Saxena Arpit, Biswas Sanchay Kumar, Chand Karam, Chauhan Ankita, Mohd Gulam, Subramaniam Saravanan, Naskar Jishnu, Mondal Bimalendu, Ramakrishnan Muthannan A, Pandey Awadh Bihari
Division of Virology, Indian Veterinary Research Institute Mukteswar, Nainital, Uttarakhand, 263 138, India; Department of Molecular and Cellular Engineering, Sam Higginbottom University of Agriculture Technology and Sciences Allahabad, Uttar Pradesh, 211 007, India.
Division of Virology, Indian Veterinary Research Institute Mukteswar, Nainital, Uttarakhand, 263 138, India.
Acta Trop. 2019 Jun;194:13-22. doi: 10.1016/j.actatropica.2019.03.018. Epub 2019 Mar 12.
Bluetongue virus (BTV) infects almost all the domestic and wild ruminants though the clinical disease is most commonly reported in sheep and some species of deer. Goat and cattle are the most common asymptomatic reservoir of the virus. Full genome sequencing and serological characterization of the virus isolates are emphasized for understanding the phylogenetic relationship and molecular epidemiology of bluetongue (BT). In this study, we report phylogenetic and phenotypic antigenic relationship of a BTV serotype-16 (PDP2/13/Ind) recovered from an apparently healthy goat from the state of Uttarakhand, a hilly terrain of sub-Himalayan India with four other BTV-16 isolates. The full genome sequence data was analyzed and the phylogenetic relationship of the goat isolate with other BTV-16 was established. Phylogenetic analysis revealed cluster of PDP2/13/Ind along with other Indian BTV-16 isolates indicating their close ancestral relationship. A cohesive ancestral relationship, irrespective of the genome segments analyzed, was also observed between Indian and Mediterranean BTV-16. The mean substitution rate of different segments of BTV-16 isolates varied from 3.231 × 10 (seg-2) to 1.129 × 10 (seg-6) substitutions per site per year. Timescale analysis indicated that all the segments had an older ancestor. No statistically significant geographic structuring of BTV-16 isolates was observed indicating frequent gene flow. The goat isolate shares highest identity (99.5%-99.8%) with G53/ABT/HSR, a BTV-16 recovered from the western part of the country whereas high level of divergence (11.9%-33.3%) at genomic segment level was observed with a Nigerian BTV-16 (NIG1982/10). Phenotypic antigenic relationship (r) of PDP2/13/Ind with other isolate-specific hyperimmune serum (HIS) determined from serum neutralization titer was 0.672 ± 0.058 to 0.948 ± 0.09. On other hand, the calculated 'r' score was 0.636 ± 0.063 to 0.814 ± 0.201 when HIS against PDP2/13/Ind was used to neutralize the other BTV-16 isolates. The percentage antigenic similarity (R) of the PDP2/13/Ind with other BTV-16 isolates was 65.39 ± 5.38-87.67 ± 14.86. Data suggests presence of subtype antigenic variation amongst the BTV-16 isolates recovered from the goats of a geographically restricted area of the state of Uttarakhand, India.
蓝舌病病毒(BTV)可感染几乎所有家养和野生反刍动物,不过临床疾病最常报道于绵羊和某些鹿种。山羊和牛是该病毒最常见的无症状宿主。强调对病毒分离株进行全基因组测序和血清学特征分析,以了解蓝舌病(BT)的系统发育关系和分子流行病学。在本研究中,我们报告了从印度次喜马拉雅山区 Uttarakhand 邦一只看似健康的山羊中分离出的 BTV 血清型 16(PDP2/13/Ind)与其他四个 BTV - 16 分离株之间的系统发育和表型抗原关系。分析了全基因组序列数据,并确定了该山羊分离株与其他 BTV - 16 的系统发育关系。系统发育分析显示 PDP2/13/Ind 与其他印度 BTV - 16 分离株聚类,表明它们有密切的祖先关系。在印度和地中海的 BTV - 16 之间,无论分析的基因组片段如何,也观察到了紧密的祖先关系。BTV - 16 分离株不同片段的平均替换率每年每个位点从 3.231×10(片段 2)到 1.129×10(片段 6)个替换不等。时间尺度分析表明所有片段都有一个更古老的祖先。未观察到 BTV - 16 分离株有统计学上显著的地理结构,表明基因流动频繁。该山羊分离株与从该国西部分离出的 BTV - 16(G53/ABT/HSR)具有最高的同一性(99.5% - 99.8%),而与尼日利亚的 BTV - 16(NIG1982/10)在基因组片段水平上观察到高度差异(11.9% - 33.3%)。根据血清中和滴度确定的 PDP2/13/Ind 与其他分离株特异性超免疫血清(HIS)的表型抗原关系(r)为 0.672±0.058 至 0.948±(此处原文有误,应为 0.09)。另一方面,当使用针对 PDP2/13/Ind 的 HIS 来中和其他 BTV - 16 分离株时,计算出的“r”值为 0.636±0.063 至 0.814±0.201。PDP2/13/Ind 与其他 BTV - 16 分离株的抗原相似性百分比(R)为 65.39±5.38 - 87.67±14.86。数据表明,从印度 Uttarakhand 邦一个地理范围有限地区的山羊中分离出的 BTV - 16 分离株之间存在亚型抗原变异。