作者: Robert S. Lanciotti , Amy J. Kerst , Roger S. Nasci , Marvin S. Godsey , Carl J. Mitchell
DOI: 10.1128/JCM.38.11.4066-4071.2000
关键词: Flavivirus 、 Reverse transcription polymerase chain reaction 、 Culex 、 Virus Cultivation 、 Virus 、 Virology 、 Biology 、 Real-time polymerase chain reaction 、 TaqMan 、 Polymerase chain reaction
摘要: The authors report on the development and application of a rapid TaqMan assay for detection West Nile (WN) virus in variety human clinical specimens field-collected specimens. Oligonucleotide primers FAM- TAMRA-labeled WN virus-specific probes were designed by using nucleotide sequence New York 1999 isolate. was compared to traditional reverse transcriptase (RT)-PCR isolation Vero cells with large number ( approximately 500) obtained from humans (serum, cerebrospinal fluid, brain tissue), mosquitoes, avian tissue samples. specific demonstrated greater sensitivity than RT-PCR method correctly identified 100% culture-positive mosquito pools 98% should be utility diagnostic laboratory complement existing testing as tool conduct surveillance United States.