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首页> 外文期刊>PLoS Pathogens >Additive Function of Vibrio vulnificus MARTXVv and VvhA Cytolysins Promotes Rapid Growth and Epithelial Tissue Necrosis During Intestinal Infection
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Additive Function of Vibrio vulnificus MARTXVv and VvhA Cytolysins Promotes Rapid Growth and Epithelial Tissue Necrosis During Intestinal Infection

机译:创伤弧菌MARTXVv和VvhA溶血素的添加功能促进肠道感染过程中的快速生长和上皮组织坏死。

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摘要

Vibrio vulnificus is a pathogen that causes both severe necrotizing wound infections and life-threatening food-borne infections. Food-borne infection is particularly lethal as the infection can progress rapidly to primary septicemia resulting in death from septic shock and multiorgan failure. In this study, we use both bioluminescence whole animal imaging and V. vulnificus bacterial colonization of orally infected mice to demonstrate that the secreted multifunctional-autoprocessing RTX toxin (MARTXVv) and the cytolysin/hemolysin VvhA of clinical isolate CMCP6 have an important function in the gut to promote early in vivo growth and dissemination of this pathogen from the small intestine to other organs. Using histopathology, we find that both cytotoxins can cause villi disruption, epithelial necrosis, and inflammation in the mouse small intestine. A double mutant deleted of genes for both cytotoxins was essentially avirulent, did not cause intestinal epithelial tissue damage, and was cleared from infected mice by 36 hours by an effective immune response. Therefore, MARTXVv and VvhA seem to play an additive role for pathogenesis of CMCP6 causing intestinal tissue damage and inflammation that then promotes dissemination of the infecting bacteria to the bloodstream and other organs. In the absence of these two secreted factors, we propose that this bacterium is unable to cause intestinal infection in humans.
机译:创伤弧菌是引起严重坏死性伤口感染和威胁生命的食源性感染的病原体。食源性感染特别致命,因为感染可以迅速发展为原发性败血症,导致败血性休克和多器官衰竭导致死亡。在这项研究中,我们使用生物发光全动物成像和口腔感染小鼠的创伤弧菌细菌定殖来证明临床分离株CMCP6的分泌的多功能自动加工RTX毒素(MARTXVv)和溶细胞素/溶血素VvhA在其中具有重要的功能。肠道促进这种病原体在体内的早期生长和传播,从小肠到其他器官。使用组织病理学,我们发现两种细胞毒素都可以在小鼠小肠中引起绒毛破坏,上皮坏死和炎症。两种细胞毒素基因的双突变体缺失基本上是无毒的,没有引起肠上皮组织损伤,并且通过有效的免疫反应在36小时内从感染的小鼠中清除了。因此,MARTXVv和VvhA似乎在CMCP6的发病机理中起着加成作用,从而引起肠道组织损伤和炎症,继而促进感染细菌向血流和其他器官的传播。在缺少这两个分泌因子的情况下,我们建议这种细菌不能引起人类肠道感染。

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