A novel pore-forming toxin in type A Clostridium perfringens is associated with both fatal canine hemorrhagic gastroenteritis and fatal foal necrotizing enterocolitis

PLoS One. 2015 Apr 8;10(4):e0122684. doi: 10.1371/journal.pone.0122684. eCollection 2015.

Abstract

A role for type A Clostridium perfringens in acute hemorrhagic and necrotizing gastroenteritis in dogs and in necrotizing enterocolitis of neonatal foals has long been suspected but incompletely characterized. The supernatants of an isolate made from a dog and from a foal that died from these diseases were both found to be highly cytotoxic for an equine ovarian (EO) cell line. Partial genome sequencing of the canine isolate revealed three novel putative toxin genes encoding proteins related to the pore-forming Leukocidin/Hemolysin Superfamily; these were designated netE, netF, and netG. netE and netF were located on one large conjugative plasmid, and netG was located with a cpe enterotoxin gene on a second large conjugative plasmid. Mutation and complementation showed that only netF was associated with the cytotoxicity. Although netE and netG were not associated with cytotoxicity, immunoblotting with specific antisera showed these proteins to be expressed in vitro. There was a highly significant association between the presence of netF with type A strains isolated from cases of canine acute hemorrhagic gastroenteritis and foal necrotizing enterocolitis. netE and netF were found in all cytotoxic isolates, as was cpe, but netG was less consistently present. Pulsed-field gel electrophoresis showed that netF-positive isolates belonged to a clonal population; some canine and equine netF-positive isolates were genetically indistinguishable. Equine antisera to recombinant Net proteins showed that only antiserum to rNetF had high supernatant cytotoxin neutralizing activity. The identifica-tion of this novel necrotizing toxin is an important advance in understanding the virulence of type A C. perfringens in specific enteric disease of animals.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacterial Toxins / chemistry
  • Bacterial Toxins / genetics*
  • Bacterial Toxins / pharmacology
  • Cell Line / drug effects
  • Clostridium perfringens / genetics*
  • Clostridium perfringens / pathogenicity
  • Dogs
  • Enterocolitis, Necrotizing / genetics
  • Enterocolitis, Necrotizing / microbiology*
  • Enterocolitis, Necrotizing / veterinary
  • Enterotoxins / genetics*
  • Enterotoxins / pharmacology
  • Gastroenteritis / genetics
  • Gastroenteritis / microbiology*
  • Gastroenteritis / veterinary
  • Genome
  • High-Throughput Nucleotide Sequencing
  • Horses
  • Nuclear Pore / drug effects

Substances

  • Bacterial Toxins
  • Enterotoxins

Grants and funding

Funding was provided from Natural Sciences and Engineering Discovery Grant, by the Ontario Ministry of Agriculture, Food and Rural Affairs (Proof of Principle grant program), and by the Ontario Centres of Excellence (C4 Proof of Principle grant program). Equine Guelph - University of Guelph funds supported the initial steps of this study.