Comparison of the Roche RealTime ready Influenza A/H1N1 Detection Set with CDC A/H1N1pdm09 RT-PCR on samples from three hospitals in Ho Chi Minh City, Vietnam. Tham, N. t., Hang, V. t. T., Khanh, T. H., Viet, D. C., Hien, T. T., Farrar, J., Chau, N. v. V., & van Doorn, H. R. Diagnostic microbiology and infectious disease, 74(2):131–136, October, 2012. doi abstract bibtex Real-time polymerase chain reaction (PCR) can be considered the gold standard for detection of influenza viruses due to its high sensitivity and specificity. Roche has developed the RealTime ready Influenza A/H1N1 Detection Set, consisting of a generic influenza virus A PCR targeting the M2 gene (M2 PCR) and a specific PCR targeting the hemagglutinin (HA) of A/H1N1-pdm09 (HA PCR, 2009 H1N1), with the intention to make a reliable, rapid, and simple test to detect and quantify 2009 H1N1 in clinical samples. We evaluated this kit against the US Centers for Disease Control and Prevention (USCDC)/World Health Organization real-time PCR for influenza virus using 419 nose and throat swabs from 210 patients collected in 3 large hospitals in Ho Chi Minh City, Vietnam. In the per-patient analysis, when compared to CDC PCR, the sensitivity and specificity of the M2 PCR were 85.8% and 97.6%, respectively; the sensitivity and specificity of HA PCR were 88.2% and 100%, respectively. In the per-sample analysis, the sensitivity and specificity in nose swabs were higher than those in throat swabs for both M2 and HA PCRs. The viral loads as determined with the M2 and HA PCRs correlated well with the Ct values of the CDC PCR. Compared with the CDC PCR, the kit has a reasonable sensitivity and very good specificity for the detection and quantification of influenza A virus and A/H1N1-pdm09. However, given the current status of 2009 H1N1, a kit that can detect all circulating seasonal influenza viruses would be preferable.
@article{tham_comparison_2012,
title = {Comparison of the {Roche} {RealTime} ready {Influenza} {A}/{H1N1} {Detection} {Set} with {CDC} {A}/{H1N1pdm09} {RT}-{PCR} on samples from three hospitals in {Ho} {Chi} {Minh} {City}, {Vietnam}.},
volume = {74},
copyright = {Copyright (c) 2012 Elsevier Inc. All rights reserved.},
issn = {1879-0070 0732-8893},
doi = {10.1016/j.diagmicrobio.2012.06.003},
abstract = {Real-time polymerase chain reaction (PCR) can be considered the gold standard for detection of influenza viruses due to its high sensitivity and specificity. Roche has developed the RealTime ready Influenza A/H1N1 Detection Set, consisting of a generic influenza virus A PCR targeting the M2 gene (M2 PCR) and a specific PCR targeting the hemagglutinin (HA) of A/H1N1-pdm09 (HA PCR, 2009 H1N1), with the intention to make a reliable, rapid, and simple test to detect and quantify 2009 H1N1 in clinical samples. We evaluated this kit against the US Centers for Disease Control and Prevention (USCDC)/World Health Organization real-time PCR for influenza virus using 419 nose and throat swabs from 210 patients collected in 3 large hospitals in Ho Chi Minh City, Vietnam. In the per-patient analysis, when compared to CDC PCR, the sensitivity and specificity of the M2 PCR were 85.8\% and 97.6\%, respectively; the sensitivity and specificity of HA PCR were 88.2\% and 100\%, respectively. In the per-sample analysis, the sensitivity and specificity in nose swabs were higher than those in throat swabs for both M2 and HA PCRs. The viral loads as determined with the M2 and HA PCRs correlated well with the Ct values of the CDC PCR. Compared with the CDC PCR, the kit has a reasonable sensitivity and very good specificity for the detection and quantification of influenza A virus and A/H1N1-pdm09. However, given the current status of 2009 H1N1, a kit that can detect all circulating seasonal influenza viruses would be preferable.},
language = {eng},
number = {2},
journal = {Diagnostic microbiology and infectious disease},
author = {Tham, Nguyen thi and Hang, Vu thi Ty and Khanh, Trong Huu and Viet, Do Chau and Hien, Tran Tinh and Farrar, Jeremy and Chau, Nguyen van Vinh and van Doorn, H. Rogier},
month = oct,
year = {2012},
pmid = {22785431},
pmcid = {PMC3444637},
keywords = {Adolescent, Adult, Aged, Child, Child, Preschool, Female, Hospitals, Humans, Infant, Influenza A Virus, H1N1 Subtype/*isolation \& purification, Influenza, Human/*diagnosis, Male, Middle Aged, Molecular Diagnostic Techniques/*methods, Nose/virology, Pharynx/virology, Real-Time Polymerase Chain Reaction/*methods, Sensitivity and Specificity, Vietnam, Virology/*methods, Young Adult},
pages = {131--136},
}
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Roche has developed the RealTime ready Influenza A/H1N1 Detection Set, consisting of a generic influenza virus A PCR targeting the M2 gene (M2 PCR) and a specific PCR targeting the hemagglutinin (HA) of A/H1N1-pdm09 (HA PCR, 2009 H1N1), with the intention to make a reliable, rapid, and simple test to detect and quantify 2009 H1N1 in clinical samples. We evaluated this kit against the US Centers for Disease Control and Prevention (USCDC)/World Health Organization real-time PCR for influenza virus using 419 nose and throat swabs from 210 patients collected in 3 large hospitals in Ho Chi Minh City, Vietnam. In the per-patient analysis, when compared to CDC PCR, the sensitivity and specificity of the M2 PCR were 85.8% and 97.6%, respectively; the sensitivity and specificity of HA PCR were 88.2% and 100%, respectively. In the per-sample analysis, the sensitivity and specificity in nose swabs were higher than those in throat swabs for both M2 and HA PCRs. 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All rights reserved.},\n\tissn = {1879-0070 0732-8893},\n\tdoi = {10.1016/j.diagmicrobio.2012.06.003},\n\tabstract = {Real-time polymerase chain reaction (PCR) can be considered the gold standard for detection of influenza viruses due to its high sensitivity and specificity. Roche has developed the RealTime ready Influenza A/H1N1 Detection Set, consisting of a generic influenza virus A PCR targeting the M2 gene (M2 PCR) and a specific PCR targeting the hemagglutinin (HA) of A/H1N1-pdm09 (HA PCR, 2009 H1N1), with the intention to make a reliable, rapid, and simple test to detect and quantify 2009 H1N1 in clinical samples. We evaluated this kit against the US Centers for Disease Control and Prevention (USCDC)/World Health Organization real-time PCR for influenza virus using 419 nose and throat swabs from 210 patients collected in 3 large hospitals in Ho Chi Minh City, Vietnam. 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