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Rapid detection of monkeypox virus and differentiation of West African and Congo Basin strains using endonuclease restriction-mediated real-time PCR-based testing.
Zhou, Juan; Xiao, Fei; Huang, Xiaolan; Fu, Jin; Jia, Nan; Sun, Chunrong; Chen, Min; Xu, Zheng; Huang, Hui; Wang, Yi.
Afiliación
  • Zhou J; Experimental Research Center, Capital Institute of Pediatrics, Beijing, 100020, P. R. China. wildwolf0101@163.com.
  • Xiao F; Experimental Research Center, Capital Institute of Pediatrics, Beijing, 100020, P. R. China. wildwolf0101@163.com.
  • Huang X; Experimental Research Center, Capital Institute of Pediatrics, Beijing, 100020, P. R. China. wildwolf0101@163.com.
  • Fu J; Experimental Research Center, Capital Institute of Pediatrics, Beijing, 100020, P. R. China. wildwolf0101@163.com.
  • Jia N; Experimental Research Center, Capital Institute of Pediatrics, Beijing, 100020, P. R. China. wildwolf0101@163.com.
  • Sun C; Experimental Research Center, Capital Institute of Pediatrics, Beijing, 100020, P. R. China. wildwolf0101@163.com.
  • Chen M; Experimental Research Center, Capital Institute of Pediatrics, Beijing, 100020, P. R. China. wildwolf0101@163.com.
  • Xu Z; Experimental Research Center, Capital Institute of Pediatrics, Beijing, 100020, P. R. China. wildwolf0101@163.com.
  • Huang H; Department of Infectious Diseases, Affiliated Children's Hospital, Capital Institute of Pediatrics, Beijing, 10020, P. R. China. huihui07@tom.com.
  • Wang Y; Experimental Research Center, Capital Institute of Pediatrics, Beijing, 100020, P. R. China. wildwolf0101@163.com.
Anal Methods ; 16(17): 2693-2701, 2024 May 03.
Article en En | MEDLINE | ID: mdl-38624185
ABSTRACT
The ongoing multi-country outbreak of monkeypox virus (MPXV) has continuously attracted global attention, highlighting the critical need for timely and accurate methods to detect MPXV and differentiate its clades. Herein, we devised a novel multiplex ET-PCR (endonuclease restriction-mediated real-time PCR) assay that integrates PCR amplification, restriction endonuclease cleavage and real-time fluorescence detection to diagnose MPXV infection and distinguish the Congo Basin and West African MPXV strains. In the MPXV ET-PCR system, three sets of specific primers were designed for MPXV, Congo Basin and West African strains. A short sequence, which could be recognized by restriction endonuclease enzyme BstUI, was added to the 5'end of amplification primers. Then, the modified primers were assigned different reporter dyes and corresponding quenching dyes to each of the three targets, enabling real-time fluorescence reporting of the results and multiplex detection. The designed assay enabled the detection of single or three targets in a single tube, with excellent specificity and analytical sensitivity in terms of plasmid and pseudotyped virus. Moreover, the clinical feasibility of our assay was validated using artificially simulated plasma, nasopharyngeal swab and skin swab samples. In conclusion, the multiplex ET-PCR assay devised here had the advantages of simple primer design, cost-effectiveness, low contamination risk, excellent sensitivity, high specificity and multiplex detection, making it a valuable and dependable tool for curbing the extensive spread of MPXV.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Monkeypox virus / Reacción en Cadena en Tiempo Real de la Polimerasa Límite: Humans País/Región como asunto: Africa Idioma: En Revista: Anal Methods Año: 2024 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Monkeypox virus / Reacción en Cadena en Tiempo Real de la Polimerasa Límite: Humans País/Región como asunto: Africa Idioma: En Revista: Anal Methods Año: 2024 Tipo del documento: Article Pais de publicación: Reino Unido