Rapid and sensitive detection of Little cherry virus 2 using isothermal reverse transcription-recombinase polymerase amplification

Journal of Virological Methods

Volumn 205, Issue , 2014, Pages 24-30

  Mekuria, Tefera A ^a,c   Zhang, Shulu ^b   Eastwell, Kenneth C ^a  

^a WASHINGTON STATE UNIVERSITY   (United States)

^b Agdia Inc   (United States)

^c Agri Analysis LLC   (United States)

Author keywords

Isothermal detection; Little cherry disease; Little cherry virus 2; Prunus avium; Recombinase polymerase amplification; Sweet cherry

Indexed keywords

COAT PROTEIN; PRIMER DNA; RECOMBINASE; VIRUS RNA;

AMPLICON; ARTICLE; CLOSTEROVIRIDAE; CONTROLLED STUDY; GENE AMPLIFICATION; INTERMETHOD COMPARISON; ISOTHERMAL REVERSE TRANSCRIPTION RECOMBINASE POLYMERASE AMPLIFICATION; LITTLE CHERRY VIRUS 2; NONHUMAN; NUCLEIC ACID ANALYSIS; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROCESS DEVELOPMENT; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SENSITIVITY ANALYSIS; SWEET CHERRY; VIRUS DETECTION; DNA SEQUENCE; GENETICS; ISOLATION AND PURIFICATION; PLANT DISEASE; PROCEDURES; SENSITIVITY AND SPECIFICITY; SEQUENCE ALIGNMENT; TIME FACTOR; VIROLOGY;

BASE SEQUENCE; CLOSTEROVIRIDAE; DNA PRIMERS; PLANT DISEASES; PRUNUS AVIUM; RECOMBINASES; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; RNA, VIRAL; SENSITIVITY AND SPECIFICITY; SEQUENCE ALIGNMENT; SEQUENCE ANALYSIS, DNA; TIME FACTORS;

EID: 84901044261     PISSN: 01660934     EISSN: 18790984     Source Type: Journal    
DOI: 10.1016/j.jviromet.2014.04.015     Document Type: Article

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