2018
DOI: 10.1016/j.cropro.2018.01.017
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Revealing new information from existing genomic data for pepper mild mottle virus pathotype determination

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Cited by 4 publications
(7 citation statements)
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“…Belonging to the Virgaviridae family and Tobamovirus genus, this pepper plant pathogen is transmitted via mechanical contact with contaminated soil and/or seed and causes fruit malformation and leaf mosaic in Capsicum species throughout Asia, Australia, Europe, Middle East, and North and South America (Adkins et al, 2001, Ahmad et al, 2015, Alonso et al, 1991, Beczner et al, 1997, Çağlar et al, 2013, Garcia-Luque et al, 1993, Genda et al, 2007, Han et al, 2017, Ichiki et al, 2009, Kaur et al, 2014, Milošević et al, 2015, Oliveira et al, 2010, Wang et al, 2006, Wetter et al, 1984, Yu et al, 2018). PMMoV has a 6,356 bp genome that encodes for a capsid, two replication-associated proteins (126 kDa and 183 kDa), and a cell-to-cell movement-associated protein (Banović Đeri et al, 2018, Oliveira et al, 2010). Given the limited genetic variability of PMMoV, it has been suggested that the PMMoV genome is highly stable (Rodriguez-Cerezo et al, 1989) and limited sequence variation has been observed among geographic regions (Yu et al, 2018).…”
Section: Pepper Mild Mottle Virus Ecology and Its Origin In Human Fecesmentioning
confidence: 99%
“…Belonging to the Virgaviridae family and Tobamovirus genus, this pepper plant pathogen is transmitted via mechanical contact with contaminated soil and/or seed and causes fruit malformation and leaf mosaic in Capsicum species throughout Asia, Australia, Europe, Middle East, and North and South America (Adkins et al, 2001, Ahmad et al, 2015, Alonso et al, 1991, Beczner et al, 1997, Çağlar et al, 2013, Garcia-Luque et al, 1993, Genda et al, 2007, Han et al, 2017, Ichiki et al, 2009, Kaur et al, 2014, Milošević et al, 2015, Oliveira et al, 2010, Wang et al, 2006, Wetter et al, 1984, Yu et al, 2018). PMMoV has a 6,356 bp genome that encodes for a capsid, two replication-associated proteins (126 kDa and 183 kDa), and a cell-to-cell movement-associated protein (Banović Đeri et al, 2018, Oliveira et al, 2010). Given the limited genetic variability of PMMoV, it has been suggested that the PMMoV genome is highly stable (Rodriguez-Cerezo et al, 1989) and limited sequence variation has been observed among geographic regions (Yu et al, 2018).…”
Section: Pepper Mild Mottle Virus Ecology and Its Origin In Human Fecesmentioning
confidence: 99%
“…Given that any of the evolutionary prediction models we are building is as good as the starting datasets and underlying bioinformatics algorithms are, securing a critical amount of relevant data is essential for any credible prediction. Besides mutations leading to amino acid replacements, synonymous nucleotide changes may also contribute to different viral pathogenicity levels, as was already shown for another positive-sense single-stranded RNA virus [30]. Therefore, all detected nucleotide changes, even the silent ones, should be taken into account when conducting data mining analysis and viral genotype−phenotype association SARS-CoV-2 studies.…”
Section: Discussionmentioning
confidence: 97%
“…A single amino acid mutation of asparagine to methionine at the 138th position (N138M) of the PMMoV-I isolate was sufficient to induce a hypersensitive response (HR) and localization of the virus in C. chinense plants with the L 3 gene (106). This mutation (N138M) is observed in all PMMoV isolates characterized as P 123 pathotypes (18,78,106,111). The mutations in PMMoV CP at the 7th position from alanine to serine (A7S), and the 81st position from serine to alanine (S81A) had L 3 -mediated resistance-inducing and -breaking abilities, respectively (112).…”
Section: Pathotypes Of Pmmov and The Role Of Viral Coat Protein In Th...mentioning
confidence: 98%
“…For instance, EcoRI restriction digestion of 836 bp amplicons of PMMoV-S genome (P 12 ) and PMMoV-Ia (P 123 ) genome obtained using primer pair P12/3 and P12/3A revealed two fragments of 260 and 570 bp, respectively, from the genome of PMMoV-Ia, whereas only a single fragment was obtained for PMMoV-S (65). The available genomic data of PMMoV were mined for identifying the informative sites in PMMoV genome for its pathotype determination (18). The findings indicate that the nucleotide composition at positions 552, 565, 639, 666, 708, 5921, 5975, and 6002 can serve as a reliable marker for distinguishing three PMMoV pathotypes, viz., P 12 , P 123 , and P 1234 (18).…”
Section: Pathotypes Of Pmmov and The Role Of Viral Coat Protein In Th...mentioning
confidence: 99%
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