2019
DOI: 10.1371/journal.pone.0214983
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Immunological detection of the Weligama coconut leaf wilt disease associated phytoplasma: Development and validation of a polyclonal antibody based indirect ELISA

Abstract: Weligama coconut leaf wilt disease (WCLWD) causes heavy losses in the coconut cultivations of southern Sri Lanka. The in-house developed and validated indirect ELISA was based on specific polyclonal antibodies raised in female New Zealand White rabbits, against partially purified WCLWD associated phytoplasma. This ELISA has the potential to distinguish secA PCR confirmed, WCLWD associated phytoplasma positive palms from phytoplasma free palms at high accuracy (93%) and sensitivity (92.7%… Show more

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Cited by 13 publications
(3 citation statements)
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“…Papaya plants have optimal cultivation temperatures of between 25°C and 30°C. Temperature, moisture, light, and wind are also major environmental factors impacting papaya production [37,38]. Temperatures lower than 16°C and higher than 36°C for extended periods negatively impact plant growth [39].…”
Section: Papaya Responses To Environment Stressesmentioning
confidence: 99%
“…Papaya plants have optimal cultivation temperatures of between 25°C and 30°C. Temperature, moisture, light, and wind are also major environmental factors impacting papaya production [37,38]. Temperatures lower than 16°C and higher than 36°C for extended periods negatively impact plant growth [39].…”
Section: Papaya Responses To Environment Stressesmentioning
confidence: 99%
“…Due to the difficulty in developing polyclonal antisera with high titre value, the application of serodiagnostics is limited in the detection of phytoplasmal diseases of palms. Enzyme-linked immunosorbent assay (ELISA) has been developed and standardized for the detection of RWD (Sasikala et al, 2010) and WCLWD of coconut (Kanatiwela-de Silva et al, 2019) and YLD of arecanut (Rajeev et al, 2011).…”
Section: Serologymentioning
confidence: 99%
“…This could be due to the lower specificity of the primers, uneven titer and the erratic distribution of the pathogen in the plant, variability in primer-binding sites, or the association of other fastidious prokaryotes with the symptomatic samples. Even though immunological detection methods [ 16 ] and a qPCR method [ 17 ] have been developed, they are not cost-effective and feasible for large-scale studies. Therefore, further improvements to the PCR-based method are required.…”
Section: Introductionmentioning
confidence: 99%