...
首页> 外文期刊>Virology Journal >Molecular analysis of partial VP-2 gene amplified from rectal swab samples of diarrheic dogs in Pakistan confirms the circulation of canine parvovirus genetic variant CPV-2a and detects sequences of feline panleukopenia virus (FPV)
【24h】

Molecular analysis of partial VP-2 gene amplified from rectal swab samples of diarrheic dogs in Pakistan confirms the circulation of canine parvovirus genetic variant CPV-2a and detects sequences of feline panleukopenia virus (FPV)

机译:从巴基斯坦腹泻犬直肠拭子样本中扩增的部分VP-2基因的分子分析证实了犬细小病毒基因变异CPV-2a的流通并检测了猫泛白细胞减少症病毒(FPV)的序列

获取原文
           

摘要

The infection in dogs due to canine parvovirus (CPV), is a highly contagious one with high mortality rate. The present study was undertaken for a detailed genetic analysis of partial VP2 gene i.e., 630?bp isolated from rectal swab samples of infected domestic and stray dogs from all areas of district Faisalabad. Monitoring of viruses is important, as continuous prevalence of viral infection might be associated with emergence of new virulent strains. In the present study, 40 rectal swab samples were collected from diarrheic dogs from different areas of district Faisalabad, Pakistan, in 2014–15 and screened for the presence of CPV by immunochromatography. Most of these dogs were stray dogs showing symptoms of diarrhea. Viral DNA was isolated and partial VP2 gene was amplified using gene specific primer pair Hfor/Hrev through PCR. Amplified fragments were cloned in pTZ57R/T (Fermentas) and completely sequenced. Sequences were analyzed and assembled by the Lasergene DNA analysis package (v8; DNAStar Inc., Madison, WI, USA). The results with immunochromatography showed that 33/40 (82%) of dogs were positive for CPV. We were able to amplify a fragment of 630?bp from 25 samples. In 25 samples the sequences of CPV-2a were detected showing the amino acid substitution Ser297Ala and presence of amino acid (426-Asn) in partial VP2 protein. Interestingly the BLAST analysis showed the of feline panleukopenia virus (FPV) sequences in 3 samples which were already positive for new CPV-2a, with 99% sequence homology to other FPV sequences present in GenBank. Phylogenetic analysis showed clustering of partial CPV-VP-2 gene with viruses from China, India, Japan and Uruguay identifying a new variant, whereas the 3 FPV sequences showed immediate ancestral relationship with viruses from Portugal, South Africa and USA. Interesting observation was that CPV are clustering away from the commercial vaccine strains. In this work we provide a better understanding of CPV prevailing in Pakistan at molecular level. The detection of FPV could be a case of real co-infection or a case of dual presence, due to ingestion of contaminated food.
机译:犬细小病毒(CPV)引起的狗感染是一种具有高传染性的动物,死亡率很高。进行本研究是为了详细分析部分VP2基因,即从Faisalabad地区所有地区的受感染家犬和流浪狗的直肠拭子样本中分离出的630bp的基因。病毒的监测非常重要,因为病毒感染的持续流行可能与新毒株的出现有关。在本研究中,2014-15年度从巴基斯坦费萨拉巴德地区不同地区的腹泻犬收集了40个直肠拭子样本,并通过免疫色谱法筛选了CPV的存在。这些狗大多数是流浪狗,表现出腹泻症状。分离病毒DNA,并使用基因特异性引物对Hfor / Hrev通过PCR扩增部分VP2基因。将扩增的片段克隆到pTZ57R / T(Fermentas)中并进行完整测序。通过Lasergene DNA分析软件包(v8; DNAStar Inc.,麦迪逊,威斯康星州,美国)分析和组装序列。免疫色谱法的结果表明,33/40(82%)的狗CPV阳性。我们能够从25个样品中扩增出630bp的片段。在25个样品中检测到CPV-2a序列,显示部分VP2蛋白中存在氨基酸取代Ser297Ala和氨基酸(426-Asn)。有趣的是,BLAST分析显示3个样本中的猫泛白细胞减少病毒(FPV)序列已经对新CPV-2a呈阳性,与GenBank中存在的其他FPV序列具有99%的同源性。系统发育分析表明,部分CPV-VP-2基因与来自中国,印度,日本和乌拉圭的病毒聚集在一起,确定了一个新的变异体,而3个FPV序列显示与来自葡萄牙,南非和美国的病毒有着直接的祖传关系。有趣的观察是,CPV正在远离商业疫苗株。在这项工作中,我们从分子水平上更好地了解了CPV在巴基斯坦盛行。由于摄入被污染的食物,FPV的检测可能是真正的共同感染或双重存在。

著录项

相似文献

  • 外文文献
  • 中文文献
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号