Zhai S-L, Zhang H, Lin T, Chen S-N, Zhou X, Chen Q-L, Lv D-H, Wen X-H, Zhou X-R, Jia C-L, Wei W-K
Guangdong Key Laboratory of Animal Disease Prevention, Animal Disease Diagnostic Center, Institute of Animal Health, Guangdong Academy of Agricultural Sciences, Guangzhou, China.
College of Veterinary Medicine, South China Agricultural University, Guangzhou, China.
Transbound Emerg Dis. 2017 Aug;64(4):1030-1036. doi: 10.1111/tbed.12663. Epub 2017 May 11.
Since the first report of porcine kobuvirus (PKV) in 2008, it has been confirmed that PKV is widely present in several countries and plays an important role in diarrhoea outbreak in pigs. Studies have shown that the biggest difference among PKVs is the presence or absence of a specific 30-amino acid (aa) sequence in the 2B region of the polyprotein gene. Based on this unique feature, most PKV sequences could be divided into two groups (Group 1 without deletion and Group 2 with deletion), but a few sequences did not follow this rule due to possible recombination. In this study, two PKV genome sequences, designated JXAT2015 (8,123 nucleotide) and JXJC2015 (8,120 nucleotide), were identified on two different commercial swine farms with the severe diarrhoea outbreak accompanying with highly PKV infection (90%, 18/20) and moderate infection (40%, 8/20) of porcine bocavirus 1 (PBoV1) in Jiangxi province of China. Sequence analysis based on the polyprotein gene showed that they shared low nucleotide similarity (86.3%-88.1%) with other known PKVs. Although both possessed the 30-aa deletion in the 2B region, phylogenetic analysis showed that JXJC2015 was distinct from Group 1 and even Group 2, and formed a new Group (designated Group 3). The findings of this study further revealed genetic diversity and the possible pathogenic role of PKV in conjunction with other pathogens in piglets.
自2008年首次报道猪杯状病毒(PKV)以来,已证实PKV在多个国家广泛存在,并在猪腹泻暴发中起重要作用。研究表明,PKV之间最大的差异在于多聚蛋白基因2B区域中是否存在特定的30个氨基酸(aa)序列。基于这一独特特征,大多数PKV序列可分为两组(第1组无缺失,第2组有缺失),但由于可能的重组,少数序列不遵循此规则。在本研究中,在中国江西省的两个不同商业猪场中鉴定出两个PKV基因组序列,分别命名为JXAT2015(8123个核苷酸)和JXJC2015(8120个核苷酸),这两个猪场发生严重腹泻暴发,同时猪博卡病毒1(PBoV1)感染率高(90%,18/20)和中等感染率(40%,8/20)。基于多聚蛋白基因的序列分析表明,它们与其他已知PKV的核苷酸相似性较低(86.3%-88.1%)。虽然两者在2B区域都有30个氨基酸的缺失,但系统发育分析表明JXJC2015与第1组甚至第2组不同,形成了一个新的组(命名为第3组)。本研究结果进一步揭示了PKV的遗传多样性及其与其他病原体联合在仔猪中的可能致病作用。