Literature DB >> 24088846

External quality assessment for Avian Influenza A (H7N9) Virus detection using armored RNA.

Yu Sun1, Tingting Jia, Yanli Sun, Yanxi Han, Lunan Wang, Rui Zhang, Kuo Zhang, Guigao Lin, Jiehong Xie, Jinming Li.   

Abstract

An external quality assessment (EQA) program for the molecular detection of avian influenza A (H7N9) virus was implemented by the National Center for Clinical Laboratories (NCCL) of China in June 2013. Virus-like particles (VLPs) that contained full-length RNA sequences of the hemagglutinin (HA), neuraminidase (NA), matrix protein (MP), and nucleoprotein (NP) genes from the H7N9 virus (armored RNAs) were constructed. The EQA panel, comprising 6 samples with different concentrations of armored RNAs positive for H7N9 viruses and four H7N9-negative samples (including one sample positive for only the MP gene of the H7N9 virus), was distributed to 79 laboratories in China that carry out the molecular detection of H7N9 viruses. The overall performances of the data sets were classified according to the results for the H7 and N9 genes. Consequently, we received 80 data sets (one participating group provided two sets of results) which were generated using commercial (n = 60) or in-house (n = 17) reverse transcription-quantitative PCR (qRT-PCR) kits and a commercial assay that employed isothermal amplification method (n = 3). The results revealed that the majority (82.5%) of the data sets correctly identified the H7N9 virus, while 17.5% of the data sets needed improvements in their diagnostic capabilities. These "improvable" data sets were derived mostly from false-negative results for the N9 gene at relatively low concentrations. The false-negative rate was 5.6%, and the false-positive rate was 0.6%. In addition, we observed varied diagnostic capabilities between the different commercially available kits and the in-house-developed assays, with the assay manufactured by BioPerfectus Technologies (Jiangsu, China) performing better than the others. Overall, the majority of laboratories have reliable diagnostic capacities for the detection of H7N9 virus.

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Year:  2013        PMID: 24088846      PMCID: PMC3838055          DOI: 10.1128/JCM.02018-13

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  15 in total

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Journal:  J Clin Microbiol       Date:  2011-08-24       Impact factor: 5.948

4.  Armored long RNA controls or standards for branched DNA assay for detection of human immunodeficiency virus type 1.

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7.  Avian influenza A virus (H7N7) associated with human conjunctivitis and a fatal case of acute respiratory distress syndrome.

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Journal:  MBio       Date:  2013-07-09       Impact factor: 7.867

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Journal:  Emerg Infect Dis       Date:  2013-08       Impact factor: 6.883

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2.  External Quality Assessment of Molecular Detection of Ebola Virus in China.

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4.  Influenza surveillance capacity improvements in Africa during 2011-2017.

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Journal:  Influenza Other Respir Viruses       Date:  2020-11-04       Impact factor: 4.380

5.  External Quality Assessment for the Detection of Measles Virus by Reverse Transcription-PCR Using Armored RNA.

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6.  Armored long non-coding RNA MEG3 targeting EGFR based on recombinant MS2 bacteriophage virus-like particles against hepatocellular carcinoma.

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7.  External quality assessment for the molecular detection of MERS-CoV in China.

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8.  External Quality Assessment for Molecular Detection of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) in Clinical Laboratories.

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  8 in total

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