Ke-Chuan Wang, Christian Clement Yde, Heli Anglenius, Krista Salli, Wesley Morovic, Matthew Poore, Svetlana Gerdes, Sebastian Meier, Henrik Max Jensen, Pernille Rose Jensen
{"title":"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","authors":"Ke-Chuan Wang, Christian Clement Yde, Heli Anglenius, Krista Salli, Wesley Morovic, Matthew Poore, Svetlana Gerdes, Sebastian Meier, Henrik Max Jensen, Pernille Rose Jensen","doi":"10.1021/acsinfecdis.4c00796","DOIUrl":null,"url":null,"abstract":"<p><p>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, <i>Bifidobacterium animalis</i> spp. <i>lactis</i> (<i>B. lactis</i>) HN019 and <i>Lacticaseibacillus rhamnosus</i> (<i>L. rhamnosus</i>) HN001 and their effect against the bacterial pathogen <i>Shigella flexneri</i> 2457T (<i>S. flexneri</i>). The CFSs from <i>B. lactis</i> HN019 exhibited a higher antibacterial effect against <i>S. flexneri</i> growth than the CFSs from <i>L. rhamnosus</i> HN001, independent of the carbon source utilized. This effect correlated with higher formate within the CFSs from <i>B. lactis</i> HN019. As expected, the antimicrobial effects of CFSs were stronger against free <i>S. flexneri</i> cells than for <i>S. flexneri</i> 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 <i>S. flexneri</i> in the presence of <i>B. lactis</i> HN019 CFSs both in the solution and under biofilm-forming conditions. The synergistic effect between different components acting on <i>S. flexneri</i> gives reasons to believe that suitably designed mixtures of probiotic metabolic products and small-molecule effectors bear promise for successfully combating pathogens.</p>","PeriodicalId":17,"journal":{"name":"ACS Infectious Diseases","volume":" ","pages":"1424-1436"},"PeriodicalIF":3.8000,"publicationDate":"2025-06-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synergistic Effect of Formate and Cell-Free Supernatant Fermented by Two Probiotics, <i>Bifidobacterium animalis</i> spp. <i>lactis</i> HN019 and <i>Lacticaseibacillus rhamnosus</i> HN001, against <i>Shigella flexneri</i> Growth.\",\"authors\":\"Ke-Chuan Wang, Christian Clement Yde, Heli Anglenius, Krista Salli, Wesley Morovic, Matthew Poore, Svetlana Gerdes, Sebastian Meier, Henrik Max Jensen, Pernille Rose Jensen\",\"doi\":\"10.1021/acsinfecdis.4c00796\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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, <i>Bifidobacterium animalis</i> spp. <i>lactis</i> (<i>B. lactis</i>) HN019 and <i>Lacticaseibacillus rhamnosus</i> (<i>L. rhamnosus</i>) HN001 and their effect against the bacterial pathogen <i>Shigella flexneri</i> 2457T (<i>S. flexneri</i>). The CFSs from <i>B. lactis</i> HN019 exhibited a higher antibacterial effect against <i>S. flexneri</i> growth than the CFSs from <i>L. rhamnosus</i> HN001, independent of the carbon source utilized. This effect correlated with higher formate within the CFSs from <i>B. lactis</i> HN019. As expected, the antimicrobial effects of CFSs were stronger against free <i>S. flexneri</i> cells than for <i>S. flexneri</i> 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 <i>S. flexneri</i> in the presence of <i>B. lactis</i> HN019 CFSs both in the solution and under biofilm-forming conditions. The synergistic effect between different components acting on <i>S. flexneri</i> gives reasons to believe that suitably designed mixtures of probiotic metabolic products and small-molecule effectors bear promise for successfully combating pathogens.</p>\",\"PeriodicalId\":17,\"journal\":{\"name\":\"ACS Infectious Diseases\",\"volume\":\" \",\"pages\":\"1424-1436\"},\"PeriodicalIF\":3.8000,\"publicationDate\":\"2025-06-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Infectious Diseases\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1021/acsinfecdis.4c00796\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/5/15 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Infectious Diseases","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1021/acsinfecdis.4c00796","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/5/15 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
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.
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.