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A Common Pathway for Activation of Host-Targeting and Bacteria-Targeting Toxins in Human Intestinal Bacteria

机译:用于活化宿主靶向和细菌靶向毒素的常见途径

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ABSTRACT Human gut microbes exhibit a spectrum of cooperative and antagonistic interactions with their host and also with other microbes. The major Bacteroides host-targeting virulence factor, Bacteroides fragilis toxin (BFT), is produced as an inactive protoxin by enterotoxigenic B. fragilis strains. BFT is processed by the conserved bacterial cysteine protease fragipain (Fpn), which is also encoded in B. fragilis strains that lack BFT. In this report, we identify a secreted antibacterial protein (fragipain-activated bacteriocin 1 [Fab1]) and its cognate immunity protein (resistance to fragipain-activated bacteriocin 1 [RFab1]) in enterotoxigenic and nontoxigenic strains of B. fragilis . Although BFT and Fab1 share no sequence identity, Fpn also activates the Fab1 protoxin, resulting in its secretion and antibacterial activity. These findings highlight commonalities between host- and bacterium-targeting toxins in intestinal bacteria and suggest that antibacterial antagonism may promote the conservation of pathways that activate host-targeting virulence factors.
机译:摘要人体肠道微生物表现出一种与其宿主的合作和拮抗相互作用以及其他微生物。主要的拟菌靶向毒力因子,植物斑纹毒素毒素(BFT),由Enterotoxigenic B.Crotilis菌株作为无活性原生毒素制备。 BFT由保守的细菌半胱氨酸蛋白酶Fropipain(FPN)加工,其在缺乏BFT的B.Fragilis菌株中也被编码。在本报告中,我们鉴定了分泌的抗菌蛋白(Fropipain-活化的菌丝1 [Fab1])及其同源免疫蛋白(抗B.Fragilis的毒性毒素菌株中的抗碎屑激活的菌株1 [RFAB1])。虽然BFT和FAB1不份数不序列同一性,但FPN还激活Fab1预氮素,导致其分泌和抗菌活性。这些发现突出了肠细菌中宿主和细菌靶向毒素之间的共性,并表明抗菌拮抗作用可以促进激活宿主靶向毒力因子的途径守恒。

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