4.5 Article

Mutagenesis Scanning Uncovers Evolutionary Constraints on Tobacco Etch Potyvirus Membrane-Associated 6K2 Protein

期刊

GENOME BIOLOGY AND EVOLUTION
卷 11, 期 4, 页码 1207-1222

出版社

OXFORD UNIV PRESS
DOI: 10.1093/gbe/evz069

关键词

bulk selection; mutagenesis; Potyvirus; TEV; virulence; virus fitness

资金

  1. Spanish Agencia Estatal de Investigacion - FEDER [BFU2015-65037-P]
  2. Generalitat Valenciana [PROMETEOII/2014/021]
  3. European Research Council Consolidator grant [616434]
  4. Spanish Ministry of Economy and Competitiveness [BFU2011-2606, SEV-2012-0208]
  5. AXA Research Fund
  6. Bettencourt Schueller Foundation
  7. Agencia de Gestio d'Ajuts Universitaris i Recerca [SGR-831]
  8. CRG Systems Biology Program
  9. CERCA Program (Generalitat de Catalunya)
  10. China Scholarship Council
  11. Chinese Academy of Agricultural Sciences
  12. Fundacion Ramon Areces
  13. CRG fellowships
  14. European Research Council (ERC) [616434] Funding Source: European Research Council (ERC)

向作者/读者索取更多资源

RNA virus high mutation rate is a double-edged sword. At the one side, most mutations jeopardize proteins functions; at the other side, mutations are needed to fuel adaptation. The relevant question then is the ratio between beneficial and deleterious mutations. To evaluate this ratio, we created a mutant library of the 6K2 gene of tobacco etch potyvirus that contains every possible single-nucleotide substitution. 6K2 protein anchors the virus replication complex to the network of endoplasmic reticulum membranes. The library was inoculated into the natural host Nicotiana tabacum, allowing competition among all these mutants and selection of those that are potentially viable. We identified 11 nonsynonymous mutations that remain in the viral population at measurable frequencies and evaluated their fitness. Some had fitness values higher than the wild-type and some were deleterious. The effect of these mutations in the structure, transmembrane properties, and function of 6K2 was evaluated in silico. In parallel, the effect of these mutations in infectivity, virus accumulation, symptoms development, and subcellular localization was evaluated in the natural host. The alpha-helixH1 in the N-terminal part of 6K2 turned out to be under purifying selection, while most observed mutations affect the link between transmembrane alpha-helices H2 and H3, fusing them into a longer helix and increasing its rigidity. In general, these changes are associated with higher within-host fitness and development of milder or no symptoms. This finding suggests that in nature selection upon 6K2 may result from a tradeoff between within-host accumulation and severity of symptoms.

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