- Research article
- Open Access
Tracking costs of virulence in natural populations of the wheat pathogen, Puccinia striiformis f.sp.tritici
© Bahri et al; licensee BioMed Central Ltd. 2009
Received: 22 August 2008
Accepted: 30 January 2009
Published: 30 January 2009
Costs of adaptation play an important role in host-parasite coevolution. For parasites, evolving the ability to circumvent host resistance may trade off with subsequent growth or transmission. Such costs of virulence (sensu plant pathology) limit the spread of all-infectious genotypes and thus facilitate the maintenance of genetic polymorphism in both host and parasite. We investigated costs of three virulence factors in Puccinia striiformis f.sp.tritici, a fungal pathogen of wheat (Triticum aestivum).
In pairwise competition experiments, we compared the fitness of near-isogenic genotypes that differed by a single virulence factor. Two virulence factors (vir4, vir6) imposed substantial fitness costs in the absence of the corresponding resistance genes. In contrast, the vir9 virulence factor conferred a strong competitive advantage to several isolates, and this for different host cultivars and growing seasons. In part, the experimentally derived fitness costs and benefits are consistent with frequency changes of these virulence factors in the French pathogen population.
Our results illustrate the variation in the evolutionary trajectories of virulence mutations and the potential role of compensatory mutations. Anticipation of such variable evolutionary outcomes represents a major challenge for plant breeding strategies. More generally, we believe that agro-patho-systems can provide valuable insight in (co)evolutionary processes in host-parasite systems.
Central to many concepts in evolutionary biology is the idea that adaptation is not cost-free [1, 2]. Costs arise if adaptation in one trait is opposed by a negative correlated response to another trait. Such trade-offs between fitness components can influence life-history evolution, ecological specialisation and more generally, the maintenance of genetic diversity .
Costs of adaptation also play an important role in host-parasite coevolution. In the host, costs of resistance refer to trade-offs between resistance and other fitness-relevant traits, conferring a selective disadvantage to resistant genotypes in the absence of the parasite. The corresponding costs in the parasite, referred to as 'costs of virulence' in the plant-pathogen literature, are trade-offs between the capacity to establish an infection and other parasite characters (e.g., within-host growth, production of transmission stages ). These costs are considered major ingredients of the coevolutionary process because they can prevent the spread to fixation of all-resistant host or all-infectious parasite genotypes and thereby preserve genetic diversity in both host and parasite populations [5–8].
While costs of resistance have been investigated in various host-parasite systems (plant: [9, 10]; (cyano)bacteria: [11, 12]; protozoa: ; drosophila: ), still little is known about costs of virulence and their role in shaping genetic structure and coevolutionary dynamics. Historically, this issue has first been addressed in plant-pathogen interactions [15, 16]. Here, virulence refers to the ability of the pathogen to circumvent host resistance and establish an infection. This ability often arises from mutational loss of function of genes that would otherwise elicit a defense reaction of the host . However, this advantage of malfunctioning can turn into a disadvantage if these genes are essential for subsequent development of infection. With the advent of molecular techniques, investigation of the precise genetic and physiological basis of costs of virulence has become possible. Induced mutagenesis of genes implicated in plant-pathogen recognition revealed that at least some of these genes are involved in within-host replication, pathogenicity or spore production [18–20]. Thus, loss of function of these genes will allow infection, but also impose a straightforward cost for subsequent development.
Given their intrinsic fitness costs, selection should eliminate unnecessary virulence genes from the pathogen population and favour pathotypes with particular virulence genes that match the resistance structure of the host population . Thus, in classical models of plant-pathogen coevolution, changes in the frequencies of resistance and virulence genes are essentially determined by the fitness trade-offs associated with these genes [6, 15]. While more recent theoretical developments balance the importance of cost with other biological features [22, 23], empirical and experimental evidence of these basic theoretical concepts is still scant. Natural populations of various pathogens often harbour genotypes carrying different numbers of virulence alleles. For pathogens of crop plants, withdrawal of a particular cultivar sometimes leads to the subsequent decrease in frequency of the genotypes carrying the corresponding virulence allele [24, 25], consistent with the idea of selection against unnecessary and costly virulence alleles. In some cases, molecular analysis suggests that costs of virulence contribute to the maintenance of genetic polymorphism in the pathogen ; in yet other cases, elimination of the function of virulence genes seems to be cost-free, suggesting that fitness costs are not universal and depend on the gene or the pathogen considered.
Only few experimental studies compared the relative fitness of naturally occurring pathogen genotypes that carry different numbers of virulence alleles. Thrall and Burdon  detected a negative correlation between virulence and spore production for the plant pathogen Melampsora lini. This trade-off may explain why relatively avirulent strains dominated susceptible host populations. Furthermore, for different plant-pathogen systems, competition experiments compared pathogen genotypes with different numbers of virulence alleles. Some of these studies demonstrated a selective advantage of simpler over complex genotypes, at least in the greenhouse [[19, 27, 28], but see ]. Typically, however, these experiments did not control for the genetic background of the competing strains and it is possible that fitness differences were caused by other genes .
Here, we investigated costs of virulence in the yellow rust fungus, Puccinia striiformis f.sp.tritici (PST), one of the most damaging wheat pathogens worldwide . This clonally reproducing pathogen rapidly evolves through stepwise mutational acquisition of new virulences [32, 33], and the resulting arms race between plant breeders and the pathogen is characterised by frequent and rapid resistance breakdowns . In North-Western Europe, the fitness advantage of being able to grow on a resistant cultivar is so strong that a new virulent mutant pathotype can replace an existing dominant pathotype within 2–3 years [33, 35]. Costs of virulence potentially slow down resistance breakdowns or at least limit the severity of epidemics. Therefore knowledge of these costs can help plant breeders to better understand evolutionary change in the pathogen and to develop more efficient strategies of resistance management.
We performed competition experiments using pathogen genotypes that differed by a single virulence gene not needed for infection. This is analogous to measuring costs of resistance in the absence of the parasite [4, 10]. If the virulence gene is costly, its carriers should be at a competitive disadvantage. We tested this hypothesis for different naturally occurring virulence genes. The specific novelty of this study is that we explicitly accounted for genetic background by competing genotypes with identical (or nearly so) profiles of molecular markers (AFLP). Because this pathogen is clonal, identical profiles indicate very close phylogenetic relationships. Further, competition assays were carried out both in the climatic chamber and in the field, on different wheat cultivars and in different years. We confront our results with changes in the frequencies of these virulence factors in natural populations over the past 20 years , and with changes in aggressiveness in a collection of isolates from this period.
1. Competition experiments
Identity of pathogen isolates in the pairwise competition experiments
Virulence factor profile2
Success of virulent isolates in pairwise competition experiments in the field
Selective value of Avir
38 ± 2.7
26 ± 0.2
24 ± 1
32 ± 10.2
26 ± 9.8
32 ± 0.2
80 ± 3.5
46 ± 6.4
74 ± 0.2
76 ± 0.3
71 ± 0.9
83 ± 0.3
85 ± 4.4
70 ± 11.6
74 ± 5.3
83 ± 3.3
83 ± 8.6
72 ± 5
70 ± 3.2
85 ± 5.1
22 ± 0.1
18 ± 0.9
23 ± 0.8
44 ± 6.3
28 ± 5.1
20 ± 0.3
17 ± 1.4
14 ± 1.9
25 ± 6.1
25 ± 0.9
29 ± 14.5
28 ± 9.9
20 ± 2.2
12 ± 1.9
Statistical analysis of competitive success of vir9 isolates in the field competition experiments
Pr > F
With two additional competition pairs (E, F) we were able to compare all possible A vir/vir combinations between the i1, i2, i5 and i6 isolates. Analysis of this set of combinations (pairs A, B, E, F) revealed a significant effect of virulence identity (i5 vs. i6; F1,8 = 142.61, p = < 0.0001), but no significant interaction between avirulence and virulence identity (F1,8 = 0.05, p = 0.832). That is, the i5 isolate was less competitive and the i6 more competitive, regardless of the identity of the avirulent counterpart in the mix.
vir4 and vir6 pathotypes
For the vir4 and vir6 pathotypes, four pairs of avirulent and virulent isolates were tested (Pairs G-J, Table 2) under field conditions. For all virulent isolates, we observed a significant decrease in the frequency (vir4: t7 = 12.76, p < 0.0001; vir6: t5 = 5.19, p = 0.0035) (Figure 2b, Table 2). Typically, their relative frequencies dropped from initially 50% to around 20–30% within a growing season, although this effect varied to some extent between years (vir4: year × cultivar interaction: F1,6 = 17.4, p = 0.0059) and host cultivars (vir6: year × pair interaction: F1,8 = 7.44, p = 0.0260). Thus, in all four pairs tested, the isolate with the additional virulence was substantially less competitive, with a selective disadvantage of 17–24%.
2. Sporulation test and genetic analysis of the vir9 pathotype
Evidence for costs of virulence
For five of the 8 virulent isolates tested, our experiments demonstrated a substantial cost of carrying an additional virulence gene, and this for different genes and different genetic backgrounds of the same gene. Despite some variation between years and cultivars, these costs appear to be quite robust and repeatable. In particular, the additional tests (pairs E, F) showed that the low performance of the virulent isolates was independent of the identity of the avirulent competitor.
Genetic variation in fitness detected in the laboratory does not always reflect the degree of variation expressed under field conditions. Under natural conditions, stress can increase the genetic variance in fitness , while confounding environmental effects might limit its detection . Here, the field assays revealed even stronger fitness differences between the competing isolates (Figure 2). The selection coefficients (13%–22%) are similar to those from laboratory studies on other organisms [39–41] and indicate potentially strong selection against these virulence genes, if redundant. The most likely cause of this competitive disadvantage is a reduction in the ability to develop on the host and produce spores. This type of cost has been detected in other pathogens [39–43] and at least for the vir9 virulence gene, we have direct evidence that costs are due to low sporulation.
Compatibility with epidemiological history of natural PST populations
In agricultural host-parasite arms races, farmers typically plant one or a few host cultivars over large geographic areas. This imposes strong, uniform selection on the pathogen to evolve the ability to attack these host genotypes. In the case of PST, the necessary virulence genes to overcome resistance can rapidly arise through mutation in large clonal populations. Once a resistance breakdown has occurred, cultivars are withdrawn and replaced by new resistant cultivars, developed by plant breeders. Indeed, one of the to date most convincing examples of such a semi-natural coevolutionary arms race has been demonstrated for the PST-wheat system , and it involves the virulence genes (vir4, vir6, vir9) studied in our experiments. With the replacement of susceptible cultivars, the vir6 and vir9 genes have become redundant at some point during the past 15 years (vir4 has always been redundant). Thus, if these genes impose fitness costs, they should have decreased in frequency in natural pathogen populations.
For the vir6 virulence gene, this seems to be the case. The competition experiment revealed a strong selective disadvantage of the virulent vir6 isolates, and this is consistent with three declines in the frequency of the vir6 gene, when cultivars carrying the corresponding resistance gene (Yr6) were retracted . In contrast, the fitness costs of the vir4 virulence gene detected in the competition experiment does not match with its epidemiological history. The vir4 gene appeared in Europe already more than 20 years ago[34, 44] and all contemporary pathotypes carry it. Interestingly, the majority of plant varieties used in France in the past 30 years did not carry the corresponding Yr4 resistance gene and thus the vir4 gene must have been mostly redundant. Given the clonal evolution of PST, it is possible that this ancestral vir4 gene has spread to fixation by hitch-hiking with new, selectively advantageous virulence genes. Originally, the vir4 gene may have immigrated from the UK, where the Yr4 resistance gene was present in several cultivars in the past (e.g., Maris Beacon, Rapier, Avalon or Brimstone [45–47]). In fact, the Yr4 has also been postulated for certain Danish wheat cultivars . This suggests that the vir4 gene may even have a selective advantage at a larger, European scale and that simple hitch-hiking is not the only explanation for its presence in the French population. It further implies that migration at larger geographical scales, such as that between the UK and continental Europe [33, 35], can influence local pathogen population structure and evolution.
For the vir9 gene, the story is more complex. After the resistance breakdowns in 1989 and 1994 and subsequent withdrawal of the susceptible cultivars, vir9 did not decrease in frequency, and currently all known PST pathotypes are fixed for this redundant virulence gene . In part, this can be explained by its hitch-hiking with a newly arisen virulence gene (vir17, [34, 35]), just like in the case of the vir4 gene. Moreover, we detected a fitness cost only for one vir9 isolate, while the other three isolates were even more competitive than their avirulent counterparts not carrying the vir9 gene. Our results further indicate that these differences are due to variation in aggressiveness and sporulation rates. The three successful isolates sporulate at high rates, while the less competitive one is among the least aggressive isolates of the vir9 collection.
Why is the vir9 gene costly in some isolates, but not in others? The answer may lie either in the gene itself or in its genetic background. First, in our four virulent isolates, the same vir9 virulence phenotype may represent different mutations, and only one imposes a fitness cost. Typically, virulence genes arise from mutations disrupting some metabolic function that would otherwise elicit a resistance reaction. It is conceivable that different mutations can bring about such modifications, and possibly not all of them come at a fitness cost . Alternatively, costs of virulence may have been balanced by compensatory mutations. Compensation may occur directly in the gene(s) responsable for the loss of function, but also indirectly in genes determining pathogen aggressiveness. Indeed, aggressiveness is known to have a multigenic basis , thus offering multiple targets for compensatory mutations. If fitness effects are sufficiently large and selection efficient, this may even bring about a net positive effect and overcompensation of the cost of virulence. The history of the vir9 gene is compatible with such a scenario. Resistance breakdown of the Yr9 gene in England occurred already two years before highly aggressive vir9 variants appeared in France. Breakdowns are usually accompanied by massive PST epidemics, with exponential population growth and up to 10 infection cycles per growing season. This may have provided sufficient time for compensatory mutations to arise in the vir9 background and to be picked up by natural selection. Indeed, for the period in question, a signature of this process can be seen by the increase of the frequency of highly aggressive isolates in the vir9 spore collection. So far, cost-compensation has been described for resistance to antibiotics or insecticides . If our interpretations are correct, this study is one of the first to suggest the compensation of costs of virulence in natural populations of a pathogen. Similar ideas about the progressive evolution of the fitness of new pathotypes of cereal rusts date back to the 1970s. Based on empirical and experimental data, it was suggested that new phenotypes were unable to spread because of their low aggressiveness [52, 53] and that adaptation to quantitative host resistance occurred gradually through polygenic changes .
Interestingly, we did not detect variation in neutral genetic markers among the isolates in the collection, despite the large number of primer combinations screened. As these isolates share the same clonal background, variation in both virulence and aggressiveness must have arisen within a relatively short time span. Indeed, Lande and Barrowclough  showed that in very large populations, heritable variation in quantitative traits can established by spontaneous mutation without leaving a trace in neutral genetic markers. Clearly, this rapid evolutionary change sets limits to our "all-else-being-equal" approach in the competition experiments, aiming at the comparison of isogenic isolates that differ only in the virulence gene in question.
First, our study demonstrates substantial fitness costs of single virulence genes on different host varieties under field conditions. In part, these costs explain changes in the genetic composition of natural PST populations, consistent with van der Plank's hypothesis of selection against redundant virulence genes . Second, however, we also found that redundant virulence genes are not automatically selected against, either because they do not have a fitness cost or because costs are compensated. Regardless of the precise mechanism, one of our main conclusions is that the fate of a particular virulence mutation may not be independent of its genetic background. This is particularly relevant for clonal pathogens, such as PST, where the whole genome is a single linkage group exposed to natural selection. Selection then perceives the sum of the costs of the different virulence genes carried by a given genotype and that of all other genes determining growth and transmission. Indeed, additional virulences may have more deleterious effects in genetic backgrounds that already carry other virulence genes [40, 42, 56] as it was the case in our study. The very different outcomes for the three virulence genes studied here indicate strong variation in the evolutionary trajectories of virulence mutations; this also stresses the need for more refined theoretical models to predict these trajectories.
Third, our results have implications for plant breeding strategies. Current large-scale programs employ inter-specific crosses and molecular engineering to develop resistance genes imposing a high cost of virulence for pathogens that overcome this resistance. This handicap may prevent the spread of such pathogen genotypes and thus increase the durability of resistance . Obviously, this approach critically hinges on the consistency and durability of costs of virulence. Our experiments indicate that costs can be quite consistent, at least for certain virulence genes. However, durability of costs of virulence can be expected to be inversely proportional to the strength of selection imposed on the pathogen to compensate these costs. We suspect that that compensation may occur rather rapidly, by hitch-hiking processes or by efficient selection on multigenic traits. Thus, if demonstrating the cost of virulence is already complicated, predicting its durability may be even more difficult.
Finally, it is often argued that agro-patho-systems are too artificial or too simple to be comparable to natural host-parasite systems. Here, we demonstrated that the seemingly straightforward genetic architecture of the cultivated host produces complex patterns of genetic change in its natural opponent. These evolutionary changes can be investigated experimentally in real-time (several pathogen generations) and they remain traceable over larger time scales in the production areas (years or decades). We therefore believe that the study of these systems can provide valuable general insights in the costs and consequences of adaptation in host-parasite systems.
Puccinia striiformis f.sp. tritici (order Uredinales, class Basidiomycetes) is strongly wheat-specific (Triticum aestivum and T. turgidum). There is no known alternate host on which the sexual cycle could be completed and thus fungal reproduction is essentially asexual. Fungal mycelia systemically grow within leaf nervures (stripes); the asexual part of the life cycle is completed within only 14 days, resulting in repeated bursts of sporulating lesions releasing urediospores that infect neighbouring plants. Typically, these clonal fungal populations experience strong between-season bottlenecks every season, and from low initial genetic diversity, new virulence mutations arise during seasonal epidemics. In Europe, resistance breakdown usually takes only 3–4 years . Even if treated the yield loss can reach 80% . To date, a complete phylogeny of this species is still lacking, but introductions of new strains occur worldwide and can be attributed to both long distance wind dispersal and accidental human contamination.
We used 16 isolates collected as uredospores from infected fields in the North of France, between 1989 and 1997 (Table 1), and stored in liquid nitrogen. Virulence gene profiles were characterised on European and World differential cultivars, using Johnson et al.'s method . We used 39 AFLP primer combinations to characterise phylogenetic relationships among the isolates [see Additional file 1]. Thus, competing pairs of virulent and avirulent isolates of the vir9 and vir6 pathotypes represented indistinguishable AFLP genotypes; for the vir4 pathotype, competing isolates differed by four AFLP bands and may therefore carry other mutations in addition to the virulence for Yr4.
We tested 8 virulent isolates, four carrying the vir9 virulence gene and two with the vir4 and vir6 virulence genes, respectively. Each virulent isolate was paired with an avirulent isolate as a competitor (Pairs A-J, Table 1). Most pairs were competed on two host cultivars and in two growing seasons (2005, 2006) under field conditions. Pairs A and B were also tested under climate chamber conditions. We established two independent replicates per pair, year and host cultivar.
Preparation of inocula
To produce fresh inocula for the experiments, uredospores were taken out of the liquid nitrogen, heat shocked (40°C, 15 min) and used to inoculate 7-day-old seedlings of the susceptible cultivar Victo. Inoculated plants were incubated in a dew chamber at 8°C for 16 h in the dark to facilitate infection ( and then transferred to the greenhouse (day: 16 h, 350 μE·m-2·s-1, 17°C; night: 8 h, 14°C). Eighteen days after inoculation, spores were collected with a vacuum collector, dried in a desiccator for 3 days at 4°C and stored in microtubes at -80°C prior to the experiments.
Climate chamber experiment (Pairs A and B, vir9virulence gene)
For each replicate, a 50:50 mixture of 20 mg uredospores of the virulent and avirulent isolate was inoculated on approx. 400 7-day-old seedlings of a given host cultivar. We used two susceptible wheat varieties, Thésée (carrying the Yr2 resistance gene) and Récital (Yr6) . We chose these cultivars because of their high susceptibility at the time of the appearance of the vir9 virulence in 1989. After incubation in a dew chamber at 8°C for 16 h, plants were placed in a climate chamber (day: 16 h, 350 μE·m-2·s-1, 17°C; night: 8 h, 14°C). Twenty days after inoculation, spores were collected and used to start a new infection cycle on the same host cultivar, as described above. We ran five cycles of competition and preserved a small sample of spores at each cycle to estimate the relative frequencies of the competing isolates.
Field experiments were conducted during two wheat seasons in 2005 and 2006, at the Grignon Institute in Northern France (48°50'N 1°55'E). A replicate consisted of a 10 × 1.5 m plot, (250 plants/m2) of a given host cultivar. Experiments were started in late March, at the end of tillering. In the center of the plot, we planted two sporulating Victo seedlings that had been inoculated with a 50:50 mix of the two competing isolates, as described above. Preliminary tests showed that sporulation on the Victo seedlings did not significantly change the 50:50 ratio (data not shown). At the end of the epidemic (early June), uredospores were harvested and stored at -80°C until further processing. The absence of infection in surrounding plots indicated that natural or cross-contamination did not occur.
Frequency assessments of the competing isolates followed the protocol by Lannou et al. (2005). For a given sample, we used an oil solution of 0.1 mg of the collected uredospores to inoculate five pots, each with 15 seedlings of a discriminating host cultivar. The cultivars Sleipner (Yr9 resistance gene), Heines Kolben (Yr2, Yr6) and Hybrid 46 (Yr4) were used for experiments with vir9, vir6 and vir4 virulence genes, respectively. On these discriminant cultivars, the virulent isolate develops sporulating lesions, whereas the avirulent isolate produces non-sporulating chloroses, indicating the failure of infection. Thus, the total number of chloroses was counted 7 days and sporulating lesions 14 days after inoculation. The frequency of the virulent isolate in the sample was taken as the ratio of sporulating chloroses/total chloroses. Each frequency was estimated on 400 chloroses on average. The goodness of the frequency assessment was previously validated for Heines Kolben and Hybrid 46 . For Sleipner, we controlled the reliability of frequency estimates by the inoculation of different ratios of Avirulent/virulent isolates [100/0; 75/25; 50/50; 25/75 and 0/100, see Additional file 2].
Estimation of the cost of virulence
We calculated the selective value (s) of the avirulent isolate from a model by Leonard , with Ln (qn/(1-qn)) = Ln (q0/(1-q0)) – n Ln (1-s); q0 is the initial frequency of the virulent isolate in the mix and qn its final frequency after n generations and (1-s) is the fitness difference between the virulent and the avirulent isolate. Following McGregor and Manners , the number of fungal generations n in the field experiments was estimated by fitting the duration of latent period (p) on the mean yearly temperature (T) at the Grignon site as: p = 28,24exp(-0,06T). From this, we obtained an estimate of five fungal generations in both years.
Analysis of the collection of vir9isolates
Of the 33 vir9 isolates analysed here, 11 were collected early after the first appearance of this pathotype in France (1989–1991). In 1992, this first epidemic was ended by a severe drought, and the remaining isolates were collected during the second epidemic period (1992–1997). The isolates all have the same virulence gene profile, as confirmed by previous analysis using the World and European differential cultivars as well as by our own tests using supplementary cultivars [Federationx4Kavkaz (Yr9), Sleipner (Yr9+), Austerlitz (Yr6+), Early Premium, Anza]. Isolates had been stored at -80°C and fresh uredospores were prepared as described above.
We used AFLP markers to investigate the neutral genetic diversity among the isolates. Ten combinations of PstI and MseI primers with two selective nucleotides were used. A subset of eight isolates was screened with 24 additional primer combinations with two selective nucleotides. The four isolates used in the competition experiments were tested with all 39 AFLP combinations. Genomic DNA extraction, DNA quantification on agarose gel and AFLP genotyping are described in detail by Enjalbert et al. [34, 64].
Variation in aggressiveness was measured as follows. Seedlings of the Clement cultivar were grown in groups of five plants in 1 dm3 pots in the greenhouse (14°C-8 h dark period and 17°C-16 h light period). When primary leaves were fully expanded, pots were exposed to a 16 h light regime and two pots per isolate were inoculated with 0.2 mg of uredospores, suspended in 300 μl of Soltrol [60, 65]. After incubation in a dark dew chamber for 24 h at 8°C, seedlings were placed back in the greenhouse. Fifteen days after inoculation, the primary leaf of each seedling was examined visually for the infection type according to a scale from 0 (no symptoms) to 9 (high sporulation) .
To calibrate the infection type index, we measured the sporulation rate of 11 isolates, including those from the competition experiment (i5, i6, i7, i8). Groups of 10 Clement seedlings were grown in 5 cm2 pots, as described above. At the 2-leaf stage (8 days), seedlings were thinned to 6 individuals per pot and exposed to a 16 h light regime. The second leaf from each seedling was removed and the first leaf attached horizontally, adaxial side up, on a Plexiglas sheet with plasticine (Ulmann, Paris, France) . Seedlings from 10 pots were inoculated together in a settling tower , with 5 mg spores of a given isolate (≈ 52 spores deposited per cm2). After incubation, seedlings were kept in a climate chamber, as described above. Eight days after their opening, we counted the number of lesions and estimated the inoculated part of the leaf surface estimated (width × length) on two leaves per pot, from which we calculated the lesion density per cm2. The pots were then placed individually under plastic jars to prevent cross-contamination. Uredospores were collected 17 and 22 days after inoculation, dried for 24 h at 5°C and then weighed. For each pot, we calculated sporulation rate as the ratio of spore production (mg) over lesion density.
Changes in (arcsine-transformed) frequency of virulent isolates in the climate chamber competition experiment were analysed by means of a repeated measure ANOVA, using the MIXED procedure of SAS statistical software . Variation in final frequencies of virulent isolates in the field competition experiments were analysed by means of Analysis of Deviance, based on a logistic regression (GENMOD procedure; SAS). Fully factorial statistical models contained the identity of competing pairs (Pair A, B, etc.), host cultivar and year. In all analyses, frequencies for a given replicate represented combined values over all pots and plants of the discriminating cultivar. We further used t-tests to test whether the final frequency of virulent isolates was significantly different from 0.5 across all replicates and pairs. Frequencies in the 1:1 mixtures at the beginning of the experiments were not significantly different from 0.5 (not shown). One-way ANOVAs were employed to compare differences in mean and variance of infection type among isolates from the two epidemic periods.
We thank Cécile Hamès, Nathalie Galet and Laurent Gerard for their help during the experimentations, as well as Aurélien Tellier and two anonymous reviewers for their comments on the manuscript. This work was supported by the European Integrated Project Bioexploit, FOOD-CT-2005-513959. The first author was supported by a grant from the "Institut Français de Coopération" in Tunisia.
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