云南省2019 - 2023年肿块性皮肤病病毒分子检测及系统发育分析

IF 2 3区 农林科学 Q2 VETERINARY SCIENCES
Jun Yao, Xue Li, Lei Tan, Lin Gao, Pei Zhu, Jiarui Xie, Rui Yan, Taoyin Yu, Fengyi Xia, Qiyun Chen, Bangquan Zeng, Jiaping Yang
{"title":"云南省2019 - 2023年肿块性皮肤病病毒分子检测及系统发育分析","authors":"Jun Yao, Xue Li, Lei Tan, Lin Gao, Pei Zhu, Jiarui Xie, Rui Yan, Taoyin Yu, Fengyi Xia, Qiyun Chen, Bangquan Zeng, Jiaping Yang","doi":"10.1007/s11259-025-10879-6","DOIUrl":null,"url":null,"abstract":"<p><p>The lumpy skin disease (LSD), caused by the lumpy skin disease virus (LSDV), represents an emerging infectious disease that poses substantial economic losses to the cattle industries in China. This study aimed to investigate the epidemiological characteristics of LSDV in Yunnan Province, Southwest China, from 2019 to 2023. A Taqman-probe-based real-time PCR (qPCR) assay was developed for the molecular detection of LSDV nucleotides. In total, 2495 samples were collected and tested using the established method. LSDV-positive samples were further analyzed by amplifying and sequencing the GPCR and p32 genes. In addition, Viral isolation was performed to explore the biological characterisitics of the isolate. The developed qPCR assay demonstrated high sensitivity, with a limit of detection of 4.83 copies/µL. Six samples (0.24%) tested positive for LSDV, all originating from skin scabs. Molecular and phylogenetic analyses of the GPCR and p32 genes revealed that these six LSDV strains were genetically related to strains previously reported from China, Russia, and Thailand. One LSDV strain, designated YUN-LSDV, was successfully isolated in primary sheep testicular (PST) cells; while the isolate exhibited insensitivity to Madin-Darby bovine kidney cells. Collectively, this study represents the first report on the epidemiological characteristics of LSDV in cattle in Yunnan Province and contributes to the development of effective prevention and control strategies for LSD.</p>","PeriodicalId":23690,"journal":{"name":"Veterinary Research Communications","volume":"49 5","pages":"297"},"PeriodicalIF":2.0000,"publicationDate":"2025-09-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Molecular detection and phylogenetic analysis of lumpy skin disease virus in Yunnan Province, China from 2019 to 2023.\",\"authors\":\"Jun Yao, Xue Li, Lei Tan, Lin Gao, Pei Zhu, Jiarui Xie, Rui Yan, Taoyin Yu, Fengyi Xia, Qiyun Chen, Bangquan Zeng, Jiaping Yang\",\"doi\":\"10.1007/s11259-025-10879-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The lumpy skin disease (LSD), caused by the lumpy skin disease virus (LSDV), represents an emerging infectious disease that poses substantial economic losses to the cattle industries in China. This study aimed to investigate the epidemiological characteristics of LSDV in Yunnan Province, Southwest China, from 2019 to 2023. A Taqman-probe-based real-time PCR (qPCR) assay was developed for the molecular detection of LSDV nucleotides. In total, 2495 samples were collected and tested using the established method. LSDV-positive samples were further analyzed by amplifying and sequencing the GPCR and p32 genes. In addition, Viral isolation was performed to explore the biological characterisitics of the isolate. The developed qPCR assay demonstrated high sensitivity, with a limit of detection of 4.83 copies/µL. Six samples (0.24%) tested positive for LSDV, all originating from skin scabs. Molecular and phylogenetic analyses of the GPCR and p32 genes revealed that these six LSDV strains were genetically related to strains previously reported from China, Russia, and Thailand. One LSDV strain, designated YUN-LSDV, was successfully isolated in primary sheep testicular (PST) cells; while the isolate exhibited insensitivity to Madin-Darby bovine kidney cells. Collectively, this study represents the first report on the epidemiological characteristics of LSDV in cattle in Yunnan Province and contributes to the development of effective prevention and control strategies for LSD.</p>\",\"PeriodicalId\":23690,\"journal\":{\"name\":\"Veterinary Research Communications\",\"volume\":\"49 5\",\"pages\":\"297\"},\"PeriodicalIF\":2.0000,\"publicationDate\":\"2025-09-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Veterinary Research Communications\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://doi.org/10.1007/s11259-025-10879-6\",\"RegionNum\":3,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"VETERINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Veterinary Research Communications","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1007/s11259-025-10879-6","RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"VETERINARY SCIENCES","Score":null,"Total":0}
引用次数: 0

摘要

由疙瘩状皮肤病病毒(LSDV)引起的疙瘩状皮肤病(LSD)是一种新兴的传染病,给中国的养牛业造成了巨大的经济损失。本研究旨在了解2019 - 2023年云南省LSDV的流行病学特征。建立了一种基于taqman探针的实时荧光定量PCR (qPCR)方法,用于LSDV核苷酸的分子检测。采用所建立的方法,共采集样品2495份。对lsvv阳性样本进行GPCR和p32基因扩增和测序。此外,还进行了病毒分离,以探索分离物的生物学特性。该方法灵敏度高,检测限为4.83 copies/µL。6个样本(0.24%)LSDV检测呈阳性,均来自皮肤痂。GPCR和p32基因的分子和系统发育分析表明,这6株LSDV与此前报道的中国、俄罗斯和泰国的LSDV有亲缘关系。在绵羊原代睾丸(PST)细胞中成功分离到一株LSDV,命名为YUN-LSDV;而分离物对马丁-达比牛肾细胞不敏感。本研究首次报道了云南省牛LSDV的流行病学特征,有助于制定有效的LSDV防治策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular detection and phylogenetic analysis of lumpy skin disease virus in Yunnan Province, China from 2019 to 2023.

The lumpy skin disease (LSD), caused by the lumpy skin disease virus (LSDV), represents an emerging infectious disease that poses substantial economic losses to the cattle industries in China. This study aimed to investigate the epidemiological characteristics of LSDV in Yunnan Province, Southwest China, from 2019 to 2023. A Taqman-probe-based real-time PCR (qPCR) assay was developed for the molecular detection of LSDV nucleotides. In total, 2495 samples were collected and tested using the established method. LSDV-positive samples were further analyzed by amplifying and sequencing the GPCR and p32 genes. In addition, Viral isolation was performed to explore the biological characterisitics of the isolate. The developed qPCR assay demonstrated high sensitivity, with a limit of detection of 4.83 copies/µL. Six samples (0.24%) tested positive for LSDV, all originating from skin scabs. Molecular and phylogenetic analyses of the GPCR and p32 genes revealed that these six LSDV strains were genetically related to strains previously reported from China, Russia, and Thailand. One LSDV strain, designated YUN-LSDV, was successfully isolated in primary sheep testicular (PST) cells; while the isolate exhibited insensitivity to Madin-Darby bovine kidney cells. Collectively, this study represents the first report on the epidemiological characteristics of LSDV in cattle in Yunnan Province and contributes to the development of effective prevention and control strategies for LSD.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Veterinary Research Communications
Veterinary Research Communications 农林科学-兽医学
CiteScore
2.50
自引率
0.00%
发文量
173
审稿时长
3 months
期刊介绍: Veterinary Research Communications publishes fully refereed research articles and topical reviews on all aspects of the veterinary sciences. Interdisciplinary articles are particularly encouraged, as are well argued reviews, even if they are somewhat controversial. The journal is an appropriate medium in which to publish new methods, newly described diseases and new pathological findings, as these are applied to animals. The material should be of international rather than local interest. As it deliberately seeks a wide coverage, Veterinary Research Communications provides its readers with a means of keeping abreast of current developments in the entire field of veterinary science.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信