Genetic mechanisms and biological processes underlying host response to ophidiomycosis (snake fungal disease) inferred from tissue‐specific transcriptome analyses

• Published in: Molecular ecology Vol. 33; no. 2; pp. e17210 - n/a
• Main Authors: Mathur, Samarth, Haynes, Ellen, Allender, Matthew C., Gibbs, H. Lisle
• Format: Journal Article
• Language: English
• Published: England Blackwell Publishing Ltd 01.01.2024
• Subjects: Amphibians; Animal diseases; Animals; Biological activity; Biological Phenomena; challenge study; Chytridiomycosis; Crotalus; Crotalus viridis; Dermatomycoses - genetics; Dermatomycoses - microbiology; Dermatomycoses - veterinary; Disease; emerging wildlife disease; Experimental infection; Fungal diseases; Fungi; Gene expression; Gene Expression Profiling; High temperature; Infections; Infectious diseases; Low temperature; Natural populations; Ophidiomyces ophidiicola; prairie rattlesnakes; Skin; snake fungal disease; Snakes; Temperature; Temperature effects; Transcriptomes; transcriptomics; Venomous Snakes; White-nose syndrome; Wildlife; challenge study; emerging wildlife disease; prairie rattlesnakes; transcriptomics; snake fungal disease; Ophidiomyces ophidiicola
• ISSN: 0962-1083; 1365-294X
• DOI: 10.1111/mec.17210

Emerging infectious diseases in wildlife species caused by pathogenic fungi are of growing concern, yet crucial knowledge gaps remain for diseases with potentially large impacts. For example, there is detailed knowledge about host pathology and mechanisms underlying response for chytridiomycosis in amphibians and white‐nose syndrome in bats, but such information is lacking for other more recently described fungal infections. One such disease is ophidiomycosis, caused by the fungus Ophidiomyces ophidiicola, which has been identified in many species of snakes, yet the biological mechanisms and molecular changes occurring during infection are unknown. To gain this information, we performed a controlled experimental infection in captive Prairie rattlesnakes (Crotalus viridis) with O. ophidiicola at two different temperatures: 20 and 26°C. We then compared liver, kidney, and skin transcriptomes to assess tissue‐specific genetic responses to O. ophidiicola infection. Given previous histopathological studies and the fact that snakes are ectotherms, we expected highest fungal activity on skin and a significant impact of temperature on host response. Although we found fungal activity to be localized on skin, most of the differential gene expression occurred in internal tissues. Infected snakes at the lower temperature had the highest host mortality whereas two‐thirds of the infected snakes at the higher temperature survived. Our results suggest that ophidiomycosis is likely a systemic disease with long‐term effects on host response. Our analysis also identified candidate protein coding genes that are potentially involved in host response, providing genetic tools for studies of host response to ophidiomycosis in natural populations.