Literature DB >> 27070102

Expanding Distribution of Lethal Amphibian Fungus Batrachochytrium salamandrivorans in Europe.

Annemarieke Spitzen-van der Sluijs, An Martel, Johan Asselberghs, Emma K Bales, Wouter Beukema, Molly C Bletz, Lutz Dalbeck, Edo Goverse, Alexander Kerres, Thierry Kinet, Kai Kirst, Arnaud Laudelout, Luis F Marin da Fonte, Andreas Nöllert, Dagmar Ohlhoff, Joana Sabino-Pinto, Benedikt R Schmidt, Jeroen Speybroeck, Frank Spikmans, Sebastian Steinfartz, Michael Veith, Miguel Vences, Norman Wagner, Frank Pasmans, Stefan Lötters.   

Abstract

Emerging fungal diseases can drive amphibian species to local extinction. During 2010-2016, we examined 1,921 urodeles in 3 European countries. Presence of the chytrid fungus Batrachochytrium salamandrivorans at new locations and in urodeles of different species expands the known geographic and host range of the fungus and underpins its imminent threat to biodiversity.

Entities:  

Keywords:  Batrachochytrium salamandrivorans; Belgium; Europe; Germany; Ichthyosaura alpestris; Lissotriton vulgaris; Salamandra salamandra; amphibian; chytridiomycosis; fungi; geographic distribution; the Netherlands

Mesh:

Year:  2016        PMID: 27070102      PMCID: PMC4918153          DOI: 10.3201/eid2207.160109

Source DB:  PubMed          Journal:  Emerg Infect Dis        ISSN: 1080-6040            Impact factor:   6.883


Amphibians provide an iconic example of disease-driven global loss in biodiversity. The recently described chytrid fungus Batrachochytrium salamandrivorans (Bsal) is an emerging pathogen that is driving amphibian populations to local extinction (,). This highly pathogenic fungus causes a lethal skin disease that has so far been restricted to urodele amphibians (newts and salamanders); the fungus was most likely introduced from East Asia into Europe via the pet trade (). In Europe, Bsal infection has led to dramatic declines of fire salamander (Salamandra salamandra) populations in the Netherlands and Belgium (). Within 7 years after the supposed introduction of the fungus, a population in the Netherlands declined by 99.9% (,). In the United Kingdom and Germany, Bsal has been detected in captive salamanders and newts (,). Infection trials suggest that Bsal represents an unprecedented threat to diversity of Western Palearctic urodeles (); nevertheless, reports of deaths among salamanders and newts in their naturalized ranges have been restricted to a few populations of a single salamander species in the southern Netherlands and adjacent Belgium (,). Using data from field surveillance, we examined the hosts and the geographic range of Bsal in Europe.

The Study

During 2010–2016, we collected samples of free-living populations of newts and salamanders from 48 sites in the Netherlands, Belgium, and adjacent regions of the Eifel region in Germany (near the border with the Netherlands and Belgium) (Figure; Technical Appendix Table 1). Site selection was based on reported amphibian deaths, apparent negative amphibian population trends, preventive Bsal surveillance in susceptible populations, or geographic proximity to known outbreak sites. Samples were also collected at 6 additional sites in Germany and 1 in the Netherlands, which were located >100 km from the nearest known outbreak (Technical Appendix Table 2). Sampling was conducted by swabbing skin (,) of live animals and collecting skin samples from dead animals. All samples were kept frozen at −20°C until they were analyzed for the presence of Bsal DNA via real-time PCR, as described ().
Figure

Study sites for collection of amphibians in Western Europe, 2010–2016. Numbers correspond to field sites at which amphibians were collected and examined for Batrachochytrium salamandrivorans (Bsal) (Technical Appendix). Solid circles, Bsal detected; open circles, Bsal not detected. Larger cities are indicated in light gray. Note that there are additional sites where the fungus remained undetected (not shown).

Study sites for collection of amphibians in Western Europe, 2010–2016. Numbers correspond to field sites at which amphibians were collected and examined for Batrachochytrium salamandrivorans (Bsal) (Technical Appendix). Solid circles, Bsal detected; open circles, Bsal not detected. Larger cities are indicated in light gray. Note that there are additional sites where the fungus remained undetected (not shown). Across all 55 sites, we tested 1,019 fire salamanders (43 dead, 976 skin swab samples); at site 14, skin swab samples instead of tissue samples were collected from 16 dead salamanders. We also collected samples from 474 alpine newts (Ichthyosaura alpestris; 18 dead, 456 skin swab samples), 239 smooth newts (Lissotriton vulgaris; 2 dead, 237 skin swab samples), 80 palmate newts (Lissotriton helveticus; all skin swab samples), 79 crested newts (Triturus cristatus; all skin swab samples), and 30 Italian crested newts (Triturus carnifex; all skin swab samples). To obtain a Bayesian 95% credible interval for prevalence (online Technical Appendix), we used the computational methods of Lötters et al. (). We ran 3 parallel Markov chains with 20,000 iterations each and discarded the first 5,000 iterations as burn-in; chains were not thinned. Bsal was found at 14 of the 55 sites; infected amphibians were fire salamanders, alpine newts, and smooth newts. Our results demonstrate that the range of Bsal distribution may be up to ≈10,000 km2 (measured as the surface of a minimum convex polygon encompassing the outermost points) across Germany, Belgium, and the Netherlands (Figure). The presence of Bsal in wild alpine newts and smooth newts shows distinct expansion of the known host range in the wild (Technical Appendix Table 1). Furthermore, we document that Bsal is present in natural fire salamander populations in Germany (confined to the Eifel region). At some sites, because of our sample sizes, the upper limit of the 95% credible interval for Bsal prevalence was as high as 0.7; therefore, we may have failed to detect Bsal at these sites (Technical Appendix Table 1). In addition, the fungus may have been present at several sites before first detection. For example, Bsal was detected at site 4, where population-monitoring efforts in the years before detection (2000–2013) showed declines in 4 newt species (http://www.ravon.nl/EID_SI_Spitzen_et_al_2016). However, because no samples were collected before 2015, we have no evidence for a causal relationship between the presence of Bsal and the declines. We have also recorded the presence of Bsal in populations with no evidence of population change so far, such as the incidental findings of dead Bsal-positive newts in fyke nets at sites 5 and 11, and the incidental findings of dead Bsal-positive fire salamanders at sites 12 and 14. Clinical signs of mycosis, such as lethargy and skin shedding (), were observed at some Bsal-positive sites (1, 2, 7, 8, 14) but not at others.

Conclusions

Our study provides evidence that Bsal among wild amphibians in Europe is more widely distributed and affects a wider host range than previously known, which can either indicate recent spread of the fungus or point to historically infected sites that hitherto remained undetected. The presence of Bsal in wild populations can easily remain unnoticed because the lesions develop only near the final stage of the disease (). This information is crucial for the design of field surveys for Bsal surveillance. Our data might be used to inform a management strategy and to implement the recommendation of the Bern Convention () to halt the spread of Bsal in Europe. Research to search for molecular evidence that the outbreak locations are connected is under way. Chytrid disease dynamics are affected by multiple factors (e.g., temperature regimes []), and yet undetermined environmental determinants might be essential for disease outbreaks (). Untangling these factors, as well as the modes of Bsal spread and its geographic distribution, are points for further research to fully map the problem and identify populations and species at risk.

Technical Appendix

Field sites in Europe at which Batrachochytrium salamandrivorans fungus was and was not detected in amphibians, 2010–2016.
  7 in total

1.  Emerging disease in UK amphibians.

Authors:  Andrew A Cunningham; Katie Beckmann; Matthew Perkins; Liam Fitzpatrick; Ruth Cromie; Jay Redbond; Michelle F O'Brien; Pria Ghosh; Jennifer Shelton; Matthew C Fisher
Journal:  Vet Rec       Date:  2015-05-02       Impact factor: 2.695

2.  Detection of Batrachochytrium dendrobatidis in Mexican bolitoglossine salamanders using an optimal sampling protocol.

Authors:  Pascale Van Rooij; An Martel; Joachim Nerz; Sebastian Voitel; Filip Van Immerseel; Freddy Haesebrouck; Frank Pasmans
Journal:  Ecohealth       Date:  2011-09-13       Impact factor: 3.184

3.  Batrachochytrium salamandrivorans sp. nov. causes lethal chytridiomycosis in amphibians.

Authors:  An Martel; Annemarieke Spitzen-van der Sluijs; Mark Blooi; Wim Bert; Richard Ducatelle; Matthew C Fisher; Antonius Woeltjes; Wilbert Bosman; Koen Chiers; Franky Bossuyt; Frank Pasmans
Journal:  Proc Natl Acad Sci U S A       Date:  2013-09-03       Impact factor: 11.205

4.  Wildlife disease. Recent introduction of a chytrid fungus endangers Western Palearctic salamanders.

Authors:  A Martel; M Blooi; C Adriaensen; P Van Rooij; W Beukema; M C Fisher; R A Farrer; B R Schmidt; U Tobler; K Goka; K R Lips; C Muletz; K R Zamudio; J Bosch; S Lötters; E Wombwell; T W J Garner; A A Cunningham; A Spitzen-van der Sluijs; S Salvidio; R Ducatelle; K Nishikawa; T T Nguyen; J E Kolby; I Van Bocxlaer; F Bossuyt; F Pasmans
Journal:  Science       Date:  2014-10-31       Impact factor: 47.728

5.  Diagnostic assays and sampling protocols for the detection of Batrachochytrium dendrobatidis.

Authors:  A D Hyatt; D G Boyle; V Olsen; D B Boyle; L Berger; D Obendorf; A Dalton; K Kriger; M Heros; H Hines; R Phillott; R Campbell; G Marantelli; F Gleason; A Coiling
Journal:  Dis Aquat Organ       Date:  2007-01-18       Impact factor: 1.802

6.  Duplex real-time PCR for rapid simultaneous detection of Batrachochytrium dendrobatidis and Batrachochytrium salamandrivorans in Amphibian samples.

Authors:  M Blooi; F Pasmans; J E Longcore; A Spitzen-van der Sluijs; F Vercammen; A Martel
Journal:  J Clin Microbiol       Date:  2013-10-09       Impact factor: 5.948

Review 7.  Amphibian chytridiomycosis: a review with focus on fungus-host interactions.

Authors:  Pascale Van Rooij; An Martel; Freddy Haesebrouck; Frank Pasmans
Journal:  Vet Res       Date:  2015-11-25       Impact factor: 3.683

  7 in total
  31 in total

Review 1.  Overview of chytrid emergence and impacts on amphibians.

Authors:  Karen R Lips
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2016-12-05       Impact factor: 6.237

Review 2.  A salamander's toxic arsenal: review of skin poison diversity and function in true salamanders, genus Salamandra.

Authors:  Tim Lüddecke; Stefan Schulz; Sebastian Steinfartz; Miguel Vences
Journal:  Naturwissenschaften       Date:  2018-09-04

3.  Disruption of skin microbiota contributes to salamander disease.

Authors:  Molly C Bletz; Moira Kelly; Joana Sabino-Pinto; Emma Bales; Sarah Van Praet; Wim Bert; Filip Boyen; Miguel Vences; Sebastian Steinfartz; Frank Pasmans; An Martel
Journal:  Proc Biol Sci       Date:  2018-08-22       Impact factor: 5.349

Review 4.  Batrachochytrium salamandrivorans and the Risk of a Second Amphibian Pandemic.

Authors:  Tiffany A Yap; Natalie T Nguyen; Megan Serr; Alexander Shepack; Vance T Vredenburg
Journal:  Ecohealth       Date:  2017-11-16       Impact factor: 3.184

5.  Exploring the Distribution of the Spreading Lethal Salamander Chytrid Fungus in Its Invasive Range in Europe - A Macroecological Approach.

Authors:  Stephan Feldmeier; Lukas Schefczyk; Norman Wagner; Günther Heinemann; Michael Veith; Stefan Lötters
Journal:  PLoS One       Date:  2016-10-31       Impact factor: 3.240

6.  Survey of Pathogenic Chytrid Fungi (Batrachochytrium dendrobatidis and B. salamandrivorans) in Salamanders from Three Mountain Ranges in Europe and the Americas.

Authors:  Joshua Curtis Parrott; Alexander Shepack; David Burkart; Brandon LaBumbard; Patrick Scimè; Ethan Baruch; Alessandro Catenazzi
Journal:  Ecohealth       Date:  2016-10-05       Impact factor: 3.184

7.  Risk of survival, establishment and spread of Batrachochytrium salamandrivorans (Bsal) in the EU.

Authors:  Simon More; Miguel Angel Miranda; Dominique Bicout; Anette Bøtner; Andrew Butterworth; Paolo Calistri; Klaus Depner; Sandra Edwards; Bruno Garin-Bastuji; Margaret Good; Virginie Michel; Mohan Raj; Søren Saxmose Nielsen; Liisa Sihvonen; Hans Spoolder; Jan Arend Stegeman; Hans-Hermann Thulke; Antonio Velarde; Preben Willeberg; Christoph Winckler; Vojtech Baláž; An Martel; Kris Murray; Chiara Fabris; Irene Munoz-Gajardo; Andrey Gogin; Frank Verdonck; Christian Gortázar Schmidt
Journal:  EFSA J       Date:  2018-04-30

Review 8.  Fungal infections in animals: a patchwork of different situations.

Authors:  Seyedmojtaba Seyedmousavi; Sandra de M G Bosco; Sybren de Hoog; Frank Ebel; Daniel Elad; Renata R Gomes; Ilse D Jacobsen; Henrik Elvang Jensen; An Martel; Bernard Mignon; Frank Pasmans; Elena Piecková; Anderson Messias Rodrigues; Karuna Singh; Vania A Vicente; Gudrun Wibbelt; Nathan P Wiederhold; Jacques Guillot
Journal:  Med Mycol       Date:  2018-04-01       Impact factor: 4.076

9.  Amphibian skin microbiota exhibits temporal variation in community structure but stability of predicted Bd-inhibitory function.

Authors:  Molly C Bletz; R G Bina Perl; Bianca Tc Bobowski; Laura M Japke; Christoph C Tebbe; Anja B Dohrmann; Sabin Bhuju; Robert Geffers; Michael Jarek; Miguel Vences
Journal:  ISME J       Date:  2017-04-07       Impact factor: 10.302

10.  Cutaneous Bacterial Communities of a Poisonous Salamander: a Perspective from Life Stages, Body Parts and Environmental Conditions.

Authors:  Eugenia Sanchez; Molly C Bletz; Laura Duntsch; Sabin Bhuju; Robert Geffers; Michael Jarek; Anja B Dohrmann; Christoph C Tebbe; Sebastian Steinfartz; Miguel Vences
Journal:  Microb Ecol       Date:  2016-09-27       Impact factor: 4.552

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