scholarly journals Design and Validation of an H5 TaqMan Real-Time One-Step Reverse Transcription-PCR and Confirmatory Assays for Diagnosis and Verification of Influenza A Virus H5 Infections in Humans

2007 ◽  
Vol 45 (5) ◽  
pp. 1535-1543 ◽  
Author(s):  
J. S. Ellis ◽  
J. W. Smith ◽  
S. Braham ◽  
M. Lock ◽  
K. Barlow ◽  
...  
2008 ◽  
Vol 5 (1) ◽  
pp. 77 ◽  
Author(s):  
Alejandra Alvarez ◽  
Marion EG Brunck ◽  
Victoria Boyd ◽  
Richard Lai ◽  
Elena Virtue ◽  
...  

2016 ◽  
Vol 55 (2) ◽  
pp. 479-484 ◽  
Author(s):  
Hee Jae Huh ◽  
Ji-Youn Kim ◽  
Hyeon Jeong Kwon ◽  
Sun Ae Yun ◽  
Myoung-Keun Lee ◽  
...  

ABSTRACTThe Allplex respiratory panels 1, 2, and 3 (Allplex) comprise a one-step real-time reverse transcription-PCR assay for the detection of respiratory viruses (RVs) and influenza A subtypes based on multiple detection temperature (MuDT) technology. The performance of the Allplex assay was compared with those of the AdvanSure RV real-time PCR kit (AdvanSure) and the PowerChek pandemic H1N1/H3N2/H5N1 real-time PCR kit (PowerChek) using 417 clinical respiratory specimens. In comparison with the AdvanSure assay for RV detection by each virus, the ranges of positive percent agreement, negative percent agreement, and kappa values with the Allplex assay were 82.8 to 100%, 95.5 to 100%, and 0.85 to 1.00, respectively. For influenza A virus (INF A) subtyping, the kappa values between the Allplex and PowerChek assays were 0.67 and 1.00 for the INF A H1N1-pdm09 and H3 subtypes, respectively. Uniplex PCR and sequencing for samples with discrepant results demonstrated that the majority of results were concordant with those from the Allplex assay. When testing 24 samples, the turnaround and hands-on time required to perform the Allplex assay were 4 h 15 min and 15 min, respectively. In conclusion, the Allplex assay produced results comparable to those from the AdvanSure and PowerChek assays.


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