4.3 Article

A sensitive and specific nanoparticle-assisted PCR assay for rapid detection of porcine parvovirus

期刊

LETTERS IN APPLIED MICROBIOLOGY
卷 58, 期 2, 页码 163-167

出版社

WILEY-BLACKWELL
DOI: 10.1111/lam.12171

关键词

nanoPCR; NS1 gene; PPV; sensitivity; specificity

资金

  1. National Natural Science Foundation of China [31001069, 31172349, 31172341]
  2. Chinese State Key Laboratory of Veterinary Biotechnology Fund [NKLVBP 201108]
  3. National High-tech RDProgram [863-2011AA10A208/2011AA10A200]
  4. Excellent Youth Foundation of Heilongjiang Scientific Committee [JC201216]
  5. National Science and Technology Achievement Transformation Project [2012GB23260557]

向作者/读者索取更多资源

A novel nanoparticle-assisted polymerase chain reaction (nanoPCR) assay to detect porcine parvovirus (PPV) is described here. Primers for this assay were designed based on the conserved region of the nonstructural protein 1 (NS1) gene of PPV, which encodes one of the nonstructural proteins. The sensitivity of the PPV nanoPCR assay was measured by using diluted recombinant plasmids in which the PPV NS1 gene had been inserted. The detection limit was 5.6 x 10(1) copies mu l(-1) for the PPV nanoPCR assay vs 5.6 x 10(3) copies mu l(-1) for conventional PCR assay. The results showed that the sensitivity of PPV nanoPCR assay was 100 times higher than that of conventional PCR assay. The PPV nanoPCR assay produced 142-bp product as expected when amplifying PPV DNA, while produced nothing when amplifying the DNA or cDNA of the following viruses: swine encephalomyocarditis virus, classical swine fever virus, porcine pseudorabies virus, porcine reproductive and respiratory syndrome virus, porcine teschovirus and porcine circovirus type II. PPV was detected in 108 of 109 clinical swine samples from Heilongjiang, Jilin and Henan provinces using the nanoPCR assay, and the results were confirmed by sequencing.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.3
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据