1. Validation and Application of a Commercial Quantitative Real-Time Reverse Transcriptase-PCR Assay in Investigation of a Large Dengue Virus Outbreak in Southern Taiwan
- Author
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You-Yuan Tsai, Huey Pin Tsai, Jung-Chin Chen, Wen Chien Ko, I-Ting Lin, Jen Ren Wang, Pin-Hwa Kuo, and Kung Chao Chang
- Subjects
0301 basic medicine ,Serotype ,RNA viruses ,Male ,Viral Diseases ,Physiology ,viruses ,Artificial Gene Amplification and Extension ,Dengue virus ,Viral Nonstructural Proteins ,medicine.disease_cause ,Pathology and Laboratory Medicine ,Antibodies, Viral ,Polymerase Chain Reaction ,Biochemistry ,Fluorophotometry ,Dengue fever ,Dengue Fever ,Disease Outbreaks ,Dengue ,Spectrum Analysis Techniques ,Immune Physiology ,Medicine and Health Sciences ,Fluorescence Resonance Energy Transfer ,Immune System Proteins ,Reverse Transcriptase Polymerase Chain Reaction ,lcsh:Public aspects of medicine ,virus diseases ,Viral Load ,Middle Aged ,Antigenic Variation ,Reverse transcription polymerase chain reaction ,Infectious Diseases ,Medical Microbiology ,Spectrophotometry ,Viral Pathogens ,Viruses ,Female ,Antibody ,Pathogens ,Viral load ,Research Article ,Neglected Tropical Diseases ,lcsh:Arctic medicine. Tropical medicine ,lcsh:RC955-962 ,030106 microbiology ,Immunology ,Taiwan ,Biology ,Research and Analysis Methods ,Microbiology ,Antibodies ,03 medical and health sciences ,Extraction techniques ,Virology ,medicine ,Antigenic variation ,Humans ,Antigens ,Molecular Biology Techniques ,Microbial Pathogens ,Molecular Biology ,Aged ,Biology and life sciences ,Flaviviruses ,Public Health, Environmental and Occupational Health ,Organisms ,Outbreak ,Proteins ,lcsh:RA1-1270 ,Reverse Transcriptase-Polymerase Chain Reaction ,Dengue Virus ,medicine.disease ,Tropical Diseases ,RNA extraction ,biology.protein ,Viral Transmission and Infection - Abstract
Background Accurate, rapid, and early diagnosis of dengue virus (DENV) infections is essential for optimal clinical care. Here, we evaluated the efficacy of the quantitative real-time PCR (qRT-PCR)-LightMix dengue virus EC kit for DENV detection using samples from a dengue outbreak in Taiwan in 2015. Methods Sera from patients with suspected DENV infection were analyzed and compared using the LightMix kit, a Dengue NS1 Ag + Ab Combo kit for detection of NS1 antigen and DENV-specific IgM and IgG antibodies, and an “in-house” qualitative DENV-specific RT-PCR assay. Results A total of 8,989, 8,954, and 1581 samples were subjected to NS1 antigen detection, IgM and IgG detection, and LightMix assays, respectively. The LightMix assay yielded a linear curve for viral loads (VL) between 102 and 106 copies/reaction, and the minimum detection limits for DENV serotype 1 (DENV1) and DENV2, DENV3, and DENV4 were 1, 10, and 100 focus forming units (FFU)/mL, respectively. There was 88.9% concordance between the results obtained using the NS1 antigen combo kit and by LightMix analysis, and the diagnostic sensitivity and specificity of the two methods were 89.4 and 100%, and 84.7 and 100%, respectively. Notably, fatal cases were attributed to DENV2 infection, and 79.5% (27/34) of these cases occurred in patients ≥ 71 years of age. Among these older patients, 82.3% (14/17) were NS1/IgM/IgG (+/-/-), exhibiting VLs between 106–109 copies/mL, which was markedly higher than the rate observed in the other age groups. Conclusions The LightMix assay was effective for early diagnosis of DENV infection. Our data indicate that high VLs during primary infection in elderly patients may be a positive predictor for severe illness, and may contribute to high mortality rates., Author Summary The LightMix dengue virus EC qRT-PCR assay is effective for early diagnosis of DENV infection. High viral loads during primary infection in elderly patients may comprise a positive predictor for severe illness, and may contribute to high mortality rates.
- Published
- 2016