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bioRxiv · 10.64898/2026.07.27.741084

Solanum americanum Bs2 and ZAR1 homologs recognize Xanthomonas euvesicatoria effectors essential for infection.

Abstract

Multiple recognition events of pathogen-secreted effectors by immune receptors confer robust disease resistance in plants. Understanding the underlying mechanisms facilitates the discovery and deployment of valuable resistance genes for crop protection. Xanthomonas euvesicatoria causes devastating bacterial spot disease in solanaceous crops but cannot infect the wild relative Solanum americanum. Here, we identified X. euvesicatoria type III effectors (T3Es) that induce cell death in S. americanum when transiently expressed in leaf. By quantifying immune responses of the S. americanum SP2273 accession to X. euvesicatoria multiple-T3E knockout mutants, we demonstrated that at least nine T3Es (AvrBs2, XopAP, XopAU, XopE1, XopJ3, XopM, XopN, XopX, and XopZ1) collectively contribute to effector-triggered immunity (ETI). Among these, AvrBs2 and XopJ3 were the primary drivers of ETI, eliciting robust cell death and defense gene expression when naturally delivered into plant cells. We next generated S. americanum lines concomitantly edited at the corresponding immune receptor loci, SaBs2 and SaZAR1 (SP2273-bz). Genetic complementation of SP2273-bz confirmed that AvrBs2 and XopJ3 are specifically recognized by each of the four SaBs2 homologs and by SaZAR1, respectively. Moreover, enhanced growth of X. euvesicatoria on the characterized SP2273-bz line indicated that both effectors are required for bacterial multiplication in S. americanum. Together, our findings provide a framework for understanding the mechanisms of ETI-mediated resistance and establish a genetic foundation for resistance breeding in solanaceous crops.

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BibTeXRIS

Koh, Y., Jo, H., Kim, J., Cho, H., Kim, I., Kim, W., Kim, C. M., Sohn, K. H., Segonzac, C.. 2026-07-28. Solanum americanum Bs2 and ZAR1 homologs recognize Xanthomonas euvesicatoria effectors essential for infection.. https://doi.org/10.64898/2026.07.27.741084

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