Disease resistance in plants depends on a molecular dialogue with microbes that involves many known chemical effectors, but the time course of the interaction and the influence of the environment are largely unknown. The outcome of host-pathogen interactions is thought to reflect the offensive and defensive capabilities of both players. When plants interact with Pseudomonas syringae, several well-characterized virulence factors contribute to early bacterial pathogenicity, including the type III secretion system (T3SS), which must be activated by signals from the plant and environment to allow the secretion of virulence effectors. The manner in which these signals regulate T3SS activity is still unclear. Here, we strengthen the paradigm of the plant-pathogen molecular dialogue by addressing overlooked details concerning the timing of interactions, specifically the role of plant signals and temperature on the regulation of bacterial virulence during the first few hours of the interaction. Whole-genome expression profiling after 1 h revealed that the perception of plant signals from kiwifruit or tomato extracts anticipated T3SS expression in P. syringae pv. actinidiae compared to apoplast-like conditions, facilitating more efficient effector transport in planta, as revealed by the induction of a temperature-dependent hypersensitive response in the nonhost plant Arabidopsis thaliana Columbia-0 (Col-0). Our results show that in the arms race between plants and bacteria, the temperature-dependent timing of bacterial virulence versus the induction of plant defenses is probably one of the fundamental parameters governing the outcome of the interaction.

Puttilli M.R., Danzi D., Correia C., Brandi J., Cecconi D., Manfredi M., et al. (2022). Plant signals anticipate the induction of the type III secretion system in Pseudomonas syringae pv. actinidiae, facilitating efficient temperature-dependent effector translocation. MICROBIOLOGY SPECTRUM, 10(6), 1-15 [10.1128/spectrum.02073-22].

Plant signals anticipate the induction of the type III secretion system in Pseudomonas syringae pv. actinidiae, facilitating efficient temperature-dependent effector translocation

Spinelli F.
Conceptualization
;
2022

Abstract

Disease resistance in plants depends on a molecular dialogue with microbes that involves many known chemical effectors, but the time course of the interaction and the influence of the environment are largely unknown. The outcome of host-pathogen interactions is thought to reflect the offensive and defensive capabilities of both players. When plants interact with Pseudomonas syringae, several well-characterized virulence factors contribute to early bacterial pathogenicity, including the type III secretion system (T3SS), which must be activated by signals from the plant and environment to allow the secretion of virulence effectors. The manner in which these signals regulate T3SS activity is still unclear. Here, we strengthen the paradigm of the plant-pathogen molecular dialogue by addressing overlooked details concerning the timing of interactions, specifically the role of plant signals and temperature on the regulation of bacterial virulence during the first few hours of the interaction. Whole-genome expression profiling after 1 h revealed that the perception of plant signals from kiwifruit or tomato extracts anticipated T3SS expression in P. syringae pv. actinidiae compared to apoplast-like conditions, facilitating more efficient effector transport in planta, as revealed by the induction of a temperature-dependent hypersensitive response in the nonhost plant Arabidopsis thaliana Columbia-0 (Col-0). Our results show that in the arms race between plants and bacteria, the temperature-dependent timing of bacterial virulence versus the induction of plant defenses is probably one of the fundamental parameters governing the outcome of the interaction.
2022
Puttilli M.R., Danzi D., Correia C., Brandi J., Cecconi D., Manfredi M., et al. (2022). Plant signals anticipate the induction of the type III secretion system in Pseudomonas syringae pv. actinidiae, facilitating efficient temperature-dependent effector translocation. MICROBIOLOGY SPECTRUM, 10(6), 1-15 [10.1128/spectrum.02073-22].
Puttilli M.R.; Danzi D.; Correia C.; Brandi J.; Cecconi D.; Manfredi M.; Marengo E.; Santos C.; Spinelli F.; Polverari A.; Vandelle E.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/996389
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