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World J Microbiol Biotechnol. 2016 Jul;32(7):108. doi: 10.1007/s11274-016-2078-4. Epub 2016 Jun 4.

Loop mediated isothermal amplification (LAMP) assay for detection of coconut root wilt disease and arecanut yellow leaf disease phytoplasma.

Author information

1
Central Plantation Crops Research Institute, Indian Council of Agricultural Research (ICAR), Kudlu P.O, Kasaragod, 671124, Kerala, India.
2
Department of Biotechnology, Sugarcane Breeding Institute, Indian Council of Agricultural Research (ICAR), Coimbatore, 641007, Tamil Nadu, India. rmanimekalaiicar@gmail.com.

Abstract

The coconut root wilt disease (RWD) and the arecanut yellow leaf disease (YLD) are two major phytoplasma associated diseases affecting palms in South India. Greatly debilitating the palm health, these diseases cause substantial yield reduction and economic loss to farmers. A rapid and robust diagnostic technique is crucial in efficient disease management. We established phytoplasma 16S rDNA targeted loop mediated isothermal amplification (LAMP) and real time LAMP based diagnostics for coconut RWD and arecanut YLD. The LAMP reaction was set at 65 °C and end point detection made using hydroxynaphthol blue (HNB) and agarose gel electrophoresis. Molecular typing of LAMP products were made with restriction enzyme HpyCH4 V. Conventional PCR with LAMP external primers and sequencing of amplicons was carried out. Real time LAMP was performed on the Genei II platform (Optigene Ltd., UK). An annealing curve analysis was programmed at the end of the incubation to check the fidelity of the amplicons. The phytoplasma positive samples produced typical ladder like bands on agarose gel, showed colour change from violet to blue with HNB and produced unique annealing peak at 85 ± 0.5 °C in the real time detection. Restriction digestion produced predicted size fragments. Sequencing and BLASTN analysis confirmed that the amplification corresponded to phytoplasma 16S rRNA gene. LAMP method devised here was found to be more robust compared to conventional nested PCR and hence has potential applications in detection of phytoplasma from symptomatic palm samples and in rapid screening of healthy seedlings.

KEYWORDS:

16S rRNA gene; LAMP; Phytoplasma; Real time LAMP

PMID:
27263003
DOI:
10.1007/s11274-016-2078-4
[Indexed for MEDLINE]

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