| Title | Development of a toxA Gene Knock-out Mutant of Pasteurella multocida and Evaluation of its Protective Effects |
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| Author | Tae Jung Kim1, Jae Il Lee2, and Bong Joo Lee*2 |
| Address | 1School of Veterinary and Biomedical Sciences, Murdoch University, Murdoch, WA 6150, Australia, 2College of Veterinary Medicine, Chonnam National University, Gwangju, 500-757, Republic of Korea |
| Bibliography | Journal of Microbiology, 44(3),320-326, 2006, |
| DOI | |
| Key Words | homologous recombination, knock-out, Pasteurella multocida toxin (PMT), toxA |
| Abstract | Pasteurella multocida is an important veterinary and opportunistic human pathogen. In particular, strains of P. multocida serogroup D cause progressive atrophic rhinitis, and produce a potent, intracellular, mitogenic toxin known as P. multocida toxin (PMT), which is encoded by the toxA gene. To further investigate the toxigenic and pathogenic effects of PMT, a toxA-deleted mutant was developed by homologous gene recombination. When administrated to mice, the toxigenicity of the toxA mutant P. multocida was drastically reduced, suggesting that the PMT constributes the major part of the toxigenicity of P. multocida. Similar results were obtained in a subsequent experiment, while high mortalities were observed when toxA(+) P. multocida bacterial culture or culture lysate were administrated. Mice immunized with toxA(? P. multocida were not protected (none survived) following challenge with toxA(+) P. multocida or bacterial culture lysate (toxin). These results suggest that the toxigenicity of P. multocida is mainly derived from PMT. |
| Download PDF | JM2006-031.pdf |