4.7 Article

Panzootic chytrid fungus exploits diverse amphibian host environments through plastic infection strategies

期刊

MOLECULAR ECOLOGY
卷 31, 期 17, 页码 4558-4570

出版社

WILEY
DOI: 10.1111/mec.16601

关键词

Batrachochytrium dendrobatidis; molecular phenotypic plasticity; multihost pathogen evolution; pathogenic fungus; transcriptomic meta-analysis

资金

  1. National Institutes of Health [NIH-5R25GM115298-5]
  2. National Science Foundation [DBI-1523551, IOS-1310036, IOS-2011278]

向作者/读者索取更多资源

This study examines the functional machinery driving the invasion of the pathogen Batrachochytrium dendrobatidis (Bd) in multiple hosts. Through a meta-analysis of Bd gene expression, the researchers identified plastic infection strategies of Bd in hosts with varying disease susceptibility. They also found that certain genes were differentially expressed in hosts with similar infection outcomes. The study provides insights into the eco-evolutionary dynamics of host-pathogen systems.
While some pathogens are limited to single species, others can colonize many hosts, likely contributing to the emergence of novel disease outbreaks. Despite this biodiversity threat, traits associated with host niche expansions are not well understood in multihost pathogens. Here, we aimed to uncover functional machinery driving multihost invasion by focusing on Batrachochytrium dendrobatidis (Bd), a pathogen that infects the skin of hundreds of amphibians worldwide. We performed a meta-analysis of Bd gene expression using data from published infection experiments and newly generated profiles. We analysed Bd transcriptomic landscapes across the skin of 14 host species, reconstructed Bd isolates phylogenetic relationships, and inferred the origin and evolutionary history of differentially expressed genes under a phylogenetic framework comprising other 12 zoosporic fungi. Bd displayed plastic infection strategies when challenged by hosts with different disease susceptibility. Our analyses identified sets of differentially expressed genes under host environments with similar infection outcome. We stressed nutritional immunity and gene silencing as important processes required to overcome challenging skin environments in less susceptible hosts. Overall, Bd genes expressed during amphibian skin exploitation have arisen mainly via gene duplications with great family expansions, increasing the gene copy events previously described for this fungal species. Finally, we provide a comprehensive gene data set that can be used to further examine eco-evolutionary hypotheses for this host-pathogen system. Our study supports the idea that host environments exert contrasting selective pressures, such that gene expression plasticity could be one of the evolutionary keys leading to the success of multihost pathogens.

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