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A functional Xop AG homologue in Xanthomonas fuscans pv. aurantifolii strain C limits host range
Author(s) -
Gochez A. M.,
Minsavage G. V.,
Potnis N.,
Canteros B. I.,
Stall R. E.,
Jones J. B.
Publication year - 2015
Publication title -
plant pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.928
H-Index - 85
eISSN - 1365-3059
pISSN - 0032-0862
DOI - 10.1111/ppa.12361
Subject(s) - biology , xanthomonas citri , xanthomonas , xanthomonas campestris , citrus paradisi , microbiology and biotechnology , citrus canker , strain (injury) , canker , virulence , botany , gene , pathogen , bacteria , genetics , rutaceae , anatomy
Citrus canker is caused by two Xanthomonas species, Xanthomonas citri , which has become the primary pathogen where citrus canker occurs (type A citrus canker, Xc‐A), and X. fuscans pv. aurantifolii (Xfa), which consists of strains B and C. The B strain is less pathogenic than the A strain, but produces symptoms in all citrus species. The C‐type cankers only infect Key lime ( Citrus aurantifolia ) and produce a hypersensitive reaction ( HR ) in grapefruit ( Citrus paradisi ) leaves. An avirulence gene, avrGf2 , was identified in a C strain that was responsible for the HR in grapefruit. AvrGf2 is a member of Xop AG effector family and shares 45% identity at amino acid level with another member of the same family, AvrGf1 from strain Xc‐A w , which was previously shown to elicit an HR in grapefruit. AvrGf2 shares sequence identity with other Xop AG effectors present in Xanthomonas vasculorum , Xanthomonas campestris pv. musacearum and Pseudomonas syringae pv. tomato . Mutagenesis of avrGf2 in C strain resulted in a compatible reaction in grapefruit. There was no observable effect on virulence when Xc‐A transconjugants containing either avirulence gene were inoculated on Key lime. Expression of avrGf1 or avrGf2 in Xc‐A resulted in a similar phenotype following infiltration into grapefruit leaves, although the avrGf2 transconjugant elicited a faster HR and lower populations than the transconjugant containing avrGf1 . Also, it was shown that all Xfa‐B strains tested contain a transposon in avrGf2 that helps to explain the differences in host range between B and C strains.