2010
DOI: 10.1186/1743-422x-7-275
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Analysis of a new strain of Euphorbia mosaic virus with distinct replication specificity unveils a lineage of begomoviruses with short Rep sequences in the DNA-B intergenic region

Abstract: BackgroundEuphorbia mosaic virus (EuMV) is a member of the SLCV clade, a lineage of New World begomoviruses that display distinctive features in their replication-associated protein (Rep) and virion-strand replication origin. The first entirely characterized EuMV isolate is native from Yucatan Peninsula, Mexico; subsequently, EuMV was detected in weeds and pepper plants from another region of Mexico, and partial DNA-A sequences revealed significant differences in their putative replication specificity determin… Show more

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Cited by 27 publications
(16 citation statements)
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“…New World BGVs are grouped in several secondary linages or "clades," such as the Squash leaf curl virus (SLCuV) clade, the Abutilon mosaic virus (AbMV) clade and the Brazil clade (Argüello-Astorga et al, 1994;Rojas et al, 2005). Members of the SLCuV clade display distinctive features in their replication origin, AC4 protein and N-terminal domain of their Rep protein (Argüello-Astorga et al, 1994;Gregorio-Jorge et al, 2010;Torres-Herrera et al, 2019). Legumoviruses and sweepoviruses are grouped by the host that they specifically infect.…”
Section: Introductionmentioning
confidence: 99%
“…New World BGVs are grouped in several secondary linages or "clades," such as the Squash leaf curl virus (SLCuV) clade, the Abutilon mosaic virus (AbMV) clade and the Brazil clade (Argüello-Astorga et al, 1994;Rojas et al, 2005). Members of the SLCuV clade display distinctive features in their replication origin, AC4 protein and N-terminal domain of their Rep protein (Argüello-Astorga et al, 1994;Gregorio-Jorge et al, 2010;Torres-Herrera et al, 2019). Legumoviruses and sweepoviruses are grouped by the host that they specifically infect.…”
Section: Introductionmentioning
confidence: 99%
“…Leaf samples of a variety of weeds exhibiting symptoms of virosis (e.g., leaf curling, yellowing, mosaics, interveinal chlorosis, growth stunting, and so on) were collected during the summer of 2007 in diverse localities of Yucatán and Morelos, México (See Section 2). The presence of BGVs was tested by PCR using a combination of both “universal” and “lineage-specific” primers designed to improve the detection of either S-Lin members or “typical” NW BGVs [30,34]. Nine out 16 examined samples produced amplicons of the expected size (~1.4 kb) with the pair of primers repSL-2150for/cpYMACrev, specific for detection of S-Lin members.…”
Section: Resultsmentioning
confidence: 99%
“…To increase the quantity of the field sample DNA, the extracts were subjected to rolling circle amplification (RCA) using the TempliPhi kit (GE Healthcare, Chicago, IL, USA). Polymerase chain reaction (PCR)-detection for begomoviruses was performed using Taq DNA Polymerase master mix (New England BioLabs, USA) and paired sets of lineage-specific primers, repSL2150for/cpYMAC-rev [30] and repDGR-for/cpYMAC-rev [34]. The PCR products were cloned in pGem-T Easy vector system (Promega, Madison, WI, USA).…”
Section: Methodsmentioning
confidence: 99%
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“…The DNA-A was amplified by PCR using two pairs of primers that produce amplicons overlapping along a ~520-bp segment, and that jointly encompass the full A genomic component. The DNA-B was PCR amplified using two sets of degenerate primers, BC1-290rev/BV1-310for and BC1-290for/BV1-470-rev, as previously described [37]; the latter primers are complementary to conserved sequences in the B genomic component of New World BGVs. The amplicons were cloned into pGEM-T Easy Vector (Promega) and analysed in restriction fragment length polymorphism (RFLP) assays using EcoRI and HinfI endonucleases.…”
Section: Methodsmentioning
confidence: 99%