針對淋巴細胞脈絡(luò)叢腦膜炎病毒（lymphocytic choriomeningitis virus,，LCMV）基因保守序列，設(shè)計特異性引物和熒光探針,，建立了LCMV實時重組聚合酶等溫擴增（real-time recombinasepolymerase amplification,，real-time RPA）檢測方法,。該檢測方法具有良好的特異性，與LCMV同步檢測的其他鼠病毒均未出現(xiàn)交叉反應(yīng),；該檢測方法具有與RT-PCR一樣的高敏感性,；通過對LCMV感染鼠組織樣本和LCMV陰性鼠血清樣本的檢測，證實建立的實時熒光RPA方法具有良好的穩(wěn)定性和可靠性,。與現(xiàn)有的核酸檢測方法相比,，該實時熒光RPA檢測方法在核酸上樣20 min內(nèi)即可判讀結(jié)果，可滿足嚙齒類動物L(fēng)CMV快速檢疫需要,。

Establishment of a Real-time RPA Method for Rapid Detection ofLymphocytic Choriomeningitis Virus

In this paper,，specificprimers and fluorescent probes were designed according to the conservativesequence of lymphocytic choriomeningitis virus（LCMV）,，and a real-time recombinase polymerase amplification assay（real-time RPA）was established. Resultsshowed that the specificity of the assay was good，andno any cross reaction with other murine viruses detected by LCMV was shown. Thesensitivity of established assay was as high as the RT-PCR method. Otherwise,，based on detection of LCMV infected murine tissues and negativeserums,，the real-time RPA showed good stability andreliability. Compared with current detection methods of nucleic acids，the test results could be interpreted within 20 minutes after loadingthe nucleic buffer using the real-time RPA,，which couldsatisfy the need of rapid LCMV inspection in rodent animals.

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