Staphylococcus aureus is an aggressive pathogen and a model organism to study cell division in sequential orthogonal planes in spherical bacteria. However, the small size of staphylococcal cells has impaired analysis of changes in morphology during the cell cycle. Here we use super-resolution microscopy and determine that S. aureus cells are not spherical throughout the cell cycle, but elongate during specific time windows, through peptidoglycan synthesis and remodelling. Both peptidoglycan hydrolysis and turgor pressure are required during division for reshaping the flat division septum into a curved surface. In this process, the septum generates less than one hemisphere of each daughter cell, a trait we show is common to other cocci. Therefore, cell surface scars of previous divisions do not divide the cells in quadrants, generating asymmetry in the daughter cells. Our results introduce a need to reassess the models for division plane selection in cocci.
Staphylococci are spherical organisms that divide sequentially in three orthogonal planes over three consecutive division cycles1,2. This mode of division is less common in bacterial cells than equatorial division, observed in many genera. Division in three planes implies that cells retain information about the positioning of the two preceding divisions to divide with precision. Given that this spatial information varies with each division, it cannot be encoded by DNA3. Peptidoglycan, the major component of the bacterial cell wall, has been proposed to encode epigenetic information in the form of protuberant, ring-like structures that mark previous division planes and are used by Staphylococcus aureus to divide accurately in sequential perpendicular planes3.
Orientation of division planes is merely one of the distinctive features of the staphylococcal cell cycle. S. aureus has been proposed to have only one cell wall synthesis machine, which incorporates peptidoglycan mostly at the division septum4,5, while rod-shaped bacteria such as Escherichia coli or Bacillus subtilis have two major cell wall synthesis machines, one for incorporation of new peptidoglycan at the division septum and another for elongation of the lateral wall4. Accordingly, S. aureus has only four native Penicillin-Binding Proteins (PBPs 1–4), described to localize at the septum, while E. coli and B. subtilis have 12 and 16 PBPs, respectively, which localize at the septum or at the lateral wall4. PBPs are enzymes involved in the last steps of peptidoglycan biosynthesis, which catalyse the polymerization of the glycan strands, as well as their crosslinking via peptide stems. Given that an elongation-specific machinery seems to be absent in S. aureus, increase of the cell surface area required for growth has been attributed to a process of reshaping the flat septum into curved hemispheres of the two daughter cells, which occurs immediately after splitting of the mother cell during division2. Reshaping of the flat septum, resulting in doubling of the external surface area of peptidoglycan, could theoretically occur in the absence of synthesis, if accompanied by changes in the angle of the glycan chains with respect to the peptide chains6. Alternatively, increase of the surface area could be driven by hydrolysis of peptidoglycan bonds catalysed by specific autolysins. At least 13 genes of the S. aureus genome encode known or putative peptidoglycan hydrolases, although the products of only three of these genes (atl, sle1 and lytM) have been characterized. Of these genes, atl encodes the major autolysin in S. aureus, which is involved in the separation of the daughter cells after division7,8. Interestingly, orthogonal rings of Atl can be observed by immunoelectron microscopy at the surface of S. aureus cells, similar to scars of previous divisions9, confirming that information regarding the localization of previous, orthogonal, division planes can be present at the cell surface.
S. aureus is an aggressive pathogen and one of the most important nosocomial bacteria causing antibiotic-resistant infections. Despite its clinical relevance, the small size of staphylococcal cells (with a ∼1 μm diameter, only four times larger than the diffraction-limited resolution of conventional light microscopy) has impaired a detailed analysis of its cell cycle and of the morphological changes that occur as S. aureus grows and divides. This lack of knowledge extends to the cell cycle of other cocci as well. Therefore detailed characterization of the mode of growth and division of S. aureus has implications for the global understanding of the cell cycle of cocci. Here, we have used super-resolution microscopy to analyse the dynamics of cell shape and size during the cell cycle of S. aureus. We found that, contrary to current thinking, S. aureus cells elongate before dividing. Furthermore, we show that the division septum generates less than one hemisphere of each daughter cell and therefore scars of previous divisions do not mark quadrants of the cell. Our results suggest that the models for division plane selection in cocci should be re-examined.
S. aureus cells elongate during the cell cycle
To follow morphology dynamics during the cell cycle of S. aureus, cells of type strain COL were labelled with the membrane dye Nile Red, placed on an agarose pad containing growth medium and imaged during growth at room temperature by Super-Resolution Structured Illumination Microscopy (SR-SIM; Fig. 1a and Supplementary Movie 1). During the initial phase of the cell cycle (here referred to as Phase 1), before initiation of division septum formation, cells were approximately spherical in shape, as determined by calculating the ratio between the longer axis of the cell (perpendicular to the division septum) and the shorter axis (coincident with the septum) and then became slightly elongated (Fig. 1c, Supplementary Fig. 1 and Supplementary Table 1). In a second stage (Phase 2), cells initiated and completed the synthesis of the division septum and did not significantly elongate. Finally, during the last stage of the cell cycle (Phase 3), cells with a complete septum elongated further, before splitting into two daughter cells. Splitting was accompanied by fast reshaping of the flat septum to become approximately one hemisphere of each daughter cell.
Although we were able to observe cells undergoing complete cell cycles by SR-SIM imaging, we noticed a delay in growth, when compared with cells on the same slide that were not exposed to laser light. Photodamage is cumulative and therefore could cause an increasing bias towards longer duration of growth phases over the course of the experiment. To overcome this limitation, all quantitative analyses were only performed on the first complete growth phase of each cell (that is, in cells observed finishing the previous phase and starting the next phase), and not on the entire cell cycle. Using this approach we measured the duration of each growth phase of the S. aureus cell cycle (Fig. 1b). Cells spent approximately half of the cell cycle in Phase 1 (47±9%), with the other half being spent in septum synthesis (Phase 2, 24±7%) and the final elongation step (Phase 3, 29±6%), with a cell cycle duration of 66±9 min. Because the cells analysed by this method were growing at room temperature on growth medium containing agarose pads, on the microscope stage, we independently confirmed the length of each phase by growing S. aureus cells in liquid culture with aeration at 37 °C, labelling cell membranes and immediately observing them by SR-SIM. The percentage of cells observed in each phase should be proportional to the fraction of the cell cycle spent in that stage. Figure 1b shows that similar results for the duration of Phases 1–3 were obtained by both methods.
Interestingly, at the timescale of this experiment, we never observed intermediate stages in the process of cell splitting and reshaping of the flat septum into a curved surface, implying that these events are likely to be extremely fast. To verify this assumption, we imaged cells, growing on an agarose pad, at 2 ms intervals (Fig. 2a and Supplementary Movie 2). S. aureus cells divided into two daughter cells in the interval between two acquisitions, indicating that splitting takes less than 2 ms (n=10). The spatial and temporal resolution of these images does not allow us to determine if (i) splitting and septum reshaping occur simultaneously, as one could expect if remodelling of the flat septum did not require any enzymatic activity and resulted solely from the increased turgor pressure imposed on the septum as it splits and becomes exposed to the external milieu or (ii) splitting and septum reshaping are two consecutive processes. We reasoned that if the latter hypothesis was correct, we should be able to capture intermediates in the division process in which the septum had already split but remained flat. For this purpose we fixed cells during exponential growth and imaged using Scanning Electron Microscopy (SEM; Fig. 2b). In agreement with previous data9, we observed recently divided cells in which the previous septum was seen as a smooth flat surface, indicating that septum splitting and reshaping are likely to be sequential events.
Septum generates less than one hemisphere of daughter cells
Previous descriptions of the S. aureus cell cycle suggested that cell wall synthesis occurred mainly, if not only, at the division septum5. Furthermore, it was assumed that the ‘new’ cell wall material, from the septum of the mother cell, formed one complete hemisphere of each of the daughter cells, while the other hemisphere was made of ‘old’ cell wall material originating from the peripheral wall of the mother cell. However, we observed that just before splitting, at the end of Phase 3, the mother cell has an ellipsoid shape, with a semi-major axis of 0.70±0.04 μm (perpendicular to the septum) and two semi-minor axes of 0.55±0.03 μm (equivalent to the radius of the septum) resulting in a septal surface area of 0.95 μm2. After splitting, at the beginning of Phase 1, each daughter cell has semi-major and semi-minor axes of 0.52±0.03 μm and 0.46±0.03 μm, respectively. Therefore, the total surface area of each daughter cell is ∼2.89 μm2 (see Methods section for Knud Thomsen approximation used for calculations), of which 0.95 μm2, or ∼33%, should be composed of new cell wall material, originating from the septum of the mother cell (in the absence of septum expansion). The remaining ∼67% of the cell surface should be composed of ‘old’ cell wall material, originating from one hemisphere of the mother cell, that is, the distribution of old and new cell wall material should not be 50% of each, as previously assumed3,5,6 (Fig. 3a).
To determine whether the mode of S. aureus growth was consistent with these assumptions, cells were labelled with a green fluorescent derivative of wheat germ agglutinin (WGA-488), a lectin that labels N-acetylglucosamine residues present in peptidoglycan and in wall teichoic acids. Importantly, WGA labels the cell wall present at the cell surface (peripheral wall) but does not diffuse into (and therefore does not label) the division septum. Cells were next washed to remove unbound WGA-488, and stained with the membrane dye Nile Red, which diffuses through the septum and therefore labels the entire membrane of the cell. Finally, cells were placed on an agarose pad containing growth medium and imaged by SR-SIM during growth (Fig. 3b). Cells whose surface was completely labelled by WGA-488 were selected for analysis, and both the perimeter of each cell as well as the fraction of the cell surface made of old cell wall (WGA-488 labelled) was measured. In agreement with our model, we found that after splitting of the mother cell, each daughter cell had 61.3±3.3% (n=30) of its surface labelled by WGA-488, that is, made of old cell wall, clearly showing that the flat septum, even after reshaping, does not contribute to half of the cell surface (Fig. 3c).
These results were confirmed in a second experiment, similar to the one described above, in which cells were labelled with Hydroxycoumarin-amino-D-alanine (HADA) instead of WGA-488. HADA is a blue fluorescent derivative of 3-amino-D-alanine that can be incorporated in the pentapeptide chain of peptidoglycan10. Selected cells whose entire surface was labelled with HADA at time zero were followed during growth for 60 min (Fig. 3d). Similar to the results obtained with WGA-488 labelling, on splitting of the mother cell 62.5±3.4% of the surface of each daughter cell was labelled with HADA.
Careful inspection of SEM images of S. aureus cells confirms that the ‘old’ cell wall constitutes more than 50% of the surface of each daughter cell (Fig. 4). Cell wall material that is at least one generation old has been described as having an irregular, rough appearance, while newly synthesized cell wall, resulting directly from the septum of the mother cell, has a smoother appearance with concentric rings3,11, with a clear border separating the two types of cell surface12. These borders, seen in Fig. 4 and denoted in blue in the schematic representation of the cells, are clearly not placed at mid cell, reinforcing the idea that more than half of the surface of S. aureus cells is at least one generation old.
We then asked if this mode of division of spherical cells, in which the division septum of the mother cell generates less than one hemisphere of each daughter cells, was restricted to S. aureus or common to other cocci. Labelling of peripheral cell walls in Sporosarcina ureae with WGA-488 showed that division of spherical cells from this organism also results in daughter cells with ∼60% of the surface made of ‘old’ cell wall (Fig. 3f).
S. aureus grows by remodelling the entire cell surface
The fact that cell wall synthesis in Staphylococci occurred mainly, if not exclusively, at the division septum5, led to the suggestion that S. aureus does not enlarge during the cell cycle and that the conversion of the flat division septum into one hemisphere of each daughter cell accounted for the doubling in volume required for cell division to take place3,5,6. Importantly, the diffraction-limited resolution of conventional light microscopy (∼250 nm)13,14 impaired, until now, detection of size variations in the range of those required for the doubling of S. aureus cell volume (see Discussion section). These variations can, however, be observed by SR-SIM, which improves the lateral (xy) resolution to ∼110 nm15. Using this technique, we observed that staphylococcal cells increased in volume during the entire cell cycle, from a volume of 0.47±0.07 μm3 at the beginning of Phase 1 to a volume of 0.91±0.12 μm3 at the end of Phase 3 (Fig. 1d and Supplementary Table 2). If enlargement of S. aureus cells was mainly due to the remodelling of the flat septum into a hemisphere, the volume increase should be essentially restricted to the process of splitting and reshaping of the septum. On the contrary, we have observed that there is no significant increase in volume when staphylococcal cells divide, that is, each of the two daughter cells has approximately half of the volume of the Phase 3 mother cell (Fig. 1d). Furthermore, the largest and fastest increase in volume occurs during Phase 3 (Δvolume=0.16±0.07 μm3 at a rate of 0.009±0.003 μm3 min−1, Supplementary Table 2), during which there is no reshaping of the flat septum, clearly indicating that other mechanisms must be involved with the enlargement of S. aureus cells.
Next, we wondered if enlargement of cells occurred via remodelling only of the material derived from the previous septum or via remodelling of the entire cell surface (Fig. 3a). In the former case, the percentage of ‘new’ cell wall should increase during the course of the cell cycle, eventually reaching half of the total cell surface, while in the latter case the ratio of new to old cell wall observed immediately after splitting of the mother cell (∼39% to ∼61%, respectively, Fig. 3b) should be maintained over the cell cycle. Therefore, following the growth of cells in which the ‘old’ cell wall was labelled with WGA-488 should allow us to determine how S. aureus cells enlarge. The perimeter of WGA-488-labelled cells increased from 3.08±0.17 μm to 3.40±0.21 μm after 60 min on the slide, confirming that the cells were growing. Under these conditions, the fraction of cell wall labelled by WGA-488 remained at 60.6±3.2%, even in cells that were already initiating the next round of division (Fig. 3b,c). Similar results were obtained with HADA-labelled cells, in which the fraction of labelled cell wall remained at 60.5±3.8% after 60 min (Fig. 3d,e), indicating that cell enlargement was due to remodelling of the entire cell surface and not exclusively of the septal material.
Cell enlargement needs peptidoglycan synthesis and autolysis
Enlargement of bacterial cells can occur via synthesis of new peptidoglycan, autolysis of old peptidoglycan or a combination of both processes. We have previously observed that peptidoglycan synthesis occurred mostly at the division septum5. Given that we have now shown that growth of staphylococcal cells occurs via remodelling of the entire cell surface, we considered the possibility that enlargement was mainly due to autolytic activity. However, autolysis without synthesis would lead to a thinning and/or increase in the porosity of the old peptidoglycan mesh over consecutive generations. Since ∼60% of old cell wall is transmitted to daughter cells in each cell division, staphylococcal cells would have regions of the surface a few generations old, which were necessarily submitted to the enlargement process multiple times. Thinning of these regions owing to peptidoglycan autolysis without synthesis could therefore endanger the integrity of the bacterial cell. Making use of newly available tools to study peptidoglycan synthesis and to image protein localization, we revisited the question regarding the localization of peptidoglycan synthesis in S. aureus.
S. aureus cells were labelled with Nitrobenzofurazan-amino-D-alanine (NADA), a green fluorescent derivative of 3-amino-D-alanine that can be incorporated by PBPs in the pentapeptide chain of peptidoglycan10. Cells in growth Phases 2 and 3, that is, cells with partial or complete septa, showed labelling mostly at the septum, in agreement with previous reports showing that the majority of PBP activity takes place at the septum4,5,16. However, peripheral signal was also observable (Fig. 5a). Labelling around the entire cell surface was even more noticeable in Phase 1 cells, lacking a septum (Fig. 5a, cells labelled with asterisks), even when the labelling period was as short as 5 min (Supplementary Fig. 2).
We then asked which of the four native S. aureus PBPs had peripheral activity. Given that PBP1 and PBP2 are essential proteins in MSSA strains and therefore cannot be depleted17,18, S. aureus mutants lacking PBP3 and PBP4 were initially tested. COLΔpbpD cells, lacking PBP4, were virtually devoid of NADA labelling away from the septum (Fig. 5b and Supplementary Fig. 3b), showing that this protein is the main enzyme responsible for the peripheral signal. Complementation of COLΔpbpD with a plasmid-encoded PBP4 resulted in recovery of the peripheral signal (Supplementary Fig. 3c,d). A comparison of the ratio of the septal versus peripheral fluorescence signal, obtained by conventional epifluorescence microscopy, in the COL parental strain (7.91±0.42) and COLΔpbpD (18.7±0.76) confirmed that incorporation of D-alanine-labelled analogues was essentially absent from the peripheral wall of the mutant lacking PBP4 (Supplementary Fig. 3e). In agreement, localization of a fluorescent derivative of PBP4 by SR-SIM showed that although this protein is mainly localized at the septum, as we have previously reported19, peripheral fluorescent signal could also be observed (Fig. 5c and Supplementary Fig. 3f). Quantification by PhotoActivated Localization Microscopy (PALM) showed that 26±11% of the total PBP4 molecules (fused to photoactivatable mCherry) in Phase 3 cells are present at the peripheral membrane (Supplementary Fig. 3g).
Furthermore, the duration of Phase 1 is longer in COLΔpbpD than in the parental strain COL (Fig. 6a) and the cell volume is smaller (Supplementary Table 2), reinforcing the hypothesis that PBP4 is one of the proteins that have a role in peripheral peptidoglycan synthesis during this growth phase.
In contrast, cell elongation is unaffected in COLΔpbpD cells (Supplementary Table 1), suggesting that additional proteins have a role in cell growth. We therefore evaluated the role of two major autolysins, Atl (ref. 7) and Sle1 (ref. 20) in cell enlargement and elongation, as well as in septum remodelling, by deleting chromosomal atl or sle1 genes of strain COL. The lack of Atl amidase and glucosaminidase activities led to larger cells that are less elongated when compared with the parental strain COL (Supplementary Tables 1 and 2), indicating that Atl autolytic activity is involved not only in cell separation, as previously shown8,9, but also in cell size homoeostasis and shape maintenance. COLΔsle1 cells remain elongated throughout the entire cell cycle, which could result from increased stiffness of peptidoglycan in the absence of Sle1 amidase activity, possibly impairing correct reshaping of the cell following division. Furthermore, these cells have a longer Phase 3 than the parental strain COL (Fig. 6a and Supplementary Fig. 4), suggesting that cell splitting is impaired in this mutant.
Interestingly, we have observed the appearance, albeit at low frequency, of cells with the shape of the letter ‘D’ in cultures of COLΔsle1 (Fig. 6b). These cells seem to be impaired in the process of reshaping of the flat septum, generated immediately after the splitting of the mother cell, into a curved hemisphere. D-shaped cells were never observed in the parental strain COL by SR-SIM. This phenotype seems to be a consequence of defects in specific autolytic enzymes whose activity is required for the reshaping of the flat septum, since asymmetric cells were also identified at higher frequencies than in the parental strains in (i) an sle1 deletion mutant in the background of a different S. aureus strain, namely NCTC8325-4 (Supplementary Fig. 5b); (ii) an NCTC8325-4 mutant lacking LytM, an autolysin with glycylglycine endopeptidase activity21 (Supplementary Fig. 5c); and (iii) a COL mutant depleted for the two-component system WalK/WalR (also known as YycG/YycF), which positively controls autolytic activity22 (Supplementary Fig. 5e). Interestingly, although WalKR is essential in RN4220 (ref. 22), strain COL grows in its absence.
To determine if turgor pressure also had a role in driving the reshaping of the flat septum, we incubated COL and COLΔsle1 in buffer containing saturating NaCl concentration. The decreased turgor pressure led to higher frequency of ‘D’ shaped or asymmetric cells both in COLΔsle1 and in parental strain COL, albeit to lower levels in the parental strain (Fig. 6d). Strain COLΔsle1 complemented with a plasmid-encoded Sle1 behaved as the parental strain COL (Supplementary Fig. 6). These results suggest that the division septum requires the action of both autolytic enzymes and turgor pressure to change from a flat to a curved surface, although we cannot exclude the possibility that the effect of NaCl is due to an impact on the activity of autolysins.
Despite its importance as a clinical pathogen, the small size of S. aureus cells has impaired a detailed analysis of the morphological changes occurring during its cell cycle, given that size variations required to double the cell volume are close to the limit of resolution of conventional optical microscopy: S. aureus cells are ∼1 μm in diameter (or 0.52 μm3 in volume). Approximating the cell shape to a sphere, an increase of the diameter to 1.26 μm is sufficient to double the cell volume. However, this 260 nm increase is close to the diffraction-limited resolution of conventional optical microscopy, which is ∼250 μm for most biocompatible fluorophores13,14.
The current model for S. aureus cell division postulates that cells do not significantly enlarge during the cell cycle and that the major variation in cell volume occurs on splitting of the mother cell, when the flat septum is reshaped into a curved surface to generate one hemisphere of each daughter cell. This model was based on the fact that both incorporation of new peptidoglycan material and localization of the major peptidoglycan synthesis enzymes, the PBPs, occurred mostly at the septum5,16,17,19,23, two observations that still hold true. However, here, by fast imaging of dividing S. aureus cells, we show that reshaping of the division septum is an extremely rapid process, on the timescale of <2 ms, and therefore not compatible with a duplication of cellular volume and the consequent abrupt changes in concentrations of cellular contents. It is therefore more likely that, similar to other bacteria, the volume of S. aureus cells gradually increases over the cell cycle, but these size variations are too small to be observable by conventional light microscopy.
Recent advances in fluorescence microscopy, specifically the introduction of super-resolution techniques, now allow an unprecedented level of detail in the analysis of bacterial cell morphology. Making use of SR-SIM, with a lateral resolution of ∼110 nm (ref. 15), we measured variations of the volume of S. aureus cells and concluded that (i) cell volume increases gradually over the entire cell cycle and (ii) there is no substantial increase in cell volume due to reshaping of the flat septum, given that on splitting of a mother cell, each newly generated daughter cell has approximately half of the mother cell’s volume. Furthermore, and contrary to previous assumptions, the cell wall material resulting from the division septum of the mother cell (new cell wall) does not constitute half of the cell surface of each daughter cell, but ∼33% (Fig. 7). Taken together, these observations suggest that other mechanisms besides septum reshaping are responsible for cell growth in S. aureus.
On division of the mother cell, S. aureus cells could grow by (i) remodelling and enlarging only the new cell wall material or (ii) remodelling the entire cell surface. In the first case, the surface area corresponding to new cell wall material would be expected to expand from 33% and eventually constitute half of the cell surface, while in the second case the 33/67 ratio of new/old cell wall would be maintained during the entire cell cycle. We have labelled peripheral cell wall with a lectin (WGA-488) as well as a fluorescent derivative of D-alanine (HADA) and confirmed that the latter hypothesis is correct.
Cell enlargement can occur by synthesis of new peptidoglycan material, autolysis of old peptidoglycan or a combination of both processes. The fact that the entire cell surface is enlarged during growth, but different sections of the surface vary in age, seems incompatible with the notion that peptidoglycan synthesis or autolysis alone are responsible for the increase in cell surface. If that were the case, then regions with different ages of the cell wall would have different thickness and/or porosity. By transmission electron microscopy, S. aureus peripheral cell wall seems homogeneous in thickness24. The porosity of new and old cell wall may be different, as the former shows a series of concentric rings while the latter appears as a network of fibres with a large number of empty spaces between them, perhaps resulting from autolytic activity11,25. However, if this autolytic activity would occur across the entire cell surface multiple times, that is, over several generations, in the absence of peptidoglycan synthesis, holes in older regions of the cell surface would presumably become larger, possibly endangering the integrity of the cell.
It therefore seems likely that peptidoglycan synthesis has to occur across the cell surface, concomitantly with autolysis. In fact, we were able to detect peripheral PBP activity through the incorporation of fluorescent derivatives of 3-amino-D-alanine10, mediated mostly by PBP4, in agreement with recent data by Gautam et al.26. It is possible that other PBPs also have a role in peripheral peptidoglycan synthesis, which is not detected in our assay given that PBP4 is the main responsible for incorporation of exogenous peptidoglycan synthesis probes26,27. It is important to note that these probes may be incorporated by PBPs in an exchange reaction that occurs outside the cell, and therefore do not necessarily reflect the sites of incorporation of lipid-linked peptidoglycan precursors. It is possible that PBP4 activity is required, not (only) to incorporate new peptidoglycan precursor molecules, therefore increasing the amount of peptidoglycan material in the cell wall, but also to make new bonds in pre-existing material that was subjected to autolytic activity during cell expansion leading to an increased mechanical strength. In fact PBP4 was shown to be responsible for the very high levels of peptidoglycan crosslinking characteristic of S. aureus28,29 and required to increase the stiffness of the cell envelope30.
Finally, we have also pondered over the question of the extremely fast process of septum reshaping into a curved hemisphere, namely if it was a purely mechanical process or if it required enzymatic activity. Previous reports using atomic force microscopy imaging have shown the presence of perforation holes around the bacterial circumference coincident with the outer edge of the division septum. These holes become larger, merge and form longer nicks in the peripheral wall as splitting of the septum proceeds25. These holes are most likely the result of activity of autolysins such as Atl, a protein required for cell separation, which localizes in rings at the division site8,9. Interestingly, Atl localizes exclusively at the external edge of the septum, not across the entire septal surface9, suggesting that its activity is only required at the initial steps of splitting. This would be in agreement with the suggestion by Matias and Beveridge that the septum of S. aureus has a middle zone that separates two adjacent septal cross walls31. Once the outer edge of the septum is cleaved by autolysins, cell separation could proceed through a merely mechanical process driven by turgor pressure on the two separate halves of the cross-wall, as no additional cleavage of peptidoglycan bonds would be required across the septum. The time required for splitting, which we have now shown to occur in <2 ms, does indeed suggest a mechanical process, probably driven by turgor pressure, in agreement with our data showing that septum reshaping is impaired in high osmolarity conditions and with recent data published while this manuscript was under revision32. However, we have also shown that autolysins such as Sle1 and LytM have a role in reshaping of the flat septum, given that mutants lacking one of these proteins, particularly when exposed to medium with high osmolarity, generate daughter cells in which the previous septum remains flatter. Nevertheless, we cannot determine if Sle1 and LytM activities occur before or during splitting. Interestingly, Bailey et al.33 have recently shown that the new cell wall material in the flat septum is stiffer than the rest of the cell wall and becomes softer when fully expanded into a hemisphere. Therefore, these authors suggest that reshaping of the flat septum cannot occur only through stretching (as this would require the flat septum to be thicker but softer than the rest of the cell wall), but instead requires partial degradation of the peptidoglycan by autolytic enzymes33.
The increase in resolution resulting from advances in super-resolution microscopy has allowed us to completely redefine the cell cycle of S. aureus, one of the most relevant bacterial pathogens, with important implications for current models of cell division in cocci. S. aureus cells divide in three orthogonal planes over three consecutive division cycles1,2, raising the question of how do the cells retain ‘memory’ of the two previous planes of division, to define a third, perpendicular, division plane. Scars of previous divisions have been proposed to contain epigenetic information regarding the previous planes of division3. Junctions of these scars at the cell poles could be used as topological cues to drive chromosome segregation in an axis perpendicular to the next division plane34. The process of nucleoid occlusion, which prevents assembly of the divisome over the chromosome, would then restrict the localization of the next division plane to a plane orthogonal to the two previous ones34. However, these models assume that scars of previous division planes are placed precisely at the centre of the cell (similar to the equator or meridians of earth, Fig. 7a), and therefore cross each other at poles of the cells. Our observation that lines dividing the S. aureus cell surface containing old/new cell wall material do not divide the cell in two equal parts (Fig. 7b), reopens the question of how staphylococci divide in orthogonal planes. Our findings may also be extended to other cocci that divide in orthogonal planes, such as Sporosarcina, and thus our observations described for S. aureus should have implications for the global understanding of cell division in other coccal bacteria.
Bacterial growth conditions
Strains and plasmids used in this study are listed in Supplementary Table 3. S. aureus strains were grown in tryptic soy broth (TSB, Difco) with aeration at 37 °C or on tryptic soy agar (Difco) at 30 or 37 °C. For microscopy experiments, overnight cultures of S. aureus strains were diluted 1:200 in fresh TSB medium and allowed to grow at 37 °C until an OD600 nm of ∼0.5. Cells were then collected and resuspended in the same medium. E. coli and S. ureae strains were grown in Luria–Bertani broth (Difco) with aeration, or Luria–Bertani agar (Difco) at 37 or 30 °C, respectively. Antibiotics ampicillin and erythromycin were added to the media at a final concentration of 100 and 10 μg ml−1, respectively, when necessary. 5-Bromo-4-chloro-3-indolyl β-D-galactopyranoside (X-gal) was used at 100 μg ml−1. Expression of PBP4 from plasmid pBCBPM115 was induced with cadmium chloride (1 μM). Expression of Sle1 from plasmid pSle1 was induced with IPTG (1 mM) in the presence of 10 μg ml−1 chloramphenicol.
Construction of S. aureus mutants
The COLΔatl, COLΔsle1 and NCTCΔlytM null mutants (Supplementary Table 3) were constructed using the pMAD vector35 containing the upstream and downstream regions of each gene of interest, to allow recombination and integration of the plasmids into the chromosome, followed by their excision with the genes to be deleted. Briefly, upstream and downstream regions of sle1 and lytM were amplified by PCR, using primers P1_sle1/P2_sle1 and P3_sle1/P4_sle1, P1_lytM/P2_lytM and P3_lytM/P4_lytM, respectively (Supplementary Table 4). The PCR fragments encoding the upstream and downstream regions of each gene were joined by overlap PCR using the pairs of primers P1_Sle1/P4_Sle1 and P1_lytM and P4_lytM. The resulting fragments were digested with NcoI and BglII (Fermentas) and cloned into the pMAD vector, giving plasmids pΔsle1 and pΔlytM, which were propagated in E. coli DC10B and whose inserts were sequenced. The plasmids, as well as pΔatl36, were then electroporated into S. aureus RN4220 strain at 30 °C, using erythromycin and X-gal selection, and transduced into COL or NCTC8325-4 using phage 80α (ref. 37). The integration of the plasmids into the chromosome and their excision was done as previously described23. Gene deletions were confirmed by PCR and sequencing of the amplified fragment.
For complementation of COLΔsle1, plasmid pBCBover was constructed by introducing a DNA fragment containing the Pspac promoter, a multiple cloning site and the lacI gene into the S. aureus replicative vector pGC2 (ref. 38). For that, two DNA fragments, one containing the Pspac coding sequence and HindIII, SmaI and XbaI restriction sites and a second one encompassing a BglII restriction site upstream of the lacI gene, were amplified from pDH88 plasmid39 by using, respectively, the pair of primers Pspac_pDH88_P9_XhoI_SalI/Pspac_pDH88_SpeI_P10 and Pspac_pDH88_SpeI_P11/Pspac-pDH88-P12-XhoI-EcoRI. These two PCR products were then joined in a second PCR, using primers Pspac-pDH88_P9_XhoI_SalI and Pspac-pDH88-P12-XhoI-EcoRI, to originate a 1,743 bp fragment in which a SpeI restriction site was introduced between XbaI and BglII restriction sites. The resulting fragment was restricted with SalI and EcoRI, cloned into the pGC2 vector and sequenced. The pSle1 plasmid was constructed by cloning the entire sle1 coding sequence downstream of Pspac promoter in pBCBover. For that, a 1,024 bp DNA fragment containing sle1 gene and its upstream ribosomal binding site was amplified from NCTC8325-4 genome using primers Sle1_FW_XmaI and Sle1_RV_XbaI, digested with SmaI and XbaI and cloned into pBCBover. The insert was then sequenced.
Both pBCBover and pSle1 plasmids were electroporated into RN4220 (selection with 10 μg ml−1 chloramphenicol) and subsequently transduced, using phage 80α, to strain COLΔsle1, generating strains COLΔsle1pBCBover and COLΔsle1pSle1, respectively.
Construction of an S. aureus COL mutant with yycFG (also known as walKR) under the control of the IPTG-inducible Pspac promoter was done using the pMUTIN4 plasmid40. A 518-bp fragment containing the ribosome binding site and 5′ end of yycF (walR) was amplified using primers yycF_fw_EcoRI and yycF_stop_rv_BamHI. The DNA fragment was then digested with EcoRI and BamHI, cloned into pMUTIN4 giving plasmid pwalKR, which was propagated in E. coli DC10B and whose insert was sequenced. Plasmid pwalKR was then electroporated into S. aureus RN4220 at 37 °C, using erythromycin selection, and transduced into COL using phage 80α. Integration of the plasmid occurred through a single crossover event, placing the walKR operon under the control of the Pspac promoter.
To study PBP4 localization in S. aureus NCTC8325-4 strain by PALM, we replaced the pbpD gene, encoding PBP4, for a gene encoding a photoactivatable derivative (pbpD-PAmCherry). For that purpose, pbpD was cloned fused to PAmCherry1 (ref. 41) in the backbone of pCNX plasmid. The pCNX plasmid was constructed by substituting the erm erythromycin resistance cassette of the pCN51 plasmid42 by the aphA-3 kanamycin cassette from pCN34 (ref. 42), using ApaI and XhoI restriction sites. To clone pbpD-PAmCherry into pCNX, a fragment encompassing a ribosomal binding site, the pbpD gene lacking the stop codon and seven codons encoding an amino-acid linker was amplified using NCTC8325-4 genomic DNA as template and primers P1pbp4pCNX and P2pbp4pCNX. A fragment encompassing PAmCherry1 was amplified from the pBAD/HisB-PAmCherry1 plasmid41 using P3pbp4pCNX and P4pbp4pCNX primers. The two fragments were joined by overlap PCR, digested with BamHI and EcoRI, ligated into the pCNX plasmid generating plasmid pBCBRP007, whose insert was sequenced. We then replaced the pbpD gene from its native locus in the S. aureus genome by the pbpD-PAmCherry fusion. For this purpose two DNA fragments were amplified, one encompassing a truncated pbpD (last 999 bp), a sequence encoding a seven-amino-acid linker and PAmCherry1 amplified from the pBCBRP007 plasmid using primers P1pMADpbp4PAmCherry and P2pMADpbp4PAmCherry and a second DNA fragment of 1,000 bp corresponding to the region downstream of pbpD amplified from the NCTC8325-4 genome using primers P3pMADpbp4PAmCherry and P4pMADpbp4PAmCherry. The two fragments were joined by overlap PCR using primers P1pMADpbp4PAmCherry and P4pMADpbp4PAmCherry, digested with BamHI and XmaI restriction enzymes and cloned into pMAD, generating pBCBRP008 plasmid. Correct sequence of the insert was confirmed and the pBCBRP008 plasmid was electroporated into RN4220 and subsequently transduced to NCTC8325-4 strain using phage 80α. Integration and excision of pBCBRP008 from the genome was performed as previously described23, colonies in which pbpD had been replaced by the pbpD-PAmCherry were identified by PCR and the strain was named NCTCΔpbpD::pbpD-PAmCherry.
To complement COLΔpbpD with a plasmid encoding PBP4, the 1.3 Kb pbp4 gene was PCR amplified from NCTC8325-4 genomic DNA using primers PBP4pCadP1BamFW and pCADPBP4wt_EcoREV and cloned into the pCNX replicative plasmid, under the control of a cadmium inducible promoter, using BamHI and EcoRI sites, generating plasmid pBCBPM115. Plasmids pCNX and pBCBPM115 were electroporated into RN4220 and then transduced into COLΔpbpD, giving rise to strains BCBPM120 (COLΔpbpDpCNX) and BCBPM138 (COLΔpbpDpPBP4).
Scanning electron microscopy
Exponentially growing S. aureus COL cells43 were collected by centrifugation, resuspended in fixative solution (2.5% glutaraldehyde in 0.2 M sodium cacodylate buffer, pH 7.4), deposited on glass discs (Marienfeld) and kept for 1 week at 4 °C. The fixative solution was subsequently removed and the cells were washed three times with sodium cacodylate solution. The sample was progressively dehydrated by immersion in a graded series of ethanol (50–100%) and then mounted on aluminium stubs with carbon adhesive discs (Agarscientific). The sample was critical-point dried under CO2 and sputter coated with gold–palladium (Polaron SC7640) for 200 s at 10 mA. SEM observations were performed using secondary electron images (2 kV) with a Hitachi S4500 instrument at the Microscopy and Imaging Platform (Micalis, B2HM, Massy, France) of the INRA research centre of Jouy-en-Josas (France).
Super-resolution structured illumination microscopy
SR-SIM imaging was performed using a Plan-Apochromat 63x/1.4 oil DIC M27 objective, in an Elyra PS.1 microscope (Zeiss). Images were acquired using either three or five grid rotations, with 34 μm grating period for the 561 nm laser (100 mW), 28 μm period for 488 nm laser (100 mW) and 23 μm period for 405 nm laser (50 mW). Images were acquired using a Pco.edge 5.5 camera and reconstructed using ZEN software (black edition, 2012, version 220.127.116.114) based on a structured illumination algorithm44, using synthetic, channel specific optical transfer functions and noise filter settings ranging from −6 to −8.
Fast time-lapse imaging of S. aureus
A 2 μl aliquot of an exponentially growing culture of S. aureus was placed on an agarose pad in TSB. Cells were imaged at 2 ms intervals for a total time of 10 s, using a Pco.edge 5.5 camera and a Plan-Apochromat 100x /1.46 NA Oil DIC ELYRA objective in an Elyra PS.1 microscope (Zeiss).
Labelling and imaging of S. aureus
For time-lapse experiments, S. aureus cells were incubated with the membrane dye Nile Red (Invitrogen) at a final concentration of 10 μg ml−1, for 5 min at 37 °C, with agitation (550 r.p.m.). Subsequently, the cells were placed on an agarose pad containing 50% TSB in phosphate buffer saline (PBS) and imaged during growth by SR-SIM. Image sets were acquired every 3 min, for a total period of 1 h, using 2% of 561 nm laser power and 50 ms exposure times. Measurements were performed on reconstructed super-resolution images using ZEN software.
To determine the fraction of old/new cell wall in S. aureus, cells were stained with either a wheat germ agglutinin Alexa Fluor 488 conjugate (WGA-488, Invitrogen) or fluorescent D-amino-acid HADA10,45 at a final concentration of 2 μg ml−1 and 250 μM, respectively. The cells were incubated at 37 °C with agitation for 5 or 30 min for WGA-488 or HADA, respectively. Unbound dye was removed from the media by washing cells with TSB and cells were then incubated with Nile Red (10 μg ml−1) for 5 min at room temperature and placed on an agarose pad containing 50% TSB in PBS. Cells showing uniform WGA-488 or HADA staining were imaged by SR-SIM at 0, 3, 6, 30 and 60 min, using 2% 561 nm laser with 50 ms exposure for Nile Red, 3% 488 nm laser with 50 ms exposure for WGA-488 and 20% 405 nm laser with 100 ms exposure for HADA.
To evaluate localization of peptidoglycan synthesis activity, S. aureus cells grown to an OD600 nm of ∼0.5 were labelled with fluorescent D-amino-acid NADA (250 μM) for 20 min at 37 °C, 550 r.p.m. Cells were then washed with PBS, placed on an agarose pad and visualized by SR-SIM, using 10% 488 nm laser, 100 ms exposure. For pulse labelling experiments, S. aureus cells were incubated with either HADA or its L-enantiomer HALA10 for 5 min at 37 °C, 550 r.p.m. and then imaged as described above.
S. aureus cell wall labelling with vancomycin was performed by incubating the cells for 2 min at room temperature with a mixture containing equal amounts of vancomycin (Sigma) and a BODIPY FL conjugate of vancomycin (Van-FL, Molecular Probes) to a final concentration of 0.8 μg ml−1. Cells were visualized by SR-SIM, using 2% 488 nm laser, 100 ms exposure.
Labelling and imaging of S. ureae
To determine the fraction of old/new cell wall in S. ureae by time-lapse microscopy, cells from cultures at OD600∼0.5 were stained with WGA-488 at a final concentration of 6 μg ml−1. The cells were incubated at 30 °C with agitation for 10 min. Unbound dye was removed from the medium by washing cells with Luria–Bertani broth. Cells were then incubated with Nile Red (10 μg ml−1) for 5 min at room temperature and placed on an agarose pad containing 50% Luria–Bertani broth in PBS. Cells showing uniform WGA-488 labelling were imaged by SR-SIM at 0, 15, 30, 45 and 60 min, using 2% 561 nm laser with 50 ms exposure for Nile Red, 3% 488 nm laser with 50 ms exposure for WGA-488.
Photoactivated localization microscopy
To observe PBP4-PAmCherry single molecules by PALM, an overnight culture of NCTCΔpbpD::pbpD-mCherryPA was diluted 1/200 in TSB and incubated at 37 °C. At mid-exponential phase (OD600 nm 0.6), 1 ml of culture was harvested by centrifugation and washed with 1 ml of PBS. Cells were resuspended in 20 μl of PBS and 1 μl was placed on a thin layer of 1.2% agarose in PBS mounted on a gene frame (Thermo Scientific). Image sequences for PALM analysis were obtained using a Zeiss Elyra PS.1 microscope with a × 100 1.46 NA objective, additional magnification of × 1.6, equipped with an electron multiplying charge-coupled device camera (Andor—iXon DU897) using the Zeiss ZEN software. For an initial bleach of auto-fluorescent molecules and unwanted preactivated fluorophores, the sample was first imaged with a 561 nm laser at ∼0.76 kW cm−2 and 33 ms exposure for 2,000 frames. After bleaching, the continuous activation and imaging of PAmCherry molecules was performed for 8,000 frames by simultaneously irradiating the sample with a 405 nm laser at ∼1.9 W cm−2 and a 561 nm laser at ∼0.76 kW cm−2, using 33 ms of exposure time. To maintain a stable density of fluorophores photo activating in each frame and compensate the depletion of PAmCherry molecules during the course of the experiment, the intensity of the 405 nm laser was gradually increased until ∼38 W cm−2. Post-processing of the last 8,000 frames was performed using the ZEN software where an xy two-dimensional-Gaussian fit was applied to the individually resolvable subdiffraction molecules present in each frame (mask of 9 pixels with a minimum signal-to-noise ratio of 6).
COL and COLΔsle1 cells were grown in TSB until an OD600 nm of ∼0.5 and then incubated for 30 min at 37 °C with agitation (700 r.p.m.) in the presence of NADA (250 μM). The cells were collected, washed once with 50 mM Tris-HCl buffer pH=7.5 containing a saturating concentration of NaCl (4.96 M) and incubated for 15 min at 37 °C. Cells were pelleted and placed on an agarose pad containing the same medium used to perform the hyperosmotic shock and imaged by SR-SIM.
Calculation of cell dimensions
To calculate the volume of each cell, an ellipse was fitted to the border limits of the cellular membrane of Nile-Red-labelled cells, overlaying the membrane dye signal. Subsequently, the shorter and longer axes were measured, coinciding with the septum and the axis perpendicular to it, respectively. The volume of the cell was obtained by an approximation to the volume of a prolate spheroid (equation (1)) where a and b correspond to the longer and shorter semi-axes, respectively.
Cell surface area was calculated using the Knud Thomsen approximation46 (equation (2)) to calculate surface area of ellipsoids, where a corresponds to the longer semi-axis and b and c correspond to shorter semi-axes, which are identical in the case of S. aureus cells.
To evaluate cellular symmetry and identify ‘D’ shaped cells, cells in Phase 1 of the cell cycle were selected and an ellipse was fit to the cell borders corresponding to the old cell wall. The ellipse centre was defined as the middle point of the longer axis and the distances from this point (along a perpendicular axis) to new peripheral cell wall and old peripheral cell wall were calculated (see Fig. 6d). Symmetry was assessed by the ratio between the distance from the centre to the old cell wall and the distance from the centre to the new cell wall. A cell was considered as asymmetric when this ratio was more than 1.33, that is, when the distance from cell centre to the new cell wall was <75% of the distance to the old cell wall.
Calculation of fluorescence ratio in NADA-labelled cells
NADA-labelled S. aureus cells were observed using a Zeiss Axio Observer microscope equipped with a Photometrics CoolSNAP HQ2 camera (Roper Scientific) and Metamorph 7.5 software (Molecular Devices). To quantitatively assess D-amino-acid incorporation, the fluorescence signal at the septum and at the peripheral cell wall was determined for 50 cells with fully formed septa. A fluorescence ratio for septal versus peripheral cell wall signals was determined as previously described47.
Statistical analyses were done using GraphPad Prism 6 (GraphPad Software). Unpaired student’s t-tests were used to evaluate the differences in cellular volume and shape between cell cycle stages and between the initial and final stages of each phase, as well as to compare fluorescence ratios between peripheral and septal wall signal intensity. One-way analysis of variance was used to compare old/new cell wall fraction at different time points. P values ≤0.05 were considered as significant for all analysis performed and were indicated with asterisks: *P≤0.05, **P≤0.01 and ***P≤0.001.
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This study was funded by the European Research Council through grant ERC-2012-StG-310987 (M.G.P.) and through research grants FCT PTDC/BIA-PLA/3432/2012 (S.R.F.) and NIH GM51986 (Y.V.B.). J.M.M., F.V., A.R.P., A.C.T., M.T.F. and H.V. were supported by FCT fellowships SFRH/BD/71993/2010, SFRH/BD/78748/2011, SFRH/BD/86416/2012, SFRH/BD/52204/2013, SFRH/BD/77849/2011 and SFRH/BPD/87374/2012, respectively. We thank Suckjoon Jun (UCSD), Adriano Henriques (ITQB) and Nathalie Reichmann (ITQB) for critically reading the manuscript. We thank T. Meylheuc from the Microscopy and Imaging Platform MIMA2 (INRA, France) for SEM observations, Rut Carballido-López and Arnaud Chastanet (Micalis Institute, INRA Jouy-en-Josas) for support for SEM observations and assistance with the preparation of the SEM samples, Luis Morgado (ITQB) for schematics in Fig. 4.
The authors declare no competing financial interests.
Supplementary Figures 1-6, Supplementary Tables 1-4 and Supplementary References (PDF 1315 kb)
Time lapse of dividing S. aureus cells imaged every 3 minutes S. aureus COL cells were labelled with Nile Red, placed on a medium-containing agarose pad and imaged during 42 minutes, at 3 minutes intervals, by Super-Resolution Structured Illumination Microscopy (SR-SIM). Scale bar 1 μm. (MOV 6044 kb)
Time lapse of dividing S. aureus cells imaged every two milliseconds A 60 ms segment of a 1 minute timelapse of S. aureus COL cells imaged at 2 milliseconds intervals, by Differential Interference Contrast (DIC) microscopy, while growing on a medium-containing agarose pad. (MOV 1012 kb)
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Monteiro, J., Fernandes, P., Vaz, F. et al. Cell shape dynamics during the staphylococcal cell cycle. Nat Commun 6, 8055 (2015). https://doi.org/10.1038/ncomms9055
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