动物乳酸双歧杆菌HN019和鼠李糖乳杆菌HN001发酵甲酸盐和无细胞上清液对福氏志贺氏菌生长的协同作用

IF 3.8 2区 医学 Q2 CHEMISTRY, MEDICINAL
ACS Infectious Diseases Pub Date : 2025-06-13 Epub Date: 2025-05-15 DOI:10.1021/acsinfecdis.4c00796
Ke-Chuan Wang, Christian Clement Yde, Heli Anglenius, Krista Salli, Wesley Morovic, Matthew Poore, Svetlana Gerdes, Sebastian Meier, Henrik Max Jensen, Pernille Rose Jensen
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引用次数: 0

摘要

益生菌代谢物、宿主健康和病原体抑制之间的相互作用越来越引起人们的兴趣,但由于这些因素之间复杂的分子相互作用,仍未得到解决。研究了乳酸双歧杆菌HN019和鼠李糖乳杆菌HN001两种益生菌的无细胞上清液(CFSs)对致病菌福氏志贺氏2457T (S. flexneri)的抑制作用。与碳源无关,B. lactis HN019的CFSs对S. flexneri的抑菌效果优于L. rhamnosus HN001。这种效应与乳酸菌HN019的CFSs中较高的甲酸有关。正如预期的那样,CFSs对游离的flexneri菌的抗菌作用强于对感染宿主细胞的flexneri菌的抗菌作用。结果表明,cfs与吲哚-3-乳酸酯和甲酸酯等有机小分子具有协同作用。CFSs与吲哚-3-乳酸和甲酸之间的相互作用反映在乳杆菌HN019 CFSs存在时,flexneri在溶液和生物膜形成条件下的代谢率改变。不同成分对flexneri的协同作用使我们有理由相信,适当设计的益生菌代谢产物和小分子效应物的混合物有望成功对抗病原体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synergistic Effect of Formate and Cell-Free Supernatant Fermented by Two Probiotics, Bifidobacterium animalis spp. lactis HN019 and Lacticaseibacillus rhamnosus HN001, against Shigella flexneri Growth.

The interplay between probiotic metabolites, host health, and inhibition of pathogens has increasingly attracted interest but remains unresolved due to the complex molecular interactions among these factors. We investigated the action of cell-free supernatants (CFSs) from two probiotic bacteria, Bifidobacterium animalis spp. lactis (B. lactis) HN019 and Lacticaseibacillus rhamnosus (L. rhamnosus) HN001 and their effect against the bacterial pathogen Shigella flexneri 2457T (S. flexneri). The CFSs from B. lactis HN019 exhibited a higher antibacterial effect against S. flexneri growth than the CFSs from L. rhamnosus HN001, independent of the carbon source utilized. This effect correlated with higher formate within the CFSs from B. lactis HN019. As expected, the antimicrobial effects of CFSs were stronger against free S. flexneri cells than for S. flexneri infecting host cells. A synergistic effect of the CFSs with additional small organic molecules such as indole-3-lactate and formate was found. Such interplay between CFSs, indole-3-lactate, and formate was reflected by altered metabolic rates by S. flexneri in the presence of B. lactis HN019 CFSs both in the solution and under biofilm-forming conditions. The synergistic effect between different components acting on S. flexneri gives reasons to believe that suitably designed mixtures of probiotic metabolic products and small-molecule effectors bear promise for successfully combating pathogens.

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来源期刊
ACS Infectious Diseases
ACS Infectious Diseases CHEMISTRY, MEDICINALINFECTIOUS DISEASES&nb-INFECTIOUS DISEASES
CiteScore
9.70
自引率
3.80%
发文量
213
期刊介绍: ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to: * Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials. * Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets. * Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance. * Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents. * Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota. * Small molecule vaccine adjuvants for infectious disease. * Viral and bacterial biochemistry and molecular biology.
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