scholarly journals First Report of Southern bean mosaic virus Infecting French Bean in Morocco

Plant Disease ◽  
2004 ◽  
Vol 88 (10) ◽  
pp. 1162-1162 ◽  
Author(s):  
E. Segundo ◽  
F. M. Gil-Salas ◽  
D. Janssen ◽  
G. Martin ◽  
I. M. Cuadrado ◽  
...  
Keyword(s):  
Mosaic Virus ◽  
Sodium Dodecyl ◽  
Plant Viruses ◽  
Enzyme Linked Immunosorbent Assay ◽  
First Report ◽  
Sequence Identity ◽  
Southern Bean Mosaic Virus ◽  
Bean Plants ◽  
Symptomatic Leaf ◽  
Das Elisa

Common bean (Phaseolus vulgaris L.) is grown on approximately 1,500 ha in commercial greenhouses and is of major economic importance in the Souss-Massa Region, Agadir, Morocco. Since October 2003, symptoms resembling a viral disease, consisting of pod mosaic and distortion and mild to severe mosaic in leaves, have been observed on bean plants in several greenhouses. Mechanical inoculation with symptomatic leaf extracts produced necrotic local lesions on P. vulgaris ‘Pinto’ and systemic symptoms similar to those observed in the naturally infected bean plants P. vulgaris ‘Donna’ (five plants per cultivar). Inoculated and naturally infected samples reacted positively using a double antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA) to Southern bean mosaic virus (SBMV) (DSMZ, Braunschweig, Germany), a member of the Sobemovirus genus that is transmitted by contact, soil, beetles, and seeds (1). Virions purified from a naturally infected ‘Donna’ plant contained a 30-kDa polypeptide that reacted positively using sodium dodecyl sulfate polyacrylamide gel electrophoresis and western blot analysis with SBMV antiserum (DSMZ). Reverse transcription-polymerase chain reaction amplification with SMBV primers as described by Verhoeven et al. (2) produced an expected 870-bp band. The amplicon was cloned, sequenced (GenBank Accession No. AJ748276), and compared to those isolates available in GenBank and had a nucleotide sequence identity of 87% and a derived amino acid sequence identity of 95% with an SBMV isolate from Spain (2). During a survey in different areas of the Souss-Massa Region, 20 symptomatic leaf and pod samples were randomly collected from 12 greenhouses (50 ha) where significant commercial losses were suffered because of this virus disease, and all samples were positive using DAS-ELISA for SBMV. To our knowledge, this is the first report of SBMV in Morocco. References: (1) J. H. Tremaine and R. I. Hamilton. Southern bean mosaic virus. No. 274 in: Descriptions of Plant Viruses. CMI/AAB, Kew, Surrey, England, 1983. (2) J. Th. J. Verhoeven et al. Eur. J. Plant Pathol. 109:935, 2003.

scholarly journals First Report of Cucumber Mosaic Virus in Eryngium amethystinum, Canna spp., and Aquilegia hybrids in Ohio

Plant Disease ◽  
1997 ◽  
Vol 81 (11) ◽  
pp. 1331-1331 ◽  
Author(s):  
J. R. Fisher ◽  
M.-C. Sanchez-Cuevas ◽  
S. T. Nameth ◽  
V. L. Woods ◽  
C. W. Ellett
Keyword(s):  
Cucumber Mosaic Virus ◽  
Mosaic Virus ◽  
Plant Viruses ◽  
Early Summer ◽  
Reservoir Host ◽  
Enzyme Linked Immunosorbent Assay ◽  
Herbaceous Plant ◽  
First Report ◽  
Severe Stunting ◽  
Banding Profile

Eryngium amethystinum (amethyst sea holly) is a herbaceous plant commonly grown as an ornamental perennial in U.S.D.A. hardiness zones 3 to 8. The plant thrives in dry areas with infertile soils and the flowers are often used in dried floral arrangements. Canna spp. (Canna), soft perennials (U.S.D.A. zone 9 and above), are becoming popular flowering plants because of their bright flowers and spectacular foliage. There are a variety of species that fall under the heading Canna spp., of which the most popular are C. glauca, C. indica, C. edulis, and C. iridiflora. Hybrids of Aquilegia (garden columbine), a hardy perennial (U.S.D.A. zones 3 to 9), flower in late spring through early summer. The genus is made up of a wide variety of cultivars. E. amethystinum exhibiting severe mosaic, yellowing, and stunting, along with Canna plants exhibiting severe stunting, chlorotic and distorted foliage, and mosaic, and garden columbine plants exhibiting stunting, leaf curl, chlorosis, and mosaic, collected from commercial plantings throughout the central Ohio area, were analyzed for the presence of virus infection with viral-associated, double-stranded RNA (dsRNA) analysis. dsRNA analysis resulted in a banding profile typical of that seen with members of the cucumovirus family of plant viruses. Plants positive for cucumovurus-like dsRNA were tested with a direct antibody sandwich enzyme-linked immunosorbent assay (ELISA). ELISA results confirmed the presence of cucumber mosaic virus (CMV) in all symptomatic plants tested. No evidence of dsRNA or CMV was found in any of the asymptomatic plants tested. Because all of these hosts are common in the perennial garden, they could serve as a reservoir host of CMV for other plants in the garden. This is the first report of CMV in E. amethystinum, Canna spp., and Aquilegia hybrids in Ohio.

scholarly journals First Report of a Begomovirus Associated with Tomato Yellow Leaf Curl Disease in Ethiopia

Plant Disease ◽  
2006 ◽  
Vol 90 (7) ◽  
pp. 974-974 ◽  
Author(s):  
S. L. Shih ◽  
S. K. Green ◽  
W. S. Tsai ◽  
L. M. Lee ◽  
J. T. Wang ◽  
...  
Keyword(s):  
Mosaic Virus ◽  
Tomato Yellow Leaf ◽  
Tomato Mosaic Virus ◽  
Enzyme Linked Immunosorbent Assay ◽  
Yellow Leaf ◽  
First Report ◽  
Sequence Identity ◽  
Pcr Product ◽  
Leaf Curl Disease ◽  
Leaf Curl

During December 2003, severe leaf yellowing, leaf curling, and stunting symptoms were observed in tomato (Lycopersicon esculentum) plantings in Melkassa (1,550 m above sea level), Ethiopia. Eleven symptomatic samples were collected and tested for the presence of a begomovirus using polymerase chain reaction (PCR) with the begomovirus-specific degenerate primer pair PAL1v1978/PAR1c715 (3). Samples were also tested for Cucumber mosaic virus (CMV), Potato virus Y (PVY), Tobacco etch virus (TEV), Pepper veinal mottle virus (PVMV), and Tomato mosaic virus (ToMV) using enzyme-linked immunosorbent assay (ELISA). All samples were negative for CMV, PVY, TEV, PVMV, and ToMV. However, the expected 1.4-kb PCR product for begomoviruses was obtained from all samples. DNA-B and DNA-beta were not detectable using PCR with the DNA-B specific primer pairs DNABLC1/DNABLV2 and DNABLC2/ DNABLV2 (2) and the DNA-beta primer pair Beta01/Beta02 (1), respectively. The 1.4-kb PCR product of one sample was cloned and sequenced. On the basis of the sequence of the 1.4-kb DNA product, specific primers were designed to complete the DNA-A sequence. The DNA-A consisted of 2,785 nucleotides (GenBank Accession No. DQ358913) and was found to contain the six predicted open reading frames (ORFs V1, V2, C1, C2, C3, and C4). A BLAST analysis was conducted with geminivirus sequences available in the GenBank database at the National Center for Biotechnology Information (Bethesda, MD), and DNAMAN software (Lynnon Corporation, Quebec, Canada) was used for further comparisons. The DNA-A sequence of the virus associated with yellow leaf curl disease of tomato from Ethiopia showed highest sequence identity (92%) with Tomato yellow leaf curl Mali virus (TYLCMLV; GenBank Accession No. AY502934). On the basis of the DNA-A sequence comparison and the ICTV demarcation of species at 89% sequence identity, the Ethiopian virus is a provisional strain of TYLCMLV described from Mali. To our knowledge, this is the first report of a begomovirus associated with tomato yellow leaf curl disease in Ethiopia. References: (1) R. W. Briddon et al. Mol. Biotechnol. 20:315, 2002. (2) S. K. Green et al. Plant Dis. 85:1286, 2001. (3) M. R. Rojas et al. Plant Dis. 77:340, 1993.

scholarly journals First Report of Cichorium endivia (Asteraceae) as a Natural Host of Groundnut ringspot orthotospovirus in Brazil.

Plant Disease ◽  
2020 ◽  
Author(s):  
Tiago Silva Jorge ◽  
Mirtes Freitas Lima ◽  
Leonardo Silva Boiteux ◽  
Maria Esther N. Fonseca ◽  
Elliot W. Kitajima
Keyword(s):  
Untranslated Region ◽  
Natural Infection ◽  
Plant Viruses ◽  
Enzyme Linked Immunosorbent Assay ◽  
Nucleotide Sequencing ◽  
Rt Pcr ◽  
Plant Materials ◽  
First Report ◽  
Cichorium Endivia ◽  
Das Elisa

Endive (Cichorium endivia L.) is a very important cash crop for small farmers in Brazil. During inspections conducted in the summer season of 2019–2020, leaf samples of C. endivia ‘La Spezia’ seedlings exhibiting typical symptoms of orthotospoviruses infection (viz. concentric chlorotic spots and apical leaf deformation; ≈ 10%) were collected in commercial greenhouses in Brasília–DF, Central Brazil. Leaves of one healthy and three symptomatic plants were initially evaluated via double antibody sandwich enzyme-linked immunosorbent assay (DAS–ELISA) with polyclonal antibodies (produced at CNPH) raised against the nucleoprotein of the three major orthotospoviruses: tomato spotted wilt orthotospovirus (TSWV), groundnut ringspot orthotospovirus (GRSV) and tomato chlorotic spot orthotospovirus (TCSV). Strong serological reactions were observed only against GRSV antibodies exclusively in extracts from symptomatic samples. In order to confirm the causal agent of those symptoms, total RNA was extracted (Trizol®; Sigma) from infected leaf samples and used in a two-step reverse transcriptase polymerase chain reaction (RT–PCR) approach. Synthesis of the cDNA was carried out with the J13 primer (5’–CCC GGA TCC AGA GCA AT–3’) (Cortez et al., 2001) followed by PCR assays with the primer pair BR60 (5’–AGA GCA ATC GTG TCA–3`) and BR65 (5’–ATC AAG CCT TCT GAA AGT CAT–3’) (Eiras et al., 2001). This primer set amplifies a fragment of 453 bp including the untranslated region at the 3’ terminus of the small RNA and the protein N–coding gene of at least five orthotospoviruses: TSWV, GRSV, TCSV, chrysanthemum stem necrosis orthotospovirus (CSNV) and zucchini lethal chlorosis orthotospovirus (ZLCV) (Eiras et al., 2001). The obtained amplicons (≈ 432 bp) were subsequently subjected to Sanger dideoxy nucleotide sequencing at CNPH. BLASTn analysis showed >99% identity with a wide array of GRSV isolates available in the GenBank. The nucleotide sequence of Tospo #1 (MT215222) and Tospo #3 (MT215224) isolates displayed 100% identity between them, whereas the Tospo #2 (MT215223) isolate displayed one non–synonymous point mutation in the 3’ untranslated region in comparison with the former two isolates. Three plants of C. endivia, Capsicum annuum L. cv. Ikeda, tomato (Solanum lycopersicum L.) cv. Santa Clara and its isoline ‘LAM–147’ (with the Sw–5 resistance gene), Nicotiana rustica L., Lactuca sativa L. (‘Vanda’ and ‘PI-342444’) and Gomphrena globosa L. were mechanically inoculated individually with each GRSV isolate in order to confirm their pathogenicity. Chlorotic lesions and mosaic were observed seven days after inoculation of all plant materials, except the tomato inbred line ‘LAM–147’, which has the Sw-5 gene that confers broad–spectrum resistance to all Brazilian orthotospoviruses (Boiteux and Giordano, 1993). The GRSV infection was confirmed via DAS–ELISA and RT–PCR 15 days after inoculation, using the same set of antibodies and the primer pair BR60 / BR65. Transmission electron microscopy of ultrathin sections from symptomatic leaf tissues, both from field–infected and experimentally inoculated endive revealed the presence of typical orthotospovirus particles, within endoplasmic reticulum cisternae. Natural infection of endive by TSWV has been reported in Greece (Chatzivassiliou et al., 2000) and by TCSV in São Paulo State, Brazil and in Florida, USA (Subramanya Sastry et al., 2019). To our knowledge, it is the first report of GRSV naturally infecting this Asteraceae species in Brazil. Confirmation of GRSV infection of C. endivia plants is a relevant piece of information aiming to design effective disease management strategies. References: Boiteux, L.S. and Giordano, L. B. 1993. Euphytica 71: 151. Eiras, M. et al. 2001. Fitopatol. Bras. 26: 170. Chatzivassiliou, E.K. et al. 2000 Ann. Appl. Biol. 137: 127. Cortez, I., et al. 2001. Arch. Virol. 146: 265. Subramanya Sastry, K., et al. 2019. Encyclopedia of plant viruses and viroids. Springer, New Delhi. https://doi.org/10.1007/978-81-322-3912-3.

scholarly journals First Report of Papaya ringspot virus W in Sponge Gourd from India

Plant Disease ◽  
2006 ◽  
Vol 90 (7) ◽  
pp. 974-974 ◽  
Author(s):  
Raj Verma ◽  
V. K. Baranwal ◽  
Satya Prakash ◽  
S. P. S. Tomer ◽  
R. P. Pant ◽  
...  
Keyword(s):  
Mosaic Virus ◽  
Zucchini Yellow Mosaic Virus ◽  
Ringspot Virus ◽  
Yellow Mosaic Virus ◽  
Enzyme Linked Immunosorbent Assay ◽  
Natural Occurrence ◽  
Papaya Ringspot Virus ◽  
First Report ◽  
Sponge Gourd ◽  
Das Elisa

During August 2004, symptoms resembling a virus disease were observed in commercial cultivation of sponge gourd (Luffa cylindrica (L.) M. Roem. [cv. Chikni]) in Pune, India. Affected plants exhibited mosaic mottling, vein banding, and downward marginal curling on leaves. The incidence of disease was 10 to 30% based on the symptoms and confirmed using enzyme-linked immunosorbent assay (ELISA). Six fields of sponge gourd were visited, and 30 samples were collected randomly. Samples from affected fields were analyzed for the presence of virus by mechanical inoculation. Symptoms typical of those observed in the original field plants appeared 10 days after inoculation on sponge gourd. The virus isolate produced local lesions on Chenopodium amaranticolor and systemic symptoms on Cucumis melo, Cucumis sativus, Cucurbita maxima, Cucurbita pepo, L. acutangula, and L. cylindrica, but did not produce symptoms on Carica papaya (cvs. CO2 and Red Lady), Nicotiana glutinosa, N. tabacum (cv. White Burley), or Vigna unguiculata. Field-infected sponge gourd and all indicator plants were tested using double-antibody sandwich (DAS)-ELISA. The virus was identified as Papaya ringspot virus-W (PRSV-W) using DAS-ELISA (Agdia, Elkhart, IN). A strong, positive reaction was obtained with antiserum to PRSV-W but not with antisera to PRSV-P, Cucumber mosaic virus, Squash mosaic virus, Zucchini yellow mosaic virus, and Groundnut bud necrosis virus. To ensure virus purity, the isolate was passed through three successive single-lesion transfers on C. amaranticolor. Flexuous filamentous particles 775 nm long were observed with electron microscopy of leaf-dip preparation from symptomatic sponge gourd leaves. The virus particles were then decorated with a second PRSV-W antiserum obtained from the Plant Virology Unit, IARI, New Delhi. PRSV-W on sponge gourd has previously been reported from Taiwan (1). To our knowledge, this is the first report of natural occurrence of PRSV-W on sponge gourd in India. Reference: (1.) C. H. Huang et al. J. Agri. Res. China 36:413, 1987.

scholarly journals Outbreak of Clover yellow vein virus in a Bean Field in Colusa County, California

Plant Disease ◽  
2001 ◽  
Vol 85 (4) ◽  
pp. 444-444 ◽  
Author(s):  
R. Crnov ◽  
R. L. Gilbertson
Keyword(s):  
Common Bean ◽  
Virus Disease ◽  
Sodium Dodecyl ◽  
Yellow Vein ◽  
Enzyme Linked Immunosorbent Assay ◽  
Rt Pcr ◽  
Systemic Necrosis ◽  
First Report ◽  
Bean Plants ◽  
Clover Yellow Vein Virus

In 1999, a severe outbreak (i.e., 100% infection) of a virus disease was observed in a single field of common bean in Colusa County, CA. The symptoms included a yellow mosaic, leaf epinasty and, in some plants, a systemic necrosis. This field was adjacent to a clover field that had been harvested early in the development of the bean plants. A preliminary serological test (enzyme-linked immunosorbent assay, ELISA) suggested that the virus infecting these bean plants was Peanut mottle virus (PeMoV). This would represent the first report of this virus in California. A range of common bean cultivars (Black Turtle Soup, Topcrop, California Early Light Red Kidney, and Sutter Pink) were inoculated with sap prepared from symptomatic leaves collected from this field. Symptoms developing on these plants ranged from systemic necrosis (cvs. Sutter Pink and Black Turtle Soup) to strong yellow green mosaic and leaf distortion (cvs. Topcrop and California Early Light Red Kidney). Furthermore, inoculated primary leaves of cv. Topcrop failed to develop local lesions, which is characteristic of PeMoV. ELISAs on all symptomatic plants with antisera against PeMoV, BYMV, BCMV, and BCMNV as well as reverse transcription polymerase chain reaction (RT-PCR) analysis with primer pairs specific for PeMoV, BYMV, BCMV, and BCMNV were negative. To further investigate the nature of this virus, a minipurification method was used to purify virions from symptomatic leaves of all four cultivars. Sodium dodecyl sulfate polyacrylamide gel electrophoresis analysis of purified virions from these cultivars revealed a 32-kDa band consistent with infection by a potyvirus. Transmission electron microscopy analysis of these preparations revealed the presence of potyvirus-like flexous rods (approximately 750 nm long and 10 nm wide). We next designed a primer pair specific for the coat protein gene of Clover yellow vein virus (ClYVV) and RT-PCR with these primers resulted in the amplification of a 630-bp DNA fragment from four isolates of the unknown potyvirus. No fragments were amplified from an uninfected control. The PCR-amplified fragments were direct-sequenced, and sequence comparisons revealed that the sequences of all four isolates were 95% identical to that of ClYVV (Genbank accession number D89541). Subsequently, a ClYVV antiserum was obtained from Simon Scott (Department of Plant Pathology, Clemson University), and ELISAs performed on leaves infected with all four isolates were positive. Finally, to assess whether the virus was seed-transmitted, seed harvested from this field was planted in a greenhouse (two lots of 400 seed each). None of the plants from these seeds developed virus symptoms, suggesting that the virus was not seed-transmitted. Together, these results indicate that the virus disease outbreak in this bean field was caused by ClYVV rather than PeMoV. The inoculum source for the virus was probably the adjacent clover field. This is the first report of ClYVV infecting common bean in California.

scholarly journals First Report of Cucumber mosaic virus in Banana from Iran

Plant Disease ◽  
2005 ◽  
Vol 89 (8) ◽  
pp. 914-914 ◽  
Author(s):  
T. Ghotbi ◽  
K. Bananej
Keyword(s):  
Cucumber Mosaic Virus ◽  
Mosaic Virus ◽  
Plant Viruses ◽  
Economic Losses ◽  
Enzyme Linked Immunosorbent Assay ◽  
Streak Virus ◽  
Serological Tests ◽  
Tropical Fruit ◽  
Test Plants ◽  
Das Elisa

Banana bunchy top virus (BBTV), Banana streak virus (BSV), and Cucumber mosaic virus (CMV) (genus Cucumovirus, family Bromoviridae [2]) cause widespread economic losses on banana (Musa sp.) throughout the world and have been reported on banana in different countries including Pakistan along its southeastern border with Iran (1). A survey was conducted from 2004–2005 to identify viruses infecting banana in greenhouses in different growing areas in northern Iran, Mazandaran Province (Sari, Babol, Behshahr, and Ghaemshahr cities). A total of 180 samples from seven banana-growing greenhouses with symptoms of mosaic, chlorosis, stunting, and fruit malformation were collected. All samples were tested for CMV with polyclonal antibodies using double-antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA) (CMV strain D subgroup I; gifted by H. Lecoq, INRA, Avignion, France). For sap inoculation onto indicator test plants, selected ELISA-positive leaf samples were ground in chilled 0.01 M phosphate buffer, pH 7.0, containing 0.15% 2-mercaptoethanol. Chlorotic and necrotic local lesions developed on Chenopodium amaranticolor and Vigna unguiculata (cv. Mashad local) 10 and 12 days postinoculation, respectively. Cucumis sativus and Nicotiana rustica also developed systemic mosaic symptoms (3). All indicator test plants were rechecked for the presence of CMV using DAS-ELISA. On the basis of serological tests and indicator host plants reactions, CMV was identified in 32% of samples including Sari (13.8%), Babol (2.7%), Behshahr (10%) and Ghahemshahr (5%), respectively. Fifty-five samples did not react with CMV antiserum but the presence of symptoms resembling BBTV and BSV (4) emphasizes the need for further investigations to confirm the presence and identities of other viruses. References: (1) J. Bird and F. L. Wellman. Phytopathology 52:286, 1962. (2) S. K. Choi et al. J. Virol. Methods 83:67, 1999. (3) A. J. Gibbs and B. D. Harrison. Descriptions of Plant Viruses. No.1. CMI/AAB, Surrey, England, 1970. (4) R. C. Ploetz et al., eds. Compendium of Tropical Fruit Diseases. The American Phytopathological Society, St. Paul, MN, 1994.

scholarly journals A Survey of Viruses Affecting French bean (Phaseolus vulgaris) in Iran Includes a First Report of Southern bean mosaic virus and Bean pod mottle virus

Plant Disease ◽  
2005 ◽  
Vol 89 (9) ◽  
pp. 1012-1012 ◽  
Author(s):  
N. Shahraeen ◽  
T. Ghotbi ◽  
A. Dezaje Elkhache ◽  
A. Sahandi
Keyword(s):  
Phaseolus Vulgaris ◽  
Mosaic Virus ◽  
Plant Viruses ◽  
French Bean ◽  
Mottle Virus ◽  
Bean Pod Mottle Virus ◽  
Southern Bean Mosaic Virus ◽  
Leaf Distortion ◽  
Test Plants ◽  
Das Elisa

A survey was conducted from 2003 to 2004 to identify viruses infecting common bean (Phaseolus vulgaris L.) in different growing areas of East Azarbaejan Province of Iran. A total of 300 French bean samples with symptoms of viral infection (mosaic, vein clearing, leaf rolling, yellowing, and leaf distortion) were collected. The samples were tested for eight viruses using the tissue-blot immunoassay procedures (TBIA) (2) and double-antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA) according to the manufacturer's instructions (DSMZ, Braun-schweig, Germany). ELISA tests for Alfalfa mosaic virus (AMV), Bean yellow mosaic virus (BYMV), Bean common mosaic virus (BCMV), Bean common mosaic necrosis virus (BCMNV), Cucumber mosaic virus (CMV), Bean leaf roll virus (BLRV), and Southern bean mosaic virus (SBMV) were used. In addition, antiserum was provided by S. A. Ghabrial (University of Kentucky, Lexington) to test for Bean pod mottle virus (BPMV). Serological tests showed that SBMV and BPMV were present in 12% (35 samples) and 5% (15 samples) of samples, respectively. BCMV, BCMNV, BYMV, BLRV, CMV, and AMV were more common and were detected in 155, 105, 80, 46, 30, and 10 samples of 300 samples, respectively. These six viruses were previously reported in other pulses and in French bean in Iran (1). The presence of SBMV and BPMV were verified in samples by transmission to French bean (Phaseolus vulgaris), cowpea (Vigna unguiculata), and soybean (Glycine max) indicator test plants (3,4). Inoculation with extracts from SBMV-positive plants produced systemic mottle and mosaic symptoms in soybean (cv. Gorgan-3) and French bean (cvs. Dubbele Witte and Cheete). In cowpea (cv. Mashad) and French bean (cv. Pinto), inoculation produced necrotic local lesions. Inoculation with extracts from BPMV-positive plants produced severe mosaic, leaf distortion, and puckering in soybean (cv. Gorgan-3) and French bean (cv. Ten-dergreen). No symptoms were observed in cowpea (cv. Mashad). Cvs. Pinto and Bountiful bean reacted with necrotic local lesions. All indicator test plants tested positive for the presence of SBMV or BPMV as expected using DAS-ELISA. To our knowledge, this is the first report of BPMV and SBMV naturally infecting French bean in Iran. These viruses can cause a serious problem to other leguminous crops grown in Iran. References: (1) W. J. Kaiser et al. Plant Dis. Rep. 52:687, 1968. (2) K. M. Makkouk and A. Comeau. Eur. J. Plant Pathol. 100:71, 1994. (3) J. S. Semancik. Bean pod mottle virus. No. 108 in: Descriptions of Plant Viruses. CMI/AAB, Kew, Surrey, England, 1972. (4) J. H. Tremain and R. I. Hamilton. Southern bean mosaic virus. No. 274 in: Descriptions of Plant Viruses. CMI/AAB, Kew, Surrey, England, 1983.

scholarly journals First Reports of Soilborne wheat mosaic virus and Wheat spindle streak mosaic virus in Africa

Plant Disease ◽  
2000 ◽  
Vol 84 (8) ◽  
pp. 921-921 ◽  
Author(s):  
R. G. Kapooria ◽  
J. Ndunguru ◽  
G. R. G Clover
Keyword(s):  
Triticum Aestivum ◽  
Mosaic Virus ◽  
Wheat Yield ◽  
Plant Viruses ◽  
Enzyme Linked Immunosorbent Assay ◽  
Infected Leaf ◽  
Mechanical Transmission ◽  
Panicum Maximum ◽  
Wheat Cultivars ◽  
Das Elisa

During 1997 and 1998, virus symptoms similar to those of Soilborne wheat mosaic virus (SBWMV) and Wheat spindle streak mosaic virus (WSSMV) were observed on nine wheat cultivars (Triticum aestivum cvs. Deka, Gamtoos, Lorie II, MM2, Nata, Nkwazi, P7, Scepter, and Scan) in the Central, Copper-Belt, Lusaka, and Southern provinces of Zambia. Symptoms were observed between June and August on wheat, which in Zambia is an irrigated crop grown during the cooler months (May to August). In fields suspected to be infected with SBWMV, irregularly distributed, circular patches of severely stunted sparse plants were observed. Because of these symptoms, the syndrome is described in Zambia as the “crater disease.” Infection was more common on light to medium sandy-loam clay soils, and affected patches were particularly common along the field edges and in poorly drained areas. Such waterlogged conditions are conducive to the multiplication and spread of Polymyxa graminis, the protist vector of SBWMV (1). Affected plants initially showed chlorotic streaks on all leaves, which became uniformly yellow and eventually necrotic. The roots of these plants were slightly swollen and enlarged and are likened to “Rastafarian pleats” locally. In fields suspected to be infected with WSSMV, symptomatic plants were observed in the border rows of affected fields. Chlorotic streaks and mosaics were observed on the leaves of affected plants, and the tips of these leaves were also frequently twisted. Using double antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA), SBWMV and WSSMV were positively identified in symptomatic plants. In total, 81 plants from the four provinces were tested, and 72 and 37% were infected with SBWMV and WSSMV, respectively. Identification was confirmed by DAS-ELISA using antisera from W. Huth (BBA-Braunschweig, Germany) and C. Rubies-Autonell (Bologna University, Italy) for SBWMV and using antisera from W. Huth (BBA-Braunschweig, Germany) and G. Bergstrom (Cornell University, New York) for WSSMV. Further confirmation of the identity of the two viruses was provided by the reaction of 12 indicator species (Chenopodium amaranticolor, C. quinoa, C. hybridum, Digitaria milanjiana, Eleusine indica, Oryza sativa (cv. IITA 212), Panicum maximum, Rottboellia cochinchinensis, Setaria verticillata, Sorghum bicolor(cv. Sima), S. halepense, and Triticum aestivum (cvs. Lucal, Kwale, Lorie II, Nkanga, 128, and GV 4–12) in mechanical transmission studies using infected leaf sap. This is the first report of SBWMV and WSSMV not only in Zambia but also Africa. The area of wheat grown in Zambia has risen in the past several years to approximately 18,000 ha per annum. However, annual wheat yield (60,000 tons) has not risen to match this increase. The effect of SBWMV and WSSMV on yield in Zambia has not yet been measured, but both viruses cause serious losses in other countries (1–3) and the severity of the symptoms suggests that significant yield reductions are likely. Furthermore, no Zambian wheat cultivars are known to be resistant to either virus. Generally, wheat production fails to meet demand in the country and therefore further yield losses due to virus infection could be disastrous. References: (1) M. K. Brakke. CMI/AAB Desc. of Plant Viruses 77, 1971. (2) J. T. Slykhuis. Phytopathology 60:319, 1970. (3) V. Vallega and C. Rubies-Autonell. Plant Dis. 69:64, 1985.

First Detection of Tobacco Mosaic Virus in Tobacco Fields in Northern Lebanon

2020 ◽  
Vol 20 ◽  
Author(s):  
Rami Obeid ◽  
Elias Wehbe ◽  
Mohamad Rima ◽  
Mohammad Kabara ◽  
Romeo Al Bersaoui ◽  
...  
Keyword(s):  
Tobacco Mosaic Virus ◽  
Mosaic Virus ◽  
Viral Genome ◽  
Virus Genome ◽  
Enzyme Linked Immunosorbent Assay ◽  
Virus Family ◽  
Crop Fields ◽  
Wide Range ◽  
Almost All ◽  
Das Elisa

Background: Tobacco mosaic virus (TMV) is the most known virus in the plant mosaic virus family and is able to infect a wide range of crops, in particularly tobacco, causing a production loss. Objectives: Herein, and for the first time in Lebanon, we investigated the presence of TMV infection in crops by analyzing 88 samples of tobacco, tomato, cucumber and pepper collected from different regions in North Lebanon. Methods: Double-antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA), revealed a potential TMV infection of four tobacco samples out of 88 crops samples collected. However, no tomato, cucumber and pepper samples were infected. The TMV+ tobacco samples were then extensively analyzed by RT-PCR to detect viral RNA using different primers covering all the viral genome. Results and Discussion: PCR results confirmed those of DAS-ELISA showing TMV infection of four tobacco samples collected from three crop fields of North Lebanon. In only one of four TMV+ samples, we were able to amplify almost all the regions of viral genome, suggesting possible mutations in the virus genome or an infection with a new, not yet identified, TMV strain. Conclusion: Our study is the first in Lebanon revealing TMV infection in crop fields, and highlighting the danger that may affect the future of agriculture.

scholarly journals First Report of Soilborne Rye Mosaic Virus in Rye in Denmark

Plant Disease ◽  
1999 ◽  
Vol 83 (11) ◽  
pp. 1074-1074 ◽  
Author(s):  
S. L. Nielsen ◽  
M. Nicolaisen ◽  
R. Koenig ◽  
W. Huth
Keyword(s):  
Mosaic Virus ◽  
Trypan Blue ◽  
Chenopodium Quinoa ◽  
Average Diameter ◽  
First Record ◽  
Plant Viruses ◽  
Polyclonal Antiserum ◽  
Polymyxa Graminis ◽  
Sequence Identity ◽  
Rigid Rod

Soilborne wheat mosaic furovirus (SBWMV)-like particles were detected in rye (Secale cereale) grown in sandy soil in West Zealand during spring 1999. Infected plants showed yellow leaf mosaic and light stunting. Electron microscopy of negatively stained crude sap preparations revealed rigid rod-shaped particles with two average lengths, 296 and 162 nm; average diameter was 23 nm. Sap-inoculation to Chenopodium quinoa and C. amaranticolor produced local leaf lesions when grown at 17°C but none when grown at 22 to 25°C. All the features agree with the description of SBWMV (1). Immunosorbent electronmicroscopy with polyclonal antiserum produced by W. Huth to furovirus-like particles isolated from rye in Germany gave a distinct decoration to particles. Light microscopy of roots cleared with 10% KOH and stained with a 0.5% solution of trypan blue in lactoglycerol revealed resting spores with a morphology and size similar to Polymyxa graminis, a furovirus vector. This is the first record of a furovirus on cereals in Denmark. The complete nucleotide sequence of the isolate was analyzed and compared with data on isolates from wheat. Sequence identity was only 74%. Therefore, the isolate was designated as soilborne rye mosaic virus. SBRMV has been recorded previously in rye and triticale in several regions of Germany (2). References: (1) M. K. Brakke. 1971. CMI/AAB Descr. Plant Viruses No. 77. (2) W. Huth. Nachrichtenbl. Dtsch. Pflanzenschutzdienstes 50:163, 1998.

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