Aphanomyces astaci, the crayfish plague pathogen, first appeared in Europe in the mid-19th century and is still responsible for mass mortalities of native European crayfish. The spread of this parasite across the continent is especially facilitated by invasive North American crayfish species that serve as its reservoir. In France, multiple cases of native crayfish mortalities have been suggested to be connected with the presence of the signal crayfish Pacifastacus leniusculus, which is highly abundant in the country. It shares similar habitats as the native white-clawed crayfish Austropotamobius pallipes and, when infected, the signal crayfish might therefore easily transmit the pathogen to the native species. We investigated the prevalence of A. astaci in French signal crayfish populations to evaluate the danger they represent to local populations of native crayfish. Over 500 individuals of Pacifastacus leniusculus from 45 French populations were analysed, plus several additional individuals of other non-indigenous crayfish species Orconectes limosus, O. immunis and Procambarus clarkii. Altogether, 20% of analysed signal crayfish tested positive for Aphanomyces astaci, and the pathogen was detected in more than half of the studied populations. Local prevalence varied significantly, ranging from 0% up to 80%, but wide confidence intervals suggest that the number of populations infected by A. astaci may be even higher than our results show. Analysis of several individuals of other introduced species revealed infections among two of these, O. immunis and P. clarkii. Our results confirm that the widespread signal crayfish serves as a key reservoir of Aphanomyces astaci in France and therefore represents a serious danger to native crayfish species, especially the white-clawed crayfish. The prevalence in other non-indigenous crayfish should also be investigated as they likely contribute to pathogen transmission in the country.
Citation: Filipová L, Petrusek A, Matasová K, Delaunay C, Grandjean F (2013) Prevalence of the Crayfish Plague Pathogen Aphanomyces astaci in Populations of the Signal Crayfish Pacifastacus leniusculus in France: Evaluating the Threat to Native Crayfish. PLoS ONE8(7): e70157. https://doi.org/10.1371/journal.pone.0070157
Editor: Martin Krkosek, University of Toronto, Canada
Received: September 6, 2012; Accepted: June 20, 2013; Published: July 23, 2013
Copyright: © 2013 Filipová et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This project has been funded by the French National Agency for Water and Aquatic Environments (ONEMA) and the Charles University in Prague (SVV 265 207). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
For more than 150 years, native crayfish in Europe have been decimated by the crayfish plague, a disease caused by the oomycete Aphanomyces astaci. The first presumed European outbreak of crayfish plague was recorded in 1859 in northern Italy, and another focus of the disease appeared in France in 1874 at Plateau des Langres , . In the following decades, the pathogen continued to spread to other European countries , , , . At present, the known carriers of the pathogen in Europe are three North American crayfish species that were introduced to the continent before 1975, the so-called “old” non-indigenous crayfish species: the spiny-cheek crayfish Orconectes limosus, the signal crayfish Pacifastacus leniusculus, and the red swamp crayfish Procambarus clarkii . Their presence in European waters facilitates the persistence and spread of the parasite, and further contributes to mortalities of native crayfish , , , , .
The largest mass mortalities of native crayfish in France took place between the 1870s and 1912 , , but after a relatively calm period up until the 1980s, new outbreaks of crayfish plague have again been reported , , . Some of these mortalities of native species were suspected to be connected with the presence of the invasive signal crayfish Pacifastacus leniusculus , , , , . The link between the presence of this species and crayfish plague spread is also apparent in other European countries , , .
The signal crayfish was introduced to France in 1972 from Sweden, and in 1974 more individuals were brought directly from North America (Lake Tahoe and Lake Donner in California); this was followed by numerous secondary introductions , . The species is now widely distributed in France , , , , , . In 2006, it was estimated to be present at about 1000 sites in 73 out of 96 French departments  representing all 22 administrative regions of continental France. Although several other non-indigenous crayfish species are found in France, Pacifastacus leniusculus represents the largest threat to native species, particularly to the white-clawed crayfish Austropotamobius pallipes . Signal crayfish may colonise similar habitats in the headwaters of rivers and therefore easily come into contact with A. pallipes populations . This facilitates the transmission of the pathogen to the native species if the invasive one is infected.
The white-clawed crayfish Austropotamobius pallipes is the most abundant indigenous European crayfish in France. In 2006, it was still found at over 2200 sites in 76 out of 96 departments, i.e., in all but one administrative region of continental France (Fig. 1; ). However, the number of its populations has significantly decreased recently and is substantially lower than that of alien crayfish . The crayfish plague is one of the major factors that contribute to the decline of A. pallipes in France ; eighty-nine per cent of crayfish mass mortalities recorded in France between the years 2001 and 2006 affected Austropotamobius pallipes, while only the remaining 11% of mortalities concerned other species .
Distribution of A. pallipes is based on a 2006 survey  (white: no known population in a department, pale green: 1–5, medium: 6–25, dark: 25–150 populations). Red crosses with years indicate mass mortalities most likely caused by crayfish plague reported since the 1990s (, , , , , , ; T. Duperray and T. Pantarotto, pers. comm.); additional mortalities ascribed to crayfish plague were reported between 2001 and 2005 from departments marked by black dots (according to ). Bold crosses mark outbreaks in which A. astaci has been confirmed by molecular detection and genotyped (see Discussion). The prevalence of Aphanomyces astaci in sampled signal crayfish populations is expressed by colour: no reliable detection of the pathogen (white triangles), low prevalence (1–30%, yellow), medium prevalence (31–60%, orange) and high prevalence (61–100%, red triangles); the number of analysed individuals in the respective population is indicated by symbol size (small triangle: <10 individuals, large triangle: 10+ individuals). Regions discussed in the text are abbreviated: Al – Alsace, Au – Auvergne, Ba-No – Basse-Normandie, Ce – Centre, Ch-Ar – Champagne-Ardenne, La-Ro – Languedoc-Rousillon, Li – Limousin, Lo – Lorraine, Po-Ch – Poitou-Charentes, Rh-Al – Rhône-Alpes; Lake Geneva (Lac Léman) is marked by L within the triangle. The distance scale depends on latitude (top: 51.5°N, bottom: 41°N) and reflects the map projection.
Despite the substantial impact the crayfish plague has on native crayfish species, reliable information on the distribution of its pathogen A. astaci in European waters is rather scattered. For many years, mortalities of native crayfish, if noticed, suggested the presence of the disease. However, the identity of the pathogen was often assumed rather than confirmed, due to difficulties with its cultivation and ambiguous morphological characteristics , . Recently, several molecular methods for the detection of Aphanomyces astaci have been developed that do not require cultivation , , , , . Very low quantities of the pathogen DNA in the sample are detectable by some of these methods, enabling large-scale screening of populations of invasive crayfish from different European countries.
Interestingly, recent molecular studies have suggested that some populations of invasive crayfish in Europe might not be infected by A. astaci or its prevalence is very low, and in those confirmed to host the pathogen the prevalence and load may vary substantially , . So far, the largest datasets have been obtained by Kozubíková et al. , , who studied crayfish plague prevalence in more than 300 individuals of Orconectes limosus and more than 100 individuals of Pacifastacus leniusculus, representing 29 Central European populations. In other studies focusing on the presence of this pathogen in invasive crayfish in Europe, only one or a few populations were analysed (e.g., , , , ).
No data on the prevalence of the crayfish plague pathogen in non-indigenous crayfish populations in France have been available so far. Therefore, we tested in the present study numerous French populations of Pacifastacus leniusculus as well as a few individuals of other non-indigenous crayfish species for the presence of Aphanomyces astaci. A quantitative TaqMan minor groove binder (MGB) real-time polymerase chain reaction (PCR) designed by Vrålstad et al.  was chosen for our analyses, as it has been shown to be the most sensitive of the available detection methods, and highly specific to this pathogen species , .
Our aim was to evaluate the threat that signal crayfish populations in different regions of France represent to native crayfish species. We specifically focused on this invasive crayfish species because its distribution and habitat preferences most overlap with native crayfish in France . Data on the prevalence of A. astaci and infection intensities expressed as pathogen levels in the hosts’ tissues may then allow targeting the most infected invasive crayfish populations for potential future eradication trials, and pinpointing native crayfish populations that are at highest risk and could be translocated to safer areas, i.e., “ark sites” . Thus, data on the distribution and prevalence of the crayfish plague pathogen in the country may contribute to improving the efficiency of conservation management of indigenous crayfish species, in particular Austropotamobius pallipes.
All experimental procedures and animal manipulations, as well as field sampling, conformed to French law. The analysed material was provided by the French National Agency for Water and Aquatic Environments (ONEMA), which is entitled to collect samples in French watercourses, including those located on privately owned land. No additional permits were required for the described field studies. The project did not involve work with endangered or protected species, apart from samples of dead individuals collected from mass mortalities of the native crayfish species Austropotamobius pallipes.
Sampling, DNA Isolation and Real-time PCR
In total, 513 signal crayfish Pacifastacus leniusculus individuals were sampled from 45 localities in France (Table 1, Fig. 1) by hand or by electrofishing. Although these sites represent only a small fraction of invaded sites in the country (see ), they cover a substantial part of most invaded regions. Most individuals came from running waters, especially brooks and several rivers. In addition, several individuals of other non-indigenous species were also analysed. These were 19 individuals of Orconectes limosus from two populations, seven individuals of O. immunis from one population, and two individuals of Procambarus clarkii from one population (Table 1). The sampled populations, their characteristics, and the numbers of analysed individuals are summarised in Table 1.
Captured crayfish were stored in 96% ethanol. Tissue from one half of the soft abdominal cuticle and one uropod (body parts most suitable for the detection of A. astaci, ) was dissected from each crayfish using sterile tools. While processing each individual, we noted the presence of black melanised spots, as possible visual symptoms of immune reaction to pathogens  and a characteristic used in the past to assess the infection status in signal crayfish (e.g., , ). Dissected tissues from each individual were collected in a single 1.5 ml tube, dried and stored in a deep freezer at −80°C. Before further processing, 360 µl of Buffer ATL from the DNeasy tissue kit (Qiagen) was added to the thawed dissected material. The mixture was then crushed by one scoop (ca 50 µl) of stainless steel beads (1.6 mm diameter) using a BBX24B Bullet Blender (Next Advance) for 10 min at maximum speed. DNA extractions from the crushed cuticle then followed the rest of the spin-column protocol of the DNeasy tissue kit, in double volume (i.e., with 40 µl of the proteinase K solution and 400 µl of Buffer AL).
The isolated material was then tested for the presence of Aphanomyces astaci by the quantitative TaqMan MGB real-time PCR , using a LightCycler® 480 Instrument (Roche). A 59 bp fragment of the internal transcribed spacer (ITS) region of A. astaci nuclear rDNA was amplified using the primers AphAstITS-39F (5′-AAG GCT TGT GCT GGG ATG TT-3′) and AphAstITS-97R (5′-CTT CTT GCG AAA CCT TCT GCT A-3′), and quantified with the pathogen-specific TaqMan® minor groove binder (MGB) probe AphAstITS-60P (5′-6-FAM-TTC GGG ACG ACC C-MGBNFQ-3′). The 25 µl reaction volume consisted of a 2x Universal PCR Master Mix (Applied Biosystems), both primers (500 nM each), TaqMan MGB-Probe (200 nM), nuclease free water, and template DNA (around 20 ng/µl). The PCR program consisted of one cycle of 10 min at 95°C, 50 cycles of 15 sec at 95°C and 60 sec at 58°C, and one final cycle of 60 sec at 40°C. In each run, two replicates of four different standards were included that served as positive controls and ensured the comparability of different runs. The quantity of the pathogen DNA in these standards, expressed in PCR forming units (PFU), were 3×410, 3×48, 3×44 and 3×42, respectively . Two negative controls (which remained negative in all runs) were included in each run to detect possible contamination. For each isolate, undiluted and a 10-fold diluted replicate were analysed to test for the impact of inhibition that might influence the efficiency of detection , . When some effects of inhibition were occasionally detected (mostly in samples with low agent level), the PFU values were estimated as described in .
Based on their PFU values, samples were classified into semi-quantitative categories of pathogen load, ranging from A0 (no traces of A. astaci DNA) to A7 (extremely high amounts of A. astaci DNA in the sample), as proposed by Vrålstad et al. . Only individuals with agent level A2 and higher were considered infected. Agent level A1 falls below the limit of detection of the method (corresponding to 5 PFU) and may not only indicate trace amounts of pathogen DNA, but also false positives or minor contamination during analyses. Therefore, agent level A1 should not be considered a confirmation of the presence of A. astaci in the sample , .
We estimated the prevalence of A. astaci in studied populations and its 95% confidence interval, using the function “epi.conf” included in the library epiR  for the statistical package R v. 3.0 . Furthermore, we evaluated the relationship between the prevalence of A. astaci in tested populations and the pathogen load in infected individuals (with agent level A2 or higher, log-transferred) from each population by calculating the logistic regression with quasibinomial distribution of errors (due to overdispersion) by generalised linear model (GLM) in R. Potential outliers were identified using Cook’s distance and leverage of residuals, and the analysis was also repeated with the dataset excluding such populations.
We detected the presence of the crayfish plague pathogen in more than half of the studied signal crayfish populations across the whole country (Fig. 1). The number of Aphanomyces astaci-positive individuals in sampled populations, agent levels detected in infected specimens and the crayfish plague prevalence for each population are summarised in Table 1.
In total, 103 signal crayfish (20% of analysed individuals) from 24 populations (i.e., 53% out of 45 tested) were found to be infected (with agent level A2 or higher) (Table 1). The pathogen prevalence in samples from the studied populations was highly variable, ranging from 0% to 80%; however, due to often low number of individuals analysed per populations, the confidence intervals for the prevalence estimates remain wide (Table 1). Thus, lack of unambiguous detection of the pathogen at a particular site cannot be considered as an evidence for its absence from the population; substantially higher sample sizes are needed to test for such scenario .
In 322 signal crayfish, no traces of Aphanomyces astaci DNA were found (agent level A0), and 88 individuals were assigned to agent level A1 (i.e., a very weak signal not considered as positive pathogen detection). Most samples (73 individuals) that tested positive contained a low amount of pathogen DNA (agent level A2), while agent level A3 was found in 28 individuals and A4 in two individuals (Table 1). Black melanised spots were observed on the cuticle of 17 signal crayfish individuals from nine localities; however, A. astaci DNA was detected in only three of such crayfish from different localities: Sarthon, Lake Geneva (Lac Léman), and Charpasonne.
The distribution of P. leniusculus populations with the highest crayfish plague prevalence (over 50%) was rather scattered, as these were located in Limousin (central France; Li in Fig. 1), Rhône-Alpes (eastern France; Rh-Al), Basse-Normandie (northwestern France; Ba-No) and the Lorraine region (northeastern France; Lo) (Table 1, Fig. 1). In some regions, A. astaci-positive individuals were found in the majority of local populations, such as in Limousin (6 infected out of 7 analysed populations), Rhône-Alpes (4/6), and Basse-Normandie (4/5). On the other hand, relatively low numbers of infected individuals were found in most populations from the Lorraine region, where only 17 individuals from 141 analysed signal crayfish tested positive for A. astaci (in 5 out of 13 analysed populations), or in populations from Champagne-Ardenne (Ch-Ar) with five infected out of 68 tested individuals, coming from a single population where 6 individuals were analysed (Table 1). In Languedoc-Rousillon (La-Ro), none of the signal crayfish tested positive for the presence of A. astaci; however, only 20 individuals from two populations were analysed from this region.
We observed a relatively weak trend of increase of A. astaci prevalence in signal crayfish populations with the average pathogen load per infected individuals from respective populations (Fig. 2); this increase was nevertheless not significant (GLM; df = 1, 23; p = 0.12). Based on criteria used to define outliers, we excluded two most influential points (populations with highest average pathogen load, shown in Fig. 2); their removal neither improved the significance of the model nor its general trend.
The equation characterising the model estimated by logistic regression (dashed line) is given in the upper right corner; removal of two outlier populations with highest average pathogen load (indicated by empty circles) did not change the model substantially (dotted line, equation not shown). Note that when a quasibinomial instead of binomial distribution of errors is used (due to overdispersion in data), the increasing trend is non-significant.
The real-time PCR analyses also confirmed the presence of A. astaci in two out of three other crayfish species analysed. None of the analysed individuals of Orconectes limosus from either of the two sampled populations (Rhône-Alpes and Centre regions) showed traces of the pathogen. However, two out of seven tested individuals (29%) of Orconectes immunis from Alsace tested positive, as did one of the two analysed individuals of Procambarus clarkii from the Centre region (Table 1).
Our results provide the first insight into the prevalence of the crayfish plague pathogen in invasive crayfish in France. We confirmed that the signal crayfish Pacifastacus leniusculus serves as an important reservoir of this disease in France, which strongly supports the notion of the key role of this invasive species in mortalities of native crayfish. We also showed independently on a recent study by Schrimpf et al.  that Orconectes immunis, a crayfish invader established only in the early 1990s , can be a carrier of A. astaci. This is the first of the “new” non-indigenous crayfish species in Europe, i.e., those introduced to the continent after 1980 , tested for this pathogen presence. Its positive infection status calls for investigating of other established North American crayfish species as well.
Our study confirms that a substantial proportion of signal crayfish from France carried Aphanomyces astaci. Despite the fact that the pathogen’s DNA was unambiguously detected in no more than 20% of analysed individuals, A. astaci presence was confirmed in 24 out of 45 studied host populations, representative for a substantial part of the invaded range in France. Furthermore, it may be assumed that the proportion of infected populations is substantially higher, given the wide confidence intervals for pathogen prevalence in individual populations. In Central European populations of this species (from the Czech Republic, Slovakia, and Hungary), Kozubíková et al.  also showed that a substantial proportion of analysed individuals tested positive for A. astaci, with 32 infected out of 153 analysed individuals, coming from 8 out of 9 sampled populations. In one population from Norway analysed by Vrålstad et al. , 38 out of 44 signal crayfish (86%) were infected; such high prevalence within a population was only rarely found in France. In contrast, no traces of the pathogen DNA were detected in 44 individuals from the river Alling Å in Denmark . The number of infected individuals of another intensively studied invasive crayfish in Central Europe, Orconectes limosus, was found to be generally higher than in signal crayfish : 116 out of 307 tested individuals (38%) were infected, coming from 16 out of 20 analysed populations . Our results are also consistent with findings that crayfish infected by A. astaci may not show any macroscopic melanisation suggesting visually the presence of a pathogen , , and, on the contrary, that crayfish individuals (of various species) exhibiting strongly melanised spots may not test positive as A. astaci carriers , , .
The present results, although clearly demonstrating the widespread presence of the crayfish plague pathogen, should be interpreted carefully because the real prevalence of A. astaci is almost certainly underestimated in many cases. As only a small number of individuals could be tested from some sites, lack of detection of A. astaci cannot be interpreted as the absence of the pathogen from the population (see the 95% confidence intervals for the prevalence in Table 1). Providing conclusive evidence that some populations of potential A. astaci hosts (North American invasive crayfish) are likely to be uninfected requires much more intensive sampling effort . Temporal fluctuations of the pathogen prevalence (or detectability) could also influence our results, as was shown for a Czech Orconectes limosus population studied over several seasons . Thus, low A. astaci prevalence detected in some French signal crayfish populations does not mean that those pose a lower threat than other more infected populations of the same species.
Moreover, only certain parts of the crayfish cuticle (from the abdomen and uropod) were analysed, the isolation efficiency might have differed among samples, and just a part of DNA isolate was used in the real-time PCR. All these factors might further contribute to underestimations. However, as uropod tissue seems to be generally more infected than other parts of the crayfish body in signal crayfish , we assume that some pathogen DNA should have been present in samples from most infected crayfish individuals analysed in our study. Other characteristics and limits of this method (such as its specificity against other closely related species of Aphanomyces, or its sensitivity) are discussed in detail elsewhere , . In general, however, the real-time PCR detection of A. astaci can be considered well validated , . Thus, although our results are based on this method only, and we did not use alternative methods to confirm the pathogen (e.g., amplification and sequencing of a longer DNA fragment), we are convinced that the positive results indeed reflect the detection of A. astaci. Furthermore, we used some of the individuals from our study to test performance of newly developed microsatellite markers for this pathogen (F. Grandjean et al., in prep.), and the allele sizes obtained from infected French P. leniusculus matched perfectly those obtained from pure culture of A. astaci strain isolated from the same host species (F. Grandjean et al., unpubl. data). We consider this a convincing evidence that such crayfish individuals were infected by the same or very closely related strain of the pathogen.
One of the localities that deserves particular attention is Lake Geneva (Lac Léman) on the Swiss-French border (marked by L in Fig. 1), where the signal crayfish has been intensively harvested . In this lake, over 31% of analysed P. leniusculus individuals tested positive for A. astaci. Although French law does not permit the transport and selling of invasive species, special prefectoral regulations allow fishermen to sell crayfish from Lake Geneva anywhere in France. They may therefore be exported alive to the rest of the country under the label “crayfish from Lac Léman” , . Such commercial activities may contribute to the spread of the crayfish plague. Indeed, one French aquaculture company who offers P. leniusculus from Lake Geneva also sells A. leptodactylus that do not seem to live long after purchase (T. Duperray, pers. comm.). More measures should therefore be taken to avoid the further spread of signal crayfish from this lake to other parts of France or beyond.
However, Lake Geneva is also interesting because of the evidence for the extended coexistence between American and European crayfish species. The signal crayfish has long been established in the lake, since 1976 . However, the narrow-clawed crayfish Astacus leptodactylus (a European species not indigenous to this region) was found in the lake at least until 2001  and it seems that the native white-clawed crayfish Austropotamobius pallipes was also present there at least until 2003 (C. Bugnon, pers. comm.). Several cases of long-term coexistence between native species and P. leniusculus have also been recorded in other European countries. In England, A. pallipes coexisted with signal crayfish for more than 5 years . In Finland, Westman & Savolainen  reported a 30-year coexistence of P. leniusculus with another native species, Astacus astacus, although the latter was finally outcompeted. In these cases, it has been suggested that the invasive species was not infected by the pathogen, similarly as in some Central European sites where native crayfish coexisted with O. limosus . The present situation in Lake Geneva, where we demonstrated the presence of A. astaci in five out of 16 analysed signal crayfish, seems thus different, although we cannot rule out that the pathogen has been introduced to the local population of P. leniusculus only recently.
It is probable that the signal crayfish as well as the spiny-cheek crayfish O. limosus, also present in the lake , have contributed to the decline of the susceptible species Astacus leptodactylus and Austropotamobius pallipes at this locality. No information on mass mortalities of these species in the lake exist, so we cannot assess if this decline was caused by plague outbreaks, competition with invasive crayfish, other reasons, or a combination of multiple factors. Nevertheless, several recent studies have demonstrated that chronic A. astaci infections of generally susceptible crayfish may be possible at some localities, as was shown for A. leptodactylus in Turkey ,  and Romania , , for Astacus astacus in Finland , , and most recently for Austropotamobius torrentium in Slovenia . Kozubíková et al.  also reported from the Czech Republic that the native noble crayfish A. astacus coexisted for at least ten years with a P. leniusculus population in which a low A. astaci agent level (A2) was recently found in two out of 23 analysed individuals (although a recent confirmation of the pathogen presence does not necessarily mean the host population has been infected during the whole period of coexistence). The presence of the crayfish plague pathogen apparently does not always result in the complete disappearance of native species at a locality. Such coexistence seems facilitated both by an increased resistance of some populations or species of European crayfish to the pathogen and a reduced virulence of some A. astaci strains , , the relative contributions of these (and possibly other) factors probably differing from site to site.
In some areas in France, Austropotamobius pallipes is still relatively abundant (although the sites occupied by invasive American crayfish are already much more numerous than those with native species ). In other regions in the country, this native species is only rare or even absent (see Fig. 1 and ). The main centres of distribution are in central and south-eastern France, the former being also occupied by many signal crayfish populations . At several sites in Rhône-Alpes and Auvergne (Rh-Al and Au in Fig. 1), regions where mortalities of A. pallipes occurred in the past (T. Duperray, T. Pantarotto, pers. comm.), we found that nearby signal crayfish populations had individuals infected by A. astaci. High priority should therefore especially be given to the protection of those localities where A. pallipes is abundant but infected P. leniusculus populations are nearby.
Apart from screening for the presence of the pathogen, molecular methods may also be used to assess the pathways and likely sources of Aphanomyces astaci. We have directly demonstrated the pathogen by real-time PCR detection in samples of A. pallipes from two crayfish plague outbreaks from France (indicated by thicker red crosses in Fig. 1). The first took place in 2001 in the Saint-Christophe river, Poitou-Charentes region, Western France (Po-Ch in Fig. 1), and was described in detail in . The second outbreak took place in July 2008 in the river Le Jabron, Rhône-Alpes region (Rh-Al in Fig. 1). In both regions, all three widespread North American crayfish species (Pacifastacus leniusculus, Orconectes limosus, and Procambarus clarkii) are present , so any of them might have been the source of the pathogen causing these mass mortalities. However, as different genotypes of A. astaci have been isolated from different host species , , genotyping of the pathogen might indicate its source. We characterised A. astaci from both French outbreaks using several variable microsatellite markers that are being developed for this species (F. Grandjean et al., unpublished), and confirmed that the first mortality was caused by the genotype group B, which is associated with P. leniusculus , and the other one by the genotype group E, originally isolated from O. limosus . Although the reliability of the pathogen genotyping approach needs thorough evaluation, these results indeed suggest that signal crayfish has been the original source of A. astaci in at least some mass mortalities recently recorded in France.
The trend of increase in crayfish plague prevalence and the pathogen load of local infected individuals in French P. leniusculus populations corresponds to findings of Kozubíková et al. , who observed similar but much more pronounced patterns in Central European O. limosus and P. leniusculus populations. This relationship might be due to increased concentrations of A. astaci zoospores in the environment released from infected individuals, increasing the likelihood of pathogen spread. However, the pattern observed in French signal crayfish populations studied by us was not significant, unlike those reported in .
Eradication of P. leniusculus from large areas is not yet possible . However, our results can contribute to the development of more efficient conservation management strategies for native crayfish in France. More attention should be paid to areas where high prevalences of the crayfish plague in tested P. leniusculus populations have been found, as these represent a greater danger to native species. The fact that we found infected individuals in more than half of the studied populations confirms that the signal crayfish plays an important role in the transmission of the crayfish plague pathogen in France, and that it represents a serious threat to native crayfish, especially to the endangered Austropotamobius pallipes. Our analysis also confirms that other non-indigenous crayfish species, including the recently established invader Orconectes immunis, likely serve as sources of the disease in France. Further studies of the prevalence of the crayfish plague in other non-indigenous host species would therefore also be important for evaluating the risk they represent for native crayfish.
We thank the French National Agency for Water and Aquatic Environments (ONEMA, Office National de l’Eau et des Milieux Aquatiques), N. Poulet, C. Souty-Grosset and M. Collas for providing samples, T. Vrålstad and E. Kozubíková for their valuable advices on the methodology, E. Gaba for providing the source map used to create Fig. 1 at Wikimedia Commons, D. Hardekopf for language revisions, and anonymous reviewers for comments on previous versions of the manuscript. F. Pozer from Laboratoire Départemental d’Analyses du Jura (LDA39), Poligny, provided the samples from crayfish plague outbreaks.
Conceived and designed the experiments: FG AP LF. Performed the experiments: LF KM CD. Analyzed the data: LF FG AP. Wrote the paper: LF AP FG.
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