TY - JOUR
T1 - Repeated gain and loss of a single gene modulates the evolution of vascular plant pathogen lifestyles
AU - Gluck-Thaler, Emile
AU - Cerutti, Aude
AU - Perez-Quintero, Alvaro L.
AU - Butchacas, Jules
AU - Roman-Reyna, Verónica
AU - Madhavan, Vishnu Narayanan
AU - Shantharaj, Deepak
AU - Merfa, Marcus V.
AU - Pesce, Céline
AU - Jauneau, Alain
AU - Vancheva, Taca
AU - Lang, Jillian M.
AU - Allen, Caitilyn
AU - Verdier, Valerie
AU - Gagnevin, Lionel
AU - Szurek, Boris
AU - Beckham, Gregg T.
AU - De La Fuente, Leonardo
AU - Patel, Hitendra Kumar
AU - Sonti, Ramesh V.
AU - Bragard, Claude
AU - Leach, Jan E.
AU - Noël, Laurent D.
AU - Slot, Jason C.
AU - Koebnik, Ralf
AU - Jacobs, Jonathan M.
N1 - Publisher Copyright:
Copyright © 2020 The Authors, some rights reserved.
PY - 2020/11/13
Y1 - 2020/11/13
N2 - 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.
AB - 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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U2 - 10.1126/sciadv.abc4516
DO - 10.1126/sciadv.abc4516
M3 - Article
C2 - 33188025
AN - SCOPUS:85096153648
SN - 2375-2548
VL - 6
JO - Science Advances
JF - Science Advances
IS - 46
M1 - eabc4516
ER -