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Molecular evolution of Pepino mosaic virus during long‐term passaging in different hosts and its impact on virus virulence
Author(s) -
Minicka J.,
Rymelska N.,
Elena S.F.,
Czerwoniec A.,
HasiówJaroszewska B.
Publication year - 2015
Publication title -
annals of applied biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.677
H-Index - 80
eISSN - 1744-7348
pISSN - 0003-4746
DOI - 10.1111/aab.12179
Subject(s) - biology , nonsynonymous substitution , virus , lineage (genetic) , genetics , virology , host (biology) , synonymous substitution , gene , mutation , negative selection , population , viral evolution , genome , demography , codon usage bias , sociology
In this study the effect of host changes and multiple passages on Pepino mosaic virus ( PepMV ) evolution was analysed. A population of a mild isolate of PepMV was used to generate five independent evolution lineages on three tomato cultivars, which differ in rate of appearance of symptoms and their severity during viral infection (Beta Lux, Moneymaker and Malinowy Ożarowski) and on Datura inoxia . Twenty serial passages were performed over a period of 217–220 days. Symptom severity was monitored along the entire experiment. After the last series of passages total RNAs from each lineage and host were isolated and the triple gene block 3 ( TGB3 ) and coat protein ( CP ) were amplified, cloned and 10 clones for each gene sequenced. Among the 400 clones for both genes, 143 individual mutations (61 synonymous and 82 nonsynonymous) were identified, with the largest number of nonsynonymous mutations being observed for the tomato cultivars Malinowy Ożarowski and Beta Lux. In two of the lineages evolving in the most susceptible variety of tomato (Beta Lux) necrotic changes in leaf blades appeared after 17 passages, leading to death of the plants. In these two lineages the mutation responsible for necrotic symptoms was K67E in TGB3 . The appearance of this convergent mutation in independently evolving lineages may suggest that selection in this experimental set up favours more aggressive PepMV variants. We found a positive association between the severity of symptoms and the amount of genetic variability contained on viral populations. Indeed, the severity of symptoms turned out to be a good predictor for several indices of molecular variability. In addition, mapping all observed mutations in CP and TGB3 protein structures revealed that most were located on the surface, indicating a possible implication in viral–viral or viral–host interactions.