A multiplex RT-PCR assay for detection and differentiation of avian H3, H5, and H9 subtype influenza viruses and Newcastle disease viruses

被引:19
作者
Tang, Qingdong [1 ]
Wang, Jinhang [1 ]
Bao, Jingnan [1 ]
Sun, Honglei [1 ]
Sun, Yipeng [1 ]
Liu, Jinhua [1 ,2 ]
Pu, Juan [1 ]
机构
[1] China Agr Univ, Coll Vet Med, Minist Agr, Key Lab Anim Epidemiol & Zoonosis, Beijing 100193, Peoples R China
[2] Shandong Anim Dis Control Ctr, Jinan 250022, Shandong, Peoples R China
关键词
Avian influenza viruses; H3; subtype; H5; H9; Newcastle disease viruses; Multiplex RT-PCR; POLYMERASE-CHAIN-REACTION; GENOME SEQUENCE-ANALYSIS; HEMAGGLUTININ GENE; OLIGONUCLEOTIDE MICROARRAYS; RAPID DETECTION; HONG-KONG; CHINA; POULTRY; EVOLUTION; CHICKENS;
D O I
10.1016/j.jviromet.2012.02.003
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Avian influenza viruses (AIVs) and Newcastle disease viruses (NDVs) co-circulate in the poultry population in China. These viruses cause repeated disease outbreaks that exhibit similar clinical symptoms and epidemiological patterns. H5 and H9 influenza viruses are the major pathogens infecting poultry stocks. Recently, H3 AIV (one of the main subtypes in waterfowl) has become endemic in chickens. A multiplex reverse-transcriptase polymerase chain reaction (mRT-PCR) assay was designed for simultaneous detection and differentiation of avian H3, H5, H9 subtype AIVs and NDVs. Four primer sets were evaluated, three of which specifically targeted the hemagglutinin genes of H3, H5 and H9 AIVs, while the other targeted the NDV fusion gene. The sensitivity and specificity of the mRT-PCR assay was determined. The assay detected the major clades or genotypes of all of the reference AIVs and NDVs currently circulating in China. In addition, the mRT-PCR results obtained from screening 380 clinical swabs and 12 experimental tracheal samples were consistent with those obtained using conventional virus isolation methods. The mRT-PCR assay was established successfully for the detection and differentiation of avian H3, H5, and H9 subtype AIVs and NDVs. The method should, therefore, provide a valuable diagnostic tool for these infections. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:164 / 169
页数:6
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