TY - JOUR
T1 - Development of conventional and real-time reverse transcription polymerase chain reaction assays to detect Tembusu virus in Culex tarsalis mosquitoes
AU - Petz, Lawrence N.
AU - Turell, Michael J.
AU - Padilla, Susana
AU - Long, Lewis S.
AU - Reinbold-Wasson, Drew D.
AU - Smith, Darci R.
AU - O'Guinn, Monica L.
AU - Melanson, Vanessa R.
AU - Lee, John S.
N1 - Publisher Copyright:
Copyright © 2014 by The American Society of Tropical Medicine and Hygiene.
PY - 2014/10/1
Y1 - 2014/10/1
N2 - Tembusu virus (TMUV) is an important emerging arthropod-borne virus that may cause encephalitis in humans and has been isolated in regions of southeast Asia, including Malaysia, Thailand, and China. Currently, detection and identification of TMUV are limited to research laboratories, because quantitative rapid diagnostic assays for the virus do not exist. We describe the development of sensitive and specific conventional and real-time quantitative reverse transcription polymerase chain reaction assays for detecting TMUV RNA in infected cell culture supernatant and Culex tarsalis mosquitoes. We used this assay to document the replication of TMUV in Cx. tarsalis, where titers increased 1,000- fold 5 days after inoculation. These assays resulted in the detection of virus-specific RNA in the presence of copurified mosquito nucleic acids. The use of these rapid diagnostic assays may have future applications for field pathogen surveillance and may assist in early detection, diagnosis, and control of the associated arthropod-borne pathogens.
AB - Tembusu virus (TMUV) is an important emerging arthropod-borne virus that may cause encephalitis in humans and has been isolated in regions of southeast Asia, including Malaysia, Thailand, and China. Currently, detection and identification of TMUV are limited to research laboratories, because quantitative rapid diagnostic assays for the virus do not exist. We describe the development of sensitive and specific conventional and real-time quantitative reverse transcription polymerase chain reaction assays for detecting TMUV RNA in infected cell culture supernatant and Culex tarsalis mosquitoes. We used this assay to document the replication of TMUV in Cx. tarsalis, where titers increased 1,000- fold 5 days after inoculation. These assays resulted in the detection of virus-specific RNA in the presence of copurified mosquito nucleic acids. The use of these rapid diagnostic assays may have future applications for field pathogen surveillance and may assist in early detection, diagnosis, and control of the associated arthropod-borne pathogens.
UR - http://www.scopus.com/inward/record.url?scp=84907684471&partnerID=8YFLogxK
U2 - 10.4269/ajtmh.13-0218
DO - 10.4269/ajtmh.13-0218
M3 - Article
C2 - 25114013
AN - SCOPUS:84907684471
SN - 0002-9637
VL - 91
SP - 666
EP - 671
JO - American Journal of Tropical Medicine and Hygiene
JF - American Journal of Tropical Medicine and Hygiene
IS - 4
ER -