scholarly journals A Polish Isolate of Zucchini yellow mosaic virus from Zucchini is Distinct from Other European Isolates

Plant Disease ◽  
2007 ◽  
Vol 91 (5) ◽  
pp. 639-639 ◽  
Author(s):  
H. Pospieszny ◽  
B. Hasiów ◽  
N. Borodynko
Keyword(s):  
Amino Acid ◽  
Mosaic Virus ◽  
Citrullus Lanatus ◽  
Zucchini Yellow Mosaic Virus ◽  
Amino Acid Identity ◽  
Plant Viruses ◽  
Yellow Mosaic Virus ◽  
Parameter Method ◽  
Acid Identity ◽  
Conserved Sequence

Zucchini yellow mosaic virus (ZYMV) is a member of the Potyvirus genus in the Potyviridae family, the largest group of plant viruses. Different isolates of this virus have been found in infected cucurbits throughout the world, including localities in Europe, America, Australia, and Asia. In August 2005, mosaic and yellowing of leaves, as well as yellow spots on green fruits, were observed on zucchini (Cucurbita pepo cv. giromontiina) growing in commercial fields in the Kujawsko-Pomorskie Region of Poland. Flexuous virus particles (~750 nm long), typical of potyviruses, were observed in leaf-dip preparations from symptomatic zucchini plants. The virus in the sap from symptomatic plants was mechanically transmitted and systemic infections were produced on Citrullus lanatus, Cucumis melo, Cucumis sativus, C. pepo cvs. giromontiina and patissoniana, C. maxima, and Nicotiana benthamiana. Severe symptoms such as severe malformation of leaves and stunting of plants were observed on zucchini plants (cv. giromontiina) infected mechanically with the virus and grown in the greenhouse. Double-antibody sandwich (DAS)-ELISA using an anti-ZYMV polyclonal antiserum (AS-0234; DSMZ, Braunschweig, Germany) identified the presence of ZYMV in mechanically infected C. pepo cv. giromontiina and N. benthamiana plants. Subsequently, a reverse transcription (RT)-PCR using a universal primer, Sprimer, designed from the consensus sequences that code for the conserved sequence GNNSGQP in the NIb region of Potyviridae family members and the M4 primer was performed (1). The 1740-bp PCR fragments were cloned into the pGEM-T vector (Promega, Madison, WI) and three randomly selected clones were sequenced on an ABI automatic sequencer. An 837-bp sequence representing the full length coat protein gene (GenBank Accession No. EF178505) was compared with homologous sequences from other ZYMV isolates using BioEdit and Mega 3.1 softwares. Genetic distances were calculated by Kimura's two-parameter method (2). Surprisingly, the Polish ZYMV isolate (ZYMV-Zug) was more closely related to ZYMV isolates from Asia than those from Europe. Pairwise comparisons of ZYMV-Zug with several other European ZYMV isolates (GenBank Accession Nos. DQ645729, AJ420020, AJ459956, AJ420014, AJ420019, DQ124239, and AJ420018) indicated an 81 to 82% nucleotide and 91 to 92% amino acid identity, while there was a 94% nucleotide and 99% amino acid identity with the Shanxi (GenBank Accession No. AY074808) and Shandong isolates (GenBank Accession No. AF513552) from China. References: (1) J. Chen et al. Arch. Virol. 146:757, 2001. (2) S. Kumar et al. Brie. Bioinform. 5:150, 2004.

scholarly journals Characterization of cucumber mosaic virus originating from cucurbits in Serbia

2011 ◽  
Vol 26 (4) ◽  
pp. 325-336 ◽  
Author(s):  
Ana Vucurovic ◽  
Aleksandra Bulajic ◽  
Ivana Stankovic ◽  
Danijela Ristic ◽  
Janos Berenji ◽  
...  
Keyword(s):  
Cucumber Mosaic Virus ◽  
Mosaic Virus ◽  
Mixed Infection ◽  
Zucchini Yellow Mosaic Virus ◽  
Amino Acid Identity ◽  
Plant Viruses ◽  
Yellow Mosaic Virus ◽  
Watermelon Mosaic Virus ◽  
Worldwide Distribution ◽  
Frequency Changes

Cucumber mosaic virus (CMV) is considered one of the most economically important plant viruses and has a worldwide distribution and a very wide host range including plants from family Cucurbitaceae. In Serbia, on cucurbits CMV was detected in single and mixed infections with Zucchini yellow mosaic virus (ZYMV) and Watermelon mosaic virus (WMV). Viruses, including CMV, are constantly present in cucurbit crops, but their frequency changes by year and locality. Surveys and sample collections were conducted in cucurbit crops in the period from 2008 to 2009 at 15 localities in Vojvodina province, and sample testing was carried out using the DAS-ELISA method and commercially available antisera for six economically most important cucurbit viruses. In 2008, a total of 51 samples were collected from 13 cucurbit crops of oilseed pumpkin Olinka variety, squash, and bottle gourd and CMV was detected in a total of 55% of tested samples with symptoms of viral infection. The most common infectious type was mixed infection with ZYMV and WMV (35.3%), and then mixed infection with ZYMV (17.7%) and WMV (2%). A total of 599 symptomatic samples of oilseed pumpkin Olinka variety, zucchini squash varieties Beogradska and Tosca, squash, and winter squash were collected in 15 cucurbits crops in 2009. CMV was present in 4.4% of total collected samples, in single infections in 1.3%, and in mixed with WMV or ZYMV in 1.3%, and 1.8%. Five CMV isolates were obtained by mechanical inoculations of N. glutinosa and one of them was selected for further biological characterization. Test plants which were described to be hosts of CMV expressed symptoms characteristic for those caused by CMV after inoculations by isolate 115-08. CMV specific primers Au1u/Au2d were used to amplify an 850 bp fragment using RT-PCR method. Amplified fragment encodes the entire viral coat protein (CP) gene and partial 5? and 3? UTRs of two selected CMV isolates. Amplified fragments were sequenced and deposited in the NCBI, where they were assigned accession numbers, HM065510 (115-08) and HM065509 (151-08). The sequences of CMV isolates from Serbia shared the highest nucleotide and amino acid identity with isolates from subgroup IA, from 99.5 to 97.4% and 99.1 to 97.4%, and the lowest identities were with the subgroup II isolates from 66.9 to 64, 5%, from 75.8 to 74.1%.

scholarly journals Evaluation of ‘AU-Performance’ Watermelon for Its Response to Virus Inoculation

2009 ◽  
Vol 19 (3) ◽  
pp. 609-612 ◽  
Author(s):  
John F. Murphy ◽  
Fenny Dane
Keyword(s):  
Mosaic Virus ◽  
Fungal Pathogens ◽  
Citrullus Lanatus ◽  
Zucchini Yellow Mosaic Virus ◽  
Systemic Infection ◽  
Yellow Mosaic Virus ◽  
Watermelon Mosaic Virus ◽  
Susceptible Parent ◽  
Resistant Parent ◽  
Systemic Symptoms

The watermelon (Citrullus lanatus var. lanatus) ‘AU-Performance’ was developed for resistance to multiple fungal pathogens and the plant virus, zucchini yellow mosaic virus (ZYMV). A greenhouse-based evaluation was carried out to determine the response of ‘AU-Performance’ to inoculation with three important cucurbit (Cucurbitaceae) viruses in the genus Potyvirus: papaya ringspot virus (PRSV), watermelon mosaic virus (WMV), and ZYMV. The evaluation included the resistant parent (PI595203), the susceptible parent (‘AU-Producer’), and varieties AU-Allsweet and Charleston Gray. Each of the three viruses systemically infected ‘AU-Performance’ with 100% infection and development of characteristic systemic symptoms. The susceptible parent (‘AU-Producer’), ‘AU-Allsweet’, and ‘Charleston Gray’ responded similarly with 100% infection and systemic symptoms. In contrast, the resistant parent (PI595203) was resistant to WMV and ZYMV; however, PRSV-inoculated plants developed a systemic infection with accompanied symptoms and high levels of PRSV accumulation in noninoculated leaves. PI595203 was shown in previous studies to be resistant to PRSV. We show in this report that under greenhouse conditions and application of virus by mechanical inoculation, ‘AU-Performance’ was not resistant to infection by the three potyviruses.

Creation of trivalent transgenic watermelon resistant to virus infection

2005 ◽  
Vol 2 (3) ◽  
pp. 179-185 ◽  
Author(s):  
Niu Sheng-Niao ◽  
Huang Xue-Sen ◽  
Wong Sek-Man ◽  
Yu Jia-Lin ◽  
Zhao Fu-Xing ◽  
...  
Keyword(s):  
Virus Infection ◽  
Mosaic Virus ◽  
Citrullus Lanatus ◽  
Zucchini Yellow Mosaic Virus ◽  
Field Trials ◽  
Yellow Mosaic Virus ◽  
Watermelon Mosaic Virus ◽  
Virus Infections ◽  
High Level ◽  
Transgenic Watermelon

AbstractA trivalent vector containing genes of Watermelon mosaic virus (WMV) coat protein (CP), and replicase genes of Zucchini yellow mosaic virus (ZYMV) and Cucumber mosaic virus (CMV), was constructed for transformation of watermelon (Citrullus lanatus) plants, mediated by Agrobacterium tumefaciens. The integrated foreign genes were identified in the regenerated progenies by polymerase chain reaction (PCR) and Southern blots. The transformation efficiency was about 1.7‰. Resistance to virus infection was determined by mechanical inoculation in the greenhouse and by field trials. The transgenic watermelon lines showed different phenotypes of susceptible, resistant, immune or recovery from virus infections in the late growth stage. A relatively high level of resistance was shown by T3 plants of the line BH1-7. This result indicates the possibility of creating, by transgenic protocols, new varieties of watermelon resistant to viral infection.

Some characteristics of Australian isolates of Zucchini Yellow Mosaic Virus

1988 ◽  
Vol 39 (6) ◽  
pp. 1085 ◽  
Author(s):  
RS Greber ◽  
DM Persley ◽  
ME Herrington
Keyword(s):  
Mosaic Virus ◽  
Citrullus Lanatus ◽  
Zucchini Yellow Mosaic Virus ◽  
Resistance Breeding ◽  
Seed Transmission ◽  
Fruit Production ◽  
Yellow Mosaic Virus ◽  
Watermelon Mosaic Virus ◽  
Marketable Fruit ◽  
Triton X

Isolates of zucchini yellow mosaic virus (ZYMV) were obtained from six cucurbit species from four states of Australia and identified by host range, electron microscopy and serology. A survey of coastal Queensland in 1986-87 showed no ZYMV north of Townsville nor around Rockhampton, but major centres of ZYMV incidence with specific pathotypes, around Ayr, Bowen and in south-east Queensland. Pathotypes were distinguished using Cucumis melo differentials, Trichosanthes anguina and Phaseolus vulgaris. Three ZYMV isolates were compared with watermelon mosaic virus 2 and papaya ringspot virus, cucurbit strain, on 20 hosts from 5 families. The effect of ZYMV on 19 cvv. of pumpkin, squash, zucchini, cucumber, rockmelon and watermelon was examined in the field where marketable fruit production was most affected in Cucurbita maxima and C. pepo, moderately in C. melo and Citrullus lanatus and least in C. moschata and C. sativus. One instance of ZYMV seed transmission in C. pepo and transmission by Aphisgossypii was demonstrated. Resistance breeding progress with C. maxima using a C. ecuadorensis source and in C. lanatus using Citrullus sp. cv. Egusi is reported. Virus purification was achieved using carbon tetrachloride and Triton X-100 clarification with sucrose pad and gradient centrifugations. An antiserum was produced and reacted well in agarose gel-diffusion tests without prior virus particle disruption.

scholarly journals Modifications of the Helper Component-Protease of Zucchini yellow mosaic virus for Generation of Attenuated Mutants for Cross Protection Against Severe Infection

2007 ◽  
Vol 97 (3) ◽  
pp. 287-296 ◽  
Author(s):  
Shih-Shun Lin ◽  
Hui-Wen Wu ◽  
Fuh-Jyh Jan ◽  
Roger F. Hou ◽  
Shyi-Dong Yeh
Keyword(s):  
Mosaic Virus ◽  
Fluorescent Protein ◽  
Zucchini Yellow Mosaic Virus ◽  
Chenopodium Quinoa ◽  
Severe Infection ◽  
Plant Viruses ◽  
Cross Protection ◽  
Yellow Mosaic Virus ◽  
Mild Strain ◽  
Helper Component

A nonpathogenic mild strain is essential for control of plant viruses by cross protection. Three amino acid changes, Arg180→Ile180 (GA mutation), Phe205→Leu205 (GB mutation), and Glu396→Asn396 (GC mutation), of the conserved motifs of the helper component-protease (HC-Pro) of a severe strain TW-TN3 of Zucchini yellow mosaic virus (ZYMV), a member of the genus Potyvirus, were generated from an infectious cDNA clone that carried a green fluorescent protein reporter. The infectivity of individual mutants containing single, double, or triple mutations was assayed on local and systemic hosts. On Chenopodium quinoa plants, the GB mutant induced necrotic lesions; the GA, GC, and GBC mutants induced chlorotic spots; and the GAB and GAC mutants induced local infection only visualized by fluorescence microscopy. On squash plants, the GA, GB, GC, and GBC mutants caused milder mosaic; the GAC mutant induced slight leaf mottling followed by recovering; and the GAB mutant did not induce conspicuous symptoms. Also, the GAC mutant, but not the GAB mutant, conferred complete cross protection against the parental virus carrying a mite allergen as a reporter. When tested on transgene-silenced transgenic squash, the ability of posttranscriptional gene silencing suppression of the mutated HC-Pro of GAC was not significantly affected. We concluded that the mutations of the HC-Pro of ZYMV reduce the degrees of pathogenicity on squash and also abolish the ability for eliciting the hypersensitive reaction on C. quinoa, and that the mutant GAC is a useful mild strain for cross protection.

scholarly journals First Report of Zucchini yellow mosaic virus in Watermelon in Serbia

Plant Disease ◽  
2012 ◽  
Vol 96 (1) ◽  
pp. 149-149 ◽  
Author(s):  
A. Vučurović ◽  
A. Bulajić ◽  
I. Stanković ◽  
D. Ristić ◽  
D. Nikolić ◽  
...  
Keyword(s):  
Amino Acid ◽  
Mosaic Virus ◽  
Sandwich Elisa ◽  
Zucchini Yellow Mosaic Virus ◽  
Yellow Mosaic Virus ◽  
Rt Pcr ◽  
Total Rna ◽  
First Report ◽  
Cp Gene ◽  
Negative Controls

During a survey of cucurbit viruses in the Gornji Tavankut locality (North Backa District), Serbia in June 2011, field-grown (a surface of 1.8 ha) watermelon plants (Citrullus lanatus [Thunb.] Matsum and Nakai) with mild mosaic symptoms were observed. Large numbers of Aphis gossypii were colonizing the crop. A total of 26 samples, six from plants exhibiting mosaic and 20 from asymptomatic plants, were analyzed by double-antibody sandwich-ELISA using polyclonal antisera virus (Bioreba AG, Reinach, Switzerland) against three cucurbit-infecting viruses known to infect Cucurbita pepo in Serbia: Zucchini yellow mosaic virus (ZYMV), Cucumber mosaic virus, and Watermelon mosaic virus (3). Commercial positive and negative controls were included in ELISA analysis. Only six symptomatic samples tested positive for ZYMV, but no other tested viruses were found. The virus was mechanically transmitted from a representative ELISA-positive watermelon sample (550-11) to five plants of C. pepo ‘Ezra F1’ and severe mosaic was noticed 10 days after inoculation. For further confirmation of ZYMV infection, total RNA from a naturally infected watermelon plant and symptomatic C. pepo ‘Ezra F1’ plants were extracted with the RNeasy Plant Mini Kit (Qiagen, Hilden, Germany). Reverse transcription (RT)-PCR was performed with the One-Step RT-PCR Kit (Qiagen) using primer pair ZY-2 and ZY-3 (2). Total RNA obtained from a Serbian isolate of ZYMV from pumpkin (GenBank Accession No. HM072432) and healthy watermelon plants were used as positive and negative controls, respectively. The expected sizes of the RT-PCR products (1,186 bp) were amplified from naturally and mechanically infected symptomatic samples, but not from healthy tissues. The amplified product that derived from isolate 550-11 was purified (QIAquick PCR Purification Kit, Qiagen), sequenced in both directions, deposited in GenBank (Accession No. JN561294), and subjected to sequence analysis using MEGA4 software. Sequence comparisons revealed a high nucleotide identity of 99.9 to 99.8% and 100 to 99.6% amino acid identity for the CP gene with Serbian ZYMV isolates from C. pepo (Accession Nos. JF308188, HM072431, and HM072432). The nucleotide and deduced amino acid sequences of the entire CP gene (837 nt) of the Serbian ZYMV isolate from watermelon shared 99.9 to 93.7% and 100 to 96.8% identity, respectively, with innumerous isolates of ZYMV deposited in the GenBank (e.g., Accession Nos. AJ420012–17 and FJ705262). To our knowledge, this is the first report of ZYMV spreading its host range to watermelon in Serbia. ZYMV infection has been responsible for severe epidemics on cucurbits throughout the world (1). The presence of ZYMV on watermelon could therefore represent a serious threat for this valuable crop in Serbia, especially considering that it is prevalent in other cucurbit crops in the country and the vectors are widespread. References: (1) H. Lecoq et al. Virus Res. 141:190, 2009. (2) K. G. Thomson et al. J. Virol. Methods 55:83, 1995. (3) A. Vučurović et al. Pestic. Phytomed. (Belgrade) 24:85, 2009.

scholarly journals First Report of Zucchini yellow mosaic virus in Cucumber (Cucumis sativus) in India

Plant Disease ◽  
2004 ◽  
Vol 88 (8) ◽  
pp. 906-906 ◽  
Author(s):  
Raj Verma ◽  
Satya Prakash ◽  
S. P. S. Tomer
Keyword(s):  
Mosaic Virus ◽  
Cucumis Sativus ◽  
Cucurbita Pepo ◽  
Citrullus Lanatus ◽  
Natural Infection ◽  
Zucchini Yellow Mosaic Virus ◽  
Yellow Mosaic Virus ◽  
Watermelon Mosaic Virus ◽  
Cucumis Sativus L ◽  
First Report

In August of 2002, cucumber (Cucumis sativus L. cv. Himangi) plants grown in commercial fields in Pune, western Maharashtra, India, exhibited chlorotic spots, veinal chlorosis, mosaic, blister formation and shoestring symptoms on leaves, stunted growth, and distortion of fruits. Incidence of virus infection in the fields varied from 25 to 38%. Crude sap extracted from infected cucumber leaf samples was inoculated mechanically onto cucumber and indicator host plants. The inoculated glasshouse-grown cucumber plants showed virus symptoms similar to those observed in the field. The virus produced chlorotic local lesions on Chenopodium amaranticolor and chlorotic spots followed by veinal chlorosis, mosaic, vein banding, and leaf distortion on Citrullus lanatus, C. melo, C. sativus, Cucurbita maxima, Cucurbita pepo, Luffa acutangula, and Trichosanthes anguina. The virus did not infect Nicotiana benthamiana, N. glutinosa, and N. tabacum cv. White Burley (1,2). Cucumber and indicator plants were tested using direct antigen coating enzyme-linked immunosorbent assays. A positive reaction was obtained with monoclonal antiserum to Zucchini yellow mosaic virus (ZYMV) but not with antisera to Papaya ringspot virus-P, Cucumber mosaic virus, and Watermelon mosaic virus (Agdia, Inc., Elkhart, IN). The disease was observed again in the field during July to September 2003. Natural infection of zucchini (Cucurbita pepo) by ZYMV has been reported previously from India (3). To our knowledge, this is the first report of ZYMV in cucumber in India. References: (1) H. Pospieszny et al. Plant Dis. 87:1399, 2003. (2) R. Provvidenti et al. Plant Dis. 68:443, 1984. (3) S. J. Singh et al. Indian Phytopathol. 56:174, 2003.

Zucchini yellow mosaic virus. [Distribution map].

2003 ◽  
Author(s):  
Keyword(s):  
New York ◽  
South Carolina ◽  
Mosaic Virus ◽  
United Arab Emirates ◽  
New Caledonia ◽  
Citrullus Lanatus ◽  
Zucchini Yellow Mosaic Virus ◽  
Peninsular Malaysia ◽  
Yellow Mosaic Virus ◽  
Distribution Map

Abstract A new distribution map is provided for Zucchini yellow mosaic virus Viruses: Potyviridae: Potyvirus Hosts: Cucurbita maximia, C. moschata, C. pepo, Cucumis melo, C. sativus and Citrullus lanatus. Information is given on the geographical distribution in EUROPE, Austria, Belgium, Bulgaria, Czechoslovakia (former), France, Germany, Greece, Hungary, Italy, Netherlands, Portugal, Slovenia, Spain, Mainland Spain, UK, ASIA, China, Hebei, Henan, Shaanxi, India, Punjab, Indonesia, Irian Jaya, Java, Iran, Israel, Japan, Hokkaido, Honshu, Kyushu, Ryukyu Archipelago, Shikoku, Jordan, Korea Republic, Lebanon, Malaysia, Peninsular Malaysia, Nepal, Oman, Saudi Arabia, Singapore, Syria, Taiwan, Turkey, United Arab Emirates, Yemen, AFRICA, Algeria, Egypt, Mauritius, Mayotte, Morocco, Reunion, South Africa, Sudan, Swaziland, Tunisia, Zimbabwe, NORTH AMERICA, Canada, Ontario, Mexico, USA, Alabama, Arkansas, California, Connecticut, Delaware, Florida, Georgia, Hawaii, Idaho, Illinois, Iowa, Kansas, Kentucky, Louisiana, Maine, Massachusetts, Michigan, Minnesota, Missouri, New Jersey, New York, North Carolina, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Vermont, Virginia, Washington, Wisconsin, CENTRAL AMERICA & CARIBBEAN, Costa Rica, Dominican Republic, Guadeloupe, Honduras, Martinique, Puerto Rico, SOUTH AMERICA, Argentina, Brazil, Maranhao, Para, Rio Grande do Norte, Sao Paulo, Chile, Venezuela, OCEANIA, Australia, Queensland, Tasmania, Western Australia, Guam, New Caledonia, New Zealand, Papua New Guinea, Samoa, Tonga.

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