Specialization of independently acquired flagellar FliC proteins in plant-associated <i>Sphingomonas</i> balances swimming and immunogenicity
Plants monitor their environment for microbial invaders using pattern-recognition receptors that detect microbe-associated molecular patterns (MAMPs). Flagellin, the main component of bacterial flagellum, contains the flg22 epitope recognized by the plant immune receptor FLS2. Immune recognition can create an evolutionary conflict, requiring bacteria to balance flagellar function and immune evasion. Here, we show that plant-associated Sphingomonads resolve this constraint by partitioning two flagellar functions, motility and colonization, across two divergent and independently acquired flagellin genes. Comparative genomics revealed widespread coexistence of FliC proteins expressing either an immunogenic variant (FliC-H) or a non-immunogenic variant (FliC-L). The non-immunogenic FliC-L is necessary and sufficient for full directional swimming, whereas FliC-H is dispensable for swimming, but sufficient for full attachment and colonization. Flagellin expression patterns mirror these functions. Thus, FLS2 recognizes the flagellar variant required for colonization rather than motility, potentially restricting colonizing bacteria from entering internal leaf and root tissues.
Authors
- Theresa Law (ORCID: https://orcid.org/0000-0003-2027-9240)
- Zihe Zheng (ORCID: https://orcid.org/0000-0003-0040-4016)
- Derek S. Lundberg (ORCID: https://orcid.org/0000-0001-7970-1595)
- Dor Russ
- Manuel Anguita-Maeso
- Karnelia Paul
- Jeffery L. Dangl
- Connor R Fitzpatrick
- Chinmay Saha
Institutions
- University of North Carolina at Chapel Hill (US)
- Howard Hughes Medical Institute (US)
- Swedish University of Agricultural Sciences (SE)
Publication Details
- Journal
- bioRxiv (Cold Spring Harbor Laboratory)
- Published
- 2026-02-24
- DOI
- https://doi.org/10.64898/2026.02.23.707200
- Primary Topic
- Plant-Microbe Interactions and Immunity
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Science Foundation
- Howard Hughes Medical Institute
- University of North Carolina at Chapel Hill
- Natural Sciences and Engineering Research Council of Canada
- Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill