Design and evaluation of consensus PCR assays for henipaviruses

被引:47
作者
Feldman, K. S. [1 ,2 ,3 ]
Foord, A. [3 ]
Heine, H. G. [3 ]
Smith, I. L. [4 ]
Boyd, V. [3 ]
Marsh, G. A. [3 ]
Wood, J. L. N.
Cunningham, A. A. [2 ]
Wang, L. -F. [3 ]
机构
[1] Univ Cambridge, Cambridge Infect Dis Consortium, Dept Vet Med, Cambridge CB3 0ES, England
[2] Zool Soc London, Inst Zool, London NW1 4RY, England
[3] CSIRO Livestock Ind, Australian Anim Hlth Lab, Geelong, Vic 3219, Australia
[4] Queensland Hlth, Coopers Plains, Qld 4108, Australia
关键词
Henipavirus; PCR; SYBR Green; Consensus PCR; HENDRA VIRUS-INFECTION; BATS PTEROPUS-POLIOCEPHALUS; NIPAH VIRUS; FRUIT BATS; FLYING-FOXES; BANGLADESH; PIGS; TRANSCRIPTION; MALAYSIA;
D O I
10.1016/j.jviromet.2009.05.014
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Henipaviruses were first discovered in the 1990s, and their potential threat to public health is of increasing concern with increasing knowledge. Old-world fruit bats are the reservoir hosts for these viruses, and spill-over events cause lethal infections in a wide range of mammalian species, including humans. In anticipation of these spill-over events, and to investigate further the geographical range of these genetically diverse viruses, assays for detection of known and potentially novel strains of henipaviruses are required. The development of multiple consensus PCR assays for the detection of henipaviruses, including both SYBR Green and TaqMan real-time PCRs and a conventional heminested PCR is described. The assays are highly sensitive and have defined specificity. In addition to being useful tools for detection of known and novel henipaviruses, evaluation of assay efficiency and sensitivity across both biological and synthetic templates has provided valuable insight into consensus PCR design and use. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:52 / 57
页数:6
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