Porcine reproductive and respiratory syndrome virus: Antigenic and molecular diversity of British isolates and implications for diagnosis

被引:14
作者
Frossard, Jean-Pierre [1 ]
Fearnley, Catherine [1 ]
Naidu, Brindha [1 ]
Errington, Jane [2 ]
Westcott, David G. [1 ]
Drew, Trevor W. [1 ]
机构
[1] Anim Hlth & Vet Labs Agcy Weybridge, New Haw KT15 3NB, Surrey, England
[2] Anim Hlth & Vet Labs Agcy Penrith, Penrith CA11 9RR, Cumbria, England
关键词
Porcine respiratory and reproductive syndrome virus; Antigenic diversity; Serologic tests; Reverse transcriptase polymerase; chain reaction; MONOCLONAL-ANTIBODIES; SEQUENCE ALIGNMENT; LELYSTAD VIRUS; PRRS VIRUS; AMERICAN; STRAINS; EUROPE; PCR;
D O I
10.1016/j.vetmic.2012.03.004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Porcine reproductive and respiratory syndrome (PRRS) is an endemic disease of pigs, caused by PRRS virus, a member of the Arteriviridae family. First seen in Britain in 1991, the disease continues to be a significant economic and welfare problem for pig producers. To date, only PRRSV genotype 1 has been found in Britain. At the genetic level, a considerable increase has been reported in the diversity of PRRS viruses isolated in Britain between 2003 and 2007, versus the early 1990s. In this study, the diversity has been shown to extend to the antigenic level too, with potential consequences for diagnostic methods. Antigenic diversity was assessed using a panel of twelve monoclonal antibodies, only one of which reacted with all isolates tested. Nine diverse viruses were compared as potential antigens in immunoperoxidase monolayer assays, where each one produced quite different results for a common panel of sera. As a single virus is used in each diagnostic assay, results must therefore be interpreted cautiously. For a real-time RT-PCR assay, published oligonucleotide primer and probe sequences were evaluated against available genetic sequences of British and European viruses, and were re-designed where considerable mismatches were found. The multiplex assay incorporating these modified primers to detect genotype 1 and 2 PRRS viruses was then validated for use with diagnostic sera and tissues. As the increasing degree of diversity exhibited by British strains is mirrored in other countries, PRRSV will continue to provide an ongoing challenge to diagnosis at a global, as well as national level. Crown Copyright (C) 2012 Published by Elsevier B.V. All rights reserved.
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收藏
页码:308 / 315
页数:8
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