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基于S基因序列分析新型猪流行性腹泻病毒的遗传演化
引用本文:周昱行,胡承哲,周群,王何欣,董沙沙,刘娟,张丹丹,任玉鹏,张斌.基于S基因序列分析新型猪流行性腹泻病毒的遗传演化[J].畜牧兽医学报,2020,51(1):109-119.
作者姓名:周昱行  胡承哲  周群  王何欣  董沙沙  刘娟  张丹丹  任玉鹏  张斌
作者单位:1. 西南民族大学生命科学与技术学院, 成都 610041;2. 国家民族事务委员会青藏高原动物疫病防控创新团队, 成都 610041
基金项目:国家自然科学基金(31772766);四川省教育厅创新团队项目(13TD0057);西南民族大学中央高校青年项目(2017NZYQN01)
摘    要:最近,笔者实验室在青藏高原地区发现两种新亚型藏猪源猪流行性腹泻病毒(PEDV),为进一步调查新型PEDV是否在四川腹泻猪群中存在或流行,对实验室2018-2019年保存的116份猪腹泻粪便或肠组织样本进行PEDV的检测及其纤突蛋白基因(spike)分子特征研究。结果表明:腹泻样本的PEDV检出率为42.2%(49/116,95% CI=33.1%~51.8%),并获得了13条完整的S基因序列,全长为4 149~4 170 bp,序列相似性为94.2%~99.9%,其中SWUN-H3-CH-SCYA-2019的S基因与藏猪源新G1亚群PEDV的序列相似性高达97.0%~98.6%。遗传演化研究结果表明13株PEDV S基因划分为G1和G2大群,其中SWUN-H3-CH-SCYA-2019位于藏猪源新G1亚群;SWUN-19-CH-SCZY-2018、SWUN-4-CH-SCXC-2018、SWUN-1-CH-SCNJ-2019和SWUN-3CH-CH-SCZG-2019位于G2亚群中一个独立的分支,且与藏猪源新G2亚群毒株有着较近的亲缘关系。为了进一步研究13株PEDV的演化过程,以贝叶斯进化分析软件包(BEAST)进行分歧时间估算,结果表明SWUN-H3-CH-SCYA-2019的分歧时间约为2012.3年,早于藏猪源新G1亚群其余毒株的最早分歧时间(2015.7年);SWUN-4-CH-SCXC-2018、SWUN-19-CH-SCZY-2018和SWUN-3CH-CH-SCZG-2019的分歧时间约为2014.2年,早于G2亚群的藏猪源毒株2014.7年,所有藏猪源PEDV的分歧时间均晚于四川毒株。本研究在四川地区首次发现了藏猪源PEDV,并且从毒株的分歧时间推断青藏高原的藏猪源PEDV来源于四川,为新型PEDV分子遗传进化的监测提供了依据。

关 键 词:猪流行性腹泻病毒  S蛋白  遗传分析  分子钟  
收稿时间:2019-07-30

Phylogenetic and Evolutionary Analysis of Novel Porcine Epidemic Diarrhea Virus Based on S Gene
ZHOU Yuxing,HU Chengzhe,ZHOU Qun,WANG Hexin,DONG Shasha,LIU Juan,ZHANG Dandan,REN Yupeng,ZHANG Bin.Phylogenetic and Evolutionary Analysis of Novel Porcine Epidemic Diarrhea Virus Based on S Gene[J].Acta Veterinaria et Zootechnica Sinica,2020,51(1):109-119.
Authors:ZHOU Yuxing  HU Chengzhe  ZHOU Qun  WANG Hexin  DONG Shasha  LIU Juan  ZHANG Dandan  REN Yupeng  ZHANG Bin
Institution:1. College of Life Science and Technology, Southwest Minzu University, Chengdu 610041, China;2. Animal Disease Prevention and Control Innovation Team in the Qinghai-Tibet Plateau of State Ethnic Affairs Commission, Chengdu 610041, China
Abstract:Recently, two novel subgroups of porcine epidemic diarrhea virus (PEDV) were identified in Tibetan pigs on the Qinghai-Tibet Plateau. We further investigated if the novel variant PEDV exists or had been prevalent in Sichuan region. One hundred and sixteen fecal and intestinal tissue samples collected in 2018-2019 from diarrheal pigs of Sichuan were detected for PEDV by RT-PCR, and the molecular characteristics of Spike genes (S) of PEDV were further investigated in this study. The results showed that the detection rate of PEDV was 42.2% (49/116, 95%CI=33.1%-51.8%) in diarrhea samples. Thirteen complete S gene sequences were obtained, and they were 4 149-4 170 bp in length, sharing 94.2%-99.9% identities with each other. Interestingly, SWUN-H3-CH-SCYA-2019 shared 97.0%-98.6% nucleotide sequence identities with those of the novel G1 subgroup of Tibetan Pig PEDVs. Phylogenetic and evolutionary analysis showed that the 13 S genes obtained in this study could be divided into G1 and G2 subgroups, one of which (SWUN-H3-CH-SCYA-2019 strain) fell into the novel G1 subgroup of Tibetan Pig PEDVs; the SWUN-19-CH-SCZY-2018, SWUN-4-CH-SCXC-2018, SWUN-1-CH-SCNJ-2019 and SWUN-3CH-CH-SCZG-2019 were clustered into an unique branch of G2 subgroup, and shared high sequence identities with the novel G2 subgroup of Tibetan Pig PEDVs. To further study the evolution process of 13 PEDVs, the BEAST software was used to estimate the divergence time. The results showed that the divergence time of SWUN-H3-CH-SCYA-2019 was about 2012.3 year, earlier than the earliest divergence time of the other novel G1 subgroup strains (2015.7 year), and the divergence time of SWUN-4-CH-SCXC-2018, SWUN-19-CH-SCZY-2018 and SWUN-3CH-CH-SCZG-2019 were about 2014.2 year, earlier than that of the novel G2 subgroup (2014.7 year). The divergence time of Tibetan pig PEDVs was later than that of strains identified in this study. Tibetan Pig PEDVs were first detected in Sichuan region, and we deduced a conclusion from different divergence time that the novel Tibetan Pig PEDVs were originated from Sichuan region. This study will provide the theoretical basis for monitoring the new variation of PEDV.
Keywords:porcine epidemic diarrhea virus  S protein  phylogenetic analysis  molecular clock  
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