Lyu Jinli, Gao Mengyu, Zhao Shaowei, Liu Xinyang, Zhao Xinlong, Zou Yuanqiang, Zhong Yiyi, Ge Lan, Zhang Hiafeng, Huang Liting, Fan Shangrong, Xiao Liang, Zhang Xiaowei
Department of Obstetrics and Gynecology, Peking University Shenzhen Hospital, Shenzhen, 518036, China.
BGI-Shenzhen, Shenzhen, 518083, China.
Heliyon. 2024 Apr 30;10(9):e30495. doi: 10.1016/j.heliyon.2024.e30495. eCollection 2024 May 15.
Vaginitis, characterized by pathogenic invasion and a deficiency in beneficial lactobacilli, has recognized lactobacilli supplementation as a novel therapeutic strategy. However, due to individual differences in vaginal microbiota, identifying universally effective strains is challenging. Traditional methodologies for probiotic selection, which heavily depend on extensive experiments, are both time-intensive and laborious. The aim of this study was to pinpoint possible vaginal probiotic candidates based on whole-genome screening. We sequenced the genomes of 98 previously isolated strains, annotating their genes involved in probiotic metabolite biosynthesis, adherence, acid/bile tolerance, and antibiotic resistance. A scoring system was used to assess the strains based on their genomic profiles. The highest-scoring strains underwent further evaluation. Consequently, two strains, LG55-27 and TM13-16, displayed an outstanding ability to produce d-lactate and adhere to human vaginal epithelial cells. They also showed higher antimicrobial activity against , , , and compared to reference strains. Their resilience to acid and bile environments highlights the potential for oral supplementation. Oral and vaginal administration of these two strains were tested in a bacterial vaginosis (BV) rat model at various doses. Results indicated that combined vaginal administration of these strains at 1 × 10 CFU/day significantly mitigated BV in rats. This research offers a probiotic dosage guideline for vaginitis therapy, underscoring an efficient screening process for probiotics using genome sequencing, testing, and BV model experimentation.
阴道炎以病原体入侵和有益乳酸杆菌缺乏为特征,已将补充乳酸杆菌作为一种新的治疗策略。然而,由于阴道微生物群的个体差异,识别普遍有效的菌株具有挑战性。传统的益生菌选择方法严重依赖大量实验,既耗时又费力。本研究的目的是基于全基因组筛选确定可能的阴道益生菌候选菌株。我们对98株先前分离的菌株进行了基因组测序,注释了它们参与益生菌代谢物生物合成、黏附、耐酸/耐胆汁和抗生素抗性的基因。使用评分系统根据菌株的基因组概况对其进行评估。得分最高的菌株进行了进一步评估。因此,LG55 - 27和TM13 - 16这两株菌株表现出出色的产生d - 乳酸和黏附人阴道上皮细胞的能力。与参考菌株相比,它们对[此处缺失具体细菌名称]也表现出更高的抗菌活性。它们对酸和胆汁环境的耐受性突出了口服补充的潜力。在细菌性阴道病(BV)大鼠模型中对这两株菌株进行了不同剂量的口服和阴道给药测试。结果表明,以1×10[此处缺失具体单位]CFU/天的剂量联合阴道给药这些菌株可显著减轻大鼠的BV。本研究为阴道炎治疗提供了益生菌剂量指南,强调了使用基因组测序、测试和BV模型实验对益生菌进行高效筛选的过程。