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231225s2006 xx |||||o 00| ||eng c |
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|a 10.1094/PD-90-1458A
|2 doi
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|a pubmed24n0980.xml
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|a (NLM)30780917
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|a DE-627
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|c DE-627
|e rakwb
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| 041 |
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|a eng
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| 100 |
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|a Pérez-Moreno, L
|e verfasserin
|4 aut
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|a First Report of Leek yellow stripe virus in Garlic in the State of Guanajuato, Mexico
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| 264 |
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|c 2006
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| 336 |
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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| 338 |
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|a ƒa Online-Ressource
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|2 rdacarrier
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|a Date Revised 20.11.2019
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|a published: Print
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|a Citation Status PubMed-not-MEDLINE
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|a Garlic (Allium sativum L.) can be affected by a virus complex (1) consisting of two potyviruses, Onion yellow dwarf virus (OYDV) and Leek yellow stripe virus (LYSV), and two carlaviruses, Garlic common latent virus (GCLV) and Shallot latent virus (SLV) (1). To identify the components of the virus complex that could be present in garlic plants in Guanajuato State, which is the second largest garlic producer in the country and where presumptive viral symptoms were initially observed in December 2004, a survey was carried out in six locations: San Miguel de Allende and San Luis de la Paz in northern Guanajuato; Irapuato and Villagrán in the central region; and Salamanca and Valle de Santiago in the southern part of the state. Enzyme-linked immunosorbent assay (ELISA) was carried out to detect LYSV, OYDV, GCLV, and SLV in 195 garlic leaf samples collected during January 2005 from plants with leaf yellow stripe, mosaic, enation, deformation, or dwarfism symptoms. A set of primers, previously reported and specific to the coat protein cistron of LYSV (1), were synthesized and used in a reverse transcriptase-polymerase chain reaction (RT-PCR). The amplified product (1,020 nucleotides) was cloned into plasmid pGEM T-Easy (Promega, Madison, WI) and sequenced (Gen-bank Accession No. DQ841554). Sequence analysis showed that the cloned DNA fragment shared 97% similarity with the coat protein cistron of LYSV isolate no. 3 from Okinawa (GenBank Accession No. AB194632). The fragment was then radioactively labelled and used as a probe in the RNA blot analysis of all samples to confirm the ELISA results of LYSV. Of the 195 samples, 64 tested positive by RNA blot analysis. Forty-one of these were also positive by ELISA for LYSV. Preliminary, positive ELISA results were also obtained for OYDV, GCLV and SLV. To our knowledge, this is the first report of LYSV in the State of Guanajuato and in Mexico. The correct identification of viruses present in garlic will help to use the appropriate strategies to reduce viral incidence in this garlic-producing region. Reference: (1) T. V. M. Fajardo et al. Fitopatol. Bras. 26:619, 2001
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|a Journal Article
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|a Córdova-Rosales, Z
|e verfasserin
|4 aut
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|a Barboza-Corona, E
|e verfasserin
|4 aut
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|a Ramírez-Malagón, Rafael
|e verfasserin
|4 aut
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| 700 |
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|a Ramírez-Lúa, J
|e verfasserin
|4 aut
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| 700 |
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|a Ruiz-Castro, S
|e verfasserin
|4 aut
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| 700 |
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|a Silva-Rosales, L
|e verfasserin
|4 aut
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| 773 |
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|i Enthalten in
|t Plant disease
|d 1997
|g 90(2006), 11 vom: 01. Nov., Seite 1458
|w (DE-627)NLM098181742
|x 0191-2917
|7 nnns
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| 773 |
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|g volume:90
|g year:2006
|g number:11
|g day:01
|g month:11
|g pages:1458
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|u http://dx.doi.org/10.1094/PD-90-1458A
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