• 제목/요약/키워드: DAS-ELISA

검색결과 25건 처리시간 0.026초

Comparison of an Immunochromatographic Assay Kit with DAS-ELISA for Large-Scale Diagnosis and Molecular Discrimination of Satsuma Dwarf Virus Collected from Citrus Orchards

  • Kato, Mitsuhiro;Tomimura, Kenta;Ishii, Kanako
    • The Plant Pathology Journal
    • /
    • 제36권5호
    • /
    • pp.509-514
    • /
    • 2020
  • Satsuma dwarf virus (SDV) seriously damages citrus production by reducing the quality and yield of fruit. To avoid contamination with SDV, mother trees are checked to be SDV-free in advance of nursery tree distribution. In this study, we compared an immunochromatographic assay (ICA) kit with double-antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA) for large-scale diagnosis of SDV in orchardgrown trees in Shizuoka Prefecture, Japan. The two methods gave conflicting results for 11 of 1,705 samples, all of which were negative by DAS-ELISA but positive by ICA. The samples scored as positive by either DAS-ELISA or ICA were analyzed by reverse transcription polymerase chain reaction and all were confirmed to be positive. These results validate the use of ICA as a screening method for large-scale diagnosis. Strain discrimination revealed that 16 of 22 isolates belonged to SDV, while citrus mosaic virus (CiMV) infection only and co-infection (SDV and CiMV) were in a minority.

Construction of Antibodies for Detection and Diagnosis of Cucumber green mottle mosaic virus from Watermelon Plants

  • Shim, Chang-Ki;Lee, Jung-Han;Hong, Sun-Min;Han, Ki-Soo;Kim, Hee-Kyu
    • The Plant Pathology Journal
    • /
    • 제22권1호
    • /
    • pp.21-27
    • /
    • 2006
  • We immunized BALB/c mice with purified Cucumber green mottle mosaic virus isolate HY1 (CGMMV-HY1). Through the selection of positive clones that were grown on the HAT medium, four sensitive monoclonal clones (CG99-01, CG99-02, CG99-03, and CG99-04) were selected from 500 Hypoxanthine-guanine phosphoribosyltransferase positive hybridoma cells. Four sensitive clones of CGMMV-HYI were determined as IgM type of the subclass of mouse immunoglobulins Ig group. The titer of monoclonal antiserum against CGMMVHY1 was estimated 1:12,800 by the indirect ELISA. Although monoclonal antibodies (MAbs) from CG99-01 and from CG99-04 cross-reacted with Zucchini green mottle mosaic virus and Kyuri green mottle mosaic virus, MAb from the cell line CG99-03 was highly specific to CGMMV. No MAbs cross-reacted with Cucumber mosaic virus-Fny. Only CG99-04 reacted with Pepper mild mottle virus weakly and CG99-02 reacted with both CGMMV and KGMMV. CGMMV was detected from the rind of watermelon fruit by DAS-ELISA of CGMMV-HY1, but not from the flesh of watermelon. Average seed transmission rate of CGMMV in watermelon was $24\%$ from symptomatic watermelon collected from 5 regions of Gyeongnam province. CGMMV was detected by DAS-ELISA with specific MAb of CGMMVHY1 periodically from root stock, during the sequential process for nursery seedling in Haman. Necrotic spots on cotyledons of root stock seedling progressed to reveal the typical symptomatology on the primary leaves of scion upon grafting. Here, we have established MAb based ELISA system, which could accurately detect CGMMV from watermelon seeds, nursery seedlings, transplants and field samples from greenhouse or open out door field as well.

풋고추 수경재배에서 발생하는 tobamovirus의 특성 (Tobamoviruses of Green Peppers Growing on Hydroponic Systems)

  • 최국선;김재현;김정수;김현란
    • 식물병연구
    • /
    • 제10권3호
    • /
    • pp.194-197
    • /
    • 2004
  • 풋고추 수경재배에서 tobamovirus 병의 발병률은 생육 후기 단계에서 100%였다 바이러스 종류별 감염 빈도는 PMMOY 34%, TMGMY 41.5% 및 이들 2종의 바이러스 복합감염이 24.5%로 나타났다. 다클론 항체로 제작된 DAS-ELISA에서 각각의 항체에 대하여 특이적인 반응을 보였다. 수경재배하는 풋고추에서 77개의 tobamovirus를 순수분리하여 tobamovirus의 pathotype을 구분한 결과, $P_{0}$은 61% 및 $P_{1,2}$는 39% 빈도로 분리되었다. 모든 TMGMV 분리주는 pathotype $P_{0}$에 속하였다. PMMOY에서 구분된 pathotype $P_{0}$$P_{1,2}$의 외피단백질유전자에 상응하는 cDNA를 합성하여 제한효소에 대한 분석을 실시한 결과, $P_{1,2}$는 TaqI 위치가 두 곳에 존재하였으나 $P_{0}$은 단지 한 곳에만 존재하였다.존재하였다.

국내에서 발생하는 배나무 바이러스병 (Occurrence of Pome Fruit Viruses on Pear Trees (Pyrus pyrifolia) in Korea)

  • 조인숙;김대현;김현란;정봉남;조점덕;최국선
    • 식물병연구
    • /
    • 제16권3호
    • /
    • pp.326-330
    • /
    • 2010
  • 2009년 가을, 배 주산단지인 나주, 울산, 안성의 3개 지역에서 신고, 원황, 추황 품종을 대상으로 배 바이러스병 발생률을 ELISA와 RT-PCR로 조사한 결과 ELISA 검정은 ACLSV, ASPV, ASGV 3종 바이러스가 검출되어 35.2%의 발생률을 보였다. RT-PCR 검정은 ELISA 검정 보다는 적은 시료로 검정을 수행하였지만 ACLSV, ASPV, ASGV 3종 바이러스가 검출되었고 86.3%의 높은 발생률을 보였다. ELISA와 RT-PCR 진단 모두 ASGV > ASPV > ACLSV 순으로 ASGV의 발생률이 높게 나타났지만 발생률에는 ELISA 22.1%, RT-PCR 74.2%로 큰 차이가 있었다. 따라서 배 바이러스 검정은 ELISA 방법 보다 RT-PCR 방법이 바이러스 검출에 적합하다. ASGV가 감염된 신고 잎에서는 부정형의 검은점 증상이 보였으며 ASPV와 ACLSV가 감염된 식물체에서는 별다른 이상증상은 보이지 않았다. RT-PCR로 증폭된 ACLSV, ASPV, ASGV 유전자는 기존에 보고된 바이러스와 83~94%의 상동을 보였고, 특히, ASPV는 국내에서 처음으로 발생이 확인되었다.

Genetic Diversity in the Coat Protein Genes of Prune dwarf virus Isolates from Sweet Cherry Growing in Turkey

  • Ozturk, Yusuf;Cevik, Bayram
    • The Plant Pathology Journal
    • /
    • 제31권1호
    • /
    • pp.41-49
    • /
    • 2015
  • Sweet cherry is an important fruit crop with increasing economical value in Turkey and the world. A number of viruses cause diseases and economical losses in sweet cherry. Prune dwarf virus (PDV), is one of the most common viruses of stone fruits including sweet cherry in the world. In this study, PDV was detected from 316 of 521 sweet cherry samples collected from 142 orchards in 10 districts of Isparta province of Turkey by double antibody sandwich-enzyme linked immunosorbent assay (DAS-ELISA). The presence of PDV in ELISA positive samples was confirmed in 37 isolates by reverse transcription- polymerase chain reaction (RT-PCR) method. A genomic region of 862 bp containing the coat protein (CP) gene of PDV was re-amplified from 21 selected isolates by RT-PCR. Amplified DNA fragments of these isolates were purified and sequenced for molecular characterization and determining genetic diversity of PDV. Sequence comparisons showed 84-99% to 81-100% sequence identity at nucleotide and amino acid level, respectively, of the CP genes of PDV isolates from Isparta and other parts of the world. Phylogenetic analyses of the CP genes of PDV isolates from different geographical origins and diverse hosts revealed that PDV isolates formed different phylogenetic groups. While isolates were not grouped solely based on their geographical origins or hosts, some association between phylogenetic groups and geographical origins or hosts were observed.

Molecular Screening and Characterization of Antiviral Potatoes

  • Tripathi, Giriraj;Li, Hongxain;Park, Jae-Kyun;Park, Yoon-Kyung;Cheong, Hyeon-Sook
    • Biotechnology and Bioprocess Engineering:BBE
    • /
    • 제11권2호
    • /
    • pp.89-95
    • /
    • 2006
  • Potato plants carrying the Ry gene are extremely resistance to a number of potyviruses, but it is not known which variety expressed the resistance. In this investigation, combined classical and molecular techniques were used to identify virus resistance potatoes. Mechanical inoculation of 32 varieties of Korean potato cultivars, with potato virus Y (PVY), induced various symptoms, such as mosaic, yellowing, necrosis, mottle, vein clearing and vein bending. Different virus spreading patterns were observed, such as highly sensitive, moderate and resistant to $PVY^o$ inoculated leaves in different cultivars. From the results of double antibody sandwich-enzyme links immunosorbant assays (DAS-ELISA), coupled with reverse transcription polymerase chain reaction (RT-PCR), Winter valley and Golden valley were found to be highly susceptible and resistant cultivars to $PVY^o$ respectively. TEM was used as a complementary method to conform the localization of the virus in leaf tissues. TEM detect virus particles in Golden valley, where, ELISA and RT-PCR were unable to detect the CP gene. However, the interior part of the tissues was severely deformed in $PVY^o$ infected Winter valley, than Golden valley The Ry gene is involved in an induced response in $PVY^o$ infected Golden valley plants. The methods described in this study could be applied for the screening and development of antiviral potatoes.

Production and Evaluation of Monoclonal Antibodies Against Recombinant Coat Protein of Lily mottle virus for Western Blotting and Immono-blot Analysis

  • Chung, Bong-Nam;Yoon, Ju-Yeon;Choi, Gug-Sun
    • The Plant Pathology Journal
    • /
    • 제25권3호
    • /
    • pp.225-230
    • /
    • 2009
  • Lily mottle virus (LMoV) causes flower quality reduction in Lilium spp. The coat protein gene was RT-PCR-amplified from total RNA extracted from infected lily leaves and the amplified fragment was cloned into the pRSET expression vector tagged with a His-MBP. The plasmid of recombinant coat protein was used to transform an Escherichia coli strain pLysS and was expressed. The coat protein was purified by affinity chromatography using a Ni-NTA resin. The identity of the purified protein was confirmed by SDS-PAGE. The in vitro-expressed protein was used for immunization of mice. The polyclonal and monoclonal antibodies reacted specifically for the detection of LMoV in lily extracts in Western blot. Moreover the monoclonal antibodies reacted with lily extracts in DAS-ELISA with no unspecific or heterologous reactions against other non-serologically related viruses, but the polyclonal antibodies revealed a weak reaction against both infected lily and healthy control.

Population of Rice Stripe Virus-Viruliferous Insect and Natural Weed Host of Rice Stripe Virus.

  • Park, Jin-Woo;Jin, Tae-sung;Shin, Dong-bum;Park, Byung-ryul;Kim, Jin-young;Oh, In-suk;Lee, B. C.;T. H. Noh;S. J. Ko
    • 한국식물병리학회:학술대회논문집
    • /
    • 한국식물병리학회 2003년도 정기총회 및 추계학술발표회
    • /
    • pp.140.2-141
    • /
    • 2003
  • Among over-wintering small brown planthoppers, population of the rice stripe virus (RSV)-viruliferous insects was surveyed throughout the country in late April of 2003 by using DAS-ELISA. Averaged population of the RSV-viruliferous insects in this year was 2.1%, which was lower than that of last year of 3.7%. However, the insect population in Seoul, Incheon and Kyeonggi areas were relatively high showing 6.7%, 6.2% and 2.6%, respectively. Based on the survey results, it was expected that overall occurrence of RSV on rice could be decreased in this year, except certain areas. Ovarial transmission rate of RSV by the insects on diseased rice samples collected from 10 areas ranged from 22.2% to 77.8%. Among 35 graminous weed species collected from rice fields in Ganghwa and Kimpo in 2002 and 2003, common reed and formosens were found to be infected by RSV. The result indicates that those weeds are potential alternative natural hosts of the RSV Further studies on ecological and pathological impacts of the alternative natural host of RSV are being processed.

  • PDF

Cowpea mosaic virus from Vegetable Soybeans in Korea

  • Cho, Eui-Kyoo;Lee, Sin-Ho
    • The Plant Pathology Journal
    • /
    • 제19권3호
    • /
    • pp.166-170
    • /
    • 2003
  • Ninety samples showing mosaic symptoms on soybean (Glycine max) cv. Sukryangputkong were collected from the Cheongsongkun area, Kyungbuk province in Korea. Initially, DAS-ELISA was conducted far detection of Soybean mosaic virus (SMV). Negative samples were chosen at random and mechanically inoculated on soybean cv. Buffalo, which reported not to produce mosaic symptoms when mechanically inoculated with SMV. An isolate of SMV, designated as B-1, from Buffalo showing mosaic and mottle symptoms was used for identification and biological characterization of the causal vim. The purified B-1 isolate had spherical particles of approximately 24nm. It positively reacted with the antiserum against Cowpea mosaic virus (CPMV) but not with Cucumber mosaic virus (CMV) and SMV antisera. CPMV was newly isolated from soybean and had been characterized by host range and by serological and electron microscopic methods. Results of this study suggest that CPMV is the possible cause of mosaic disease in vegetable soybean and that based on sympto-matology, a difference between the typical mosaic and rugose symptoms caused by SMV and CPMV was observed. This is first report of CPMV from soybean in Korea.