Vibrio cholerae use pili and flagella synergistically to effect motility switching and conditional surface attachment
Andrew S. Utada,
Rachel R. Bennett,
Jiunn C. N. Fong,
Maxsim L. Gibiansky,
Fitnat H. Yildiz (),
Ramin Golestanian () and
Gerard C. L. Wong ()
Additional contact information
Andrew S. Utada: California NanoSystems Institute, University of California
Rachel R. Bennett: Rudolf Peierls Centre for Theoretical Physics, University of Oxford
Jiunn C. N. Fong: University of California
Maxsim L. Gibiansky: California NanoSystems Institute, University of California
Fitnat H. Yildiz: University of California
Ramin Golestanian: Rudolf Peierls Centre for Theoretical Physics, University of Oxford
Gerard C. L. Wong: California NanoSystems Institute, University of California
Nature Communications, 2014, vol. 5, issue 1, 1-8
Abstract:
Abstract We show that Vibrio cholerae, the causative agent of cholera, use their flagella and mannose-sensitive hemagglutinin (MSHA) type IV pili synergistically to switch between two complementary motility states that together facilitate surface selection and attachment. Flagellar rotation counter-rotates the cell body, causing MSHA pili to have periodic mechanical contact with the surface for surface-skimming cells. Using tracking algorithms at 5 ms resolution we observe two motility behaviours: ‘roaming', characterized by meandering trajectories, and ‘orbiting’, characterized by repetitive high-curvature orbits. We develop a hydrodynamic model showing that these phenotypes result from a nonlinear relationship between trajectory shape and frictional forces between pili and the surface: strong pili–surface interactions generate orbiting motion, increasing the local bacterial loiter time. Time-lapse imaging reveals how only orbiting mode cells can attach irreversibly and form microcolonies. These observations suggest that MSHA pili are crucial for surface selection, irreversible attachment, and ultimately microcolony formation.
Date: 2014
References: Add references at CitEc
Citations:
Downloads: (external link)
https://www.nature.com/articles/ncomms5913 Abstract (text/html)
Related works:
This item may be available elsewhere in EconPapers: Search for items with the same title.
Export reference: BibTeX
RIS (EndNote, ProCite, RefMan)
HTML/Text
Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:5:y:2014:i:1:d:10.1038_ncomms5913
Ordering information: This journal article can be ordered from
https://www.nature.com/ncomms/
DOI: 10.1038/ncomms5913
Access Statistics for this article
Nature Communications is currently edited by Nathalie Le Bot, Enda Bergin and Fiona Gillespie
More articles in Nature Communications from Nature
Bibliographic data for series maintained by Sonal Shukla () and Springer Nature Abstracting and Indexing ().