Genetic dissection of the tissue-specific roles of type III effectors and phytotoxins in the pathogenicity ofPseudomonas syringaepv.syringaeto cherry

Abstract

AbstractWhen compared with other phylogroups (PGs) of thePseudomonas syringae (Ps)species complex,Pspv. syringaestrains within PG2 have a reduced repertoire of type III effectors (T3Es) but produce several phytotoxins. Effectors within the cherry pathogenPss9644 were grouped based on their frequency in strains fromPrunusas: the conserved effector locus (CEL) common to mostPspathogens; a CORE of effectors common to PG2; a set of PRUNUS effectors common to cherry pathogens; and a FLEXIBLE set of T3Es.Pss9644 also contains gene clusters for biosynthesis of toxins syringomycin/syringopeptin and syringolin A. After confirmation of virulence gene expression, mutants with a sequential series of T3E and toxin deletions were pathogenicity tested on wood, leaves and fruits of sweet cherry (Prunus avium) and leaves of ornamental cherry (Prunus incisa). The toxins had a key role in disease development in fruits but were less important in leaves and wood. An effectorless mutant retained some pathogenicity to fruit but not wood or leaves. Striking redundancy was observed amongst effector groups. The CEL effectors have important roles during the early-stages of leaf infection and acted synergistically with toxins in all tissues. Deletion of separate groups of T3Es had much more effect inPrunus incisathan in sweet cherry. Mixed inocula were used to complement the toxin mutationsin transand indicated that strain mixtures may be important in the field. Our results highlight the niche-specific role of toxins in cherry tissues and the complexity of effector redundancy in the pathogenPss9644.