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      A new mode of swimming in singly flagellated Pseudomonas aeruginosa

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          Significance

          The monotrichous Pseudomonas aeruginosa was usually thought to swim in a pattern of “run and reverse” (possibly with pauses in between), where straight runs alternated with reverses with angular changes of swimming direction near 180°. Here, by simultaneously tracking the cell swimming and the morphology of its flagellum, we discovered a swimming mode in P. aeruginosa—the wrap mode, during which the flagellar filament wrapped around the cell body and induced large fluctuation of the body orientation. The wrap mode randomized swimming direction, resulting in a broad distribution of angular changes over 0 to 180° with a peak near 90°. This allowed the bacterium to explore the environment more efficiently, which we confirmed by stochastic simulations of P. aeruginosa chemotaxis.

          Abstract

          Bacterial motility and chemotaxis are important for many biological processes such as the exploration of the environment and the spreading of bacterial infections. Different bacterial species usually adopt different swimming strategies. As an opportunistic pathogen, the singly flagellated Pseudomonas aeruginosa was recently found to swim in a “run–reverse” or “run–reverse–pause” pattern. Here, by simultaneously tracking the position of the cell body and the conformation of its flagellum, we discovered a swimming mode—the wrap mode, during which the filament wrapped around the cell body. We measured the behavioral characteristics of the wrap mode and found that it randomized the swimming direction, thereby allowing the bacterium to explore its neighborhood efficiently. We confirmed by stochastic simulations of P. aeruginosa chemotaxis that the wrap mode enhanced its chemotaxis performance. Therefore, the wrap mode we discovered here represents an efficient strategy for polar-flagellated bacteria to explore the environment.

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          Most cited references36

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          Swimming in circles: motion of bacteria near solid boundaries.

          Near a solid boundary, Escherichia coli swims in clockwise circular motion. We provide a hydrodynamic model for this behavior. We show that circular trajectories are natural consequences of force-free and torque-free swimming and the hydrodynamic interactions with the boundary, which also leads to a hydrodynamic trapping of the cells close to the surface. We compare the results of the model with experimental data and obtain reasonable agreement. In particular, the radius of curvature of the trajectory is observed to increase with the length of the bacterium body.
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            Bacterial motility on a surface: many ways to a common goal.

            When free-living bacteria colonize biotic or abiotic surfaces, the resultant changes in physiology and morphology have important consequences on their growth, development, and survival. Surface motility, biofilm formation, fruiting body development, and host invasion are some of the manifestations of functional responses to surface colonization. Bacteria may sense the growth surface either directly through physical contact or indirectly by sensing the proximity of fellow bacteria. Extracellular signals that elicit new gene expression include autoinducers, amino acids, peptides, proteins, and carbohydrates. This review focuses mainly on surface motility and makes comparisons to features shared by other surface phenomenon.
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              • Record: found
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              Bacteria swim by rotating their flagellar filaments.

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                Author and article information

                Journal
                Proc Natl Acad Sci U S A
                Proc Natl Acad Sci U S A
                pnas
                PNAS
                Proceedings of the National Academy of Sciences of the United States of America
                National Academy of Sciences
                0027-8424
                1091-6490
                29 March 2022
                5 April 2022
                29 September 2022
                : 119
                : 14
                : e2120508119
                Affiliations
                [1] aDepartment of Physics, University of Science and Technology of China , Hefei 230026, China
                Author notes
                2To whom correspondence may be addressed. Email: jhyuan@ 123456ustc.edu.cn or rjzhang@ 123456ustc.edu.cn .

                Edited by Steven Block, Stanford University, Stanford, CA; received November 9, 2021; accepted February 18, 2022

                Author contributions: R.Z. and J.Y. designed research; M.T. and Z.W. performed research; M.T., Z.W., R.Z., and J.Y. contributed new reagents/analytic tools; M.T. and Z.W. analyzed data; and M.T., Z.W., R.Z., and J.Y. wrote the paper.

                1M.T. and Z.W. contributed equally to this work.

                Article
                202120508
                10.1073/pnas.2120508119
                9168846
                35349348
                25975d8a-1349-4ed6-b657-7ff58ac468ac
                Copyright © 2022 the Author(s). Published by PNAS.

                This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND).

                History
                : 18 February 2022
                Page count
                Pages: 10
                Funding
                Funded by: National Natural Science Foundation of China (NSFC) 501100001809
                Award ID: 11925406
                Award ID: 11872358
                Award ID: 12090053
                Award Recipient : Maojin Tian Award Recipient : Zhengyu Wu Award Recipient : Rongjing Zhang Award Recipient : Junhua Yuan
                Categories
                408
                Biological Sciences
                Biophysics and Computational Biology

                bacterial motility,chemotaxis,flagellar,buckling instability

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