Cheun-Arom Thaniwan, Temeeyasen Gun, Tripipat Thitima, Kaewprommal Pavita, Piriyapongsa Jittima, Sukrong Suchada, Chongcharoen Wanchai, Tantituvanont Angkana, Nilubol Dachrit
Department of Veterinary Microbiology, Faculty of Veterinary Science, Bangkok, Thailand.
Genome Technology Research Unit, National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Pathumthani, Thailand.
Infect Genet Evol. 2016 Oct;44:114-121. doi: 10.1016/j.meegid.2016.06.046. Epub 2016 Jun 25.
Porcine epidemic diarrhea virus (PEDV) has continued to cause sporadic outbreaks in Thailand since 2007 and a pandemic variant containing an insertion and deletion in the spike gene was responsible for outbreaks. In 2014, there were further outbreaks of the disease occurring within four months of each other. In this study, the full-length genome sequences of two genetically distinct PEDV isolates from the outbreaks were characterized. The two PEDV isolates, CBR1/2014 and EAS1/2014, were 28,039 and 28,033 nucleotides in length and showed 96.2% and 93.6% similarities at nucleotide and amino acid levels respectively. In total, we have observed 1048 nucleotide substitutions throughout the genome. Compared to EAS1/2014, CBR1/2014 has 2 insertions of 4 ((56)GENQ(59)) and 1 ((140)N) amino acid positions 56-59 and 140, and 2 deletions of 2 ((160)DG(161)) and 1 ((1199)Y) amino acid positions 160-161 and 1199. The phylogenetic analysis based on full-length genome of CBR1/2014 isolate has grouped the virus with the pandemic variants. In contrast, EAS1/2014 isolate was grouped with CV777, LZC and SM98, a classical variant. Our findings demonstrated the emergence of EAS1/2014, a classical variant which is novel to Thailand and genetically distinct from the currently circulating endemic variants. This study warrants further investigations into molecular epidemiology and genetic evolution of the PEDV in Thailand.
自2007年以来,猪流行性腹泻病毒(PEDV)在泰国持续引发散发性疫情,一种在刺突基因中存在插入和缺失的大流行变异株是疫情的罪魁祸首。2014年,该病在彼此相隔四个月的时间内又出现了进一步的疫情爆发。在本研究中,对来自这些疫情爆发的两个基因不同的PEDV分离株的全长基因组序列进行了特征分析。这两个PEDV分离株,CBR1/2014和EAS1/2014,长度分别为28,039和28,033个核苷酸,在核苷酸和氨基酸水平上分别显示出96.2%和93.6%的相似性。我们总共在整个基因组中观察到1048个核苷酸替换。与EAS1/2014相比,CBR1/2014在氨基酸位置56 - 59和140处有2个4个氨基酸((56)GENQ(59))和1个1个氨基酸((140)N)的插入,在氨基酸位置160 - 161和1199处有2个2个氨基酸((160)DG(161))和1个1个氨基酸((1199)Y)的缺失。基于CBR1/2014分离株全长基因组的系统发育分析将该病毒与大流行变异株归为一组。相比之下,EAS1/2014分离株与CV777、LZC和SM98(一种经典变异株)归为一组。我们的研究结果表明,EAS1/2014这一经典变异株在泰国出现,它对泰国来说是新的,并且在基因上与目前流行的地方变异株不同。本研究有必要对泰国PEDV的分子流行病学和基因进化进行进一步调查。