TY - JOUR
T1 - Genetic rearrangements in Pseudomonas amygdali pathovar aesculi shape coronatine plasmids
AU - Nielsen, Tue Kjærgaard
AU - Winther-Have, Caroline S.
AU - Thomsen, Iben Margrete
AU - Jackson, Robert W.
AU - Rabiey, Mojgan
AU - Hennessy, Rosanna Catherine
AU - Bak, Frederik
AU - Kot, Witold
AU - Nicolaisen, Mette Haubjerg
AU - Carstens, Alexander Byth
AU - Hansen, Lars Hestbjerg
N1 - Publisher Copyright:
© 2023
PY - 2023
Y1 - 2023
N2 - Plant pathogenic Pseudomonas species use multiple classes of toxins and virulence factors during host infection. The genes encoding these pathogenicity factors are often located on plasmids and other mobile genetic elements, suggesting that they are acquired through horizontal gene transfer to confer an evolutionary advantage for successful adaptation to host infection. However, the genetic rearrangements that have led to mobilization of the pathogenicity genes are not fully understood. In this study, we have sequenced and analyzed the complete genome sequences of four Pseudomonas amygdali pv. aesculi (Pae), which infect European horse chestnut trees (Aesculus hippocastanum) and belong to phylogroup 3 of the P. syringae species complex. The four investigated genomes contain six groups of plasmids that all encode pathogenicity factors. Effector genes were found to be mostly associated with insertion sequence elements, suggesting that virulence genes are generally mobilized and potentially undergo horizontal gene transfer after transfer to a conjugative plasmid. We show that the biosynthetic gene cluster encoding the phytotoxin coronatine was recently transferred from a chromosomal location to a mobilizable plasmid that subsequently formed a co-integrate with a conjugative plasmid.
AB - Plant pathogenic Pseudomonas species use multiple classes of toxins and virulence factors during host infection. The genes encoding these pathogenicity factors are often located on plasmids and other mobile genetic elements, suggesting that they are acquired through horizontal gene transfer to confer an evolutionary advantage for successful adaptation to host infection. However, the genetic rearrangements that have led to mobilization of the pathogenicity genes are not fully understood. In this study, we have sequenced and analyzed the complete genome sequences of four Pseudomonas amygdali pv. aesculi (Pae), which infect European horse chestnut trees (Aesculus hippocastanum) and belong to phylogroup 3 of the P. syringae species complex. The four investigated genomes contain six groups of plasmids that all encode pathogenicity factors. Effector genes were found to be mostly associated with insertion sequence elements, suggesting that virulence genes are generally mobilized and potentially undergo horizontal gene transfer after transfer to a conjugative plasmid. We show that the biosynthetic gene cluster encoding the phytotoxin coronatine was recently transferred from a chromosomal location to a mobilizable plasmid that subsequently formed a co-integrate with a conjugative plasmid.
KW - Coronatine
KW - Mobile genetic elements
KW - Nanopore sequencing
KW - Phytotoxins
KW - Plant pathogens
KW - Plasmid
KW - Pseudomonas
KW - Virulence
U2 - 10.1016/j.meegid.2023.105486
DO - 10.1016/j.meegid.2023.105486
M3 - Journal article
C2 - 37541538
AN - SCOPUS:85166959238
VL - 113
JO - Infection, Genetics and Evolution
JF - Infection, Genetics and Evolution
SN - 1567-1348
M1 - 105486
ER -