Khalifa Khalda A, Sidahmed Abdelrahim Egbal, Badwi Magdi, Mohamed Amal M
Veterinary Research Institute (VRI), P.O. Box 806, Khartoum, Sudan.
J Vet Med. 2013;2013:208026. doi: 10.1155/2013/208026. Epub 2013 Sep 18.
The current study described the isolation and molecular detection of Mycoplasma gallisepticum (Mg) and Mycoplasma synoviae from tracheal swabs of diseased birds showing signs of respiratory distress in selected commercial (layer and broiler) farms and from yolk and an open air of pens of vaccinated breeder flocks in Sudan. A number of 45 Mycoplasma isolates were recovered from chickens in Khartoum, Gezira, and Equatoria states in Sudan. Of these, eight Mg and three Ms isolates were identified using growth inhibition and rapid serum agglutination (RSA) tests. The conventional PCR technique was applied to amplify 140 bp and 720 bp DNA fragments for the Mg and Ms, respectively. This research confirmed vertical and horizontal transmission of Mg from breeder farms through detection of Mg in yolk of fertile eggs and an air of pens despite previous vaccination. PCR is considered a rapid, sensitive, and cheap method and it will improve the diagnosis of Mycoplasma in chickens.
本研究描述了从苏丹选定的商业(蛋鸡和肉鸡)养殖场出现呼吸窘迫症状的患病禽类气管拭子中,以及从苏丹接种疫苗的种鸡群的蛋黄和鸡舍空气中分离和分子检测鸡毒支原体(Mg)和滑液支原体。从苏丹喀土穆、杰济拉和赤道州的鸡中分离出45株支原体。其中,通过生长抑制和快速血清凝集(RSA)试验鉴定出8株Mg和3株Ms分离株。应用常规PCR技术分别扩增Mg和Ms的140 bp和720 bp DNA片段。本研究通过检测受精鸡蛋蛋黄和鸡舍空气中的Mg,证实了种鸡场Mg的垂直和水平传播,尽管之前进行了疫苗接种。PCR被认为是一种快速、灵敏且廉价的方法,它将改善鸡支原体的诊断。