Conjugative plasmids of Gram-negative bacteria have both vertical and horizontal modes of transmission: they are segregated to daughter cells during division, and transferred between hosts by plasmid-encoded conjugative machinery. Despite maintaining horizontal mobility, many plasmids carry fertility inhibition (fin) systems that repress their own conjugative transfer. To assess the ecological basis of self-transfer repression, we compared the invasion of bacterial populations by fin+ and fin− variants of the plasmid R1 using a computational model and co-culture competitions. We observed that the fin+ variant had a modest cost to the host (measured by reduction in growth rate), while the fin− variant incurred a larger cost. In simulations and empirical competitions the fin− plasmid invaded cultures quickly, but was subsequently displaced by the fin+ plasmid. This indicated a competitive advantage to reducing horizontal transmission and allowing increased host replication. Computational simulations predicted that the advantage associated with reduced cost to the host would be maintained over a wide range of environmental conditions and plasmid costs. We infer that vertical transmission in concert with competitive exclusion favour decreased horizontal mobility of plasmids. Similar dynamics may exert evolutionary pressure on parasites, such as temperate bacteriophages and vertically transmitted animal viruses, to limit their rates of horizontal transfer.
Gram-negative bacteria host a wide variety of plasmids that encode conjugative self-transfer systems (Lawley et al., 2004). The ecology of these plasmids is of medical interest as they are of prime importance in the prevalence of drug resistance in bacterial populations (Levin and Andreasen, 1999; Mazel and Davies, 1999; Wise, 2004). Bacteria and their conjugative plasmids can also provide a tractable model of a host–parasite system. These genetic elements can persist in suitable hosts for many generations without conferring a selective advantage (Turner et al., 2002; Dahlberg and Chao, 2003; De Gelder et al., 2004; Bahl et al., 2007).
Conjugative plasmids in Gram-negative bacteria are vertically transmitted to daughter cells during division, but also horizontally transmitted to neighbouring cells by self-encoded type IV secretion systems known as ‘tra’ (for transfer) systems. The persistence and diversity of the tra systems suggests that their horizontal transfer capabilities have been valuable to plasmids over evolutionary time. However, many plasmids repress their own conjugative transfer with cis-encoded ‘fertility inhibition’ (fin) systems. Fin genes inhibit expression and assembly of their cognate tra systems, and have been described in Gram-negative plasmids spanning the F, I and X incompatibility (Inc) groups; IncP plasmids also carry genes that limit tra expression (Firth et al., 1996; Lawley et al., 2004). The effects of fin systems can be dramatic: the finOP system of the well-studied plasmid R1 reduces conjugative efficiency about 1000-fold (Dionisio et al., 2002).
In essence, fin systems antagonize a plasmid's capacity for horizontal transfer; the conservation of fin genes suggests that they provide conjugative plasmids with an evolutionary advantage. Why would it be advantageous to repress horizontal transfer? Lundquist and Levin (1986) postulated that fin systems represent a compromise between the benefits of horizontal transfer (to the plasmid) and the associated costs to the host, which could manifest themselves in a variety of ways. Expression of tra genes makes cells susceptible to certain bacteriophages and can induce both cytoplasmic and extracytoplasmic stress–response pathways with pleiotropic effects on the host (Anderson, 1968; Campbell, 1996; Zahrl et al., 2006). Avoiding either of these factors might provide the evolutionary pressure for tra repression. Furthermore, increased horizontal transfer might reduce vertical transmission by slowing host growth; such tradeoffs have been predicted and observed for diverse parasites (Bull et al., 1991; Kover et al., 1997; Kover and Clay, 1998; Messenger et al., 1999; Dahlberg and Chao, 2003; Jensen et al., 2006). Plasmids display a tradeoff between conjugation rate and vertical transfer (Turner et al., 1998; Turner, 2004), and have been shown to evolve reduced cost to the host at the expense of horizontal transfer when the environment limits conjugative spread (Dahlberg and Chao, 2003).
To assess the ecological role of transfer–repression systems, we computationally simulated competitions between fin+ and fin− plasmids. We modelled an environment in which the plasmid offers no growth advantage to its host; the plasmid is, in this case, a parasitic genetic element. These simulations indicated a broad competitive advantage for fin+ plasmids in the absence of phages or inducers of stress–response pathways, suggesting that the tradeoff between horizontal and vertical transmission is itself strong enough to select for the maintenance of fin systems. In addition to simulated competitions, we competed the naturally occurring fin+ plasmid R1 with its fin-deficient derivative R1-16 in laboratory-grown populations of Escherichia coli. R1 and R1-16 compete through mutual exclusion from host cells, as the presence of one conjugative plasmid prevents entry by related plasmids (Clark, 1985; Firth et al., 1996). Empirical competitions between R1 and R1-16 agreed well with our theoretical predictions and showed a competitive advantage for R1. Our results indicate that competition between plasmids for limited hosts exerts a downward evolutionary pressure on horizontal transfer rates, which helps explain the persistence of fin systems in nature. We hypothesize that vertical transfer and mutual exclusion play key roles in shaping the dynamics of plasmid competitions in nature.
Materials and methods
Growth media, bacteria and plasmids
Rich broth (LB) was used as a growth medium (Miller, 1972). Medium supplements were used at the following concentrations: 30 μg ml−1, chloramphenicol (Cml); 40 μg ml−1, kanamycin (Kan). E. coli were the K12-derived strain XK1502 (Panicker and Minkley, 1985). Plasmids were wild-type R1 (IncFII, transfer-proficient, fin+ KanR CmlR) and the R1-derived R1-16 (IncFII, transfer-proficient, fin− KanR CmlS) (Blohm and Goebel, 1978). R1-16 carries the R1 surface exclusion system (Bayer et al., 1995); we verified that R1 cannot efficiently conjugate into and be maintained in cells carrying R1-16 (data not shown).
Simulation design and programming
Our model was inspired by the mass-action chemostat models of Levin et al. (1979) and Hansen and Hubbell (1980), but adapted to serial-transfer experiments such as those performed by Turner (2004) and Dahlberg and Chao (2003). Our model considered the growth of bacterial populations in the presence of a limiting nutrient C, with periodic dilution into fresh medium with a nutrient concentration C0 every 24 h. Simulated cultures contained up to four distinct populations: plasmid-free cells (N), cells hosting a tra-repressed plasmid Pfin+ (P1b), new recipients of Pfin+ not yet repressed by fin (P1a), and cells hosting a tra-derepressed plasmid Pfin− (P2). Related plasmids prevent one another from entering the same cell by surface exclusion mechanisms (Clark, 1985; Firth et al., 1996), so we assumed that cells carrying one plasmid would not be recipients in further conjugative transfers. Variables used in the model are defined in Table 1, and the differential equations that describe cell and resource concentrations are shown below.
Plasmid-free cells (N):
Recent recipients of plasmid 1, not yet fin-repressed (P1a):
Cells carrying fin-repressed plasmid 1 (P1b):
Cells carrying the fin-deficient plasmid 2 (P2):
Growth-limiting carbon source (C) (replenished every 24 h):
Transfer of diverse conjugative plasmids is inhibited by stationary phase and high-cell densities (Sudarshana and Knudsen, 1995; Frost and Manchak, 1998). To incorporate this dynamic into our simulations, we included a switch that reduced conjugation rates 1000-fold when C fell below 1/10th of the Km value (see Table 1 for variable definitions). To account for observed cell death in stationary phase (see Results), a 1-log drop in CFU ml−1 at the 24-h time point was incorporated into the computational simulations. Bloodshed Dev-C++ version 188.8.131.52 was used for programming and compiling computational simulations.
Determination of plasmid cost and stationary-phase survival
Plasmid cost was measured as the increase in generation time relative to the plasmid-free progenitor strain. Growth rates were measured by monitoring the OD600 of cultures growing in LB (without antibiotics) after 100-fold dilution from overnight cultures in LB (supplemented with Kan for strains bearing R1 or R1-16). Only time points corresponding to logarithmic growth were used in calculating doubling times. To monitor stationary-phase survival, overnight cultures of XK1502, XK1502 R1 and XK1502 R1-16 were diluted 1:10 in fresh LB. Viable cell counts were determined by plating aliquots of each culture at 0, 6, 12, 18 and 24 h post-dilution.
Plasmid invasion and competition experiments
Overnight cultures of XK1502 were diluted 1:100 into fresh LB and mixed with 1:10 000 dilutions of XK1502 R1 and/or XK1502 R1-16 overnight cultures. Cultures grew at 37 °C, in 10 ml glass culture tubes containing 2 ml volumes of culture, aerated by slow rolling (45 r.p.m.), and diluted 100-fold into fresh broth every 24 h. After 8 h, aliquots were removed to determine viable cell counts before stationary phase (see below for viable count method). Viable counts were also determined at 24, 48, 72 and 96 h.
For each time point, dilutions of the cultures were plated in quadruplicate to non-selective, Kan-containing and Cml-containing media. Cells containing R1 grew on all plates, cells containing R1-16 were killed by Cml, and plasmid-free cells were killed by both antibiotics. Colony counts from the three types of plates were used to calculate cell densities by the following formulae: R1-containing cells=Cml plate counts; R1-16-containing cells=Kan plate counts minus Cml plate counts; plasmid-free cells=non-selective plate counts minus Kan plate counts. This method, while repeatable, led to some uncertainty in plasmid-free cell numbers when they fell to 2% or less of plasmid-bearing levels. In ambiguous cases, colonies from non-selective plates were patched to Kan and Cml to more precisely determine the densities of plasmid-bearing and plasmid-free cells. On a few occasions a minority population was beneath the level of detection; we omitted these data points from the analysis (as noted in Figure 3 and its legend).
Computational simulations predict a competitive advantage for fin-mediated repression
We examined the fitness of parasitic fin+ and fin− plasmids by comparing their abilities to invade host populations, individually and in competitive co-cultures. We use the term ‘invasion’ to refer to the increase in prevalence of an initially rare plasmid in a host population, and the subsequent maintenance of that plasmid over time. Invasion as we define it can thus be achieved by horizontal transfer and/or vertical transmission of plasmids.
We first approached plasmid invasion using computational simulations. Our model considered two variants of a parasitic conjugative plasmid: a fin+ (transfer-repressed) plasmid Pfin+ and a fin− (transfer-derepressed) plasmid Pfin−. We used simulations to predict the ability of conjugative plasmids to invade a plasmid-free population in three distinct scenarios: Pfin+ alone, Pfin− alone or both plasmids in co-culture. Initially, we set parameters to simulate fin+ and fin− variants of the naturally occurring IncFII plasmid R1 in a population of E. coli. R1 and its derivatives have been used in several studies on plasmid invasion (Levin et al., 1979; Lundquist and Levin, 1986; Dionisio et al., 2002; Dahlberg and Chao, 2003; Turner, 2004). Conjugation rates for such plasmids have been measured earlier (Levin et al., 1979), and we empirically determined costs for R1 and the fin− mutant R1-16 in an E. coli K12 strain (see below).
We simulated growth under relatively nutrient-rich conditions (resulting in stationary-phase cell densities similar to those observed in LB), with plasmid-bearing cells initially making up 1% of the population. The resultant simulations are shown as Figure 1. When present alone Pfin+ and Pfin− both invaded a plasmid-free population, with Pfin+ achieving a majority by day 3 and Pfin− achieving a majority in <1 day (Figures 1a and b). Plasmids were maintained over ∼3500 simulated generations, with plasmid-free cells persisting at a stable plasmid-specific level. When both plasmids were present together, Pfin− quickly assumed the majority, but within a few days Pfin− was overtaken by Pfin+; Pfin+ went on to dominate the mixed culture in the long term (Figure 1c).
These results predict a long-term competitive advantage for Pfin+ in spite of earlier takeover by Pfin−. However, these simulations represent only one of a variety of possible plasmid–host-environment combinations. The success of actual plasmid invasions is mainly determined by plasmid cost, host density and conjugation rates (Levin et al., 1979; Lundquist and Levin, 1986; Turner, 2004; Bahl et al., 2007). We therefore wished to determine and compare the effects of bacterial density and plasmid cost on invasion by Pfin+ and Pfin−, which represent plasmids with differing conjugation rates.
To explore this wider parameter space, we first ran iterative simulations in which we varied the initial resource concentration C0. Increasing C0 increases the population density reached by simulated bacteria before they exhaust their limiting resource and stop dividing. We considered each plasmid separately and then both in co-culture. At the end of each simulation, we tallied one of three outcomes: no plasmid persisted, plasmid Pfin+ persisted as the most numerous or plasmid Pfin− persisted as the most numerous. The results of these iterative simulations are summarized in Figure 2. Neither plasmid persisted at the lowest C0 value, and increasing nutrient concentrations were advantageous for both plasmids (Figure 2a). Although Pfin− was the more costly plasmid, its high conjugation rate allowed it to invade cultures at C0⩾40, whereas Pfin+ could only invade at C0⩾100. Populations containing both plasmids displayed a striking result: in environments where only Pfin− would have invaded alone, Pfin+ dominated mixed cultures. In these competitions, Pfin− first spread through the population and Pfin+ cells then displaced their less-fit Pfin− competitors, whereas uninfected cells were in the minority (data not shown). At intermediate resource levels (40⩽C0⩽80), this dynamic allowed Pfin+ to invade mixed cultures when it could not have persisted alone. Resource-variant simulations thus indicated that, in contrast to single-plasmid systems, co-culture conditions broadly favoured vertical transfer over horizontal transfer.
To investigate the role played by plasmid cost, we simulated cultures containing both Pfin+ and Pfin− in the presence of a plasmid-free majority, varying the costs of each plasmid independently (and tallying the most numerous plasmid at the end of each simulation). We defined cost as the fractional reduction in growth rate of a plasmid-bearing strain relative to the plasmid-free strain. We set C0=200, such that stationary-phase cell densities were comparable with those empirically observed in LB (see below), and both plasmids could invade given growth rate costs of <50%. When plasmid costs were equal, Pfin− spread rapidly through the population and was not displaced by Pfin+ (Figure 2b). However, a very modest reduction in cost allowed Pfin+ to outcompete Pfin−, in spite of the fact that Pfin− had a ∼1000-fold greater conjugation rate. Even a cost reduction of 0.01 (the smallest interval tested) provided a clear advantage for Pfin+. These results supported our earlier observations that decreasing cost to the host provides a competitive advantage to a parasitic plasmid.
On the basis of our simulations, we were able to make a number of predictions about the behaviour of conjugative plasmids in bacterial populations, assuming horizontal transfer is costly to the host. A fin− plasmid should invade more quickly, and under a wider range of conditions, than a fin+ relative. A fin+ plasmid, however, should have a long-term competitive advantage over a fin− relative. And finally, the presence of a fin− plasmid may facilitate invasion by its fin+ relative under certain conditions.
The fin+ plasmid R1 has a competitive advantage over its fin− mutant R1-16
We tested our predictions using the conjugative plasmids, and we considered in our initial simulations: R1 and its fin-deficient derivative R1-16. R1 and R1-16 replicate stably in E. coli, and can be differentiated by selectable markers (R1 is KanR CmlR, whereas R1-16 is KanR CmlS). To aid in building our simulations, and in preparation for empirical tests, we determined the growth cost of each plasmid in E. coli growing in LB in the absence of antibiotics. In the K12 strain XK1502, doubling times during logarithmic growth were as follows: XK1502, 28.5±0.2 min; XK1502 R1, 29.6±0.3 min; XK1502 R1-16, 32.0±0.7 min (data are the mean±s.e. of three biological replicates). Increased doubling times of plasmid-containing strains indicate that both R1 and R1-16 are costly to the host, with R1-16 being the more costly plasmid.
Our simulations using these growth costs predicted that R1 and R1-16 would individually invade plasmid-free populations, and in a mixed culture R1-16 would invade cultures rapidly only to be overtaken by R1 (Figure 1). To test these predictions, we performed plasmid invasion/competition assays with R1 and R1-16. We did not select for plasmid maintenance; under these conditions, plasmid costs should be equal to those we measured empirically. Three different experimental scenarios were tested, corresponding to the three scenarios simulated computationally (see Figures 1 and 2): R1 only; R1-16 only; or both plasmids together.
The results of these competition experiments are shown in Figure 3. Our experimental data agreed well with the simulated competitions. For each plasmid individually, horizontal transfer was sufficient to overcome plasmid cost in dense E. coli cultures. Alone, R1 invaded and was present in the majority of cells after 3 days, whereas R1-16 alone achieved majority within a day; these dynamics agree almost exactly with our predictions (compare Figures 1 and 3). Our prediction that in a mixed culture R1-16 would invade rapidly and then be outcompeted by R1 was also borne out in these experiments. Population dynamics in experimental cultures were highly repeatable, with all four biological replicates of each competition following the same path as the mean presented here (data not shown).
One aspect of the actual competition between R1 and R1-16 that differed from our computational predictions was the rapidity of R1 takeover after R1-16 invasion (in comparison with simulations with Pfin+/Pfin−; compare Figure 1c with Figure 3c). One clue to this disparity is the behaviour of the competitors between the 8 and 24 h time points: XK1502 R1-16 densities decreased significantly more than XK1502 R1 densities between 8 and 24 h in the co-culture competitions (Figure 3c; R1 slope=0.007, R1-16 slope=−0.034, d.f.=3, P=0.04). In these co-culture competitions, R1-bearing cells survived the 8–24 h period better than in R1-only invasion experiments (Figure 3a; R1 slope=−0.030, Figure 3c; R1 slope 0.007, d.f.=6, P=0.004). Computational simulations indicated that this increase in survival could account for the relatively rapid timing of R1 takeover in the presence of R1-16 (data not shown).
Why R1-bearing cells survived stationary phase so well in these competitions is unclear. In control experiments, monitoring stationary-phase survival, R1-bearing cells survived no better than plasmid-free or R1-16-bearing cells (data not shown). R1-bearing cells died normally in the competitions in which R1-16 was not present (Figure 3a), ruling out the possibility that our R1-bearing strain had acquired a GASP phenotype (Zambrano and Kolter, 1996; Zahrl et al., 2006) or some similar mutation that gave it a general advantage under stationary-phase conditions. Because IncF conjugation is strongly inhibited during stationary phase (Frost and Manchak, 1998), the disparity in plasmid persistence probably did not arise from plasmid transfer events. We posit instead that R1-bearing cells had an advantage in survival or proliferation over R1-16-bearing cells. This could have resulted from environmental modifications by cells carrying R1-16 that disproportionately benefited cells carrying R1. One candidate effect of R1-16 that we noted in our assays was the formation of macroscopic cellular aggregates when cells carrying R1-16 reached high densities in liquid media (data not shown). While stationary-phase clumping would not a priori benefit R1-bearing cells, it may have given them some unexpected advantage in competitions.
In summary, both R1 and R1-16 invaded plasmid-free populations even though they were demonstrably costly under the growth conditions used. The loss of fin-mediated tra repression allowed R1-16 to invade a plasmid-free population quickly, but put it at a competitive disadvantage in the presence of R1, its wild-type parent with a functioning fin system.
Our results shed light on a conundrum in plasmid evolution: why plasmids do not maximize their own conjugative transfer rates. Several groups have seen plasmid-bearing populations evolve to minimize plasmid cost to the host, which is generally associated with a reduction in conjugation rates (Freter et al., 1983; Turner et al., 1998; Dahlberg and Chao, 2003; Turner, 2004; Dionisio et al., 2005). Furthermore, many natural plasmids repress expression of their self-transfer functions (Firth et al., 1996; Lawley et al., 2004). These observations are surprising given that increased rates of conjugation aid plasmids in invading and persisting within host populations, as demonstrated by this work and others’ (Stewart and Levin, 1977; Dionisio et al., 2002; De Gelder et al., 2007, 2008; Miki et al., 2007). Here we show that, in a population of plasmid-bearing cells, a variant plasmid with a decreased conjugation rate can give its hosts a competitive edge. Increased replication of hosts carrying low-conjugation plasmid variants can thus explain the experimental observations of conjugation rate reduction and the evolutionary persistence of fin systems in conjugative plasmids of Gram-negative bacteria. Cells bearing fin+ plasmids grow more quickly than cells carrying fin− relatives, outcompeting them and increasing the prevalence of the fin+ plasmid. The extreme of this dynamic is represented in some of our simulated competitions, which suggest that under certain culture conditions Pfin+ would be unable to invade unless Pfin− were present to help it become established (Figure 2a, 40⩽C0⩽80).
One notable result we did not predict was that R1-bearing cells enjoyed increased survival during stationary phase if (and only if) R1-16-bearing cells were present at a high density (see Results). To the best of our knowledge, this interaction between hosts carrying competing R plasmids has not been described earlier. Unexpected interactions such as this highlight the importance of empirical competitions, even when good theoretical predictions are available. The reasons behind the preferential survival of R1-bearing cells are unclear, and can be addressed in future work.
It is important to note that various aspects of plasmid ecology not considered by our model might influence the outcome of plasmid competitions in natural communities. Our experimental system allows bacteria to spread and propagate in new environments, but does not include immigration of new strains into established populations. Although we observe a benefit associated with fin systems, fin-deficient plasmids might be favoured if there were a regular influx of plasmid-free recipients (Turner et al., 1998; Bergstrom et al., 2000). This sort of dynamic may explain the existence of naturally tra-derepressed conjugative plasmids such as F, which carries an IS3 insertion in its finO gene (Firth et al., 1996). However, we believe that natural environments would generally increase the advantageousness of fin genes for the following reasons. (i) Derepressed tra expression in E. coli cells has been shown to elicit stress responses, indicating pleiotropic negative effects of fin mutants on their hosts (Zahrl et al., 2006). (ii) Many plasmids carry genes such as antibiotic-resistance markers that make them advantageous under certain conditions (Eberhard, 1990); sporadic selection for plasmids would help them rise to high levels in a population, which we have shown favours tra repression. Transient selection can also allow plasmids to evolve increased stability in non-optimal hosts (De Gelder et al., 2008). (iii) The presence of plasmid-specific phages in natural environments would increase the fitness of tra-repressed cells by preferentially killing highly piliated fin mutants (Anderson, 1968; Campbell, 1996). Furthermore, other environmental variables not present in our model may allow fin+ plasmids to attain high rates of transfer, potentially increasing their invasion potential in the absence of fin− competitors. Variations in host strains allow some donors to be functionally fin-deficient (Dionisio et al., 2002; Dionisio, 2005; Harr and Schlotterer, 2006). Also, structured environments allowing the development of aggregates or biofilms can increase the spread of wild-type conjugative plasmids in bacterial populations (Molin and Tolker-Nielsen, 2003). Our model assumes mass-action kinetics associated with well-mixed populations; the kinetics of plasmid spread can be quite different on surfaces (Simonsen, 1990; Krone et al., 2007; Fox et al., 2008).
Returning from the specific to the general, our results are consistent with the proposal that fin systems represent a compromise between the interests of the plasmid and those of the host (Lundquist and Levin, 1986). Characteristics of the plasmid–host relationship that set the stage for this compromise are the obligate intracellular nature of plasmids, the pairing of vertical and horizontal modes of transfer and the surface exclusion. Future experiments could determine which of these is most important in biasing the system towards a competitive reduction in plasmid transfer. Such work would provide insights that might help to understand and control the spread of antibiotic resistance in clinically relevant environments.
This work also has implications outside of plasmid biology, in which our mathematical model could apply to any host–parasite system that fits its basic assumptions. In general terms, we predict that a parasite may be selected for in the environment if it provides protection from a more virulent pathogen. The competitive advantage we observed for a low-cost (that is, low-virulence) parasitic element provides a valuable contrast to studies that predict or demonstrate an increase in virulence under competitive pressure for other parasites (Kover et al., 1997; Kover and Clay, 1998; Kerr et al., 2006; Coombs et al., 2007; Bull and Ebert, 2008). We postulate that the importance of vertical transmission and the resistance of the infected host to superinfection are key factors that support a competitive reduction in virulence in our system. Theoretical work suggests that frequent vertical inheritance under competitive conditions might limit virulence in other parasites as well (Frank, 1996). Understanding factors that drive evolution of virulence or temperance will provide insights into the spread of infectious diseases and allow us to better determine which infectious agents require particular attention as new pathogens emerge.
Anderson ES . (1968). The ecology of transferable drug resistance in the Enterobacteria. Annu Rev Microbiol 22: 131–180.
Bahl MI, Hansen LH, Sorensen SJ . (2007). Impact of conjugal transfer on the stability of IncP-1 plasmid pKJK5 in bacterial populations. FEMS Microbiol Lett 266: 250–256.
Bayer M, Eferl R, Zellnig G, Teferle K, Dijkstra A, Koraimann G et al. (1995). Gene 19 of plasmid R1 is required for both efficient conjugative DNA transfer and bacteriophage R17 infection. J Bacteriol 177: 4279–4288.
Bergstrom CT, Lipsitch M, Levin BR . (2000). Natural selection, infectious transfer and the existence conditions for bacterial plasmids. Genetics 155: 1505–1519.
Blohm D, Goebel W . (1978). Restriction map of the antibiotic resistance plasmid R1drd-19 and its derivatives pKN102 (R1drd-19B2) and R1drd-16 for the enzymes BamHI, HindIII, EcoRI and SalI. Mol Gen Genet 167: 119–127.
Bull JJ, Ebert D . (2008). Invasion thresholds and the evolution of nonequilibrium virulence. Evol App 1: 172–182.
Bull JJ, Molineux IJ, Rice WR . (1991). Selection of benevolence in a host-parasite system. Evolution 45: 875–882.
Campbell A . (1996). Bacteriophages. In: Neidhardt FC, Curtiss III R, Ingraham JL, Lin ECC, Low KB, Magasanik B et al. (eds). Escherichia Coli and Salmonella Typhimurium: Cellular and Molecular Biology. ASM Publications: Washington, DC, pp 2402–2405.
Clark AJ . (1985). Conjugation and its aftereffects in E. coli. In: Halvorson HO, Monroy A (eds). The Origins and Evolutions of Sex. Alan R. Liss Inc.: New York, NY, pp 47–68.
Coombs D, Gilchrist MA, Ball CL . (2007). Evaluating the importance of within- and between-host selection pressures on the evolution of chronic pathogens. Theor Popul Biol 72: 576–591.
Dahlberg C, Chao L . (2003). Amelioration of the cost of conjugative plasmid carriage in Escherichia coli K12. Genetics 165: 1641–1649.
De Gelder L, Ponciano JM, Abdo Z, Joyce P, Forney LJ, Top EM . (2004). Combining mathematical models and statistical methods to understand and predict the dynamics of antibiotic-sensitive mutants in a population of resistant bacteria during experimental evolution. Genetics 168: 1131–1144.
De Gelder L, Ponciano JM, Joyce P, Top EM . (2007). Stability of a promiscuous plasmid in different hosts: no guarantee for a long-term relationship. Microbiology 153: 452–463.
De Gelder L, Williams JJ, Ponciano JM, Sota M, Top EM . (2008). Adaptive plasmid evolution results in host-range expansion of a broad-host-range plasmid. Genetics 178: 2179–2190.
Dionisio F . (2005). Plasmids survive despite their cost and male-specific-phages due to heterogeneity of bacterial populations. Evolution Ecol Res 7: 1–19.
Dionisio F, Conceicao IC, Marques AC, Fernandes L, Gordo I . (2005). The evolution of a conjugative plasmid and its ability to increase bacterial fitness. Biol Lett 1: 250–252.
Dionisio F, Matic I, Radman M, Rodrigues OR, Taddei F . (2002). Plasmids spread very fast in heterogeneous bacterial communities. Genetics 162: 1525–1532.
Eberhard WG . (1990). Evolution in bacterial plasmids and levels of selection. Q Rev Biol 65: 3–22.
Firth N, Ippen-Ihler K, Skurray RA . (1996). Structure and function of the F-Factor and mechanisms of conjugation. In: Neidhardt FC, Curtiss III R, Gross CA, Ingraham JL, Lin ECC, Low KB et al. (eds). Escherichia coli and Salmonella typhimurium: Cellular and Molecular Biology. ASM Publications: Washington, DC, pp 2377–2382.
Fox RE, Zhong X, Krone SM, Top EM . (2008). Spatial structure and nutrients promote invasion of IncP-1 plasmids in bacterial populations. ISME J 2: 1024–1039.
Frank SA . (1996). Models of parasite virulence. Q Rev Biol 71: 37–78.
Freter R, Freter RR, Brickner H . (1983). Experimental and mathematical models of Escherichia coli plasmid transfer in vitro and in vivo. Infect Immun 39: 60–84.
Frost LS, Manchak J . (1998). F− phenocopies: characterization of expression of the F transfer region in stationary phase. Microbiology 144: 2579–2587.
Hansen SR, Hubbell SP . (1980). Single-nutrient microbial competition: qualitative agreement between experimental and theoretically forecast outcomes. Science 207: 1491–1493.
Harr B, Schlotterer C . (2006). Gene expression analysis indicates extensive genotype-specific crosstalk between the conjugative F-plasmid and the E. coli chromosome. BMC Microbiol 6: 80.
Jensen KH, Little T, Skorping A, Ebert D . (2006). Empirical support for optimal virulence in a castrating parasite. PLoS Biol 4: e197.
Kerr B, Neuhauser C, Bohannan BJ, Dean AM . (2006). Local migration promotes competitive restraint in a host-pathogen ‘tragedy of the commons’. Nature 442: 75–78.
Kovářová K, Zehnder AJ, Egli T . (1996). Temperature-dependent growth kinetics of Escherichia coli ML 30 in glucose-limited continuous culture. J Bacteriol 178: 4530–4539.
Kover PX, Clay K . (1998). Trade-off between virulence and vertical transmission and the maintenance of a virulent plant pathogen. Am Nat 152: 165–175.
Kover PX, Dolan TE, Clay K . (1997). Potential versus actual contribution of vertical transmission to pathogen fitness. Proc R Soc Lond B 264: 903–909.
Krone SM, Lu R, Fox R, Suzuki H, Top EM . (2007). Modelling the spatial dynamics of plasmid transfer and persistence. Microbiology 153: 2803–2816.
Lawley T, Wilkins BM, Frost LS . (2004). Bacterial conjugation in Gram-negative bacteria. In: Funnell BE and Phillips GJ (eds). Plasmid Biology. ASM Press: Washington, DC, pp 203–226.
Levin BR, Stewart FM, Rice VA . (1979). The kinetics of conjugative plasmid transmission: fit of a simple mass action model. Plasmid 2: 247–260.
Levin SA, Andreasen V . (1999). Disease transmission dynamics and the evolution of antibiotic resistance in hospitals and communal settings. Proc Natl Acad Sci USA 96: 800–801.
Lundquist PD, Levin BR . (1986). Transitory derepression and the maintenance of conjugative plasmids. Genetics 113: 483–497.
Mazel D, Davies J . (1999). Antibiotic resistance in microbes. Cell Mol Life Sci 56: 742–754.
Messenger SL, Molineux IJ, Bull JJ . (1999). Virulence evolution in a virus obeys a trade-off. Proc R Soc Lond B 266: 397–404.
Miki T, Ueki M, Kawabata Z, Yamamura N . (2007). Long-term dynamics of catabolic plasmids introduced to a microbial community in a polluted environment: a mathematical model. FEMS Microbiol Ecol 62: 211–221.
Miller JH . (1972). Experiments in Molecular Genetics. Cold Spring Harbor Laboratory: Cold Spring Harbor, NY.
Molin S, Tolker-Nielsen T . (2003). Gene transfer occurs with enhanced efficiency in biofilms and induces enhanced stabilisation of the biofilm structure. Curr Opin Biotechnol 14: 255–261.
Olsson JA, Paulsson J, Nordstrom K . (2004). Effect of the CopB auxiliary replication control system on stability of maintenance of Par+ plasmid R1. J Bacteriol 186: 207–211.
Panicker MM, Minkley Jr EG . (1985). DNA transfer occurs during a cell surface contact stage of F sex factor-mediated bacterial conjugation. J Bacteriol 162: 584–590.
Simonsen L . (1990). Dynamics of plasmid transfer on surfaces. J Gen Microbiol 136: 1001–1007.
Stewart FM, Levin BR . (1977). The population biology of bacterial plasmids: a priori conditions for the existence of conjugationally transmitted factors. Genetics 87: 209–228.
Sudarshana P, Knudsen GR . (1995). Effect of parental growth on dynamics of conjugative plasmid transfer in the pea spermosphere. Appl Environ Microbiol 61: 3136–3141.
Turner PE . (2004). Phenotypic plasticity in bacterial plasmids. Genetics 167: 9–20.
Turner PE, Cooper VS, Lenski RE . (1998). Tradeoff between horizontal and vertical modes of transmission in bacterial plasmids. Evolution 52: 315–329.
Turner SL, Bailey MJ, Lilley AK, Thomas CM . (2002). Ecological and molecular maintenance strategies of mobile genetic elements. FEMS Microbiol Ecol 42: 177–185.
Willetts NS . (1974). The kinetics of inhibition of Flac transfer by R100 in E. coli.. Mol Gen Genet 129: 123–130.
Wise R . (2004). The relentless rise of resistance? J Antimicrob Chemother 54: 306–310.
Zahrl D, Wagner M, Bischof K, Koraimann G . (2006). Expression and assembly of a functional type IV secretion system elicit extracytoplasmic and cytoplasmic stress responses in Escherichia coli. J Bacteriol 188: 6611–6621.
Zambrano MM, Kolter R . (1996). GASPing for life in stationary phase. Cell 86: 181–184.
Ellen Zechner kindly provided plasmids R1 and R1-16. We thank Gene Nester, Eva Top and Stephen Krone for critical reading of the manuscript. This work was supported by the National Science Foundation (MCB-0345018). R Haft was supported in part by the National Institute of General Medical Sciences (NRSA T32 GM07270).
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Haft, R., Mittler, J. & Traxler, B. Competition favours reduced cost of plasmids to host bacteria. ISME J 3, 761–769 (2009). https://doi.org/10.1038/ismej.2009.22
- microbial ecology
- parasite evolution
- plasmid biology
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