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基于ORF3基因和S1基因的中国中部地区猪流行性腹泻病毒的检测与系统发育分析

Detection and phylogenetic analysis of porcine epidemic diarrhea virus in central China based on the ORF3 gene and the S1 gene.

作者信息

Su Yunfang, Liu Yunchao, Chen Yumei, Zhao Baolei, Ji Pengchao, Xing Guangxu, Jiang Dawei, Liu Chang, Song Yapeng, Wang Guoqiang, Li Dongliang, Deng Ruiguang, Zhang Gaiping

机构信息

College of Veterinary Medicine, Northwest Agriculture and Forestry University, Yangling, Shaanxi, 712100, China.

Henan Provincial Key Laboratory of Animal Immunology, Henan Academy of Agricultural Science, Zhengzhou, 450002, China.

出版信息

Virol J. 2016 Nov 25;13(1):192. doi: 10.1186/s12985-016-0646-8.

Abstract

BACKGROUND

Porcine epidemic diarrhea (PED) has increased in severity in China since 2010. To investigate further the infectivity, genetic diversity and molecular epidemiology of its causative agent, the porcine epidemic diarrhea virus (PEDV), we assessed 129 clinical samples, which were the intestinal tissue of piglets with severe diarrhea, from 17 cities in central China. Both the spike (S) glycoprotein (S1, 1-789 amino acids (aa)) and the full-length ORF3 gene of 21 representative field strains from 21 farms in 11 cities were sequenced and analysed.

METHODS

PEDV was detected by reverse transcription-polymerase chain reaction (RT-PCR), and S1 and ORF3 sequences were processed by the Clustal W method via DNAMAN 8 software, and phylogenetic trees were constructed by the neighbor-joining method using MEGA 6 software.

RESULTS

The prevalence of PEDV was 92.25% and was detected in 119 of 129 samples, with 94.03% (63 of 67) of pig farms harbouring the disease. According to the phylogenetic analysis of the S1 genes, our isolates all fell into group G2 (variants) and showed a close relationship to isolates from Chinese (HN1303, CH/ZMDZY/11 and AJ1102), Korean (AD01), American (MN, IA1, IA2 and 13-019349) sources, and these isolates differed genetically from other Chinese (LZC, CH/HNZZ/2011 and SD-M) and Korean (SM98) strains as well Japanese (83-P5 and MK) strains. In addition, our isolates differed from attenuated vaccine strains, CV777 (used in China) and DR13 (used in Korea). According to our derived amino acid sequence analysis, we detected one novel variant PEDV, viz: CH/HNLY, with 4-aa insertion/deletion (RSSS/T) at position 375 and 1-aa (D) deletion at position 430 compared to the CV777 attenuated strain. These mutations were located on the receptor binding domain. Our ORF3 gene analyses showed that the prevalent PEDV isolates were variants, and the isolated strains differed genetically from the vaccine strains.

CONCLUSIONS

These findings illustrated the existence of genetic diversity among geographically distinct PEDV strains, and our study has provided an impetus to conduct further research on the PEDV receptor binding protein and on the new and efficacious vaccines design.

摘要

背景

自2010年以来,猪流行性腹泻(PED)在中国的严重程度有所增加。为了进一步研究其病原体猪流行性腹泻病毒(PEDV)的传染性、遗传多样性和分子流行病学,我们评估了来自中国中部17个城市的129份临床样本,这些样本是患有严重腹泻的仔猪的肠道组织。对来自11个城市21个养殖场的21株代表性田间毒株的刺突(S)糖蛋白(S1,1 - 789个氨基酸(aa))和全长ORF3基因进行了测序和分析。

方法

通过逆转录 - 聚合酶链反应(RT - PCR)检测PEDV,S1和ORF3序列通过DNAMAN 8软件的Clustal W方法进行处理,并使用MEGA 6软件通过邻接法构建系统发育树。

结果

PEDV的流行率为92.25%,在129份样本中的119份中检测到该病毒,67个猪场中有94.03%(63个)感染了该病。根据S1基因的系统发育分析,我们的分离株均属于G2组(变异株),与来自中国(HN1303、CH/ZMDZY/11和AJ1102)、韩国(AD01)、美国(MN、IA1、IA2和13 - 019349)的分离株关系密切,并且这些分离株在基因上与其他中国(LZC、CH/HNZZ/2011和SD - M)、韩国(SM98)毒株以及日本(83 - P5和MK)毒株不同。此外,我们的分离株与减毒疫苗株CV777(在中国使用)和DR13(在韩国使用)不同。根据我们推导的氨基酸序列分析,我们检测到一种新型变异PEDV,即:CH/HNLY,与CV777减毒株相比,在375位有4个氨基酸的插入/缺失(RSSS/T),在430位有1个氨基酸(D)缺失。这些突变位于受体结合域。我们的ORF3基因分析表明,流行的PEDV分离株是变异株,分离株在基因上与疫苗株不同。

结论

这些发现说明了地理上不同的PEDV毒株之间存在遗传多样性,我们的研究为进一步研究PEDV受体结合蛋白以及新型高效疫苗设计提供了动力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/534f/5123408/42fd8af22f0a/12985_2016_646_Fig1_HTML.jpg

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