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Loop-mediated isothermal amplification assay in combination with lateral flow dipstick in HSV type 1
被引:0
|作者:
Gao, Fei
[1
,3
]
Wang, Zhuoshi
[2
]
Zhang, Mingqi
[2
]
Zhao, Yan
[2
]
Yao, Tao
[1
]
Xu, Ling
[1
]
He, Xiangdong
[2
]
Wang, Bing
[3
]
He, Wei
[1
,2
]
机构:
[1] He Univ, HE Eye Hosp, Clin Res Ctr, Shenyang, Liaoning, Peoples R China
[2] He Univ, Precis Med Innovat Inst, Stem Cell Res Ctr, Shenyang, Liaoning, Peoples R China
[3] Northeastern Univ, Coll Life Sci & Hlth, Shenyang, Liaoning, Peoples R China
关键词:
HSV type 1;
herpetic keratitis;
lateral flow dipstick;
loop-mediated isothermal amplification;
quantitative PCR;
HERPES-SIMPLEX-VIRUS;
DIAGNOSIS;
KERATITIS;
LAMP;
D O I:
10.2217/fvl-2022-0100
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Aim: Diagnostic methods for HSV-1 need to be updated. Materials & methods: Serial dilutions of HSV-1 DNA and ocular pathogenic microorganisms were tested by loop-mediated isothermal amplification-lateral flow dipstick assay (LAMP-LFD assay). The reliability of the LAMP-LFD assay and quantitative real-time PCR (qPCR) for HSV-1 detection was also validated using 30 clinical swab samples. Results: The LAMP reaction is optimal at 65 degrees C and 30 min. And the LAMP-LFD assay could detect HSV-1 up to 10 copies/mu l and no cross-reactivity with other pathogens was observed. Moreover, LAMP-LFD had similar positive rates to qPCR in clinical samples, and sensitivity and specificity were highly consistent with those of qPCR. Conclusion: LAMP-LFD assay is a rapid technique for the diagnosis of HSV-1.
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页码:39 / 50
页数:12
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