4.8 Article

Repeated gain and loss of a single gene modulates the evolution of vascular plant pathogen lifestyles

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SCIENCE ADVANCES
卷 6, 期 46, 页码 -

出版社

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/sciadv.abc4516

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资金

  1. NSF Postdoctoral Fellowship in Biology [1306196]
  2. U.S. Fulbright Scholar Award
  3. USDA NIFA Postdoctoral Fellowship [2017-67012-26116]
  4. COST SUSTAIN travel grant
  5. USDA NIFA through NSF/NIFA Plant Biotic Interactions Program [2018-67013-28490]
  6. NSF [DEB-1638999]
  7. Fonds de Recherche du Quebec-Nature et Technologies Doctoral Research Scholarship
  8. NEPHRON project [ANR-18-CE20-0020-01]
  9. University Grants Commission of India
  10. J. C. Bose Fellowship
  11. French Ministry of National Education and Research
  12. TULIP LabEx [ANR-10LABX-41, ANR-11-IDEX-0002-02]
  13. Science and Engineering Research Board, Government of India [SB/52/JCB-12/2014]
  14. COST (European Cooperation in Science and Technology) [CA16107 EuroXanth]
  15. U.S. Department of Energy (DOE) [DE-AC36-08GO28308]
  16. U.S. Department of Energy Office of Energy Efficiency and Renewable Energy Bioenergy Technologies Office
  17. Div Of Biological Infrastructure
  18. Direct For Biological Sciences [1306196] Funding Source: National Science Foundation

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Vascular plant pathogens travel long distances through host veins, leading to life-threatening, systemic infections. In contrast, nonvascular pathogens remain restricted to infection sites, triggering localized symptom development. The contrasting features of vascular and nonvascular diseases suggest distinct etiologies, but the basis for each remains unclear. Here, we show that the hydrolase CbsA acts as a phenotypic switch between vascular and nonvascular plant pathogenesis. cbsA was enriched in genomes of vascular phytopathogenic bacteria in the family Xanthomonadaceae and absent in most nonvascular species. CbsA expression allowed nonvascular Xanthomonas to cause vascular blight, while cbsA mutagenesis resulted in reduction of vascular or enhanced nonvascular symptom development. Phylogenetic hypothesis testing further revealed that cbsA was lost in multiple nonvascular lineages and more recently gained by some vascular subgroups, suggesting that vascular pathogenesis is ancestral. Our results overall demonstrate how the gain and loss of single loci can facilitate the evolution of complex ecological traits.

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