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The attachment of bacteria to surfaces provides advantages such as increasing nutrient access and resistance to environmental stress. Attachment begins with a reversible phase, often mediated by surface structures such as flagella and pili, followed by a transition to irreversible attachment, typically mediated by polysaccharides. Here we show that the interplay between pili and flagellum rotation stimulates the rapid transition between reversible and polysaccharide-mediated irreversible attachment. We found that reversible attachment of Caulobacter crescentus cells is mediated by motile cells bearing pili and that their contact with a surface results in the rapid pili-dependent arrest of flagellum rotation and concurrent stimulation of polar holdfast adhesive polysaccharide. Similar stimulation of polar adhesin production by surface contact occurs in Asticcacaulis biprosthecum and Agrobacterium tumefaciens. Therefore, single bacterial cells respond to their initial contact with surfaces by triggering just-in-time adhesin production. This mechanism restricts stable attachment to intimate surface interactions, thereby maximizing surface attachment, discouraging non-productive self-adherence, and preventing curing of the adhesive.
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Many organisms derive important competitive advantages from their attachment to surfaces and the mechanisms by which they settle on a surface are subject to important regulation. For example, in sessile marine and aquatic invertebrates such as mussels, barnacles and oysters, it is well established that during the transition from the free swimming larval stage to the sessile adult, the larva reversibly contact the surface, testing and responding to the physical and chemical composition of its environment, prior to cementation and an irreversible commitment to stationary life (Morse, 1990; Tamburri et al., 1992). Surface attachment is also advantageous for bacteria because it increases nutrient access and resistance to environmental stress, and they have evolved many strategies that improve the efficiency of the attachment process.
Decades of research have clearly determined that bacterial attachment proceeds in two stages, a reversible stage that involves transient surface interactions and an irreversible stage that depends on adhesins responsible for mediating permanent attachment (van Loosdrecht et al., 1990a,b; Vigeant et al., 2002; Hinsa et al., 2003; Agladze et al., 2005; Beloin et al., 2008; Otto, 2008; Van Dellen et al., 2008). Flagellar motility and thin surface structures such as pili often mediate the reversible adhesion phase and allow cells to overcome the electrostatic repulsion as they approach a surface. In addition, bacteria produce exopolymers, such as adhesive polysaccharides, to mediate the transition from reversible to irreversible binding and increase their strength of adhesion to surfaces. The temporal mechanism by which this transition occurs however has remained mysterious (Karatan and Watnick, 2009).
In this study, Caulobacter crescentus is used as a model bacterium to study the dynamics of cell-to-surface binding. C. crescentus exhibits a dimorphic life cycle in which each cell division produces a motile swarmer cell and a sessile stalked cell (Fig. 1). Swarmer cells (SW) harbour pili and a flagellum at the same pole. These cells are unable to initiate DNA replication and are motile for approximately 25–30 min under the conditions used in these studies, unless they attach to a surface. After the motile period, swarmer cells differentiate into stalked cells (ST) by shedding their flagellum, retracting their pili and synthesizing an adhesive polysaccharide holdfast and a stalk at the same pole. The holdfast is composed at least in part of a polysaccharide of N-acetylglucosamine that is required for irreversible adhesion to surfaces (Merker and Smit, 1988). Stalked cells initiate DNA replication, elongate and eventually synthesize a flagellum at the pole opposite the stalk, forming the pre-divisional cell (PD). Flagellum rotation is initiated just prior to the completion of cell division, which always produces a swarmer cell and a stalked cell. Initial surface adhesion occurs during the swarmer phase (Bodenmiller et al., 2004; Levi and Jenal, 2006) and permanent adhesion is cemented by the holdfast, which binds to surfaces with an impressive strength in the µN range (Tsang et al., 2006). Therefore, the availability of a portion of the life cycle in which the adhesive polysaccharide is absent allows the investigation of factors that regulate its synthesis and its correlation with surface adhesion.
Here, we take advantage of the fact that C. crescentus and several species of alphaproteobacteria synthesize polar adhesive polysaccharides (Laus et al., 2006; Brown et al., 2009; Tomlinson and Fuqua, 2009) to show that surface contact triggers the rapid production of adhesins and to investigate the mechanism that drives the transition between reversible and irreversible attachment. We find that the interplay between pili and the flagellum during initial surface interactions causes the rapid, just-in-time production of the C. crescentus adhesin, the holdfast polysaccharide, thereby driving the transition from reversible to irreversible attachment. We show that the surface contact stimulation of adhesive polysaccharides is a general phenomenon as it also occurs in two other bacterial genera, the stalked bacterium Asticcacaulis biprosthecum and the plant pathogen Agrobacterium tumefaciens.
Results and discussion
Surface contact stimulates the rapid, protein synthesis independent deployment of the holdfast adhesin
In order to determine if surface contact influences the biosynthesis of the holdfast polysaccharide adhesin, C. crescentus swarmer cells, which do not harbour a holdfast, were collected following synchronization and divided into two treatments. To monitor holdfast production in attached cells, an aliquot of swarmer cells was placed on a coverslip for 5 min to allow cells to attach. Unattached cells were washed away and the attached cells were grown, followed by labelling for holdfasts. To observe holdfast production in unattached cells, synchronized swarmer cells were diluted 100-fold in peptone-yeast extract (PYE) medium such that few cells could contact the surfaces until they were labelled for holdfasts. The holdfasts of both populations were labelled at specific time points with fluorescein-conjugated WGA lectin (fluorescein-WGA), which specifically binds to holdfast polysaccharide (Umbreit and Pate, 1978; Merker and Smit, 1988). Fluorescence microscopy analysis indicated that attached cells produce a holdfast much earlier than unattached cells; more than 90% of attached cells had a holdfast within 7.5 min in contrast to only 2% of unattached cells. Unattached cells took ∼37.5 min to reach a level similar to that of attached cells at 2 min (Fig. 1).
To improve the time resolution of the study of holdfast synthesis in single cells, total internal reflection fluorescence (TIRF) microscopy was used to observe and quantify holdfast production in real time by measuring the integrated fluorescence intensity of the labelled holdfast of individual attached cells in the presence of fluorescein-WGA (Fig. 2A and Movie S1). During the first ∼20 min after the synchrony, virtually all cells lacked holdfast prior to their contact with the surface (Figs 2B–D and S1A). Throughout this time interval, the timing of holdfast production depended on the time of attachment to the surface, rather than the age of the cell, and it occurred within 1–2 min of contact (Figs 2D and S1A). Furthermore, stimulation of holdfast production did not require de novo protein synthesis since holdfast synthesis was still triggered by surface contact in the presence of a growth inhibiting concentration of kanamycin (Fig. 3A). This observation is consistent with previous work showing that addition of kanamycin, choloramphenicol or tetracycline had no effect on attachment or holdfast biogenesis during the cell cycle of planktonic C. crescentus cells (Levi and Jenal, 2006). Thus, surface contact stimulates rapid holdfast production by a post-translational mechanism that would involve activating the holdfast polysaccharide biosynthesis or export machinery (Smith et al., 2003; Toh et al., 2008). In contrast, 25 min after synchronization, nearly all C. crescentus cells, including the unattached cells in suspension, had detectable holdfast (Figs 1, 2C and D and S1A). This observation is readily explained by cell cycle-dependent holdfast production, which occurs slightly prior to swarmer-to-stalk cell differentiation (Levi and Jenal, 2006).
The results presented above imply that the initial attachment of newborn swarmer cells to surfaces is not mediated by the holdfast, whose synthesis or export must be stimulated in order to transit from reversible attachment to holdfast-mediated permanent attachment. In order to test this model, we observed attachment of an ΔhfsA mutant, which is deficient in holdfast synthesis (Smith et al., 2003), using a quantitative dark-field microscopy assay. After processing overlays of sequential images (see Experimental procedures) attached cells appear as stationary foci and are readily distinguished from swimming cells, which generate trajectories (Fig. S2). Swarmer cells of the ΔhfsA mutant initially attached to the glass surface nearly as efficiently as wild type (Fig. 4B). However, they did not permanently adhere and progressively detached from the surface (Fig. 4C). In contrast, once attached, the number of attached wild-type cells remained the same for at least 90 min (data not shown). Thus, the holdfast is not required for the initial reversible weak attachment, suggesting that the stimulation of holdfast production drives the transition to the permanent adhesion stage.
How is reversible attachment mediated when cells encounter a surface? We used video microscopy to observe the dynamics of single cell attachment in real time. As C. crescentus wild-type cells attached to the surface, they rapidly became tethered (Movie S2). Immediately after attachment, the cell body continued to rotate due to the rotation of the flagellar motor. The majority of attached cells stopped rotation within a few seconds and formed a stable association with the surface, whereas a low proportion of cells continued rotation for a short period, but then detached and swam away. In order to quantify the efficiency of surface attachment in a population, synchronized cells were placed between two glass surfaces separated by 12 µm and were observed with dark-field microscopy with a 10× objective, allowing cells at any depth in the field of view to be imaged. Surface attachment was extremely rapid; 68% of the swarmer cells had attached to the surface within 1 min, and virtually all the cells had attached within 5 min (Fig. 4A).
Caulobacter crescentus pili are colocalized with the flagellum at the future pole of holdfast synthesis and are required for efficient surface attachment (Bodenmiller et al., 2004; Entcheva-Dimitrov and Spormann, 2004; Levi and Jenal, 2006). In order to assess the role of pili in the dynamics of single cell attachment, we synchronized swarmer cells of a mutant lacking pili, ΔpilA, and observed the cells by video microscopy. ΔpilA cells were rarely found attached to the surface. Occasionally, a ΔpilA cell became tethered to the surface by its flagellum, but the motor continued to rotate until the cell detached and swam away (Movie S3). Notably, the flagellum motor of tethered ΔpilA cells rotates considerably slower (60 Hz) than the motor of free-swimming ΔpilA cells (∼330 Hz) (Li and Tang, 2006). Thus, the decrease in flagellum motor rotation upon tethering of ΔpilA cells does not lead to permanent attachment. In contrast, the complete stopping of motor rotation following tethering of wild-type cells results in permanent adhesion (Movie S2). Thus, we infer that pili are required to arrest flagellum rotation when cells are bound to a surface.
Quantitative cell attachment assays using dark-field microscopy indicated that, in stark contrast to wild-type cells, the effective attachment of ΔpilA swarmer cells only began to occur more than 20 min after cell division and occurred at a 24-fold lower rate than wild type (Fig. 4A). The timing of attachment of ΔpilA swarmer cells was consistent with the timing of holdfast synthesis of unattached cells (Figs 1, 2C and 5), suggesting that contact between a preexisting holdfast, whose synthesis was triggered by the developmental pathway, and the surface is responsible for the attachment. This hypothesis is supported by the fact that a mutant synthesizing neither pili nor holdfasts (ΔpilA ΔhfsDAB) does not bind to surfaces since both initial reversible attachment and permanent attachment have been abolished (data not shown). Thus, we conclude that pili-mediated initial attachment is followed by rapid holdfast production that drives the transition from reversible to permanent adhesion.
How does the initial reversible attachment stimulate holdfast production and the transition to permanent attachment? Video microscopy of the ΔpilA mutant binding to surfaces revealed that attachment of the flagellum filament enables transient attachment of the cell to the surface (Movie S3). Since the objective is focused on the surface and the cell pole remains out of focus, we infer that the flagellum-mediated attachment is not sufficient to bring the cell body into close proximity with the surface. Notably, tethering by the filament, even though it slows down flagellum rotation, appears insufficient to stimulate holdfast production since attachment of the ΔpilA mutant only becomes efficient once developmental regulation has triggered holdfast synthesis ∼20 min after cell division (Figs 4 and 5). Like the ΔpilA mutant, cells from a double ΔpilA ΔflgE mutant attached at a slow rate (Fig. 4D). In contrast to wild-type and ΔpilA cells, which swam to the surface and whose behaviour is consistent with tethering (Movies S2 and S3), cells from the ΔpilA ΔflgE mutant simply diffused to the surface. We hypothesize that adhesion by the pili brings the flagellum filament in close proximity to the surface, thereby increasing the probability of filament adhesion. Indeed, the aggregate interaction of the filament and the pili with the surface causes the rapid inhibition of motor rotation (Movie S2). This pure mechanical force may be sufficient to inhibit flagellum rotation, although it is possible that the mechanism involves a clutch or a brake type mechanism (Blair et al., 2008; Paul et al., 2010) regulated at the post-translational level. However, the rapidity by which the cell body is immobilized to the surface by the pili precludes the distinction between these mechanisms by video microscopy. Irrespective of the mechanism, inhibition of flagellum rotation is immediately followed by stimulation of holdfast synthesis, independent of the stage of the cell cycle.
Polymer crowding agents that arrest flagellum rotation stimulate holdfast synthesis
Inhibition of the flagellar motor has been reported to trigger various changes in bacteria (McCarter et al., 1988; Anderson et al., 2010). To test if stopping flagellar rotation could stimulate holdfast production independent of surface attachment, we used the observation that polymer crowding agents can cause bacteria to aggregate in solution (Eboigbodin et al., 2005; Schwarz-Linek et al., 2010), due to osmotic pressure caused by the crowding polymers being excluded from the space between neighbouring cells, an effect called the depletion effect (Tang et al., 1997; Hosek and Tang, 2004). We found that C. crescentus cells formed aggregates in 10% Ficoll within 1 min after the addition of the polymer. Single cells and some aggregates continued to move (Movie S4), propelled by the rotating flagellar filaments in the aggregates. Almost all the cells and aggregates stopped moving at 4 min (Movie S5), indicating that all flagella in the aggregates stopped rotation. The cells at age 17.5 min were labelled with fluorescein-WGA for fluorescence microscopy. The majority of the cells (78%) showed clear holdfasts in contrast to free swimming cells in medium without crowding agent of which only 29% had holdfast (Table 1 and Fig. 6).
Table 1. Effect of various polymers on holdfast synthesis.
% with holdfast
Motility at age 17.5 min
PEG (8000 Da), 3.5%
Some moving aggregates and cells
PEG (35 000 Da), 5%
No moving aggregates or cells
Dextran (100 000–200 000 Da), 5%
No moving aggregates or cells
Ficoll (400 000 Da), 5%
No moving aggregates or cells
Ficoll (400 000 Da), 10%
No moving aggregates or cells
The stimulation of holdfast production was also observed with polymers of different chemical composition that stopped flagellar motor rotation (Table 1). In contrast, polymers that did not stop flagellum rotation despite being added to a similar viscosity did not stimulate holdfast production (Table 1). The dependence of holdfast production on the inhibition of flagellum rotation triggered by viscous solution supports the notion that arrest of flagellum rotation is required for contact-dependent holdfast production. However, it is possible that the osmotic shock induced by the introduction of the viscous solution may trigger membrane stress (or another physiological change) responsible for stimulating holdfast production, although not all polymer crowding agents had this effect.
These results were confirmed with TIRF microscopy experiments in the presence of Ficoll. In contrast to what was observed in complex medium, cells in the presence of 10% Ficoll arrived at the surface with a holdfast (Figs 3B and S3A), indicating that holdfast synthesis was stimulated prior to surface contact. Ficoll had a similar effect on ΔpilA cells, which also arrived at the surface with holdfasts already formed and adhered permanently to the surface (Figs 3C and S3B). Therefore, pili are not required for the stimulation of holdfast synthesis by viscous agents as they are for the surface contact stimulation. This result also supports our earlier inference that, prior to the developmental trigger of holdfast synthesis, ΔpilA cells do not adhere productively upon surface contact because they are unable to stimulate holdfast synthesis.
We conclude that the loss of flagellum rotation upon surface contact triggers holdfast synthesis. In addition, our results suggest that on surfaces pili are mediating the arrest of flagellum rotation, but with viscosity agents the flagellum is intrinsically impeded and the need for the pili in stimulating holdfast synthesis is bypassed. Future studies will utilize fla and mot mutants to directly determine the contribution of the flagellum filament and motor in initial binding and the transition to permanent adhesion. At present, these experiments are complicated by the fact that these mutants have a delay in cell separation and cannot be synchronized via either the plate synchrony or density centrifugation methods. Furthermore, these mutants have altered timing of cell cycle-dependent holdfast production (data not shown). We are currently exploring alternative methods of cell synchrony to enable these studies.
Surface-contact stimulation probably activates previously assembled holdfast synthesis machinery since it does not require de novo protein synthesis. Indeed, at least the holdfast anchoring machinery (Hardy et al., 2010) and the outer membrane export protein HfsD (J. Javens, Z. Wan and Y.V. Brun, in preparation) are already localized at the flagellar pole in newborn swarmer cells, in close proximity to the flagellum and the pili.
Surface contact stimulation of adhesin synthesis in other bacterial genera
To determine if surface contact stimulated adhesin synthesis is a general phenomenon, we observed polar polysaccharide formation in A. biprosthecum and A. tumefaciens. A. biprosthecum has a dimorphic life cycle similar to that of C. crescentus; however, this bacterium produces two lateral stalks and the holdfast is made at the pole of the cell body (Pate et al., 1973). The unipolar polysaccharide (UPP) of the plant pathogen A. tumefaciens is rarely detected in single planktonic cells, but is frequently detected in cells attached to each other in rosettes or single cells attached to a surface (Tomlinson and Fuqua, 2009). Stimulation of holdfast and UPP production following contact with a surface was readily observed in both species using TIRF microscopy. For A. biprosthecum, nearly every cell arrived at the surface without a holdfast, but these were detected as early as 2 min after contact, irrespective of cell age (Figs 2E and S1B; Movie S6). For A. tumefaciens, most cells produced UPP within 3 min of attaching to a glass surface (Figs 2F and S1C; Movie S7). We also tested whether the production of UPP was stimulated by contact with Arabidopsis roots, a more natural surface for A. tumefaciens attachment. UPP production occurred preferentially among cells attached to an Arabidopsis root when compared with unattached cells from the same population (Fig. 7A; Movie S8) and UPP production occurred after initial attachment of A. tumefaciens cells to the Arabidopsis root (Fig. 7B; Movie S9). These data indicate that surface contact-dependent stimulation of polar polysaccharide production is conserved in multiple bacterial species.
Advantages of surface contact stimulation of adhesin synthesis
We have shown that the ability to rapidly produce a permanent adhesin is shared among at least three members of the Alphaproteobacteria, in which motile cells differentiate to become sessile cells. For many motile bacteria, initial attachment is reversible, allowing cells to detach and sample other surfaces (Korber et al., 1994; Hinsa et al., 2003). The ability to rapidly deploy a permanent adhesin may be advantageous for swimming cells that have encountered a favourable environment, enabling colonization.
Another advantage of just-in-time adhesin deployment upon surface contact is that it reduces the chances that the adhesive will be inactivated. Once exported from the cell, two main factors can reduce the adhesiveness of an adhesin: curing, as observed in the mussel byssal thread (Kamino, 2008) and also with man-made glues, and occlusion of the adhesin with microscopic particles after random collision events. Either mechanism would be expected to decrease adhesiveness over time, limiting productive interactions with a surface. Indeed, previous experiments showed that permanent surface adhesion is highest during the swarmer phase of the C. crescentus developmental cycle and drops dramatically during the stalked cell stage despite the presence of a holdfast on stalked cells (Bodenmiller et al., 2004; Levi and Jenal, 2006). These results support the hypothesis that holdfast adhesiveness decreases with time after export and suggest that the ability to rapidly stimulate adhesin formation upon initial contact with a surface dramatically improves the efficiency of surface interaction and colonization.
Polar attachment of single bacterial cells as a prelude to the transition from reversible to irreversible attachment has also been seen in other proteobacteria such as Escherichia coli (Agladze et al., 2005) and Pseudomonas aeruginosa (Caiazza and O'Toole, 2004). Therefore, contact-dependent adhesin deployment may be a commonly utilized strategy to improve adhesion. As surface-associated adhesins may also act to stimulate host defence responses, this timing may also come into play during pathogenesis to ensure that potential antigens are not prematurely exposed to the host immune system.
Bacterial strains and synchronization
Caulobacter crescentus strains were grown at 30°C in PYE medium (Poindexter, 1964) with 10 µg ml−1 kanamycin when indicated. The following C. crescentus strains were used in this study: YB135 (CB15 wild type), YB4038 (CB15 ΔpilA), YB5086 (CB15 ΔpilA ΔflgE) and YB2833 (CB15 ΔhfsA). A. biprosthecum strain JH2 (YB1113) was grown at 26°C in PYE. A. tumefaciens strain C58 (YB2951) was grown at 26°C in LB. Synchronized newborn cells were obtained using the plate release technique (Degnen and Newton, 1972). Briefly, cultures were grown for ∼10 h with shaking at 100 r.p.m. Three millilitres of the culture was added to 20 ml of fresh growth medium in a 9 cm diameter plastic Petri dish and grown at room temperature overnight (or 48 h for A. tumefaciens with medium changes every 12 h) with shaking at 60 r.p.m. After growth, a monolayer of cells was attached to the surface of the Petri dish. The Petri dish was washed thoroughly with water to remove loosely attached and unattached cells. Twenty millilitres of fresh medium was added to the Petri dish and the cells were grown further at room temperature for ∼4 h with shaking at 60 r.p.m. The Petri dish was then grown for 1 more hour at 30°C for C. crescentus and 26°C for A. biprosthecum and A. tumefaciens. The Petri dish was washed repeatedly with oxygenated fresh medium to remove unattached cells and 1 ml fresh medium was added to the plate, which was incubated for 5 min without shaking. The synchronized cells were harvested from the 1 ml of fresh medium. The resulting newborn cells differ in age by a maximum 5 min after cell division.
Fluorescence labelling and fluorescence microscopy
Labelling holdfasts of attached cells. The holdfast is composed of a polysaccharide containing N-acetylglucosamine (GlcNac), which can be labelled with fluorescein-conjugated wheat germ agglutinin lectin (fluorescein-WGA) (Merker and Smit, 1988; Ong et al., 1990). A drop of culture containing synchronized swarmer cells was placed on a coverslip for 5 min to allow some cells to attach to the glass surface. The unattached cells were rinsed with PYE. The cells attached to the coverslips were then grown in oxygenated PYE at 30°C for various amounts of time. After growth, the coverslips were rinsed with water and the cells were labelled with 0.02 mg ml−1 fluorescein-WGA (Molecular Probes) and 0.05% w/v of the bacteriocide sodium azide on ice for 15 min. After labelling, the coverslips were rinsed with 0.05% w/v sodium azide three times and antiphotobleaching solution (20 µg ml−1 catalase, 0.5 mg ml−1 glucose, 0.1 mg ml−1 glucose oxidase and 0.25% v/v mercaptoethanol) was added to the slide for fluorescence microscopy.
Labelling holdfasts of unattached cells. One millilitre of synchronized swarmer cells was added to 100 ml of oxygenated PYE and grown at 30°C without agitation for various amounts of time. In this large volume, very few cells get sufficiently close to the surface to attach. After growth, the unattached cells were supplemented with 0.05% w/v sodium azide and transferred to a pre-cooled glass beaker. Fluorescein-WGA was added to a final concentration of 20 µg ml−1 and the cells were labelled for 15 min on ice. The solution was then passed through an Isopore membrane of 0.4 µm pore size (Millipore) to collect the cells. The collected cells on the membrane were further washed with cold 0.05% w/v sodium azide solution to remove excess dyes. Antiphotobleaching solution was added for fluorescence microscopy.
Attachment of C. crescentus on a glass surface
Immediately after synchronization, an aliquot of synchronized cells was placed between a coverslip and a glass slide that had been cleaned with a solution of 6.5 g of Nochromix (Godax Laboratories) in 100 ml of sulphuric acid for 30 min, rinsed thoroughly with water and dried in air before use. The slide sample was quickly transferred to a warm stage kept at 30°C and observed with dark-field microscopy with a 10× objective, allowing cells at any depth in the field of view to be imaged. To monitor the attachment process, a 1-s-long video was taken at 10 frames per second every 2–3 min. To identify attached cells, an average image was obtained by overlaying the 10 frames of a video and dividing the intensity of the overlay by 10. Since the swimming cells are moving, the brightness of swimming cells is 10 times weaker than that of attached cells in the average image, and therefore the attached cells can be identified by appropriately scaling the image to show only the bright spots (Fig. S2A and B). The attached cells were counted from such images. Attached cells can be distinguished from unattached non-swimming cells because the later drift randomly due to Brownian motion, while attached cells do not. To image the swimming cells, we removed the attached cell from the video by subtracting the average image from each frame. Three consecutive frames were then overlaid and the number of trajectories was counted as the number of swimming cells (Fig. S2C and D). The thickness of the sample was measured using phase-contrast microscopy with a 100× objective by focusing on the top and bottom surfaces respectively (Li and Tang, 2004).
The strain YB2833 (ΔhfsA) lacks a holdfast, is unable to form a stable monolayer and therefore cannot be synchronized by the plate release method. To quantify its attachment, YB2833 cells were grown to exponential phase in a mixed culture, centrifuged and resuspended in fresh PYE. An aliquot was confined between a coverslip and a glass slide and the sample was observed by dark-field microscopy at 30°C. The culture at mid-exponential phase is a mixture of swarmer cells, stalked cells and pre-divisional cells. We measured the decrease in the number of swimming cells as a measure of attachment by counting the number of cell trajectories as described above. The attached cells could easily be washed off the surface, unlike similarly treated wild-type cells, which are tightly attached through their holdfast. Although this strain is able to attach to glass surface through pili, the attachment is not permanent. To quantify the detachment, we added a drop of cell culture at mid-exponential phase to a coverslip, allowed it to sit for 2 min and rinsed gently to remove unattached cells. The number of attached cells was recorded under the light microscope over time.
Labelling holdfast in viscous media
The test viscosity agents used included Percoll (GE), PEGs of molecular weight 8000 Da and 35 000 Da (Fluka), dextran of molecular weight 100 000–200 000 Da (Sigma) and Ficoll of molecular weight 400 000 Da (Fluka). The viscosity was measured with the falling ball method (Tang et al., 1999), except for PEG 8000 (Gunduz, 1996) and Ficoll (Chen and Berg, 2000), which are obtained from the literature. Synchronized C. crescentus wild-type cells were mixed with these agents at the designated concentration and 10 µg ml−1 fluorescein-WGA in PYE in a 1 ml tube. A portion of the mixture was taken out to make slide samples at different times to observe cell swimming and aggregation. To observe holdfast labelling 15 min after mixing, the mixture was passed through a 0.44 µm microfilter (Millipore), followed by passing 60 ml of water to wash the cells trapped by the filter. About 100 µl of water was left in the filter to collect the cells, which became dispersed by the procedure. The cells were then dried on a coverslip for microscopic observation.
A Nikon Eclipse E800 epifluorescence microscope with a 100× oil immersion objective lens (Plan Apo) was used to image the fluorescently labelled holdfast. A highly sensitive and linear CoolSnap camera controlled by MetaMorph software (Universal Imaging, PA) was used to record labelled holdfast fluorescence. The fluorescence images were taken at 0.1 s exposure time. To keep the same photobleaching time for each sample, we focused on the holdfast by taking successive pictures under fluorescence microscopy after readjusting the sample stage height between pictures. If the holdfast was in focus prior to the 11th exposure, subsequent exposures were taken and the picture taken at the 11th exposure was used to measure the fluorescence intensity.
TIRF microscopy was performed with a Nikon E2000 inverted microscope with a TIRF objective (NA = 1.49). Two hundred microlitres of synchronized swarmer cells (2.5 ± 2.5 min old) in 20 µg ml−1 fluorescein-WGA lectin solution in PYE was added to a cleaned coverslip sitting on top of the TIRF objective. Some of the dye adsorbed to the coverslip, facilitating focusing of the microscope. After focusing, the TIRF illumination was kept on for 2 min to photobleach the adsorbed dye. Since the TIRF setting varies from experiment to experiment, it is hard to control the light intensity on the holdfast and inconsistent levels of photobleaching are observed. Light microscopy images and TIRF images were taken alternately with 30 s interval to get a time series. The integrated intensity of the TIRF image of individual holdfasts was measured over time. For experiments in the presence of polymers, cells were mixed with the polymers as indicated and 20 µg ml−1 fluorescein-WGA lectin prior to TIRF observation. All the experiments were performed at approximately 22°C.
A. tumefaciens UPP production during attachment to an Arabidopsis root
Sterilized Arabidopis thaliana seeds were placed on ½ MS salts plates with 1% agar and 1% sucrose and allowed to germinate and grow until the roots were approximately 3 cm long (Ramey et al., 2004). Wild-type A. tumefaciens cells were grown in LB medium at 26°C until reaching exponential phase. Two hundred microlitres of cell culture was washed and resuspended in a solution containing 1 mM calcium chloride and 0.4% sucrose. The bacterial cell suspension was spotted into a Petri dish and a root segment was floated in the bacterial cell suspension. The root segments were incubated in the bacterial culture overnight in the dark at room temperature. The root segments were rinsed in 1 mM calcium chloride and 0.4% sucrose to remove unattached cells and placed on an agarose pad containing Alexa Fluor 488 conjugated-WGA. The attachment of A. tumefaciens cells to the root segments was observed using time-lapse microscopy. A. tumefaciens attachment to the root occurs prior to the formation of UPP and this structure is rarely observed in the unattached cells (Fig. 7).
Initial stages of this work were supported by National Institutes of Health grant GM51986 and an Indiana University Faculty Research Support Program grant to Y.V.B., and by a grant from the Indiana METACyt Initiative of Indiana University (funded in part through a major grant from the Lilly Endowment) to C.F. and Y.V.B. The major portion of this work was supported by National Institutes of Health Grant GM077648 to Y.V.B. and J.X.T. and GM080546 to C.F. P.J.B.B. was supported by a postdoctoral National Institutes of Health National Research Service Award number F32AI072992 from the National Institute of Allergy and Infectious Diseases. The authors thank Peter Merritt for his assistance in growing Arabidopsis thaliana, Daniel Kearns, and members of their laboratories for critical reading of the manuscript.