Literature DB >> 33288623

Flagellar Structures from the Bacterium Caulobacter crescentus and Implications for Phage ϕ CbK Predation of Multiflagellin Bacteria.

Eric J Montemayor1,2, Nicoleta T Ploscariu1, Juan C Sanchez1,3, Daniel Parrell1, Rebecca S Dillard4, Conrad W Shebelut5, Zunlong Ke4,6, Ricardo C Guerrero-Ferreira4, Elizabeth R Wright7,2,3,4,8.   

Abstract

Caulobacter crescentus is a Gram-negative alphaproteobacterium that commonly lives in oligotrophic fresh- and saltwater environments. C. crescentus is a host to many bacteriophages, including ϕCbK and ϕCbK-like bacteriophages, which require interaction with the bacterial flagellum and pilus complexes during adsorption. It is commonly thought that the six paralogs of the flagellin gene present in C. crescentus are important for bacteriophage evasion. Here, we show that deletion of specific flagellins in C. crescentus can indeed attenuate ϕCbK adsorption efficiency, although no single deletion completely ablates ϕCbK adsorption. Thus, the bacteriophage ϕCbK likely recognizes a common motif among the six known flagellins in C. crescentus with various 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 posttranslational 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 investigations of how phage ϕCbK infects C. crescentus at the molecular level.IMPORTANCE Bacterial flagellar filaments serve as an initial attachment point for many bacteriophages to bacteria. Some bacteria harbor numerous flagellin genes and are therefore able to generate flagellar filaments with complex compositions, which is thought to be important for evasion from bacteriophages. This study characterizes the importance of the six flagellin genes in C. crescentus for infection by bacteriophage ϕCbK. We find that filaments containing the FljK flagellin are the preferred substrate for bacteriophage ϕCbK. We also present a high-resolution structure of a flagellar filament containing only the FljK flagellin, which provides a platform for future studies on determining how bacteriophage ϕCbK attaches to flagellar filaments at the molecular level.
Copyright © 2021 American Society for Microbiology.

Entities:  

Keywords:  Caulobacter crescentus; bacteria; bacteriophage; cryo-electron microscopy; cryo-electron tomography; flagellum; helical reconstruction; single particle

Mesh:

Substances:

Year:  2021        PMID: 33288623      PMCID: PMC7890551          DOI: 10.1128/JB.00399-20

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  83 in total

1.  FlbT, the post-transcriptional regulator of flagellin synthesis in Caulobacter crescentus, interacts with the 5' untranslated region of flagellin mRNA.

Authors:  P E Anderson; J W Gober
Journal:  Mol Microbiol       Date:  2000-10       Impact factor: 3.501

Review 2.  Protein glycosylation in bacteria: sweeter than ever.

Authors:  Harald Nothaft; Christine M Szymanski
Journal:  Nat Rev Microbiol       Date:  2010-11       Impact factor: 60.633

Review 3.  Flagellin glycosylation with pseudaminic acid in Campylobacter and Helicobacter: prospects for development of novel therapeutics.

Authors:  Abu Iftiaf Md Salah Ud-Din; Anna Roujeinikova
Journal:  Cell Mol Life Sci       Date:  2017-10-27       Impact factor: 9.261

4.  A new class of Caulobacter crescentus flagellar genes.

Authors:  G Leclerc; S P Wang; B Ely
Journal:  J Bacteriol       Date:  1998-10       Impact factor: 3.490

5.  CryoEM structure of the Methanospirillum hungatei archaellum reveals structural features distinct from the bacterial flagellum and type IV pilus.

Authors:  Nicole Poweleit; Peng Ge; Hong H Nguyen; Rachel R Ogorzalek Loo; Robert P Gunsalus; Z Hong Zhou
Journal:  Nat Microbiol       Date:  2016-12-05       Impact factor: 17.745

6.  SP3: a flagellotropic bacteriophage of Bacillus subtilis.

Authors:  T B Shea; E Seaman
Journal:  J Gen Virol       Date:  1984-11       Impact factor: 3.891

7.  Both the extracellular leucine-rich repeat domain and the kinase activity of FSL2 are required for flagellin binding and signaling in Arabidopsis.

Authors:  L Gómez-Gómez; Z Bauer; T Boller
Journal:  Plant Cell       Date:  2001-05       Impact factor: 11.277

8.  Obstruction of pilus retraction stimulates bacterial surface sensing.

Authors:  Courtney K Ellison; Jingbo Kan; Rebecca S Dillard; David T Kysela; Adrien Ducret; Cecile Berne; Cheri M Hampton; Zunlong Ke; Elizabeth R Wright; Nicolas Biais; Ankur B Dalia; Yves V Brun
Journal:  Science       Date:  2017-10-27       Impact factor: 47.728

9.  Phase-variable surface structures are required for infection of Campylobacter jejuni by bacteriophages.

Authors:  Chris Coward; Andrew J Grant; Craig Swift; Jennifer Philp; Rebecca Towler; Mohammad Heydarian; Jennifer A Frost; Duncan J Maskell
Journal:  Appl Environ Microbiol       Date:  2006-07       Impact factor: 4.792

10.  Structural and Functional Comparison of Salmonella Flagellar Filaments Composed of FljB and FliC.

Authors:  Tomoko Yamaguchi; Shoko Toma; Naoya Terahara; Tomoko Miyata; Masamichi Ashihara; Tohru Minamino; Keiichi Namba; Takayuki Kato
Journal:  Biomolecules       Date:  2020-02-06
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  4 in total

1.  Convergent evolution in the supercoiling of prokaryotic flagellar filaments.

Authors:  Mark A B Kreutzberger; Ravi R Sonani; Junfeng Liu; Sharanya Chatterjee; Fengbin Wang; Amanda L Sebastian; Priyanka Biswas; Cheryl Ewing; Weili Zheng; Frédéric Poly; Gad Frankel; B F Luisi; Chris R Calladine; Mart Krupovic; Birgit E Scharf; Edward H Egelman
Journal:  Cell       Date:  2022-09-02       Impact factor: 66.850

Review 2.  Biological foundations of successful bacteriophage therapy.

Authors:  Carola Venturini; Aleksandra Petrovic Fabijan; Alicia Fajardo Lubian; Stefanie Barbirz; Jonathan Iredell
Journal:  EMBO Mol Med       Date:  2022-05-27       Impact factor: 14.260

Review 3.  Flagellotropic Bacteriophages: Opportunities and Challenges for Antimicrobial Applications.

Authors:  Nathaniel C Esteves; Birgit E Scharf
Journal:  Int J Mol Sci       Date:  2022-06-25       Impact factor: 6.208

4.  Identification of Receptor Binding Proteins in Flagellotropic Agrobacterium Phage 7-7-1.

Authors:  Floricel Gonzalez; Birgit E Scharf
Journal:  Viruses       Date:  2021-06-29       Impact factor: 5.048

  4 in total

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