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源自乳酸杆菌的细胞外囊泡增强宿主对耐万古霉素肠球菌的免疫反应。

Lactobacillus-derived extracellular vesicles enhance host immune responses against vancomycin-resistant enterococci.

作者信息

Li Ming, Lee Kiho, Hsu Min, Nau Gerard, Mylonakis Eleftherios, Ramratnam Bharat

机构信息

Division of Infectious Diseases, The Warren Alpert Medical School of Brown University, Providence, RI, 02903, USA.

COBRE Center for Cancer Research, Rhode Island Hospital, Warren Alpert Medical School of Brown University, Providence, RI, 02903, USA.

出版信息

BMC Microbiol. 2017 Mar 14;17(1):66. doi: 10.1186/s12866-017-0977-7.

Abstract

BACKGROUND

Probiotic bacteria are known to modulate host immune responses against various pathogens. Recently, extracellular vesicles (EVs) have emerged as potentially important mediators of host-pathogen interactions. In this study, we explored the role of L. plantarum derived EVs in modulating host responses to vancomycin-resistant Enterococcus faecium (VRE) using both Caenorhabditis elegans and human cells.

RESULTS

Our previous work has shown that probiotic conditioning C. elegans with L. acidophilus NCFM prolongs the survival of nematodes exposed to VRE. Similarly, L. plantarum WCFS1 derived extracellular vesicles (LDEVs) also significantly protected the worms against VRE infection. To dissect the molecular mechanisms of this EV-induced protection, we found that treatment of C. elegans with LDEVs significantly increased the transcription of host defense genes, cpr-1 and clec-60. Both cpr-1 and clec-60 have been previously reported to have protective roles against bacterial infections. Incubating human colon-derived Caco-2 cells with fluorescent dye-labeled LDEVs confirmed that LDEVs could be transported into the mammalian cells. Furthermore, LDEV uptake was associated with significant upregulation of CTSB, a human homologous gene of cpr-1, and REG3G, a human gene that has similar functions to clec-60.

CONCLUSIONS

We have found that EVs produced from L. plantarum WCFS1 up-regulate the expression of host defense genes and provide protective effects on hosts. Using probiotic-derived EVs instead of probiotic bacteria themselves, this study provides a new direction to treat antimicrobial resistant pathogens, such as VRE.

摘要

背景

已知益生菌可调节宿主针对各种病原体的免疫反应。最近,细胞外囊泡(EVs)已成为宿主-病原体相互作用中潜在的重要介质。在本研究中,我们使用秀丽隐杆线虫和人类细胞探索了植物乳杆菌衍生的细胞外囊泡在调节宿主对耐万古霉素屎肠球菌(VRE)反应中的作用。

结果

我们之前的工作表明,用嗜酸乳杆菌NCFM对秀丽隐杆线虫进行益生菌预处理可延长暴露于VRE的线虫的存活时间。同样,植物乳杆菌WCFS1衍生的细胞外囊泡(LDEVs)也显著保护线虫免受VRE感染。为了剖析这种由细胞外囊泡诱导的保护作用的分子机制,我们发现用LDEVs处理秀丽隐杆线虫可显著增加宿主防御基因cpr-1和clec-60的转录。先前已有报道称,cpr-1和clec-60均对细菌感染具有保护作用。用荧光染料标记的LDEVs孵育人结肠来源的Caco-2细胞证实,LDEVs可被转运到哺乳动物细胞中。此外,LDEVs的摄取与CTSB(cpr-1的人类同源基因)和REG3G(与clec-60具有相似功能的人类基因)的显著上调有关。

结论

我们发现植物乳杆菌WCFS1产生的细胞外囊泡上调宿主防御基因的表达并对宿主提供保护作用。本研究使用益生菌衍生的细胞外囊泡而非益生菌本身,为治疗耐抗菌性病原体(如VRE)提供了一个新方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a198/5348868/c679f3c961c5/12866_2017_977_Fig1_HTML.jpg

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