2018
DOI: 10.1007/s00705-018-3838-2
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Identification and molecular characterization of a novel varicosa-like virus from red clover

Abstract: During aetiological study of diseased red clover (Trifolium pratense L.) using high throughput sequencing, a novel virus with a 10 kb genome divided into two segments was discovered. The virus, tentatively named red clover associated varicosavirus (RCaVV), is phylogenetically related to classifiable members of the genus Varicosavirus (family Rhabdoviridae, order Mononegavirales). Analysis of mRNA levels from the individual RCaVV genes suggested possible differences in transcription regulation between rhabdovir… Show more

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Cited by 20 publications
(34 citation statements)
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“…A considerable disadvantage of growing clover is its limited persistence, due in large measure to its susceptibility to viral and phytoplasma diseases (Edwardson & Christie, ; Taylor & Quesenberry, ; Fránová et al , ; Jones, ). More than 30 viruses are known to infect red clover (Edwardson & Christie, ), and this list could certainly be extended with further discoveries (Fránová et al , ; Fránová & Jakešová, ; Koloniuk & Fránová, ; Lenz et al , ; Koloniuk et al , ,).…”
Section: Introductionmentioning
confidence: 99%
“…A considerable disadvantage of growing clover is its limited persistence, due in large measure to its susceptibility to viral and phytoplasma diseases (Edwardson & Christie, ; Taylor & Quesenberry, ; Fránová et al , ; Jones, ). More than 30 viruses are known to infect red clover (Edwardson & Christie, ), and this list could certainly be extended with further discoveries (Fránová et al , ; Fránová & Jakešová, ; Koloniuk & Fránová, ; Lenz et al , ; Koloniuk et al , ,).…”
Section: Introductionmentioning
confidence: 99%
“…Missing sequence segments were obtained by PCR amplification using the Q5 High-Fidelity Master Mix (NEB, Ipswich, MA, USA). The 5′-termini were completed and sequenced with a 5′ rapid amplification of complementary DNA (cDNA) ends (RACE) kit (Invitrogen, Carlsbad, CA, USA), and the 3′-ends were derived as previously described [ 17 ]. Sequence verification and gap-filling were done through Sanger sequencing of PCR amplicons or cloned into a pGEM T-Easy vector system (Promega, Road Madison, WI, USA).…”
Section: Methodsmentioning
confidence: 99%
“…As shown in Figure 6, there were nine major components (1)(2)(3)(4)(5)(6)(7)(8)(9) in the T. pratense L. extract. After the use of methanol to denature the enzyme and dislodge the specifically bound compounds and the ultrasonication of the extract with COX-2-coated magnetic nanoparticles, two main peaks, 4 and 6, completely disappeared in the supernatant, while the peak area of 8 and 9 were significantly reduced.…”
Section: Analysis Of Binding Compounds From Trifolium Pratense L Extmentioning
confidence: 99%