Samit Kundu, Gonçalo Dos Santos Correia, Yun S Lee, Sherrianne Ng, Lynne Sykes, Denise Chan, Holly Lewis, Richard G Brown, Lindsay Kindinger, Anne Dell, Ten Feizi, Stuart M Haslam, Yan Liu, Julian R Marchesi, David A MacIntyre, Phillip R Bennett
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引用次数: 0
摘要
FUT2基因突变导致组织血型抗原在分泌的糖蛋白上缺乏表达,可能会塑造阴道微生物群,从而影响出生结果。为了验证这一点,我们分析了302名不同种族的孕妇的分泌物状态、阴道微生物群和妊娠长度之间的关系,其中包括82名早产孕妇。在非分泌性细菌中,发现产气乳杆菌和延氏乳杆菌与其他微生物类群有明显的共生模式。此外,在妊娠早期,乳酸菌缺乏高多样性阴道微生物群的非分泌型孕妇的妊娠长度明显短于乳酸菌占优势的非分泌型孕妇(平均241.54天(sd=47.14) vs . 266.21天(23.61);假定值= 0.0251)。阴道多样性高的非分泌物组与乳酸菌占优势的分泌物组的妊娠期差异相似(平均262.52天(SD=27.73);p值=0.0439)或衰竭(平均266.05天(SD=20.81);假定值= 0.0312)。我们的数据强调,在早产风险的背景下,分泌状态和血型抗原表达是阴道微生物-宿主相互作用的重要介质。
Secretor status is a modifier of vaginal microbiota-associated preterm birth risk.
Mutations in the FUT2 gene that result in a lack of expression of histo-blood group antigens on secreted glycoproteins may shape the vaginal microbiota with consequences for birth outcome. To test this, we analysed the relationship between secretor status, vaginal microbiota and gestational length in an ethnically diverse cohort of 302 pregnant women, including 82 who delivered preterm. Lactobacillus gasseri and L. jensenii were found to have distinct co-occurrence patterns with other microbial taxa in non-secretors. Moreover, non-secretors with Lactobacillus spp. depleted high diversity vaginal microbiota in early pregnancy had significantly shorter gestational length than Lactobacillus spp. dominated non-secretors (mean of 241.54 days (sd=47.14) versus 266.21 (23.61); P-value=0.0251). Similar gestational length differences were observed between non-secretors with high vaginal diversity and secretors with Lactobacillus spp. dominance (mean of 262.52 days (SD=27.73); p-value=0.0439) or depletion (mean of 266.05 days (SD=20.81); p-value=0.0312). Our data highlight secretor status and blood-group antigen expression as being important mediators of vaginal microbiota-host interactions in the context of preterm birth risk.
期刊介绍:
Microbial Genomics (MGen) is a fully open access, mandatory open data and peer-reviewed journal publishing high-profile original research on archaea, bacteria, microbial eukaryotes and viruses.