• 제목/요약/키워드: Clubroot(Plasmodiophora brassicae)

검색결과 62건 처리시간 0.026초

Occurrence of Clubroot on Shepherd's-purse Caused by Plasmodiophora brassicae

  • Kim, Wan-Gyu;Lee, Sang-Yeob;Choi, Hyo-Won;Hong, Sung-Kee;Lee, Young-Kee
    • Mycobiology
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    • 제39권3호
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    • pp.233-234
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    • 2011
  • Clubroot symptoms were frequently observed on roots of shepherd's-purse (Capsella bursa-pastoris) grown in a field in Nonsan, Chungnam province, Korea in March, 2009. Many resting spores were found in the cells of the root gall tissues collected from the field. The clubroot pathogen was identified as Plasmodiophora brassicae based on its morphological and pathological characteristics. This is the first report that P. brassicae causes clubroot of shepherd's-purse in Korea.

Occurrence of Clubroot on Pak-Choi Caused by Plasmodiophora brassicae

  • Kim, Wan-Gyu;Moon, Mi-Hwa;Kim, Jin-Hee;Choi, Hyo-Won;Hong, Sung-Kee
    • Mycobiology
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    • 제37권1호
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    • pp.69-71
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    • 2009
  • Clubroot symptoms occurred severely on roots of Pak-Choi (Brassica campestris ssp. chinensis) grown in greenhouses in Gwangju city, Gyeonggi province, Korea in September, 2008. The incidence of the disease symptoms reached as high as 90% in three greenhouses investigated. The root galls collected from the greenhouses were sectioned using a scalpel and observed by light microscope. Many resting spores were found in the cells of the root gall tissues. Suspension of resting spores was prepared from the root galls and inoculated to roots of healthy Pak-Choi plants. Each of five resting spore suspensions caused clubroot symptoms on the roots, which were similar to those observed during the greenhouse survey. Resting spores of the pathogen were observed in the cells of the affected roots. The clubroot pathogen was identified as Plasmodiophora brassicae based on its morphological and pathological characteristics. This is the first report that Plasmodiophora brassicae causes clubroot of Pak-Choi.

Occurrence of Clubroot Caused by Plasmodiophora brassicae in Baecheongchae

  • Kim, Wan-Gyu;Oh, Sang-Keun;Semunyana, Marc;Han, Man-Jong;Lee, Gyo-Bin;Cho, Weon-Dae
    • 한국균학회지
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    • 제48권4호
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    • pp.499-503
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    • 2020
  • Clubroot symptoms were frequently observed on the roots of Baecheongchae plants grown in vinyl greenhouses of a farmer located in Yangpyeong area of Korea during a disease survey in June 2019. The incidence of diseased Baecheongchae plants ranged from 30 to 90% in the vinyl greenhouses investigated. Many resting spores were found in the tissue of root galls collected. The resting spores were hyaline and spherical and measured 2.5-4.2 ㎛ in diameter. Three inoculum suspensions of resting spores prepared from the root galls were inoculated to the roots of healthy Baecheongchae plants. All the inoculum suspensions caused clubroot symptoms to appear on the roots of the inoculated Baecheongchae plants. The symptoms on the roots induced by artificial inoculation were similar to those observed in the plants of the vinyl greenhouses during the disease survey. Resting spores of the pathogen were recovered from the root galls of the inoculated plants. Three root gall isolates obtained from the inoculated plants were used for molecular identification. Comparing the isolates to the Plasmodiophora brassicae strains in GenBank, the amplification products demonstrated 100% similarity with the internal transcribed spacer (ITS2) sequences. The clubroot pathogen was identified as P. brassicae according to its morphological, pathological, and molecular characteristics. This is the first report of P. brassicae causing clubroot in Baecheongchae.

PCR을 이용한 Plasmodiophora brassicae의 검출 (Detection of Plasmodiophora brassicae by Using Polymerase Chain Reaction)

  • 지희윤;김완규;조원대;지형진;최용철
    • 한국식물병리학회지
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    • 제14권6호
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    • pp.589-593
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    • 1998
  • DNA amplification by polymerase chain reaction (PCR) was used to specifically detect Plasmodiophora brassicae, causing clubroot of crucifers. On the basis of DNA sequence informations, an oligonucleotide primer set specific for the pathogen was designed form small subunit gene (18S-like) and internal transcribed spacer (ITS) region of ribosomal DNA. Primer ITS 5/PB-C produced an amplification product of approximately 520 bp in length with DNA from P. brassicae. However, no amplification product was produced with DNAs from several soil-borne fungi, Didymella bryoniae and Rhizopus stolonifer. Using these primers, the clubroot pathogen was readily detected from infected roots of crucifers, but not from healthy roots. Southern hybridization analysis further confirmed that the amplification product was originated from P. brassicae.

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배추 무사마귀병의 발생상황과 병원균(Plasmodiophora brassicae)의 병원성 및 배추품종의 병저항성 (Incidence, Pathogenicity of Clubroot Fungus(Plasmodiophora brassicae) and Varietal Resistance in Chinese Cabbage)

  • 김두욱;오정행
    • 한국식물병리학회지
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    • 제13권2호
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    • pp.95-99
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    • 1997
  • To obtain a basic information of breeding for resistance to clubroot in Chinese cabbage, disease incidence, pathogenicity, and varietal response to the pathogen were studied. Incidence of clubroot was observed at 3 districts in Gyeonggi-Do, 2 districts in Kangwon-Do, and 1 district each in Gyeongnam, Geongbuk and Jeonbuk, respectively. Disease infection rate and diseased ara were most severe in northern part of Gyeonggi-Do. The isolates of clubroot collected from 8 different districts were not different in their virulence one another in view of their infection rate and disease severity in Chinese cabbage. The clubroot fungus had a wide host range for the cruciferous vegetables. Disease severity was high in rape, turnip and mustard, moderate in Chinese cabbage and broccoli, and low in kale and cauliflower. All of Korean hybrids of Chinese cabbage tested were highly susceptible to clubroot, but Japanese varieties were resistant to the highly pathogenic isolate (EJ-93) which was isolated from the Chinese cabbage in Korea. The hybrid(F1) between clubroot resistant line(930WG) and the susceptible line(332MS) showed completely resistant reaction, which indicated that clubroot resistance was governed by a dominant gene.

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배추 뿌리혹병균 Plasmodiophora brassicae의 종 특이적 프라이머 개발 (Development of Species-Specific Primers for Plasmodiophora brassicae, Clubroot Pathogen of Kimchi Cabbage)

  • 최진수;양슬기;송정영;김홍기
    • 식물병연구
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    • 제20권1호
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    • pp.21-24
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    • 2014
  • Plasmodiophora brassicae는 십자화과 작물에 뿌리혹병을 일으키는 주요 병원균이다. 본 연구에서는 뿌리혹병균의 신속 정확한 검출을 위해서 뿌리혹병균에 대한 새로운 종 특이적 프라이머를 개발하고자 하였다. 새롭게 개발된 프라이머들은 10종의 주요 토양병원균을 비롯하여 기주인 배추 DNA와는 반응하지 않고 P. brassicae와만 반응하는 특이성을 갖고 있었다. 그 가운데 Primer ITS1-1/1-2는 민감도 검정 결과, 10 spores/ml의 DNA까지 검출이 가능함으로써, first round PCR용임에도 불구하고 이전의 검출법 보다 감도가 높고 정확한 결과를 얻었다. Quantitative real-time PCR로 분석할 경우에는 더 적은 수의 포자까지 안정적으로 검출해 낼 수 있어 새로운 P. brassicae 종 특이적 프라이머로서의 유용성을 확인할 수 있었다.

배추뿌리혹병균(Plasmodiophora brassicae)의 인공접종을 위한 효율적인 저장조건 (Optimal Storage Condition of Clubroot Pathogen, Plasmodiophora brassicae for Artificial Inoculation)

  • 양슬기;박주영;서문원;김홍기
    • 한국균학회지
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    • 제43권4호
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    • pp.286-289
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    • 2015
  • 순활물기생체인 Plasmodiophora brassicae는 병원성 검정을 위해서 반드시 뿌리혹을 장기적으로 보관하는 것이 매우 중요하기 때문에 그동안 병원성을 유지하는 것이 관건이다. 특히 기존의 방법은 100년 이상 사용되어온 저장법으로 개선이 필요하여 그 효율적인 방법을 밝히고자 하였다. 이 결과 장기적으로 병원성의 저하를 최소화하며 장기간 뿌리혹을 저장할 수 있는 방법은 $-70^{\circ}C$ 냉동고에 보관하는 것으로 확인되었고, 저장 조건은 뿌리혹을 그대로 보관하거나 뿌리혹을 갈아 균질화한 후 여러 겹의 거즈에 거른 것이 6가지 저장조건 중에 가장 효과적인 저장법으로 밝혀졌다.

Plasmodiophora brassicae에 의한 콜라비 뿌리혹병 발생 (Ocurrence of Clubroot Caused by Plasmodiophora brassicae on Kohlrabi in Korea)

  • 송민아;최인영;송정흡;이귀재;신현동
    • 식물병연구
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    • 제25권1호
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    • pp.33-37
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    • 2019
  • 2016년부터 2018년까지 제주도내 농가포장에서 재배되고 있는 콜라비에 뿌리혹병 지속적으로 발생(최고발병률 27.2%)했다. 초기 감염은 뿌리털 부분이 정상주 뿌리털에 비해 비대했으며, 병이 진전되면서 뿌리 중심부에 혹이 형성되고, 잎이 시들고 끝이 누렇게 변했다. P. brassicae 휴면포자 현탁액을 이용한 병원성 검정결과 접종 50일 후에 병원성을 나타냈다. 병원균은 콜라비 세포조직 안에 빈 곳 없이 무수히 많은 휴면포자를 형성하며, 휴면포자는 단세포로 무색, 원형 또는 타원형, 크기는 직경 $3-5{\mu}m$이다. 콜라비 뿌리혹병원균의 ITS rDNA 염기서열 분석, 계통수 작성 결과 P. brassicae로 동정했다. 따라서 균학적 특징, 병원성 검정, ITS rDNA 염기서열 비교분석 등의 결과를 바탕으로 이 병은 우리나라에서 지금까지 보고되지 않은 'Plasmodiophora brassicae에 의한 콜라비 뿌리혹병'으로 명명하고자 한다.

Development of an In Planta Molecular Marker for the Detection of Chinese Cabbage (Brassica campestris ssp. pekinensis) Club Root Pathogen Plasmodiophora brassicae

  • Kim, Hee-Jong;Lee, Youn-Su
    • Journal of Microbiology
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    • 제39권1호
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    • pp.56-61
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    • 2001
  • Plasmodiophora brassicae is an obligate parasite, a causal organism of clubroot disease in crucifers that can survive in the soil as resting spores for many years. P. brassicae causes great losses in susceptible varieties of crucifers throughout the world. In this present study, an in planta molecular marker for the detection of P. bassicae was developed using an oligonucleotide primer set foam the small subunit gene (18S like) and internal transcribed spacer (ITS) region of rDNA. The specific primer sequences determined were TCAGCTTGAATGCTAATGTG (ITS5) and CTACCTCATTTGAGATCCTTTGA (PB-2). This primer set was used to specifically detect p. bassicae in planta. The amplicon using the specific primer set was about 1,000 bp. However, the test plant and other soil-borne fungi including Fusarium spp. and Rhizoctonia app., as well as bacteria such as Pseudomonas app. and Erwinia sup. did not show any reaction with the primer set.

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관주 접종법을 이용한 효율적인 배추 뿌리혹병 저항성 검정법 (Convenient Screening Method of Chinese Cabbage for Resistance to Plasmodiophora brassicae Using Soil-Drenching Inoculation)

  • 조수정;장경수;최용호;김진철;최경자
    • 식물병연구
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    • 제16권3호
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    • pp.279-284
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    • 2010
  • Plasmodiophora brassicae에 의한 배추 뿌리혹병은 전 세계적으로 발생하여 큰 피해를 주고 있다. 본 연구에서는 관주 접종을 이용한 효율적인 배추 뿌리혹병 저항성 검정법을 확립하기 위하여, 레이스 9인 GN-1 균주를 사용하여 토양 종류, 접종원 농도, 배추 생육시기, 접종 후 배양 기간 등의 발병 조건에 따른 뿌리혹병 발생을 조사하였다. 혼합토양(원예용 상토:밭 토양=1:1, v/v)과 달리, 원예용 상토에서는 P. brassicae 접종농도가 증가함에 따라 배추 뿌리혹병 발생도 증가하였다. 접종원 농도는 폿트 당 $4.0{\times}10^8$개의 포자로 접종하였을 때 그리고 접종을 위한 배추는 파종 후 10일 유묘가 적합하였다. 안정적인 발병을 위해서, 접종한 배추 유묘는 3일 동안 $20^{\circ}C$ 생육상에서 하루에 12시간 광을 처리하며 배양한 후 온실($25{\pm}5^{\circ}C$)에서 5주 동안 재배한 후에 병조사하는 것이 요구되었다. 확립한 배추 뿌리혹병 저항성 검정법을 이용하여, 시판 중인 뿌리혹병 저항성 품종 25종과 감수성 품종3종의 P. brassicae GN-1 균주에 대한 저항성 정도를 실험한 결과, 모든 저항성 품종들은 뿌리혹병에 대하여 뚜렷한 저항성을 나타내었고, 감수성 품종들은 발병도 3.5 이상의 높은 감수성을 보였다. 따라서 이 방법은 배추의 뿌리혹병 저항성을 검정하기 위한 효율적인 검정법임을 알 수 있었다.