Reverse transcription genome exponential amplification reaction assay for rapid and universal detection of human rhinoviruses
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  • 作者:Li Guan ; Lin-Qing Zhao ; Hang-Yu Zhou ; Kai Nie ; Xin-Na Li ; Dan Zhang…
  • 刊名:Archives of Virology
  • 出版年:2016
  • 出版时间:July 2016
  • 年:2016
  • 卷:161
  • 期:7
  • 页码:1891-1898
  • 全文大小:1,147 KB
  • 刊物类别:Biomedical and Life Sciences
  • 刊物主题:Biomedicine
    Virology
    Medical Microbiology
    Infectious Diseases
  • 出版者:Springer Wien
  • ISSN:1432-8798
  • 卷排序:161
文摘
Human rhinoviruses (HRVs) have long been recognized as the cause of more than one-half of acute viral upper respiratory illnesses, and they are associated with more-serious diseases in children, such as asthma, acute otitis media and pneumonia. A rapid and universal test for of HRV infection is in high demand. In this study, a reverse transcription genome exponential amplification reaction (RT-GEAR) assay targeting the HRV 5′ untranslated region (UTR) was developed for pan-HRV detection. The reaction was performed in a single tube in one step at 65 °C for 60 min using a real-time fluorometer (Genie®II; Optigene). The RT-GEAR assay showed no cross-reactivity with common human enteroviruses, including HEV71, CVA16, CVA6, CVA10, CVA24, CVB5, Echo30, and PV1-3 or with other common respiratory viruses including FluA H3, FluB, PIV1-4, ADV3, RSVA, RSVB and HMPV. With in vitro-transcribed RNA containing the amplified regions of HRV-A60, HRV-B06 and HRV-C07 as templates, the sensitivity of the RT-GEAR assay was 5, 50 and 5 copies/reaction, respectively. Experiments to evaluate the clinical performance of the RT-GEAR assay were also carried out with a panel of 143 previously verified samples, and the results were compared with those obtained using a published semi-nested PCR assay followed by sequencing. The tested panel comprised 91 HRV-negative samples and 52 HRV-positive samples (18 HRV-A-positive samples, 3 HRV-B-positive samples and 31 HRV-C-positive samples). The sensitivity and specificity of the pan-HRVs RT-GEAR assay was 98.08 % and 100 %, respectively. The kappa correlation between the two methods was 0.985. The RT-GEAR assay based on a portable Genie®II fluorometer is a sensitive, specific and rapid assay for the universal detection of HRV infection.AbbreviationsHRVsHuman rhinovirusesRT-GEARReverse transcription genome exponential amplification reactionRT-LAMPReverse transcription loop-mediated isothermal amplificationUTRUntranslated regionHEVHuman enterovirusCVACoxsackievirus ACVBCoxsackievirus BEchoEchovirusPVPoliovirusFluA H3Influenza A virus H3FluBInfluenza B virusPIVParainfluenza virusADVAdenovirusRSVRespiratory syncytial virusHMPVHuman metapneumovirusCOPDChronic obstructive pulmonary disease
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