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Dams threaten salmonids by triggering temperature-dependent proliferative kidney disease


Abstract

Dams provide different services for human society, but they also significantly disrupt ecosystems by altering natural flow and temperature regimes. Here, we describe a novel, unappreciated threat posed by reservoirs to one of the world’s most popular game fish, brown trout (Salmo trutta). We show that small river impoundments elevate downstream water temperature during summer, which increases the prevalence and abundance of Tetracapsuloides bryosalmonae parasite triggering proliferative kidney disease (PKD), an emerging disorder in salmonids across North America and Europe. Our study highlights the role of reservoirs in creating parasite and disease hotspots, while providing limited evidence that dams act as barriers to parasite spread. This makes downstream areas from reservoirs valuable sentinel sites for monitoring climate impacts on riverine ecosystems. Ultimately, the assessment of dams requires a more holistic approach, where the disease risks are included in the decision-making process balancing human needs with the health of aquatic ecosystems.

Data availability

All data and code supporting the findings of this study are available in the Figshare repository under the https://doi.org/10.6084/m9.figshare.28595468.v4. Source data for all figures and analyses can be accessed directly through this repository. Any additional information is available from the corresponding author upon reasonable request.

References

  1. Belletti, B. et al. More than one million barriers fragment Europe’s rivers. Nature 588, 436–441 (2020).

    Google Scholar 

  2. Grill, G. et al. Mapping the world’s free-flowing rivers. Nature 569, 215–221 (2019).

    Google Scholar 

  3. Zarfl, C. et al. Future large hydropower dams impact global freshwater megafauna. Sci. Rep. 9, 18531 (2019).

  4. Su, G. et al. Human impacts on global freshwater fish biodiversity. Science 371, 835–838 (2021).

    Google Scholar 

  5. Auffray, M., Senécal, J.-F., Turgeon, K., St-Hilaire, A. & Maheu, A. Reservoirs regulated by small dams have a similar warming effect than lakes on the summer thermal regime of streams. Sci. Total Environ. 869, 161445 (2023).

    Google Scholar 

  6. Bednarek, A. Undamming rivers: a review of the ecological impacts of dam removal. Environ. Manag. 27, 803–814 (2001).

    Google Scholar 

  7. Barbarossa, V. et al. Impacts of current and future large dams on the geographic range connectivity of freshwater fish worldwide. Proc. Natl. Acad. Sci. USA 117, 3648–3655 (2020).

    Google Scholar 

  8. Palmer, M. A. et al. Climate change and the world’s river basins: anticipating management options. Front. Ecol. Environ. 6, 81–89 (2008).

    Google Scholar 

  9. Deemer, B. R. et al. Greenhouse gas emissions from reservoir water surfaces: a new global synthesis. BioScience 66, 949–964 (2016).

    Google Scholar 

  10. Olden, J. D. & Naiman, R. J. Incorporating thermal regimes into environmental flows assessments: modifying dam operations to restore freshwater ecosystem integrity. Freshw. Biol. 55, 86–107 (2010).

    Google Scholar 

  11. Sinokrot, B. A., Stefan, H. G., McCormick, J. H. & Eaton, J. G. Modeling of climate change effects on stream temperatures and fish habitats below dams and near groundwater inputs. Clim. Change 30, 181–200 (1995).

    Google Scholar 

  12. Zaidel, P. A. et al. Impacts of small dams on stream temperature. Ecol. Indic. 120, 106878 (2021).

    Google Scholar 

  13. Pereira, H. R., Gomes, L. F., Barbosa, H. D. & Agostinho, A. A. Research on dams and fishes: determinants, directions, and gaps in the world scientific production. Hydrobiologia 847, 579–592 (2020).

    Google Scholar 

  14. Marcos-López, M., Gale, P., Oidtmann, B. C. & Peeler, E. J. Assessing the impact of climate change on disease emergence in freshwater fish in the United Kingdom. Transbound. Emerg. Dis. 57, 293–304 (2010).

    Google Scholar 

  15. Bartholomew, J. L. et al. Deconstructing dams and disease: predictions for salmon disease risk following Klamath River dam removals. Front. Ecol. Evol. 11 https://doi.org/10.3389/fevo.2023.1245967 (2023).

  16. Ros, A., Schmidt-Posthaus, H. & Brinker, A. Mitigating human impacts including climate change on proliferative kidney disease in salmonids of running waters. J. Fish Dis. 45, 497–521 (2022).

    Google Scholar 

  17. Hartikainen, H., Johnes, P., Moncrieff, C. & Okamura, B. Bryozoan populations reflect nutrient enrichment and productivity gradients in rivers. Freshw. Biol 54, 2320–2334 (2009).

    Google Scholar 

  18. Bettge, K., Segner, H., Burki, R., Schmidt-Posthaus, H. & Wahli, T. Proliferative kidney disease (PKD) of rainbow trout: temperature- and time-related changes of Tetracapsuloides bryosalmonae DNA in the kidney. Parasitology 136, 615–625 (2009).

    Google Scholar 

  19. Okamura, B., Hartikainen, H., Schmidt-Posthaus, H. & Wahli, T. Life cycle complexity, environmental change and the emerging status of salmonid proliferative kidney disease. Freshw. Biol. 56, 735–753 (2011).

    Google Scholar 

  20. Waldner, K., Borkovec, M., Borgwardt, F., Unfer, G. & El-Matbouli, M. Effect of water temperature on the morbidity of Tetracapsuloides bryosalmonae (Myxozoa) to brown trout (Salmo trutta) under laboratory conditions. J. Fish Dis. 44, 1005–1013 (2021).

    Google Scholar 

  21. Ros, A. et al. Current and projected impacts of the parasite Tetracapsuloides bryosalmonae (causative to proliferative kidney disease) on Central European salmonid populations under predicted climate change. Freshw. Biol 66, 1182–1199 (2021).

    Google Scholar 

  22. Isaak, D. J. et al. Global warming of salmon and trout rivers in the northwestern U.S.: road to ruin or path through purgatory?. Trans. Am. Fish. Soc. 147, 566–587 (2018).

    Google Scholar 

  23. Donadi, S. et al. Contrasting long-term trends in juvenile abundance of a widespread cold-water salmonid along a latitudinal gradient: effects of climate, stream size and migration strategy. Ecography,2023, e06522 (2023).

  24. Hedrick, R., MacConnell, E. & De Kinkelin, P. Proliferative kidney disease of salmonid fish. Annu. Rev. Fish Dis. 3, 277–290 (1993).

    Google Scholar 

  25. Zarri, L. J., Palkovacs, E. P., Post, D. M., Therkildsen, N. O. & Flecker, A. S. The evolutionary consequences of dams and other barriers for riverine fishes. BioScience 72, 431–448 (2022).

    Google Scholar 

  26. Lessard, J. L. & Hayes, D. B. Effects of elevated water temperature on fish and macroinvertebrate communities below small dams. River Res. Appl. 19, 721–732 (2003).

    Google Scholar 

  27. Schmidt-Posthaus, H., Hirschi, R. & Schneider, E. Proliferative kidney disease in brown trout: infection level, pathology and mortality under field conditions. Dis. Aquat. Org. 114, 139–146 (2015).

    Google Scholar 

  28. Strepparava, N. et al. Temperature-related parasite infection dynamics: the case of proliferative kidney disease of brown trout. Parasitology 145, 281–291 (2018).

    Google Scholar 

  29. Økland, J. & Økland, K. A. Freshwater bryozoans (Bryozoa) of Norway V: review and comparative discussion of the distribution and ecology of the 10 species recorded. Hydrobiologia 534, 31–55 (2005).

    Google Scholar 

  30. Engel, F. et al. Phytoplankton gross primary production increases along cascading impoundments in a temperate, low-discharge river: Insights from high frequency water quality monitoring. Sci. Rep. 9, 6701 (2019).

  31. Davis, J. M., Rosemond, A. D., Eggert, S. L., Cross, W. F. & Wallace, J. B. Long-term nutrient enrichment decouples predator and prey production. Proc. Natl. Acad. Sci. USA 107, 121–126 (2009).

    Google Scholar 

  32. Wood, T. S. Digestion and nutrition in freshwater bryozoans (Phylactolaemata). Invertebr. Biol. 140, e12314 (2021).

  33. Duval, E. et al. When does a parasite become a disease? eDNA unravels complex host-pathogen dynamics across environmental stress gradients in wild salmonid populations. Sci. Total Environ. 946, 174367 (2024).

    Google Scholar 

  34. Carraro, L. et al. Integrated field, laboratory, and theoretical study of PKD spread in a Swiss prealpine river. Proc. Natl. Acad. Sci. USA 114, 11992–11997 (2017).

    Google Scholar 

  35. Ahmad, F. et al. The strength and form of natural selection on transcript abundance in the wild. Mol. Ecol. 30, 2724–2737 (2020).

    Google Scholar 

  36. Bailey, C., Segner, H., Casanova-Nakayama, A. & Wahli, T. Who needs the hotspot? The effect of temperature on the fish host immune response to Tetracapsuloides bryosalmonae the causative agent of proliferative kidney disease. Fish Shellfish Immunol. 63, 424–437 (2017).

    Google Scholar 

  37. Bruneaux, M. et al. Parasite infection and decreased thermal tolerance: impact of proliferative kidney disease on a wild salmonid fish in the context of climate change. Funct. Ecol. 31, 216–226 (2016).

    Google Scholar 

  38. Nagrodski, A., Raby, G. D., Hasler, C. T., Taylor, M. K. & Cooke, S. J. Fish stranding in freshwater systems: sources, consequences, and mitigation. J. Environ. Manag. 103, 133–141 (2012).

    Google Scholar 

  39. Huntingford, F. A. et al. How juvenile Atlantic salmon, Salmo salar L., respond to falling water levels: experiments in an artificial stream. Fish. Manage. Ecol. 6, 357–364 (1999).

    Google Scholar 

  40. Jonsson, B. & Jonsson, N. A review of the likely effects of climate change on anadromous Atlantic salmon Salmo salar and brown trout Salmo trutta, with particular reference to water temperature and flow. J. Fish Biol. 75, 2381–2447 (2009).

    Google Scholar 

  41. Schisler, G. J., Walker, P. G., Chittum, L. A. & Bergersen, E. P. Gill ectoparasites of juvenile rainbow trout and brown trout in the upper Colorado River. J. Aquat. Anim. Health 11, 170–174 (1999).

    Google Scholar 

  42. Marcogliese, D. J. The impact of climate change on the parasites and infectious diseases of aquatic animals. Rev. Sci. Tech. 27, 467–484 (2008).

    Google Scholar 

  43. Anderson, R. M. & May, R. M. The invasion, persistence and spread of infectious diseases within animal and plant communities. Philos. Trans. R. Soc. Lond. B Biol. Sci. 314, 533–570 (1986).

    Google Scholar 

  44. Schmidt-Posthaus, H. et al. The role of migration barriers for dispersion of Proliferative Kidney Disease—Balance between disease emergence and habitat connectivity. PLoS ONE 16, e0247482 (2021).

    Google Scholar 

  45. Bellmore, J. R. et al. Conceptualizing ecological responses to dam removal: if you remove it, what’s to come?. BioScience 69, 26–39 (2018).

    Google Scholar 

  46. Dolan, E. J., Soto, I., Dick, J. T. A., He, F., Cuthbert, R. N. Riverine barrier removals could proliferate biological invasions. Glob. Change Biol. 31, e70093 (2025).

  47. Altizer, S., Bartel, R. & Han, B. A. Animal migration and infectious disease risk. Science 331, 296–302 (2011).

    Google Scholar 

  48. Oexle, S., Ros, A. & Brinker, A. Evidence that wild salmonids seek cool water refuges to reduce parasite virulence: the proliferative kidney disease case. Freshw. Biol. 70, 7 (2025).

    Google Scholar 

  49. Kalny, G. et al. The influence of riparian vegetation shading on water temperature during low flow conditions in a medium sized river. Knowl. Manag. Aquat. Ecosyst. 418, 5 (2017).

    Google Scholar 

  50. Wohl, E., Lane, S. N. & Wilcox, A. C. The science and practice of river restoration. Water Resour. Res. 51, 5974–5997 (2015).

    Google Scholar 

  51. Myrstener, M., Greiser, C. & Kuglerová, L. Downstream temperature effects of boreal forest clearcutting vary with riparian buffer width. Water Resour. Res. 61, e2024WR037705 (2025).

    Google Scholar 

  52. Wahli, T., Bernet, D., Steiner, P. A. & Schmidt-Posthaus, H. Geographic distribution of Tetracapsuloides bryosalmonae infected fish in Swiss rivers: an update. Aquat. Sci. 69, 3–10 (2007).

    Google Scholar 

  53. Mo, T. A. & Jørgensen, A. A survey of the distribution of the PKD-parasite Tetracapsuloides bryosalmonae (Cnidaria: Myxozoa: Malacosporea) in salmonids in Norwegian rivers – additional information gleaned from formerly collected fish. J. Fish Dis. 40, 621–627 (2016).

    Google Scholar 

  54. Gorgoglione, B., Bailey, C. & Ferguson, J. A. Proliferative kidney disease in Alaskan salmonids with evidence that pathogenic myxozoans may be emerging north. Int. J. Parasitol. 50, 797–807 (2020).

    Google Scholar 

  55. Philpott, D. et al. Effects of different preservatives during ecological monitoring of malacosporean parasite Tetracapsuloides bryosalmonae causing proliferative kidney disease (PKD) in salmonids. J. Fish Dis. 48, e14095 (2025).

  56. Hutchins, P. R., et al. Exploration of the 2016 Yellowstone River fish kill and proliferative kidney disease in wild fish populations. Ecosphere 12, e03436 (2021).

  57. Schager, E., Peter, A. & Burkhardt-Holm, P. Status of young-of-the-year brown trout (Salmo trutta fario) in Swiss streams: factors influencing YOY trout recruitment. Aquat. Sci. 69, 41–50 (2007).

    Google Scholar 

  58. Waldner, K. et al. A brown trout (Salmo trutta) population faces devastating consequences due to proliferative kidney disease and temperature increase: a case study from Austria. Ecol. Freshw. Fish 29, 465–476 (2019).

    Google Scholar 

  59. Szklo, M., Nieto, F. J. Epidemiology: Beyond the basics 3rd edn. 139 (Jones & Bartlett Learning, 2014).

  60. Soomro, S. et al. Are global influences of cascade dams affecting river water temperature and fish ecology? Appl. Water Sci, 13, 106 (2023).

  61. Carolli, M. et al. Impacts of existing and planned hydropower dams on river fragmentation in the Balkan Region. Sci. Total Environ. 871, 161940 (2023).

    Google Scholar 

  62. Fiske, P. et al. Novel large-scale mapping highlights poor state of sea trout populations. Aquat. Conserv. Mar. Freshw. Ecosyst. 34, e4067 (2024).

  63. Lõhmus, M. & Björklund, M. Climate change: what will it do to fish-parasite interactions?. Biol. J. Linn. Soc. 116, 397–411 (2015).

    Google Scholar 

  64. Lauringson, M. et al. Spatial and intra-host distribution of myxozoan parasite Tetracapsuloides bryosalmonae among Baltic sea trout (Salmo trutta). J. Fish Dis. 46, 1073–1083 (2023).

    Google Scholar 

  65. Dash, M. & Vasemägi, A. Proliferative kidney disease (PKD) agent Tetracapsuloides bryosalmonae in brown trout populations in Estonia. Dis. Aquat. Org. 109, 139–148 (2014).

    Google Scholar 

  66. Sergeant, E. S. G. Epitools Epidemiological Calculators, Ausvet. http://epitools.ausvet.com.au (2018).

  67. Debes, P., Gross, R. & Vasemägi, A. Quantitative genetic variation in, and environmental effects on, pathogen resistance and temperature-dependent disease severity in a wild trout. Am. Nat. 190, 000–000 (2017).

    Google Scholar 

  68. Schneider, C. A., Rasband, W. S. & Eliceiri, K. W. NIH Image to ImageJ: 25 years of image analysis. Nat. Methods 9, 671–675 (2012).

    Google Scholar 

  69. Hutchins, P. R., Sepulveda, A. J., Martin, R. M. & Hopper, L. R. A probe-based quantitative PCR assay for detecting Tetracapsuloides bryosalmonae in fish tissue and environmental DNA water samples. Conserv. Genet. Resour. 10, 317–319 (2018).

    Google Scholar 

  70. Hutchins, P. R., Sepulveda, A. J., Martin, R. M. & Hopper, L. R. Improved conventional PCR assay for detecting Tetracapsuloides bryosalmonae DNA in fish tissues. J. Aquat. Anim. Health 30, 164–170 (2018).

    Google Scholar 

  71. Klymus, K. E. et al. Reporting the limits of detection and quantification for environmental DNA assays. Environ. DNA 2, 271–282 (2020).

    Google Scholar 

  72. Merkes, C. et al. Reporting the Limits of Detection (LOD) and Quantification (LOQ) for Environmental DNA Assays: Data: U.S. Geological Survey Data Release (U.S. Geological Survey, 2019).

  73. Bates, D., Mächler, M., Bolker, B. & Walker, S. Fitting linear mixed-effects models using lme4. J. Stat. Softw. 67, 1–48 (2015).

    Google Scholar 

  74. Kuznetsova, A., Brockhoff, P. B. & Christensen, R. H. B. lmerTest package: tests in linear mixed effects models. J. Stat. Softw. 82, 1–26 (2017).

    Google Scholar 

  75. Fox, J., Weisberg, S., Price, B. car: Companion to Applied Regression. R package version 3.1-3 (2024).

  76. Wickham, H. ggplot2: Elegant Graphics for Data Analysis (Springer-Verlag, New York, 2016).

  77. Wilke, C. cowplot: Streamlined Plot Theme and Plot Annotations for ‘ggplot2’. R package version 1.1.3 (2024).

  78. Hartig, F. DHARMA: Residual Diagnostics for Hierarchical (Multi-Level / Mixed) Regression Models. R package (2024). version 0.4.7.

  79. Lenth, R. emmeans: Estimated Marginal Means, aka Least-Squares Means. R package (2025). version 1.10.7.

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Acknowledgements

We thank Alfonso Diaz Suarez, Gustav Lauringson, Karl-Erik Aavik, Tanel Ader, Herki Tuus and Veljo Kisand for their assistance and support, Põlula Fish Rearing Centre of State Forest Management Centre (RMK) for logistical support and Oksana Burimski for laboratory assistance. Vihula III dam and reservoir photo (10.6 ha) at the Mustoja river, shown in Fig. 1G, is based on a drone photo from 10.07.2023, kindly provided by Gunnar Laak. The study was funded by Estonian Ministry of Regional Affairs and Agriculture, contract no. 4-1/22/6, Estonian Research Council, grant no. PSG849, PRG852, PRG3078 and Swedish research council for sustainable development FORMAS, grant no. 2021-01643.

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Open access funding provided by Swedish University of Agricultural Sciences.

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A.V. and M.L. contributed equally to this work. A.V. and M.L. conceived the study. Methodology was developed by A.V., J.N., L.P., M.L. Investigation was carried out by A.V., L.P., M.L., R.G. and S.K. Visualization was performed by A.V., J.N. and M.L. The original draft was written by A.V., J.N. and M.L., and all authors contributed to review and editing.

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Anti Vasemägi.

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Lauringson, M., Näslund, J., Pukk, L. et al. Dams threaten salmonids by triggering temperature-dependent proliferative kidney disease.
Commun Biol (2026). https://doi.org/10.1038/s42003-025-09470-1

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