2020
DOI: 10.1007/s42161-020-00668-2
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First report of grapevine virus L in grapevine in Turkey

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Cited by 3 publications
(6 citation statements)
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“…Son yıllarda (2010'lu yıllardan sonra) uluslararası çalışmalara paralel olarak yeni belirlenen bağ virüslerinin (GVB; GVD; GVL; GPGV; GRLDaV; GRSPaV, GSyV-1 gibi) ve bağları enfekte eden diğer bir viroid olan AGVd'nin teşhisleri, hassas ve güvenilir teknikler kullanılarak bu zaman diliminde gerçekleştirilmiştir [47,18,37,17,24,74,16,72,75,44]. Moleküler çalışmaların yanında [30], serolojik çalışmalara da devam edilmiştir [45,61,73].…”
Section: Türkiye'de Asma Virüs çAlışmalarının Tarihsel Gelişimi Ve Karşılaşılan Sorunlarunclassified
“…Son yıllarda (2010'lu yıllardan sonra) uluslararası çalışmalara paralel olarak yeni belirlenen bağ virüslerinin (GVB; GVD; GVL; GPGV; GRLDaV; GRSPaV, GSyV-1 gibi) ve bağları enfekte eden diğer bir viroid olan AGVd'nin teşhisleri, hassas ve güvenilir teknikler kullanılarak bu zaman diliminde gerçekleştirilmiştir [47,18,37,17,24,74,16,72,75,44]. Moleküler çalışmaların yanında [30], serolojik çalışmalara da devam edilmiştir [45,61,73].…”
Section: Türkiye'de Asma Virüs çAlışmalarının Tarihsel Gelişimi Ve Karşılaşılan Sorunlarunclassified
“…GVL is a newly identified member of the genus Vitivirus whose genome sequence was first identified in publicly available RNAseq libraries of grapevine samples from China, Croatia, USA (a Canadian grapevine sample), and New Zealand [3]. Since then, additional GVL isolates from grapevine samples from the USA (California and Texas) [13,14], Tunisia [15], Turkey [16], South Africa [17], Korea [18], and France [19] have been characterized. The GVL genome is 7,607 nt long and has a genome organization that is typical of members of the genus Vitivirus.…”
mentioning
confidence: 99%
“…For confirmation of the presence of GVL in single and composite samples, total RNA was extracted from leaf, petiole, or phloem tissue scrapings of each sample (depending on the sampling season), using the extraction method described above and the one-step reverse transcription polymerase chain reaction (RT-PCR) procedure described by Ilbagi et al [16], using a set of primers (GVL_F_6750/ GVL_R_6938, Table 1) that amplify a 189-bp-long fragment of the GVL CP gene (ORF4). One GVL isolate that was detected using the above reaction in all of the composite samples analyzed by HTS (GB15 from pool GeA, X10 from pool XA, and Ks14 from PKs1) and in the two isolates retrieved from the individual samples analyzed by HTS (AG-1 and AUTH69) were selected for confirmation of a larger part of the genome sequence by Sanger sequencing.…”
mentioning
confidence: 99%
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