Clostridium perfringens type C necrotic enteritis in pigs: diagnosis, pathogenesis, and prevention
| Autor: | Julia Bruggisser, Basma Tarek, Sonja Kittl, Horst Posthaus |
|---|---|
| Jazyk: | angličtina |
| Rok vydání: | 2020 |
| Předmět: | |
| Zdroj: | Posthaus, Horst; Kittl, Sonja; Tarek, Basma; Bruggisser, Julia (2020). Clostridium perfringens type C necrotic enteritis in pigs: diagnosis, pathogenesis, and prevention. Journal of veterinary diagnostic investigation, 32(2), pp. 203-212. Sage 10.1177/1040638719900180 J Vet Diagn Invest |
| DOI: | 10.1177/1040638719900180 |
| Popis: | Clostridium perfringens type C causes severe and lethal necrotic enteritis (NE) in newborn piglets. NE is diagnosed through a combination of pathology and bacteriologic investigations. The hallmark lesion of NE is deep, segmental mucosal necrosis with marked hemorrhage of the small intestine. C. perfringens can be isolated from intestinal samples in acute cases but it is more challenging to identify pathogenic strains in subacute-to-chronic cases. Toxinotyping or genotyping is required to differentiate C. perfringens type C from commensal type A strains. Recent research has extended our knowledge about the pathogenesis of the disease, although important aspects remain to be determined. The pathogenesis involves rapid overgrowth of C. perfringens type C in the small intestine, inhibition of beta-toxin (CPB) degradation by trypsin inhibitors in the colostrum of sows, and most likely initial damage to the small intestinal epithelial barrier. CPB itself acts primarily on vascular endothelial cells in the mucosa and can also inhibit platelet function. Prevention of the disease is achieved by immunization of pregnant sows with C. perfringens type C toxoid vaccines, combined with proper sanitation on farms. For the implementation of prevention strategies, it is important to differentiate between disease-free and pathogen-free status of a herd. The latter is more challenging to maintain, given that C. perfringens type C can persist for a long time in the environment and in the intestinal tract of adult animals and thus can be distributed via clinically and bacteriologically inapparent carrier animals. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|