2022
DOI: 10.3390/jof8040335
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Morphological and Molecular Identification of Plant Pathogenic Fungi Associated with Dirty Panicle Disease in Coconuts (Cocos nucifera) in Thailand

Abstract: Dirty panicle disease in coconuts (Cocos nucifera) was first observed in the KU-BEDO Coconut BioBank, Nakhon Pathom province, Thailand. The occurrence of the disease covers more than 30% of the total coconut plantation area. The symptoms include small brown to dark brown spots and discoloration of male flowers. Herein, three fungal strains were isolated from infected samples. Based on the morphological characteristics the fungal isolates, they were classified into two genera, namely, Alternaria (Al01) and Fusa… Show more

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Cited by 14 publications
(7 citation statements)
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“…Currently, the identification of fungal pathogens causing diseases in plants relies on both morphology and molecular techniques in addition to pathogenicity testing to determine whether Koch’s postulates are fulfilled [ 19 , 31 , 46 ]. The molecular details of multiple DNA sequences have been applied in identifying fungal species [ 42 , 43 ].…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Currently, the identification of fungal pathogens causing diseases in plants relies on both morphology and molecular techniques in addition to pathogenicity testing to determine whether Koch’s postulates are fulfilled [ 19 , 31 , 46 ]. The molecular details of multiple DNA sequences have been applied in identifying fungal species [ 42 , 43 ].…”
Section: Discussionmentioning
confidence: 99%
“…To test whether fungal isolates can cause disease in rubber tree leaves, pathogenicity testing was conducted according to the agar plug (0.5 mm) method [ 30 , 31 ] to determine fulfillment of Koch’s postulates. Healthy rubber tree leaves were disinfected using 70% ethanol.…”
Section: Methodsmentioning
confidence: 99%
“…A total of ten symptomatic samples were collected. The causal fungus was isolated using the tissue transplanting method [ 15 , 16 ]. The infected tissue samples were cut into small pieces (0.3 × 0.3 cm), and their surfaces were disinfected with 70% ethanol followed by 1% sodium hypochlorite (NaOCl).…”
Section: Methodsmentioning
confidence: 99%
“…The three isolates were grown in 100 mL potato-dextrose broth (PDB; prepared as PDA medium but in the absence of agar) at 26 °C and 200 rpm in darkness for 48 h. The genomic DNA was extracted using the Ezup Column Fungi Genomic DNA Purification Kit (Sangon Biotech, China) according to the manufacturer’s instructions. Internal transcribed spacer ( ITS ) region of rDNA, elongation factor 1-α ( EF1-α ) and RNA polymerase II second largest subunit ( RPB2 ) partial sequences were amplified using the ITS1/ITS4 (5′-TCCGTAGCTGAACCTGCGG-3′ and 5′-TCCTCCGCTTATTGATATGC-3′, respectively), EF1-728F/EF1-986R (5′-CATCGAGAAGTTCGAGAAGG-3′ and 5′-TACTTGAAGGAACCCTTACC-3′, respectively) and fRPB2-7CF/fRPB2-11aR (5′-ATGGGYAARCAAGCYATGGG-3′ and 5′-GCRTGGATCTTRTCRTCSACC-3′, respectively) primers [ 27 , 28 , 29 ].…”
Section: Methodsmentioning
confidence: 99%