Development of TaqMan® MGB fluorescent real-time PCR assay for the detection of anatid herpesvirus 1

被引:32
|
作者
Guo, Yufei [1 ,2 ]
Cheng, Anchun [1 ,2 ]
Wang, Mingshu [1 ,2 ]
Shen, Chanjuan [2 ]
Jia, Renyong [1 ]
Chen, Shun [1 ]
Zhang, Na [1 ]
机构
[1] Sichuan Agr Univ, Avian Dis Res Ctr, Coll Vet Med, Yaan 625014, Peoples R China
[2] Sichuan Agr Univ, Key Lab Anim Dis & Human Hlth Sichuan Prov, Yaan 625014, Peoples R China
来源
VIROLOGY JOURNAL | 2009年 / 6卷
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
POLYMERASE-CHAIN-REACTION; DUCK VIRUS ENTERITIS; EPSTEIN-BARR-VIRUS; PLAGUE VIRUS; RT-PCR; DNA; WATERFOWL; QUANTITATION; CYTOMEGALOVIRUS; DISEASE;
D O I
10.1186/1743-422X-6-71
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Anatid herpesvirus 1 (AHV-1) is an alphaherpesvirus associated with latent infection and mortality in ducks and geese and is currently affecting the world-wide waterfowl production severely. Here we describe a fluorescent quantitative real-time PCR (FQ-PCR) method developed for fast measurement of AHV-1 DNA based on TaqMan MGB technology. Results: The detection limit of the assay was 1 x 101 standard DNA copies, with a sensitivity of 2 logs higher than that of the conventional gel-based PCR assay targeting the same gene. The real-time PCR was reproducible, as shown by satisfactory low intra-assay and inter-assay coefficients of variation. Conclusion: The high sensitivity, specificity, simplicity and reproducibility of the AHV-1 fluorogenic PCR assay, combined with its wide dynamic range and high throughput, make this method suitable for a broad spectrum of AHV-1 etiologically related application.
引用
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页数:8
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