Jeong Hee Gon, Oh Man Hwan, Kim Byoung Sik, Lee Min Young, Han Ho Jae, Choi Sang Ho
Department of Agricultural Biotechnology, Center for Agricultural Biomaterials, Research institute for Agriculture and Life Sciences, Seoul National University, South Korea.
Infect Immun. 2009 Aug;77(8):3209-17. doi: 10.1128/IAI.00109-09. Epub 2009 Jun 1.
N-acetylneuraminic acid (Neu5Ac, sialic acid) could provide a good substrate for enteropathogenic bacteria in the intestine, when the bacteria invade and colonize in human gut. In order to analyze the role of Neu5Ac catabolism in Vibrio vulnificus pathogenesis, a mutant with disruption of the nanA gene encoding Neu5Ac lyase was constructed by allelic exchanges. The nanA mutant was not able to utilize Neu5Ac as a sole carbon source and revealed an altered colony morphotype with reduced opacity in the presence of Neu5Ac. Compared to the wild type, the nanA mutant exhibited a low level of cytotoxicity toward INT-407 epithelial cells in vitro and reduced virulence in a mouse model. The disruption of nanA also resulted in a substantial decrease in histopathological damage in jejunum and colon tissues from the mouse intestine. These results indicated that NanA plays an important role in V. vulnificus pathogenesis. In addition, the nanA mutant was significantly diminished in growth with and adherence to INT-407 epithelial cells in vitro, and was defective for intestinal colonization, reflecting the impaired ability of the mutant to grow and survive with, persist in, and adhere to the intestine in vivo. Consequently, the combined results suggest that NanA and the capability of catabolic utilization of Neu5Ac contribute to V. vulnificus virulence by ensuring growth, adhesion, and survival during infection.
当肠道致病菌侵入并定殖于人体肠道时,N-乙酰神经氨酸(Neu5Ac,唾液酸)可为其提供良好的底物。为了分析Neu5Ac分解代谢在创伤弧菌致病过程中的作用,通过等位基因交换构建了编码Neu5Ac裂解酶的nanA基因缺失突变体。nanA突变体不能利用Neu5Ac作为唯一碳源,并且在Neu5Ac存在的情况下呈现出菌落形态改变,不透明度降低。与野生型相比,nanA突变体在体外对INT-407上皮细胞的细胞毒性较低,并且在小鼠模型中的毒力降低。nanA基因的缺失还导致小鼠肠道空肠和结肠组织的组织病理学损伤显著减少。这些结果表明,NanA在创伤弧菌致病过程中起重要作用。此外,nanA突变体在体外与INT-407上皮细胞共培养时生长和黏附能力显著降低,并且在肠道定殖方面存在缺陷,这反映出该突变体在体内与肠道共生、存活和黏附的能力受损。因此,综合结果表明,NanA和Neu5Ac的分解代谢利用能力通过确保感染期间的生长、黏附和存活,对创伤弧菌的毒力有贡献。