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High-quality RT-PCR with chemically modified RNA controls.
Luo, Guangcheng; Zhang, Jun; Zhang, Shun; Hu, Bei; Hu, Lillian; Huang, Zhen.
  • Luo G; Key Laboratory of Bio-Resource and Eco-environment of Ministry of Education, College of Life Sciences, Sichuan University, Chengdu, Sichuan, 610064, PR China; Department of Clinical Laboratory, Affiliated Hospital of North Sichuan Medical College, Nanchong, Sichuan, China.
  • Zhang J; Key Laboratory of Bio-Resource and Eco-environment of Ministry of Education, College of Life Sciences, Sichuan University, Chengdu, Sichuan, 610064, PR China.
  • Zhang S; Key Laboratory of Bio-Resource and Eco-environment of Ministry of Education, College of Life Sciences, Sichuan University, Chengdu, Sichuan, 610064, PR China.
  • Hu B; Key Laboratory of Bio-Resource and Eco-environment of Ministry of Education, College of Life Sciences, Sichuan University, Chengdu, Sichuan, 610064, PR China.
  • Hu L; SeNA Research Institute, Atlanta, GA, 30303, USA.
  • Huang Z; Key Laboratory of Bio-Resource and Eco-environment of Ministry of Education, College of Life Sciences, Sichuan University, Chengdu, Sichuan, 610064, PR China; SeNA Research Institute, Atlanta, GA, 30303, USA. Electronic address: huang@senaresearch.org.
Talanta ; 224: 121850, 2021 Mar 01.
Article in English | MEDLINE | ID: covidwho-919513
ABSTRACT
In detecting infectious diseases, such as coronavirus 2019 (COVID-19), real-time reverse-transcription polymerase chain reaction (RT-PCR) is one of the most important technologies for RNA detection and disease diagnosis. To achieve high quality assurance, appropriate positive and negative controls are critical for disease detection using RT-PCR kits. In this study, we have found that commercial kits often adopt DNAs instead of RNAs as the positive controls, which can't report the kit problems in reverse transcription, thereby increasing risk of the false negative results when testing patient samples. To face the challenge, we have proposed and developed the chemically modified RNAs, such as phosphoroselenaote and phosphorothioate RNAs (Se-RNA and S-RNA), as the controls. We have found that while demonstrating the high thermostability, biostability, chemostability and exclusivity (or specificity), both Se-RNA and S-RNA can be fine templates for reverse transcription, indicating their potentials as both positive and negative controls for RT-PCR kits.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: RNA, Viral / Reverse Transcriptase Polymerase Chain Reaction / Real-Time Polymerase Chain Reaction / COVID-19 Nucleic Acid Testing / COVID-19 Type of study: Diagnostic study / Prognostic study Limits: Humans Language: English Journal: Talanta Year: 2021 Document Type: Article Affiliation country: J.talanta.2020.121850

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Full text: Available Collection: International databases Database: MEDLINE Main subject: RNA, Viral / Reverse Transcriptase Polymerase Chain Reaction / Real-Time Polymerase Chain Reaction / COVID-19 Nucleic Acid Testing / COVID-19 Type of study: Diagnostic study / Prognostic study Limits: Humans Language: English Journal: Talanta Year: 2021 Document Type: Article Affiliation country: J.talanta.2020.121850