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Artigos de revistas sobre o tema "Cucumoviruses"

Autor: Grafiati

Publicado: 4 de junho de 2021

Última modificação: 28 de janeiro de 2023

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1

Haase, Anita, and Frank Rabenstein. "Serotype-specific monoclonal antibodies against two cucumoviruses: (Short communication)." Archives Of Phytopathology And Plant Protection 24, no. 2 (January 1988): 167–69. http://dx.doi.org/10.1080/03235408809437803.

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2

Dietzgen, Ralf G., Ben Callaghan, Colleen M. Higgins, Robert G. Birch, Kunrong Chen, and Zeyong Xu. "Differentiation of Peanut Seedborne Potyviruses and Cucumoviruses by RT-PCR." Plant Disease 85, no. 9 (September 2001): 989–92. http://dx.doi.org/10.1094/pdis.2001.85.9.989.

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Seedborne peanut viruses pose important constraints to peanut production and safe movement of germ plasm. They also pose a risk of accidental introduction into previously disease-free regions. We have developed reverse transcription-polymerase chain reaction (RT-PCR) assays based on identical cycling parameters which identified peanut stripe, Peanut mottle, Peanut stunt, and Cucumber mosaic viruses through production of specific DNA fragments of 234 bp, 327 bp, 390 bp, and 133 bp, respectively. Assay sensitivity in the picogram range was achieved. The two potyviruses and two cucumoviruses coul

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3

White, P. Scott, Francisco Morales, and Marilyn J. Roossinck. "Interspecific Reassortment of Genomic Segments in the Evolution of Cucumoviruses." Virology 207, no. 1 (February 1995): 334–37. http://dx.doi.org/10.1006/viro.1995.1088.

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4

KAMEYA-IWAKI, Mitsuro, Kimiaki MURAKAMI, Shin-ichi ITO, Kaoru HANADA, and Shuhei TANAKA. "Semipersistency of Myzus persicae Transmission of Cucumoviruses Systemically Infecting Leguminous Plants." Journal of General Plant Pathology 66, no. 1 (February 2000): 64–67. http://dx.doi.org/10.1007/pl00012922.

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5

Shi, B. J., R. H. Symons, and S. W. Ding. "In vivo expression of an overlapping gene encoded by the cucumoviruses." Journal of General Virology 78, no. 1 (January 1, 1997): 237–41. http://dx.doi.org/10.1099/0022-1317-78-1-237.

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6

FUKUMOTO, Fumiyoshi, and Hiroshi TOCHIHARA. "Similarity of the Conditions for Freeze-drying Preservation among Three Cucumoviruses." Japanese Journal of Phytopathology 58, no. 3 (1992): 366–72. http://dx.doi.org/10.3186/jjphytopath.58.366.

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7

Codoñer, Francisco M., and Santiago F. Elena. "The promiscuous evolutionary history of the family Bromoviridae." Journal of General Virology 89, no. 7 (July 1, 2008): 1739–47. http://dx.doi.org/10.1099/vir.0.2008/000166-0.

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Recombination and segment reassortment are important contributors to the standing genetic variation of RNA viruses and are often involved in the genesis of new, emerging viruses. This study explored the role played by these two processes in the evolutionary radiation of the plant virus family Bromoviridae. The evolutionary history of this family has been explored previously using standard molecular phylogenetic methods, but incongruences have been found among the trees inferred from different gene sequences. This would not be surprising if RNA exchange was a common event, as it is well known t

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8

Pacios, Luis F., and Fernando García-Arenal. "Comparison of properties of particles of Cucumber mosaic virus and Tomato aspermy virus based on the analysis of molecular surfaces of capsids." Journal of General Virology 87, no. 7 (July 1, 2006): 2073–83. http://dx.doi.org/10.1099/vir.0.81621-0.

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The plant RNA viruses Cucumber mosaic virus (CMV) and Tomato aspermy virus (TAV) (genus Cucumovirus) have similar icosahedral particles, the crystal structures of which have been reported recently. Similarity in particle structure agrees with reports of stable capsids assembled from their capsid proteins and of viable recombinant viruses with chimeric capsid proteins derived from CMV and TAV. However, differences between the cucumoviruses have been reported for physicochemical properties. Here, structural and electrostatic features of the molecular surfaces are studied to investigate their rel

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9

Salánki, Katalin, Ákos Gellért, Emese Huppert, Gábor Náray-Szabó, and Ervin Balázs. "Compatibility of the movement protein and the coat protein of cucumoviruses is required for cell-to-cell movement." Journal of General Virology 85, no. 4 (April 1, 2004): 1039–48. http://dx.doi.org/10.1099/vir.0.19687-0.

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For the cell-to-cell movement of cucumoviruses both the movement protein (MP) and the coat protein (CP) are required. These are not reversibly exchangeable between Cucumber mosaic virus (CMV) and Tomato aspermy virus (TAV). The MP of CMV is able to function with the TAV CP (chimera RT), but TAV MP is unable to promote the cell-to-cell movement in the presence of CMV CP (chimera TR). To gain further insight into the non-infectious nature of the TR recombinant, RNA 3 chimeras were constructed with recombinant MPs and CPs. The chimeric MP and one of the CP recombinants were infectious. The other

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10

Gellért, Á., K. Salánki, E. Huppert, G. Náray-Szabó, and E. Balázs. "Applied homology modelling in the study of cell-to-cell movement of cucumoviruses." Acta Crystallographica Section A Foundations of Crystallography 60, a1 (August 26, 2004): s127. http://dx.doi.org/10.1107/s0108767304097508.

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11

Bernal, J. J., E. Moriones, and F. Garcia-Arenal. "Evolutionary relationships in the cucumoviruses: nucleotide sequence of tomato aspermy virus RNA 1." Journal of General Virology 72, no. 9 (September 1, 1991): 2191–95. http://dx.doi.org/10.1099/0022-1317-72-9-2191.

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12

Aaziz, R., and M. Tepfer. "Recombination between Genomic RNAs of Two Cucumoviruses under Conditions of Minimal Selection Pressure." Virology 263, no. 2 (October 1999): 282–89. http://dx.doi.org/10.1006/viro.1999.9973.

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13

Leiser, R. M., and J. Schumacher. "DETECTION OF CUCUMBER MOSAIC AND TOMATO ASPERMY CUCUMOVIRUSES BY MEANS OF POLYMERASE CHAIN REACTION." Acta Horticulturae, no. 377 (October 1994): 221–22. http://dx.doi.org/10.17660/actahortic.1994.377.24.

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14

Fukumoto, Fumiyoshi. "Preservation of Alfalfa mosaic virus by freezing and freeze-drying and similarities to Cucumoviruses." Journal of General Plant Pathology 74, no. 2 (March 4, 2008): 164–70. http://dx.doi.org/10.1007/s10327-008-0082-8.

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15

Chen, B., J. W. Randles, and R. I. B. Francki. "Mixed-subunit capsids can be assembled in vitro with coat protein subunits from two cucumoviruses." Journal of General Virology 76, no. 4 (April 1, 1995): 971–73. http://dx.doi.org/10.1099/0022-1317-76-4-971.

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16

Sackey, S. T., and R. I. B. Francki. "Interaction of cucumoviruses in plants: persistence of mixed infections of cucumber mosaic and tomato aspermy viruses." Physiological and Molecular Plant Pathology 36, no. 5 (May 1990): 409–19. http://dx.doi.org/10.1016/0885-5765(90)90069-a.

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17

Hsu, H. T., L. Barzuna, Y. H. Hsu, W. Bliss, and K. L. Perry. "Identification and Subgrouping of Cucumber mosaic virus with Mouse Monoclonal Antibodies." Phytopathology® 90, no. 6 (June 2000): 615–20. http://dx.doi.org/10.1094/phyto.2000.90.6.615.

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Using a mixture of isolates of Cucumber mosaic virus (CMV) from subgroups I and II as immunogens, 20 mouse hybridoma cell lines secreting monoclonal antibodies were produced. A reliable method for efficient detection and accurate subgrouping of CMV isolates has been developed. Tests with 12 well-characterized strains of CMV and other cucumoviruses demonstrated the presence of epitopes that were virus and subgroup specific. Analyses of 109 accessions of CMV isolates collected from various parts of the world revealed 70% were subgroup I, with 20% identified as subgroup II. Seven isolates (6%) di

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18

Ram, Raja, Anupama Sharma, R. K. Singh, Daizy Chauhan, and A. A. Zaidi. "Cucumber Mosaic Virus on Asiatic Hybrid Lilies in India." Plant Disease 83, no. 1 (January 1999): 78. http://dx.doi.org/10.1094/pdis.1999.83.1.78a.

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Asiatic hybrid lilies are popular cut flowers with a range of bright colors. Of the several viruses reported from lily (2,3), cucumber mosaic virus (CMV) reduces flower quality and yield (1). Classical symptoms of CMV were observed in recently introduced plants of Asiatic hybrid lilies in Kangra Valley, Himachal Pradesh. The symptoms were mild leaf mosaic, ring spot, transient vein yellowing, occasionally with growth deformation, and flower breaking. Leaf samples from cvs. MonteNegro, Yellow Present, Apeldoorn, Toscana, Connecticut King, and Adelina were collected randomly on the basis of symp

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19

Chang, Peta-Gaye S., Wayne A. McLaughlin, and Sue A. Tolin. "Tissue blot immunoassay and direct RT-PCR of cucumoviruses and potyviruses from the same NitroPure nitrocellulose membrane." Journal of Virological Methods 171, no. 2 (February 2011): 345–51. http://dx.doi.org/10.1016/j.jviromet.2010.11.018.

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20

Shi, Bu-Jun, Peter Palukaitis, and Robert H. Symons. "Differential Virulence by Strains of Cucumber mosaic virus is Mediated by the 2b Gene." Molecular Plant-Microbe Interactions® 15, no. 9 (September 2002): 947–55. http://dx.doi.org/10.1094/mpmi.2002.15.9.947.

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The approximately 12-kDa 2b protein, encoded by all cucumoviruses, had been shown to play an important role in viral long-distance movement, hypervirulence, and suppression of post-transcriptional gene silencing. The role of the 2b gene in the hypervirulence of Cucumber mosaic virus (CMV) and whether hypervirulence was linked to movement were analyzed using a hybrid virus (CMV-qw), generated by replacing the 2b gene in a subgroup II strain, Q-CMV, with the 2b gene from a subgroup IA strain, WAII-CMV. CMV-qw was more virulent than Q-CMV or WAII-CMV on most of the host plant species tested. Nort

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21

Shi, Bu-Jun, Jane Miller, Robert H. Symons, and Peter Palukaitis. "The 2b Protein of Cucumoviruses Has a Role in Promoting the Cell-to-cell Movement of Pseudorecombinant Viruses." Molecular Plant-Microbe Interactions® 16, no. 3 (March 2003): 261–67. http://dx.doi.org/10.1094/mpmi.2003.16.3.261.

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Pseudorecombinant viruses (i.e., those containing a reas-sorted genome of closely related multipartite viruses) are often not as competitive as the parental viruses. The role of the 2b gene in hypervirulence and maintenance of a progressive infection was assessed in a pseudorecombinant virus formed between RNAs 1 plus 2 of Cucumber mosaic virus (CMV) and RNA 3 of Tomato aspermy virus (TAV). The presence of RNA 3 of TAV was found to affect the level of RNA accumulation but not the level of virulence. By contrast, the 2b genes of both TAV and a hypervirulent strain of CMV (WAII-CMV) were found t

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22

Choi, Seung Kook, Jang Kyung Choi, Won Mok Park, and Ki Hyun Ryu. "RT–PCR detection and identification of three species of cucumoviruses with a genus-specific single pair of primers." Journal of Virological Methods 83, no. 1-2 (December 1999): 67–73. http://dx.doi.org/10.1016/s0166-0934(99)00106-8.

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23

Suzuki, Masashi, Tadaaki Hibi, and Chikara Masuta. "RNA recombination between cucumoviruses: possible role of predicted stem-loop structures and an internal subgenomic promoter-like motif." Virology 306, no. 1 (February 2003): 77–86. http://dx.doi.org/10.1016/s0042-6822(02)00050-8.

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24

Gao, Shuangyu, Jinda Lu, Xiaodong Cheng, Zhouhang Gu, Qiansheng Liao, and Zhiyou Du. "Heterologous Replicase from Cucumoviruses can Replicate Viral RNAs, but is Defective in Transcribing Subgenomic RNA4A or Facilitating Viral Movement." Viruses 10, no. 11 (October 28, 2018): 590. http://dx.doi.org/10.3390/v10110590.

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Interspecific exchange of RNA1 or RNA2 between the cucumoviruses cucumber mosaic virus (CMV) and tomato aspermy virus (TAV) was reported to be non-viable in plants previously. Here we investigated viability of the reassortants between CMV and TAV in Nicotiana benthamiana plants by Agrobacterium-mediated viral inoculation. The reassortants were composed of CMV RNA1 and TAV RNA2 plus RNA3 replicated in the inoculated leaves, while they were defective in viral systemic movement at the early stage of infection. Interestingly, the reassortant containing TAV RNA1 and CMV RNA2 and RNA3 infected plant

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25

Martín-Hernández, Ana Montserrat, and Belén Picó. "Natural Resistances to Viruses in Cucurbits." Agronomy 11, no. 1 (December 24, 2020): 23. http://dx.doi.org/10.3390/agronomy11010023.

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Cucurbit viruses cause considerable economic losses worldwide. The most common viral diseases affecting this crop family are Potyviruses, Cucumoviruses, Criniviruses, Ipomoviruses, Tobamoviruses, and the emerging Begomoviruses. Four main cucurbit crops are grown worldwide, namely melon, cucumber (Cucumis), watermelon (Citrullus), and squash (Cucurbita). Huge natural variation is also available within each genus, providing valuable sources of genetic resistance to these diseases. Intraspecific and intrageneric diversity and crossability are key factors to select the optimum breeding strategies.

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26

Thompson, Jeremy R., and Fernando García-Arenal. "The Bundle Sheath-Phloem Interface of Cucumis sativus Is a Boundary to Systemic Infection by Tomato Aspermy Virus." Molecular Plant-Microbe Interactions® 11, no. 2 (February 1998): 109–14. http://dx.doi.org/10.1094/mpmi.1998.11.2.109.

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The progress of infection of two cucumoviruses in cucumber plants was analyzed immunohistochemically. Strain Fny of cucumber mosaic virus (CMV, FFF) was found to infect cucumber tissues systemically by 6 days postinoculation (dpi), while a reassortant virus with RNAs 1+2 of Fny-CMV plus RNA3 of strain 1 of tomato aspermy virus (FFT) was unable to move long distance and infect cucumber plants systemically. FFF infection of the vasculature was detected 6 dpi in the phloem of a low percentage of both minor (order VII–VI) and major (order V–IV) veins. At 9 dpi, infection was detected in phloem cel

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27

Shimura, Hanako, Chikara Masuta, Naoto Yoshida, Kae Sueda, and Masahiko Suzuki. "The 2b protein of Asparagus virus 2 functions as an RNA silencing suppressor against systemic silencing to prove functional synteny with related cucumoviruses." Virology 442, no. 2 (August 2013): 180–88. http://dx.doi.org/10.1016/j.virol.2013.04.015.

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28

Liu, Sijun, Xiaohua He, Gyungsoon Park, Caroline Josefsson, and Keith L. Perry. "A Conserved Capsid Protein Surface Domain of Cucumber Mosaic Virus Is Essential for Efficient Aphid Vector Transmission." Journal of Virology 76, no. 19 (October 1, 2002): 9756–62. http://dx.doi.org/10.1128/jvi.76.19.9756-9762.2002.

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ABSTRACT A prominent feature on the surfaces of virions of Cucumber mosaic virus (CMV) is a negatively charged loop structure (the βH-βI loop). Six of 8 amino acids in this capsid protein loop are highly conserved among strains of CMV and other cucumoviruses. Five of these amino acids were individually changed to alanine or lysine (an amino acid of opposite charge) to create nine mutants (the D191A, D191K, D192A, D192K, L194A, E195A, E195K, D197A, and D197K mutants). Transcripts of cDNA clones were infectious when they were mechanically inoculated onto tobacco, giving rise to symptoms of a mot

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29

Damayanti, Tri Asmira, Anastasya Hondo, and Yusmani Prayogo. "Infeksi Alami Pepper Yellow Leaf Curl Virus dan Sweet potato virus C Pada Ubi Jalar di Malang, Jawa Timur." Jurnal Fitopatologi Indonesia 15, no. 6 (December 11, 2019): 248–54. http://dx.doi.org/10.14692/jfi.15.6.248-254.

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Gejala tulang daun kuning (vein yellowing) dan malformasi daun yang diduga disebabkan oleh virus ditemukan pada ubi jalar IR Melati di daerah Kendalpayak, Malang, Jawa Timur. Amplifikasi DNA/cDNA menggunakan primer universal Begomovirus, Potyvirus, dan Cucumovirus menunjukkan positif teramplifikasi DNA dengan primer universal Begomovirus, dan Potyvirus, namun negatif dengan primer universal Cucumovirus. Berdasarkan runutan sikuen nukleotida, gejala tulang daun kuning dan malformasi daun disebabkan oleh infeksi ganda Pepper yellow leaf curl virus (PYLCV) dan Sweet potato virus C (SPVC). Analisi

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30

Aebig, Joan A., Kathryn Kamo, and Hei-Ti Hsu. "Biolistic inoculation of gladiolus with cucumber mosaic cucumovirus." Journal of Virological Methods 123, no. 1 (January 2005): 89–94. http://dx.doi.org/10.1016/j.jviromet.2004.09.010.

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31

Varveri and Boutsika. "Characterization of cucumber mosaic cucumovirus isolates in Greece." Plant Pathology 48, no. 1 (February 1999): 95–100. http://dx.doi.org/10.1046/j.1365-3059.1999.00308.x.

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32

Holcomb, G. E., and R. A. Valverde. "Natural Infection of Salvia uliginosa with Cucumber Mosaic Cucumovirus." HortScience 33, no. 7 (December 1998): 1215–16. http://dx.doi.org/10.21273/hortsci.33.7.1215.

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Salvia uliginosa Benth. plants, in an experimental planting of Salvia species, exhibited virus-like symptoms of chlorotic line patterns and ringspots. The suspect virus was mechanically transmitted to several experimental hosts and was identified as cucumber mosaic cucumovirus (CMV) based on dsRNA gel patterns, positive reaction with CMV antiserum, and particle morphology as observed by transmission electron microscopy.

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33

REI, F. T., M. I. E. C. HENRIQUES, F. A. LEITÃO, J. F. SERRANO, and M. F. POTES. "Immunodiagnosis of cucumber mosaic cucumovirus in different olive cultivars." EPPO Bulletin 23, no. 3 (September 1993): 501–4. http://dx.doi.org/10.1111/j.1365-2338.1993.tb01360.x.

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34

Diaz-Ruiz, J. R., M. J. Avila-Rincon, and I. Garcia-Luque. "Subcellular localization of cucumovirus-associated satellite double-stranded RNAs." Plant Science 50, no. 3 (January 1987): 239–48. http://dx.doi.org/10.1016/0168-9452(87)90079-3.

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35

Karasawa, Akira, Kazuhiro Nakaho, Tetsuji Kakutani, Yuzo Minobe, and Yoshio Ehara. "Nucleotide sequence of RNA 3 of peanut stunt cucumovirus." Virology 185, no. 1 (November 1991): 464–67. http://dx.doi.org/10.1016/0042-6822(91)90800-q.

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36

Linthorst, H. J. M., and J. M. Kaper. "Cucumovirus Satellite RNAs Cannot Replicate Autonomously in Cowpea Protoplasts." Journal of General Virology 66, no. 8 (August 1, 1985): 1839–42. http://dx.doi.org/10.1099/0022-1317-66-8-1839.

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37

Megahed, A. A., Kh A. El Dougdoug, B. A. Othman, S. M. Lashin, M. A. Ibrahim, and A. R. Sofy. "A New Egyptian Satellite Strain of Cucumber Mosaic Cucumovirus." International Journal of Virology 8, no. 3 (June 15, 2012): 240–57. http://dx.doi.org/10.3923/ijv.2012.240.257.

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38

Sanchez-Cuevas, M.-C., and S. G. P. Nameth. "Virus-associated Diseases of Double Petunia: Frequency and Distribution in Ohio Greenhouses." HortScience 37, no. 3 (June 2002): 543–46. http://dx.doi.org/10.21273/hortsci.37.3.543.

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Double petunia plants expressing virus-like symptoms were collected in greenhouses and garden centers throughout Ohio in Spring 1997 and 1998 in an effort to determine the frequency and distribution of petunia viruses present in the state. Direct antibody-sandwich and indirect enzyme-linked immunosorbent assay (ELISA) were conducted with commercial antisera made against 13 viruses, a potyvirus kit capable of detecting 80 different potyviruses, and our antiserum raised against a tobamo-like virus inducing severe mosaic in double petunia. Viral-associated double-stranded ribonucleic acid (dsRNA)

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39

Chan, Yuan-Li, Nurali Saidov, Li-Mei Lee, Fu-Hsun Kuo, Su-Ling Shih, and Lawrence Kenyon. "Survey of Viruses Infecting Tomato, Cucumber and Mung Bean in Tajikistan." Horticulturae 8, no. 6 (June 6, 2022): 505. http://dx.doi.org/10.3390/horticulturae8060505.

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Viral diseases are major constraints to tomato, cucumber and mung bean production in most areas where these crops are grown. To identify the viruses on the crops in Tajikistan, a field survey was conducted in 2019. Samples of cucumber, mung bean and tomato with virus-like symptoms were collected and the viruses present were diagnosed by RT-PCR and PCR. Across all the samples, a very high proportion of the samples were infected with viruses from the genera Cucumovirus and Potyvirus. Cucumber mosaic virus (CMV; Cucumovirus) was very common in the collected samples of the three crops. As for Poty

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40

Shafie, Radwa, Aly Hamed, and Hany El-Sharkawy. "Inducing Systemic Resistance against Cucumber Mosaic Cucumovirus using Streptomyces spp." Egyptian Journal of Phytopathology 44, no. 1 (June 30, 2016): 127–42. http://dx.doi.org/10.21608/ejp.2016.91931.

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41

Khalid, S., T. Yasmin, and M. H. Soomro. "First report of cucumber mosaic cucumovirus in banana from Pakistan." EPPO Bulletin 29, no. 1-2 (March 1999): 207–9. http://dx.doi.org/10.1111/j.1365-2338.1999.tb00820.x.

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42

Perry, K. L., and R. I. B. Francki. "Insect-mediated transmission of mixed and reassorted cucumovirus genomic RNAs." Journal of General Virology 73, no. 8 (August 1, 1992): 2105–14. http://dx.doi.org/10.1099/0022-1317-73-8-2105.

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43

., M. Osman, Kh EI-Dougdoug ., E. T. Abd EI-Salam ., R. M. Taha ., and R. M. El-Hamid . "Histo-Cytopathological Effects Of Cucumber Mosaic Cucumovirus On Squash Leaves." International Journal of Virology 1, no. 1 (December 15, 2004): 34. http://dx.doi.org/10.3923/ijv.2005.34.34.

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44

Gillaspie, A. G., and S. A. Ghabrial. "First Report of Peanut Stunt Cucumovirus Naturally Infecting Desmodium sp." Plant Disease 82, no. 12 (December 1998): 1402. http://dx.doi.org/10.1094/pdis.1998.82.12.1402a.

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Plant species in the genus Desmodium (Fabaceae) are used as forage and cover crops and include a number of common weeds such as beggarweed (D. tortuosum) and beggarlice (D. intortum). Accessions of the genus are part of the plant genetic resources collection maintained at Griffin, GA. Peanut stunt cucumovirus (PSV) was detected in naturally infected plants of Desmodium sp. PI 322505 (from Brazil) in a germ plasm regeneration plot by a direct antigen coating-enzyme-linked immunosorbent assay (DAC-ELISA) with an antiserum against PSV strain ER (subgroup I) originally isolated from cowpea in Geor

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45

Wilson, C. R. "First Report of Cucumber Mosaic Cucumovirus on Wasabi in Australia." Plant Disease 82, no. 5 (May 1998): 590. http://dx.doi.org/10.1094/pdis.1998.82.5.590a.

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Wasabi (Wasabia japonica (Miquel) Matsum.), a native perennial of Japan and Shakhalin Island used to produce a condiment for Japanese dishes, is under commercial development in Tasmania, Australia. Plants propagated within shade houses showed systemic necrotic flecks and veinal necrosis in leaves and sunken necrotic stem lesions similar to those, reported in Japan (1), caused by cucumber mosaic cucumovirus (CMV). Necrosis progressed rapidly, resulting in death of plants transferred to or mechanically inoculated in a glasshouse (15 to 30°C) under full light. Disease progression in plants mainta

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ZIEGLER, A., L. TORRANCE, S. M. MACINTOSH, G. H. COWAN, and M. A. MAYO. "Cucumber Mosaic Cucumovirus Antibodies from a Synthetic Phage Display Library." Virology 214, no. 1 (December 1995): 235–38. http://dx.doi.org/10.1006/viro.1995.9935.

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Tzanetakis, I. E. "First Report of Cucumber mosaic virus in Anemone sp. in the United States." Plant Disease 93, no. 4 (April 2009): 431. http://dx.doi.org/10.1094/pdis-93-4-0431b.

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In the spring of 2008, more than a dozen, aphid-infested, anemone plants (Anemone sp.) grown at the campus of the University of Arkansas in Fayetteville showed stunting and mosaic, whereas only two were asymptomatic. Leaf homogenates from four symptomatic plants were inoculated onto Nicotiana benthamiana that became stunted and developed severe mosaic approximately 7 days postinoculation, whereas buffer-inoculated plants remained asymptomatic. Double-stranded RNA (dsRNA) extraction (4) from symptomatic anemone revealed the presence of four predominant bands of approximately 3.2, 2.9, 2.2, and

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Emad, Al Dalain, A. Bysov, O. Shevchenko, T. Shevchenko, and V. Polischuk. "Several viral diseases of Lycopersicon esculentum circulating in Ukraine." Bulletin of Taras Shevchenko National University of Kyiv. Series: Biology 68, no. 3 (2014): 96–98. http://dx.doi.org/10.17721/1728_2748.2014.68.96-98.

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This paper describes detection of some typical plant viruses infecting Lycopersicon esculentum Mill. plants in Ukraine. Diagnostics using enzyme-linked immunosorbent assay (ELISA) confirmed presence of antigens of viruses belonging to Tobamovirus (PMMoV, ToMV), Cucumovirus (CMV) and Tobravirus (TRV) genera in sap of tomato plants. When studying viral diseases of tomatoes, monoinfection was shown to be prevalent. Tomato mosaic virus (ToMV) was most common.

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Burgyán, József, and Fernando García-Arenal. "Template-Independent Repair of the 3′ End of Cucumber Mosaic Virus Satellite RNA Controlled by RNAs 1 and 2 of Helper Virus." Journal of Virology 72, no. 6 (June 1, 1998): 5061–66. http://dx.doi.org/10.1128/jvi.72.6.5061-5066.1998.

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ABSTRACT RNA viruses which do not have a poly(A) tail or a tRNA-like structure for the protection of their vulnerable 3′ termini may have developed a different strategy to maintain their genome integrity. We provide evidence that deletions of up to 7 nucleotides from the 3′ terminus of cucumber mosaic cucumovirus (CMV) satellite RNA (satRNA) were repaired in planta in the presence of the helper virus (HV) CMV. Sequence comparison of 3′-end-repaired satRNA progenies, and of satRNA and HV RNA, suggested that the repair was not dependent on a viral template. The 3′ end of CMV satRNA lacking the l

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Kassim, N. A. "EFFECT OF SOME PLANT EXTRACT AND ANTIBIOTIC ON Cucumber Mosaic Cucumovirus." Mesopotamia Journal of Agriculture 34, no. 4 (December 28, 2006): 134–39. http://dx.doi.org/10.33899/magrj.2006.26437.

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