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Comparison of Primer-Probe Sets among Different Master Mixes for Laboratory Screening of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2).
Cuong, Hoang Quoc; Hai, Nguyen Duc; Linh, Hoang Thuy; Anh, Nguyen Hoang; Hieu, Nguyen Trung; Thang, Cao Minh; Thao, Nguyen Thi Thanh; Lan, Phan Trong.
Afiliación
  • Cuong HQ; Directorial board, Pasteur Institute in Ho Chi Minh City, Vietnam.
  • Hai ND; Planning Division, Pasteur Institute in Ho Chi Minh City, Vietnam.
  • Linh HT; Medical Analysis Department, Pasteur Institute in Ho Chi Minh City, Vietnam.
  • Anh NH; Microbiology and Immunology Department, Pasteur Institute in Ho Chi Minh City, Vietnam.
  • Hieu NT; Microbiology and Immunology Department, Pasteur Institute in Ho Chi Minh City, Vietnam.
  • Thang CM; Microbiology and Immunology Department, Pasteur Institute in Ho Chi Minh City, Vietnam.
  • Thao NTT; Microbiology and Immunology Department, Pasteur Institute in Ho Chi Minh City, Vietnam.
  • Lan PT; Directorial board, Pasteur Institute in Ho Chi Minh City, Vietnam.
Biomed Res Int ; 2020: 7610678, 2020.
Article en En | MEDLINE | ID: mdl-33029522
BACKGROUND: There is a shortage of chemical reagents for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) diagnosis and a surge of SARS-CoV-2 cases, especially in limited-resource settings. Therefore, the combination of an optimal assay kit is necessary. METHODS: We compared the ability to screen SARS-CoV-2 among three primer-probe sets in two different master mixes, Invitrogen™ SuperScript™ III One-Step RT-PCR and LightCycler Multiplex RNA Virus Master. RESULTS: The assay with TIB-Molbiol, IDT, and Phu Sa sets for LightCycler Multiplex RNA Virus Master or Invitrogen™ SuperScript™ III One-Step RT-PCR showed positive results from a single reaction of triplicate in the three days of 4.8 copies per reaction. R squared and amplification efficiency were 0.97 and ranged from 107 to 108%, respectively. CONCLUSIONS: Our findings indicated that TIB-Molbiol, IDT, and Phu Sa primer-probe sets could be beneficial for the laboratory screening of SARS-CoV-2 by RT-qPCR assay of E gene. There is a need to consider the combination of these reagent sets as a new strategy to increase the testing capacity of screening programs for COVID-19.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neumonía Viral / Sondas ARN / Cartilla de ADN / Infecciones por Coronavirus / Técnicas de Laboratorio Clínico / Betacoronavirus Tipo de estudio: Diagnostic_studies / Screening_studies Límite: Humans Idioma: En Revista: Biomed Res Int Año: 2020 Tipo del documento: Article País de afiliación: Vietnam Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neumonía Viral / Sondas ARN / Cartilla de ADN / Infecciones por Coronavirus / Técnicas de Laboratorio Clínico / Betacoronavirus Tipo de estudio: Diagnostic_studies / Screening_studies Límite: Humans Idioma: En Revista: Biomed Res Int Año: 2020 Tipo del documento: Article País de afiliación: Vietnam Pais de publicación: Estados Unidos