• Research in Plant Disease
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• v.29 no.1
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• pp.52-59
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• 2023

Cucurbit chlorotic yellows virus (CCYV) is a plant virus that causes damage to cucurbit crops such as watermelon and cucumber, and is transmitted by an insect vector known as the whitefly. Since CCYV was first detected on cucumber in Chungbuk in 2018, it has been reported in other areas including Gyeongsang in Korea. In 2020, we performed field surveys of yellowing diseases in the greenhouses growing melon and watermelon in Chungbuk (Jincheon and Eumseong). Reverse transcription-polymerase chain reaction analysis of 79 collected samples including melon, watermelon, and weeds resulted in detection of CCYV in 4 samples: Three samples were singly infected with CCYV and one samples was mixed infected with CCYV, Cucurbit aphid borne yellows virus, and Watermelon mosaic virus. The complete genome sequences of the four collected CCYV melon isolates (ES 1-ES 4) were determined and genetically compared with those of previously reported CCYV isolates retrieved from GenBank. Phylogenetic analyses of RNA 1 and 2 sequences revealed that four ES isolates were clustered in one group and closely related to the CCYV isolates from China. The analysis also revealed very low genetic diversity among the CCYV ES isolates. In general, CCYV isolates showed little genetic diversity, regardless of host or geographic origins. CCYV has the potential to pose a serious threat to melon, watermelon, and cucumber production in Korea. Further studies are needed to examine the pathogenicity and transmissibility of CCYV in weeds and other cucurbits including watermelon.

• Journal of Korean Society of Forest Science
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• v.48 no.1
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• pp.29-39
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• 1980

This study was initiated to find out the possible insect vector and other means of transmission of jujube witches'-broom disease. 1. Eight species of leafhoppers were found to feed on both healthy and diseased jujube trees. Among these, rhombic marked leafhoppers (Hishimonus sellatus Uhler) were most abundant throughout the growing season of jujube trees in all localities surveyed. H. sellatus was far more abundant on diseased trees than healthy ones. 2. Jujube witches'-broom mycoplasma(JWM) was transmitted to jujube seedlings by Hishimonus sellatus. Jujube seedlings inoculated with H. sellatus which had been fed for 14-21 days on diseased jujube plants, developed smaller, chlorotic leaves 40-60 days after inoculation. Electron microscopy of midveins and petioles of the infected jujube seedlings revealed the presence of numerous mycoplasmalike organisms in phloem tissues. 3. Jujube witches'-broom mycoplasma was also transmitted to Vinca rosea plants by H. sellatus. Infected Vinca rosea plants developed vein clearing and marginal chlorosis of upper leaves 25-38 days after inoculation and followed by stunting and ultimate wilting and death of plant. Electron microscopy of petioles and midveins of infected Vinca rosea plant revealed the presence of numerous mycoplasmalike organisms in phloem tissues. 4. H. sellatus survived more than 30 days on jujube, Vinca rosea, carrot, celery, eggplant, hop, Calystegia japonica, Humulus japonicus, Astragalus sinicus, white clover, red clover, and radino clover. Many second generation nymphs of H. sellatus were also abserved on these plants but clovers. 5. Jujube seeds collected from witches'-broom diseased jujube trees yielded healthy seedlings.

• Journal of Korean Society of Forest Science
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• v.100 no.3
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• pp.352-358
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• 2011

Field Cage plots ($1m{\times}1m{\times}1m$) were established (7 units) to find the lowest limit time about the tending of red pine forest (Pinus densiflora) which can no longer be used as a habitat by Monochamus alternatus, vector insect of pine wilt disease at the experimental forest of the southern forest research center of the Korea forest research institute in February in 2010. Thinning slashes (length, 1 m; diameter, 5~10 cm) tended at the different times were put in cages, and 4~6 couples of adult M. alternatus were put into each the cage in June. Presence or absence the larval entrance holes and larval were determined in November in 2010. Incase of the combination 24, 18, 12 and 6-month-old thinning slashes from thinning times to the time of adult emergence inside a single cage, larval entrance holes were found in the 6-month-old and 12-month-old thinning slashes but larvae were found only in the 6-month-old thinning slashes (treatment 1). In case of the combination 24, 18, 15 and 12-month-old thinning slashes inside a single cage, larval entrance holes were found in the 15-month-old and 12-month-old thinning slashes but larvae were found only in the 12-month-old (treatment 2). When 24, 18, 15, 12 and 6-month-old thinning slashes with treated dry and humid condition were put separately inside each cage, larval entrance holes were found in the 18, 15, 12, 6-month-old thinning slashes without the relation of the dry and humid conditions. But larvae were found in the 15, 12, 6-month-old thinning slashes in the dry conditions and only in the 6-month-old thinning slashes in the humid conditions. Results indicated the lowest limit time which can no longer be used as a habitat by M. alternatus is before 24 month from the time of adult emergence.