根據(jù)GenBank登錄的豬德爾塔冠狀病毒（PDCoV）毒株M基因設(shè)計(jì)特異性引物，建立了PDCoV納米PCR檢測(cè)方法并進(jìn)行了臨床樣品檢測(cè)。結(jié)果顯示：該方法對(duì)標(biāo)準(zhǔn)品檢測(cè)的最低濃度可達(dá)102 copies/μL，與其他幾種常見豬病病毒無交叉反應(yīng)；用該方法檢測(cè)國內(nèi)豬場(chǎng)62份腹瀉糞便樣品，相比常規(guī)PCR方法，該納米PCR方法的檢出率更高，而兩種方法對(duì)268份進(jìn)境活豬糞拭子樣品檢測(cè)均為陰性。結(jié)果表明，本研究所建立的納米PCR檢測(cè)方法適用于國內(nèi)豬場(chǎng)的PDCoV檢測(cè)和進(jìn)境活豬的監(jiān)控檢測(cè)，可作為PDCoV實(shí)驗(yàn)室檢測(cè)的有力技術(shù)手段。
Establishment of Nanoparticle-assisted PCR Assay for Detection ofPorcine Deltacoronavirus
In this paper，a pair ofprimers were designed according to the M gene sequence of porcinedeltacoronavirus（PDCoV）that waspublished in Genbank，then a kind ofnanoparticle-assisted PCR assay was established. The results showed that thestandard samples with minimum concentration of 102 copies/μL could be detected by this method，and therewas no any cross-reaction with other common swine disease viruses. Compared toregular PCR assay，the nanoparticle-assisted PCR assaypresented a higher detection rate when 62 diarrhea feces collected fromdomestic swine farms were tested. When 268 fecal swab samples of imported livepigs were tested by both the two methods，the detectionresults all showed negative. Therefore，thenanoparticle-assisted PCR assay established in the paper could be used indetecting PDCoV in domestic swine farms and monitoring imported live pigs，which would be a strong technical tool for laboratory detection ofPDCoV.
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