comprises a group of filamentous plant pathogens that cause serious crop diseases worldwide. It is widely known that a complex effector repertoire was secreted by pathogens to manipulate plant immunity and determine resistance and susceptibility. It is also recognized that pathogens may inhabit natural niches within complex environmental microbes, including bacteria. However, how pathogens interact with their cohabited microbes remains poorly understood. Here, we present such an intriguing case by using -bacteria interaction as a working system. We found that under co-culture laboratory conditions, several pathogens appeared to block the contact of an ecologically relevant bacterium, including and a model ... More
comprises a group of filamentous plant pathogens that cause serious crop diseases worldwide. It is widely known that a complex effector repertoire was secreted by pathogens to manipulate plant immunity and determine resistance and susceptibility. It is also recognized that pathogens may inhabit natural niches within complex environmental microbes, including bacteria. However, how pathogens interact with their cohabited microbes remains poorly understood. Here, we present such an intriguing case by using -bacteria interaction as a working system. We found that under co-culture laboratory conditions, several pathogens appeared to block the contact of an ecologically relevant bacterium, including and a model bacterium, . We further observed that utilizes a conserved Crinkler (CRN) effector protein, PsCRN63, to impair bacterial growth. deploys another CRN effector, PcCRN173, to interfere with bacterial flagellum- and/or type IV pilus-mediated motility whereas a -derived RxLR effector, PcAvh540, inhibits bacterial swimming motility, but not twitching motility and biofilm formation, suggesting functional diversification of effector-mediated -bacteria interactions. Thus, our studies provide a first case showing that the filamentous pathogens could deploy effectors to interfere with bacterial growth and motility, revealing an unprecedented effector-mediated inter-kingdom interaction between pathogens and bacterial species and thereby uncovering ecological significance of effector proteins in filamentous plant pathogens besides their canonical roles involving pathogen-plant interaction.
