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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:
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.
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页数:8
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