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Optimization of RT–PCR for the Detection of Bean leaf roll virus in Plant Hosts and Insect Vectors
Author(s) -
Ortiz V.,
Castro S.,
Romero J.
Publication year - 2005
Publication title -
journal of phytopathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.53
H-Index - 60
eISSN - 1439-0434
pISSN - 0931-1785
DOI - 10.1111/j.1439-0434.2004.00929.x
Subject(s) - biology , aphis , luteovirus , nucleic acid , virus , polymerase chain reaction , plant virus , vector (molecular biology) , potato virus y , aphid , virology , aphis gossypii , aphididae , insect , reverse transcriptase , botany , homoptera , gene , genetics , pest analysis , recombinant dna
The detection of luteoviruses by reverse transcription polymerase chain reaction (RT–PCR) depends on the adequate quality and quantity of extracted viral nucleic acids. We have optimized the detection of Bean leaf roll virus (BLRV) using selective precipitation by LiCl of viral RNA from a small quantity of infected plant tissues and insect vectors. The optimal template for PCR was 15 μ l of RT reaction mixture. BLRV was detected in different plant hosts and aphid vectors and Aphis fabae , previously considered to be a non‐vector of BLRV, was found to acquire the virus from infected plants.