.
Pagés H, et al. Biostrings: efficient manipulation of biological strings. 2023.
Wickham H, et al. Welcome to the Tidyverse. J Open Source Softw. 2019;4(43):1686. DOI
Paradis E, Schliep K. Ape 5.0: an environment for modern phylogenetics and evolutionary analyses in R. Bioinformatics. 2019;35(3):526–8. PubMed DOI
Xu S, et al. Ggtree: a serialized data object for visualization of a phylogenetic tree and annotation data. iMeta. 2022;1(4):e56. PubMed DOI
Ruan Z, et al. Clonality and distribution of clinical Ureaplasma isolates recovered from male patients and infertile couples in China. PLoS ONE. 2017;12(8):e0183947. PubMed DOI
Yang T, et al. Clonal diversity of Ureaplasma species and its relationship with oligozoospermia and semen quality in Chinese infertile males. Eur J Clin Microbiol Infect Dis. 2018;37(10):1957–63. PubMed DOI
Kong Y, et al. Correlation between Ureaplasma spp. sub-group 1 and preterm pre-labour rupture of membranes revealed by an eMLST scheme. Infect Genet Evol. 2019;68:172–6. PubMed DOI
Tantengco OAG, Menon R. Breaking down the barrier: the role of cervical infection and inflammation in preterm birth. Front Glob Womens Health. 2021;2:777643. PubMed DOI
Oh KJ, et al. Intraamniotic infection with genital mycoplasmas exhibits a more intense inflammatory response than intraamniotic infection with other microorganisms in patients with preterm premature rupture of membranes. Am J Obstet Gynecol. 2010;203(3):e2111–8. DOI
Matulova J, et al. Birth weight and intra-amniotic inflammatory and infection-related complications in pregnancies with preterm prelabor rupture of membranes: a retrospective cohort study. J Matern Fetal Neonatal Med. 2022;35(25):7571–81. PubMed DOI
Yoneda N, et al. Polymicrobial amniotic fluid infection with mycoplasma/ureaplasma and other bacteria induces severe intra-amniotic inflammation associated with poor perinatal prognosis in preterm labor. Am J Reprod Immunol. 2016;75(2):112–25. PubMed DOI
Noda-Nicolau NM, et al. Combinations and loads of bacteria affect the cytokine production by fetal membranes: an in vitro study. Am J Reprod Immunol. 2016;76(6):504–11. PubMed DOI
Noda-Nicolau NM, et al. Polybacterial stimulation suggests discrete IL-6/IL-6R signaling in human fetal membranes: potential implications on IL-6 bioactivity. J Reprod Immunol. 2018;126:60–8. PubMed DOI
Kwak DW, et al. Co-infection with vaginal Ureaplasma urealyticum and Mycoplasma hominis increases adverse pregnancy outcomes in patients with preterm labor or preterm premature rupture of membranes. J Matern Fetal Neonatal Med. 2014;27(4):333–7. PubMed DOI
Andrade Y, et al. Multilocus sequence typing characterizes diversity of Ureaplasma diversum strains, and intra-species variability induces different immune response profiles. BMC Vet Res. 2020;16(1):163. PubMed DOI PMC
Sung TJ, et al. Frequency of ureaplasma serovars in respiratory secretions of preterm infants at risk for bronchopulmonary dysplasia. Pediatr Infect Dis J. 2011;30(5):379–83. PubMed DOI PMC