Salem Mohamed A, El-Deeb Wael M, Zaghawa Ahmed A, Housawi Fadel M, Alluwaimi Ahmed M
Veterinary Teaching Hospital, King Faisal University, Al-Hasa, Kingdom of Saudi Arabia.
Department of Medicine and Infectious Diseases, Faculty of Veterinary Medicine, Cairo University, Cairo, Egypt.
Vet World. 2019;12(2):218-223. doi: 10.14202/vetworld.2019.218-223. Epub 2019 Feb 9.
subspecies (MAP) causes Johne's disease in ruminants. This study aimed to investigate infection in clinically infected camels on the immunological, conventional bacteriological, and molecular biological basis.
A total of 30 Arabian camels () were examined in this study. The camels were suffering from signs ranging from mild to severe infections (that did not respond to antibiotic treatment) to chronic or intermittent diarrhea. Camels were grouped into three groups based on their age, sex, and breed. Detection of anti-MAP antibodies in camels' serum, Ziehl-Neelsen (ZN) staining technique on rectal scraps, direct recognition of MAP in stool and tissue specimens by IS900 polymerase chain reaction (PCR) assay, and finally isolation and molecular description of MAP from fecal and tissue samples were carried out.
Five MAP isolates were recovered from these investigated camel samples giving an isolation rate of 16.6%, while eight camels were identified by PCR (26.6%). Five camels yielded MAP in their feces by ZN fecal staining (16.6%), whereas ELISA detected anti-MAP antibodies in nine camels only (30%).
From the obtained results, we concluded that the gold standard for the diagnosis of MAP is the culture method despite its limitations. Molecular diagnosis (PCR) could be a useful tool in the identification of truly positive and negative camels; however, great care should be given regarding the primers specificity and sensitivity.
副结核分枝杆菌亚种(MAP)可引起反刍动物的副结核病。本研究旨在从免疫学、传统细菌学和分子生物学角度调查临床感染骆驼中的MAP感染情况。
本研究共检查了30头阿拉伯骆驼。这些骆驼表现出从轻度到重度感染(对抗生素治疗无反应)到慢性或间歇性腹泻等症状。根据骆驼的年龄、性别和品种将其分为三组。检测骆驼血清中的抗MAP抗体,对直肠刮片进行齐-尼(ZN)染色技术检测,通过IS900聚合酶链反应(PCR)分析直接识别粪便和组织标本中的MAP,最后从粪便和组织样本中分离MAP并进行分子鉴定。
从这些被调查的骆驼样本中分离出5株MAP,分离率为16.6%,而通过PCR鉴定出8头骆驼感染(26.6%)。5头骆驼的粪便经ZN粪便染色检测出MAP(16.6%),而酶联免疫吸附测定(ELISA)仅在9头骆驼中检测到抗MAP抗体(30%)。
根据所得结果,我们得出结论,尽管存在局限性,但MAP诊断的金标准仍是培养方法。分子诊断(PCR)可能是识别真正阳性和阴性骆驼的有用工具;然而,应特别注意引物的特异性和敏感性。