• The Plant Pathology Journal
• /
• 제30권3호
• /
• pp.261-268
• /
• 2014

This work was conducted to identify mungbean genotypes showing yield stability and resistance to mungbean yellow mosaic virus (MYMV) disease. Sixteen genotypes were evaluated in a randomized complete block design with two replications for two years (2011 and 2012) at three locations (Gazipur, Ishurdi and Madaripur) of the Bangladesh Agricultural Research Institute. An analysis of variance exhibited significant effects of genotype (G), environment (E), and genotype ${\times}$ environment ($G{\times}E$) on grain yield. Among eight agronomic characters, the principal component 1 (PC1) was always higher than the PC2. Considering $G{\times}E$ interaction, BM6 was the best genotype at all three locations in both years. Based on grain yield and stability performance, BM6 ranked first while the worst performing genotypes were BM1 and G10. Based on discrimination and representation, Gazipur was identified as an ideal environment for these mungbeans. Relationship between soil-plant analysis developments (SPAD) value was positive with yield but negative with MYMV severity. BM6, G1 and G2 were considered as promising sources of resistance for low disease score and stable response across the environments. The environment proved to have an influence on MYMV infection under natural infestation. A positive correlation was observed between disease score and the temperature under natural growing condition.

• 한국식물병리학회지
• /
• 제3권3호
• /
• pp.223-235
• /
• 1987

황색 모자이크 괴저조반, 위축, 기형, colour breaking의 병미을 나타내고 있는 나리류를 한국의 남부지역에서 채집하였다. 전자현미경에 의해 2종의 바이러스 입자가 분리되어, 이들의 기주범위, 혈청반응, 조즙액중의 부활화 한계, 진딧물의 전반성, 감염엽세포에 있어서 바이러스 입자의 소재양식에 의하여 2종의 바이러스를 동정하였다. Broad bean wilt virus(BBWV) : 이 바이러스는 즙액접종에 의해 8과 23종의 검정식물에 감염이 확인되었다. 복숭아혹진딧물에 의해 쉽게 전반되었다. 내열성은 $70\%$, 내희석성은 1,000배, 내보존성은 6일이였다. 바이러스 입자의 형태는 직경 약 28nm의 소구형이다. 혈청시험에서 본 바이러스는 BBWV의 항혈청과 특이적인 반응대를 형성했다. 병엽절편의 전자현미경적관찰에서는 엽육세포의 세포질, 액포, 핵내에서 바이러스 입자의 응집괴 및 결정배열상이 확인되엇고, 특히 세포질내에서는 vesicular body의 발달이 확인되었다. Cncumber mosaic virus(CMV) : 이 바이러스 입자의 형태는 직경 약30nm의 소구형이다. 본 바이러스 CMV-Y의 항혈청과 특이적인 반응대를 형성했다. 감염엽조직의 전자현미경적관찰에서는 엽육세포의 세포질 및 액포내에서 바이러스 입자의 응집괴 도는 결정배열상이 확인되었다. BBWV와 CMV를 건전한 나리류(Lilium tigrium, L. concolor, L. auratum)에 재접종한 결과 BBWV의 접종주에서는 가벼운 병징 또는 colour breaking를 나타내었고, CMV의 접종수에서는 황색 모자이크 또는 괴저조반을 나타냈다.

• 식물병연구
• /
• 제15권2호
• /
• pp.72-76
• /
• 2009

국내 보리 재배지에 분포하는 BaYMV strain에 대한 BaYMV 저항성 유전자별 반응을 조사하였다. 지역별 바이러스 검정 결과 BaYMV가 전체 약 51%로 가장 높은 발생을 보였으며 BaMMV와의 혼합감염도 38.8%의 높은 비율을 나타내었다. BaMMV 단독 감염은 1.4%로 낮게 조사되었다. BaYMV 4개의 strain별 저항성 유전자의 반응을 조사한 결과 BaYMV-N type에 대해 검정한 결과 rym 1+5(Mokusekko-3), rym 3(Ea 52, Baitori), rym 5a(Solan)가 저항성을 보였다. -H strain은 rym 2(Mihori Hadaka 3), rym 3(Ea 52, Haganemugi, Baitori), rym 4m (Diana, Franka), rym 5a(Solan), rym 7(Hor 3365), rym 9 (Bulgarian 347), rym 12(Jochiwon Covered 2) 등 7종의 유전자가 저항성을 보여 다른 strain에 비해 효율적인 저항성이 많게 나타났다. -I strain의 경우 rym 1+5(Mokusekko-3), rym 3(Ea 52, Baitori), rym 5a(Hakei I-41, Solan) 등 3종의 유전자가 저항성을 보였다. -M starin에서는 rym 3(Chosen, Ea 52, Haganemugi, Baitori, Ishukushirazu), rym 4m(Diana), rym 5a(Hakei I-41) 등 3종의 유전자가 저항성을 보였다.

• 한국작물학회지
• /
• 제48권3호
• /
• pp.156-159
• /
• 2003

1. 4개년 조사 기간 중 보리호위축병 발병율은 6.6%-62.5%로 연차간 기상조건에 따라 큰 변이를 나타내었다. 2. 면역혈청학적 검정 결과 보리호위축병의 감염이 확인되었으며, 일부 품종은 BaMMV와의 혼합 감염이 발생하였으나 보리호위축병에 비해 상대적으로 발생이 낮은 경향이었다. 3. 월동전 보리 초기 생육 기간의 기상 조건과 발병율의 변화 조사 결과 평균기온이 바이러스의 감염과 유의성 있는 상관을 나타내었다. 4. 월동기중에는 기상조건과 발병율과는 어떤 요인도 유의성 있는 상관을 나타내지 않았다. 5. 생육재생기 이후의 발병율은 최고기온과 유의성 있는 상관을 나타내어 병징 발현에는 최고기온이 영향을 미치는 것으로 조사되었다.

• The Plant Pathology Journal
• /
• 제25권4호
• /
• pp.369-375
• /
• 2009

The potential antiviral effects of the culture filtrates (CF) from Serratia marcescens strain Gsm01 against yellow strain of Cucumber mosaic virus (CMV-Y) were investigated. The culture filtrate of S. marcescens strain Gsm01 applied on Chenopodium amaranticolor showed high inhibitory activity, likewise no necrosis appeared when applied on the tobacco plants 2 days before CMV-Y inoculation. When plants were challenge inoculated with CMV-Y for eighteen days, the disease incidence in plants with culture filtrate of S. marcescens Gsm01 did not exceed 59%, whereas 100% of control plants were severely infected. The results of double antibody sandwich-enzyme linked immunosorbent assay (DAS-ELISA), reverse transcriptase polymerase chain reaction (RT-PCR), dot blotting, and western blotting showed that culture filtrate treatment highly affected the accumulation of CMV-Y or its CP protein gene in the treated plant leaves. It was also observed that the culture filtrate had no RNase activity on genomic RNAs of CMV-Y, suggesting that culture filtrate may not contain ribosome inactivating proteins (RIPs) or proteins with RNase activity. These data shows that culture filtrate of S. marcescens strain Gsm01 seems to be a promising source of antiviral substance for the practical use.

• The Plant Pathology Journal
• /
• 제21권3호
• /
• pp.262-269
• /
• 2005

An antiviral producing bacterial strain was isolated from a ginseng rhizosphere in Kangwon province of Republic of Korea. In order to identify the bacterial strain, microbiological, physiological and biochemical tests were performed, along with RAPD, 16S rRNA, 16S-23S rRNA ITS (intergenic spacer region) and DNA-DNA hybridization analyses. The bacterium was found to be a strain of Pseudomonas fluorescens, which was designated as Gpf01. The strain was grown in Muller-Hinton (MH) broth, and the culture supernatant obtained was filtered through a $0.45{\mu}l$ filter. It was further boiled at $100^{\circ}C$ and tested in two experiments for its ability to control a yellow strain of Cucumber mosaic virus (CMV-Y). In the first experiment, boiled culture filtrate (RCF) was treated on one half of the leaves of Chenopodium amaranticolor followed by CMV- Y inoculation on both halves. In the second experiment, BCF was treated on the lower leaves of Nicotiana tobacum var. Xanthi-nc, with the CMV-Y mechanically inoculated onto the upper untreated leaves. In the first experiment, BCF treatment was able to considerably reduce the number of viral lesion, and in the second experiment, plants treated with BCF showed no visible viral symptoms compared to the Muller-Hinton (MH) media treated controls 15 days post inoculation (dpi), and remained symptomless throughout the study period. Thus, Gpf01, identified as P. fluorescence, was able to produce an antiviral component in the culture filtrate, which was found to be heat stable, non-phytotoxic and effective in local as well as systemic hosts of CMV.

• The Plant Pathology Journal
• /
• 제29권2호
• /
• pp.193-200
• /
• 2013

Trichoderma asperellum SKT-1 is a microbial pesticide that is very effective against various diseases. Our study was undertaken to evaluate T. asperellum SKT-1 for induction of resistance against yellow strain of Cucumber mosaic virus (CMV-Y) in Arabidopsis plants. Disease severity was rated at 2 weeks post inoculation (WPI). CMV titre in Arabidopsis leaves was determined by indirect enzyme-linked immunosorbent assay (ELISA) at 2 WPI. Our results demonstrated that among all Arabidopsis plants treated with barley grain inoculum (BGI) of SKT-1 NahG and npr1 plants showed no significant reduction in disease severity and CMV titre as compared with control plants. In contrast, disease severity and CMV titre were significantly reduced in all Arabidopsis plants treated with culture filtrate (CF) of SKT-1 as compared with control plants. RT-PCR results showed increased expression levels of SA-inducible genes, but not JA/ET-inducible genes, in leaves of BGI treated plants. Moreover, expression levels of SA- and JA/ET-inducible genes were increased in leaves of CF treated plants. In conclusion, BGI treatment induced systemic resistance against CMV through SA signaling cascade in Arabidopsis plants. While, treatment with CF of SKT-1 mediated the expression of a majority of the various pathogen related genes, which led to the increased defense mechanism against CMV infection.

• 식물병연구
• /
• 제13권1호
• /
• pp.71-73
• /
• 2007

전라남도 호박 주산단지의 2000년 바이러스병 발생포장율은 노지재배 76.1%,억제재배 55%,반촉성재배는 발생이 없었으며, 포장별 이병주율은 반촉성재배 3.6%, 노지재배 100%이었다. 포장에서 채집된 시료에 대한 RT-PCR 검정결과 노지재배는 40점 시료 중 WMV 16점, ZYMV 10점, PRSV 2점이 각각 검출되었으며, WMV, ZYMV, PRSV의 2개 또는 3개 바이러스에 중복감염된 시료도 7점이었다. 억제재배는 21점 시료중 WMV 7점, ZYMV 6점, PRSV 6점, WMV와 PRSV의 2개 바이러스에 중복감염된 시료가 1점이었으며, CMV는 검출되지 않았다.

• The Plant Pathology Journal
• /
• 제18권5호
• /
• pp.237-243
• /
• 2002

A survey of virus infection in garlic plants cultivated in Korea was conducted for three years. Most virus-infected garlic plants (Allium sativum) showed typical symptoms on the leaves such as yellow mosaic, stripes, and distortion. Through immunosorbent electron micro-scopy and RT-PCR analysis, the complex mixtures of viruses including garlic viruses of the genus Allerivirus, gaylic strain of Leek yellow stripe virus of the genus Potyvirus, and Garlic latent virus of the genus Carlavirus were identified in the virus-infected garlic plants. Among these viruses, Allexivirus was the most frequently detect-ed in the regions surveyed. Using sets of differential primers for Allexivirus genomes, two members of the genus were amplified and sequenced from the purified viruses. The deduced amino acid sequences for the coat proteins and the nucleic acid binding proteins of two viruses showed high homologies to Garlic virus A (CarV-A) and Garlic virus D (GarV-D) of Allekivirus. This is the first report of GarV-A and GarV-D in Korea. This suggests that Allexivirus in gavlic plants in Korea was mixed and varied. Phylogenetic analyses showed that the genus Allexivirus was diversi(ied by the processes of accumulation and evolution of viruses in garlic plants due to the long period of repeated vegetative propagation.

• The Plant Pathology Journal
• /
• 제27권1호
• /
• pp.93-97
• /
• 2011

For quarantine purpose, we selected five plant RNA viruses including Cucumber vein yellowing virus (CVYV), Cucurbit yellow stunting disorder virus (CYSDV), Potato aucuba mosaic virus (PAMV), Potato yellow dwarf virus (PYDV), and Tomato chlorosis virus (ToCV), which are not reported in Korea and cause serious economic losses to the family Cucurbitaceae or Solanaceae. To detect those viruses, we employed RT-PCR technique with specific oligonucleotide primer pairs and tested their detection efficiency for each virus. To design RT-PCR primers, coat protein was used for CVYV, CYSDV, and ToCV whereas RNA polymerase and nucleocapsid regions were used for PAMV and PYDV, respectively. The development of an RT-PCR based method proved a useful tool for rapid detection and identification of quarantine virus infections.