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Parasitology Research

, Volume 117, Issue 12, pp 3695–3704 | Cite as

Agents of swimmer’s itch—dangerous minority in the Digenea invasion of Lymnaeidae in water bodies and the first report of Trichobilharzia regenti in Poland

  • Anna Marszewska
  • Tomasz Strzała
  • Anna Cichy
  • Grażyna B. Dąbrowska
  • Elżbieta Żbikowska
Open Access
Original Paper

Abstract

Trichobilharzia spp. have been identified as a causative agent of swimmers’ itch, a skin disease provoked by contact with these digenean trematodes in water. These parasites have developed a number of strategies to invade vertebrates. Since we have little understanding of the behavior of these parasites inside the human body, the monitoring of their invasion in snail host populations is highly recommended. In our research, lymnaeid snails were collected from several Polish lakes for two vegetation seasons. The prevalence of bird schistosomes in snail host populations was significantly lower than that of other digenean species. We were the first to detect the presence of the snails emitted Trichobilharzia regenti (potentially the most dangerous nasal schistosome) in Poland. In addition, by sequencing partial rDNA genes, we confirmed the presence of the snails positive with Trichobilharzia szidati in Polish water bodies, showing that swimmer’s itch is more frequent during summer months and that large snails are more often infected with bird schistosomes than small ones.

Keywords

Trichobilharzia Lymnaeidae Molecular identification Prevalence Seasonality Shell size 

Introduction

Digenea include parasites with a complex life cycle. Generally, they use snails as their first intermediate hosts, and vertebrates, as final (Cheng 1986; Cichy et al. 2011). Many digenetic trematodes pose threat to animal and human health (Cheng 1986). These parasites include bird schistosomes, whose invasion on humans has been recently reported in many countries (Rao et al. 2007; Valdovinos and Balboa 2008; Gohardehi et al. 2013; Marie et al. 2015; Marszewska et al. 2016; Caron et al. 2017). The disease caused by cercariae of these trematodes occurs globally and is considered to be re-emerging (Kolářová et al. 2010).

The first intermediate hosts of widely spread Trichobilharzia spp. include freshwater snail species of the family Lymnaeidae (Horák et al. 2002). Their final hosts include waterfowl of the families Ardeidae, Podicipedidae, Ciconiidae, and Anatidae (Sulgostowska and Czaplińska 1987; Rudolfová et al. 2007; Jouet et al. 2009). The specificity of bird schistosomes is much lower in relation to the final than to the intermediate host. According to Horák et al. (2002), the same species can develop and sexually reproduce in representatives of different bird families. Cercariae of the parasites are released from snails and seek their final vertebrate hosts using chemoreceptors. They respond to external stimuli (e.g., shadow) and signals from a potential host (e.g., fatty acids) (Horák et al. 2008). When the search is complete, larvae penetrate the host through the skin. In this process, the products of parasite’s penetration glands are activated (Horák et al. 1997; Mikeš et al. 2005). The similarity between some lipid components in the integument of humans and birds makes the parasites attack people wading, swimming, or working in water (Haas and van de Roemer 1998). The consequence of such invasions is a skin disease known as swimmers’ itch (Kolářová et al. 2010), whose first symptoms appear within 2 h after the exposure to cercariae. Within the next 2 days, the symptoms worsen. The rash, which initially causes only redness and itching, develops into small, red bumps (Żbikowska et al. 2002). The severity of symptoms may vary, depending on the number of parasites attacking the skin (Żbikowska 2003). The affected area is warm, swollen, and painful. A pricking, tingling, and sometimes burning sensation leads to discomfort and even insomnia (Żbikowska et al. 2002). The condition may be accompanied by other symptoms including swollen lymph nodes, diarrhea, nausea, or fever (Horák et al. 2002; Żbikowska et al. 2002). Occasionally, anaphylactic shocks or respiratory system disorders may also be observed (Bayssade–Dufour et al. 2001). The disease intensity depends on the individual susceptibility of the host (Kolářová et al. 2013a).

The swimmer’s itch is a recurrent disease listed also in Poland. Therefore, there are several reasons for monitoring the prevalence of these parasites Trichobilharzia spp. in snail populations: (i) the abundance of snails releasing cercariae of Trichobilharzia spp., (ii) the abundance of water birds, (iii) frequent cases of itchy rashes (with a range of symptoms), especially in children, (iv) the lack of data on the behavior of cercariae invading humans through the skin. It is recommended that monitoring should be conducted in two ways: (i) using molecular method to identify particularly dangerous nasal schistosomes and (ii) conducting environmental inspection of recreational water bodies. The present study was aimed at investigating the diversity of Trichobilharzia species in Poland and highlighting the risk of swimmer’s itch based on the spread of bird schistosomes in intermediate snail host populations (prevalence and seasonal fluctuations of parasite invasion, shell size of snail hosts) and in comparison with overall risk of Digenea invasion.

Material and methods

Field sampling

Lymnaeid snails (intermediate hosts of Tricholilharzia spp.), namely Lymnaea stagnalis, Radix spp., and Stagnicola palustris were collected monthly from May to September in 2016 and 2017. In 2016, they were collected from seven lakes of central and northern Poland: Głuszyńskie (52° 29′ 8″ N, 18° 38′ 13″ E), Ostrowąskie (52° 49′ 46″ N, 18° 42′ 3″ E), Służewskie (52° 51′ 14″ N, 18° 38′ 38″ E), Skulskie (52° 28′ 0″ N, 18° 19′ 18″ E) (Kuyavian-Pomeranian Voivodeship), Skulska Wieś (52° 28′ 58″ N, 18° 19′ 34″ E) (Greater Poland Voivodeship), Szymbarskie (53° 36′ 52″ N, 19° 30′ 39″ E) (Warmian-MasurianVoivodeship), and Wodna Dolina (Water Valley) (54° 10′ 45″ N, 16° 11′ 15″ E) (West Pomeranian Voivodeship), while in 2017, from three lakes: Głuszyńskie, Skulskie, and Skulska Wieś. Research sites were selected based on a combination of factors such as preliminary parasitological tests of snails in 2015, the presence of waterfowl, and previous reports of swimmer’s itch episodes.

The snails, collected from the littoral zone (depth of ca. 0.5–1.5 m) of each lake by two researchers within the span of 1 h and under stable weather conditions, were transported to the laboratory in containers with lake water and examined for Digenea invasion.

Snail/cercaria examination

Piechocki’s and Wawrzyniak-Wydrowska’s (2016) and Jackiewicz’s (2000) keys were used for morphological and anatomical identification of snails. Shell sizes (shell lengths) were measured using an electronic caliper (accuracy of 0.1 mm). Snails were placed individually in beakers with a small amount of conditioned tap water and exposed to artificial light for 3 h to stimulate the release of cercariae. Larval species were preliminarily determined using a light microscope (Primostar Carl Zeiss) and available keys, descriptions, and pictures from numerous publications on these parasites (Combes 1980; Našincová 1992; Faltýnková et al. 2007, 2008; Cichy and Żbikowska 2016). When no cercariae were released into water, an autopsy of snail hepatopancreas and gonads was carried out. The digenetic species were identified from fully developed cercariae. Morphologically classified larvae of bird schistosomes were subjected to molecular identification.

DNA extraction, PCR amplification, sequencing, and phylogenetic analyses

The suspension of bird schistosome cercariae was centrifuged. The isolated larvae were preserved in ethanol (96%) and frozen (at − 20 °C) for subsequent molecular identification (Jouet et al. 2008). Several dozens of cercariae were used for DNA extraction. Prior to DNA extraction, cercariae were centrifuged at 5000g for 5 min and washed three times in PBS buffer (pH 7.4). Total genomic DNA was isolated with Sherlock AX (A&A Biotechnology, Gdynia, Poland), according to the manufacturer’s instruction. The quality and quantity of the isolated DNA was assessed in gel electrophoresis (1% agarose gel). The partial nuclear ribosomal 28S rDNA (D1–D3) gene (28SrDNA) of cercariae released from Radix spp. was amplified using the forward primer DLS1 (5′-ACCCGCTGAACTTAAGCATATCACTAAGC-3′) (Laskowski and Rocka 2014) and the reverse primer 1500R (5′-GCTATCCTGAGGGAAACTTCG-3′) (Tkach et al. 2003). A fragment of the ribosomal DNA of bird schistosomes invading L. stagnalis, spanning the sequences of internal transcribed spacers 1, 2, and 5.8S (ITS), was amplified using the forward primer its5Trem (5′-GGAAGTAAAAGTCGTAACAAGG-3′) and the reverse primer its4Trem (5′-TCCTCCGCTTATTGATATGC-3′) (Dvorák et al. 2002) according to PCR conditions described by Dvorák et al. (2002).The amplified products were purified with Clean-Up (A&A Biotechnology, Gdynia, Poland) according to the producer’s manual. DNA product sequencing in both directions was carried out by Genomed S. A., Warsaw. From the obtained genetic material, one sample from each research site for each snail species was used for sequencing. Furthermore, species membership of the analyzed individuals was identified with phylogenetic approach within two datasets (28rDNA and ITS). Newly sequenced haplotypes, along with homological DNA sequences from GenBank (Supplementary Material 1, 2), were first aligned using Muscle algorithm (Edgar 2004) implemented in Seaview software (Gouy et al. 2010). After the alignment, the sequences were cut to obtain a uniform block of sequences and a model of nucleotide substitution was chosen for each dataset using jModelTest 2.1.10 (Darriba et al. 2012). Next, both datasets were analyzed with MrBayes 3.2.6 (Ronquist et al. 2012) using GTR +G as the best-fit model. Two independent runs of four chains starting from different random trees were used. The trees were sampled every 100th generation for 25,000,000 generations of Markov chain steps and all trees making up the final tree were probed when the average standard deviation between the runs was much lower than 0.01.

Statistical analysis

Seasonal infection fluctuations were calculated and the results were analyzed using Friedman rank test followed by post-hoc Wilcoxon signed-rank test. A chi-square test of contingency table was used to determine statistical differences in the number of snails infected with bird schistosomes and uninfected ones between four shell size classes. The same analysis was used to compare the numbers of snails infected and uninfected with Digenea. Next, post hoc test based on standardized residuals was used. Standardized residuals presented the degree to which an observed value deviates from the expected value in terms of a z score (Sidanius et al. 2008). A standardized residual (SR) of plus or minus 1.96 presented a significant deviation from 0 at the p = 0.05 level (Sidanius et al. 2008). Statistical analysis was prepared based only on data on bird schistosomes from L. stagnalis. The term prevalence was used for the description of one snail species invaded by one parasite species.

Results

Larval trematode infection in Lymnaeidae

We collected a total of 3456 snails (2484 in the first and 972 in the second year of study): 2325 individuals of L. stagnalis, 890 Radix spp., and 240 S. palustris. Over 30% of the collected Lymneaidae were infected with Digenea. The infection was most frequent among L. stagnalis (36.34%) (Table S1), followed by S. palustris (21.25%) (Table S2), and Radix spp. (18.08%) (Table S3). The following species were most frequent in L. stagnalis: Diplostomum pseudospathaceum Niewiadomska, 1984 (in 27.3% of infected snails), Opisthioglyphe ranae (Frolich, 1791) (20%), Plagiorchis elegans (Rudolphi, 1802) (12.5%), and Echinoparyphium aconiatum (Dietz, 1909) (11.5%). Radix spp. were most frequently invaded by O. ranae (19.9%), Cotylurus sp. (13.7%), Echinoparyphium recurvatum (Linstow, 1873) (12.4%), and P. elegans (8.1%), while S. palustris, by D. pseudospathaceum (27.5%), E. aconiatum (9.8%), Hypoderaeum conoideum (Bloch, 1782) (9.8%), Molinella anceps (Molin, 1859) (9.8%), and O. ranae (9.8%). Bird schistosomes were recorded in 1.24% of all examined snails. L. stagnalis were the most common host of bird schistosomes (1.68%), followed by Radix spp. (0.44%). S. palustris were not infected with these parasites (Fig. 1). L. stagnalis were found in all seven studied lakes, while Radix spp., only in two (Fig. 1).
Fig. 1

The number of Lymnaeidae infected with bird schistosomes at all research sites

Molecular analyses of cercariae of bird schistosomes

As a result of sequencing, we revealed four haplotypes for the ITS and one haplotype for the 28SrDNA (GenBank accession numbers: MH190224, MH190225, MH190226, MH190227, MH190228). Phylogenetic tree created with 28S rDNA (Fig. 2) (Table S4) showed that the one haplotype presented in this study belonged to Trichobiharzia regenti. Haplotype from our study, along with sequence of T. regenti possessed from GenBank NCBI, created one clade with the highest possible probability (100%) of the common node. Similarly, phylogenetic tree created for ITS (Fig. 3) (Table S5) allowed to determine species belonging of four revealed in this study haplotypes as Trichobiharzia szidati. All four haplotypes from this study connected with five sequences of T. szidati from GenBank and formed very well-supported (100% posterior probability) and distinct genetic clade.
Fig. 2

Bayesian phylogenetic tree of dataset X consisted of 33 sequences of bird schistosomes. Three sequences from representatives of Bivitellobriharzia nairi were used as an outgroup. Numbers along the nodes are posterior probability of the node. DNA sequence revealed in this study is marked with a star

Fig. 3

Bayesian phylogenetic tree of dataset X consisted of 34 sequences of bird schistosomes. Three sequences from representatives of Dendrirobiharzia pulverulenta and Anserobiharzia brantae were used as an outgroup. Numbers along the nodes are posterior probability of the node. DNA sequence revealed in this study is marked with a star

Seasonal fluctuations of Digenea larvae invasion in L. stagnalis

Snails infected with bird schistosomes were found in all research months in 2016. Statistically significant seasonal fluctuations of schistosome infection were observed (N = 7, χ2 = 12.036, df = 4, p = 0.017) (Fig. 4a). A similar trend (Fig. 4b) is reflected in statistically significant differences for seasonal infection of all Digenea species found inside L. stagnalis individuals (N = 7, χ2 = 14.857, df = 4, p = 0.005). The post hoc test indicated that L. stagnalis infected with Digenea larvae was most frequently recorded in July and August.
Fig. 4

Seasonal infection of Lymnaea stagnalis with a Trichobilharzia szidati and b all digenean species in the growing season 2016. *Statistically different from May and June (post hoc Wilcoxon signed-rank test, p < 0.05)

Infection of L. stagnalis with Digenea larvae related to four shell size classes

Bird schistosomes were found in snails whose shell length ranged from 30.9 to 63.1 mm. We identified four shell size classes: class size I < 40.0 mm of shell length, class size II 40.1–44.9 mm, class size III 45.0–49.9 mm, and class size IV ≥ 50.0 mm. The number of bird schistosome hosts from individual size classes was significantly different (χ2 = 9.42, df = 3, p = 0.02). The post hoc test indicated that infected individuals of the highest shell size class were statistically significant. Similarly, the number of L. stagnalis infected with all Digenea (Fig. 5) was significantly dependent on correlated with shell size classes (χ2 = 119.83, df = 3, p < 0.001). Moreover, the post hoc test indicated that individuals from the highest and also lowest classes were statistically significant (Fig. 5).
Fig. 5

Infection of Lymnaea stagnalis of different shell size classes with a Trichobilharzia szidati and b all digenean species in the growing season 2016. Asterisks (*) indicate groups significantly contributing to the differences in the parasite presence (z-scores of standardized residuals)

Discussion

Symptoms of swimmer’s itch caused by bird schistosomes depend greatly on their species. Since morphological and anatomical identifications of cercariae are unreliable (Dvorák et al. 2002; Horák et al. 2002; Rudolfová et al. 2005; Podhorský et al. 2009), human health risk assessment should be based on a molecular analysis of these larvae. Recent reports (Jouet et al. 2008, 2015; Christiansen et al. 2016) show much higher species diversity within the genus Trichobilharzia in Europe than previously thought. The following species have been recorded: Trichobilharzia anseri (Jouet et al. 2015), Trichobilharzia franki (Müller and Kimmig 1994), Trichobilharzia mergi (Kolářová et al. 2013b), Trichobilharzia salmanticensis (Simon-Martin and Simon-Vicente 1999), T. regenti (Horák et al. 1998), and T. szidati (Neuhaus 1952). Our study is the first to report the presence of T. regenti in Polish water bodies. The results also confirm widespread occurrence of T. szidati in Polish freshwater snails. What is surprising, despite the examination of nearly 1000 Radix sp. individuals, none of them was infected with T. franki—a bird schistosome widely distributed in the European populations of snail and waterfowl (Jouet et al. 2010). Both recorded species, as well as mentioned T. franki are widely recognized as causal agents of swimmer’s itch (Müller and Kimmig 1994; Żbikowska 2004). Bird schistosomes have been found in the majority of Polish lymnaeid species, but many reports have been limited to giving their complex name T. ocellata (Żbikowska 2004; Żbikowska et al. 2006; Cichy 2013). Only isolated cases of the presence of T. szidati in L. stagnalis (Żbikowska 2005) and S. palustris (Cichy 2013) as well as T. franki in R. auricularia (Żbikowska 2004) have been reported. In our previous study (Marszewska et al. 2016), we made an assumption that cercariae found in R. balthica belonged to the nasal bird schistosome species T. regenti. Molecular analysis performed in the present study confirmed this assumption. Also, the successful experimental infection of R. balthica by miracidia of T. regenti confirms the developing of this bird schistosome inside this species of Radix snails (Marszewska et al. 2018). However, the lack of molecular diagnosis of the Radix individuals naturally infected with T. regenti larvae does not allow to give the species name of hosts, that the conchological and anatomical data indicate that they were not snails belonging to the R. auricularia (Jackiewicz 2000; Piechocki and Wawrzyniak-Wydrowska 2016). For humans, the invasion of T. regenti may be more dangerous than that of other bird schistosomes. Nasal schistosomes migrate inside the final host through the nervous system (Kolářová et al. 2001; Leontovyč et al. 2016). Experimental studies have indicated that the movement of T. regenti within the nervous system of unusual mammalian hosts led to leg paralysis (Kouřilová et al. 2004; Lichtenbergová et al. 2011; Horák and Kolářová 2001). Although so far bird schistosomes have not been found inside the human body (Horák et al. 2015), it should be emphasized that in laboratory larvae of Trichobilharzia sp. invaded mammals through the skin and migrated to their internal organs (Horák and Kolářová 2001). In an experiment using mice, schistosomules of bird schistosomes were found in the lungs (Appleton and Brock 1986; Haas and Pietsch 1991; Horák and Kolářová 2000), heart, kidneys, liver, and intestines of these rodents (Haas and Pietsch 1991). According to Olivier (1953), they have also been found in the lungs of other mammalian hosts including hamsters, guinea pigs, rabbits, and even rhesus monkeys.

In Polish lakes, the prevalence of bird schistosomes was very low (Fig. 1), which corresponds to the observations of other European water bodies. The prevalence of Trichobilharzia spp. in intermediate hosts ranges from 0.05 to 5% (Soldánová et al. 2013) and is far lower than that of other Digenea. It should be noted that low prevalence of snails infected with these parasites does not exclude high risk of swimmer’s itch (Chamot et al. 1998; Lévesque et al. 2002; Farahnak and Essalat 2003; Skírnisson and Kolárová 2005; Jouet et al. 2008). This can be explained by very high bird schistosome cercarial emission (significantly higher than of other Digenean species) (Żbikowska 2005). Even low prevalence of invaded snails is sufficiently balanced by high intensity of cercarial release.

On the other hand, high risk of swimmer’s itch in European lakes results from seasonal fluctuations of the invasion. The results of our present and previous studies (Żbikowska 2004) confirm bird schistosome infection in snails collected from May to September, with the highest prevalence in the peak of the summer season (Fig. 4a). Therefore, risk assessment and preventive measures (e.g., removing snails from lakes) are extremely important (Chamot et al. 1998; Lévesque et al. 2002; Caumes et al. 2003; Verbrugge et al. 2004; Jouet et al. 2008).

Many authors have described seasonal changes in the prevalence of bird schistosomes and other Digenean species in snail hosts, indicating the highest rate during the warmest and the lowest during the coldest months (Loy and Haas 2001; Żbikowska et al. 2006; Żbikowska and Nowak 2009; Brown et al. 2010). This results from the fact that temperature has a huge impact on the life cycle of trematodes (Mas-Coma et al. 2009; Żbikowska and Cichy 2012). High temperature facilitates the transmission of parasites in the environment (Poulin 2006; Cichy et al. 2016) and stimulates the production of cercariae inside molluscs (Kendall and McCullough 1951; Lo and Lee 1996; Poulin 2006).

Finally, bird schistosome invasion inside host snails is an important factor affecting swimmer’s itch risk level. Our research shows that large snails are more often infected with flukes than small ones (Fig. 5), which is in line with the observations of other researchers (Loker 1983; Brown et al. 1988; Sorensen and Minchella 1998; Graham 2003; Sichun et al. 2005). According to Sichun et al. (2005), this correlation is beneficial for the parasite. Larger host snails provide greater energy resources and/or more space for the production of invasive cercariae (Graham 2003; Sichun et al. 2005). More intensive invasion of Digenea in snail hosts results in a bigger number of cercariae released into water and therefore with a higher risk of swimmer’s itch. The fact that larger snails are more often infected with these trematodes depends on many factors (Sturrock 1966; Baudoin 1975; Wilson and Denison 1980; McCarthy et al. 2004; Żbikowska et al. 2006; Miura and Chiba 2007). First of all, it may be connected to the preferences of parasites, which choose larger host snails over small ones (Baudoin 1975). On the other hand, it is well-know that the parasite may affect the host’s phenotypic traits, for example as the size of the shell (Miura and Chiba 2007). Scientists postulate that digenetic trematodes contribute to the abnormally large shells of host molluscs, known as parasitic gigantism (Wilson and Denison 1980; McCarthy et al. 2004; Żbikowska et al. 2006). However, when the snails are not yet infected, bigger snails are usually older snails and have more time to meet potentially a larger number of invasive larvae (Graham 2003; Sichun et al. 2005). Finally, smaller (younger) host snails are characterized by greater mortality because of the parasite (Sturrock 1966; Baudoin M; 1975) and as a result, smaller infected individuals are harder to find in the environment. This point of view is supported by our observation that large specimens of L. stagnalis invaded with bird schistosomes were collected in early May. Taking into account that the development of bird schistosomes from miracidia to cercariae takes about 7 weeks (Amen and Meuleman 1992), we can assume that snails releasing cercariae in May were invaded in autumn (McMullen and Beaver 1945; Jarcho and van Burkalow 1952) and survived winter (Horák et al. 2002). This situation is beneficial for bird schistosomes and increases the risk of swimmer’s itch, especially in the situation of recent climate change, and the earlier beginning of the recreational season in the temperate zone.

In conclusion, there are numerous indicators of real risk of swimmer’s itch including the following: (i) recent detection of the presence of potentially most dangerous nasal schistosome T. regenti in Poland, (ii) widespread presence of snails infected with T. szidati in Polish water bodies, (iii) widespread presence of these parasites during the summer season, (iv) frequent presence of these parasites in larger (more resistant) hosts. In view of these facts, we believe that it is necessary to develop effective methods of protection against cercarial dermatitis.

Notes

Acknowledgements

We would like to thank Daria Owczarek, MSc, of Wrocław University of Environmental and Life Sciences for help and instructions in laboratory work as well as Jarosław Kobak, PhD professor UMK, of Nicolaus Copernicus University in Toruń for statistical consultations.

Funding information

This project was supported by statutory funds from the Ministry of Science and Higher Education (PL) for the research programs of the Department of Invertebrate Zoology, Nicolaus Copernicus University in Torun, PL, including Grant Nos. 2832-B and 2572-B (Principal Investigator—Anna Marszewska).

Compliance with ethical standards

Conflict of interest

The authors declare that they have no conflict of interest.

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Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

Authors and Affiliations

  • Anna Marszewska
    • 1
  • Tomasz Strzała
    • 2
  • Anna Cichy
    • 1
  • Grażyna B. Dąbrowska
    • 3
  • Elżbieta Żbikowska
    • 1
  1. 1.Department of Invertebrate Zoology, Faculty of Biology and Environment ProtectionNicolaus Copernicus University in ToruńToruńPoland
  2. 2.Department of Genetics, Faculty of Biology and Animal ScienceWrocław University of Environmental and Life SciencesWrocławPoland
  3. 3.Department of Genetics, Faculty of Biology and Environment ProtectionNicolaus Copernicus University in ToruńToruńPoland

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