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Item type:Publication, Postharvest detection of anthracnose (Colletotrichum asianum) on mango fruit (Mangifera indica L. cv Namdokmai Sithong) using near-infrared response(2026-12-01) ;Junto, Apiwat ;Phanomsophon, Thitima ;Sharma, Sneha ;Kaewsorn, KannapotJongyingcharoen, Jiraporn SripinyowanichAnthracnose disease, caused by fungi of the genus Colletotrichum, poses a major threat to mango production and export industries, with Colletotrichum asianum being among the most significant pathogenic species. This work proposes the hypothesis that the simple difference in absorption between anthracnose-infected and noninfected mangoes illustrated by the average near-infrared (NIR) spectra obtained from hyperspectral images could be used for simple differentiation of the two groups. The method of depositing fungal spores by spraying the spores over the fruit surface, not a small area or specific point, allows for the number of spores per unit area to be harmonized and to detect infected or noninfected spores on every pixel of the mango surface using a hyperspectral imaging camera. Important wavelengths for differentiation included water bands of 970, 1190, and 1200 nm which resulted in the greatest difference in absorbance, and bands of chitin, the major component of the fungal cell wall; 1195 nm was the most important band. In addition, the vibration bands of 868 (protein in the fungal cell wall), 1134 (sugar and starch of the mango substrate), 1320 (NIR absorbers in the fungus-sprayed and mango substrate, not specifically defined) and 1069 nm (crystallinity and N-acetyl methyl groups in the fungal chitin and constituents of the mango), differed from each other. These wavelengths can be used for modelling, which can lead to high performance in quantifying the concentration of anthracnose and classifying the strength levels of anthracnose infection. The microbiological mechanism of anthracnose growth on infected mangoes corresponding to changes in the NIR spectrum during the 4 days after spore infection is comprehensively discussed. These results can aid in enhancing early detection and classification techniques for anthracnose-infected mangoes from noninfected mangoes using hyperspectral image sensors. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, In vitro assessment of crude extract from Gomphrena weed (Gomphrena celosioides Mart.) for control of plant pathogenic fungi causing chili diseases(2023-03-01) ;Apithanasakulngeon, P. ;Somnuek, S. ;Kongtragoul, P.Jaenaksorn, T.The phytochemical screening of both the flowers and other aerial parts of the Gomphrena weed extract (Gomphrena celosioides Mart.) presented alkaloids, flavonoids, saponins, phenolics/tannins, and terpenoids. The extracts from both parts at 80, 160, and 240 mg/ml were significantly inhibited the mycelial growth of C. gloeosporioides and Fusarium sp. compared to inoculated control by paper disc diffusion. The extract from both parts of the Gomphrena weed at the highest concentration (160 mg/ml) significantly showed the greatest inhibitory effect on mycelial growth of Sclerotium sp. (100 percent), followed by C. gloeosporioides (82.5 percent), Cercospora sp. (41.16 percent), and Fusarium sp. (24.41 percent) when tested using the poisoned food technique. The spore germination test revealed both parts of the weed extract yielded concentrations which were completely inhibited (100 percent) on the spore germination of C. capsici, C. gloeosporioides, and Fusarium sp. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Resistance to quinone-outside inhibitor (Qoi) fungicides in colletotrichum species isolated from anthracnose disease occurring in Thailand(2020-01-01) ;Kongtragoul, Pornprapa ;Imamoto, KazuumiIshii, HideoColletotrichum species are plant pathogens causing anthracnose diseases in many crops that result in significant reduction of quality and quantity of the crop products. Management of these diseases has become increasingly difficult recently due to the development of fungicide resistance in pathogens. Thus, monitoring for fungicide sensitivity in the pathogen is important to manage these diseases. The isolates of Colletotrichum species were isolated from anthracnose disease on various crops collected during 2016-2017 in central and southern Thailand. They were tested for their mycelium growth sensitivity to azoxystrobin, a quinone-outside inhibitor (QoI) fungicide and their internal transcribed spacer (ITS) and 5.8S regions of rDNA were analyzed. The results showed that eleven out of twenty four isolates of Colletotrichum species were resistant to azoxystrobin. They were able to grow on PDA amended with 100 mg/l azoxystrobin in the presence of salicylhydroxamic acid (SHAM) at 100 mg/l. Moreover, two isolates of azoxystrobin-resistant Colletotrichum spp. produced much larger lesions than azoxystrobin-sensitive isolates on mango fruits after treatment with 100 mg/l azoxystrobin. This is the first report on the occurrence of azoxystrobin resistance in Colletotrichum species present in Thailand and will contribute to the management of these important diseases in the future. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Postharvest control of anthracnose in mangoes by fumigation with vinegar and ethanol vapours(2019-01-01) ;Suwapanich, Rachit ;Krusong, WarawutThompson, Anthony KeithAnthracnose disease of mangoes is caused by Collectotrichum gloeosporioides. A control method that does not include synthetic fungicides would be beneficial therefore fumigation, in an especially designed vapour exposure box, with vapour from upland rice vinegar and ethanol were tested in vitro on C. gloeosporioides isolated from mangoes and cultured on PDA. Fumigation times were 0, 5, 6, 7, 8, 9 or 10 min for ethanol and vinegar vapours separately and in mixtures at different ratios for 0, 10, 11, 12, 13, 14 or 15 min. Exposure to either ethanol vapour or vinegar vapour controlled both mycelial growth and conidia germination during subsequent storage for seven days at 28°C–32°C, but ethanol was more effective than vinegar and ethanol was more effective alone than in any of the combinations with vinegar. These results provide a successful organic anthracnose control method, but in vivo testing is recommended before commercial application - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Biological control of anthracnose disease on banana var 'Namwa Mali-Ong' by Neosartorya species(2018-12-01) ;Pattarasaikul, W. ;Soytong, K.Poeaim, S.The anthracnose disease caused by Colletotrichum musae on banana was controlled by biological control agents. Seven isolates of C. musae were collected from banana growing area in Suphanburi, Nakhonpathom, Ratchaburi and Nonthaburi province, Thailand. Pathogenicity was tested on fresh banana, and proved that isolates CMDC-01 and CMNM-01 were most aggressive isolates. These isolates were molecular phylogeny confirmed species. In vitro test was done by dual culture tecnique, two isolates of pathogen were tested against ten isolates of antagonistic fungi (Neosartorya hiratsukae, N. pseudofischeri, N, aureola, N. spinosa, N. fenneliae, Talaromyces muroii and T. trachyspermus). The result showed the best antagonistic isolate was N. pseudofischeri EU13 which inhibited C. musae CMDC-01 of 51.23% and N. fenneliae CHA03-A11 inhibited C. musae CMNM-01 of 59.85%. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Application of a new bio-formulation of chaetomium cupreum for biocontrol of colletotrichum gloeosporioides causing coffee anthracnose on arabica variety in Laos(2017-01-01) ;Vilavong, SomlitSoytong, KasemThe anthracnose pathogen was isolated from coffee leave and bean symptoms. Morphological and molecular phylogenetic data confirmed the species as Colletotrichum gloeosporioides. The pathogenicity of the isolate was also confirmed by detached leaf method which inoculated the virulent isolate into coffee leaves. The crude extracts with hexane, ethyl acetate and methanol solvents from Chaetomium cupreum CC3003 resulted significantly inhibited C. gloeosporioides that the ED<inf>50</inf> values of 13, 11 and 28 ppm, respectively. The bioactive substances of C. cupreum CC3003 expressed antifungal activity against C. gloeosporioides as can be seen in the abnormal appearance of spores. A powder bio-formulation of C. cupreum significantly resulted to reduce anthracnose disease of 54.77 %. The application of nano-rotiorinol, nano-trichotoxin and a spore suspension of C. cupreum reduced anthracnose incidence of 46.23, 42.71 and 18.59 %, respectively while the inoculated control had high anthracnose disease. The application of bio-formulation of C. cupreum in powder form, nano-rotiorinol, and nano-trichotoxin to reduce coffee anthracnose was reported for the first time in Lao PDR.
