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Abstract
Aim:
The study aims to standardize a Real-Time LAMP assay for effective, highly
sensitive, and rapid detection of BBTV in North-east India.
Methodology: Forty samples of banana showing BBTV like symptoms
were collected from Assam, India and subjected to conventional PCR for
confirmation. Six sets of BBTV LAMP primers were designed and the PCR
positive samples were subjected to Real-Time LAMP assay for detection of
BBTV. Finally, a sensitivity test of BBTV LAMP assay and comparison of BBTV
LAMP assay with conventional PCR was done using seven 10-fold dilutions of
total genomic DNA of leaf samples with the highest dilution starting from 100
ng µl-1.
Results:
Initially a total of twenty six out of forty banana samples were tested
positive for BBTV with conventional PCR method. The Real-Time LAMP assay for
BBTV detection resulted in typical sigmoidal amplification curves with the
peak values ranging between 8.00 to 12.15 min and annealing derivatives
ranging between 83.3oC to 84.3oC in the tested samples.
Sensitivity testing and comparison of BBTV Real-Time LAMP assay with
conventional PCR revealed that the BBTV LAMP assay could efficiently detect
up to 0.0001ng µl-1 of total DNA against 0.01ng µl-1 in
conventional PCR.
Interpretation: The findings highlight rapid, sensitive,
accurate and effective diagnosis of BBTV using Real-Time LAMP method. This
method can be preferred over conventional diagnostic techniques like PCR or
ELISA for rapid large scale detection of BBTV in banana plants in North-east
India.
Key words: Banana, Banana bunchy top virus, Rapid
detection, Real-Time LAMP assay
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