為準(zhǔn)確檢測(cè)豬圓環(huán)病毒2型（PCV2）并分析其基因序列情況，在序列比對(duì)分析的基礎(chǔ)上，設(shè)計(jì)一對(duì)簡(jiǎn)并引物和一條探針，經(jīng)體系優(yōu)化建立了PCV2的熒光PCR方法。該方法可檢出10拷貝的PCV2質(zhì)粒DNA，不與豬瘟病毒等多種病毒發(fā)生交叉反應(yīng)。對(duì)送檢的2批次45份病死豬臟器進(jìn)行檢測(cè)，檢出25份陽性樣品，與套式PCR方法的復(fù)合率為95.6%；對(duì)3份強(qiáng)陽性樣品使用一對(duì)全基因組擴(kuò)增引物，擴(kuò)增了PCV2型全基因片段；經(jīng)克隆測(cè)序后分析，發(fā)現(xiàn)3個(gè)病毒基因分別屬于2種基因亞型（PCV2b和PCV2d）。本研究對(duì)于PCV2的準(zhǔn)確檢測(cè)及其變異特征的了解具有參考意義。
Detection ofPorcine Circovirus Type 2 in Dead Pigs and Analysis on ItsComplete Genome Sequence
In order toaccurately detect porcine circovirus type 2（PCV2）and to analyze its genome sequence，a pair of degenerate primers and aprobe were designed based on sequence alignment analysis，after systematic optimization，a real-time PCR method was established，which could detect 10 copies ofplasmid DNA of PCV2，with no anycross reaction with classical swine fever virus and other viruses. Then twobatches of 45 organ samples collected from dead pigs were tested by establishedmethod，and 25 samples were detected to bepositive，the coincidence rate with nested-PCRwas 95.6%；for the three strong-positive samples，their complete gene fragments of PCV2were amplified by a pair of primers，then weresequenced and analyzed，and it wasfound that the genes of the three viruses were classified into two differentsubtypes（PCV2b and PCV2d）. Therefore，it was of certain significance toconfirm relevant test results and recognize any variation of PCV2 by the abovemethod.
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