• The Plant Pathology Journal
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• 제18권5호
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• pp.293-299
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• 2002

A survey of Fusarium wilt of perilla was conducted in 12 locations in Korea from 1999 to 2001. The disease occurred in 74 out of 187 fields in the 12 locations surveyed, and incidence of the disease reached up to 30% at its maximum in some perilla fields in Seosan and Dangjin. Incidence of the disease in the other locations ranged from 0.2 to 20%. A total of 327 isolates of Fusarium spp. were obtained from stems and roots of the diseased perilla plants. The isolates were identified based on their morphological characteristics. Out of the 327 isolates of Fusarium, 277 isolates from 12 locations were identified as F. oxysporum, 11 isolates from three locations as F. solani,17 isolates from two locations as F. equiseti, 4 isolates from one location as F. avenaceum and 6 isolates from one location as F. subglutinans. The other 12 isolates of Fusarium from four locations were unidentified. Twelve isolates of F. oxysporum and two isolates each of the other Fusarium spp. were tested for their pathogenicity to five cultivars of perilla. Seven isolates of F. oxysporum were strongly pathogenic to some perilla cultivars, but the other five isolates were weakly or not pathogenic. One isolate of F. solani was strongly pathogenic to all the perilla cultivars tested, but another isolate was not pathogenic. All the isolates of F. equiseti, F. avenaceum, and F. Subglutinans tested were not pathogenic to any of the perilla cultivars tested. Symptoms on the perilla plants induced by artificial inoculation with strongly pathogenic isolates of F. oxysporum and F. solani appeared as wilt, stem blight, and root yet, which were similar to those observed in the fields. The isolates which induced symptoms by artificial inoculation were re-isolated from the lesions of the perilla plants inoculated. All the isolates of F. oxysporum tested were not pathogenic to eight other crops inoculated. Results of this study reveal that F. oxysporum is the main pathogen of perilla wilt and that it is host specific to perilla. forma specialis of F. oxysporum causing wilt of perilla is proposed as perillae.

• 한국식물병리학회지
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• 제3권3호
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• pp.174-179
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• 1987

1978년부터 1985년까지 8년간 전국에서 수집 분리한 도열병균 4,885균주를 공시하여 레이스를 판별하였다. $1978\~1980$년까지 일본 구판별품종에 의한 레이스 판별 결과는 통일계품종 침해레이스 6, T-레이스군 2, C-레이스군 5, N-레이스군 2 등 15개 레이스였고 $1981\~1985$년까지 한국 판별품종에 의한 레이스 판별 결과는 통일계품종과 일반계품종에 병원성이 있는 KI-레이스군 11, 일반계품종에만 병원성이 있는 KJ-레이스군 7종 등 18개 레이스로 판별되었다. 시험기간 중 우점레이스는 도열병이 다발된 $1978\~1979$년은 레이스 $N-2^{+t},\;1980\~1985$년은 레이스 KJ-301이었으며 현재 재배되고 있는 통일계품종 대부분에 병원성을 갖는 레이스 KI-315a, ki-315b가 1983년에 출현 그 분포가 증가하였다. 레이스의 지역적 분포는 강원도 지역에는 저항성유전인자 Pi-k, Pi-i를 갖는 품종을 침해하는 레이스 KJ-105, KJ-201의 분포가 많았고, 충북, 전남 지역에는 레이스 KI-315b가 타지역보다 많이 분포하였다.

• 식물병연구
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• 제15권2호
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• pp.130-133
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• 2009

Nano-silver 용액의 식물병원성 세균에 대한 항균 활성 검정을 하기 위해 Clavibacter michiganensis subsp. michiganensis를 포함한 10가지 균주를 대상으로 실험을 수행 하였다. Nano-silver용액은 바이오 (주)플러스에서 제공된 WA-CV-WA13B, WA-AT-WB13R과 WA-PR-WB13R용액을 사용하였으며, 10 ppm, 25 ppm, 50 ppm, 100 ppm 농도로 nano-silver 용액을 배지에 첨가하여 nano-silver 배지를 제조한 후 실험대상 세균 균주를 72 h 배양 후 생장억제 정도를 관찰하기 위하여 세균의 colony 수를 세었다. 실험 결과, WA-CV-WA13B 용액의 경우 C-1에 대하여 10 ppm에서도 높은 생장 억제 효과를 나타냈고, P-6, X-1, 그리고 X-2에 대해서도 생장억제 효과를 나타냈고, WA-AT-WB13R용액의 경우 10 ppm의 농도에서 P-6에 대하여 살균효과가 나타났다. 10 ppm의 농도에서는 C-1, X-1, 그리고 X-2에 대해서 약간의 생장억제 효과가 관찰 되었다. WA-PR-WB13R용액의 경우 10 ppm 혹은 그이상의 농도가 P-5, P-6, 그리고 X-2 균주에 대하여 살균효과를 나타내었다. 실험에 사용된 3가지 nano-silver 용액 모두 25 ppm 이상에서 모든 실험대상 식물병원성 세균에 대하여 살균효과를 나타내었으며, 이러한 결과는 nano-silver 용액을 식물병원성 세균의 방제제로 활용할 수 있는 가능성을 보여주는 결과라고 판된다.

• 식물병연구
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• 제26권3호
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• pp.134-143
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• 2020

본 논문에서는 종자전염 식물병원세균을 규정하였다. 국내 금지병해충 목록에서 세균 4종 및 파이토플라즈마 2종, 그리고 관리병해충 목록 중 세균 35종 및 파이토플라즈마 17종을 대상으로 종자내부 또는 유묘에서 병원세균을 검출한 문헌조사를 실시하였다. 금지 식물병원세균 2종, 관리 식물병원세균 18종 및 관리 파이토플라즈마 1종이 종자전염 식물병원세균으로 판명되었다. 이에 이들 종자전염 식물병원세균들에 대한 근거를 제시하였으며, 향후 수입종자의 검역을 위한 기본자료로 활용될 수 있을 것으로 생각된다.

• Journal of Microbiology and Biotechnology
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• 제5권6호
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• pp.324-334
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• 1995

The actinomycete strain A 11 was antagonistic to plant pathogenic fungi Phytophthora capsid and Magnaporthe grisea. Based on the diaminopimelic acid (DAP) type and morphological characteristics examined by scanning electron microscopy, the strain A 11 was confirmed to belong to the genus Streptomyces. Based on Willcox probability and similarity level, the strain A 11 was numerically identified as Streptomyces flaveus using TAXON program of Ward and Goodfellow. Antibiotic production of S. flaveus strain A 11 was most favorable when cultured on glycerol yeast extract peptone (GYP) agar for 20 days at $28^{\circ}C$. The crude antibiotics from solid GYP agar cultures of the strain A 11 were most effective against Phytophthora capsici and Sclerotinia sclerotiorum among the fungi tested. Antifungal activity of the antibiotics against Alternaria solani, Botryosphaeria dothidea, Cercospora capsici, Magnaporthe grisea, and Rhizoctonia solani was somewhat high, whereas Colletotrichum gloeosporioides and Fusarium oxysporum f. sp. cucumerinum were rarely inhibited even at high concentrations.

• 한국작물학회:학술대회논문집
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• 한국작물학회 2017년도 9th Asian Crop Science Association conference
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• pp.134-134
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• 2017

Recently, host-induced gene silencing (HIGS) system has been successfully applied into development of resistant crops against insects, fungal and viral pathogens. To test HIGS-mediated resistance in rice against rice blast fungus, Magnaporthe oryzae, we first tested possibility of movement of small non-coding RNA from rice cells to rice blast fungus. The rice blast fungus expressing GFP transgene were inoculated to transgenic rice plants ectopically expressing dsRNAi construct targeting fungal GFP gene. Expression of dsRNAi construct for GFP gene in transgenic plants significantly suppressed GFP expression in infected fungal cells indicating that small RNAs generated in plant cells can move into infected fungal cells and efficiently suppress the expression of fungal GFP gene. Consistent with these results, expression of dsRNAi constructs against 3 fungal pathogenic genes of M. oryzae in transgenic rice specifically and efficiently suppressed not only the expression of fungal pathogenic genes, but also fungal infection. The conidia of M. oryzae applied on leaf sheath of transgenic rice expressing dsRNAs against 3 fungal pathogenic genes showed abnormal development of primary hyphae and malfunction of appressorium, which is consistent with the phenotypes of corresponding fungal knock-out mutants. Taken these results together, here, we suggest a novel strategy for development of antifungal crops by means of HIGS system.

• Applied Biological Chemistry
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• 제41권8호
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• pp.600-604
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• 1998

Methanol extracts from 53 species of oriental medicinal plants in 34 families were tested for their fungicidal activities against Pyricularia grisea, Rhizoctonia solani, Phytophthora capsici, Phytophthora infestans, Collectotrichum dematium, Botryospaeria dothidea, Fusarium oxysporum f. sp. cucumerinum, Botrytis cinerea, Puccinia recondita, and Erysiphe graminis. In in vitro study using impregnated paper disc method, the efficacy varied with both plant pathogen and plant species tested. Methanol extracts of Asarum sieboldii roots, Sinomenium acutum roots, Pinus densiflora leaves, Rheum undulatum root barks, Coptis japonica roots, and Phellodendron amurense barks showed potent fungicidal activities against the various pathogens when treated with 10 mg/disc. In a whole plant test, methanol extracts of P. densiflora leaves and roots and C. japonica roots were highly effective against a variety of plant pathogens. As a naturally occurring fungicide, P. densiflora- and C. japonica-derived materials could be useful as new fungicidal products against various plant diseases induced by plant pathogenic fungi.

• 식물병연구
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• 제10권3호
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• pp.203-208
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• 2004

붉은 고추 탄저병균의 우점종인 Colletotrichum gloeosporioides는 C. acutatum에 비해 병원성이 강하였다. C. gloeosporioides는 G와 R계통이 존재하였으며, G계통이 R계통보다 더욱 강한 병원성을 보였다. 붉은 고추 품종간의 병원성 검정 결과, 금세기 품종이 가장 감수성이었고, 파페트 품종이 가장 약한 감수성이었다. 참깨, 홍화, 마, 그리고 딸기와 같은 다른 기주에서 분리되어진 C. gloeosporioides는 붉은 고추에 감염을 일으켰다.

• The Plant Pathology Journal
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• 제19권2호
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• pp.75-78
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• 2003

A lichen-forming fungus was successfully isolated by discharged spore method from Korean lichen (Hetero-dermia sp.) and cultivated in pure culture. The isolate JR0012 inhibited mycelial growth of several plant-pathogenic fungi. Mycelial growth of the four Pythium spp. tested was completely inhibited. Potato dextrose broth was found to be the medium favorable for large-scale production of antibiotics from the isolate. Anti-fungal substances produced in axenic culture were partially purified. This is the first report in Korea of lichen-forming fungus successfully isolated and which exhibited strong antifungal activity against plant-pathogenic fungi, especially the four Pythium spp..

• 한국식물병리학회지
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• 제10권3호
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• pp.197-210
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• 1994

This experiment was carried out to study the cause of degeneration and rot of cultivated mushroom. Among 597 bacterial isolates derived from the rots of Button mushroom (Agaricus bisporus), Oyster mushroom (Pleurotus ostreatus) and Oak mushroom (Lentinus edodes) collected from markets of 5 cities (Seoul, Suwon, Taegu, Pohang and Pusan) in Korea (1991~1993), 111 bacterial isolates (18.5%) were proved as pathogenic bacteria. These pathogenic bacteria causing bacterial rots of cultivated mushrooms were identified as Pseudomonas tolasii, P. agarici, and Eriwinia sp., and the main causal bacteria were P. tolaasii. P. fluorescens and Klebsiella plenticola were confirmed as saprophytic non-pathogenic bacteria. One hundred fifty nine isolates (Group No. 39) of the 486 saprophytic bacterial isolates were classified as P. fluorescens, and this species was most often found rot area of cultivated mushrooms. P. tolaasii, the causal organism of bacterial blotch, was classified into two groups; One group can be differentiated from the other by the formation of white precipitation band by white line reacting organisms of Pseudomonas Agar F media. P. tolaasii attacked the cultivated mushrooms relatively well at lower incubation temperature such as 5$^{\circ}C$, but P. agarici rarely attack at below 1$0^{\circ}C$. The temperature for the infection commercial cultivated mushrooms by P. agarici was higher than that of P. tolaasii. Optimum temperature for the infection of mushrooms by P. tolaasii and P. agarici were 2$0^{\circ}C$ and $25^{\circ}C$, respectively.