A real-time PCR assay for the detection of Neisseria gonorrhoeae by LightCycler


Autoria(s): Whiley, David M.; LeCornec, Genevera M.; Mackay, Ian M.; Siebert, David J.; Sloots, Theo P.
Contribuinte(s)

Ronald N. Jones

Data(s)

01/02/2002

Resumo

The detection of Neisseria gonorrhoeae by the polymerase chain reaction (PCR) is now recognized as a sensitive and specific method of diagnosing infection by the organism. In this Study 152 urine specimens were examined for N. gonorrhoeae by a real-time PCR method using the LightCycler platform and results were compared to an in-house PCR assay using an ELISA-based detection method. N. gonorrhoeae DNA was detected in 29 (19%) specimens by LightCycler PCR (LC-PCR) and in 31 (20%) specimens by the in house PCR method. The LightCycler assay proved to be specific and 94% sensitive when compared to the in house PCR method. These features combined with the rapid turn-around time for results makes the LC-PCR particularly suitable for the detection of N. gonorrhoeae in a routine clinical laboratory. (C) 2002 Elsevier Science Inc. All rights reserved.

Identificador

http://espace.library.uq.edu.au/view/UQ:61346

Idioma(s)

eng

Publicador

Elsevier Science Inc.

Palavras-Chave #Neisseria Gonorrhoeae #Real-time Pcr #Lightcycler #Diagnosis #Infectious Diseases #Microbiology #Chlamydia-trachomatis #Multicenter Evaluation #Virus-infections #Amplicor #Amplification #Specimens #C1 #270303 Virology #730101 Infectious diseases #730204 Child health
Tipo

Journal Article