Showing posts with label motility. Show all posts
Showing posts with label motility. Show all posts

Sunday, July 22, 2012

100 (micro)meter dash

A fun read in the current issue of Nature Reviews Microbiology is an essay entitled "The Microbial Olympics, " just in time for the Summer Olympics.  You will find stories about microbes competing in boxing, javelin, pathogen relay, diving, and other Olympic events.  Flagellated bacteria compete in the 100 micrometer dash, which you can watch below.  (Note that some of the contestants were genetically modified.)


Lane assignments:
  1. E. coli chimera (has sodium-driven flagellar motors instead of its normal proton-driven motors)
  2. E. coli (proton-driven flagellar motors)
  3. Vibrio alginolyticus, puller (clockwise-locked flagellum "pulls" cell body from front)
  4. Vibrio alginolyticus, pusher (counterclockwise-locked flagellum "pushes" cell body from back)
  5. Pseudomonas aeruginosa
  6. Rhodobacter sphaeroides
  7. Rhodospirillum rubrum
  8. Yersinia enterocolitica

Reference

Youle M, Rohwer F, Stacy A, Whiteley M, Steel BC, Delalez NJ, Nord AL, Berry RM, Armitage JP, Kamoun S, Hogenhout S, Diggle SP, Gurney J, Pollitt EJG, Boetius A, and Cary SC (August 2012).  Nature Reviews Microbiology 10(8):583-588.  DOI: 10.1038/nrmicro2837

Friday, February 12, 2010

The Lyme disease spirochete has flagella but doesn't use them to penetrate the gut of the feeding tick

ResearchBlogging.orgThe Lyme disease agent Borrelia burgdorferi possesses flagella, which are the thin motility structures owned by many members of the bacteria world.  Flagella propel bacteria towards their destination by spinning (read this post to see how flagella function in Borrelia).  It has been assumed B. burgdorferi spin their flagella whenever they need to move from one location to another.  A recent paper in The Journal of Clinical Investigation has demonstrated otherwise, at least for B. burgdorferi in the midgut of a feeding Ixodes (blacklegged) tick.

Borrelia burgdorferi spends much of its life cycle lying dormant in the midgut of Ixodes ticks.  The spirochetes lightly pepper the inner surface of the midgut cell lining, with a few spirochetes also hiding between cells.  None live at the base of the cells at the basement membrane surrounding the midgut.  The spirochetes wake up and multiply only when the tick attaches to an animal or human and imbibes blood.  A few days into the blood meal, some spirochetes eventually breech the basement membrane and enter the hemocoel, the fluid-filled space between the tick organs where they must avoid the phagocytes patrolling the area.  From there the spirochetes invade the salivary glands, which can then release B. burgdorferi-tainted saliva into the skin of the victim.  After completing its satisfying meal of blood, the tick detaches from the skin of the victim, who may end up suffering from Lyme disease.

Dunham-Ems and colleagues wanted to follow the spirochetes in the midgut as ticks took their meal of blood.  They engineered a strain of B. burgdorferi expressing green fluorescent protein so that they could watch the spirochetes in the gut by fluorescence microscopy.  They allowed ticks with the green B. burgdorferi strain in their midguts to feed on laboratory mice.  24, 48, and 72 hours after the ticks were placed on the mice, the investigators removed the midguts and examined the organ by fluorescence microscopy to see what the spirochetes were doing.  Surprisingly, they never saw motile spirochetes in the midgut even though the spirochetes eventually found their way at 72 hours into the hemocoel, where they were highly motile.

If the spirochetes in the midgut remained nonmotile during tick feeding, how did they reach the basement membrane? The few spirochetes that initially populated the midgut multiplied exponentially and formed growing networks of spirochetes on the cell surfaces as the tick drank blood from the mice.  By 72 hours the networks eventually coalesced, encasing many gut cells in spirochetes (see the figures below).  Spirochetes at the base of the encased cells were poised to penetrate the basement membrane and invade the hemocoel.  All of this happened without B. burgdorferi ever spinning its flagella.  Only when they broke through into the hemocoel did the flagella start spinning.

Figure 4F-H from Dunham-Ems 2009.  Confocal fluorescence microscopy of a midgut from a nymph that fed on a mouse for 72 hours.  Panel F shows a network of spirochetes (green) attached to the inner surface of the midgut.  An optical section taken 24-26 µm into the lining of the midgut (panel G) reveals aggregates of spirochetes surrounding the cells. Panel H shows that some spirochetes have made it to the basement membrane, which is found 50 µm below the surface.  The midgut cell membrane is stained in red.  Scale bars = 25 µm.  Some of the gut cells are extremely large because they are differentiating as part of the digestion process.



Figure 5 A and B from Dunham-Ems 2009.  Silver stain of sections from ticks that fed for 48 hours (panel A) and 72 hours (panel B).  The edges of the epithelial cells are easier to see than in the previous figure.  Arrows point to aggregates of spirochetes (hairy bodies).  At 72 hours at least one cell is encased in spirochetes.  Scale bars = 25 µm.  Some of the cells are extremely large because they are differentiating as part of the normal digestion process of the tick (dc, differentiated cells; uc, undifferentiated cells). 

The investigators also found that something in the tick midgut inhibited the motility of B. burgdorferi.  They placed a bit of minced midgut from a tick that had been feeding on a mouse for 72 hours at the edge of a gelatin matrix containing motile fluorescent B. burgdorferi.  (Because of their helical shape, spirochetes love to move about in viscous substances such as gelatin.)  Most of the spirochetes near the tissue ceased moving and remained motionless throughout the 15 minute viewing period.  In contrast, the spirochetes continued moving when mouse blood was placed at the edge of the gelatin matrix.

Why does B. burgdorferi employ a nonmotile mode of penetration of the cell lining of the tick midgut?  Is there some advantage for the spirochete to avoid using their flagella?  As blood is known to be a powerful chemoattractant for B. burgdorferi, the authors offered the following explanation:

These results, although counterintuitive at first blush, make sense; if blood in the midgut acted as a chemoattractant, spirochetes would never disseminate during feeding.
Hence the "inhibitor" of motility released by the tick gut serves as a signal to the spirochete to not spin their flagella.

To me, this explanation isn't satisfying.  It would seem simple for B. burgdorferi to have evolved a regulatory scheme that would allow the spirochete to temporarily uncouple blood chemotaxis from flagellar motility so that they could bore through the gut lining in minutes rather than days. There must be a reason why B. burgdorferi chooses to take its time to penetrate the gut lining.

Perhaps B. burgdorferi delays its journey to the salivary glands to allow the feeding tick to properly prepare the skin, which is an inhospitible environment for both tick and spirochete.  As the tick feeds, it releases a brew of anti-immune factors into the skin to protect itself from attack by the immune system.  Early arrival of B. burgdorferi to the salivary gland would release the spirochetes into the skin before the anti-immune factors have taken full effect, potentially allowing the host immune system to eliminate the spirochetes before they could establish an infection.

Reference

Dunham-Ems, S.M., Caimano, M.J., Pal, U., Wolgemuth, C.W., Eggers, C.H., Balic, A., & Radolf, J.D. (2009). Live imaging reveals a biphasic mode of dissemination of Borrelia burgdorferi within ticks. Journal of Clinical Investigation. 119(12):3652-3665. DOI: 10.1172/JCI39401

Sunday, February 22, 2009

Viewing the arrangement of Borrelia burgdorferi flagella by electron cryotomography

ResearchBlogging.orgThe most peculiar feature of spirochetes may be the location of their flagella, the thin motility structures that propel bacteria through liquids. Flagella typically extend out from the surface of bacteria into the surroundings. Spirochetes, being not so typical, keep their flagella hidden in the periplasm between the cytoplasmic and outer membranes (see figure). For example, the Lyme disease spirochete Borrelia burgdorferi has 7-11 flagella attached near each end of the "protoplasmic" or cell cylinder, with each flagellum extending through the periplasm towards the center of the spirochete. The flagella impose a flat-wave shape (not a spiral shape!) on B. burgdorferi by wrapping around its protoplasmic cylinder.


How do flagella that are located in the periplasm drive the spirochete through the medium? B. burgdorferi motility is thought to require the rotation of its flagella against the cell cylinder, causing the cell body to gyrate.

B. burgdorferi flagella often appear as a bundle when observed by standard transmission electron microscopy. Here is one such image from a 2000 study revealing at least 10 flagella in a cross section of B. burgdorferi. With the flagella arranged in this manner, it is difficult to imagine how the flagella that are not in direct contact with the cell cylinder could contribute to its gyration.

A study by Charon and colleagues in the January 2009 issue of Journal of Bacteriology suggests that the flagellar bundle is an artifact of the standard techniques used to prepare the samples for electron microscopy. They employed the emerging technique of electron cryotomography to avoid the fixation and staining procedures that often introduce artifacts into samples. Electron cryotomography consists of the following steps:
  1. To preserve structure, the specimen is plunge frozen at -165°C or less. Fixing or staining is not necessary.
  2. While maintaining the sample at the ultralow temperature, 2D projections of the sample are obtained at different angles by transmission electron microscopy.
  3. Computer software assembles the 3D structure of the specimen from the 2D projections.
The software also permits slices of the specimen to be observed without having to actually perform thin sectioning.

Here's a cross-section of B. burgdorferi as viewed by electron cryotomography. Note that the flagella are arranged in a single layer within the periplasm, not in a bundle.

Figure 1 of Charon et al. Bar, 50 nm.
PFs, periplasmic flagella; PS, periplasmic space; PM, plasma (or cytoplasmic) membrane; OM, outer membrane.

A longitudinal slice through the periplasm of B. burgdorferi reveals nine flagella neatly arranged in a parallel fashion along the surface of the protoplasmic cylinder. The authors refer to this array as a "flat ribbon." Each flagellum in the ribbon is separated by ~3 nm, allowing each to rotate in the same direction without interference from neighboring flagella.

Figure 5 of Charon et al. Bar, 200 nm.

3D reconstruction of a section of the spirochete illustrates the flat ribbon of flagella (in red) wrapping around the cell cylinder (in blue). Only a section of the cell cylinder is shown, and the outer membrane has been removed from the image.



These new images support a model for for B. burgdorferi motility that was first described back in the 1990s. In this model, the rotation of the flagella against the cell cylinder generates gyrating waves that progress backwards along the cell body. As explained in the discussion of the Charon et al. paper, it is conceivable that all 7-11 flagella must lie against the cell cylinder as a flat ribbon to exert the force necessary to generate the waves; a flagella bundle may not exert enough force. The torque generated by the rotating flagella causes a counter rotation of the cell cylinder (panel a below). The backward-propagating, gyrating waves push the spirochete through the medium. Flagella arranged in a bundle would not generate enough torque because of potential interference between rotating flagella (panel b).

Figure 8 of Charon et al. a. Flagella arranged in a flat ribbon. b. Flagella arranged in a bundle.

This model also explains why B. burgdorferi moves so well through viscous gel-like material such as the extracellular matrix; the gel provides traction for the backward-progressing waves to drive the spirochete through the medium.

Here's a movie animating B. burgdorferi motility, first presented at a meeting in 2001 .


SOURCE

You can also see real B. burgdorferi gyrating and generating backward-moving waves in a movie embedded in Dr. Nyles Charon's website.

Reference

N. W. Charon, S. F. Goldstein, M. Marko, C. Hsieh, L. L. Gebhardt, M. A. Motaleb, C. W. Wolgemuth, R. J. Limberger, N. Rowe (2009). The Flat-Ribbon Configuration of the Periplasmic Flagella of Borrelia burgdorferi and Its Relationship to Motility and Morphology Journal of Bacteriology, 191 (2), 600-607 DOI: 10.1128/JB.01288-08