Amphibians are facing an extinction crisis, and conservation breeding programmes are a tool used to prevent imminent species extinctions. Compared to mammals and birds, amphibians are considered ideal candidates for these programmes due to their small body size and low space requirements, high fecundity, applicability of reproductive technologies, short generation time, lack of parental care, hard wired behaviour, low maintenance requirements, relative cost effectiveness of such programmes, the success of several amphibian conservation breeding programmes and because captive husbandry capacity exists. Superficially, these reasons appear sound and conservation breeding has improved the conservation status of several amphibian species, however it is impossible to make generalisations about the biology or geo-political context of an entire class. Many threatened amphibian species fail to meet criteria that are commonly cited as reasons why amphibians are suitable for conservation breeding programmes. There are also limitations associated with maintaining populations of amphibians in the zoo and private sectors, and these could potentially undermine the success of conservation breeding programmes and reintroductions. We recommend that species that have been assessed as high priorities for ex situ conservation action are subsequently individually reassessed to determine their suitability for inclusion in conservation breeding programmes. The limitations and risks of maintaining ex situ populations of amphibians need to be considered from the outset and, where possible, mitigated. This should improve programme success rates and ensure that the limited funds dedicated to ex situ amphibian conservation are allocated to projects which have the greatest chance of success.

SummaryThe fungus Batrachochytrium dendrobatidis (Bd) causes chytridiomycosis, a lethal epizootic disease of amphibians. Rapid identification of the pathogen and biosecurity is essential to prevent its spread, but current laboratory‐based tests are time‐consuming and require specialist equipment. Here, we describe the generation of an IgM monoclonal antibody (mAb), 5C4, specific to Bd as well as the related salamander and newt pathogen Batrachochytrium salamandrivorans (Bsal). The mAb, which binds to a glycoprotein antigen present on the surface of zoospores, sporangia and zoosporangia, was used to develop a lateral‐flow assay (LFA) for rapid (15 min) detection of the pathogens. The LFA detects known lineages of Bd and also Bsal, as well as the closely related fungus Homolaphlyctis polyrhiza, but does not detect a wide range of related and unrelated fungi and oomycetes likely to be present in amphibian habitats. When combined with a simple swabbing procedure, the LFA was 100% accurate in detecting the water‐soluble 5C4 antigen present in skin, foot and pelvic samples from frogs, newts and salamanders naturally infected with Bd or Bsal. Our results demonstrate the potential of the portable LFA as a rapid qualitative assay for tracking these amphibian pathogens and as an adjunct test to nucleic acid‐based detection methods.