Ahmed Mohamed S, Body Mohammad H, El-Neweshy Mahmoud S, ALrawahi Abdulmajeed H, Al-Abdawani Mohsin, Eltahir Hatim A, ALmaewaly Mahir G
Animal Health Research Center, Directorate General of Agriculture and Livestock Research, Ministry of Agriculture and Fisheries, Muscat, Sultanate of Oman.
Department of Pathology, Faculty of Veterinary Medicine, Kafrelsheikh University, Kafr El Sheikh, 33516, Egypt.
Trop Anim Health Prod. 2020 Jul;52(4):2163-2168. doi: 10.1007/s11250-020-02239-0. Epub 2020 Mar 2.
The accurate and early diagnosis of rabies is critical for undertaking public health measures in animals. The aim of the current study was to identify the molecular characterization of the circulating rabies virus (RABV) among camels (Camelus dromedaries) in Oman and to evaluate the efficacy of the histopathology and reverse transcription polymerase chain reaction (RT-PCR) as diagnostic tools of acute rabies encephalitis in camels in comparison with direct fluorescent antibody test (dFAT). Of the forty-five brain samples from suspected camels submitted to the Animal Health Research Center in Oman (2009-2013), 22 cases were positive by dFAT and RT-PCR. Two positive samples were subjected for N gene nucleotide sequencing and phylogenetic analysis (accession numbers GU353156 and KC883998 for brain samples collected in 2009 and 2011, respectively). The specificity and sensitivity of histopathology were 100% and 81%, respectively, while in RT-PCR were 100% and 100%, respectively. The neuropathological changes were presence of intracytoplasmic inclusions (Negri bodies) in the pyramidal neurons of the hippocampus beside prominent cerebral and cerebellar congestion and hemorrhage. Neuronal necrosis with satellitosis and neuronophagia were also noticed in the cerebrum of affected brains. Conclusively, there was one genetic group of RABV with 99% homology circulating in Omani camels. Also, it is concluded that histopathological examination is a safe and reliable diagnostic tool when only formalin-fixed and paraffin-embedded material is available, but the negative results should be reaffirmed by dFAT or RT-PCR.
狂犬病的准确早期诊断对于采取动物公共卫生措施至关重要。本研究的目的是确定阿曼单峰骆驼( Camelus dromedaries )中流行的狂犬病病毒(RABV)的分子特征,并评估组织病理学和逆转录聚合酶链反应(RT-PCR)作为骆驼急性狂犬病脑炎诊断工具的有效性,同时与直接荧光抗体试验(dFAT)进行比较。在提交给阿曼动物健康研究中心(2009 - 2013年)的45份疑似骆驼脑样本中,22例通过dFAT和RT-PCR检测呈阳性。对两份阳性样本进行了N基因核苷酸测序和系统发育分析(2009年和2011年采集的脑样本的登录号分别为GU353156和KC883998)。组织病理学的特异性和敏感性分别为100%和81%,而RT-PCR的特异性和敏感性分别为100%和100%。神经病理学变化表现为海马锥体细胞内存在胞浆内包涵体(内基小体),同时伴有明显的大脑和小脑充血及出血。在受影响大脑的大脑中还观察到神经元坏死伴卫星现象和噬神经细胞现象。总之,阿曼骆驼中存在一个同源性为99%的RABV基因群。此外,得出的结论是,当只有福尔马林固定和石蜡包埋的材料可用时,组织病理学检查是一种安全可靠的诊断工具,但阴性结果应通过dFAT或RT-PCR再次确认。