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Enterococcus faecium C171: Modulating the Immune Response to Acute Lethal Viral Challenge

International journal of antimicrobial agents(2023)

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摘要
Commensal bacteria modulate acute immune responses to infection in hosts. In this study, Enterococcus faecium C171 was screened and isolated. This strain has similar basic characteristics to the reference pro-biotic, including strong anti-inflammatory and anti-infective effects. E. faecium C171 inhibits the produc-tion of pro-Caspase-1 and significantly reduces the production of interleukin-1 beta (IL-1 beta) in vitro. These reactions were confirmed using the Transwell system. Live E. faecium C171 mainly exerted an inhibitory effect on acute inflammation, whereas the anti-infective and immune-activating effects were primarily mediated by the E. faecium C171-produced bacterial extracellular vesicles (Efm-C171-BEVs). Furthermore, in the specific pathogen-free (SPF) chicken model, oral administration of E. faecium C171 increased the relative abundance of beneficial microbiota (Enterococcus and Lactobacillus), particularly Enterococcus, the most important functional bacteria of the gut microbiota. E. faecium C171 significantly inhibited the acute inflammatory response induced by a highly virulent infectious disease, and reduced mortality in SPF chickens by 75%. In addition, E. faecium C171 induced high levels of CD3+ ,CD4-, and CD8- immunoreg- ulatorycells and CD8+ killer T cells, and significantly improved the proliferative activity of T cells in peripheral blood mononuclear cells, and the secretion of interferon-gamma. These findings indicate that E. fae-cium C171 and Efm-C171-BEVs are promising candidates for adjuvant treatment of acute inflammatory diseases and acute viral infections.(c) 2023 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license ( http://creativecommons.org/licenses/by-nc-nd/4.0/ )
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关键词
Probiotics,Enterococcus faecium,Acute inflammation,Anti-inflammatory,Anti-infective,Immunomodulatory,Infectious bursal disease virus,IBDV,Bacterial extracellular vesicles
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