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A Rapid and Specific Assay for the Detection of MERS-CoV.

Identifieur interne : 000A37 ( PubMed/Checkpoint ); précédent : 000A36; suivant : 000A38

A Rapid and Specific Assay for the Detection of MERS-CoV.

Auteurs : Pei Huang [République populaire de Chine] ; Hualei Wang [République populaire de Chine] ; Zengguo Cao [République populaire de Chine] ; Hongli Jin [République populaire de Chine] ; Hang Chi [République populaire de Chine] ; Jincun Zhao [République populaire de Chine] ; Beibei Yu [République populaire de Chine] ; Feihu Yan [République populaire de Chine] ; Xingxing Hu [République populaire de Chine] ; Fangfang Wu [République populaire de Chine] ; Cuicui Jiao [République populaire de Chine] ; Pengfei Hou [République populaire de Chine] ; Shengnan Xu [République populaire de Chine] ; Yongkun Zhao [République populaire de Chine] ; Na Feng [République populaire de Chine] ; Jianzhong Wang [République populaire de Chine] ; Weiyang Sun [République populaire de Chine] ; Tiecheng Wang [République populaire de Chine] ; Yuwei Gao [République populaire de Chine] ; Songtao Yang [République populaire de Chine] ; Xianzhu Xia [République populaire de Chine]

Source :

RBID : pubmed:29896174

Abstract

Middle East respiratory syndrome coronavirus (MERS-CoV) is a novel human coronavirus that can cause human respiratory disease. The development of a detection method for this virus that can lead to rapid and accurate diagnosis would be significant. In this study, we established a nucleic acid visualization technique that combines the reverse transcription loop-mediated isothermal amplification technique and a vertical flow visualization strip (RT-LAMP-VF) to detect the N gene of MERS-CoV. The RT-LAMP-VF assay was performed in a constant temperature water bath for 30 min, and the result was visible by the naked eye within 5 min. The RT-LAMP-VF assay was capable of detecting 2 × 101 copies/μl of synthesized RNA transcript and 1 × 101 copies/μl of MERS-CoV RNA. The method exhibits no cross-reactivities with multiple CoVs including SARS-related (SARSr)-CoV, HKU4, HKU1, OC43 and 229E, and thus exhibits high specificity. Compared to the real-time RT-PCR (rRT-PCR) method recommended by the World Health Organization (WHO), the RT-LAMP-VF assay is easy to handle, does not require expensive equipment and can rapidly complete detection within 35 min.

DOI: 10.3389/fmicb.2018.01101
PubMed: 29896174


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pubmed:29896174

Le document en format XML

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<name sortKey="Feng, Na" sort="Feng, Na" uniqKey="Feng N" first="Na" last="Feng">Na Feng</name>
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<name sortKey="Sun, Weiyang" sort="Sun, Weiyang" uniqKey="Sun W" first="Weiyang" last="Sun">Weiyang Sun</name>
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<name sortKey="Wang, Tiecheng" sort="Wang, Tiecheng" uniqKey="Wang T" first="Tiecheng" last="Wang">Tiecheng Wang</name>
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<name sortKey="Gao, Yuwei" sort="Gao, Yuwei" uniqKey="Gao Y" first="Yuwei" last="Gao">Yuwei Gao</name>
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<name sortKey="Yang, Songtao" sort="Yang, Songtao" uniqKey="Yang S" first="Songtao" last="Yang">Songtao Yang</name>
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<name sortKey="Xia, Xianzhu" sort="Xia, Xianzhu" uniqKey="Xia X" first="Xianzhu" last="Xia">Xianzhu Xia</name>
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<div type="abstract" xml:lang="en">Middle East respiratory syndrome coronavirus (MERS-CoV) is a novel human coronavirus that can cause human respiratory disease. The development of a detection method for this virus that can lead to rapid and accurate diagnosis would be significant. In this study, we established a nucleic acid visualization technique that combines the reverse transcription loop-mediated isothermal amplification technique and a vertical flow visualization strip (RT-LAMP-VF) to detect the N gene of MERS-CoV. The RT-LAMP-VF assay was performed in a constant temperature water bath for 30 min, and the result was visible by the naked eye within 5 min. The RT-LAMP-VF assay was capable of detecting 2 × 10
<sup>1</sup>
copies/μl of synthesized RNA transcript and 1 × 10
<sup>1</sup>
copies/μl of MERS-CoV RNA. The method exhibits no cross-reactivities with multiple CoVs including SARS-related (SARSr)-CoV, HKU4, HKU1, OC43 and 229E, and thus exhibits high specificity. Compared to the real-time RT-PCR (rRT-PCR) method recommended by the World Health Organization (WHO), the RT-LAMP-VF assay is easy to handle, does not require expensive equipment and can rapidly complete detection within 35 min.</div>
</front>
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</PubDate>
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<Title>Frontiers in microbiology</Title>
<ISOAbbreviation>Front Microbiol</ISOAbbreviation>
</Journal>
<ArticleTitle>A Rapid and Specific Assay for the Detection of MERS-CoV.</ArticleTitle>
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<MedlinePgn>1101</MedlinePgn>
</Pagination>
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<Abstract>
<AbstractText>Middle East respiratory syndrome coronavirus (MERS-CoV) is a novel human coronavirus that can cause human respiratory disease. The development of a detection method for this virus that can lead to rapid and accurate diagnosis would be significant. In this study, we established a nucleic acid visualization technique that combines the reverse transcription loop-mediated isothermal amplification technique and a vertical flow visualization strip (RT-LAMP-VF) to detect the N gene of MERS-CoV. The RT-LAMP-VF assay was performed in a constant temperature water bath for 30 min, and the result was visible by the naked eye within 5 min. The RT-LAMP-VF assay was capable of detecting 2 × 10
<sup>1</sup>
copies/μl of synthesized RNA transcript and 1 × 10
<sup>1</sup>
copies/μl of MERS-CoV RNA. The method exhibits no cross-reactivities with multiple CoVs including SARS-related (SARSr)-CoV, HKU4, HKU1, OC43 and 229E, and thus exhibits high specificity. Compared to the real-time RT-PCR (rRT-PCR) method recommended by the World Health Organization (WHO), the RT-LAMP-VF assay is easy to handle, does not require expensive equipment and can rapidly complete detection within 35 min.</AbstractText>
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<ForeName>Pei</ForeName>
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</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Key Laboratory of Jilin Province for Zoonosis Prevention and Control, Institute of Military Veterinary, Academy of Military Medical Sciences, Changchun, China.</Affiliation>
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<LastName>Wang</LastName>
<ForeName>Hualei</ForeName>
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</AffiliationInfo>
<AffiliationInfo>
<Affiliation>College of Veterinary Medicine, Jilin University, Changchun, China.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Disease and Zoonoses, Yangzhou, China.</Affiliation>
</AffiliationInfo>
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<LastName>Cao</LastName>
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</AffiliationInfo>
<AffiliationInfo>
<Affiliation>College of Veterinary Medicine, Jilin University, Changchun, China.</Affiliation>
</AffiliationInfo>
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</AffiliationInfo>
<AffiliationInfo>
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</AffiliationInfo>
<AffiliationInfo>
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</AffiliationInfo>
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</AffiliationInfo>
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<LastName>Yan</LastName>
<ForeName>Feihu</ForeName>
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</AffiliationInfo>
<AffiliationInfo>
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<LastName>Jiao</LastName>
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<AffiliationInfo>
<Affiliation>College of Veterinary Medicine, Jilin University, Changchun, China.</Affiliation>
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<LastName>Xu</LastName>
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</AffiliationInfo>
<AffiliationInfo>
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</AffiliationInfo>
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<LastName>Zhao</LastName>
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</AffiliationInfo>
<AffiliationInfo>
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<LastName>Sun</LastName>
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<AffiliationInfo>
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<AffiliationInfo>
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<LastName>Xia</LastName>
<ForeName>Xianzhu</ForeName>
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<AffiliationInfo>
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</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Disease and Zoonoses, Yangzhou, China.</Affiliation>
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<li>République populaire de Chine</li>
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<li>Dongbei</li>
<li>Guangdong</li>
<li>Jilin</li>
<li>Zhejiang</li>
</region>
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<li>Changchun</li>
<li>Hangzhou</li>
<li>Jiangmen</li>
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<li>Université de Zhejiang</li>
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<name sortKey="Cao, Zengguo" sort="Cao, Zengguo" uniqKey="Cao Z" first="Zengguo" last="Cao">Zengguo Cao</name>
<name sortKey="Chi, Hang" sort="Chi, Hang" uniqKey="Chi H" first="Hang" last="Chi">Hang Chi</name>
<name sortKey="Feng, Na" sort="Feng, Na" uniqKey="Feng N" first="Na" last="Feng">Na Feng</name>
<name sortKey="Gao, Yuwei" sort="Gao, Yuwei" uniqKey="Gao Y" first="Yuwei" last="Gao">Yuwei Gao</name>
<name sortKey="Hou, Pengfei" sort="Hou, Pengfei" uniqKey="Hou P" first="Pengfei" last="Hou">Pengfei Hou</name>
<name sortKey="Hu, Xingxing" sort="Hu, Xingxing" uniqKey="Hu X" first="Xingxing" last="Hu">Xingxing Hu</name>
<name sortKey="Jiao, Cuicui" sort="Jiao, Cuicui" uniqKey="Jiao C" first="Cuicui" last="Jiao">Cuicui Jiao</name>
<name sortKey="Jin, Hongli" sort="Jin, Hongli" uniqKey="Jin H" first="Hongli" last="Jin">Hongli Jin</name>
<name sortKey="Sun, Weiyang" sort="Sun, Weiyang" uniqKey="Sun W" first="Weiyang" last="Sun">Weiyang Sun</name>
<name sortKey="Wang, Hualei" sort="Wang, Hualei" uniqKey="Wang H" first="Hualei" last="Wang">Hualei Wang</name>
<name sortKey="Wang, Jianzhong" sort="Wang, Jianzhong" uniqKey="Wang J" first="Jianzhong" last="Wang">Jianzhong Wang</name>
<name sortKey="Wang, Tiecheng" sort="Wang, Tiecheng" uniqKey="Wang T" first="Tiecheng" last="Wang">Tiecheng Wang</name>
<name sortKey="Wu, Fangfang" sort="Wu, Fangfang" uniqKey="Wu F" first="Fangfang" last="Wu">Fangfang Wu</name>
<name sortKey="Xia, Xianzhu" sort="Xia, Xianzhu" uniqKey="Xia X" first="Xianzhu" last="Xia">Xianzhu Xia</name>
<name sortKey="Xu, Shengnan" sort="Xu, Shengnan" uniqKey="Xu S" first="Shengnan" last="Xu">Shengnan Xu</name>
<name sortKey="Yan, Feihu" sort="Yan, Feihu" uniqKey="Yan F" first="Feihu" last="Yan">Feihu Yan</name>
<name sortKey="Yang, Songtao" sort="Yang, Songtao" uniqKey="Yang S" first="Songtao" last="Yang">Songtao Yang</name>
<name sortKey="Yu, Beibei" sort="Yu, Beibei" uniqKey="Yu B" first="Beibei" last="Yu">Beibei Yu</name>
<name sortKey="Zhao, Jincun" sort="Zhao, Jincun" uniqKey="Zhao J" first="Jincun" last="Zhao">Jincun Zhao</name>
<name sortKey="Zhao, Yongkun" sort="Zhao, Yongkun" uniqKey="Zhao Y" first="Yongkun" last="Zhao">Yongkun Zhao</name>
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