Alexandra Alexiev, Tina Melie, Rachel Martindale, Cameron Delacey, C. Alisha Quandt, Valerie J. McKenzie
{"title":"Mr. Toad's wild fungi: Fungal isolate diversity on Colorado boreal toads and their capacity for pathogen inhibition","authors":"Alexandra Alexiev, Tina Melie, Rachel Martindale, Cameron Delacey, C. Alisha Quandt, Valerie J. McKenzie","doi":"10.1016/j.funeco.2023.101297","DOIUrl":null,"url":null,"abstract":"<div><p>The amphibian skin pathogen <span><em>Batrachochytrium dendrobatidis</em></span> (<em>Bd</em>) has caused an ongoing biodiversity crisis, including in the locally endangered Colorado boreal toad (<span><em>Anaxyrus</em><em> boreas</em></span>). Although researchers have investigated the bacteria living on amphibian skin and how they interact with <em>Bd</em><span>, there is less information about fungal community members. This study describes (1) the diversity of culturable fungi from boreal toad skin, (2) which subset of these isolates is </span><em>Bd</em>-inhibitory, and (3) how <em>Bd</em><span><span> affects these isolates' growth and morphology. Most isolates were from the orders Capnodiales, </span>Helotiales<span>, and Pleosporales. Of 16 isolates tested for </span></span><em>Bd</em>-inhibition, two from the genus <em>Neobulgaria</em> and three from <em>Pseudeurotium</em> inhibited <em>Bd</em><span>. Fungal growth in co-culture with </span><em>Bd</em> varied with weak statistical support for <em>Neobulgaria</em> sp. (isolate BTF_36) and cf <em>Psychrophila</em><span> (isolate BTF_60) (p-values = 0.076 and 0.092, respectively). Fungal morphology remained unchanged in co-culture with </span><em>Bd</em>, however, these results could be attributed to low replication per isolate. Nonetheless, two fungal isolates’ growth may have been affected by <em>Bd</em>, implying that fungal growth changes in <em>Bd</em> co-culture could be a variable worth measuring in the future (with higher replication). These findings add to the sparse but growing literature on amphibian-associated fungi and suggest further study may uncover the relevance of fungi to amphibian health and <em>Bd</em> infection.</p></div>","PeriodicalId":55136,"journal":{"name":"Fungal Ecology","volume":"66 ","pages":"Article 101297"},"PeriodicalIF":1.9000,"publicationDate":"2023-11-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fungal Ecology","FirstCategoryId":"93","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1754504823000740","RegionNum":3,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ECOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
The amphibian skin pathogen Batrachochytrium dendrobatidis (Bd) has caused an ongoing biodiversity crisis, including in the locally endangered Colorado boreal toad (Anaxyrus boreas). Although researchers have investigated the bacteria living on amphibian skin and how they interact with Bd, there is less information about fungal community members. This study describes (1) the diversity of culturable fungi from boreal toad skin, (2) which subset of these isolates is Bd-inhibitory, and (3) how Bd affects these isolates' growth and morphology. Most isolates were from the orders Capnodiales, Helotiales, and Pleosporales. Of 16 isolates tested for Bd-inhibition, two from the genus Neobulgaria and three from Pseudeurotium inhibited Bd. Fungal growth in co-culture with Bd varied with weak statistical support for Neobulgaria sp. (isolate BTF_36) and cf Psychrophila (isolate BTF_60) (p-values = 0.076 and 0.092, respectively). Fungal morphology remained unchanged in co-culture with Bd, however, these results could be attributed to low replication per isolate. Nonetheless, two fungal isolates’ growth may have been affected by Bd, implying that fungal growth changes in Bd co-culture could be a variable worth measuring in the future (with higher replication). These findings add to the sparse but growing literature on amphibian-associated fungi and suggest further study may uncover the relevance of fungi to amphibian health and Bd infection.
期刊介绍:
Fungal Ecology publishes investigations into all aspects of fungal ecology, including the following (not exclusive): population dynamics; adaptation; evolution; role in ecosystem functioning, nutrient cycling, decomposition, carbon allocation; ecophysiology; intra- and inter-specific mycelial interactions, fungus-plant (pathogens, mycorrhizas, lichens, endophytes), fungus-invertebrate and fungus-microbe interaction; genomics and (evolutionary) genetics; conservation and biodiversity; remote sensing; bioremediation and biodegradation; quantitative and computational aspects - modelling, indicators, complexity, informatics. The usual prerequisites for publication will be originality, clarity, and significance as relevant to a better understanding of the ecology of fungi.