Necrotic enteritis locus 1 diguanylate cyclase and phosphodiesterase (cyclic-di-GMP) gene mutation attenuates virulence in an avian necrotic enteritis isolate of Clostridium perfringens

•Clostridium perfringens isolates that cause avian necrotic enteritis have a large pathogenicity locus NELoc-1.•Mutation of the dgc and pde genes on NELoc-1 completely attenuated the ability of strain CP1 to cause necrotic enteritis.•Complementation with the relevant gene fully restored virulence.•N...

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Veröffentlicht in:Veterinary microbiology 2017-09, Vol.208, p.69-73
Hauptverfasser: Parreira, Valeria R., Ojha, Shivani, Lepp, Dion, Mehdizadeh Gohari, Iman, Zhou, Hongzhuan, Susta, Leonardo, Gong, Jianhua, Prescott, John F.
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Sprache:eng
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Zusammenfassung:•Clostridium perfringens isolates that cause avian necrotic enteritis have a large pathogenicity locus NELoc-1.•Mutation of the dgc and pde genes on NELoc-1 completely attenuated the ability of strain CP1 to cause necrotic enteritis.•Complementation with the relevant gene fully restored virulence.•NetB production was unaffected in the two mutants.•c-di-GMP signaling is thus important in the pathogenesis of necrotic enteritis in chickens. Necrotic enteritis (NE) caused by netB-positive strains of Clostridium perfringens is an important disease of intensively-reared broiler chickens. It is widely controlled by antibiotic use, but this practice that has come under increasing scrutiny and alternative approaches are required. As part of the search for alternative approaches over the last decade, advances have been made in understanding its pathogenesis but much remains to be understood and applied to the control of NE. The objective of this work was to assess the effect on virulence of mutation of the cyclic-di-GMP signaling genes present on the large pathogenicity locus (NELoc-1) in the tcp-encoding conjugative virulence plasmid, pNetB. For this purpose, the diguanylate cyclase (dgc) and phosphodiesterase (pde) genes were individually insertionally inactivated and the two mutants were subsequently complemented with their respective genes. Southern blotting showed that a single gene insertion was present. Mutation of either gene resulted in almost total attenuation of the mutants to cause NE in experimentally-infected broiler chickens, which was fully restored in each case by complementation of the respective mutated gene. Production of NetB-associated cytotoxicity for Leghorn male hepatoma (LMH) cells was unaffected in mutants. We conclude that the cyclic-di-GMP signaling system is important in controlling virulence in a NE C. perfringens strain and might be a target for control of the disease.
ISSN:0378-1135
1873-2542
DOI:10.1016/j.vetmic.2017.07.012