A field diagnostic method for rapid and sensitive detection of mpox virus

Author:

Zhao Fei12ORCID,Xu Fengwen12ORCID,Wang Xinming3,Song Rui4,Hu Yamei12,Wei Liang12,Xie Yu12,Huang Yu12,Mei Shan12,Wang Liming12,Wang Lingwa12,Gao Zhao12,Guo Li3,Fang Jugao5,Ren Lili3,Jin Ronghua4ORCID,Wang Jianwei3ORCID,Guo Fei12

Affiliation:

1. Key Laboratory of Pathogen Infection Prevention and Control (Ministry of Education) State Key Laboratory of Respiratory Health and Multimorbidity Beijing China

2. NHC Key Laboratory of Systems Biology of Pathogens, National Institute of Pathogen Biology and Center for AIDS Research Chinese Academy of Medical Sciences & Peking Union Medical College Beijing People's Republic of China

3. Christophe Mérieux Laboratory, National Institute of Pathogen Biology Chinese Academy of Medical Sciences & Peking Union Medical College Beijing People's Republic of China

4. Beijing Ditan Hospital Capital Medical University Beijing People's Republic of China

5. Department of Otolaryngology Head and Neck Surgery Capital Medical University Beijing People's Republic of China

Abstract

AbstractThe mpox outbreak has subdued with fewer reported cases at the present in high‐income countries. It is known that mpox virus (MPXV) infection has been epidemic for more than 50 years in African countries. The ancestral MPXV strain has changed into multiple clades, indicating the ongoing evolution of MPXV, which reflects the historical neglect of mpox in Africa, especially after smallpox eradication, and bestows the danger of more severe mpox epidemics in the future. It is thus imperative to continue the development of mpox diagnostics and treatments so we can be prepared in the event of a new mpox epidemic. In this study, we have developed an MPXV detection tool that leverages the recombinase‐aid amplification assay by integrating lateral flow strips (RAA‐LF) and one‐step sample DNA preparation, with visible readout, no need of laboratory instrument, and ready for field deployment. The detection limit reaches 10 copies per reaction. The performance of our RAA‐FL assay in diagnosing mpox clinical samples is on par with that of the quantitative polymerase chain reaction (PCR) assay. Taken together, we have developed a point‐of‐care RAA‐LF method of high accuracy and sensitivity, readily deployable for field detection of MPXV. This diagnostic tool is expected to improve and accelerate field‐ and self‐diagnosis, allow timely isolation and treatment, reduce the spread of MPXV, thus effectively mitigate MPXV outbreak in the future.

Publisher

Wiley

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