Flagellar structures from the bacteriumCaulobacter crescentusand implications for phage ϕCbK predation of multi-flagellin bacteria

Author:

Montemayor Eric J.,Ploscariu Nicoleta T.,Sanchez Juan C.,Parrell Daniel,Dillard Rebecca S.,Shebelut Conrad W.,Ke Zunlong,Guerrero-Ferreira Ricardo C.,Wright Elizabeth R.ORCID

Abstract

ABSTRACTCaulobacter crescentusis a gram-negative alpha-proteobacterium that commonly lives in oligotrophic fresh and salt-water environments.C. crescentusis a host to many bacteriophages, including ϕCbK and ϕCbK-like bacteriophages, which first adsorb to cells by interaction with the bacterial flagellum. It is commonly thought that the six paralogs of the flagellin gene present inC. crescentusare important for bacteriophage evasion. Here, we show that deletion of specific flagellins inC. crescentuscan indeed attenuate ϕCbK adsorption efficiency, although no single deletion completely ablates ϕCbK adsorption. Thus, bacteriophage ϕCbK likely recognizes a common motif amongst the six known flagellins inC. crescentuswith varying degrees of efficiency. Interestingly, we observe that most deletion strains still generate flagellar filaments, with the exception of a strain that contains only the most divergent flagellin, FljJ, or a strain that contains only FljN and FljO. To visualize the surface residues that are likely recognized by ϕCbK, we determined two high-resolution structures of the FljK filament, with and without an amino acid substitution that induces straightening of the filament. We observe post-translational modifications on conserved surface threonine residues of FljK that are likely O-linked glycans. The possibility of interplay between these modifications and ϕCbK adsorption is discussed. We also determined the structure of a filament composed of a heterogeneous mixture of FljK and FljL, the final resolution of which was limited to approximately 4.6 Å. Altogether, this work builds a platform for future investigation of how phage ϕCbK infectsC. crescentusat the molecular level.

Publisher

Cold Spring Harbor Laboratory

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