Jielu Ling1, Siyi Chen, Qingqing Gao, Huiqing Xu, Song Gao, Xiufan Liu. 1. Key Laboratory of Avian Bioproducts Development, Ministry of Agriculture, College of Veterinary Medicine, Yangzhou University, Yangzhou 225009, China. lingjielu@126.com
Abstract
OBJECTIVE: To elucidate the pathogenesis role of the vir region of APEC 02 strain E058. METHODS: The gene aerobactin/sitABC operon knockout mutants E058deltavir of APEC E058 strain was generated using Red recombination system. A series of pathogenicity tests including chick embryo inoculation, the competition experiment and the colonization and persistence in vivo were used to evaluate the pathogenicity of APEC E058deltavir and the wild-type strain E058. RESULTS: E058deltavir was similar to its parental strain E058 in the growth curves, invasion assays of HD-11 cell and in vitro competition assay. In the colonization and persistence test, the recovery colonies of E058deltavir were significantly decreased in all of the organs tested (P < 0.001). CONCLUSIONS: These results indicate that the virulence factors encoded by aerobactin/sit operon genes were important for the pathogenesis of APEC E058.
OBJECTIVE: To elucidate the pathogenesis role of the vir region of APEC 02 strain E058. METHODS: The gene aerobactin/sitABC operon knockout mutants E058deltavir of APEC E058 strain was generated using Red recombination system. A series of pathogenicity tests including chick embryo inoculation, the competition experiment and the colonization and persistence in vivo were used to evaluate the pathogenicity of APEC E058deltavir and the wild-type strain E058. RESULTS: E058deltavir was similar to its parental strain E058 in the growth curves, invasion assays of HD-11 cell and in vitro competition assay. In the colonization and persistence test, the recovery colonies of E058deltavir were significantly decreased in all of the organs tested (P < 0.001). CONCLUSIONS: These results indicate that the virulence factors encoded by aerobactin/sit operon genes were important for the pathogenesis of APEC E058.