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Symptom expression of yellow speckle disease was studied in a row of 32 individual Vitis vinifera cv. Chardonnay vines in the warmer summer of 2009/2010 as compared with the cooler summer of 2011/2012 in South Australia. RT-PCR analysis showed that all these vines were positive for hop stunt viroid, grapevine yellow speckle viroid 1 (GYSVd-1) and grapevine rupestris stem pitting-associated virus. Four vines named Vines 1, 8, 11 and 15 were selected for further analyses. Vines 1 and 8 had never shown yellow speckle (YS) symptoms, Vine 11 had always been symptomatic, and Vine 15 showed YS symptoms only in the summer of 2009/2010, but not in 2011/2012. Analysis of partial nucleotide (nt) sequence of GYSVd-1 from these vines showed two major sequence polymorphisms in the pathogenicity domain coinciding with the YS symptoms and the prevailing temperature in each season. One group designated UA group had a uridine (U) at position 309 and an adenine (A) at position 311, while another group designated AU group had the other way around: an "A" at position 309 and a "U" at position 311. The AU group had never been reported before. The AU group was a minor variant in the GYSVd-1 population and not present in symptomatic Vine 11. In contrast, the UA group was dominant and present in all the vine samples. Surprisingly, all the asymptomatic vines, but not symptomatic vines, had the signature of the AU group. Whether the AU group is associated with the YS symptom expression is interesting. Our result provides a new insight into the sequence variability of viroid-inducing symptoms during two significantly different growing seasons.
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http://dx.doi.org/10.1016/j.virusres.2014.03.028 | DOI Listing |
Pathogens
August 2025
Laboratory of Biotechnology and Molecular Genetics, M. Aitkhozhin Institute of Molecular Biology and Biochemistry, Almaty 050012, Kazakhstan.
Grapevine ( L.) cultivation is an important agricultural sector worldwide. Its expansion into new areas, like Kazakhstan, brings significant phytosanitary risks.
View Article and Find Full Text PDFTo date, the use of CRISPR/Cas9 technology in ecological-model species for validating genotype to phenotype connections has focused primarily on visual phenotypes using G mutations, coupled with analyses of resulting mosaic phenotypes. However, studies of physiological phenotypes necessitate germline mutations in order to assess non-visible phenotypic effects, and thus, dedicated efforts to develop efficient germline mutations in ecological model species are needed. Here, we applied the CRISPR/Cas9 technology to an ecological model species, the speckled wood butterfly ().
View Article and Find Full Text PDFPhytomedicine
August 2025
College of Life Science and Engineering, Southwest Jiaotong University, Chengdu 610031, China. Electronic address:
Background: Ischemic stroke induced irreversible damage or loss of neurons, severely causing high death rates. Natural medicine has rapidly risen for stroke therapy. Given the activation of neural cells, it is crucial to reveal the neuroregulation and molecular mechanisms of natural medicine for developing effective therapeutical approaches for stroke.
View Article and Find Full Text PDFArch Virol
September 2024
ICAR-Indian Agricultural Research Institute, New Delhi, 110012, India.
A novel grapevine viroid was discovered in an asymptomatic grapevine of Indian rootstocks. The whole genome sequence of the viroid (370 nt) was determined by high-throughput sequencing as well as RT-PCR followed by cloning and Sanger sequencing. The terminal conserved region (TCR), central conserved region (CCR) upper strand, and CCR lower strand are conserved regions found in the viroid that are unique to the members of the genus Apscaviroid.
View Article and Find Full Text PDFVirus Genes
December 2024
Institute for Plant Protection, National Agriculture and Food Research Organization (NARO), Akitsu, Higashihiroshima, Hiroshima, 739-2494, Japan.
Virome analysis was performed on 174 grape genetic resources from the National Agriculture and Food Research Organization, Japan. A total of 20 bulk samples was prepared by grouping the vines into batches of 6-10 plants. Each of the bulk samples was analyzed using high-throughput sequencing, which detected 27 viruses and 5 viroids, including six viruses and one viroid reported in Japan for the first time (grapevine viruses F, L, and T, grapevine Kizil Sapak virus, grapevine Syrah virus 1, grapevine satellite virus, and grapevine yellow speckle viroid 2).
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