• Title/Summary/Keyword: stripe virus

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Studies on the Host Range of Rice Stripe Virus (벼 줄무의잎마름병 바이러스의 기주범위에 관한 연구)

  • Chung Bong Cho;Lee Soon Hyung
    • Korean journal of applied entomology
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    • v.10 no.2
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    • pp.85-89
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    • 1971
  • An investigation was carried out to know the host range of the rice stripe virus as a basis of the disease control. 1. In order to investigate the host range of the rice stripe virus 30 species including gramineaceae and forage crop and weeds were inoculated with viruliferous Laodelphax sriatellus Fallen. As a result, 21 out of 30 species showed typical symptoms. 2. Cyperus amuricus Maximowicz var. laxus., Pycreus sanguinolentus Nees. and Eriocaulon robustius Makino, not belonging to gramineaceae were known to be new host plants of rice stripe virus. The highest infection occurred on Pycreus sanguinolentus grown widly in the wet paddy fold. 3. The number of vectors inoculated on the plants was decreased after 48 hours than that of 24 hours.

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Serological detection of barley stripe mosaic virus infection in the seeds of barley and wheat cultivars grown in Korea (혈청학적방법에 의한 보리와 밀종자의 보리${\cdot}$줄무늬 모자이크 바이러스 감염상조사)

  • La Yong-Joon;Park Yang-Kyo
    • Korean journal of applied entomology
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    • v.18 no.1 s.38
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    • pp.29-33
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    • 1979
  • An attempt was made to find out whether barley stripe mosaic virus (BSMV) occurs in barley and wheat cultivars in Korea. Modified Hamilton's technique for serological detection of barley stripe mosaic virus was used to assay for BSMV in mature seed embryos. Of the 51 barley and wheat seed lots assayed, BSMV was detected in 34 of them. BSMV was detected in covered, naked, and matting barley as well as in wheat. The level of BSMV infection in the infected cultivars varied from $2\~35\%$. This is the first reported occurrence of barley stripe mosaic virus in Korea.

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Comparison of Rice Stripe Disease Occurrence and Yield under Different Rice (Oryza sativa L.) Cultivars (이앙시기에 따른 벼 품종별 줄무늬잎마름병 발생 및 수량 비교)

  • Cha, Kwang-Hong;Oh, Hwan-Jung;Park, Heung-Gyu;Jung, Woo-Jin
    • Korean Journal of Organic Agriculture
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    • v.18 no.1
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    • pp.75-82
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    • 2010
  • The purpose of this study is to investigate an occurrence rate of rice stripe virus disease under different rice transplanting time and different rice cultivars. After final harvest, the yield of rice infected by rice stripe virus was obtained on Wangchal cultivar compared to uninfected rice. The results obtained as following: 1) Yield of rice infected by rice stripe virus was decreased by 64% with reduction of culm length, pancile length, number of spike, number of spikelet, and grain filling compared to uninfected rice, 2) An occurrence rate of rice stripe virus disease under different rice planting season was high as order of May 30 > June 15 > July 1. In additional, to reduce a rice stripe virus disease on higher disease occurrence region and susceptible cultivars, rice planting season will be accepted on and after June 15, and 3) Eighteen cultivars were resistance cultivars such as Hwayeongbyeo, Onnuri, Ilmibyeo, Nampyongbyeo, Dongjin2ho, Hopumbyeo, Hwangkeumnuri, Malgeumi, Saenuri, Pungmi1ho, Haechanmulgyeo, Hwangkeumnodeul, Chilbobyeo, Dongjinbyeo, Younganbyeo, Junambyeo, Samkwangbyeo, and Nakdongbyeo. Twenty-one cultivars were susceptible cultivars such as Odaebyeo, Unkwangbyeo, Shinungbong1ho, Manabyeo, Hopyongbyeo, Borami, Damibyeo, Hwangchalbyeo, Sulgengbyeo, Nongrim6ho, Sasanishigi, Yunishigari, Chungmubyeo, Dongjin1ho, Huknambyeo, Guromy, Shanghehanghulna, Heukchalbyeo, Heukhwangbyeo, and Aranghwangchalbyeo.

Cloning and Sequencing of Coat Protein Gene of the Korean Isolate of Rice stripe virus

  • Hong, Yeon-Kyu;Kwak, Do-Yeon;Park, Sung-Tae;Choi, Jo-Im;Lee, Key-Woon;Lee, Bong-Choon
    • The Plant Pathology Journal
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    • v.20 no.4
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    • pp.313-315
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    • 2004
  • The coat protein gene of Korean isolate of Ricer stripe virus (RSV-Kr) was cloned and its nucleotide sequence was determined. Total RNA was extracted from infected leaves and RSV viral RNA was detected by using RT-PCR with specific primer of coat protein gene. The result of RT-PCR showed a specific band. Purified RT-PCR products of coat protein gene were ligated into the pGEM-T Easy plasmid vector and cloned cDNA was obtained for nucleotide sequence determination. Coat protein gene of RSV-Kr consisted of 969 bp long encoding a protein of 322 amino acids. RSV-Kr showed 94%-99% sequence identities to that of Japanese- and Chinese isolates.

Detection of Rice Stripe Virus using RT-PCR (RT-PCR에 의한 벼 줄무늬잎마름병 정밀진단)

  • Lee, Bong-Choon;Hong, Yeon-Kyu;Kwak, Do-Yeon;Oh, Byeong-Geun;Park, Sung-Tae;Kim, Soon-Chul
    • Research in Plant Disease
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    • v.10 no.1
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    • pp.30-33
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    • 2004
  • Until now, occurrence of rice stripe virus (RSV) is limitted in southern part of Korea. However, recently the occurrence of RSV is increased and spreaded in central part of Korea including Chungcheong and Kyonggi province. It is very difficult to distinguish RSV symptoms on virus symptom physiological damage of rice. We detected RSV viral RNA from infected rice and its insect vector Laodelphax striatellus using specific primer of RSV-polymerase and coat protein gene with reverse transcription (RT)-PCR. The result of RT-PCR, we observed specific band including RSV-polymerase (1,,023 bp) and CP (969 bp) in both host of rice and insect vector.

Transcriptome Analysis of the Small Brown Planthopper, Laodelphax striatellus Carrying Rice stripe virus

  • Lee, Joo Hyun;Choi, Jae Young;Tao, Xue Ying;Kim, Jae Su;Kim, Woojin;Je, Yeon Ho
    • The Plant Pathology Journal
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    • v.29 no.3
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    • pp.330-337
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    • 2013
  • Rice stripe virus (RSV), the type member of the genus Tenuivirus, transmits by the feeding behavior of small brown planthopper (SBPH), Laodelphax striatellus. To investigate the interactions between the virus and vector insect, total RNA was extracted from RSV-viruliferous SBPH (RVLS) and non-viruliferous SBPH (NVLS) adults to construct expressed sequence tag databases for comparative transcriptome analysis. Over 30 million bases were sequenced by 454 pyrosequencing to construct 1,538 and 953 of isotigs from the mRNA of RVLS and NVLS, respectively. The gene ontology (GO) analysis demonstrated that both libraries have similar GO structures, however, the gene expression pattern analysis revealed that 17.8% and 16.8% of isotigs were up- and down-regulated significantly in the RVLS, respectively. These RSV-dependently regulated genes possibly have important roles in the physiology of SBPH, transmission of RSV, and RSV and SBPH interaction.

An Inexpensive System for Rapid and Accurate On-site Detection of Garlic-Infected Viruses by Agarose Gel Electrophoresis Followed by Array Assay

  • Kazuyoshi Furuta;Shusuke Kawakubo;Jun Sasaki;Chikara Masuta
    • The Plant Pathology Journal
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    • v.40 no.1
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    • pp.40-47
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    • 2024
  • Garlic can be infected by a variety of viruses, but mixed infections with leek yellow stripe virus, onion yellow dwarf virus, and allexiviruses are the most damaging, so an easy, inexpensive on-site method to simultaneously detect at least these three viruses with a certain degree of accuracy is needed to produce virus-free plants. The most common laboratory method for diagnosis is multiplex reverse transcription polymerase chain reaction (RT-PCR). However, allexiviruses are highly diverse even within the same species, making it difficult to design universal PCR primers for all garlic-growing regions in the world. To solve this problem, we developed an inexpensive on-site detection system for the three garlic viruses that uses a commercial mobile PCR device and a compact electrophoresis system with a blue light. In this system, virus-specific bands generated by electrophoresis can be identified by eye in real time because the PCR products are labeled with a fluorescent dye, FITC. Because the electrophoresis step might eventually be replaced with a lateral flow assay (LFA), we also demonstrated that a uniplex LFA can be used for virus detection; however, multiplexing and a significant cost reduction are needed before it can be used for on-site detection.

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
    • Proceedings of the Korean Society of Plant Pathology Conference
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    • 2003.10a
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    • pp.140.2-141
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    • 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.

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First Report of the Peanut Stripe Strain of Bean common mosaic virus (BCMVPSt) Infecting Mungbean in Korea

  • Choi, Hong-Soo;Kim, Mi-Kyeong;Park, Jin-Woo;Lee, Su-Heon;Kim, Kook-Hyung;Kim, Jeong-Soo;Were, Hassan Karakacha;Choi, Jang-Kyung;Takanami, Yoichi
    • The Plant Pathology Journal
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    • v.22 no.1
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    • pp.46-50
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    • 2006
  • A virus causing chlorotic ringspot, yellow mosaic and vein clearing symptoms was prevalent on mungbean plants around Taean, Korea. The isolate caused mosaic on Chenopodium quinoa, Nicotiana benthamiana, Phaseolus vulgaris and Vida laba but no symptoms on peanut plants. Inclusion bodies such as scroll, pinwheel and laminated aggregates induced by the virus in the host cells were similar to those produced by members of the Potyvirus subdivision III. Multiple alignment as well as cluster dendrograms of the 709 nucleotide region comprising part of the coat protein gene and 3'untranslated region (UTR) showed that the isolate belongs to the BCMV-PSt subgroup. Altogether, these results support the identification of the causal virus as peanut stripe strain of Bean common mosaic virus (BCMV-PSt).

Rice Stripe Virus (RSV) Acquisition and Infection Rates According to Wing Form, Sex and Life Stage of Small Brown Planthopper (Laodelphax striatellus) (애멸구의 날개형태, 성별, 그리고 발육단계별 Rice stripe virus (RSV) 보독률과 이병률)

  • Yi, Hwi-Jong;Kang, Mi-Hyeong;Choi, Man-Young;Koo, Hyun-Na;Kim, Gil-Hah
    • Korean journal of applied entomology
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    • v.54 no.4
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    • pp.419-423
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    • 2015
  • Small brown planthopper (SBPH), Laodelphax striatellus, gives a lot of damage to the rice by insect vector of rice stripe virus (RSV). This study compared the RSV acquisition and infection rates according to wing form, sex, and life stage of SBPH. The RSV acquisition rate in macropterous and brachypterous was 60.7% and 63.1%, respectively. The RSV acquisition rate by sex was 61.9% in female and 52.2% in male. However, there was no difference in significance. The RSV acquisition rate of nymphs and adults was 51.2% and 58.7%, respectively. The RSV infection rate by wing form was 53.3.% in macropterous and 48.2% in brachypterous. According to life stage, nymphs was 38.2% and adults was 42.6%. There was no difference in significance. On the other hand, female and male of RSV infection rate was 50.5% and 22.3%, respectively. There was a significant difference. Additionally, developmental periods of SBPH by RSV infection, the longest when inoculated with RSV-infected SBPH in healthy rice, while the shortest when inoculated healthy SBPH in healthy rice.