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1.
Nature ; 497(7449): 388-391, 2013 May 16.
Artículo en Inglés | MEDLINE | ID: mdl-23657259

RESUMEN

Bacterial biofilms are surface-associated, multicellular, morphologically complex microbial communities. Biofilm-forming bacteria such as the opportunistic pathogen Pseudomonas aeruginosa are phenotypically distinct from their free-swimming, planktonic counterparts. Much work has focused on factors affecting surface adhesion, and it is known that P. aeruginosa secretes the Psl exopolysaccharide, which promotes surface attachment by acting as 'molecular glue'. However, how individual surface-attached bacteria self-organize into microcolonies, the first step in communal biofilm organization, is not well understood. Here we identify a new role for Psl in early biofilm development using a massively parallel cell-tracking algorithm to extract the motility history of every cell on a newly colonized surface. By combining this technique with fluorescent Psl staining and computer simulations, we show that P. aeruginosa deposits a trail of Psl as it moves on a surface, which influences the surface motility of subsequent cells that encounter these trails and thus generates positive feedback. Both experiments and simulations indicate that the web of secreted Psl controls the distribution of surface visit frequencies, which can be approximated by a power law. This Pareto-type behaviour indicates that the bacterial community self-organizes in a manner analogous to a capitalist economic system, a 'rich-get-richer' mechanism of Psl accumulation that results in a small number of 'elite' cells becoming extremely enriched in communally produced Psl. Using engineered strains with inducible Psl production, we show that local Psl concentrations determine post-division cell fates and that high local Psl concentrations ultimately allow elite cells to serve as the founding population for initial microcolony development.


Asunto(s)
Biopelículas/crecimiento & desarrollo , Polisacáridos Bacterianos/metabolismo , Pseudomonas aeruginosa/citología , Pseudomonas aeruginosa/crecimiento & desarrollo , Algoritmos , Adhesión Bacteriana/fisiología , Rastreo Celular , Retroalimentación Fisiológica , Colorantes Fluorescentes , Coloración y Etiquetado
2.
Proc Natl Acad Sci U S A ; 110(6): 2330-5, 2013 Feb 05.
Artículo en Inglés | MEDLINE | ID: mdl-23341622

RESUMEN

Myxococcus xanthus is a bacterium capable of complex social organization. Its characteristic social ("S")-motility mechanism is mediated by type IV pili (TFP), linear actuator appendages that propel the bacterium along a surface. TFP are known to bind to secreted exopolysaccharides (EPS), but it is unclear how M. xanthus manages to use the TFP-EPS technology common to many bacteria to achieve its unique coordinated multicellular movements. We examine M. xanthus S-motility, using high-resolution particle-tracking algorithms, and observe aperiodic stick-slip movements. We show that they are not due to chemotaxis, but are instead consistent with a constant TFP-generated force interacting with EPS, which functions both as a glue and as a lubricant. These movements are quantitatively homologous to the dynamics of earthquakes and other crackling noise systems. These systems exhibit critical behavior, which is characterized by a statistical hierarchy of discrete "avalanche" motions described by a power law distribution. The measured critical exponents from M. xanthus are consistent with mean field theoretical models and with other crackling noise systems, and the measured Lyapunov exponent suggests the existence of highly branched EPS. Such molecular architectures, which are common for efficient lubricants but rare in bacterial EPS, may be necessary for S-motility: We show that the TFP of leading "locomotive" cells initiate the collective motion of follower cells, indicating that lubricating EPS may alleviate the force generation requirements on the lead cell and thus make S-motility possible.


Asunto(s)
Myxococcus xanthus/fisiología , Algoritmos , Fimbrias Bacterianas/clasificación , Fimbrias Bacterianas/fisiología , Modelos Biológicos , Estructura Molecular , Movimiento/fisiología , Mutación , Myxococcus xanthus/genética , Polisacáridos Bacterianos/química , Polisacáridos Bacterianos/genética , Polisacáridos Bacterianos/fisiología
3.
Proc Natl Acad Sci U S A ; 108(31): 12617-22, 2011 Aug 02.
Artículo en Inglés | MEDLINE | ID: mdl-21768344

RESUMEN

Bacteria optimize the use of their motility appendages to move efficiently on a wide range of surfaces prior to forming multicellular bacterial biofilms. The "twitching" motility mode employed by many bacterial species for surface exploration uses type-IV pili (TFP) as linear actuators to enable directional crawling. In addition to linear motion, however, motility requires turns and changes of direction. Moreover, the motility mechanism must be adaptable to the continually changing surface conditions encountered during biofilm formation. Here, we develop a novel two-point tracking algorithm to dissect twitching motility in this context. We show that TFP-mediated crawling in Pseudomonas aeruginosa consistently alternates between two distinct actions: a translation of constant velocity and a combined translation-rotation that is approximately 20× faster in instantaneous velocity. Orientational distributions of these actions suggest that the former is due to pulling by multiple TFP, whereas the latter is due to release by single TFP. The release action leads to a fast "slingshot" motion that can turn the cell body efficiently by oversteering. Furthermore, the large velocity of the slingshot motion enables bacteria to move efficiently through environments that contain shear-thinning viscoelastic fluids, such as the extracellular polymeric substances (EPS) that bacteria secrete on surfaces during biofilm formation.


Asunto(s)
Adhesión Bacteriana/fisiología , Fimbrias Bacterianas/fisiología , Modelos Biológicos , Pseudomonas aeruginosa/fisiología , Algoritmos , Adhesión Bacteriana/genética , Proteínas Bacterianas/genética , Proteínas Bacterianas/fisiología , Biopelículas , Modelos Lineales , Movimiento/fisiología , Mutación , Pseudomonas aeruginosa/genética
4.
Biophys J ; 100(7): 1608-16, 2011 Apr 06.
Artículo en Inglés | MEDLINE | ID: mdl-21463573

RESUMEN

Bacterial biofilms are structured multicellular communities that are responsible for a broad range of infections. Knowing how free-swimming bacteria adapt their motility mechanisms near a surface is crucial for understanding the transition from the planktonic to the biofilm phenotype. By translating microscopy movies into searchable databases of bacterial behavior and developing image-based search engines, we were able to identify fundamental appendage-specific mechanisms for the surface motility of Pseudomonas aeruginosa. Type IV pili mediate two surface motility mechanisms: horizontally oriented crawling, by which the bacterium moves lengthwise with high directional persistence, and vertically oriented walking, by which the bacterium moves with low directional persistence and high instantaneous velocity, allowing it to rapidly explore microenvironments. The flagellum mediates two additional motility mechanisms: near-surface swimming and surface-anchored spinning, which often precedes detachment from a surface. Flagella and pili interact cooperatively in a launch sequence whereby bacteria change orientation from horizontal to vertical and then detach. Vertical orientation facilitates detachment from surfaces and thereby influences biofilm morphology.


Asunto(s)
Membrana Celular/metabolismo , Fimbrias Bacterianas/metabolismo , Flagelos/metabolismo , Pseudomonas aeruginosa/citología , Pseudomonas aeruginosa/metabolismo , Biopelículas , División Celular , Movimiento
5.
Sci Rep ; 6: 17790, 2016 Jan 29.
Artículo en Inglés | MEDLINE | ID: mdl-26821939

RESUMEN

Myxococcus xanthus performs coordinated social motility of cell groups through the extension and retraction of type IV pili (TFP) on solid surfaces, which requires both TFP and exopolysaccharides (EPS). By submerging cells in a liquid medium containing 1% methylcellulose, M. xanthus TFP-driven motility was induced in isolated cells and independently of EPS. We measured and analyzed the movements of cells using community tracking algorithms, which combine single-cell resolution with statistics from large sample populations. Cells without significant multi-cellular social interactions have surprisingly complex behaviors: EPS(-) cells exhibited a pronounced increase in the tendency to stand vertically and moved with qualitatively different characteristics than other cells. A decrease in the EPS secretion of cells correlates with a higher instantaneous velocity, but with lower directional persistence in trajectories. Moreover, EPS(-) cells do not adhere to the surface as strongly as wild-type and EPS overproducing cells, and display a greater tendency to have large deviations between the direction of movement and the cell axis, with cell velocity showing only minimal dependence on the direction of movement. The emerging picture is that EPS does not simply provide rheological resistance to a single mechanism but rather that the availability of EPS impacts motility pattern.


Asunto(s)
Fimbrias Bacterianas/metabolismo , Myxococcus xanthus/citología , Myxococcus xanthus/fisiología , Polisacáridos Bacterianos/metabolismo , Adhesión Bacteriana/efectos de los fármacos , Fenómenos Biomecánicos/efectos de los fármacos , Fimbrias Bacterianas/efectos de los fármacos , Metilcelulosa/farmacología , Movimiento , Myxococcus xanthus/efectos de los fármacos
6.
Nat Commun ; 5: 4913, 2014 Sep 19.
Artículo en Inglés | MEDLINE | ID: mdl-25234699

RESUMEN

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.


Asunto(s)
Fimbrias Bacterianas/fisiología , Flagelos/fisiología , Vibrio cholerae/fisiología , Algoritmos , Biopelículas , Proteínas Fimbrias/metabolismo , Flagelina/metabolismo , Fricción , Hidrodinámica , Lectina de Unión a Manosa/metabolismo , Movimiento , Mutación , Fenotipo
7.
Science ; 330(6001): 197, 2010 Oct 08.
Artículo en Inglés | MEDLINE | ID: mdl-20929769

RESUMEN

Bacterial biofilms are structured multicellular communities involved in a broad range of infections. Knowing how free-swimming bacteria adapt their motility mechanisms near surfaces is crucial for understanding the transition between planktonic and biofilm phenotypes. By translating microscopy movies into searchable databases of bacterial behavior, we identified fundamental type IV pili-driven mechanisms for Pseudomonas aeruginosa surface motility involved in distinct foraging strategies. Bacteria stood upright and "walked" with trajectories optimized for two-dimensional surface exploration. Vertical orientation facilitated surface detachment and could influence biofilm morphology.


Asunto(s)
Biopelículas , Fimbrias Bacterianas/fisiología , Pseudomonas aeruginosa/fisiología , Algoritmos , Adhesión Bacteriana , División Celular , Bases de Datos Factuales , Microscopía , Películas Cinematográficas , Movimiento , Mutación , Pseudomonas aeruginosa/genética , Pseudomonas aeruginosa/ultraestructura
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