Detection of Enterovirus using Real-Time Nucleic Acid Sequence-based Amplification.
10.5145/KJCM.2010.13.2.53
- Author:
Sun Hee JUN
1
;
Kee Hyung SUNG
;
Sang Hoon SONG
;
Kyoung Un PARK
;
Hong Bin KIM
;
Junghan SONG
;
Eun Hwa CHOI
;
Sung Sup PARK
;
Eui Chong KIM
Author Information
1. Department of Laboratory Medicine, Seoul National University Bundang Hospital, Seongnam, Korea. m91w95pf@snu.ac.kr
- Publication Type:Original Article
- Keywords:
Enterovirus;
Real-time PCR;
Nucleic acid sequence-based amplification;
Aseptic meningitis
- MeSH:
Enterovirus;
Humans;
Meningitis, Aseptic;
Meningitis, Viral;
Polymerase Chain Reaction;
Real-Time Polymerase Chain Reaction;
Reverse Transcription;
RNA;
RNA, Viral;
Self-Sustained Sequence Replication
- From:Korean Journal of Clinical Microbiology
2010;13(2):53-58
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
BACKGROUND: Enteroviruses are the most frequent etiologic agents of aseptic meningitis and are estimated to be the cause of 70% to 90% of viral meningitis cases. Enterovirus diagnosis can be difficult because clinical features vary according to patient immunity and age. The purpose of this study was to evaluate the performance of the real-time nucleic acid sequence-based amplification (NASBA) assay compared to that of the real-time nested RT-PCR assay for enterovirus detection. METHODS: This study was performed on 96 patients suspected of aseptic meningitis based on clinical features. RNA was extracted using NucliSENS EasyMAG and real-time NASBA assay was performed using NucliSENS EasyQ Enterovirus and NucliSENS EasyQ Basic 2. We also executed in-house real-time nested RT-PCR assay for RNA extracted via QIAamp Viral RNA Mini. RESULTS: The positive rate of real-time NASBA assay was 45.8% for enterovirus detection. The positive rate of first real-time reverse transcription PCR was 22.9% and the second real-time PCR was 57.3%. The concordant rate of the real-time NASBA assay and first real-time reverse transcription PCR was 75.0%. The concordant rate of the real-time NASBA assay and second real-time PCR was 86.5%. CONCLUSION: The detection of enteroviruses using the real-time NASBA assay is less prone to cross-contamination and is simple, without the need for reverse transcription. We conclude that the NASBA assay is an effective method for the rapid diagnosis of aseptic meningitis.
