Serveur d'exploration MERS

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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.

Identifieur interne : 000D83 ( PubMed/Curation ); précédent : 000D82; suivant : 000D84

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.

Auteurs : Mohammad Sadegh Hashemzadeh ; Rahimeh Rasouli ; Bentolhoda Zahraei ; Morteza Izadi ; Mahdi Tat ; Seyed Hassan Saadat ; Mohammad Najarasl ; Behzad Khansari Nejad ; Ruhollah Dorostkar

Source :

RBID : pubmed:28191331

Abstract

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.

DOI: 10.5812/ircmj.23874
PubMed: 28191331

Links toward previous steps (curation, corpus...)


Links to Exploration step

pubmed:28191331

Curation

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Mohammad Sadegh Hashemzadeh
<affiliation>
<nlm:affiliation>Applied Virology Research Center, Baqiyatallah University of Medical Sciences, Tehran, IR Iran.</nlm:affiliation>
<wicri:noCountry code="subField">IR Iran</wicri:noCountry>
</affiliation>
Rahimeh Rasouli
<affiliation>
<nlm:affiliation>Applied Virology Research Center, Baqiyatallah University of Medical Sciences, Tehran, IR Iran.</nlm:affiliation>
<wicri:noCountry code="subField">IR Iran</wicri:noCountry>
</affiliation>
Bentolhoda Zahraei
<affiliation>
<nlm:affiliation>Applied Virology Research Center, Baqiyatallah University of Medical Sciences, Tehran, IR Iran.</nlm:affiliation>
<wicri:noCountry code="subField">IR Iran</wicri:noCountry>
</affiliation>
Morteza Izadi
<affiliation>
<nlm:affiliation>Health Research Center, Baqiyatallah University of Medical Sciences, Tehran, IR Iran.</nlm:affiliation>
<wicri:noCountry code="subField">IR Iran</wicri:noCountry>
</affiliation>
Mahdi Tat
<affiliation>
<nlm:affiliation>Applied Virology Research Center, Baqiyatallah University of Medical Sciences, Tehran, IR Iran.</nlm:affiliation>
<wicri:noCountry code="subField">IR Iran</wicri:noCountry>
</affiliation>
Seyed Hassan Saadat
<affiliation>
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<wicri:noCountry code="subField">IR Iran</wicri:noCountry>
</affiliation>
Mohammad Najarasl
<affiliation>
<nlm:affiliation>Applied Virology Research Center, Baqiyatallah University of Medical Sciences, Tehran, IR Iran.</nlm:affiliation>
<wicri:noCountry code="subField">IR Iran</wicri:noCountry>
</affiliation>
Behzad Khansari Nejad
<affiliation>
<nlm:affiliation>Department of Microbiology and Immunology, Arak University of Medical Sciences, Arak, IR Iran.</nlm:affiliation>
<wicri:noCountry code="subField">IR Iran</wicri:noCountry>
</affiliation>
Ruhollah Dorostkar
<affiliation>
<nlm:affiliation>Applied Virology Research Center, Baqiyatallah University of Medical Sciences, Tehran, IR Iran.</nlm:affiliation>
<wicri:noCountry code="subField">IR Iran</wicri:noCountry>
</affiliation>

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<name sortKey="Hashemzadeh, Mohammad Sadegh" sort="Hashemzadeh, Mohammad Sadegh" uniqKey="Hashemzadeh M" first="Mohammad Sadegh" last="Hashemzadeh">Mohammad Sadegh Hashemzadeh</name>
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<name sortKey="Saadat, Seyed Hassan" sort="Saadat, Seyed Hassan" uniqKey="Saadat S" first="Seyed Hassan" last="Saadat">Seyed Hassan Saadat</name>
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<name sortKey="Khansari Nejad, Behzad" sort="Khansari Nejad, Behzad" uniqKey="Khansari Nejad B" first="Behzad" last="Khansari Nejad">Behzad Khansari Nejad</name>
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<name sortKey="Dorostkar, Ruhollah" sort="Dorostkar, Ruhollah" uniqKey="Dorostkar R" first="Ruhollah" last="Dorostkar">Ruhollah Dorostkar</name>
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<title level="j">Iranian Red Crescent medical journal</title>
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<div type="abstract" xml:lang="en">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.</div>
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<PMID Version="1">28191331</PMID>
<DateRevised>
<Year>2019</Year>
<Month>11</Month>
<Day>20</Day>
</DateRevised>
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<Journal>
<ISSN IssnType="Print">2074-1804</ISSN>
<JournalIssue CitedMedium="Print">
<Volume>18</Volume>
<Issue>11</Issue>
<PubDate>
<Year>2016</Year>
<Month>Nov</Month>
</PubDate>
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<Title>Iranian Red Crescent medical journal</Title>
<ISOAbbreviation>Iran Red Crescent Med J</ISOAbbreviation>
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<ArticleTitle>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.</ArticleTitle>
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<ELocationID EIdType="doi" ValidYN="Y">10.5812/ircmj.23874</ELocationID>
<Abstract>
<AbstractText Label="BACKGROUND" NlmCategory="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.</AbstractText>
<AbstractText Label="OBJECTIVES" NlmCategory="OBJECTIVE">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).</AbstractText>
<AbstractText Label="MATERIALS AND METHODS" NlmCategory="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.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="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.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="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.</AbstractText>
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<LastName>Hashemzadeh</LastName>
<ForeName>Mohammad Sadegh</ForeName>
<Initials>MS</Initials>
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<KeywordList Owner="NOTNLM">
<Keyword MajorTopicYN="N">Diagnosis</Keyword>
<Keyword MajorTopicYN="N">Hajj Pilgrimage</Keyword>
<Keyword MajorTopicYN="N">MERS-CoV</Keyword>
<Keyword MajorTopicYN="N">ORF1b</Keyword>
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