Bacterial Infection Disrupts Clock Gene Expression to Attenuate Immune Responses

ROMANOWSKI, ANDRÉS; SUN, HEQUAN; SCHNEEBERGER, KORBINIAN; HERNANDO, C. ESTEBAN; SOVERNA, ANA FAIGÓN; DE LEONE, MARÍA JOSÉ; VÁZQUEZ, MARTÍN; CARENO, DANIEL A.; BOLOGNA, NICOLÁS G.; YANOVSKY, MARCELO J.

CURRENT BIOLOGY

CELL PRESS

Año: 2020 vol. 30 p. 1740 - 1747

0960-9822

The circadian clock modulates immune responses in plants and animals; however, it is unclear how host-pathogen interactions affect the clock. Here we analyzed clock function in Arabidopsis thaliana mutants with defective immune responses and found that enhanced disease susceptibility 4 ( eds4) displays alterations in several circadian rhythms. Mapping by sequencing revealed that EDS4 encodes the ortholog of NUCLEOPORIN 205, a core component of the inner ring of the nuclear pore complex (NPC). Consistent with the idea that the NPC specifically modulates clock function, we found a strong enrichment in core clock genes, as well as an increased nuclear to total mRNA accumulation, among genes that were differentially expressed in eds4 mutants. Interestingly, infection with Pseudomonas syringae in wild-type (WT) plants downregulated the expression of several morning core clock genes as early as 1 h post-infection, including all members of the NIGHT LIGHT-INDUCIBLE AND CLOCK-REGULATED ( LNK) gene family, and this effect was attenuated in eds4. Furthermore, lnk mutants were more susceptible than the WT to P. syringae infection. These results indicate that bacterial infection, acting in part through the NPC, alters core clock gene expression and/or mRNA accumulation in a way that favors bacterial growth and disease susceptibility.