Malik Yashpal Singh, Kumar Naveen, Sharma Kuldeep, Saurabh Sharad, Dhama Kuldeep, Prasad Minakshi, Ghosh Souvik, Bányai Krisztián, Kobayashi Nobumichi, Singh Raj Kumar
Indian Veterinary Research Institute, Izatnagar 243 122, Uttar Pradesh, India.
National Institute of High Security Animal Diseases, Bhopal, Madhya Pradesh, India.
Infect Genet Evol. 2016 Jul;41:63-72. doi: 10.1016/j.meegid.2016.03.023. Epub 2016 Mar 28.
Rotavirus-A (RVAs), are the major cause of severe gastroenteritis in the young of mammals and birds. RVA strains possessing G6, G8, and G10 genotypes in combination with P[1] or P[11] have been commonly detected in cattle. During a routine surveillance for enteric viruses in a bovine population on North-Western temperate Himalayan region of India, an uncommon bovine RVA strain, designated as RVA/Cow-wt/IND/M1/09/2009 was detected in a diarrhoeic crossbred calf. The examination of nearly complete genome sequence of this RVA strain revealed an unusual G-P combination (G3P[11]) on a typical bovine RVA genotype backbone (I2-R2-C2-M2-A11-N2-T6-E2-H3). The VP7 gene of M1/09 isolate displayed a maximum nucleotide sequence identity of 73.8% with simian strain (RVA/Simian-tc/USA/RRV/1975/G3P[3]). The VP4 and NSP5 genes clustered with an Indian pig strain, RVA/Pig-wt/IND/AM-P66/2012/G10P[11] (99.6%), and a caprine strain, RVA/Goat-tc/BGD/GO34/1999/G6P[1] (98.9%) from Bangladesh, respectively, whilst the, VP6, NSP1, NSP3 and NSP4 genes were identical or nearly identical to Indian bovine strains (RVA/Cow-wt/IND/B-72/2008/G10P[X], RVA/Cow-wt/IND/B85/2010/GXP[X], and RVA/Cow-wt/IND/C91/2011/G6P[X]). The remaining four genes (VP1, VP2, VP3 and NSP2) were more closely related to RVA/Human-wt/ITA/PAI11/1996/G2P[4] (93.5%), RVA/Sheep-wt/CHN/LLR/1985/G10P[15] (88.8%), RVA/Human-tc/SWE/1076/1983/G2P2A[6] (93.2%) and RVA/Human-wt/AUS/CK20003/2000/G2P[4] (91.2%), respectively. Altogether, these findings are suggestive of multiple independent interspecies transmission and reassortment events between co-circulating bovine, porcine, ovine and human rotaviruses. The complete genome sequence information is necessary to establish the evolutionary relationship, interspecies transmission and ecological features of animal RVAs from different geographical regions.
A组轮状病毒(RVAs)是哺乳动物和鸟类幼崽严重肠胃炎的主要病因。在牛群中,通常检测到具有G6、G8和G10基因型并与P[1]或P[11]组合的RVA毒株。在对印度喜马拉雅西北温带地区牛群的肠道病毒进行常规监测期间,在一头腹泻的杂交小牛中检测到一种罕见的牛RVA毒株,命名为RVA/Cow-wt/IND/M1/09/2009。对该RVA毒株近乎完整的基因组序列进行检测,结果显示在典型的牛RVA基因型主干(I2-R2-C2-M2-A11-N2-T6-E2-H3)上存在不寻常的G-P组合(G3P[11])。M1/09分离株的VP7基因与猿猴毒株(RVA/Simian-tc/USA/RRV/1975/G3P[3])的核苷酸序列一致性最高,为73.8%。VP4和NSP5基因分别与来自印度的猪毒株RVA/Pig-wt/IND/AM-P66/2012/G10P[11](99.6%)以及来自孟加拉国的山羊毒株RVA/Goat-tc/BGD/GO34/1999/G6P[1](98.9%)聚类,而VP6、NSP1、NSP3和NSP4基因与印度牛毒株(RVA/Cow-wt/IND/B-72/2008/G10P[X]、RVA/Cow-wt/IND/B85/2010/GXP[X]和RVA/Cow-wt/IND/C91/2011/G6P[X])相同或几乎相同。其余四个基因(VP1、VP2、VP3和NSP2)分别与RVA/Human-wt/ITA/PAI11/1996/G2P[4](93.5%)、RVA/Sheep-wt/CHN/LLR/1985/G10P[15](88.8%)、RVA/Human-tc/SWE/1076/1983/G2P2A[6](93.2%)和RVA/Human-wt/AUS/CK20003/2000/G2P[4](91.2%)关系更密切。总之,这些发现表明在同时流行的牛、猪、羊和人轮状病毒之间存在多次独立的种间传播和重配事件。完整的基因组序列信息对于确定来自不同地理区域的动物RVA的进化关系、种间传播和生态特征至关重要。