Amplified effect of Brownian motion in bacterial near-surface swimming

259

292

We investigate swimming and chemotactic behaviors of the polarly flagellated marine bacteria Vibrio alginolyticus in an aqueous medium. Our observations show that V. alginolyticus execute a cyclic, three-step (forward, reverse, and flick) swimming pattern that is distinctively different from the run-tumble pattern adopted by Escherichia coli. Specifically, the bacterium backtracks its forward swimming path when the motor reverses. However, upon resuming forward swimming, the flagellum flicks and a new swimming direction is selected at random. In a chemically homogeneous medium (no attractant or repellent), the consecutive forward t f and backward t b swimming times are uncorrelated. Interestingly, although t f and t b are not distributed in a Poissonian fashion, their difference Δt ¼ jt f − t b j is. Near a point source of attractant, on the other hand, t f and t b are found to be strongly correlated, and Δt obeys a bimodal distribution. These observations indicate that V. alginolyticus exploit the time-reversal symmetry of forward and backward swimming by using the time difference to regulate their chemotactic behavior. By adopting the three-step cycle, cells of V. alginolyticus are able to quickly respond to a chemical gradient as well as to localize near a point source of attractant.bacterial chemotaxis | bacterial swimming pattern E nteric bacteria, such as Escherichia coli, swim by rotating a set of flagella that forms a bundle when the flagellar motors turn in the counterclockwise (CCW) direction (1-3). The bundle falls apart when one or more motors turns in the clockwise (CW) direction, and the bacterium tumbles (4). A new swimming direction is selected upon resuming the CCW rotation of the flagellar motors. By modulating the CCW and CW intervals according to external chemical cues, the cells are able to migrate toward attractants or away from repellents (5, 6).Certain bacterial species possess a single polar flagellum with a bidirectional motor similar to E. coli. Being single polarly flagellated, low Reynolds number (Re) hydrodynamics dictates that, aside from random thermal motions, the bacterium can only backtrack its trajectory when the motor reverses. This raises an interesting question concerning how this type of cells performs chemotaxis. Studies of motility patterns of single polarly flagellated bacteria Pseudomonas citronellolis showed that the bacteria change the swimming direction by a brief reversal between two long runs. From the published trajectories (7), each reversal typically results in a small change in cell orientation, and thus several reversals appear to be necessary for a significant change in the swimming direction. Backtracking was also observed in a number of single flagellated marine bacteria such as Shewanella putrefaciens, Pseudoalteromonas haloplanktis, and Vibrio alginolyticus, which execute the so-called run-reverse steps when following attractants released from porous beads and from algae (8-10). A pioneering experiment in V. alginolyticus revealed that the timereversal s...

mentioning

confidence: 69%

Bacterial flagellum as a propeller and as a rudder for efficient chemotaxis

Xie

Altindal²,

Chattopadhyay³

et al. 2011

259

292

“…The circular trajectories consistently observed in PGM solution could be a surface effect because of swimming close to the solid boundaries of the microscope slide or coverslip. This near surface swimming has been established to give rise to circular motion (34) with f luctuations in the radius of curvature driven by amplified coupling of Brownian motion with hydrodynamic interactions (35). It is interesting to note that in PGM solution, H. pylori were observed to undergo long continuous runs punctuated only by occasional brief tumbling events, while in a previous study pronounced run and tumble behavior was observed in (nonmucin) solution (33).…”

Section: H Pylori Is Highly Motile In Gastric Mucin Solution Whilementioning

confidence: 87%

Helicobacter pylori moves through mucus by reducing mucin viscoelasticity

Celli

Turner

Afdhal

et al. 2009

374

326

The ulcer-causing gastric pathogen Helicobacter pylori is the only bacterium known to colonize the harsh acidic environment of the human stomach. H. pylori survives in acidic conditions by producing urease, which catalyzes hydrolysis of urea to yield ammonia thus elevating the pH of its environment. However, the manner in which H. pylori is able to swim through the viscoelastic mucus gel that coats the stomach wall remains poorly understood. Previous rheology studies on gastric mucin, the key viscoelastic component of gastric mucus, indicate that the rheology of this material is pH dependent, transitioning from a viscous solution at neutral pH to a gel in acidic conditions. Bulk rheology measurements on porcine gastric mucin (PGM) show that pH elevation by H. pylori induces a dramatic decrease in viscoelastic moduli. Microscopy studies of the motility of H. pylori in gastric mucin at acidic and neutral pH in the absence of urea show that the bacteria swim freely at high pH, and are strongly constrained at low pH. By using two-photon fluorescence microscopy to image the bacterial motility in an initially low pH mucin gel with urea present we show that the gain of translational motility by bacteria is directly correlated with a rise in pH indicated by 2 ,7 -Bis-(2-Carboxyethyl)-5-(and-6)-carboxyfluorescein (BCECF), a pH sensitive fluorescent dye. This study indicates that the helicoidal-shaped H. pylori does not bore its way through the mucus gel like a screw through a cork as has previously been suggested, but instead achieves motility by altering the rheological properties of its environment.H. pylori ͉ bacterial motility ͉ rheology ͉ pH ͉ gelation

“…The dish was allowed to sit for 5 min to allow daughter swarmer cells to separate from the attached predivisional cells. The fresh swarmer cells (mostly at the same stage of their life cycle) were then harvested in their suspension for measurement (22). A drop of sample was sealed between a glass slide and a coverslip using either vacuum grease (separation, d, ∼20 μm) or a spacer with hollow square center cut from a sheet of Parafilm M laboratory film (separation, d, ∼150 μm).…”

Section: Methodsmentioning

confidence: 99%

Helical motion of the cell body enhances Caulobacter crescentus motility

Liu

Gulino

Morse

et al. 2014

Self Cite

We resolve the 3D trajectory and the orientation of individual cells for extended times, using a digital tracking technique combined with 3D reconstructions. We have used this technique to study the motility of the uniflagellated bacterium Caulobacter crescentus and have found that each cell displays two distinct modes of motility, depending on the sense of rotation of the flagellar motor. In the forward mode, when the flagellum pushes the cell, the cell body is tilted with respect to the direction of motion, and it precesses, tracing out a helical trajectory. In the reverse mode, when the flagellum pulls the cell, the precession is smaller and the cell has a lower translation distance per rotation period and thus a lower motility. Using resistive force theory, we show how the helical motion of the cell body generates thrust and can explain the direction-dependent changes in swimming motility. The source of the cell body precession is believed to be associated with the flexibility of the hook that connects the flagellum to the cell body.microorganisms | kinematics | fluid mechanics | torque | flicking