Establishment of recombinase polymerase amplification assay for five hemorrhagic fever-related viruses
10.11855/j.issn.0577-7402.2017.06.09
- VernacularTitle:五种出血热病毒重组酶聚合酶等温扩增方法的建立
- Author:
Xuefeng CAO
;
Xiaoping KANG
;
Yuchang LI
;
Sen ZHANG
;
Yi HU
;
Jing LI
;
Xiaoyan WU
;
Yinhui YANG
- Keywords:
recombinase polymerase assay;
isothermal amplification;
hemorrhagic fever virus
- From:
Medical Journal of Chinese People's Liberation Army
2017;42(6):526-531
- CountryChina
- Language:Chinese
-
Abstract:
Objective To establish a one-step recombinase polymerase amplification (RPA) method for pathogen screening and rapid detection in the field targeting for five hemorrhagic fever related viruses (Zaire ebola virus, Sudan ebola virus, Marburg virus, Lassa virus and Yellow fever virus). Methods The specific nucleic acid (NA) fragments of each virus were selected as target genes by genome sequence analysis, and the primers and probes for RPA assays were designed according to the sequence. A series of diluted template genes were used for RPA detection to determine the sensitivity. The hemorrhagic fever-related viral nucleic acids were used for RPA detection to determine the specificity. The amplification experiments were carried out at different temperature ranging from 37℃ to 42℃ to validate the reaction temperature range. Results The RPA reaction systems of the five hemorrhagic fever viruses could effectively amplify the target genes, the sensitivities were between 1.5×102 and 1.5×103 copies. No cross reactions existed with the other hemorrhagic fever-related viral genes. Meanwhile, RPA assay could effectively amplify the target genes at 37-42℃. Conclusion The isothermal RPA assays of five hemorrhagic fever viruses are established, which may amply target genes fast and react at a wide temperature range, and be potentially useful for in field pathogens detection.
