Dalal Anita, Maan Sushila, Bansal Nitish, Kumar Vinay, Kumar Aman, Maan Narender Singh, Kakker Naresh Kumar
Department of Veterinary Microbiology, College of Veterinary Sciences, Lala Lajpat Rai University of Veterinary and Animal Sciences, Hisar - 125 004, Haryana, India.
Department of Animal Biotechnology, College of Veterinary Sciences, Lala Lajpat Rai University of Veterinary and Animal Sciences, Hisar - 125 004, Haryana, India.
Vet World. 2017 Nov;10(11):1389-1393. doi: 10.14202/vetworld.2017.1389-1393. Epub 2017 Nov 27.
The present study was designed to characterize the genome segment 3 (Seg-3) of bluetongue virus (BTV) serotype 12 isolates from different outbreaks of Bluetongue disease in Haryana, India.
Blood and swab samples were collected from goat and sheep suspected to be suffering of BT from different outbreaks from Gurugram, Sirsa, Hisar, and Karnal districts of Haryana. The samples were grown in insect and mammalian cell lines. After preliminary identification, serotyping was done using BTV type-specific quantitative reverse transcription-polymerase chain reaction (qRT-PCR) assays. Sequencing was performed using terminal and walking internal primers specific for Seg-3 on ABI Capillary Sequencer 3130 using a "BigDye cycle sequencing kit." The obtained sequence data were analyzed with various bioinformatic tools.
Real-time PCR results confirmed the samples to be positive for BTV-12. The Seg-3 of Indian isolates was most closely related to that of a south Indian isolate of BTV-12 from Andhra Pradesh (KC662614) with 97% nucleotide identity.
The study confirmed the circulation of BTV-12 in Haryana, India. The variations shown in genome Seg-3 of BTV-12 isolates may have some significance and need to be further explored.
本研究旨在对来自印度哈里亚纳邦不同蓝舌病疫情的蓝舌病毒12型(BTV-12)分离株的基因组片段3(Seg-3)进行特征分析。
从哈里亚纳邦古鲁格拉姆、锡尔萨、希萨尔和卡纳尔地区不同疫情中疑似感染蓝舌病的山羊和绵羊采集血液和拭子样本。样本在昆虫和哺乳动物细胞系中培养。初步鉴定后,使用BTV型特异性定量逆转录聚合酶链反应(qRT-PCR)检测进行血清分型。使用针对Seg-3的末端引物和步移内部引物,在ABI 3130毛细管测序仪上使用“BigDye循环测序试剂盒”进行测序。利用各种生物信息学工具对获得的序列数据进行分析。
实时PCR结果证实样本为BTV-12阳性。印度分离株的Seg-3与来自安得拉邦的一株南印度BTV-12分离株(KC662614)关系最为密切,核苷酸同一性为97%。
该研究证实了BTV-12在印度哈里亚纳邦的传播。BTV-12分离株基因组Seg-3中显示的变异可能具有一定意义,需要进一步探索。