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Journal articles on the topic 'Dahlia mosaic virus'

Author: Grafiati

Published: 4 June 2021

Last updated: 9 February 2022

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1

Pappu, H. R., K. R. W. Hammett, and K. L. Druffel. "Dahlia mosaic virus and Tobacco streak virus in Dahlia (Dahlia variabilis) in New Zealand." Plant Disease 92, no. 7 (2008): 1138. http://dx.doi.org/10.1094/pdis-92-7-1138b.

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Dahlia (Dahlia variabilis Hort.) is a significant ornamental plant in New Zealand. Symptoms such as mosaic, ring spots, mottling, and veinal chlorosis, suggestive of a viral infection, are often seen in various dahlia collections. To better understand the incidence of viruses in dahlia in New Zealand, several popularly grown cultivars were evaluated for viruses that are known to infect dahlia. Viruses that were tested included Cucumber mosaic virus (CMV), Dahlia mosaic virus (DMV), Impatiens necrotic spot virus (INSV), Tobacco streak virus (TSV), and Tomato spotted wilt virus (TSWV). At least

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2

Eid, Sahar, Keri L. Druffel, Dayle E. Saar, and Hanu R. Pappu. "Incidence of Multiple and Distinct Species of Caulimoviruses in Dahlia (Dahlia variabilis)." HortScience 44, no. 5 (2009): 1498–500. http://dx.doi.org/10.21273/hortsci.44.5.1498.

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Dahlia mosaic is a serious disease affecting dahlias. In addition to the Dahlia mosaic virus (DMV) reported previously, we characterized two putative new caulimoviruses, tentatively designated as DMV-D10 and Dahlia common mosaic virus (DCMV), from dahlia. To better understand their relative incidence in dahlia, a total of 213 samples were collected during 2007 and 2008 from several varieties of cultivated dahlia (D. variabilis) in the United States. Samples were tested for the three caulimoviruses using virus-specific primers in a polymerase chain reaction. Amplicons were cloned and sequenced

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3

Pappu, H. R., S. D. Wyatt, and K. L. Druffel. "Dahlia Mosaic Virus: Molecular Detection and Distribution in Dahlia in the United States." HortScience 40, no. 3 (2005): 697–99. http://dx.doi.org/10.21273/hortsci.40.3.697.

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Dahlia is an important ornamental crop in the U.S. The economic value of the crop is often affected by viral diseases. Of several viruses that infect dahlia, dahlia mosaic virus (DMV) is of most concern. However, little or no information is available about its distribution. A survey of dahlias in several states in the U.S. was carried out during 2003 and 2004. Samples from CA, GA, MD, ME, MT, NM, PA, OR, and WA were tested for DMV. To develop a molecular detection assay, the viral genome was cloned and sequenced and based on the sequence information, DMV-specific primers were used in a PCR-bas

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4

Ara, MR, MMH Masud, and AM Akanda. "Detection of Plant Viruses in Some Ornamental Plants That Act as Alternate Hosts." Agriculturists 10, no. 2 (2012): 46–54. http://dx.doi.org/10.3329/agric.v10i2.13141.

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A study was conducted at the Bangabandhu Sheikh Mujibur Rahman Agricultural University (BSMRAU), Salna, Gazipur to detect virus infecting ornamental plants. Enzyme-linked Immunosorbant Assay (ELISA) and symptomalogy were used for detection. Five viruses namely TPVV (Tomato Purple Vein Virus), CMV-Y (Cucumber Mosaic Virus-Y), OYVCMV (Okra Yellow Vein clearing Mosaic Virus), MYMV (Mung bean Yellow Mosaic Virus), TYLCV (Tomato Yellow Leaf Curl Virus) were detected on Tagetes erecta (Marigold), Salvia splendens (Salvia), Dahlia hybrida (Dahlia), Helichrysum bracteatum (Straw flower), Impatiens bal

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5

Pahalawatta, V., K. Druffel, and H. R. Pappu. "Seed Transmission of Dahlia mosaic virus in Dahlia pinnata." Plant Disease 91, no. 1 (2007): 88–91. http://dx.doi.org/10.1094/pd-91-0088.

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Dahlia is an economically important ornamental crop in the United States and several other countries in the world. Among the viral diseases that affect dahlia, Dahlia mosaic virus (DMV) is considered to be the most widespread and to have the greatest impact on flower production. Using grow-out tests followed by polymerase chain reaction (PCR)-based testing of the seedlings, dahlia seed obtained from three different sources were shown to contain DMV. Additionally, the distribution of DMV in various parts of the dahlia seed was determined by PCR. Growout tests revealed a high rate of seed transm

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6

& et al., Nerway. "IN VITRO ELIMINATION OF DAHLIA MOSAIC VIRUS BY USING MERISTEM CULTURE, ELECTROTHERAPY AND CHEMOTHERAPY." IRAQI JOURNAL OF AGRICULTURAL SCIENCES 51, no. 2 (2020): 665–74. http://dx.doi.org/10.36103/ijas.v51i2.994.

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This study was conducted to investigate the effect of different in vitro techniques on elimination of dahlia mosaic virus. Meristems of Dahlia mosaic virus (DMV) infected dahlias, with 0.2-0.3 mm in length, were cultured on Murashige and Skoog (MS) medium. Based on DAS-ELISA, 100% of the survived plantlets by meristem culture were virus-free. DMV infected stem segments with two axillary buds were treated at three different levels of electric currents (15, 25 and 35 mA) and two time courses (10 and 20 min) in an electrophoresis tank and cultured on MS medium. The treatment of 35 mA for 20 min w

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7

Nicolaisen, M. "Partial Molecular Characterization of Dahlia mosaic virus and Its Detection by PCR." Plant Disease 87, no. 8 (2003): 945–48. http://dx.doi.org/10.1094/pdis.2003.87.8.945.

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Dahlia mosaic virus (DMV) is the causal agent of one of the most important diseases of Dahlia pinnata. The nucleotide sequence of a 1,195-bp fragment of its genome was amplified and characterized. Based on this sequence, polymerase chain reaction (PCR) assays were developed for detection of DMV. The nucleotide sequence confirmed the classification of DMV as a member of genus Caulimovirus since it was similar to a region covering partly open reading frames (ORFs) IV and V found in caulimoviruses. The two most closely related viruses on the basis of comparison of ORF V fragments were shown to be

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8

Pahalawatta, V., R. Miglino, K. B. Druffel, A. Jodlowska, A. R. van Schadewijk, and H. R. Pappu. "Incidence and Relative Prevalence of Distinct Caulimoviruses (Genus Caulimovirus, Family Caulimoviridae) Associated with Dahlia Mosaic in Dahlia variabilis." Plant Disease 91, no. 9 (2007): 1194–97. http://dx.doi.org/10.1094/pdis-91-9-1194.

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Dahlia mosaic, caused by Dahlia mosaic virus (DMV), is one of the most important viral diseases of dahlia. Molecular characterization of DMV showed the association of two distinct caulimoviruses (DMV-D10, DMV-Portland) and a D10-like sequence variant (DMV-Holland) with the disease. Using primers specific to these two viruses and the sequence variant, a polymerase chain reaction–based assay was used to determine their relative incidence in several dahlia samples from the United States and the Netherlands. Testing was done on samples collected in 2005 and 2006 in the United States and in 2006 in

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9

Bogunov, Yu V. "Identification of dahlia mosaic virus by molecular methods." Molecular Biology 40, no. 1 (2006): 162–63. http://dx.doi.org/10.1134/s0026893306010225.

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10

Mokra, V., B. Gotzova, V. Bezdekova, P. Dedic, and J. Ptacek. "First Report of Tobacco streak virus on Dahlia in the Czech Republic." Plant Disease 92, no. 3 (2008): 484. http://dx.doi.org/10.1094/pdis-92-3-0484b.

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Dahlia is an important ornamental crop in the Czech Republic where they have been grown for more than 150 years. New dahlia cultivars have been selected by Czech plant breeders. Virus diseases, including mosaic and stunt caused mostly by Dahlia mosaic virus, have been a problem. From 2003 to 2005, color breaking was observed in several dahlia cultivars of foreign and Czech origin. White stripes in blossoms were most frequently expressed in the second half of the flowering season. No symptoms are visible in flowers of white and yellow cultivars. It was difficult to characterize symptoms on leav

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11

Kuluev, B. R., and A. V. Chemeris. "Amplification and cloning of dahlia mosaic virus and carnation etched ring virus promoters." Russian Journal of Genetics 43, no. 12 (2007): 1413–14. http://dx.doi.org/10.1134/s1022795407120113.

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12

Khadanga, Badrinath, Jeky Chanwala, I. Sriram Sandeep, and Nrisingha Dey. "Synthetic Promoters from Strawberry Vein Banding Virus (SVBV) and Dahlia Mosaic Virus (DaMV)." Molecular Biotechnology 63, no. 9 (2021): 792–806. http://dx.doi.org/10.1007/s12033-021-00344-5.

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13

Hadfield, James, Daphné Linderme, Dionne N. Shepherd, et al. "Complete genome sequence of a dahlia common mosaic virus isolate from New Zealand." Archives of Virology 156, no. 12 (2011): 2297–301. http://dx.doi.org/10.1007/s00705-011-1112-y.

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14

Asano, S., Y. Matsushita, Y. Hirayama, and T. Naka. "Simultaneous detection ofTomato spotted wilt virus,Dahlia mosaic virusandChrysanthemum stunt viroidby multiplex RT-PCR in dahlias and their distribution in Japanese dahlias." Letters in Applied Microbiology 61, no. 2 (2015): 113–20. http://dx.doi.org/10.1111/lam.12442.

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15

Kuluev, B. R., A. V. Knyazev, and A. V. Chemeris. "Activity of promoters of carnation etched ring virus and dahlia mosaic virus in tobacco protoplasts and transgenic plants." Russian Journal of Plant Physiology 55, no. 5 (2008): 687–93. http://dx.doi.org/10.1134/s1021443708050130.

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16

Raikhy, Gaurav, Charles Krause, and Scott Leisner. "The Dahlia mosaic virus gene VI product N-terminal region is involved in self-association." Virus Research 159, no. 1 (2011): 69–72. http://dx.doi.org/10.1016/j.virusres.2011.04.026.

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17

Kuluev, B. R., A. V. Knyazev, A. A. Iljassowa, and A. V. Chemeris. "Constitutive expression of the ARGOS gene driven by dahlia mosaic virus promoter in tobacco plants." Russian Journal of Plant Physiology 58, no. 3 (2011): 507–15. http://dx.doi.org/10.1134/s1021443711030083.

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18

Sahoo, Dipak Kumar, Shayan Sarkar, Sumita Raha, et al. "Analysis of Dahlia Mosaic Virus Full-length Transcript Promoter-Driven Gene Expression in Transgenic Plants." Plant Molecular Biology Reporter 33, no. 2 (2014): 178–99. http://dx.doi.org/10.1007/s11105-014-0738-9.

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19

Maricle, Keri L., and Eric T. Gillock. "Phylogenetic Distribution of DMV-D10, an Endogenous Strain of Dahlia Mosaic Virus, in Members of Asteraceae." Transactions of the Kansas Academy of Science 123, no. 1-2 (2020): 165. http://dx.doi.org/10.1660/062.123.0113.

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20

Zhang, S., D. Zhang, Y. Liu, et al. "First Report of Chili Pepper (Capsicum annuum) as a Natural Host Plant for Dahlia mosaic virus." Plant Disease 99, no. 6 (2015): 898. http://dx.doi.org/10.1094/pdis-11-14-1134-pdn.

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21

Kuluev, B. R., A. V. Knyazev, A. V. Chemeris, and V. A. Vakhitov. "Morphological features of transgenic tobacco plants expressing the AINTEGUMENTA gene of rape under control of the dahlia mosaic virus promoter." Russian Journal of Developmental Biology 44, no. 2 (2013): 86–89. http://dx.doi.org/10.1134/s1062360413020070.

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22

Banerjee, Joydeep, Dipak Kumar Sahoo, Sumita Raha, Shayan Sarkar, Nrisingha Dey, and Indu B. Maiti. "A Region Containing an as-1 Element of Dahlia Mosaic Virus (DaMV) Subgenomic Transcript Promoter Plays a Key Role in Green Tissue- and Root-Specific Expression in Plants." Plant Molecular Biology Reporter 33, no. 3 (2014): 532–56. http://dx.doi.org/10.1007/s11105-014-0766-5.

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23

Nikoloudakis, Nikolaos, Polyxeni Pappi, Emmanouil A. Markakis, et al. "Structural Diversity and Highly Specific Host-Pathogen Transcriptional Regulation of Defensin Genes Is Revealed in Tomato." International Journal of Molecular Sciences 21, no. 24 (2020): 9380. http://dx.doi.org/10.3390/ijms21249380.

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Defensins are small and rather ubiquitous cysteine-rich anti-microbial peptides. These proteins may act against pathogenic microorganisms either directly (by binding and disrupting membranes) or indirectly (as signaling molecules that participate in the organization of the cellular defense). Even though defensins are widespread across eukaryotes, still, extensive nucleotide and amino acid dissimilarities hamper the elucidation of their response to stimuli and mode of function. In the current study, we screened the Solanum lycopersicum genome for the identification of defensin genes, predicted

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24

Runia, W. T., E. A. van Os, and G. J. Bollen. "Disinfection of drainwater from soilless cultures by heat treatment." Netherlands Journal of Agricultural Science 36, no. 3 (1988): 231–38. http://dx.doi.org/10.18174/njas.v36i3.16674.

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In closed systems with soilless cultures, recirculation of drainwater favours the spread of root-infecting pathogens. An installation was designed for disinfection of drainwater by heat treatments at high temperatures (more than 90 degrees C) for short periods (approx. 10 secs). The energy input was low because of efficient use of heat exchangers. Preliminary results of glasshouse experiments showed that tobacco mosaic virus and Verticillium dahliae were effectively controlled. Longer exposure times are probably required for complete elimination of Fusarium oxysporum f. sp. melongenae. (Abstra

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25

Erb, W. Alan, and Randall C. Rowe. "Screening Tomato Seedlings for Multiple Disease Resistance." Journal of the American Society for Horticultural Science 117, no. 4 (1992): 622–27. http://dx.doi.org/10.21273/jashs.117.4.622.

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Two procedures for screening tomato (Lycopersicon esculentum Mill.) seedlings for resistance to three pathogens were developed. In one scheme, seeds were sprayed with a spore suspension of Fusarium oxysporum f. sp. radicis-lycopersici Jarvis & Shoemaker (fusarium crown and root rot). Resistant seedlings were root-dipped 2.5 weeks later in a spore suspension of Verticillium dahliae Kleb. (verticillium wilt), and 1 week following the root dip, leaves were rubbed with tobacco mosaic virus. In the other scheme, 2-week-old seedlings were dipped in a spore suspension of F. oxysporum Schlecht f.

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26

Santos, Lucas S., Roberto A. Melo, Paulo R. Santos, José LS Carvalho Filho, and Dimas Menezes. "Tolerance to high temperature in F5 inbred lines of tomato." Horticultura Brasileira 32, no. 2 (2014): 152–58. http://dx.doi.org/10.1590/s0102-05362014000200005.

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High temperatures in the growing tomato have caused a reduction in fruit set and consequently productivity. This work aimed to evaluate F5 lines of tomato to fruit set and high temperature tolerance in two culture environments. Two experiments were carried out, one in cultivation in greenhouse and the other in the field conditions, from February to June 2012. We evaluated 20 lines F5 of tomato, originating from the segregation of hybrid SE 1055 F1, developed for the hot and humid conditions, with resistance to Fusarium oxysporum f.sp. lycopersici race 2, the tomato mosaic virus (ToMV), the Ver

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27

Yamamoto, Daiki, Yutaro Neriya, Tomohiro Suzuki, Hisashi Nishigawa, and Tomohide Natsuaki. "Construction of an infectious dahlia common mosaic virus clone." Archives of Virology, September 8, 2021. http://dx.doi.org/10.1007/s00705-021-05225-5.

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