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阴道乳杆菌对双歧杆菌的益生元活性:从概念到配方。

Prebiotic Activity of Vaginal Lactobacilli on Bifidobacteria: from Concept to Formulation.

机构信息

Department of Pharmacy and Biotechnology, Alma Mater Studiorum, University of Bologna, Bologna, Italy.

Section of Microbiology, Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, Italy.

出版信息

Microbiol Spectr. 2023 Feb 14;11(1):e0200922. doi: 10.1128/spectrum.02009-22. Epub 2023 Jan 5.

DOI:10.1128/spectrum.02009-22
PMID:36602371
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9927276/
Abstract

The gut of babies born vaginally is rapidly colonized by spp. after birth, while in infants born by cesarean section (C-section), the presence of bifidobacteria drops dramatically, increasing the risk of developing gastrointestinal disorders. Considering that newborns naturally come into contact with maternal lactobacilli as they pass through the birth canal, the aim of this work is to exploit for the first time the bifidogenic activity exerted by the cell-free supernatants (CFSs) from lactobacilli of vaginal origin, belonging to the species Lactobacillus crispatus, Lactobacillus gasseri, Limosilactobacillus vaginalis, and Lactiplantibacillus plantarum. CFSs were recovered after 7 h, 13 h, and 24 h of fermentation and assessed for the ability to stimulate the planktonic growth and biofilms of strains belonging to species widely represented in the gut tract. A bifidogenic effect was observed for all CFSs; such activity was maximal for CFSs recovered in exponential phase and was strongly dependent on the species of lactobacilli. Importantly, no stimulating effects on an intestinal Escherichia coli strain were observed. CFSs from L. vaginalis BC17 showed the best bifidogenic profile since they increased bifidobacterial planktonic growth by up to 432% and biofilm formation by up to 289%. The CFS at 7 h from BC17 was successfully formulated with a hyaluronic acid-based hydrogel aimed at preventing and treating breast sores in lactating women and exerting bifidogenic activity in infants born mainly by C-section. Bifidobacteria in the gut tract of infants play crucial roles in the prevention of gastrointestinal diseases and the maturation of the immune system. Consequently, strategies to trigger a bifidogenic shift in the infant gut are highly desirable. Evidences suggest that the presence of a maternal vaginal microbiota dominated by health-promoting lactobacilli and the development of a bifidobacterium-enriched gut microbiota in newborns are interconnected. In this context, we found out that the cell-free supernatants from lactobacilli of vaginal origin were able to effectively stimulate the proliferation of spp. grown in free-floating and biofilm forms. The cell-free supernatant from BC17 showed excellent bifidogenic behavior, which was preserved even after its incorporation into a nipple formulation for lactating women. Lactobacilli derivatives, such as cell-free supernatants, have gained increasing interest by virtue of their safer profile than that of living cells and can be proposed as an ecosustainable approach to favor gut colonization of infants by bifidobacteria.

摘要

阴道自然分娩的婴儿肠道在出生后迅速被 spp 定植,而剖宫产(C -section)出生的婴儿双歧杆菌数量显著下降,增加了胃肠道疾病的发病风险。考虑到新生儿在通过产道时自然会接触到母体乳杆菌,本研究旨在首次利用阴道来源的乳杆菌(属于 Lactobacillus crispatus、Lactobacillus gasseri、Limosilactobacillus vaginalis 和 Lactiplantibacillus plantarum 物种)的无细胞上清液(CFS)发挥其双歧杆菌促生作用。CFS 在发酵 7 小时、13 小时和 24 小时后回收,并评估其刺激广泛存在于肠道中的 菌株浮游生长和生物膜形成的能力。所有 CFS 均显示出双歧杆菌促生作用;这种活性在指数生长期回收的 CFS 中最大,并强烈依赖于乳杆菌的种类。重要的是,未观察到对肠道大肠杆菌菌株的刺激作用。L. vaginalis BC17 的 CFS 显示出最佳的双歧杆菌特性,因为它们将双歧杆菌浮游生长增加了高达 432%,生物膜形成增加了高达 289%。成功地用透明质酸基水凝胶将 BC17 的 7 小时 CFS 制成配方,旨在预防和治疗哺乳期妇女的乳头疮,并在主要通过 C 节段出生的婴儿中发挥双歧杆菌促生作用。婴儿肠道中的双歧杆菌在预防胃肠道疾病和免疫系统成熟方面发挥着关键作用。因此,触发婴儿肠道中双歧杆菌转变的策略是非常可取的。有证据表明,以促进健康的乳杆菌为主导的母体阴道微生物群的存在以及新生儿中双歧杆菌丰富的肠道微生物群的发展是相互关联的。在这种情况下,我们发现阴道来源的乳杆菌的无细胞上清液能够有效地刺激游离浮游和生物膜形式生长的 spp 的增殖。BC17 的无细胞上清液表现出极好的双歧杆菌行为,即使将其掺入用于哺乳期妇女的乳头配方中,这种行为也得以保留。无细胞上清液等乳杆菌衍生物因其比活细胞更安全的特性而受到越来越多的关注,并且可以作为一种生态可持续的方法来促进双歧杆菌对婴儿肠道的定植。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0ba/9927276/abddd09d1cbb/spectrum.02009-22-f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0ba/9927276/064fcc50de0b/spectrum.02009-22-f001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0ba/9927276/1bd0d77248db/spectrum.02009-22-f004.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0ba/9927276/064fcc50de0b/spectrum.02009-22-f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0ba/9927276/48f5b51cf42d/spectrum.02009-22-f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0ba/9927276/2d6e3a2db4d1/spectrum.02009-22-f003.jpg
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