development of dual taqman based one-step rrt-pcr assay panel for rapid and accurate diagnostic test of mers-cov: a novel human coronavirus, ahead of hajj pilgrimage

نویسندگان

mohammad sadegh hashemzadeh applied virology research center, baqiyatallah university of medical sciences, tehran, ir iran

rahimeh rasouli applied virology research center, baqiyatallah university of medical sciences, tehran, ir iran

bentolhoda zahraei applied virology research center, baqiyatallah university of medical sciences, tehran, ir iran

morteza izadi health research center, baqiyatallah university of medical sciences, tehran, ir iran

چکیده

conclusions this study showed that the developed rrt-pcr assays are rapid, reliable, reproducible, specific, sensitive, and simple tools for detection of mers-cov. finally, a kit consisting of two assay signatures and controls was assembled, which can be distributed to public health laboratories in iran to support international mers-cov surveillance and public health response. results the upe and orf1b based one-step rrt-pcr assays were optimized by testing several times via different synthetic rnas, and validation results were highly successful. the sensitivity obtained for upe was fewer than ten copies of rna template per reaction and for orf1b was 50 or fewer copies per reaction. background coronaviruses (covs) are large ribonucleic acid (rna) viruses causing primarily respiratory disease in humans. a novel human coronavirus, subsequently named middle east respiratory syndrome coronavirus (mers-cov), was first reported in saudi arabia in september of 2012. with increasing numbers of infections and deaths from mers-cov, development of a rapid and reliable kit was crucial to prevent further spread of mers-cov. materials and methods in this experimental study, acquiring patient samples was difficult; thus, according to who recommendations and standard protocols, we synthesized rna sequences of upe and orf1b genes as the template signatures and taqman based-diagnostic rrt-pcr assays were carried out using these synthetic genes for detection of mers-cov. in this research, we also inaugurated a cell-free system to transcribe these rna sequences using the dna templates synthesized. objectives in this study, we present two real-time reverse-transcription polymerase chain reaction (rrt-pcr) assays for in-house rapid and sensitive diagnostic testing of mers-cov, detecting the regions upstream of the envelope gene (upe) and open reading frame (orf) 1b, respectively, for initial screening and final confirmation of mers-cov infection, as recommended by the world health organization (who).

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Development of Dual TaqMan Based One-Step rRT-PCR Assay Panel for Rapid and Accurate Diagnostic Test of MERS-CoV: A Novel Human Coronavirus, Ahead of Hajj Pilgrimage

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عنوان ژورنال:
iranian red crescent medical journal

جلد ۱۸، شماره ۱۱، صفحات ۰-۰

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