EVALUATION OF A REVERSE TRANSCRIPTASE-POLYMERASE CHAIN-REACTION ASSAYFOR DETECTING ST-LOUIS ENCEPHALITIS-VIRUS USING FIELD-COLLECTED MOSQUITOS (DIPTERA, CULICIDAE)

Citation
Sj. Nawrocki et al., EVALUATION OF A REVERSE TRANSCRIPTASE-POLYMERASE CHAIN-REACTION ASSAYFOR DETECTING ST-LOUIS ENCEPHALITIS-VIRUS USING FIELD-COLLECTED MOSQUITOS (DIPTERA, CULICIDAE), Journal of medical entomology, 33(1), 1996, pp. 123-127
Citations number
17
Categorie Soggetti
Entomology
ISSN journal
00222585
Volume
33
Issue
1
Year of publication
1996
Pages
123 - 127
Database
ISI
SICI code
0022-2585(1996)33:1<123:EOARTC>2.0.ZU;2-U
Abstract
A reverse transcriptase-polymerase chain reaction assay (RT-PCR) was c ompared with a tissue culture assay (TC) and an enzyme immunoassay (ET A) to detect St. Louis encephalitis virus (SLEV) in mosquito pools. Ov erall, 1,725 mosquito pools with a low viral prevalence (3.3%-5.0%) we re tested. The comparison of the EIA to TC showed that the EIA was 0.9 47 sensitive, 0.988 specific, and 0.987 accurate. Comparison of RT-PCR to TC showed that the RT-PCR was 0.947 sensitive, 0.980 specific, and 0.979 accurate. Comparison of the RT-PCR to EIA showed that the RT-PC R was 0.878 sensitive, 0.987 specific, and 0.982 accurate. Because of speed, accuracy, and cost, either the RT-PCR or the EIA is recommended as the primary screen. RT-PCR has an advantage over EIA, because the amplified product contains sequence information which can confirm its identity. TC, EIA, or both can be applied as a 2nd assay for the confi rmation of samples suspected as positives by the RT-PCR.