Cargando…

Inhibitory Bacterial Diversity and Mucosome Function Differentiate Susceptibility of Appalachian Salamanders to Chytrid Fungal Infection

Mucosal defenses are crucial in animals for protection against pathogens and predators. Host defense peptides (antimicrobial peptides, AMPs) as well as skin-associated microbes are key components of mucosal immunity, particularly in amphibians. We integrate microbiology, molecular biology, network-t...

Descripción completa

Detalles Bibliográficos
Autores principales: Jiménez, Randall R., Carfagno, Amy, Linhoff, Luke, Gratwicke, Brian, Woodhams, Douglas C., Chafran, Liana Soares, Bletz, Molly C., Bishop, Barney, Muletz-Wolz, Carly R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9040618/
https://www.ncbi.nlm.nih.gov/pubmed/35348389
http://dx.doi.org/10.1128/aem.01818-21
_version_ 1784694371523756032
author Jiménez, Randall R.
Carfagno, Amy
Linhoff, Luke
Gratwicke, Brian
Woodhams, Douglas C.
Chafran, Liana Soares
Bletz, Molly C.
Bishop, Barney
Muletz-Wolz, Carly R.
author_facet Jiménez, Randall R.
Carfagno, Amy
Linhoff, Luke
Gratwicke, Brian
Woodhams, Douglas C.
Chafran, Liana Soares
Bletz, Molly C.
Bishop, Barney
Muletz-Wolz, Carly R.
author_sort Jiménez, Randall R.
collection PubMed
description Mucosal defenses are crucial in animals for protection against pathogens and predators. Host defense peptides (antimicrobial peptides, AMPs) as well as skin-associated microbes are key components of mucosal immunity, particularly in amphibians. We integrate microbiology, molecular biology, network-thinking, and proteomics to understand how host and microbially derived products on amphibian skin (referred to as the mucosome) serve as pathogen defenses. We studied defense mechanisms against chytrid pathogens, Batrachochytrium dendrobatidis (Bd) and B. salamandrivorans (Bsal), in four salamander species with different Batrachochytrium susceptibilities. Bd infection was quantified using qPCR, mucosome function (i.e., ability to kill Bd or Bsal zoospores in vitro), skin bacterial communities using 16S rRNA gene amplicon sequencing, and the role of Bd-inhibitory bacteria in microbial networks across all species. We explored the presence of candidate-AMPs in eastern newts and red-backed salamanders. Eastern newts had the highest Bd prevalence and mucosome function, while red-back salamanders had the lowest Bd prevalence and mucosome function, and two-lined salamanders and seal salamanders were intermediates. Salamanders with highest Bd infection intensity showed greater mucosome function. Bd infection prevalence significantly decreased as putative Bd-inhibitory bacterial richness and relative abundance increased on hosts. In co-occurrence networks, some putative Bd-inhibitory bacteria were found as hub-taxa, with red-backs having the highest proportion of protective hubs and positive associations related to putative Bd-inhibitory hub bacteria. We found more AMP candidates on salamanders with lower Bd susceptibility. These findings suggest that salamanders possess distinct innate mechanisms that affect chytrid fungi. IMPORTANCE How host mucosal defenses interact, and influence disease outcome is critical in understanding host defenses against pathogens. A more detailed understanding is needed of the interactions between the host and the functioning of its mucosal defenses in pathogen defense. This study investigates the variability of chytrid susceptibility in salamanders and the innate defenses each species possesses to mediate pathogens, thus advancing the knowledge toward a deeper understanding of the microbial ecology of skin-associated bacteria and contributing to the development of bioaugmentation strategies to mediate pathogen infection and disease. This study improves the understanding of complex immune defense mechanisms in salamanders and highlights the potential role of the mucosome to reduce the probability of Bd disease development and that putative protective bacteria may reduce likelihood of Bd infecting skin.
format Online
Article
Text
id pubmed-9040618
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-90406182022-09-29 Inhibitory Bacterial Diversity and Mucosome Function Differentiate Susceptibility of Appalachian Salamanders to Chytrid Fungal Infection Jiménez, Randall R. Carfagno, Amy Linhoff, Luke Gratwicke, Brian Woodhams, Douglas C. Chafran, Liana Soares Bletz, Molly C. Bishop, Barney Muletz-Wolz, Carly R. Appl Environ Microbiol Environmental Microbiology Mucosal defenses are crucial in animals for protection against pathogens and predators. Host defense peptides (antimicrobial peptides, AMPs) as well as skin-associated microbes are key components of mucosal immunity, particularly in amphibians. We integrate microbiology, molecular biology, network-thinking, and proteomics to understand how host and microbially derived products on amphibian skin (referred to as the mucosome) serve as pathogen defenses. We studied defense mechanisms against chytrid pathogens, Batrachochytrium dendrobatidis (Bd) and B. salamandrivorans (Bsal), in four salamander species with different Batrachochytrium susceptibilities. Bd infection was quantified using qPCR, mucosome function (i.e., ability to kill Bd or Bsal zoospores in vitro), skin bacterial communities using 16S rRNA gene amplicon sequencing, and the role of Bd-inhibitory bacteria in microbial networks across all species. We explored the presence of candidate-AMPs in eastern newts and red-backed salamanders. Eastern newts had the highest Bd prevalence and mucosome function, while red-back salamanders had the lowest Bd prevalence and mucosome function, and two-lined salamanders and seal salamanders were intermediates. Salamanders with highest Bd infection intensity showed greater mucosome function. Bd infection prevalence significantly decreased as putative Bd-inhibitory bacterial richness and relative abundance increased on hosts. In co-occurrence networks, some putative Bd-inhibitory bacteria were found as hub-taxa, with red-backs having the highest proportion of protective hubs and positive associations related to putative Bd-inhibitory hub bacteria. We found more AMP candidates on salamanders with lower Bd susceptibility. These findings suggest that salamanders possess distinct innate mechanisms that affect chytrid fungi. IMPORTANCE How host mucosal defenses interact, and influence disease outcome is critical in understanding host defenses against pathogens. A more detailed understanding is needed of the interactions between the host and the functioning of its mucosal defenses in pathogen defense. This study investigates the variability of chytrid susceptibility in salamanders and the innate defenses each species possesses to mediate pathogens, thus advancing the knowledge toward a deeper understanding of the microbial ecology of skin-associated bacteria and contributing to the development of bioaugmentation strategies to mediate pathogen infection and disease. This study improves the understanding of complex immune defense mechanisms in salamanders and highlights the potential role of the mucosome to reduce the probability of Bd disease development and that putative protective bacteria may reduce likelihood of Bd infecting skin. American Society for Microbiology 2022-03-29 /pmc/articles/PMC9040618/ /pubmed/35348389 http://dx.doi.org/10.1128/aem.01818-21 Text en Copyright © 2022 Jiménez et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Environmental Microbiology
Jiménez, Randall R.
Carfagno, Amy
Linhoff, Luke
Gratwicke, Brian
Woodhams, Douglas C.
Chafran, Liana Soares
Bletz, Molly C.
Bishop, Barney
Muletz-Wolz, Carly R.
Inhibitory Bacterial Diversity and Mucosome Function Differentiate Susceptibility of Appalachian Salamanders to Chytrid Fungal Infection
title Inhibitory Bacterial Diversity and Mucosome Function Differentiate Susceptibility of Appalachian Salamanders to Chytrid Fungal Infection
title_full Inhibitory Bacterial Diversity and Mucosome Function Differentiate Susceptibility of Appalachian Salamanders to Chytrid Fungal Infection
title_fullStr Inhibitory Bacterial Diversity and Mucosome Function Differentiate Susceptibility of Appalachian Salamanders to Chytrid Fungal Infection
title_full_unstemmed Inhibitory Bacterial Diversity and Mucosome Function Differentiate Susceptibility of Appalachian Salamanders to Chytrid Fungal Infection
title_short Inhibitory Bacterial Diversity and Mucosome Function Differentiate Susceptibility of Appalachian Salamanders to Chytrid Fungal Infection
title_sort inhibitory bacterial diversity and mucosome function differentiate susceptibility of appalachian salamanders to chytrid fungal infection
topic Environmental Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9040618/
https://www.ncbi.nlm.nih.gov/pubmed/35348389
http://dx.doi.org/10.1128/aem.01818-21
work_keys_str_mv AT jimenezrandallr inhibitorybacterialdiversityandmucosomefunctiondifferentiatesusceptibilityofappalachiansalamanderstochytridfungalinfection
AT carfagnoamy inhibitorybacterialdiversityandmucosomefunctiondifferentiatesusceptibilityofappalachiansalamanderstochytridfungalinfection
AT linhoffluke inhibitorybacterialdiversityandmucosomefunctiondifferentiatesusceptibilityofappalachiansalamanderstochytridfungalinfection
AT gratwickebrian inhibitorybacterialdiversityandmucosomefunctiondifferentiatesusceptibilityofappalachiansalamanderstochytridfungalinfection
AT woodhamsdouglasc inhibitorybacterialdiversityandmucosomefunctiondifferentiatesusceptibilityofappalachiansalamanderstochytridfungalinfection
AT chafranlianasoares inhibitorybacterialdiversityandmucosomefunctiondifferentiatesusceptibilityofappalachiansalamanderstochytridfungalinfection
AT bletzmollyc inhibitorybacterialdiversityandmucosomefunctiondifferentiatesusceptibilityofappalachiansalamanderstochytridfungalinfection
AT bishopbarney inhibitorybacterialdiversityandmucosomefunctiondifferentiatesusceptibilityofappalachiansalamanderstochytridfungalinfection
AT muletzwolzcarlyr inhibitorybacterialdiversityandmucosomefunctiondifferentiatesusceptibilityofappalachiansalamanderstochytridfungalinfection