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Pathogenic Leptospira species in rodents from Corsica (France)

  • Elena Izquierdo-Rodríguez ,

    Contributed equally to this work with: Elena Izquierdo-Rodríguez, Ángela Fernández-Álvarez

    Roles Data curation, Formal analysis, Writing – original draft, Writing – review & editing

    Affiliations Instituto Universitario de Enfermedades Tropicales y Salud Pública de Canarias, Universidad de La Laguna, La Laguna, Canary Islands, Spain, Department Obstetricia y Ginecología, Pediatría, Medicina Preventiva y Salud Pública, Toxicología, Medicina Legal y Forense y Parasitología, Facultad de Farmacia, Universidad de La Laguna, La Laguna, Canary Islands, Spain

  • Ángela Fernández-Álvarez ,

    Contributed equally to this work with: Elena Izquierdo-Rodríguez, Ángela Fernández-Álvarez

    Roles Data curation, Investigation, Resources

    Affiliations Instituto Universitario de Enfermedades Tropicales y Salud Pública de Canarias, Universidad de La Laguna, La Laguna, Canary Islands, Spain, UMR SPE 6134, CNRS-Université de Corse, Projet GEM, 20250 Corte, France

  • Natalia Martín-Carrillo,

    Roles Writing – review & editing

    Affiliations Instituto Universitario de Enfermedades Tropicales y Salud Pública de Canarias, Universidad de La Laguna, La Laguna, Canary Islands, Spain, Department Obstetricia y Ginecología, Pediatría, Medicina Preventiva y Salud Pública, Toxicología, Medicina Legal y Forense y Parasitología, Facultad de Farmacia, Universidad de La Laguna, La Laguna, Canary Islands, Spain

  • Bernard Marchand,

    Roles Writing – review & editing

    Affiliation UMR SPE 6134, CNRS-Université de Corse, Projet GEM, 20250 Corte, France

  • Carlos Feliu,

    Roles Conceptualization, Resources, Writing – review & editing

    Affiliations Departament de Biologia, Sanitat i Medi Ambient, Facultat de Farmàcia i Ciències de l’Alimentació, Secció de Parasitologia, Universitat de Barcelona, Barcelona, Spain, IRBio, Facultat de Biologia, Universitat de Barcelona, Barcelona, Spain

  • Jordi Miquel,

    Roles Resources, Writing – review & editing

    Affiliations Departament de Biologia, Sanitat i Medi Ambient, Facultat de Farmàcia i Ciències de l’Alimentació, Secció de Parasitologia, Universitat de Barcelona, Barcelona, Spain, IRBio, Facultat de Biologia, Universitat de Barcelona, Barcelona, Spain

  • Pilar Foronda ,

    Roles Conceptualization, Funding acquisition, Methodology, Project administration, Writing – original draft, Writing – review & editing

    pforonda@ull.edu.es

    Affiliations Instituto Universitario de Enfermedades Tropicales y Salud Pública de Canarias, Universidad de La Laguna, La Laguna, Canary Islands, Spain, Department Obstetricia y Ginecología, Pediatría, Medicina Preventiva y Salud Pública, Toxicología, Medicina Legal y Forense y Parasitología, Facultad de Farmacia, Universidad de La Laguna, La Laguna, Canary Islands, Spain

  • Yann Quilichini

    Roles Funding acquisition, Project administration, Supervision, Writing – review & editing

    Affiliation UMR SPE 6134, CNRS-Université de Corse, Projet GEM, 20250 Corte, France

Abstract

Leptospirosis is a worldwide emerging zoonotic disease caused by Leptospira species, that in some patients develop severe forms with high mortality. In France, Corsica is the area where the highest incidences have been reported. The present study was focused on the analysis of pathogenic Leptospira species in rodents of Corsica, as these micromammals are the main natural reservoirs of the bacteria, in order to identify the circulating species and to locate possible risk focuses of transmission, as no previous study on the presence of Leptospira species has been carried out in the island. Rattus rattus, Rattus norvegicus, Apodemus sylvaticus and Mus musculus domesticus were captured in the proximity of water sources along Corsica, the detection of pathogenic Leptospira species was carried out by amplification of the LipL32 gene. The bacteria were found in all the rodent species analyzed and widely. The general prevalence was 10.4%, reaching the maximum value in Bastia (45%). Leptospira interrogans and Leptospira borgpetersenii were identified by phylogenetic analysis, but also two sequences which corresponded to an unnamed Leptospira species, only previously found in rodents of New Caledonia. The high incidence of human leptospirosis in Corsica could be partially explained by the wide distribution of pathogenic Leptospira species identified in this study. Also, the presence of an unknown pathogenic species of Leptospira in an area with high prevalence, may be involved in the higher incidence of Leptospirosis in this island, however, the zoonotic capacity of this species remains unknown. The results obtained are interesting for public health since all positive samples were found near water sources and one of the routes of transmission of leptospirosis is contact with contaminated water. This information could help the competent entities to take preventive measures, reducing the incidence of human leptospirosis in Corsica.

Introduction

Leptospirosis is the most prevalent bacterial zoonosis worldwide [1]. It is an emerging infectious disease caused by Leptospira spp. spirochetes, which can infect both humans and animals. Pathogenic species cause a nonspecific self-limiting illness in human in most cases, but some patients develop systemic disease and even a severe form, including Weil´s disease and severe pulmonary hemorrhagic syndrome, with high mortality rates, >10% and >74%, respectively [2].

In Europe, the number of human leptospirosis cases has increased probably caused by climate change, the higher sensibility of the diagnostic tests and/or due to the increase in the aquatic activities [3]. Concretely in France, both in continental area and the Mediterranean island of Corsica, human leptospirosis has been reported, in cases which included mild clinical signs, as headache, to severe forms, as meningitis or myocarditis [3]. In 2017, 602 cases of leptospirosis were reported in French metropolitan areas [4].

Although a large variety of mammals have been described as Leptospira reservoirs, rodents are believed to be the main reservoirs [1], keeping the bacteria in the kidneys, releasing it through the urine, which constitute a source of infection for humans and other animals [2].

In order to identify the circulating species of Leptospira present in Corsica, the aim of the present work was to analyse rodents as the main natural reservoirs of this bacterium, as well as to aware of possible hotspots for the transmission of Leptospira species to humans and domestic animals in Corsica.

Material and methods

The study was carried out in 24 locations along Corsica island (France). Between February to June 2016, a total of 115 rodents belonging to the species Rattus rattus (80), Rattus norvegicus (2), Mus musculus domesticus (20) and Apodemus sylvaticus (13) were captured alive using Tomahawk and Sherman traps along Corsica (Fig 1). The trap setting was performed at proximity (<500 m) of ponds, river mouths and lakes. Once captured, rodents were euthanized by cervical dislocation or CO2 inhalation and bladders containing urine were extracted and stored in absolute ethanol until analyzed. This study was carried out in strict accordance with the recommendations of the guidelines of animal welfare in experimental science and the European Union legislation (Directive 86/609/EEC). The protocol was approved by “Comité de Ética de la Investigación y Bienestar Animal” of Universidad de La Laguna (Protocol Number: CEIBA2018-0330).

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Fig 1. Map of Corsica showing the sampled areas along the island, with positive (●) and negative (○) results for LipL32 presence.

(1. Rizzanese, 2. Taravo, 3. Porticcio, 4. Ajaccio, 5. Liamone, 6. Calacuccia, 7. Corte, 8. Foce, 9. Padula, 10. Saint Florent, 11. Tettola, 12. Biguglia, 13. Golo, 14. Chiatra, 15. Matra, 16. Canale di Verde, 17. Terrenzana, 18. Diane, 19. Urbino, 20. Prunelli- di- Fiumorbo, 21. Gradugine, 22. Palo, 23. Pinarellu, 24. Saint Cyprien.). (The original image was took from Wikipedia https://de.wikipedia.org/wiki/Datei:Corsica-locator.svg in which the original author authorized its use for any purpose. From which it was edited by Photoshop CS6).

https://doi.org/10.1371/journal.pone.0233776.g001

Genomic DNA was isolated using a semi-automated extraction system with the QIAamp 96 DNA QIAcube HT Kit (Qiagen Sciences, Inc., Germantown, MD, USA) using the TissueLysser II (Quiagen Sciences, Inc., Germantown, MD, USA), following the manufacturer's instructions. A LipL32 fragment (423 bp), which is present only in pathogenic leptospires, was amplified by PCR according to the method of Levett et al. [5] by using the LipL32-270F (5´-CGCTGAAATGGGAGTTCGTATGATT-3´) and LipL32-692R (5´-CCAACAGATGCAACGAAAGATCCTTT-3´) primers in a MyCycler thermocycler (Bio-Rad, Hercules, CA, USA). Leptospira interrogans serovar Icterohemorragiae (RGA strain) was used as a positive control.

The resulting PCR products were sequenced by both sides at Macrogen (Korea), sequences were then aligned by MEGA-X and compared with those available at GenBank by BLAST. New sequences were submitted to GenBank under the accession numbers MN527294-MN527304. A Bayesian analysis of the 354-bp fragment obtained from the LipL32 gene of the species included in this study was set. Sequences from previously published Leptospira species were added. The K2 + G was selected as the best-fit model for our sequences and Leptospira santarosai (AY461927) was set as an outgroup. The Ngen was set to 30 million and the first 25% trees were discarded.

The confidence intervals (CI) for prevalences were obtained using the Clopper-Pearson exact method (95%). For the comparison of the prevalences obtained in this study Chi square tests were applied setting the P value in 0.05.

Results

Pathogenic Leptospira species were found in 12 out of the 115 rodents analyzed (10.43%; CI: 5.51–17.52), and widely distributed along Corsica (Fig 1). The prevalence was 25% (CI: 66–49.10) for M. m. domesticus, 7.69% (CI: 0.19–36.03) for A. sylvaticus and 7.32% (CI: 2.73–15.25) for Rattus species (5/80 (6.25%; CI: 2.06–13.99) for R. rattus and 1/2 (50%; CI: 1.26–98.74) for R. norvegicus) (Table 1). The total prevalence of Leptospira sp. in male rodents was 11.48% (CI: 4.74–22.22) (7/61), while in female rodents was 9.43% (CI: 3.13–20.66) (5/53), no significant differences were found when comparing both sexes.

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Table 1. Distribution of the animals captured in Corsica, divided by rodent species, as well as the location of the positive samples, which were tested by the amplification of the LipL32 gene.

https://doi.org/10.1371/journal.pone.0233776.t001

Geographically, Leptospira species were homogeneously distributed along Corsica, and similar prevalence values were found between Upper Corsica (11.24%) and Southern Corsica areas (7.69%), without statistical differences. Nevertheless, the highest prevalence was found in North Corsica, as in Bastia (Biguglia pond and Golo river mouth), Saint Florent (Saint Florent and Tettola) and Foce beach, where the prevalence values were 45.45%, 22.22% and 10%, respectively. In the pond areas of Eastern Corsica (including Terrenzana, Diane, Gradugine, Prunelli-di-Fium'Orbu, Palo and Urbino lakes) the general prevalence was 3.2%, while in Western Corsica the prevalence for Ajaccio (including Ajaccio and Porticcio) and Liamone was 14.3%. However, none of the 30 animals captured in higher inner areas (Corte, Calacuccia, Matra, Chiatra, Canale di Verde and Padula) hosted the bacteria (Fig 1 and Table 1). Significant differences were found when comparing the prevalence of Bastia to Eastern Corsica (Chi square = 5.3619; p = 0.0207).

Bayesian phylogenetic analysis (Fig 2) showed that eight of the sequences obtained in this study belonging to three host species, M. m. domesticus, R. rattus and A. sylvaticus, clustered with L. borgpetersenii. It is remarkable that two different haplotypes for L. borgpetersenii were found in Corsica, one of them identical to those obtained in different areas worldwide, such as Brazil (DQ286415) [6], India (EU526390) [7] and the Canary Islands, Spain (HQ231748) [8], among others; while the other (L32 from M. m. domesticus from Palo) showed 5 mutations in the 354bp fragment of the LipL32 gene. Another sequence from R. norvegicus was identified as L. interrogans, and the two remaining sequences obtained from M. m. domesticus and R. rattus were included in a different node as a different species related with L. interrogans and L. kirschneri, these two sequences (L29 and L64) showed 97.80% of identity by BLAST analysis with both L. interrogans and L. kirschneri, and 100% with an unnamed Leptospira species found in New Caledonia (JN092329) [9].

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Fig 2. Bayesian analysis based on a 354-bp fragment of the LipL32 gene of Leptospira spp. in rodents from Corsica.

Sequences belonging to this study are shown in bold and Leptospira santarosai (AY461927) was used as outgroup. The K2 + G was selected as the best-fit model. The Ngen was set to 30 million and the first 25% trees were discarded.

https://doi.org/10.1371/journal.pone.0233776.g002

Discussion

During the last years, the incidence of human leptospirosis has increased along France, reaching the highest value since 1920, 0.9 cases per 100 000 inhabitants. The island of Corsica reported one of the highest incidences of leptospirosis in France on 2017, being 1.87 cases per 100 000 inhabitants, doubling the national mean (0.9) [4].

The presence of Leptospira species distributed in wildlife in the proximity of water sources along Corsica may imply a risk of transmission to other animal species and humans, and also may be one of the reasons under the high incidence of human leptospirosis in Corsica, especially considering that one of the many tourist attractions of the island are rivers and beaches. Indeed, in 2017, 8.7 million travellers were registered at Corsican airports [10], so the finding of Leptospira species in rodents in near-water locations may imply the transmission of these bacteria not only for locals (farmers, veterinary, fishermen, hunters), but to anyone who visits the island or practice outdoor activities (swimming, kayaking, camping), as outbreaks of human leptospirosis related to recreational activities such as triathlon has been reported in many countries, such as United States [11], Malaysia [12], Germany [13] and Austria [14] in the last decades.

According to the “Institut National de la Statistique et des Etudes Economiques” (INSEE), the total population in Bastia on 2015 was 58098 people, which represents the 17.75% of Corsican population [15]. This agglomeration coincides with the highest Leptospira prevalence found in the whole island, where 45.45% of the rodents analyzed were positive for LipL32 gene, setting a possible focus of infection. Besides, this prevalence was found significantly different (p<0.05) when compared to the East of the island, less inhabited [15]. However, only 11 rodents were captured in Bastia area, so further investigation should be done in order to confirm this location as a hotspot for the transmission of Leptospira spp.

All positive samples were found in low-altitude locations of Corsica (<400 m), while none of the rodents analyzed in higher locations hosted the bacteria. These results may be correlated with local climate conditions and reveal the possible risk of transmission to human in lower areas presenting high risk of floods. Indeed, despite the complex environmental transmission pathways of Leptospira, floods appeared to be among the important drivers on islands [16]. Nevertheless, further investigations should be done on these issues, as the number of samples belonging to this study is limited, and also there are more species that can act as host for Leptospira [1]. Also, this study was done in urinary bladders instead of kidneys, which is the organ in which Leptospira sp. is the most concentrated, so the incidence for this bacterium may have been under-reported.

Although in humans, significant differences in the prevalence of leptospirosis are observed regarding sex of the individuals [4] no significant differences were found when this comparison was made in rodents. This result may mean that the differences observed in humans are not due to physiological reasons but more related to the fact that men are more likely to have high risk jobs for the transmission of leptospirosis, such as fishermen.

The new Leptospira species detected has only been recorded in rodents of New Caledonia [9] and Corsica, islands which are more than 16 thousand kilometres apart. This fact may be explained by the transport of rodents (or other reservoir) between New Caledonia (a French colony) and the European French territory. Further investigations of European rodents should be done in order to determine if this new Leptospira species can also be found in rodents of the continent, especially in France. This Leptospira species has not been found causing human leptospirosis, so its zoonotic capacity is unknown, nevertheless, it expresses the LipL32 protein, which is involved in pathogenesis of the genus Leptospira [17]. Also, taking into consideration that Corsica has reported a higher prevalence of human leptospirosis than the national mean [4], the genotypes of human leptospirosis occurring in Corsica should be studied in order to determine if this Leptospira species may be somehow responsible of the high incidence of human leptospirosis in the island.

It is remarkable that both Leptospira species found in Palo pond are different to those normally identified in rodents, as one of them was the new Leptospira species from New Caledonia and the other correspond to a L. borgpetersenii haplotype never recorded before. This situation may be due to the isolation that this area experienced during the barbarian invasions, when the villages close to the sea were abandoned and the Corsican population hid in the mountains. It is recorded that during those times other diseases, such as malaria and plague, were present in the island [18]. The presence of rats probably infected with Leptospira species and the isolation could be the reason under the finding of the new haplotype, and the constant attacks that the island suffered may have brought rodents from different areas of the world. The presence of new haplotypes of Leptospira species due to isolation is also present in the Canary Islands [8], an Atlantic archipelago where the L. interrogans haplotype found in rodents (HQ231747) (Fig 2) also showed differences when compared to all the sequences uploaded to the GenBank data base.

Considering that early diagnostic of leptospirosis for establishing an effective treatment is vital for patients, the finding of possible risk focuses could help clinicians to familiarize on early recognition of the disease. Also, preventive measures should be applied in order to reduce the high incidence of human leptospirosis in Corsica, such as rodent control and vaccination, which is advised by the French calendar of vaccination and vaccine recommendation for workers in closed and repetitive contact with contaminated environments, such as fishermen, or people practicing ludic activities as rafting, diving, triathlon and other sports which imply humid environments [19].

Acknowledgments

CF and JM are members of the 2017-SGR-1008 research group.

References

  1. 1. Cosson JF, Picardeau M, Mielcarek M, Tatard C, Chaval Y, Suputtamongkol Y, et al. Epidemiology of Leptospira transmitted by rodents in Southeast Asia. PLoS Negl Trop Dis. 2014;8(6):e2902. pmid:24901706
  2. 2. Bomfim MRQ, Barbosa-Stancioli EF, Koury MC. Detection of pathogenic leptospires in urine from naturally infected cattle by nested PCR. Vet J. 2007;178:251–6. pmid:17869555
  3. 3. Abgueguen P, Delbos V, Blanvillain J, Chennebault JM, Cottin J, Fanello S, et al. Clinical aspects and prognostic factors of leptospirosis in adults. Retrospective study in France. J Infect. 2008;57(3):171–8. pmid:18656263
  4. 4. Centre National de Référence de la Leptospirose. Rapport annuel d’activité. Année d’exercice 2017. Paris: Institut Pasteur; 2018;38.
  5. 5. Levett PN, Morey RE, Galloway RL, Turner DE, Steigerwalt AG, Mayer LW. Detection of pathogenic leptospires by real time quantitative PCR. J Med Microbiol. 2005;54:45–9. pmid:15591254
  6. 6. Bomfim MRQ & Cota Koury MC. Evaluation of LSSP-PCR for identification of Leptospira spp. in urine samples of cattle with clinical suspicion of leptospirosis. Vet Microbiol. 2006;118(3–4):278–88. pmid:16962259
  7. 7. Vedhagiri K, Natarajaseenivasan K, Prabhakaran SG, Selvin J, Narayanan R, Shouche YS, et al. Characterization of Leptospira borgpetersenii isolates from field rats (Rattus norvegicus) by 16s rRNA and LipL32 gene sequencing. Braz J Microbiol. 2010;41:150–7. pmid:24031475
  8. 8. Foronda P, Martin-Alonso A, del Castillo-Figueruelo B, Feliu C, Gil H, Valladares B. Pathogenic Leptospira spp. in wild rodents, Canary Islands, Spain. Emerg Infect Dis. 2011;17(9):1781–2. pmid:21888829
  9. 9. Perez J, Brescia F, Becam J, Mauron C, Goarant C. Rodent Abundance Dynamics and Leptospirosis Carriage in an Area of Hyper-Endemicity in New Caledonia. PLoS Negl Trop Dis. 2011;5(10):1371.
  10. 10. Institut National de la Statistique et des Etudes Economiques. Bilan annuel du tourisme. 2018a;5. French.
  11. 11. Morgan J, Bornstein SL, Karpati AM, Bruce M, Bolin CA, Austin CC, et al. Leptospirosis Working Group. Outbreak of Leptospirosis among Triathlon Participants and Community Residents in Springfield, Illinois, 1998. Arch Clin Infect Dis. 2002;34(12):1593–9.
  12. 12. Sevjar J, Bancroft E, Winthrop K, Bettinger J, Bajani M, Bragg S, et al. Leptospirosis in “Eco-Challenge” Athletes, Malaysian Borneo, 2000. Emerg Infect Dis. 2003;9(6):702–7. pmid:12781010
  13. 13. Brockmann S, Piechotowski I, Bock-Hensley O, Winter C, Oehme R, Zimmermann S, et al. Outbreak of leptospirosis among triathlon participants in Germany. BMC Infect Dis. 2010;10(1):91.
  14. 14. Radl C, Müller M, Revilla-Fernandez S, Karner-Zuser S, de Martin A, Schauer U, et al. Outbreak of leptospirosis among triathlon participants in Langau, Austria, 2010. Wien Klin Wochenschr. 2011;123(23–24):751–5. pmid:22105111
  15. 15. Institut National de la Statistique et des Etudes Economiques. Portrait des 19 intercommunalités de Corse. 2018b;8,17,41. French.
  16. 16. Mwachui MA, Crump L, Hartskeerl R, Zinsstag J, Hattendorf J. Environmental and Behavioural Determinants of Leptospirosis Transmission: A Systematic Review. PLoS Negl Trop Dis. 2015;9(9):e0003843. pmid:26379035
  17. 17. Yang C, Wu M, Pan M, Hsieh W, Vandewalle A, Huang C. The Leptospira Outer Membrane Protein LipL32 Induces Tubulointerstitial Nephritis-Mediated Gene Expression in Mouse Proximal Tubule Cells. J Am Soc Nephrol. 2002;13:2037–45. pmid:12138134
  18. 18. Jaujou CMJ. La lutte antipaludique en Corse. Bull World Health Organ. 1954;11(‎4–5)‎:635–77. French. pmid:13209316
  19. 19. Ministére des solidarités et la santé. Candelier des vaccinations et recommandations vaccinales. 2019;19. French.