Diseases of Brinjals (Eggplant) and Their Management

Kumar, Narender; Kumar, Ajay; Chand, Gireesh; Biswas, SK

doi:10.1201/9780429322181-18

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(2 citation statements)

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“…avoiding the risk of cross contamination, 3) reduction of the assay labor and material costs, and 4) in-crease the sensitivity and speci city and allows the accurate quanti cation the target pathogen (Kumar et al, 2016).…”

Section: Discussionmentioning

confidence: 99%

“…In addition to eld, greenhouse, and controlled climatic circumstances (Pande et al 2011a;Kaur et al 2014;Varshney et al 2014), molecular techniques like Real-Time PCR and Marker Assisted Selection (MAS) is also utilized in breeding projects to screen genetic material for the presence of the AB (Kumar et al, 2016). Field conditions arti cial inoculation test method used to screen breeding material for disease was developed by ICARDA and ICRISAT (Nene et al, 1981;Singh et al, 1984).…”

Section: Introductionmentioning

confidence: 99%

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Comparison of Different Screening Methods for Selection of Ascochyta Blight Disease on Chickpea (Cicer arietinum L.) Genotypes

Aydoğan

2024

Preprint

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Chickpea (Cicer arietinum L.) is the second most important and commonly grown edible food legume crop all over the world. However, chickpea cultivation and production are mainly affected by Ascochyta Blight (AB) disease that results in up to 100% loss in areas having high humidity and warm temperature conditions. Various screening methods are used in the selection of chickpea genotypes for resistance to AB disease. These methods are Natural Field Condition (NFC), Artificial Epidemic Field Condition (AEFC), Marker Assisted Selection (MAS), and Real-Time PCR (RT-PCR). The study was conducted between the 2014 to 2016 growing seasons with 88 chickpea test genotypes. The results of the screening were used to sort the genotypes into the three categories susceptible (S), moderately resistant (MR), and resistant (R). Using MAS screening, 13, 21, and 54 chickpea genotypes were identified as S, MR, and R, respectively. For RT-PCR screening, 39 was S, 31 was MR, and 18 genotypes were R. NFC screening revealed 7, 17, and 64 genotypes that were S, MR, and R while 74 and 6 genotypes were S and MR, 8 genotypes were R to AB disease in the AEFC method.

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Section: Discussionmentioning

confidence: 99%