2009Hebei Nongye Daxue xuebaoRequires access

The establishment of detecting method for porcine reproductive and respiratory syndrome virus(PRRSV)

Deming Zhao

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Abstract

Based on highly conservative ORF6 gene sequence of PRRSV on GeneBank,a pair of primers was designed and synthesized.The RT-PCR method for detecting PRRSV was established.PRRSV-QD RNA was extracted from virus-infected Marc-145 cell and then amplified by RT-PCR.The positive 266bp specific fragment was obtained as expected.Under the same conditions,however,the results for detection of PRV,PPV,PCV and Marc-145 cell by RT-PCR were all negative.The amplified sequence of PCR product of PRRSV-QD shares 94.4%-97.4% homology with the published sequence of other PRRSV strains from GeneBank.The results indicate that RT-PCR method in this research has high sensitivity and specificity,and could be further applied for PRRSV clinical diagnosis.

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What this paper is about

Based on highly conservative ORF6 gene sequence of PRRSV on GeneBank,a pair of primers was designed and synthesized.The RT-PCR method for detecting PRRSV was established.PRRSV-QD RNA was extracted from virus-infected Marc-145 cell and then amplified by RT-PCR.The positive 266bp specific fragment was obtained as expected.Under the same conditions,however,the results for detection of PRV,PPV,PCV and Marc-145 cell by RT-PCR were all negative.The amplified sequence of PCR product of PRRSV-QD shares 94.4%-97.4% homology with the published sequence of other PRRSV strains from GeneBank.The results indicate that RT-PCR method in this research has high sensitivity and specificity,and could be further applied for PRRSV clinical diagnosis.

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Available abstract

Based on highly conservative ORF6 gene sequence of PRRSV on GeneBank,a pair of primers was designed and synthesized.The RT-PCR method for detecting PRRSV was established.PRRSV-QD RNA was extracted from virus-infected Marc-145 cell and then amplified by RT-PCR.The positive 266bp specific fragment was obtained as expected.Under the same conditions,however,the results for detection of PRV,PPV,PCV and Marc-145 cell by RT-PCR were all negative.The amplified sequence of PCR product of PRRSV-QD shares 94.4%-97.4% homology with the published sequence of other PRRSV strains from GeneBank.The results indicate that RT-PCR method in this research has high sensitivity and specificity,and could be further applied for PRRSV clinical diagnosis.

Key concepts: Porcine reproductive and respiratory syndrome virus, Virology, Biology, Virus, Gene sequence, Gene, Highly pathogenic, Homology (biology)

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