Cargando…

Diversity in growth patterns among strains of the lethal fungal pathogen Batrachochytrium dendrobatidis across extended thermal optima

The thermal sensitivities of organisms regulate a wide range of ecological interactions, including host–parasite dynamics. The effect of temperature on disease ecology can be remarkably complex in disease systems where the hosts are ectothermic and where thermal conditions constrain pathogen reprodu...

Descripción completa

Detalles Bibliográficos
Autores principales: Voyles, Jamie, Johnson, Leah R., Rohr, Jason, Kelly, Rochelle, Barron, Carley, Miller, Delaney, Minster, Josh, Rosenblum, Erica Bree
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487841/
https://www.ncbi.nlm.nih.gov/pubmed/28424893
http://dx.doi.org/10.1007/s00442-017-3866-8
_version_ 1783246530381086720
author Voyles, Jamie
Johnson, Leah R.
Rohr, Jason
Kelly, Rochelle
Barron, Carley
Miller, Delaney
Minster, Josh
Rosenblum, Erica Bree
author_facet Voyles, Jamie
Johnson, Leah R.
Rohr, Jason
Kelly, Rochelle
Barron, Carley
Miller, Delaney
Minster, Josh
Rosenblum, Erica Bree
author_sort Voyles, Jamie
collection PubMed
description The thermal sensitivities of organisms regulate a wide range of ecological interactions, including host–parasite dynamics. The effect of temperature on disease ecology can be remarkably complex in disease systems where the hosts are ectothermic and where thermal conditions constrain pathogen reproductive rates. Amphibian chytridiomycosis, caused by the pathogen Batrachochytrium dendrobatidis (Bd), is a lethal fungal disease that is influenced by temperature. However, recent temperature studies have produced contradictory findings, suggesting that our current understanding of thermal effects on Bd may be incomplete. We investigated how temperature affects three different Bd strains to evaluate diversity in thermal responses. We quantified growth across the entire thermal range of Bd, and beyond the known thermal limits (T (max) and T (min)). Our results show that all Bd strains remained viable and grew following 24 h freeze (−12 °C) and heat shock (28 °C) treatments. Additionally, we found that two Bd strains had higher logistic growth rates (r) and carrying capacities (K) at the upper and lower extremities of the temperature range, and especially in low temperature conditions (2–3 °C). In contrast, a third strain exhibited relatively lower growth rates and carrying capacities at these same thermal extremes. Overall, our results suggest that there is considerable variation among Bd strains in thermal tolerance, and they establish a new thermal sensitivity profile for Bd. More generally, our findings point toward important questions concerning the mechanisms that dictate fungal thermal tolerances and temperature-dependent pathogenesis in other fungal disease systems. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00442-017-3866-8) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5487841
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Springer Berlin Heidelberg
record_format MEDLINE/PubMed
spelling pubmed-54878412017-07-03 Diversity in growth patterns among strains of the lethal fungal pathogen Batrachochytrium dendrobatidis across extended thermal optima Voyles, Jamie Johnson, Leah R. Rohr, Jason Kelly, Rochelle Barron, Carley Miller, Delaney Minster, Josh Rosenblum, Erica Bree Oecologia Physiological Ecology - Original Research The thermal sensitivities of organisms regulate a wide range of ecological interactions, including host–parasite dynamics. The effect of temperature on disease ecology can be remarkably complex in disease systems where the hosts are ectothermic and where thermal conditions constrain pathogen reproductive rates. Amphibian chytridiomycosis, caused by the pathogen Batrachochytrium dendrobatidis (Bd), is a lethal fungal disease that is influenced by temperature. However, recent temperature studies have produced contradictory findings, suggesting that our current understanding of thermal effects on Bd may be incomplete. We investigated how temperature affects three different Bd strains to evaluate diversity in thermal responses. We quantified growth across the entire thermal range of Bd, and beyond the known thermal limits (T (max) and T (min)). Our results show that all Bd strains remained viable and grew following 24 h freeze (−12 °C) and heat shock (28 °C) treatments. Additionally, we found that two Bd strains had higher logistic growth rates (r) and carrying capacities (K) at the upper and lower extremities of the temperature range, and especially in low temperature conditions (2–3 °C). In contrast, a third strain exhibited relatively lower growth rates and carrying capacities at these same thermal extremes. Overall, our results suggest that there is considerable variation among Bd strains in thermal tolerance, and they establish a new thermal sensitivity profile for Bd. More generally, our findings point toward important questions concerning the mechanisms that dictate fungal thermal tolerances and temperature-dependent pathogenesis in other fungal disease systems. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00442-017-3866-8) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2017-04-19 2017 /pmc/articles/PMC5487841/ /pubmed/28424893 http://dx.doi.org/10.1007/s00442-017-3866-8 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Physiological Ecology - Original Research
Voyles, Jamie
Johnson, Leah R.
Rohr, Jason
Kelly, Rochelle
Barron, Carley
Miller, Delaney
Minster, Josh
Rosenblum, Erica Bree
Diversity in growth patterns among strains of the lethal fungal pathogen Batrachochytrium dendrobatidis across extended thermal optima
title Diversity in growth patterns among strains of the lethal fungal pathogen Batrachochytrium dendrobatidis across extended thermal optima
title_full Diversity in growth patterns among strains of the lethal fungal pathogen Batrachochytrium dendrobatidis across extended thermal optima
title_fullStr Diversity in growth patterns among strains of the lethal fungal pathogen Batrachochytrium dendrobatidis across extended thermal optima
title_full_unstemmed Diversity in growth patterns among strains of the lethal fungal pathogen Batrachochytrium dendrobatidis across extended thermal optima
title_short Diversity in growth patterns among strains of the lethal fungal pathogen Batrachochytrium dendrobatidis across extended thermal optima
title_sort diversity in growth patterns among strains of the lethal fungal pathogen batrachochytrium dendrobatidis across extended thermal optima
topic Physiological Ecology - Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487841/
https://www.ncbi.nlm.nih.gov/pubmed/28424893
http://dx.doi.org/10.1007/s00442-017-3866-8
work_keys_str_mv AT voylesjamie diversityingrowthpatternsamongstrainsofthelethalfungalpathogenbatrachochytriumdendrobatidisacrossextendedthermaloptima
AT johnsonleahr diversityingrowthpatternsamongstrainsofthelethalfungalpathogenbatrachochytriumdendrobatidisacrossextendedthermaloptima
AT rohrjason diversityingrowthpatternsamongstrainsofthelethalfungalpathogenbatrachochytriumdendrobatidisacrossextendedthermaloptima
AT kellyrochelle diversityingrowthpatternsamongstrainsofthelethalfungalpathogenbatrachochytriumdendrobatidisacrossextendedthermaloptima
AT barroncarley diversityingrowthpatternsamongstrainsofthelethalfungalpathogenbatrachochytriumdendrobatidisacrossextendedthermaloptima
AT millerdelaney diversityingrowthpatternsamongstrainsofthelethalfungalpathogenbatrachochytriumdendrobatidisacrossextendedthermaloptima
AT minsterjosh diversityingrowthpatternsamongstrainsofthelethalfungalpathogenbatrachochytriumdendrobatidisacrossextendedthermaloptima
AT rosenblumericabree diversityingrowthpatternsamongstrainsofthelethalfungalpathogenbatrachochytriumdendrobatidisacrossextendedthermaloptima