Copper selects for siderophore-mediated virulence in Pseudomonas aeruginosa
BMC Microbiology volume 22, Article number: 303 (2022)
Iron is essential for almost all bacterial pathogens and consequently it is actively withheld by their hosts. However, the production of extracellular siderophores enables iron sequestration by pathogens, increasing their virulence. Another function of siderophores is extracellular detoxification of non-ferrous metals. Here, we experimentally link the detoxification and virulence roles of siderophores by testing whether the opportunistic pathogen Pseudomonas aeruginosa displays greater virulence after exposure to copper. To do this, we incubated P. aeruginosa under different environmentally relevant copper regimes for either two or twelve days. Subsequent growth in a copper-free environment removed phenotypic effects, before we quantified pyoverdine production (the primary siderophore produced by P. aeruginosa), and virulence using the Galleria mellonella infection model.
Copper selected for increased pyoverdine production, which was positively correlated with virulence. This effect increased with time, such that populations incubated with high copper for twelve days were the most virulent. Replication of the experiment with a non-pyoverdine producing strain of P. aeruginosa demonstrated that pyoverdine production was largely responsible for the change in virulence.
We here show a direct link between metal stress and bacterial virulence, highlighting another dimension of the detrimental effects of metal pollution on human health.
Iron is essential for the growth of almost all bacteria as it serves as a cofactor for many enzymes [1, 2]. However, as iron most commonly exists in the insoluble form Fe3+, it is of relatively low bioavailability in the majority of environments [1,2,3,4,5,6,7]. It is therefore essential for bacteria to actively sequester Fe3+ from the environment [8, 9], with many bacteria producing iron-chelating siderophore compounds to do this . Siderophores aid iron recovery by forming extracellular complexes with Fe3+ which are then taken up by the cell and reduced to the bioavailable form Fe2+ . The extracellular nature of siderophores means they can benefit the group around the producer, with only the producer paying the cost of production. As a result, siderophore production can be a cooperative trait subject to social evolution [12, 13]. Therefore as increased siderophore production evolves under iron limitation to benefit the producer and its kin, genotypes with reduced production can also evolve to exploit these producers and gain a fitness advantage . Due to the importance of iron for microbial growth, one of the first lines of host defence is to withhold iron from invading pathogens . This often involves the production of molecules such as lactoferrin and transferrin that bind to iron with very high association constants [6, 14,15,16]. Such nutritional immunity can be overcome by pathogens through the production of siderophores, as their very high iron affinity enables ‘stealing’ iron from the host . Siderophores are therefore an important virulence factor in both gram-negative- [17,18,19] and gram-positive human pathogens [20, 21].
In addition to iron, siderophores are known to bind to a range of potentially toxic metals . Crucially, these complexes cannot passively diffuse into the cell (i.e. not without active use of transport proteins) and consequently the metal is detoxified extracellularly . As a result, siderophore production has been shown to increase in the presence of toxic levels of a wide range of non-ferrous metals [2, 3, 9, 22]. As many of the metal ions that can be bound by siderophores are essential in small amounts, siderophore production is adjusted in response to metal bioavailability , with either active uptake of metal-siderophore complexes or other metal chelating compounds used to acquire these micronutrients when they are scarce [7, 25]. Adjustments in production can be due to both genetic changes and phenotypic plasticity, with genetics dictating the limits of siderophore production and phenotypic plasticity used to regulate production within those limits . Although the upper limit of production initially increases with metal toxicity, eventually a threshold is reached as the rising metabolic cost of siderophore production can result in selection for reduced production  – analogous to the evolutionary response to iron deficiency . This cost is further exacerbated when competitors of the producer benefit from the siderophore . Consequently, when there is strong selection for siderophore production in the community, such as when toxic metals are at high concentrations, per capita siderophore production can be reduced both through phenotypic and genotypic change [8, 27, 28]. Phenotypic changes in production occur quickly in response to alterations in the environment, including the abundance of metals and population densities, and allow the cost of production to be minimised [23, 28].
Despite strong evidence both for siderophores playing an important role in metal detoxification [3, 8, 22, 24] and for siderophore production being an important determinant for bacterial virulence [16, 29, 30], whether the presence of toxic metals in non-host environments affects virulence remains untested. Here we aim to experimentally link these dual effects of siderophore production, by testing the effects of copper on the virulence of the opportunistic human pathogen Pseudomonas aeruginosa. To quantify virulence we used the insect infection model Galleria mellonella – an established model system for the mammalian innate immune system [31, 32] that has previously been used to quantify bacterial virulence, including P. aeruginosa [33, 34]. P. aeruginosa is of clinical significance capable of surviving in a range of environments including soil, water and fomites in hospitals [35, 36]. In clinical settings it is frequently responsible for severe and fatal infections of patients with cystic fibrosis (CF) , burns , and immunosuppressive illnesses . It is important to note that many CF infections are caused by P. aeruginosa acquired from the environment , and so an understanding of how selection for siderophore production outside of the host could alter virulence is of great importance.
The production of pyoverdine, the main P. aeruginosa siderophore, has been shown to rapidly evolve . We therefore test virulence after both two days (~ 7 generations), when little genotypic change is expected to have occurred, and twelve days (~ 40 generations), where genotypic changes in production are expected [12, 42]. To allow us to exclude phenotypic changes to production, at each timepoint (two and twelve days) populations are transferred to a common garden environment (copper free media) for 24 h prior to assays. By quantifying pyoverdine production in every population before the virulence assay, we are able to test whether its production is associated with virulence. We then further test for an association by repeating the experiment using a P. aeruginosa strain that cannot produce either pyoverdine or pyochelin (P. aeruginosa’s secondary siderophore ), and testing whether copper has the same effect on virulence. Moreover, we test if this association is the same across two environmentally relevant copper concentrations that span those found in agricultural soil  and in water .
Copper selected for increased pyoverdine production
Here we tested the evolutionary consequences of copper stress on Pseudomonas aeruginosa by incubating it with copper for either two or twelve days, and then without copper for one day. All results shown here therefore display the evolutionary consequences of copper stress, as the phenotypic effects are removed by growing populations in copper-free common garden environment. Unless otherwise stated, data from the non-pyoverdine producing strain are only shown in the final section of the results. In line with previous findings , pyoverdine production evolved to be significantly greater as a function of copper concentration (copper main effect: χ2 = 35.4, d.f. = 2, p < 0.001). This effect was consistent across the two- and twelve-day treatments; however, production was significantly greater after twelve days compared to two days (time main effect: χ2 = 161, d.f. = 1, p < 0.001; Fig. 1). Pyoverdine production was significantly higher in the high copper treatment compared to both the control (two days: p < 0.001; twelve days: p < 0.001) and the low copper treatment (two days: p = 0.032; twelve days: p = 0.032). Likewise, the low copper treatment was always significantly higher than the control (two days: p = 0.004; twelve days: p = 0.004). The non-independence of observations between day two and day twelve samples accounted for only a small amount of the total variation (SD = 0.029) in this model.
Virulence is higher in populations exposed to copper and this effect increases with time
To test whether copper stress caused differences in P. aeruginosa virulence, populations were assayed using the Galleria mellonella virulence model. Copper significantly increased virulence (copper main effect: χ2 = 20.8, d.f. = 2, p < 0.001) and this effect increased with time (copper-time interaction: χ2 = 6.90, d.f. = 2, p = 0.031; Fig. 2). After two days, virulence was significantly higher in the two copper treatments compared to the control (p < 0.001 for both comparisons) but these treatments did not differ themselves (p = 0.34). After twelve days virulence was again significantly higher in the two copper treatments than the control (p < 0.001 for both comparisons), however the high copper treatment was found to be significantly more virulent than the low copper treatment (p = 0.027). We note these treatment effects were found despite the random effect of repeatedly measuring the same population accounting for a large amount of the variation (SD = 0.42).
The effect of copper on population density differs over time
The effect of copper on population density differed as function of time (copper-time interaction: χ2 = 20.5, d.f. = 2, p < 0.001; Fig. 3). After two days, population densities did not significantly differ between any copper treatment (p = > 0.060 for all contrasts), whereas after twelve days of growth density was significantly lower in the two copper treatments compared to the control (high copper—control: p = 0.013 and low copper—control: p = 0.002) but did not differ themselves (p = 0.48). The effect of measuring the same populations at two time points did not explain any of the overall variation in this model (SD = 0.0), but to account for non-independency of observations it was retained in the model. These results demonstrate that the common garden environment is sufficient to allow P. aeruginosa to recover from the antimicrobial effect of copper after two-days of co-culture, but not after twelve-days of co-culture.
Virulence is associated with increased in vitro pyoverdine production but not in vitro pathogen density
Next, we tested whether increased virulence was associated with increased pyoverdine production by replacing ‘copper’ as an explanatory variable in our GLMM with per capita pyoverdine production and included density as a covariate in this model. We note that both pyoverdine production and density were measured pre-injection, and so describe traits of the initial infection populations and not those that have been exposed to the host. Despite there being substantial variation across populations in virulence (SD = 0.86), virulence increased as a function of pyoverdine production (pyoverdine main effect: χ2 = 13.9, d.f. = 1, p < 0.001; Fig. 4), and this effect did not change with time (pyoverdine-time interaction: X2 = 0.009, d.f. = 1, p = 0.93) although virulence was higher after twelve days (time main effect: X2 = 5.40, d.f. = 1, p = 0.02). Population density had no significant effect on virulence (main effect of density in GLMM: X2 = 1.09, d.f. = 2, p = 0.30).
The high copper treatment decreased the virulence of the non-pyoverdine producing strain
Finally, to confirm at least part of the change in virulence was due to pyoverdine production, we tested whether a non-pyoverdine producing mutant strain of P. aeruginosa evolved under the same copper regime exhibited similar changes in virulence. The fluorescence assay used to detect pyoverdine detected some fluorescence (mean = 431 ± 91.6 SD RFU), but since this was on average 94.5% lower than populations of the wild-type producer (mean = 7763 ± 2979 SD RFU), and P. aeruginosa PAO1ΔpvdDΔpchEF is unable to produce pyoverdine, it was deemed to be negligible fluorescence due to other non-pyoverdine metabolites. Once again, we found a significant effect of copper on virulence (copper main effect: χ2 = 66.6, d.f. = 2, p < 0.001; Fig. 5) however, this time the effect was negative, and decreased with time (copper-time interaction: χ2 = 6.45, d.f. = 2, p = 0.040; Fig. 5). Despite a slight decrease in the effect of copper over time, we found the same qualitative pattern in the virulence of the non-pyoverdine producing strain across copper treatments after two and twelve days: virulence was not significantly different between the low copper treatment and the control (two days: p = 0.087; twelve days: p = 0.48), but was significantly lower in the high copper treatment compared to both the low copper treatment and the control (p = < 0.001 for all contrasts; Fig. 5). As with the virulence model for the pyoverdine producing strain, the random effect of repeatedly measuring the same population accounted for a large amount of the variation (SD = 0.44). Note that injections with pyoverdine producing and non-pyoverdine producing strains were done in different batches of G. mellonella, and so statistical comparison between the results from the wild-type and mutant infections is inappropriate.
Here, we experimentally tested whether copper causes the evolution of increased siderophore-mediated virulence in Pseudomonas aeruginosa. We found copper to select for increased per capita pyoverdine production, which was associated with greater levels of death in the Galleria mellonella infection assay. Moreover, pyoverdine production was found to increase with time, such that populations exposed to copper for twelve days were more virulent than those exposed for two days. In addition to this overall increase in virulence with time, high copper caused significantly greater virulence than low copper in the twelve-day treatment but not in the two-day treatment. As a result, the twelve-day high copper treatment demonstrated the greatest virulence. Furthermore, we found that when using a non-pyoverdine producing mutant strain of P. aeruginosa, high copper reduced virulence, and low copper had little effect on virulence. Our results therefore demonstrate that copper stress increases pyoverdine production and consequently virulence, and that this effect increases with exposure time and copper concentration.
Finding copper-mediated increases in pyoverdine production is consistent with a role of pyoverdine in detoxification of copper in P. aeruginosa populations . Here, we show that a prolonged need for copper detoxification leads to the continued evolution of greater siderophore production. The resulting cost of these genotypic changes to a metabolically costly trait is a likely explanation for the reduced densities in the twelve-day copper treatments. We note that our finding of increased pyoverdine production with copper differs to that of previous work . Likely explanations for this are the fewer observed generations in our study (40 opposed to 200), culturing under static (versus shaken) conditions, which favours public goods production, and transfers occurring every two days compared to daily. In addition to copper, pyoverdine production has been shown to be up-regulated in response to a range of other metals . This suggests that these metals may also increase P. aeruginosa virulence, and may cause selection for increased production over longer exposure periods. Furthermore, it is likely that mixtures of metals, which are frequently encountered in polluted environments, might additively select for pyoverdine production and thereby virulence. It is also plausible that the effect of metal pollution on pyoverdine production could depend on the structure of the environment, as has been found with iron concentrations .
The positive association between pyoverdine production and virulence is consistent with previous findings, including in murine models . As well as directly aiding pathogen growth within a host by increasing iron uptake, pyoverdine production can increase virulence by causing the upregulation of additional virulence factors such as Exotoxin A and PrpL protease [49, 50]. Finding per capita pyoverdine production to be a better predictor of virulence than population density in this system shows the cost of evolving greater production on density is inconsequential in a host. Furthermore, finding the virulence of the non-pyoverdine producing mutant to not be affected by low copper, and to be decreased by high copper, strongly suggests that virulence has changed as a consequence of the evolutionary change in pyoverdine production. However, we note that in addition to pyoverdine production, copper stress has been shown to change the expression of over 300 genes in P. aeruginosa , and it is plausible these also have implications for virulence.
In addition to P. aeruginosa, toxic metals have also been shown to induce the production of (non-pyoverdine) siderophores in other species , with siderophore production being shown to increase proportionally with toxic metal pollution in natural microbial communities . As the copper concentrations used in this study were chosen for their environmental relevance, we suggest our findings could be relevant to natural communities inhabiting polluted environments. We note that remediation techniques, principally lime addition, are used in some metal-polluted areas to reduce their toxic effect , and this can lower community siderophore production . Extending experiments such as those described here to the level of natural communities could shed light on the consequences of metal pollution and metal remediation on bacterial siderophore production and virulence.
In conclusion, we experimentally show that copper can increase the virulence of the pathogen Pseudomonas aeruginosa by selecting for increased production of a metal-detoxifying siderophore. We therefore demonstrate a direct link between toxic metal stress and virulence in an opportunistic pathogen of significant clinical importance. Furthermore, we show that the effect of metal exposure on virulence increases with exposure time and copper concentration. This raises further concern for the effect of ever-increasing metal pollution on bacterial pathogens, and highlights further work is needed to understand the role of metals in bacterial virulence.
Pseudomonas aeruginosa PAO1  was grown shaking at 180 rpm for 24 h at 28 °C in glass microcosms containing 6 mL of King’s medium B (KB; 10 g glycerol, 20 g proteose peptone no. 3, 1.5 g K2HPO4,1.5 g MgSO4, per litre). After homogenisation by vortexing, 60µL of undiluted culture was added to 18 microcosms containing KB mixed with sterilised copper sulphate (CuSO4; Alfa Aesar, Massachusetts, United States) to final concentrations of either 0.0, 0.1 or 1.0 g/L. Inoculated microcosms were kept static at 28 °C for 48 h before being thoroughly homogenised and 60µL (1% by volume) transferred into fresh media (Fig. 6). Microcosms were incubated at 28 °C, rather than the more common 37 °C, in order for our experiment to be more representative of environmental conditions. Transfers occurred every two days for twelve days. To control for the physiological effects of copper stress, on days two and twelve each microcosm was homogenised and 60µL transferred into a common garden environment (6 mL of KB medium without copper). These cultures were grown for 24 h at 28 °C before pyoverdine production was quantified and aliquots were frozen at -80 °C in glycerol at a final concentration of 25% for virulence assays and to quantify density. We then repeated this experiment with an isogenic mutant strain of P. aeruginosa (PAO1ΔpvdDΔpchEF ) with the ability to produce pyoverdine, and the secondary siderophore pyochelin, knocked out (a non-pyoverdine producing strain). All experimental work was carried out in sterile conditions.
Pyoverdine production was quantified after both two and twelve days. Following 24 h in a common garden environment, cultures were thoroughly homogenised before 600µL was transferred into a 96 well-plate (200µL into three separate wells). The optical density at 600 nm (OD600) and the fluorescence at 460 nm following excitation at 400 nm of each of the cultures in the 96-well plate was measured using a BioTek Synergy 2 plate reader (BioTek, Vermont, U.S.A.). Pyoverdine, which fluoresces green, is the only culture component quantified using these excitation and emission parameters . Each culture was measured three times (one reading of each of three wells per culture), and the average of three sterile media readings was used as a reference and subtracted from each culture value. The optical density measurements were used to estimate pyoverdine production per cell (i.e. per capita pyoverdine production) using: RFU / OD600. The average of the three technical replicates was used in the analysis. We chose to quantify pyoverdine production at the population level (rather than for individual clones) as it represents the most relevant measure of the Galleria mellonella inoculum (see Galleria mellonella virulence assay below). We repeated this assay with the non-pyoverdine producing strain to confirm it produced negligible quantities of pyoverdine.
Galleria mellonella virulence assay
To quantify virulence of both the pyoverdine producing and non-producing strains, we used the insect infection model Galleria mellonella . Briefly, defrosted samples were diluted 105-fold in M9 salt buffer (3 g KH2PO4, 6 g Na2HPO4, 5 g NaCl per litre) before 10µL was injected into each of 20 final instar larvae per sample using a 50µL Hamilton syringe (Hamilton, Nevada, USA). Larvae were then incubated at 37 °C and mortality quantified 18 h post-injection, as at this timepoint there was a large variation in the number of alive larvae between the populations (all populations had caused at least one death, and some had caused 100% mortality). Larvae were classed as dead when mechanical stimulation of the head caused no response . M9-injected and non-injected controls were used to confirm mortality was not due to injection trauma or background G. mellonella mortality; > 10% control death was the threshold for re-injecting (no occurrences). Pyoverdine producing and non-producing strains were injected into different G. mellonella groups.
Quantifying Pseudomonas aeruginosa density
The density of P. aeruginosa in the common garden environment was quantified by plating onto agar. To do this, samples were defrosted, serially diluted with M9 salt buffer and plated onto KB agar. After 48 h incubation at 28 °C colonies were counted and the number of colony forming units (CFU) standardised to CFUs per mL. Note we only quantified the density of the pyoverdine producing strain.
The effect of copper on per capita pyoverdine production (RFU / OD600) and density (CFU/mL) of P. aeruginosa populations was tested using linear mixed effects models (LMEM) with copper and time as explanatory variables (both factors), as well as their 2-way interaction. To determine how copper affected virulence we used a binomial generalised linear mixed model (GLMM), with number of G. mellonella dead versus alive as binomial response variable, and copper and time as explanatory variables, as well as their two-way interaction. To analyse the combined effect of pyoverdine production and density on virulence, we used a similar framework and included pyoverdine production, total CFU and time, along with a two-way pyoverdine-time interaction, as explanatory variables. In all analyses, pyoverdine production and population density were log10-transformed to improve normality, and random intercepts were fitted for individual replicates to account for non-independency of observations over time.
For all analyses, we used the ‘DHARMa’ package  to check residual behaviour, after which the most parsimonious model was arrived at by sequentially deleting terms and comparing model fits using χ -tests. These were followed by Tukey post hoc comparisons adjusted for multiple comparisons using the Benjamini and Hochberg method. All analyses were carried out in R version 3.3.3 , with the ‘lme4’ package used for the LMEMs and GLMMs .
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LL would like to thank the NERC FRESH GW4 award no. NE/R011524/1, EH the UKRI Future Leaders Fellowship award MR/V022482/1, AB the NERC award NE/V012347/1, and MV the NERC award NE/T008083/1.
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Lear, L., Hesse, E., Buckling, A. et al. Copper selects for siderophore-mediated virulence in Pseudomonas aeruginosa. BMC Microbiol 22, 303 (2022). https://doi.org/10.1186/s12866-022-02720-w
- Evolution of virulence
- Opportunistic pathogen
- Metal detoxification
- Coincidental selection