CovidV1, Main, Exploration, bibRecord, 000760

Rapid detection of tomato leaf curl Bengaluru virus through loop mediated isothermal amplification assay

Identifieur interne : 000760 ( Main/Exploration ); précédent : 000759; suivant : 000761

Rapid detection of tomato leaf curl Bengaluru virus through loop mediated isothermal amplification assay

Auteurs : R. Arutselvan ; M. Krishna Reddy [Inde] ; T. Makeshkumar

Source :

VirusDisease [ 2347-3584 ] ; 2017.

RBID : PMC:5684993

Abstract

A loop-mediated isothermal amplification (LAMP) technique was employed to develop a simple and rapid method for the detection of tomato leaf curl Bangalore virus (ToLCBaV) in diseased plants of tomato (Solanum lycopersicum). Six sets of primers were designed for LAMP technique targeting the conserved AC1 region and successfully detected ToLCBaV. No reaction was detected in the tissues of healthy plants by either the LAMP or the polymerase chain reaction (PCR). The LAMP products can be visualized by presence or absence of turbidity and staining (0.2 μL for 25 μL LAMP product) directly in the tube with nucleic acid stain dye which allowed easy detection. Sensitivity of LAMP assay is 100 times of conventional PCR technique. Although, both the LAMP and the PCR methods were capable of detecting ToLCBaV in infected tissues of tomato, the LAMP method would be more useful than the PCR method for detection of ToLCBaV infection in tomato plants because it is more rapid, simple and accurate method.

Url:

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5684993

DOI: 10.1007/s13337-017-0385-5
PubMed: 29291217
PubMed Central: 5684993

Affiliations:

Inde

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<front><div type="abstract" xml:lang="en"><p id="Par1">A loop-mediated isothermal amplification (LAMP) technique was employed to develop a simple and rapid method for the detection of tomato leaf curl Bangalore virus (ToLCBaV) in diseased plants of tomato (<italic>Solanum lycopersicum</italic>
). Six sets of primers were designed for LAMP technique targeting the conserved AC1 region and successfully detected ToLCBaV. No reaction was detected in the tissues of healthy plants by either the LAMP or the polymerase chain reaction (PCR). The LAMP products can be visualized by presence or absence of turbidity and staining (0.2 μL for 25 μL LAMP product) directly in the tube with nucleic acid stain dye which allowed easy detection. Sensitivity of LAMP assay is 100 times of conventional PCR technique. Although, both the LAMP and the PCR methods were capable of detecting ToLCBaV in infected tissues of tomato, the LAMP method would be more useful than the PCR method for detection of ToLCBaV infection in tomato plants because it is more rapid, simple and accurate method.</p>
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Rapid detection of tomato leaf curl Bengaluru virus through loop mediated isothermal amplification assay

Rapid detection of tomato leaf curl Bengaluru virus through loop mediated isothermal amplification assay

Source :

Abstract

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