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微菌素介导炎症肠道中肠杆菌科细菌之间的竞争。

Microcins mediate competition among Enterobacteriaceae in the inflamed gut.

作者信息

Sassone-Corsi Martina, Nuccio Sean-Paul, Liu Henry, Hernandez Dulcemaria, Vu Christine T, Takahashi Amy A, Edwards Robert A, Raffatellu Manuela

机构信息

Department of Microbiology and Molecular Genetics, University of California Irvine, Irvine, California 92697, USA.

Institute for Immunology, University of California Irvine, Irvine, California 92697, USA.

出版信息

Nature. 2016 Dec 8;540(7632):280-283. doi: 10.1038/nature20557. Epub 2016 Oct 31.

Abstract

The Enterobacteriaceae are a family of Gram-negative bacteria that include commensal organisms as well as primary and opportunistic pathogens that are among the leading causes of morbidity and mortality worldwide. Although Enterobacteriaceae often comprise less than 1% of a healthy intestine's microbiota, some of these organisms can bloom in the inflamed gut; expansion of enterobacteria is a hallmark of microbial imbalance known as dysbiosis. Microcins are small secreted proteins that possess antimicrobial activity in vitro, but whose role in vivo has been unclear. Here we demonstrate that microcins enable the probiotic bacterium Escherichia coli Nissle 1917 (EcN) to limit the expansion of competing Enterobacteriaceae (including pathogens and pathobionts) during intestinal inflammation. Microcin-producing EcN limits the growth of competitors in the inflamed intestine, including commensal E. coli, adherent-invasive E. coli and the related pathogen Salmonella enterica. Moreover, only therapeutic administration of the wild-type, microcin-producing EcN to mice previously infected with S. enterica substantially reduced intestinal colonization by the pathogen. Our work provides the first evidence that microcins mediate inter- and intraspecies competition among the Enterobacteriaceae in the inflamed gut. Moreover, we show that microcins can act as narrow-spectrum therapeutics to inhibit enteric pathogens and reduce enterobacterial blooms.

摘要

肠杆菌科是一类革兰氏阴性菌,其中包括共生菌以及原发性和机会性病原体,它们是全球发病和死亡的主要原因之一。尽管肠杆菌科细菌在健康肠道微生物群中通常占比不到1%,但其中一些细菌可在发炎的肠道中大量繁殖;肠杆菌的增殖是微生物失衡(即生态失调)的一个标志。微菌素是一类小的分泌型蛋白质,在体外具有抗菌活性,但其在体内的作用尚不清楚。在此,我们证明微菌素可使益生菌大肠杆菌Nissle 1917(EcN)在肠道炎症期间限制竞争性肠杆菌科细菌(包括病原体和致病共生菌)的增殖。产生微菌素的EcN可限制发炎肠道中竞争者的生长,包括共生大肠杆菌、黏附侵袭性大肠杆菌以及相关病原体肠炎沙门氏菌。此外,只有向先前感染肠炎沙门氏菌的小鼠治疗性施用野生型、产生微菌素的EcN,才能显著减少该病原体在肠道的定植。我们的研究首次证明微菌素可介导发炎肠道中肠杆菌科细菌种间和种内的竞争。此外,我们还表明微菌素可作为窄谱治疗剂来抑制肠道病原体并减少肠杆菌的大量繁殖。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab26/5145735/a34f45f9ef1a/nihms825334f5.jpg

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