scholarly journals New Natural Hosts of Pepino mosaic virus in Spain

Plant Disease ◽  
2004 ◽  
Vol 88 (8) ◽  
pp. 906-906 ◽  
Author(s):  
M. C. Córdoba ◽  
Ll. Martínez-Priego ◽  
C. Jordá
Keyword(s):  
Mosaic Virus ◽  
Enzyme Linked Immunosorbent Assay ◽  
Weed Species ◽  
Convolvulus Arvensis ◽  
Pepino Mosaic Virus ◽  
Chenopodium Murale ◽  
Natural Hosts ◽  
Weed Hosts ◽  
Heliotropium Europaeum ◽  
Diplotaxis Erucoides

Pepino mosaic virus (PepMV) was first detected in Spain in 2000 (1). The virus infects tomato (Lycopersicon esculentum Mill.) crops and causes a variety of symptoms including leaf distortion, chlorosis, mosaic, blistering of the leaf surface, green striations on the stem and sepals, and fruit discoloration. PepMV is present along the southern and eastern regions of Spain (provinces of Granada, Almeria, Murcia, Alicante, Valencia, and Barcelona), Balearic, and the Canary Islands. In the summer and autumn of 2001 and 2002, virus-like symptoms were observed in native plants growing in or around tomato fields in Murcia and Almeria provinces. To study the alternate hosts that may serve as virus reservoirs, 62 samples of 42 common weed species, including asymptomatic plants, were collected and analyzed for PepMV using double-antibody sandwich enzyme-linked immunosorbent assay with a commercial antiserum (DSMZ As-0554; Biologische Bundesantstal, Braunschweig, Germany). The following weed hosts tested positive for PepMV: Bassia scoparia (L.) Voss., Calystegia sepium (L.) R.Br., Chenopodium murale L., Convolvulus althaeoides L., Convolvulus arvensis L., Conyza albida Willd. ex Spreng., Coronopus sp., Diplotaxis erucoides (L.) DC, Echium creticum L., E. humile Desf., Heliotropium europaeum L., Moricandia arvensis (L.) DC., Onopordum sp., Piptatherum multiflorum (Cav.) Beauv., Plantago afra L., Rumex sp., Sisymbrium irio L., Sonchus tenerrimus L., and Taraxacum vulgare (Lam.) Schrank. The presence of PepMV in these weed species was confirmed using reverse transcription-polymerase chain reaction with primers specific for PepMV (2). Although the number of samples examined may be insufficient to assess precisely the role of weed reservoirs in outbreaks of PepMV, these findings reveal potential virus sources and contribute to further understanding of PepMV epidemiology in Spain. References: (1) C. Jordá et al. Plant Dis. 85:1292, 2001. (2) P. Martínez-Culebras et al. Eur. J. Plant Pathol. 108:887, 2002.

scholarly journals First Report of Pepino mosaic virus on Natural Hosts

Plant Disease ◽  
2001 ◽  
Vol 85 (12) ◽  
pp. 1292-1292 ◽  
Author(s):  
C. Jordá ◽  
A. Lázaro Pérez ◽  
P. V. Martínez Culebras ◽  
A. Lacasa
Keyword(s):  
Mosaic Virus ◽  
Solanum Nigrum ◽  
Enzyme Linked Immunosorbent Assay ◽  
New Disease ◽  
Nicotiana Glauca ◽  
Pepino Mosaic Virus ◽  
Tomato Plants ◽  
First Report ◽  
Sonchus Oleraceus ◽  
Chenopodium Murale

Pepino mosaic virus (PepMV) is a potexvirus recently identified as the causal agent of a new disease occurring in protected tomato (Lycopersicon esculentum Mill.) crops in the Netherlands (2). PepMV has been subsequently identified in England, Germany, Italy, Morocco, Portugal, and Spain. The new disease has become a serious problem for tomato production in Europe. Most infected tomato plants expressed leaf distortion, chlorosis, and yellow mosaic. Other plants expressed mosaic and bubbling of the leaf surface. Tomato fruits showing severe discoloration and mosaic were observed in protected tomato crops. Symptoms attenuated in tomato plants as the ambient temperature increased. At present, only Solanum muricatum Ait. (Peruvian pepino) and L. esculentum are affected by PepMV.To determine possible reservoir hosts for this virus, 70 samples from Amaranthus sp., A. viridis (L.) Britton et al., Chenopodium murale L., Convolvulus arvensis L., Malva parviflora L., Nicotiana glauca Grah., Polypogon monspeliensis (L.) Desf., Senecio vulgaris L., Sisybrium sp., Solanum nigrum L., and Sonchus oleraceus L. were analyzed. The plants were collected around greenhouses affected by PepMV from different regions in Spain (Murcia and Canary Islands). The samples were analyzed for PepMV by double-antibody sandwich enzyme-linked immunosorbent assay with a commercial antiserum (DSMZ AS-0554, Biologische Bundesantstal, Braunschweig, Germany). Only Amaranthus sp., M. parviflora, N. glauca, Solanum nigrum, and Sonchus oleraceus tested postive. The presence of PepMV in these weed species was confirmed by electron microscopy and reverse transcription-polymerase chain reaction using degenerate primers for potexvirus (1). All the hosts analyzed were asymptomatic. However, symptoms were reproduced by mechanically inoculating tomato plants with sap from naturally infected weeds. To our knowledge, this is the first report of natural infection of weeds by PepMV. References: (1) A. Gibbs et al. J. Virol. Methods 74:67, 1998. (2) R. A. A. Van der Vlugt et al. Plant Dis. 84:103, 2000.

scholarly journals New Natural Hosts of Tomato spotted wilt virus

Plant Disease ◽  
2000 ◽  
Vol 84 (4) ◽  
pp. 489-489
Author(s):  
C. Jordá ◽  
I. Font ◽  
A. Lázaro ◽  
M. Juarez ◽  
A. Ortega ◽  
...  
Keyword(s):  
Tomato Spotted Wilt Virus ◽  
Enzyme Linked Immunosorbent Assay ◽  
Growth Reduction ◽  
Weed Species ◽  
Tomato Spotted Wilt ◽  
Natural Hosts ◽  
Young Leaves ◽  
Diplotaxis Erucoides ◽  
Sonchus Arvensis ◽  
Wilt Virus

Tomato spotted wilt virus (TSWV) has caused epidemics in recent years in many crops throughout the Mediterranean Region. Tomato, pepper, and lettuce are the crops most affected in Spain. To determine the reservoir hosts for the virus in the area, 210 samples from 95 species of plants were collected and tested for TSWV by double-antibody sandwich enzyme-linked immunosorbent assay with commercial antisera (Loewe Biochemica, Germany: BR-01, serogroup I or TSWV-L). Twenty-one species tested positive, and among them were thirteen newly identified hosts for TSWV (1). Weed species were among the 13 new hosts and included Diplotaxis erucoides (L.) DC., Beta maritima L., Phragmites communis Trin., Malva sylvestris L., Sonchus arvensis L., Sorghum halepense L., Panicum repens L., Atriplex patula L., Coronopus squamatus (Forssk.) Ascherson, Cuscuta sp., Xanthium spinosum L., Suaeda vera J.F., and Ecballium elaterium (L.) A. Rich. Most of these plants were asymptomatic hosts, but the Sonchus sp. showed typical symptoms of TSWV, such as yellows, bronzing, ring spots, necrosis, curling of young leaves, and growth reduction. D. erucoides, B. maritima, M. sylvestris, X. spinosum, and E. elaterium showed chlorosis and growth reduction. Reference: (1) C. Jorda et al. 1998. Anexo no. 3. Pages 381–386 in: The Health of Tomato Crops. Phytoma-España S. L., Valencia, Spain.

scholarly journals Pepino mosaic virus on Tomato Seed: Virus Location and Mechanical Transmission

Plant Disease ◽  
2008 ◽  
Vol 92 (12) ◽  
pp. 1701-1705 ◽  
Author(s):  
Kai-Shu Ling
Keyword(s):  
Mosaic Virus ◽  
Large Scale ◽  
Seed Transmission ◽  
Enzyme Linked Immunosorbent Assay ◽  
Mechanical Transmission ◽  
Tomato Seed ◽  
Tomato Production ◽  
Pepino Mosaic Virus ◽  
Infectivity Assay ◽  
Seed Coats

In just a few years, Pepino mosaic virus (PepMV) has become a major threat to greenhouse tomato production around the world. Although tomato seed is suspected to spread the disease, its importance as an initial virus inoculum for PepMV has not been established. To determine the potential for seed transmission, a tomato seed lot highly contaminated with PepMV was used for large-scale seedling grow-out tests. None of 10,000 grow-out seedlings was infected as determined by symptom expression, enzyme-linked immunosorbent assay (ELISA), or infectivity assay on Nicotiana benthamiana. Even though PepMV was not seed transmitted on tomato, the virus was effectively transmitted to tomato and N. benthamiana seedlings through mechanical transmission with seed extract. To examine the exact location where PepMV particles accumulated on the tomato seed, seed coats and embryos were carefully isolated and tested separately by ELISA, real-time RT-PCR, and bioassay on N. benthamiana. PepMV was detected in the seed coat fraction in both immature and mature tomato seeds, but not in the embryo. However, in N. benthamiana, the virus was neither seedborne nor seed-transmitted. Because PepMV is seedborne in tomato, efficient mechanical transmission of PepMV from the virus-contaminated tomato seed to seedlings could initiate a disease epidemic in a new tomato growing area. Thus, it is important to plant certified tomato seed that has been tested free of PepMV.

scholarly journals First Report of Pepino mosaic virus on Tomato in Spain

Plant Disease ◽  
2001 ◽  
Vol 85 (12) ◽  
pp. 1292-1292 ◽  
Author(s):  
C. Jordá ◽  
A. Lázaro Pérez ◽  
P. Martínez-Culebras ◽  
P. Abad ◽  
A. Lacasa ◽  
...  
Keyword(s):  
Mosaic Virus ◽  
Canary Islands ◽  
Plant Protection ◽  
Polyclonal Antibodies ◽  
Datura Stramonium ◽  
Enzyme Linked Immunosorbent Assay ◽  
Chenopodium Amaranticolor ◽  
Pepino Mosaic Virus ◽  
Tomato Plants ◽  
First Report

At the beginning of 2000, a damaging disease developed on protected tomato (Lycopersicon esculentum) crops grown in polyethylene greenhouses in different regions of Spain. Production losses were estimated at 15 to 80%. The tomato plants showed a variety of symptoms. The most common symptoms were leaf distortion, chlorosis, and mosaic. Some plants showed a dark green mosaic and bubbling of the leaf surface. Green striations were also observed on the stem and sepals. Most of the diseased plants had discolored fruits. Symptoms decreased as environmental temperature increased. The involvement of Pepino mosaic virus (PepMV) was suspected. To identify the etiological agent, ≈500 symptomatic tomato plants were collected from several locations in Alicante, Murcia, Almeria and the Canary Islands. Flexuous viral particles 510 nm long were observed by transmission electron microscopy, suggesting the presence of a potexvirus in the tissue extracts analyzed. All samples were tested by ELISA (enzyme-linked immunosorbent assay), using polyclonal antibodies to Narcissus mosaic virus (Adgen, Auchincriuve, Scotland), a virus serologically related to PepMV, and two antisera specific to PepMV (Adgen, Scotland and DMSZ, Braunschweig, Germany). PepMV was detected in 35% of the samples. Like PepMV, the virus infected (as confirmed by ELISA) greenhouse-grown Datura stramonium, Nicandra physalodes, Nicotiana benthamiana, N. clevelandii, Solanum tuberosum, and Vigna sinensis and did not infect Capsicum anuum, Cucumis sativus, Chenopodium amaranticolor, C. quinoa, Petunia × hybrida, Phaseolus vulgaris, Physalis floridana, N. glutinosa, N. rustica, or N. tabacum. The virus did infect Gomphrena globosa, which normally is not infected by PepMV. The first report of PepMV was on pepino (Solanum muricatum) in Peru in 1974 (1), but this virus has been recently reported in the Netherlands, England, Germany, and France on protected tomato crops (2). To our knowledge, this is the first report of PepMV in Spain, including the Canary Islands. References: (1) R. A. C. Jones et al. Ann. Appl. Biol. 94:61, 1980. (2) European and Mediterranean Plant Protection Organisation (EPPO). Alert List Viruses. On-line publication/2000/003.

scholarly journals New Polish Isolate of Pepino mosaic virus Highly Distinct from European Tomato, Peruvian, and US2 Strains

Plant Disease ◽  
2006 ◽  
Vol 90 (8) ◽  
pp. 1106-1106 ◽  
Author(s):  
H. Pospieszny ◽  
N. Borodynko
Keyword(s):  
Mosaic Virus ◽  
Chenopodium Quinoa ◽  
Viral Disease ◽  
Amino Acid Identity ◽  
Polyclonal Antiserum ◽  
Enzyme Linked Immunosorbent Assay ◽  
Sequence Information ◽  
Pepino Mosaic Virus ◽  
The United Kingdom ◽  
Symptomless Infection

Pepino mosaic virus (PepMV, genus Potexvirus) was first described on pepino (Solanum muricatum) in Peru during 1980. Since 1999, the virus was reported in several European countries and in North and South America as an agent of viral disease of tomato crops. In Poland in 2002, the PepMV-SW isolate that was genetically similar to European isolates (approximately 99% identity) was identified (3). In November 2005, in the western part of the Wielkopolska Region, a virus with flexuous filamentous particles approximately 500 nm long was isolated from tomato fruits exhibiting symptoms of discoloration. Crude sap from Nicotiana benthamiana leaves was used for mechanical inoculation of indicator plants. The virus caused symptoms on N. benthamiana, N. clevelandii, Datura inoxia, and Lycopersicon esculentum. Symptomless infection on N. tabacum cv. Xanthi nc, N. tabacum cv. White Burley, and N. debneyi was confirmed by back-inoculation on N. benthamiana. The virus did not infect N. glutinosa, Physalis floridana, Petunia hybrida, Capsicum annuum, Chenopodium quinoa, Cucumis sativus, or Phaseolus vulgaris. The virus was initially identified using double-antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA) with polyclonal antiserum against PepMV (DSMZ, Braunschweig, Germany). Positive serological reactions were obtained with sap from inoculated N. benthamiana, L. esculentum, and N. clevelandii plants. The serological identification was confirmed using a reverse transcription-polymerase chain reaction (RT-PCR) with primers generated from a sequence of the RNA polymerase region of an isolate of PepMV reported in the United Kingdom (1). Sequence information obtained from the amplified fragment of the virus designated PepMV-PK (GenBank Accession No. DQ387870), showed only 81% nt identity and 89% amino acid identity with PepMV-SW (GenBank Accession No. DQ387869). PepMV isolates can be divided into three strains including European tomato, Peruvian, and US2 based on their genetic diversity (2). The PepMV-PK isolate resulted in nucleotide identities ranging from 79 to 81% with isolates of the European tomato strain (GenBank Accession Nos. AJ438767, AF340024, AF484251, AJ271991, AJ606359, and AJ290424), 81% with the Peruvian strain (GenBank Accession Nos. AM109896 and AJ606361), and 78% identity with each of the U.S. isolates US1 (GenBank Accession No. AY509926) and US2 (GenBank Accession No. AY509927). These results show that the new Polish isolate is distinct from all other PepMV isolates reported to date. References: (1) C. J. French et al. Plant Dis. 85:1121, 2001. (2) L. Pagan et al. Phytopathology 96:274, 2006. (3) H. Pospieszny et al. Phytopathol. Pol. 26:91, 2002.

scholarly journals First Report of Cucumber mosaic virus in Garlic Mustard in Ohio

Plant Disease ◽  
2000 ◽  
Vol 84 (9) ◽  
pp. 1047-1047 ◽  
Author(s):  
M. J. Boehm ◽  
S. T. Nameth
Keyword(s):  
Cucumber Mosaic Virus ◽  
Mosaic Virus ◽  
Plant Species ◽  
Enzyme Linked Immunosorbent Assay ◽  
Garlic Mustard ◽  
Weed Species ◽  
Alternate Host ◽  
First Report ◽  
Molecular Weights ◽  
Symptomatic Tissue

Garlic mustard (Alliaria officinalis) is a common weed species associated with woodland borders, hedge rows, and suburban gardens. Garlic mustard plants expressing foliar symptoms of leaf mosaic and vein banding were collected from Franklin and Cuyahoga counties in Ohio. Analysis of symptomatic tissue using viral-associated double-stranded RNA (dsRNA) analysis on 5% polyacrylamide gels and stained with ethidium bromide resulted in the production of a banding profile (four dsRNA bands with molecular weights of 2.6, 2.0, 1.5, and 0.7 × 106 daltons) similar to that of Cucumber mosaic virus (CMV) (1). Symptomatic tissue suspected of being infected with CMV was analyzed with an indirect enzyme-linked immunosorbent assay (iELISA) employing commercially produced antiserum (Agdia Inc.) against the common strain of CMV antiserum confirmed the presence of CMV. Nonsymptomatic tissue reacted negatively to CMV. This is the first report of CMV in garlic mustard in Ohio. Due to the extensive range of this weed and the wide host range of CMV in ornamental and food-plant species, garlic mustard could serve as an alternate host for CMV in many commercially important plant species. Reference: (1) T. J. Morris et al. Plant Mol. Biol. Rep. 1:27–30, 1983.

scholarly journals Seed Transmission of Pepino mosaic virus and Efficacy of Tomato Seed Disinfection Treatments

Plant Disease ◽  
2007 ◽  
Vol 91 (10) ◽  
pp. 1250-1254 ◽  
Author(s):  
Maria del Carmen Córdoba-Sellés ◽  
Ana García-Rández ◽  
Ana Alfaro-Fernández ◽  
Concepción Jordá-Gutiérrez
Keyword(s):  
Seed Germination ◽  
Lycopersicon Esculentum ◽  
Mosaic Virus ◽  
Transmission Rate ◽  
Seed Transmission ◽  
Trisodium Phosphate ◽  
Enzyme Linked Immunosorbent Assay ◽  
Tomato Seed ◽  
Pepino Mosaic Virus ◽  
Seed Disinfection

Rates of seed transmission for Pepino mosaic virus (PepMV) were estimated in seedlings grown from seeds obtained from symptomatic tomato (Lycopersicon esculentum) fruits of plants naturally infected with the virus. The proportion of seeds infected with PepMV was at least 25% as estimated from enzyme-linked immunosorbent assay (ELISA) analysis of grouped seeds. The seeds from symptomatic fruits were planted, and seedlings at the cotyledon and transplant stage were assayed for PepMV by ELISA. Three of 168 seedlings grown from infected seeds were PepMV-positive, corresponding to a seed-to-seedling transmission rate of 1.84%. Various tomato seed treatments were evaluated for their ability to prevent seed transmission of PepMV. This virus was largely eradicated by immersing the seeds in 10% trisodium phosphate for 3 h. Although heat treatments of 24 h at 80°C and 48 h at 74°C eliminated PepMV in seedlings, these treatments did not eradicate the virus in whole seeds. The three treatments did not adversely affect seed germination. The results suggest that trisodium phosphate can be used to eradicate PepMV in tomato seed without hindering germination.

scholarly journals Reservoir Weed Hosts for Turnip mosaic virus in Iran

Plant Disease ◽  
2005 ◽  
Vol 89 (3) ◽  
pp. 339-339 ◽  
Author(s):  
Sh. Farzadfar ◽  
K. Ohshima ◽  
R. Pourrahim ◽  
A. R. Golnaraghi ◽  
S. Sajedi ◽  
...  
Keyword(s):  
Mosaic Virus ◽  
Plant Viruses ◽  
Turnip Mosaic Virus ◽  
Cauliflower Mosaic Virus ◽  
Universal Primers ◽  
Enzyme Linked Immunosorbent Assay ◽  
Natural Occurrence ◽  
Leaf Extracts ◽  
Chenopodium Amaranticolor ◽  
Weed Hosts

During the summer of 2003, weed samples of Rapistrum rugosum and Sisymbrium loeselii showing severe mosaic, malformation, and stunting were collected from cauliflower fields in Tehran Province of Iran. Using double-antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA) with specific polyclonal antibodies, the samples were tested for the presence of Beet western yellows virus, Cauliflower mosaic virus, Radish mosaic virus, Turnip crinkle virus, Turnip mosaic virus (TuMV) (DSMZ, Braunschweig, Germany), Cucumber mosaic virus, and Tobacco mosaic virus (Sanofi Diagnostics Pasteur, Marnes-La-Coquette, France). Leaf extracts were used for mechanical inoculation and they produced chlorotic local lesions on Chenopodium amaranticolor, necrotic lesions on leaves and shoot apex necrosis on Nicotiana glutinosa, leaf deformation, mosaic, and stunting on Petunia hybrida, and severe mosaic, distortion, and stunting on Brassica rapa. These symptoms were similar to those that were described previously for TuMV (4). ELISA results showed that the original leaf samples and inoculated indicator plants reacted positively with TuMV antibodies, but not with antibodies for any of the other viruses listed above. Also, reverse transcription-polymerase chain reaction of total RNA extracted from the collected leaf samples using the universal primers for potyviruses (3) resulted in the amplification of two fragments of the expected sizes, approximately 700 and 1,700 bp. TuMV, a member of the genus Potyvirus in the family Potyviridae, is transmitted by aphids in a nonpersistent manner (4). This virus is geographically widespread with a wide host range that can infect 318 species in 156 genera of 43 plant families including, Brassicaceae, Chenopodiaceae, Asteraceae, Cucurbitaceae, and Solanaceae (2,4). R. rugosum and S. loeselii, two annual or biennial plants in the Brassicaceae family, were common and widely distributed in the fields surveyed. The presence of TuMV-infected weed hosts in cauliflower fields may impact disease management strategies. TuMV was first observed on stock plants (Matthiola sp.) in Iran (1). To our knowledge, this is the first report of natural occurrence of TuMV on weed hosts in Iran. References: (1) M. Bahar et al. Iran. J. Plant Pathol. 21:11, 1985. (2) J. R. Edwardson and R. G. Christie. The potyvirus group. Fla. Agric. Exp. Stn. Monogr. Ser. No. 16, 1991. (3) A. Gibbs and A. Mackenzie. J. Virol. Methods 63:9, 1997. (4) J. A. Tomlinson. Turnip mosaic virus. No. 8 in: Descriptions of Plant Viruses. CMI/AAB, Surrey, England, 1970.

Viruses infecting winter tomato crops in the North West Frontier Province of Pakistan

2002 ◽  
Vol 53 (3) ◽  
pp. 333 ◽  
Author(s):  
A. Ali ◽  
S. Hassan
Keyword(s):  
Mosaic Virus ◽  
Potato Virus ◽  
Potato Virus X ◽  
Tomato Mosaic Virus ◽  
Enzyme Linked Immunosorbent Assay ◽  
Weed Species ◽  
Tomato Production ◽  
North West ◽  
The North ◽  
North West Frontier Province

Malakand Agency is a unique production area in the North West Frontier Province (NWFP) of Pakistan that is frost-free and in which tomato is grown as a winter crop. Tomato production in this area has been affected by virus-like diseases for the last 10 years. Tomato nurseries and fields at 11 locations in Malakand Agency were surveyed for tomato viruses during 1994–95. A total of 1071 samples from nurseries and 5083 samples from 142 fields were tested by indirect enzyme-linked immunosorbent assay (ELISA). In nurseries, 3 viruses, Potato virus X (PVX), Potato virus Y (PVY), and Tomato mosaic virus (ToMV), were detected with an incidence range of 9.8–22.3, 0–36.6, and 16.5–51.3%, respectively. In the field, 5 viruses [Cucumber mosaic virus (CMV), PVX, PVY, ToMV, and Tomato yellow top virus (TYTV)] were frequently found with an incidence range of 0–13.3%, 2.6–16.7%, 0.4–13.8%, 26.1–41.3%, and 1.7–11.3%, respectively. All 5 viruses except TYTV were also detected from weed species in tomato fields or in the nearby vicinity. Of 12 commercial tomato varieties screened against CMV, PVX, PVY, and ToMV, 2 varieties (Florist and Forset) were resistant to 4 of the viruses including ToMV, for which the highest incidence was recorded in nurseries and field. These 2 varieties represent a previously undescribed and potentially useful source of resistance to the 4 inoculated viruses.

scholarly journals Occurrence, Distribution and Properties of Alfalfa Mosaic Virus

2002 ◽  
Vol 7 (1) ◽  
pp. 47
Author(s):  
A.D. Zadjaii ◽  
A.R. Matrooshi ◽  
S.M. Moghal
Keyword(s):  
Mosaic Virus ◽  
Thermal Inactivation ◽  
Aphis Gossypii ◽  
Alfalfa Mosaic Virus ◽  
Weed Species ◽  
High Concentration ◽  
Ammi Majus ◽  
Thermal Inactivation Point ◽  
Heliotropium Europaeum

Alfalfa Mosaic Virus (AlflMV) was recorded on 21 hosts comprising of four field crops, 14 vegetables, one ornamental plant and two new weed species (Heliotropium europaeum and Ammi majus) belonging to nine families. The virus was identified and confirmed on the basis of its biological, serological (ELISA) and physical properties. The leaves, stem and crown from systemically infected alfalfa plant contained high concentration of the virus. It was nonpersistently transmitted by cotton aphids (Aphis gossypii). The wide host range, including virus reservoirs, seed-borne infection and insect transmission account for high incidence and distribution of AlfMV in the country. The virus isolate had a dilution end point between 1 x 10-3 to l x 10-4, 65-67 °C thermal inactivation point and a few days in-vitro longevity and appears to be similar to the AlfMV-S strain.  

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