Construction and characterization of avian pathogenic Escherichia coli mutants with iro and/or tsh gene mutation.
- Author:
Xiang CHEN
1
;
Jing LIU
;
Song GAO
;
Zhiming PAN
;
Xin'an JIAO
;
Xiufan LIU
Author Information
1. Animal Infectious Disease Laboratory of Ministry of Agriculture, Jiangsu Key Laboratory of Zoonoses, Yangzhou University, Yangzhou 225009, China.
- Publication Type:Journal Article
- MeSH:
Adhesins, Escherichia coli;
genetics;
Animals;
Chickens;
Escherichia coli;
genetics;
pathogenicity;
Escherichia coli Infections;
microbiology;
veterinary;
Genes, Bacterial;
genetics;
Mutation;
Nucleic Acid Hybridization;
methods;
Organisms, Genetically Modified;
Poultry Diseases;
microbiology;
Transformation, Genetic;
Virulence Factors;
genetics
- From:
Chinese Journal of Biotechnology
2008;24(3):401-408
- CountryChina
- Language:Chinese
-
Abstract:
Iro system and temperature-sensitive hemagglutinin (Tsh) genes were identified by suppression subtractive hybridization (SSH) and selective capture of transcribed sequences (SCOTS). To get more insights in the distribution and the occurrence of the iroC and tsh genes, we examined 243 avian E. coli strains for the presences of the these genes. Among 243 avian E. coli isolates, iroC gene was present in 84.4% strains (205/243). Of the 205 iroC-positive isolates, iroC gene was found in 184 (89.8%), 18(8.8%) and 3 (1.5%) isolates with high, intermediate and low pathogenicity, respectively. Of the 167 tsh-positive isolates, tsh gene was detected in 146 (87.4%), 21 (12.6%) and 0 (0%) isolates with high, intermediate and low pathogenicity, respectively. Among tsh-positive isolates, 89.5 to 100% of the highly pathogenic isolates of O1, O2 or O78 serogroups had the tsh gene, while 53.3% of the highly pathogenic isolates of non-O1, O2 and O78 serogroups had the tsh gene (P<0.01). Suicide vectors for deletion of the iroBCDEN or tsh genes were constructed as follows. The 715-bp fragments of iroB and 603-bp fragment of the iroN were generated by PCR respectively. Both of these two fragments together with EGFP gene were cloned into pUC18, termed pUC18-iroBNEGFP. A resultant suicide vector containing the iroB-EGFP-iroN fragment was obtained and named pMEG375-iroBNEGFP. Similarly, both of the 685-bp fragment of tshF and the 692-bp fragment of the tshR together with gentamycin gene were cloned into pUC18, resulting in pUC18-tshFRGm. A resultant suicide vector containing the tshF-Gm-tshR fragment was named pMEG375-tshFRGm. Mutant derivatives of strain E037 were generated by allelic replacements and were named E037(Deltairo), E037(Deltatsh) and E037(DeltairoDeltatsh). The 50% lethal dose (LD50) of E037, E037(Deltairo), E037(Deltatsh) and E037(DeltairoDeltatsh) in commercial day-old chickens experimentally inoculated via intratrachea were determined to be 10(5.6), 10(8.4), 10(9.0) and 10(9.5)CFU, respectively. In the chicken challenging model, the mutants were tested to determine the individual role of this system for virulence and persistence in chickens. The result suggested that Iro system and Tsh were important in the pathogenicity of APEC.
