Sharma Amrita, Singla L D, Kaur Paramjit, Bal M S
Department of Veterinary Parasitology, College of Veterinary Sciences, Guru Angad Dev Veterinary and Animal Sciences University, Ludhiana, Punjab 141004, India.
ScientificWorldJournal. 2015;2015:352519. doi: 10.1155/2015/352519. Epub 2015 Feb 25.
This investigation demonstrates the status of bovine anaplasmosis caused by A. marginale in bovines from Submountain and Undulating Zone of Punjab. Out of 184 suspected animals, 25 (19.51%), 47 (31.71%), and 78 (68.75%) were positive by microscopy, indirect ELISA, and PCR assay, respectively. The microscopy showed 29% sensitivity and 99% specificity, while ELISA showed 32% sensitivity and 79% specificity in concordance with PCR assay. Five false negative samples by msp1β PCR were reconfirmed for Anaplasma spp. targeting 16S rRNA gene. The sequence analysis showed the presence for A. marginale specific restriction site, indicating variation in the local strains of the organism resulting in no amplification with msp1β gene primers. Of 82 samples positive by PCR, 57 were negative by ELISA indicating lower efficacy of ELISA to detect early anaplasmosis. The assessment of risk factor with results of PCR technique indicated that cattle (Odds ratio = 2.884), particularly those of age > 1 years (Odds ratio = 2.204) of district Pathankot (Odds ratio = 3.182) of Submountain Zone (Odds ratio = 2.086), were at high risk of anaplasmosis. All three districts of Submountain Zone are at higher risk indicating the impact of biotic and abiotic factors on the incidence of disease.
本研究揭示了旁遮普邦山麓和丘陵地带牛群中由边缘无浆体引起的牛无浆体病状况。在184头疑似动物中,分别通过显微镜检查、间接酶联免疫吸附测定(ELISA)和聚合酶链反应(PCR)检测,有25头(19.51%)、47头(31.71%)和78头(68.75%)呈阳性。显微镜检查显示敏感性为29%,特异性为99%;而ELISA与PCR检测结果一致,敏感性为32%,特异性为79%。对msp1β PCR检测呈5例假阴性的样本,针对16S rRNA基因对无形体属进行了重新确认。序列分析显示存在边缘无浆体特异性限制性位点,表明该生物体当地菌株存在变异,导致msp1β基因引物无法扩增。在82份PCR检测呈阳性的样本中,57份ELISA检测呈阴性,表明ELISA检测早期无浆体病的效能较低。利用PCR技术结果对风险因素进行评估表明,牛(优势比 = 2.884),特别是山麓地带帕坦科特地区(优势比 = 3.182)年龄>1岁的牛(优势比 = 2.204),无浆体病感染风险较高。山麓地带的所有三个区风险都较高,表明生物和非生物因素对疾病发病率有影响。