bioRxivEcologyPreprint
Development and worldwide use of a non-lethal and minimal population-level impact protocols for the isolation of chytrids from amphibians
Matthew C. FisheriD, Pria Ghosh, Jennifer M. G. Shelton, Kieran Bates, Lola Brookes, Claudia Wierzbicki, Gonçalo M. Rosa, Rhys A. FarreriD, David M. AanenseniD, Mario Alvarado-Rybak, Arnaud BatailleiD, Lee BergeriD, Susanne Böll, Jaime BoschiD, France C. Clare, Elodie Courtois, Angelica CrottiniiD, Andrew A. Cunningham, Thomas M. Doherty-Bone, Fikirte Gebresenbet, David J. GoweriD, Jacob Höglund, Timothy Y. JamesiD, Thomas S. JenkinsoniD, Tiffany A. KoschiD, , Trenton W.J. GarneriD
Abstract
Parasitic chytrid fungi have emerged as a significant threat to amphibian species worldwide, necessitating the development of techniques to isolate these pathogens into sterile culture for research purposes. However, early methods of isolating chytrids from their hosts relied on killing amphibians. We modified a pre-existing protocol for isolating chytrids from infected animals to use toe clips and biopsies from toe webbing rather than euthanizing hosts, and distributed the protocol to interested researchers worldwide as part of the BiodivERsA project RACE - here called the RML protocol. In tandem, we developed a lethal procedure for isolating chytrids from tadpole mouthparts. Reviewing a database of use a decade after their inception, we find that these methods have been widely applied across at least 5 continents, 23 countries and in 62 amphibian species, and have been successfully used to isolate chytrids in remote field locations. Isolation of chytrids by the non-lethal RML protocol occured in 18% of attempts with 207 fungal isolates and three species of chytrid being recovered. Isolation of chytrids from tadpoles occured in 43% of attempts with 334 fungal isolates of one species (Batrachochytrium dendrobatidis) being recovered. Together, these methods have resulted in a significant reduction and refinement of our use of threatened amphibian species and have improved our ability to work with this important group of emerging fungal pathogens.
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