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IntroductionBatrachochytrium salamandrivorans(Bsal) poses a major threat to global amphibian biodiversity. It is essential we understandBsaltransmission to develop better-informed management strategies. Infected carcasses are an important source of transmission for several human and wildlife disease systems; however, they have not been examined as sources forBsalexposure. Here, we evaluated whether infected newt carcasses could contribute toBsaltransmission dynamics. MethodsWe cohoused infected carcasses with susceptible newts in two cohousing chamber types (partitioned or non-partitioned) at three timepoints post-mortem ([0,24[, [24,48, [48,72] hrs). The partitioned chamber prevented newt-to-newt contact hence only allowed indirect, waterborne transmission of zoospores. We measured shedding rates of infected carcasses at each post-mortem timepoint and monitored infection status and mortality of susceptible newts which were exposed during cohousing events. ResultsOur results indicate carcasses are capable of transmittingBsalto susceptible newts up to at least 72 hrs post-mortem, even without live newts directly contacting carcasses. All susceptible newts in each chamber type and post-mortem period became infected and >90% experienced disease-induced mortality.Bsalgenomic copies/uL in skin swabs taken from infected carcasses were high, averaging 7.4x105, 8.6x105, and 2.0x106at 24, 48, and 72 hrs post-mortem, respectively. Water samples collected from cohousing chambers averaged 2743Bsalgenomic copies/uL (approximately 1357 zoospores) and did not decline over 72 hrs. DiscussionOur results indicateBsalinfection can occur rapidly between infected carcasses and susceptible aquatic salamanders via indirect and direct transmission pathways, and carcasses may prolong outbreaks by increasing the duration that infected individuals remain infectious. Carcass removal may be a strategy to reduceBsaltransmission and the impacts of outbreaks.
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Environmental DNA ‐based detection of pathogens in trade and captive settings: Best practices and validation for Batrachochytrium salamandrivorans
Abstract Detecting pathogens in the live animal trade is critical for tracking and preventing their movement, introduction and spillover into susceptible fauna. However, the scale of the live animal trade makes individually testing animals infeasible for all but the most economically important taxa. For instance, while the fungal pathogen,Batrachochytrium salamandrivorans(Bsal), threatens amphibian, particularly caudate diversity, in Europe and the Americas, screening even a fraction of the millions of live amphibians imported into the United States, alone, is impractically laborious and expensive. A promising alternative to individual‐level sampling (e.g. swabbing the skin of salamanders) is to instead collect DNA from the animals' environment (e.g. housing container or water) which allows us to screen a whole group of animals at a time.We used a series of experiments withBsal‐spiked water and substrates and experimentally infected rough‐skinned newts (Taricha granulosa) to determine which methods yield the mostBsalenvironmental DNA (eDNA) and evaluate the capacity of these methods to detectBsal‐infected animals in conditions found in captive settings and trade.We found that filtering water housing infected animals for even an hour can consistently recover detectable levels ofBsaleDNA, that there is little evidence ofBsaleDNA being clumped in housing containers or swamped or inhibited by dirty housing containers, and that eDNA‐based methods achieves an equivalent or higher chance of detectingBsalinfections in a (virtual) population of co‐housed newts with fewer samples than individual swabs.By sampling the genetic materials accumulated from a whole group of animals, eDNA‐based methods are a powerful means of detecting pathogens, such asBsal, in shipments and captive populations. These methods bring routine pathogen surveillance into reach in many more contexts and can thus be an important tool in conservation and disease control.
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- Award ID(s):
- 1754474
- PAR ID:
- 10472205
- Publisher / Repository:
- Wiley-Blackwell
- Date Published:
- Journal Name:
- Methods in Ecology and Evolution
- Volume:
- 14
- Issue:
- 11
- ISSN:
- 2041-210X
- Format(s):
- Medium: X Size: p. 2787-2799
- Size(s):
- p. 2787-2799
- Sponsoring Org:
- National Science Foundation
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