- Research article
- Open Access
Patterning of mutually interacting bacterial bodies: close contacts and airborne signals
- Jaroslav J Čepl†1,
- Irena Pátková†1,
- Anna Blahůšková1,
- Fatima Cvrčková2 and
- Anton Markoš1Email author
© Čepl et al; licensee BioMed Central Ltd. 2010
- Received: 2 March 2010
- Accepted: 12 May 2010
- Published: 12 May 2010
Bacterial bodies (colonies) can develop complex patterns of color and structure. These patterns may arise as a result of both colony-autonomous developmental and regulatory processes (self-patterning) and environmental influences, including those generated by neighbor bodies. We have studied the interplay of intra-colony signaling (self-patterning) and inter-colony influences in related clones of Serratia rubidaea grown on rich media.
Colonies are shaped by both autonomous patterning and by signals generated by co-habitants of the morphogenetic space, mediating both internal shaping of the body, and communication between bodies sharing the same living space. The result of development is affected by the overall distribution of neighbors in the dish. The neighbors' presence is communicated via at least two putative signals, while additional signals may be involved in generating some unusual patterns observed upon encounters of different clones. A formal model accounting for some aspects of colony morphogenesis and inter-colony interactions is proposed.
The complex patterns of color and texture observed in Serratia rubidaea colonies may be based on at least two signals produced by cells, one of them diffusing through the substrate (agar) and the other carried by a volatile compound and absorbed into the substrate. Differences between clones with regard to the interpretation of signals may result from different sensitivity to signal threshold(s).
- Critical Diameter
- Close Encounter
- Colony Development
- Mixed Suspension
- Conditioned Agar
Bacteria can display a plethora of multicellular forms (colonies, mats, stromatolites, etc.); their structure and appearance depends on factors such as the presence of nutrients or neighbors. Concepts of "body" and "community", as developed for multicellular sexual eukaryots, became, however, somewhat blurred upon attempts of their application to microorganisms. Is differentiation of multicellular units in bacteria comparable to embryonic development, to the establishment of an ecosystem? Is it even the place of Darwinian evolution on a micro-scale?
Multicellular bacterial bodies can be viewed as ecosystems negotiated by myriads of (presumably genetically different and selfish) specialists (e.g. [1–6]). Each cell is understood as an individual playing its own game according to resources, energy costs, and complicated informational interactions with others. However, patterning of multicellular bodies remains beyond interest, at the most being viewed as a passive outcome of physical forces.
A multicellular bacterial community may, however, be also perceived as the prevalent form of bacterial existence, with a genuine ontogeny. To create and maintain such elaborated structures, a great deal of communication, regulations, mutual understanding, and cooperation takes place in bacterial morphogenesis. Differentiation in such a bacterial body (as a body, not a population of cells) may proceed via genetically differing subclones fulfilling different roles, and appearing reproducibly at characteristic periods of cultivation [7–10]. Sophisticated networks of chemical signals [11–13], the scaffolding of extracellular matrix  and even cell-to-cell contacts [15, 16] may enable attaining and maintaining the integrity of the body. Research in this direction has been greatly accelerated in last two decades by the discovery of the phenomenon of quorum sensing (see [17–19]; for Serratia see ). Bacterial populations react to such signals - and build multispecies bodies accordingly - in a context-dependent manner . A plethora of quorum-modulating signals, such as indole or furanole derivatives, was also described [12, 21, 22]. The study of model monoclonal populations may contribute to understanding colony morphogenesis, providing the possibility to examine how, and even why, bacteria exert themselves towards "species-specific" appearances.
We have previously demonstrated that colonies of Serratia marcescens can be viewed as multicellular bodies with genuine embryonic development . Colonies displayed finite growth and clone-specific formative processes; even a disorganized cell slurry (up to 107 cells) could establish a regular pattern and embark on a typical developmental pathway. Under standardized culture conditions on rich semi-solid media, the final shape and patterning of bacterial bodies depended essentially on four initial settings: (1) amount, density, and distribution pattern of founder cells; (2) the configuration of surrounding free medium; (3) the presence and character of other bacterial bodies sharing the same niche; and (4) self-perception, resulting in delimitation towards other bodies.
Here we further investigate the development of bacterial bodies and their interaction with close or distant neighbors of identical, or different, clonal origin. We also propose a formal model that can account for some of our experimental results.
Colony patterning in clonal variants of Serratia rubidaea
As the F morphotype plays a central role in this study, its development deserves a closer scrutiny. No matter how the colony was planted, in days 1-3 it grows as a central navel: a compact body on the agar plate only slowly propagating sideways. This phase is followed in days 3-5 by spreading of the flat interstitial circle. Microscopic observations revealed a margin of extracellular material containing small swarms of bacteria at the colony periphery at this stage (M. Schmoranz, AM and FC, unpublished observations), a phenomenon well established in Serratia sp. (e.g. [8, 13]). In days 5-7 this lateral propagation comes to end and the peripheral rim is formed; the central navel grows red in this phase. In following days, the rim also turns red and the growth proceeds towards a halt. The flat interstitial ring remains colorless (Figure 1).
Close encounters of bacterial bodies
In dense plantings, clonal rimmed colonies tend to merge into confluent colonies (Figure 2a, left). In a mix of lines differing in color (F, Fw), the origin of each participating colony is revealed by the color of its rim. If colonies were dotted close (ca 1 mm) to a growing previously planted colony (24, 48, or 72 h old; Figure 2b, left), the resulting fused body resembled a confluent colony, with a common rim and separate centers. The effect was more profound with younger colonies.
If a similar protocol was followed with the rimless clones, colonies remained thoroughly delimited, whether in a single culture (RR), or in an RW mixture (Figure 2a, middle): no fusions were observed, and clearly distinguishable furrows developed between bodies in contact. Similarly, dots applied close to an older colony became inhibited in growth, but kept distinct from its growing older neighbor (Figure 2b, middle).
Upon close encounters between rimless and rimmed bodies (RF or RFw), the R colonies grow faster and influence rimmed colonies in four ways: (i) If planted early enough, R colonies can engulf an immature rimmed colony; its body, however, survives and cells can be recovered from such a mixed body (Figure 2b, right). (ii) If F colonies are allowed to grow in the vicinity of an R colony as independent bodies up to 3rd day of cultivation (irrespective if they later grow to confluence or not), they develop to a new colony phenotype with a massive white rim with a thin colored ring at the inner side (a pattern dubbed X here and below; arrows in Figure 2a). Cells from X colonies restore the original F phenotype upon subsequent planting. (iii) A rimless (R) dot added to a rimmed colony (F or Fw) tends to proliferate around the older partner and block its further growth (Figure 2b, right); the younger the rimmed colony is, the more profound the effect. Similar results were obtained with W dots (not shown). Again, the rimmed colony remains compact (though overgrown) and contains live cells. (iv) The engulfment potential of the rimless colony is even more profound in a reverse arrangement, i.e. dotting of a rimmed colony to an older rimless partner (Figure 2b, right).
Planting of mixed suspensions
Mixed suspensions of two rimmed clones (F, Fw) produced varying and unpredictable colony patterns (Figure 2c, left), suggesting an extreme sensitivity of such mixtures to initial conditions (e.g. minor inhomogeneities in the suspension). Samples taken from both center and periphery of such chimeras revealed the presence of cells belonging to both clones in the central zone, and sometimes also in the periphery (not shown). These results contrast with previous findings on a different strain : in that case, however, both subclones tended to establish separated "areas of influence", essentially as referred below for RW mixtures.
If a colony was established from a mixture of two rimless clones RW, the center of the colony remained a mixture of both clones, sending radial monoclonal sectors as the colony grew (Figure 2c, middle), as if rimless clones were reluctant to cooperate towards a common end.
If a mixed suspension of rimmed (F) and rimless (R) suspension is dropped to initiate a colony, the cells of the rimmed clone remained confined to the central area, whereas the growing periphery is composed exclusively of R cells (Figure 2c, right), similar to the above-described engulfment of rimmed colonies by rimless ones. Again, the inhibited strain confined to the center remains viable and can be recovered upon re-planting. The behavior of RFw, WF and WFw colonies is analogous to the RF mixture (not shown).
Effects of planting layout
We have also confirmed the previously described phenomenon of "ghost" colonies , originally documented on a different strain. Briefly, colonies planted at the background of multiple (hundreds) colonies became inhibited, or even "dissolved" on the background (Figure 3b). This is the case even in synchronous cultures if, at the beginning, the background is represented by at least about 100 colony-forming units. Such a background can keep at bay a plant as dense as 100 000 cells, preventing its development towards a colony. The effect is more profound when background colonies are older. With this information in mind, we return to ring colonies.
A colony was planted into the center of a ring colony of greater diameter, or a ring colony was blotted around a growing F colony. Both bodies represent a "background" to each other, depending on the succession of plating. Results in Figure 3d show that the synchronous planting of both structures leads to disruption of the structure of the central colony, but no change in the structure of the ring. Colonies planted on the background of older rings became inhibited. On the other hand, when the ring is planted around an older colony, it develops into a typical structure, only with more profound reddening of the inner rim - again confirming that a developing colony can perceive the presence and layout of its neighbors.
Long-distance interactions between colonies and maculae
To examine the putative long-distance signals between bacterial bodies, colonies (F) were planted to the vicinity of maculae of two different Serratia clones (F, R) or an unrelated bacterial strain (E. coli). Maculae and colonies either shared the same agar plate, or were separated by a septum.
The R macula, as well as a macula of E. coli, induced, again, formation of the X phenotype in colonies of the F clone (Figure 4b, left; compare to Figure 2). No such X-like structures were observed when R colonies were planted in the vicinity of an E. coli macula (not shown).
Communication across obstacles
Nature of signals between bodies
In further experiments, we investigated the longevity of a putative macula-derived signal. A macula was grown for 3 days on a cellulose membrane laid on the agar on one side of a septum, then removed, leaving empty macula-conditioned agar. Immediately after macula removal, colonies were dotted into the neighboring compartment containing free macula-exposed agar (i.e. agar that was exposed - across the septum - to volatiles from the membrane-grown macula; Figure 5a). The results are indistinguishable from controls shown in Figure 4a, i.e. from the situation when the macula persisted in the neighboring compartment.
To test the obvious possibility that such free, but macula-exposed agar "took the smell" during macula growth, medium in the non-inoculated compartment was removed at the time of the macula removal, and replaced by "virgin" agar transferred from another, empty plate. As also shown in Figure 5a, the development of colonies was essentially the same as on macula-exposed agar. Thus, macula-conditioned agar can release sufficient amount of signal to influence the colony development on virgin agar. However, macula-exposed agar alone was unable to pass the effect further, to the virgin agar in the neighboring compartment (not shown).
The effect of conditioned agar suggests that the signals between bacterial bodies are chemical rather than physical (e.g., electric or electromagnetic pulses and/or vibrations such as sound). Since the effects is transmitted in the absence of living source bacteria, the most obvious candidate is some compound(s) soluble in the agar medium, readily evaporating (from the macula-occupied or conditioned agar), diffusing across the septum and becoming trapped in the free agar beyond. To exclude the possibility of transmission via surface of the septum, we rendered the septum hydrophobic by medical-grade vaseline (Herbacos-Biofarma). Since this did not affect the outcome of the experiment (not shown), we are left with the hypothesis of an airborne compound playing the role of the carrier of signal (or sign) for the recipient colony.
In a preliminary experiment, we tried to remove such putative compound(s) by placing possible absorbents into an adjacent compartment (Figure 5b): agar (control), water, 20% citric acid solution, or 30% KOH. As shown in Figure 5b, both citric acid and KOH appeared to be powerful inhibitors of colony development, while water or agar exhibited no effect.
Modeling colony ontogeny
In the course of the F colony development, a bacterial cell enters a succession of distinct states as follows (Figure 6a). In State 1, corresponding to freshly inoculated or "young" growing cells, the bacteria divide exponentially, resulting in a juvenile colony increasing in both its height and diameter. Cells in state 1 produce moderate amounts of a diffusible factor (further referred to as the "quorum") that spreads slowly through the substrate and inhibits their own growth if above a threshold concentration (Qlim in the model). When reaching Qlim, or as a result of nutrient limitation (approximated by a maximum colony thickness N in the model), cells stop dividing and enter State 2, corresponding to the early stationary phase and characterized by increased production of the quorum signal. At this stage, the developing colony consists of a core of non-growing cells in state 2, with a margin containing still-growing state 1 bacteria. Remarkably, over a range of parameters, thickness of the margin becomes soon limited by the quorum signal, while the colony keeps spreading laterally, resulting in a "hat-like" profile (not shown). Cells remain in state 2 for a limited time window (until reaching the "age" A), and then move on to State 3 - the mature stationary phase, where the production of the quorum signal ceases altogether but the bacteria start to emit another signaling compound - the volatile "odor" signal that is produced into the gas phase and readily absorbed into the agar across the whole dish (so that its concentration at any place reflects the total sum of production by all state 3 cells). Both state 1 and state 2 cells respond to a limiting concentration of the odor signal (Olim1) by entering State 4, or a refractory growing state, where the bacteria either keep dividing (if previously in state 1) or restore division (from state 2), but no longer produce any signaling compounds. They also do not respond to the quorum signal any more, while retaining sensitivity to the odor. Finally, upon reaching either the maximum colony thickness (N) or a second odor threshold (Olim2), state 4 cells cease growing and enter mature stationary phase (state 3), finishing thus colony development.
Computer simulations based on these assumptions yielded often colony profiles reminiscent of the observed behavior of F colonies (for an example see Figure 6b, c colonies 1 and 2). We cannot yet provide any rigorous estimate of the robustness of the F-like outcomes, as we have not systematically examined the space of model parameters; the reader is invited to do so using the provided program (Additional file 1). We obtained, however, "realistic" looking outcomes, though sometimes with distorted ratios of central, interstitial and peripheral colony zones, with a variety of parameters. We thus hope that the model might adequately describe a general aspect of the colony morphogenesis rather than an fortuitous outcome of a specific combination of parameters. Moreover, we were able to generate a "rimless" (R) phenotype solely by modifying the quorum and odor sensitivity limits while all the other parameters have been kept constant (Figure 6b, c colony 3).
Simulation of specific features of rimmed colonies
While experimenting with varying layout of the initial inoculum (using parameters that generated rimmed colonies), we have observed three worthwhile additional phenomena (Figure 7a, b): (i) multiple inocula sharing the same dish developed into colonies of perfect shape but smaller size (compare Figure 1b); (ii) under some circumstances, colonies initiated close to each other "developed" a common rim (compare Figure 1b and Figure 2a); (iii) a simulation of dropping or dotting an extended inoculum yielded "rimmed colonies" from inocula smaller than the interstitial ring of a single cell-initiated colony but maculae for larger inocula. We have observed a similar phenomenon also in laboratory experiments aimed at estimating the area of planting that still allows cells in a slurry on the surface of semi-solid medium to coordinate their behavior.
Highly structured bacterial bodies (mats, plaques, stromatolites, colonies, etc., containing astronomical amounts of cells belonging to hundreds of species) apparently represent the "default" way of living of most bacteria [25–34]. How do such bodies come into existence? Are they ad hoc contraptions, molded solely, or predominantly, by the external environment? A result from an ecological succession, a game played by well-trained players? Or, finally, may an analogy of ontogeny be assumed , similar to ontogeny in, e.g. mycobacteria, streptomycetes, slime molds, yeasts, or even plants or animals?
Our experiments with a single clone or a pair of clones, each giving well-developed colonies with finite growth, may provide initial insight into the processes of bacterial body formation. Apparently, there exists an elaborated network of communicative signals mutually affecting bacterial bodies, so the first hypothesis can be safely dismissed. As to the "ecology" of cells: a colony, whose diversity resembles rather a carefully managed cornfield than a natural landscape, may not seem to be a good model at the first sight. Yet, our two interacting clones remind of theoretical models like "hawks-doves" or "prisoners dilemma" (or even interaction of a monoculture with weeds or pathogens). The third possibility - regular patterns of colony ontogeny - allows even genuine convergent development entering the game.
Our observations suggest that development of bacterial bodies in Serratia sp. includes both events taking place within a body, and transmission of signals between distinct bodies. Signals act at a distance, i.e. they do not require physical contact (as reported, e.g., in [16, 35, 36]). Experiments with conditioned agar show that signals do not require simultaneous presence of living entities; hence, actively emitted light, sound, electrical or even chemical pulses of whatever nature can be excluded as carriers of the signal. We are left with a compound or a cocktail of compounds, emitted by living entities into their environment, persisting there for some time, and being actively interpreted by recipients that happen to be present in their range. While our observations do not provide any hints yet as to the chemical identity of these signals, they at least point towards some of their properties. Experiments with signaling across the septum suggest that the signal from the macula spreads via the gas phase. For a different bacterial system, indole could be the carrier of a volatile signal (; however, this conclusion was later questioned ). Ammonia appeared to be the signal carrier in yeast colonies . As a first step towards characterizing our signal, we demonstrated that it is readily cleared away by non-volatile acid or alkali traps.
We propose a simple model capable of simulating some aspects of our experimentally characterized examples of bacterial body morphogenesis (the F and R colonies). This model involves two factors carrying information for both morphogenesis and mutual influencing of neighbors, generated in bodies at certain developmental stages, and diffusible to the environment. One of the signals travels (slowly) through the substrate, the other is transmitted via the gas phase. These bearers of the signals (or even a sign) are perceived by all cells, allowing their orientation and behavior in the developing colony; timing may be the second critical factor at play. While several theoretical models of microbial colony morphogenesis have been published, they mostly focus on such aspects as kinetics of colony expansion controlled by nutrient diffusion through the colony and surrounding medium [40–43], intra-colony spatial organization of cells [44, 45] or fine patterning of the colony margin based on interplay of nutrient and signal diffusion and, in some cases, also swarming behavior of the bacteria [46–48]. To our knowledge, none of the published models accessible to us predicts or explains formation of "fountain" colonies of finite size (although some predict repetitive ring patterns - e.g. [49–51]), and none includes an interplay of diffusible (substrate-borne) and volatile (air-borne/substrate-absorbed) signals, albeit chemotaxis or quorum sensing has been incorporated in some simulations (e.g. [44, 45, 50]).
So far, our model does not account for modifications of the colony's "body plan" upon interaction with different clones (or even species), where additional signals diffusible in agar (or modulation of the response(s) to one signal by the other), may contribute (e.g. our X pattern, or mutual inhibition occurring upon encounter of two rimless colonies; the later has been explained by others  as a possible consequence of bacteria interpreting local nutrient concentration as a signal inducing growth rate changes). Notably, our model includes, as one of the central parameters, some kind of cellular memory - bacteria that have recently ceased dividing behave differently from their sisters that have spent a longer time in the stationary phase.
Let us suppose that in closely related bacterial clones used in our study the basic morphogenetic signals are the same, i.e. particular clones differ in the signal interpretation. Remarkably, some combinations of quorum and odor sensitivity parameters in our model produce rimless bodies while other parameters are kept the same as for rimmed ones (Figure 6).
Changes in the rate of lateral spreading during colony development have been observed or predicted especially for microbes exhibiting extensive swarming; however, we have not incorporated this phenomenon into our model since both our observations (Figure 1) and data reported by others  document a more-less constant rate of lateral growth of Serratia colonies under conditions leading to the development of compact colonies (as in our study).
The present model does not yet allow simulations involving more than one "clone" (defined by a specific set of parameters). Nevertheless, the experimentally observed "aggressive" phenotype of rimless bodies upon encounter with rimmed ones is consistent with the model assuming that the rimless clone is less sensitive to the (inhibitory) diffusible quorum signal spreading through the substrate. A "rimless" phenotype has been previously observed also in a S. marcescens strain capable of forming "fountain" colonies on standard media, when this strain was grown in the absence of glucose ; the same happened also in our F clone on glucose-free media (data not shown). It is tempting to speculate that glucose (or another effective energy source) may be required to develop full sensitivity to the diffusible quorum signal. Alternatively, production of such a signal may be diminished on poor media (since what matters in our model are not absolute values of quorum signal production but the ratio between production per bacterium and the sensitivity threshold value).
The difference in "worldviews" between rimmed and rimless clones is best demonstrated when mixed suspensions or colonies planted close together are forced towards establishing a new body. The rimless partners segregate in radial clonal sectors from a mixture, and keep separated upon close encounter. On the other hand, two rimmed clones are much closer to each other in interpreting their morphospace than two rimless clones, as they can build a common rim when planted as a mixed suspension or upon close encounters.
We have experimentally defined several additional qualitative prerequisites for establishing and maintaining the typical "body plan" of bacterial colonies; some of them can be evaluated in the light of our model.
The presence of a bacterial body in the neighborhood of a developing colony of F clone results in its quicker ripening, i.e. reddening. Very close encounters lead to disruption of both its growth and pattering: most profound is the effect on colonies planted close to older bodies, or inside ring-bodies. In case of two rimmed partners, the older the neighbor was, the more profound the growth inhibition of the younger colony, which, nevertheless, remained recognizable even when overgrown by the older partner.
Development of geometrically constrained bodies (such as those originated by ring-shaped, elongated or cruciform inocula) can be interpreted as a conflict of two ways of recognizing the "body" across the hole: as a part of "self" (resulting in a symmetric colony, or a colony with a hole, for small rings), or as a neighbor. In ring plantings up to a certain diameter, cells in the inner diameter of the ring are sufficient to produce a "virtual navel" controlling the development of the body. In large rings, the "non-self" tendency prevails: such bodies take the inner empty space for outer space outside of their morphogenetic field. New colonies planted into such an area are treated as foreign, and their pattern resembles those planted in the vicinity of other type of bodies.
While our model does not currently allow simulating development of multiple inocula differing in genotype (i.e. parameters), size, shape or time of planting, we could at least reproduce the faster ripening and smaller size of two colonies sharing a confined space, compared to a solitary colony.
We have also confirmed our previous results  showing that the growth of colonies is strongly inhibited, even abolished, if the surrounding area is evenly occupied by "background" bacterial bodies - even if their total population (biomass) is much smaller than the colony inoculum. Hence, bacteria in the background emit a signal that efficiently disturbs the organizing potential of the multicellular plant, while keeping the background colonies in an underdeveloped - "dormant" - state. Experiments with effects of colonies grown in the presence of maculae (sharing the substrate or separated by a septum), macula-exposed and "virgin" agar suggest that this effect could be identical with the gas-borne signal of our model.
Finally, we have shown that the planting area necessary for the cell population to maintain the "feeling" of belonging to a single body, roughly corresponds to the outer diameter of a mature interstitial circle (Figure 7c). Exceeding this critical diameter leads to the loss of structure and breakdown to a macula; however, even in such a case the body is self-inhibited as to lateral spreading. This may perhaps be understood as the last remnants of its "feeling of integrity"; the results of our computer simulations suggests that even this seemingly complex effect may be produced by the interplay of mere two signals.
Some isolates of Serratia sp. produce colonies exhibiting finite growth and clone-specific appearance, which is easily evaluated thanks to their conspicuous coloration. The shape and patterning of developing colonies and other multicellular bodies is easily malleable by experimental conditions. The appearance of a developing colony results from (i) its internal morphogenetic potential and (ii) the character of neighbor bodies and their overall distribution on the dish.
The development of colonies exhibiting finite growth and both rimmed and rimless patterns, the difference between the former and the latter being in the intensity of signal production and/or sensitivity towards the signal(s).
Dependence of colony size upon the number of colonies sharing common morphospace, and development of confluent colonies from closely planted inocula of a rimmed strain.
The phenomenon of "critical planting area" which must not be exceeded should a colony develop a typical rimmed pattern.
Our observations are thus consistent with bacterial colonies behaving, in some aspects, as true multicellular bodies whose patterning is controlled by positional information; the nature of the relevant signals remains to be established.
Strains, media and culture conditions
The strain Serratia rubidaea here labeled R (rimless "wild type" phenotype for the purpose of this study), as well as E. coli strain 281, were obtained from the collection of the Department of Genetics and Microbiology, Faculty of Sciences, Charles University. The R strain, originally described as S. marcescens, has been determined as S. rubidaea on the basis of metabolical markers and gyrB gene sequencing (A. Nemec, National Health Institute, Prague, personal communication). The remaining three Serratia sp. clones are morphologically distinct derivatives of R selected after prolonged serial cultivation in liquid media with subsequent plating; the F and W clones have been confirmed to be derived from the R clone by comparison of SpeI RFLP patterns obtained using pulsed-field gel electrophoresis (A. Nemec and M. Schmoranz, personal communication). Details of the strain genealogy and characterization will be reported in a future study focused on variability of Serratia sp. colony morphology (M. Schmoranz, Z. Neubauer, AB and AM, in preparation).
Bacteria have been grown under previously described standard conditions  on Nutrient Agar No2 (Imuna Pharm a.s., Order No T 382100001020) supplemented with 0.5% glucose, or on a medium obtained by solidifying Nutrient broth No2 (Imuna Pharm a.s., Order No V 382100000098) by addition of 1,5% agar, supplemented with 0,5% glucose, with the same results. The standard colony patterns have been also reproduced on standard LB medium with 0.5% glucose (not shown). Bacterial stocks have been maintained at -80°C as described previously .
New colonies were initiated (1) as clones from single cells, by classical sowing of bacterial suspension (in phosphate buffer); (2) by dropping such suspension on a defined place; (3) by dotting: from material taken by a sterile needle from an older body; (4) by streaking a mass of bacteria from an older colony using a sterile bacteriological loop; (5) by blotting from a continuous carpet of bacteria using plastic matrices of required shape (made of disposable plastic tubes or pipette tips). To obtain conditioned agar, the agar plate was covered by cellulose membrane (Blanka, CSN 646811, Chemosvit), and macula was sown (by dropping) on top of the membrane. After 3 days, cellulose membrane with bacterial mass was removed. Signaling across compartments was studied in septum-divided Petri dishes providing isolated agar compartments, but sharing the gas phase (Gama Group a.s., order No 400901).
Plates were photographed in situ using an Olympus digital camera under ambient or penetrating light (Fomei, LP-400 light panel, cold cathode light) or under magnification using a binocular magnifier. Figures shown were selected from an extensive collection of primary photos from several repetitions of each experiment. Photoshop software was used to assemble the plates but no image doctoring was performed except automatic adjustment of brightness and contrast in some cases.
The model (see Additional file 1) has been developed and modeling performed in the freely available Python 2.6.4 environment  on a Windows-based PC. The model is designed as a one-dimensional continuous cellular automaton, where the row of "cells" represents a projection of the developing colony cross-section onto a level parallel with the substrate surface. Each "cell" is characterized by discrete values of (i) bacterial layer thickness (number of bacteria), (ii) state of the bacteria (depending on local conditions and in some cases also recent history; see Results), and (iii) in case of recently stationary bacteria also their "age", i.e. time elapsed since growth cessation. Two continuous variables represent (iv) concentration of the diffusible "quorum" signal in the substrate and (v) amount of the volatile "odor" signal that is by definition equal across all cells. The model develops in a series of generations, each consisting of four steps: (1) evaluation of the state of bacteria in each cell according to their age (if defined) and concentration of quorum and odor signals; (2) division of bacteria in each cell according to their state, followed by migration of one daughter bacterium into the neighboring cell if this cell is empty and if no limitation by diffusible factors occurs; (3) production of quorum and odor signals by bacteria in each cell; (4) diffusion of the quorum signal, itself approximated by a nested multi-step process where each step represents migration of a fixed fraction of the difference in quorum signal concentration down the concentration gradient between each two neighboring cells. Raw data produced by the model have been evaluated and graphically represented using MS Excel.
Supported by the Grant agency of Czech Republic 408/08/0796 (JČ, IP, AB, AM), by the Czech Ministry of education MSM 0021620845 (AM, AB); MSM 0021620858 and LC06034 (FC). The authors thank Zdeněk Neubauer, Zdeněk Kratochvíl, and Josef Lhotský for invaluable comments, Alexander Nemec for strain determination, and Radek Bezvoda for programming advice.
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