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Methods Mol Biol ; 2142: 165-179, 2020.
Article in English | MEDLINE | ID: mdl-32367367

ABSTRACT

Molecular detection of Zika virus (ZIKV) is a key element of outbreak management. Multiple PCR and isothermal ZIKV assays targeting different ZIKV sequences have been published. In this study, we compared a qRT-PCR, 2 RT-LAMP assays (based on different primer design approaches), and an RT-RPA for the detection of African and Asian/American lineages of ZIKV isolates from human, mosquito, and monkey. Results showed that RT-LAMP detected 100% of samples with a time threshold (Tt) of 18.01 ± 11.71 min while qRT-PCR detected 88.88% of samples with a Tt of 58.30 ± 16.58 min and RT-RPA 50% of samples with a Tt of 3.70 ± 0.44 min.


Subject(s)
Molecular Diagnostic Techniques/methods , Nucleic Acid Amplification Techniques/methods , Real-Time Polymerase Chain Reaction/methods , Zika Virus Infection/diagnosis , Zika Virus/genetics , Animals , Brazil , Cells, Cultured , Cote d'Ivoire , Culicidae , Haplorhini , Humans , Recombinases/metabolism , Reproducibility of Results , Senegal , Uganda , Zika Virus/isolation & purification , Zika Virus Infection/virology
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