• 제목/요약/키워드: Potato virus X

검색결과 50건 처리시간 0.043초

Fungi에 의한 식물성 virus의 전파 (Dissemination of plant viruses by fungi)

  • 이미순
    • 미생물학회지
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    • 제9권4호
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    • pp.179-188
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    • 1971
  • There is a good evidence that tabacco necrosis virus, lettuce big vein virus, and tabacoo stunt virus are transmitted by Oplidium brassicae, although absolute proof in aspetic condition is lakcing. Some evidence suggests that polymyxa graminis may be involved in transmission of wheat mosaic virus. One report claims that Synchytrium endobioticum can transmit potato virus X. The cultivated mushroom, Agaricus bisporus, is known to act as a hose of a virus and is apparently involved in the spread of the virus.

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Development of a Rapid Detection Method for Potato virus X by Reverse Transcription Loop-Mediated Isothermal Amplification

  • Jeong, Joojin;Cho, Sang-Yun;Lee, Wang-Hyu;Lee, Kui-jae;Ju, Ho-Jong
    • The Plant Pathology Journal
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    • 제31권3호
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    • pp.219-225
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    • 2015
  • The primary step for efficient control of viral diseases is the development of simple, rapid, and sensitive virus detection. Reverse transcription loop-mediated isothermal amplification (RT-LAMP) has been used to detect viral RNA molecules because of its simplicity and high sensitivity for a number of viruses. RT-LAMP for the detection of Potato virus X (PVX) was developed and compared with conventional reverse transcription polymerase chain reaction (RT-PCR) to demonstrate its advantages over RT-PCR. RT-LAMP reactions were conducted with or without a set of loop primers since one out of six primers showed PVX specificity. Based on real-time monitoring, RT-LAMP detected PVX around 30 min, compared to 120 min for RT-PCR. By adding a fluorescent reagent during the reaction, the extra step of visualization by gel electrophoresis was not necessary. RT-LAMP was conducted using simple inexpensive instruments and a regular incubator to evaluate whether RNA could be amplified at a constant temperature instead of using an expensive thermal cycler. This study shows the potential of RT-LAMP for the diagnosis of viral diseases and PVX epidemiology because of its simplicity and rapidness compared to RT-PCR.

Identification of Potato mop-top virus from Solanum tuberosum cv. Gawon in Korea

  • Lee, Young-Gyu;Park, Jong-A;Yoon, Young-Nam;Cheon, Jeong-Uk;Lee, Key-Woon
    • 한국식물병리학회:학술대회논문집
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    • 한국식물병리학회 2003년도 정기총회 및 추계학술발표회
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    • pp.138.1-138
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    • 2003
  • Potato mop-top virus(PMTV) was identified from Solanum tuberosum cv. Gawon showing bright chlorotic mottle symptom in Namwon, Korea. Samples were collected green-house in February, 2003. Electron microscopic examination of negatively stained preparation revealed that PMTV were rigid-rod shaped particles about 100-150, 250-300 nm x 18-20 nm in length. In ultrathin sections of leaf tissue from diseased potato plants, cluster of viruses particles were observed in the cytoplasm. TAS-ELISA determined that the virus was serologically related to PMTV. PMTV produced double ring necrotic local lesion in inoculated leaf of Chenopodium amaranticolor in incubated at 15$^{\circ}C$. The PMTV could be detected with RT-PCR using PMTV detectable primer set designed to amplify about 540 bp of the partial CP gene of PMTV

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Characterization of Pathogenesis and Plant Defence-related Genes Against Potato virus X infection empolying Potato X virus expresssin vector

  • Park, Mi-Ri;Kwon, Sun-Jung;Kim, Kook-Hyung
    • 한국식물병리학회:학술대회논문집
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    • 한국식물병리학회 2003년도 정기총회 및 추계학술발표회
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    • pp.74.1-74
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    • 2003
  • Differential display (DD) of mRNA is a technique in which mRNA species expressed by a cell population are reverse transcribed and then amplified by many separate polymerase chain reactions (PCR). Using DD-RT-PCR we obtained many genes that expressed differentially in healthy and PVX-infected Nicotiana benthamima, using total RNAs extracted from healthy and PVX-infected N. benthamiana plants. Three hundred and twenty-five DNA fragments isolated from DD-RT-PCR were cloned and sequenced for further characterization. Several host genes including SKPI-like protein, heat shock transcription factor and Avr9/Cf-9 rapidly elicited protein were selected to obtain full-length open reading frame and to characterize their potential involvement in virus disease development and/or host's defense against virus infection employing PVX-based expression vector. Transcrips from wild-type and clones containing each selected gene were inoculated onto N. benthamiana Levels of virus replication were confirmedby RT-PCR and RNA blot analysis, Expression profiles and potential role(s) of selected genes upon PVX infection will be discussed.

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Regulatory Viral and Cellular Elements Required for Potato Virus X Replication

  • Kim, Kook-Hyung
    • The Plant Pathology Journal
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    • 제17권3호
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    • pp.115-122
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    • 2001
  • Potato virus X (PVX) is a flexuous rod-shaped virus containing a single plus-strand RNA. Viral RNA synthesis is precisely regulated by regulatory viral sequences and by viral and/or host proteins. RNA sequence element as well as stable RNA stem-loop structure in the 5' end of the genome affect accumulation of genomic RNA and subgenomic RNA (sgRNA). The putative sgRNA promoter regions upstream of the PVX triple gene block (TB) and coat protein (CP) gene were critical for both TB and CP sgRNA accumulation. Mutations that disrupted complementarity between a region at the 5' end of the genomic RNA and the sequences located upstream of each sgRNA initiation site is important for PVX RNA accumulation. Compensatory mutations that restore complementarity restored sgRNA accumulation levels. However, the extent of reductions in RNA levels did not directly correlate with the degree of complementarity, suggesting that the sequences of these elements are also important. Gel-retardation assays showed that the 5' end of the positive-strand RNA formed an RNA-protein complex with cellular proteins, suggesting possible involvement of cellular proteins for PVX replication. Future studies on cellular protein binding to the PVX RNA and their role in virus replication will bring a fresh understanding of PVX RNA replication.

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연초의 감자바이러스 Y 저항성 웅성불임 일대잡종 KB 109 육성 (Breeding for Potato Virus Y Resistant Male-sterile $F_1$ Hybrid KB 109 in Nicotiana tabacum L.)

  • 조천준;김대송;정석훈;최상주;조명조
    • 한국연초학회지
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    • 제16권2호
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    • pp.134-138
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    • 1994
  • Potato Virus Y(PVY), vein necrosis strain, in Korea causes severe symptoms on burley tobacco(Nicotiana tabacum L.). As the results, programs to incorporate PVY resistance into commercial cultivars were initiatEd. But the development of the homozygous fertile line resistant to PVY is time consumming. This study was conducted whether the Fl hybrid could be used to reduce the yield losses caused by PVY. Four F1 hybrids were made between male - sterile(ms) NC 107 and KB 107 as maternal parent, and TC 612 and TC 613 as Pollen donor, respectively, and were evaluated for their PVY resistance and negatively associated traits. (ms NC 107 X TC 612) F1, named as KB 109, Ivas applied to yield trial and compared with commercial cultivars for the level of disease resistance, agronomic characteristics, chemical contents and physical properties. All Fl hybrid could be used commercially as the PVY resistant cultivar. Especially KB 109 have the resistance against PVY, tobacco mosaic virus and black shank(Phytophthora parasitica var. nicotianae). It had wider leaves, flowered one day later, and yield of acceptable quality was higher than that of Burley 21, standard cultivar in Korea.

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혈청학적 방법에 의한 고추의 바이러스병 감염상 조사 (Serological Investigation of Virus Diseases of Pepper Plant (Capsicum annum L.) in Korea)

  • 라용준
    • Journal of Plant Biology
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    • 제15권1호
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    • pp.23-27
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    • 1972
  • A total of 163 virus infected pepper plants(Capsicum annuum L.) collected from various pepper growing regions in Korea were investigated on the presence of tobacco mosaic virus (TMV), cucumber mosaic virus (CMV), potato virus X(PVX), potato virus Y(PVY) and alfalfa mosaic virus (AMV) by serological methods. Van Slogteren's microprecipitin test was applied for the testing of TMV, PVX and PVY from infected plants, and Ouchterlony agar double diffusion test was used for CMV and AMV. Results obtained are as follows: 1. TMV, CMV, PVX, PVY and AMV were found to occur on the pepper plants growing in Korea. 2. The prevalence of each of these viruses among the 163 pepper plants investigated was in the order of CMV: 93 plants(57.0%)>TMV: 91 plants (55.8%)>AMV: 58 plants (35.6%)>PVY: 40 plants (24.5%)> PVX:6 plants(3.7%). 3. Among the 163 plants investigated, 72 plants (44%) showed infection with one kind of virus and 91 plants (56%) showed mixed infection with more than two different viruses. In general, heavier damage of the plants was observed from mixed infection. 4. The results of serological identification of pepper viruses coincided with those results obtained by sap inoculation experiment conducted at the Horticultural Experiment Station along with present investigation. Thus the serological techniques applied in this experiment proved to be very reliable for the identification of TMV, CMV, PVX, PVY and AMV from pepper plants infected with these viruses.

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Solanum acaule 색소체 유전자형 선발을 위한 특이적 분자마커 개발 (PCR-based markers to select plastid genotypes of Solanum acaule)

  • 박태호
    • Journal of Plant Biotechnology
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    • 제49권3호
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    • pp.178-186
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    • 2022
  • 볼리비아 유래의 4배체 감자 야생종 중 하나인 Solanum acaule는 서리, 감자역병, 감자바이러스X, 감자바이러스Y, 감자잎말림바이러스, 감자걀쭉병, 선충 등에 대한 저항성과 같이 감자의 신품종 육성에 매우 유용한 형질들을 가지고 있어 감자 육종에 많이 이용되고 있다. 그러나 이러한 유용 형질들을 재배종 감자에 전통적인 교잡에 의해 도입하는 것은 야생종과 재배종 간의 서로 다른 EBN에 따라 매우 제한적이다. 따라서, 이러한 생리적 장벽을 극복하기 위해서는 체세포융합을 이용할 수 있는데, 육종에 활용할 적절한 체세포융합체를 선발하기 위해서는 적절한 분자마커의 개발이 필수적이다. 이에, 본 연구에서는 앞서 차세대 유전체 기술에 의해 완성되어 보고된 S. acaule의 엽록체 전장 유전체 정보를 기반으로 이를 다른 8개의 Solanum 종의 엽록체 전장 유전체 정보와 비교를 통해 S. acaule 특이적인 분자마커를 개발하였다. S. acaule의 엽록체 전장 유전체 총 길이는 155,570 bp였으며, 총 158개의 유전자로 구성되어 있었다. 전체적인 구조와 유전자의 구성은 다른 Solanum 종들과 매우 유사하였고 12종의 다른 가지과에 속해 있는 종과의 계통수 분석에서 다른 Solanum 종과 매우 가까운 유연관계를 가지는 것을 확인하였다. S. acaule의 엽록체 전장 유전체와 다른 7개 Solanum 종의 엽록체 전장 유전체 다중 정렬의 결과로 각각 4개와 79개의 S. acaule 특이적인 InDel 및 SNP 영역이 확인되었으며, 이 정보를 이용하여 각각 1개씩의 InDel 및 SNP 영역 유래의 PCR 기반의 분자마커를 개발하였다. 본 연구의 결과는 S. acaule의 진화적 측면에서의 연구와 S. acaule를 이용한 감자품종 육성 연구에 기여를 할 수 있을 것이다.

Tobacco mosaic virus Detected in Vegetatively Propagated Petunia Hybrids 'Surfinia'

  • Chung, Bong-Nam;Kim, Jeong-Soo;Cho, Jeom-Deog;Cheong, Seung-Ryong;Jeong, Myeong-Il
    • The Plant Pathology Journal
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    • 제23권1호
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    • pp.34-36
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    • 2007
  • Introduction of vegetatively propagated Petunia hybrids since 1992 led to increasing virus infections of propagation material. Petunia hybrid 'Surfinia' cultivated for pot-plant showed yellowing symptom along with stunt. Flowers were smaller in size and showed color-break symptom. Tobacco mosaic virus(TMV-pet) was isolated from the diseased petunia. Healthy petunia plants inoculated with TMV-pet induced mottle on leaves and color-break on flowers, and plants were stunted. Nucleotide sequences of coat protein gene amplified from RNA prepared from Nicotiana tabacum cv. Samsun infected with TMV-pet were determined(GenBank accession no. DQ981481). It showed 99.0% nucleotide sequence homology with TMV-potato3-2(GenBank accession no. AF318215) isolated from potato showing yellow mosaic and stunt symptom, and with a TMV Korean strain(GenBank accession no. X68110). This is the first reported observation of TMV from vegetatively propagated petunia in Korea.