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PCV2a、PCV2b和PCV2d多重PCR检测方法的建立及应用

谭健梅 雷红宇 苏建明 王乃东 湛洋 赵雨欣 黄艳玲 周小汇 陈媛 雷磊 罗施乐 郝裕波 杜红梅

中国兽医科学2024,Vol.54Issue(7):896-904,9.
中国兽医科学2024,Vol.54Issue(7):896-904,9.DOI:10.16656/j.issn.1673-4696.2024.0124

PCV2a、PCV2b和PCV2d多重PCR检测方法的建立及应用

Establishment and application of multiplex PCR assay for PCV2a,PCV2b and PCV2d

谭健梅 1雷红宇 1苏建明 1王乃东 1湛洋 1赵雨欣 1黄艳玲 1周小汇 1陈媛 2雷磊 1罗施乐 2郝裕波 1杜红梅3

作者信息

  • 1. 湖南农业大学动物医学院,湖南长沙 410128||兽用蛋白质工程疫苗湖南省重点实验室,湖南长沙 410128
  • 2. 湖南派智生物科技有限公司,湖南长沙 410205
  • 3. 常德市畜牧水产事务中心,湖南常德 415000
  • 折叠

摘要

Abstract

The purpose of this study was to develop a rapid detection method for identification of PCV2a,PCV2b and PCV2d,three sets of specific primers were designed for the three genotypes of PCV2a,PCV2b and PCV2d,respectively.The optimized sets of primers were selected by constructed positive standard plasmids,and a multiplex PCR method for identification of PCV2 genotypes was established.The reaction conditions were optimized and the specificity experiments,sensitivity experiments and re-peatability experiments were verified,and clinical samples were used for preliminary application by this method.The results showed that a multiplex PCR detection method was established by using the opti-mal sets of primers,which could specifically amplify three target fragments:PCV2a(321 bp),PCV2b(190 bp)and PCV2d(561 bp).Furthermore,the optimum annealing temperature was 60 ℃ and cycle number was 25.This method had no cross-reaction with other pathogens(PPV,PRV,PEDV,TGEV,PRRSV,CSFV),and the limit of detection was 103 copies by using the positive standard plasmid.Besides,this method had good repeatability with coefficients of three repeatability tests using the same template.The PCV2 strains prevalent in 2 pig farms were detected by the method,the main genotype was determined,and the accuracy of the detection method was further verified by sequencing and evolutionary analysis.The multiplex PCR detection method developed in this study was conducive to the rapid identified diagnosis of PCV2a,PCV2b and PCV2d,and provided technical support for the control of PCV2 and epidemiological studies.

关键词

PCV2a/PCV2b/PCV2d/共感染/多重PCR

Key words

PCV2a/PCV2b/PCV2d/co-infection/multiple PCR

分类

农业科技

引用本文复制引用

谭健梅,雷红宇,苏建明,王乃东,湛洋,赵雨欣,黄艳玲,周小汇,陈媛,雷磊,罗施乐,郝裕波,杜红梅..PCV2a、PCV2b和PCV2d多重PCR检测方法的建立及应用[J].中国兽医科学,2024,54(7):896-904,9.

基金项目

国家自然科学基金项目(32202790) (32202790)

湖南省自然科学基金项目(2022JJ40183) (2022JJ40183)

湖南省技术攻关"揭榜挂帅"项目(2021NK1030) (2021NK1030)

湖南省青年科技人才项目(2022RC1046) (2022RC1046)

湖南省教育厅科学研究重点项目(23A0194) (23A0194)

中国兽医科学

OA北大核心CSTPCD

1673-4696

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