The interrelation between microbial immunoglobulin coating, vaginal microbiota, ethnicity, and preterm birth.

IF 13.8 1区 生物学 Q1 MICROBIOLOGY Microbiome Pub Date : 2024-05-28 DOI:10.1186/s40168-024-01787-z
H J Schuster, A C Breedveld, S P F Matamoros, R van Eekelen, R C Painter, M Kok, P J Hajenius, P H M Savelkoul, M van Egmond, R van Houdt
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Abstract

Background: Vaginal microbiota composition is associated with spontaneous preterm birth (sPTB), depending on ethnicity. Host-microbiota interactions are thought to play an important underlying role in this association between ethnicity, vaginal microbiota and sPTB.

Methods: In a prospective cohort of nulliparous pregnant women, we assessed vaginal microbiota composition, vaginal immunoglobulins (Igs), and local inflammatory markers. We performed a nested case-control study with 19 sPTB cases, matched based on ethnicity and midwifery practice to 19 term controls.

Results: Of the 294 included participants, 23 pregnancies ended in sPTB. We demonstrated that Lactobacillus iners-dominated microbiota, diverse microbiota, and ethnicity were all independently associated with sPTB. Microbial Ig coating was associated with both microbiota composition and ethnicity, but a direct association with sPTB was lacking. Microbial IgA and IgG coating were lowest in diverse microbiota, especially in women of any ethnic minority. When correcting for microbiota composition, increased microbial Ig coating correlated with increased inflammation.

Conclusion: In these nulliparous pregnant women, vaginal microbiota composition is strongly associated with sPTB. Our results support that vaginal mucosal Igs might play a pivotal role in microbiota composition, microbiota-related inflammation, and vaginal community disparity within and between ethnicities. This study provides insight in host-microbe interaction, suggesting that vaginal mucosal Igs play an immunomodulatory role similar to that in the intestinal tract. Video Abstract.

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微生物免疫球蛋白涂层、阴道微生物群、种族与早产之间的相互关系。
背景:阴道微生物群的组成与自发性早产(sPTB)有关,这取决于种族。宿主与微生物群之间的相互作用被认为在种族、阴道微生物群与自发性早产(sPTB)之间的关系中起着重要的潜在作用:方法:我们在一个无阴道孕妇前瞻性队列中评估了阴道微生物群的组成、阴道免疫球蛋白(Igs)和局部炎症标记物。我们对 19 例 sPTB 病例进行了巢式病例对照研究,并根据种族和助产实践与 19 例足月对照组进行了配对:结果:在纳入的 294 名参与者中,有 23 名孕妇最终患上了母婴传播性肺炎。我们发现,以乳酸杆菌为主的微生物群、多样化的微生物群和种族都与母婴传播性肺结核有独立的关联。微生物 Ig 涂层与微生物群组成和种族都有关系,但与 sPTB 没有直接联系。微生物 IgA 和 IgG 涂层在多样化微生物群中最低,尤其是在少数民族妇女中。当校正微生物群组成时,微生物 Ig 涂层的增加与炎症的增加相关:结论:在这些无阴道的孕妇中,阴道微生物群的组成与 sPTB 密切相关。我们的研究结果表明,阴道粘膜 Igs 可能在微生物群组成、微生物群相关炎症以及种族内和种族间阴道群落差异中起着关键作用。这项研究深入揭示了宿主与微生物之间的相互作用,表明阴道粘膜Igs发挥着与肠道类似的免疫调节作用。视频摘要。
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来源期刊
Microbiome
Microbiome MICROBIOLOGY-
CiteScore
21.90
自引率
2.60%
发文量
198
审稿时长
4 weeks
期刊介绍: Microbiome is a journal that focuses on studies of microbiomes in humans, animals, plants, and the environment. It covers both natural and manipulated microbiomes, such as those in agriculture. The journal is interested in research that uses meta-omics approaches or novel bioinformatics tools and emphasizes the community/host interaction and structure-function relationship within the microbiome. Studies that go beyond descriptive omics surveys and include experimental or theoretical approaches will be considered for publication. The journal also encourages research that establishes cause and effect relationships and supports proposed microbiome functions. However, studies of individual microbial isolates/species without exploring their impact on the host or the complex microbiome structures and functions will not be considered for publication. Microbiome is indexed in BIOSIS, Current Contents, DOAJ, Embase, MEDLINE, PubMed, PubMed Central, and Science Citations Index Expanded.
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