4.7 Article

A functional molecular marker for detecting blister blight disease resistance in tea (Camellia sinensis L.)

Journal

PLANT CELL REPORTS
Volume 40, Issue 2, Pages 351-359

Publisher

SPRINGER
DOI: 10.1007/s00299-020-02637-6

Keywords

Biotic stress resistance; EST-SSR marker; Exobasidium fungi; Marker assisted selection; Molecular breeding

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Funding

  1. National Research Council, Sri Lanka [NRC 09-066]

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Identification of an EST-SSR molecular marker associated with Blister blight in tea plants allows for marker-assisted selection, marking a significant advancement in tea molecular breeding. This marker, EST-SSR073, was found to be effective in identifying tea plants resistant or susceptible to Blister blight, providing a valuable tool for improving disease management and breeding efforts in tea.
Key message Identification of an EST-SSR molecular marker associated with Blister blight, a common fungal disease of tea, facilitating marker-assisted selection, marking a milestone in tea molecular breeding. lister blight (BB) leaf disease of tea, caused by the fungus Exobasidium vexans, results in 25-30% crop loss annually. BB is presently controlled by Cu based fungicides, but genetic resistance is the most viable option in disease management. Tea is a naturally out-crossing, woody perennial necessitating a long time for completion of a breeding programme. Marker-assisted selection (MAS) is vital to expedite breeding programmes and also for better accuracy in gene identification. The aim of the current research was to derive marker-trait associations using an F-1 population segregating for BB. The population was genotyped at 11 expressed sequence tag simple sequence repeat loci followed by detecting the alleles by fragment analysis. The genotypic and phenotypic data were subjected to single-marker analysis resulting in the identification of EST-SSR073 as a diagnostic marker amplifying three alleles of the sizes, 168, 170 and 190 bp in F-1. Of them, alleles 190 and 168 bp were confirmed to concur BB resistance and susceptibility, respectively. The alleles were validated in a panel of 64 tea cultivars, resulting in the amplification of 12 alleles at EST-SSR073. The EST-SSR073 allele sequences matched with Camellia sinensis photosystem-I reaction center subunit-II. The marker EST-SSR073 can be effectively used in breeding tea against BB, recording a milestone in MAS in tea.

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