Value of CODEHOP RT-pCR in detection of Flavivirus.
- Author:
Qun HU
;
Jian-Ning ZHEN
;
Si-Jie MA
;
Hui HAN
;
Xiao-Hong SUN
- Publication Type:Journal Article
- MeSH:
DNA Primers;
genetics;
Flavivirus;
classification;
genetics;
isolation & purification;
Flavivirus Infections;
virology;
Humans;
Molecular Sequence Data;
Phylogeny;
Reverse Transcriptase Polymerase Chain Reaction;
methods;
Viral Nonstructural Proteins;
genetics
- From:
Chinese Journal of Virology
2014;30(2):171-176
- CountryChina
- Language:Chinese
-
Abstract:
This study aims to analyse the value of CODEHOP RT-PCR in the detection of Flavivirus. According to the amino acid sequences of polyproteins of different flaviviruses published in GenBank, a pair of primers was designed using the CODEHOP method. One-step RT-PCR was used to detect Japanese encephalitis virus strain JEV1201, Dengue virus strain JKD001, and yellow fever virus vaccine YV6161. BLAST analysis and phylogenetic analysis were performed after the RT-PCR products of nucleocapsid genes were sequenced. The results showed that this method could amplify Flavivirus specifically, and the size and sequence of the target fragment accorded with the anticipated result. JEV1201 had the highest homology to Japanese encephalitis virus strain YL2009-4/YC2009-3, belonging to the branch of the phylogenetic tree of Japanese encephalitis virus strains. JKD001 had the highest homology to Dengue virus strain DENV-2/ID/1022DN/1975, belonging to the branch of the phylogenetic tree of Dengue virus strains. YV6161 had the highest homology to Yellow fever virus strain 17D, belonging to the branch of the phylogenetic tree of Yellow fever virus strains. In conclusion, the method of CODEHOP RT-PCR can be effectively used to detect, identify, and phylogenetically analyse Flavivirus.
