Molecular Analysis of Classical Swine Fever Virus Associated Field Infections Evidence Novel CSFV Sub Genotype in Tamil Nadu, Southern India

IF 2.1 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
S. Parthiban, B. Kowsalya, M. Parthiban, A. Ramesh, P. Raja, K. Gopal, S. Jaisree, R. Thangathurai, K. Senthilkumar
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引用次数: 0

Abstract

Classical swine fever (CSF) is an endemic and major viral infection of Indian swine husbandry, contributing to great economic losses with multiple genotypes associated with vast clinical and subclinical outcomes. Molecular detection and genotyping of CSF virus directly from field samples has great application in disease monitoring and control measures hence this study aimed to isolate and characterize CSFV genotypes circulating in southern states of India. Fifty-seven porcine post-mortem tissues (lymph nodes, spleens, livers, lungs, and kidneys) collected from pigs suspected of systemic infections and sudden death with the history of live attenuated CSF vaccination from different regions of Tamil Nadu were used in this study. An NS5B gene based CSFV specific RT-PCR screening confirmed CSFV positivity in 7% (4/57) of samples with a specific amplicon of 449 bp. Further molecular screening for other viral co-infections such as PCV2, PPV and PRRSV done by specific individual PCR assays to all the samples. Non-involvement of above screened three viral pathogens in all four field samples which showed positivity for CSFV confirming CSFV as primary pathogen. Two RT-PCR positive samples (TNI-4 and CHNL-2) selected randomly and sequenced. Aligned contig sequences of both samples were subjected to BLAST homology search and phylogentic characterization. BLAST study of TNI-4 sequence revealed 99% sequence identity with Indian CSFV sequences of genotype 1 and CHNL-2 showed 98% sequence identity with Indian CSFV sequences of genotype 2. Phylogenetic analysis of the TNI-4 and CHNL-2 sequences obtained in this study along with 38 published CSFV sequences consisting of all 5 new genotypes and 14 sub genotypes through the Maximum Likelihood tree method in MEGA 11 revealed that TNI-4 clustering together with 1.7 sub genotypes and CHNL-2 clustering together with 2.2 sub genotypes. TNI-4 and CHNL-2 partial NS5B gene sequences obtained in this study deposited in the GenBank database under accession numbers of MW822568 and MW822569 respectively. The study is the first to report CSF infections associated with the newer 1.7 sub genotype in Tamil Nadu, southern India. It is possible that vaccination could affect the genetic diversity of the CSFV through recombination and point mutations for immune evasion.

Abstract Image

印度南部泰米尔纳德邦古典猪瘟病毒相关田间感染的分子分析证明了新型 CSFV 亚基因型
典型猪瘟(CSF)是印度养猪业中的一种地方性主要病毒感染,造成了巨大的经济损失,多种基因型与不同的临床和亚临床结果相关。直接从野外样本中对 CSF 病毒进行分子检测和基因分型在疾病监测和控制措施中具有重要应用价值,因此本研究旨在分离和鉴定印度南部各邦流行的 CSFV 基因型。本研究使用了 57 份猪死后组织(淋巴结、脾脏、肝脏、肺脏和肾脏),这些组织来自泰米尔纳德邦不同地区的疑似全身感染猪和有 CSF 减毒活疫苗接种史的猝死猪。基于 NS5B 基因的 CSFV 特异性 RT-PCR 筛查证实,7%(4/57)的样本中 CSFV 呈阳性,特异性扩增片段为 449 bp。通过对所有样本进行特异性单独 PCR 检测,进一步对其他病毒合并感染(如 PCV2、PPV 和 PRRSV)进行了分子筛查。四份现场样本均未检出上述三种病毒病原体,其中 CSFV 呈阳性,证实 CSFV 为主要病原体。随机选择了两个 RT-PCR 阳性样本(TNI-4 和 CHNL-2)并进行了测序。对这两个样本的等位基因序列进行了 BLAST 同源搜索和系统特性分析。BLAST研究显示,TNI-4序列与印度CSFV基因型1序列的一致性为99%,而CHNL-2与印度CSFV基因型2序列的一致性为98%。通过在 MEGA 11 中使用最大似然树法,对本研究中获得的 TNI-4 和 CHNL-2 序列以及 38 个已发表的 CSFV 序列(包括所有 5 个新基因型和 14 个亚基因型)进行系统进化分析,发现 TNI-4 与 1.7 个亚基因型聚类,CHNL-2 与 2.2 个亚基因型聚类。本研究获得的 TNI-4 和 CHNL-2 部分 NS5B 基因序列已存入 GenBank 数据库,登录号分别为 MW822568 和 MW822569。该研究首次报告了印度南部泰米尔纳德邦与较新的 1.7 亚基因型相关的 CSF 感染。接种疫苗可能会通过重组和点突变影响 CSFV 的遗传多样性,从而逃避免疫。
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来源期刊
Indian Journal of Microbiology
Indian Journal of Microbiology BIOTECHNOLOGY & APPLIED MICROBIOLOGY-MICROBIOLOGY
CiteScore
6.00
自引率
10.00%
发文量
51
审稿时长
1 months
期刊介绍: Indian Journal of Microbiology is the official organ of the Association of Microbiologists of India (AMI). It publishes full-length papers, short communication reviews and mini reviews on all aspects of microbiological research, published quarterly (March, June, September and December). Areas of special interest include agricultural, food, environmental, industrial, medical, pharmaceutical, veterinary and molecular microbiology.
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