Abstract

This study aimed to diagnoseSarcina ventriculiin lambs with haemorrhagic abomasitis using histopathological and real-time PCR methods. The material used in this study consisted of 43 abomasum tissues recovered from lambs presenting bleeding, ulcer, gas or a combination of these in the abomasum, that were brought for necropsy to the Department of Pathology of the Veterinary Faculty, Selcuk University. The recovered samples were stored in a 10% formaldehyde solution for histopathological examinations and in Eppendorf tubes at −20 °C for PCR examinations. All the samples were analyzed by histopathological and PCR methods. WhileS. ventriculipyruvate decarboxylase (PDC) amplicon was determined by real-time PCR in 17 cases, the packaged form ofSarcina-like bacteria was found microscopically in 3 cases only. In this study, the diagnosis ofS. ventriculiin cases of lambs presenting bleeding, ulcers and gas in the abomasum or haemorrhagic abomasitis simultaneously at the necropsy was performed using histopathological and real-time PCR methods; in parallel, the real-time PCR method for the diagnosis ofS. ventriculi-derived haemorrhagic abomasitis in lambs was also optimized.

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