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Early life skin microbial trajectory as a function of vertical and environmental transmission in Bornean foam-nesting frogs
BACKGROUND: The amphibian skin microbiome is an important mediator of host health and serves as a potential source of undiscovered scientifically significant compounds. However, the underlying modalities of how amphibian hosts obtain their initial skin-associated microbiome remains unclear. Here, we...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8686334/ https://www.ncbi.nlm.nih.gov/pubmed/34930504 http://dx.doi.org/10.1186/s42523-021-00147-8 |
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author | McGrath-Blaser, Sarah Steffen, Morgan Grafe, T. Ulmar Torres-Sánchez, María McLeod, David S. Muletz-Wolz, Carly R. |
author_facet | McGrath-Blaser, Sarah Steffen, Morgan Grafe, T. Ulmar Torres-Sánchez, María McLeod, David S. Muletz-Wolz, Carly R. |
author_sort | McGrath-Blaser, Sarah |
collection | PubMed |
description | BACKGROUND: The amphibian skin microbiome is an important mediator of host health and serves as a potential source of undiscovered scientifically significant compounds. However, the underlying modalities of how amphibian hosts obtain their initial skin-associated microbiome remains unclear. Here, we explore microbial transmission patterns in foam-nest breeding tree frogs from Southeast Asia (Genus: Polypedates) whose specialized breeding strategy allows for better delineation between vertically and environmentally derived microbes. To facilitate this, we analyzed samples associated with adult frog pairs taken after mating—including adults of each sex, their foam nests, environments, and tadpoles before and after environmental interaction—for the bacterial communities using DNA metabarcoding data (16S rRNA). Samples were collected from frogs in-situ in Brunei, Borneo, a previously unsampled region for amphibian-related microbial diversity. RESULTS: Adult frogs differed in skin bacterial communities among species, but tadpoles did not differ among species. Foam nests had varying bacterial community composition, most notably in the nests’ moist interior. Nest interior bacterial communities were discrete for each nest and overall displayed a narrower diversity compared to the nest exteriors. Tadpoles sampled directly from the foam nest displayed a bacterial composition less like the nest interior and more similar to that of the adults and nest exterior. After one week of pond water interaction the tadpole skin microbiome shifted towards the tadpole skin and pond water microbial communities being more tightly coupled than between tadpoles and the internal nest environment, but not to the extent that the skin microbiome mirrored the pond bacterial community. CONCLUSIONS: Both vertical influence and environmental interaction play a role in shaping the tadpole cutaneous microbiome. Interestingly, the interior of the foam nest had a distinct bacterial community from the tadpoles suggesting a limited environmental effect on tadpole cutaneous bacterial selection at initial stages of life. The shift in the tadpole microbiome after environmental interaction indicates an interplay between underlying host and ecological mechanisms that drive community formation. This survey serves as a baseline for further research into the ecology of microbial transmission in aquatic animals. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s42523-021-00147-8. |
format | Online Article Text |
id | pubmed-8686334 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-86863342021-12-21 Early life skin microbial trajectory as a function of vertical and environmental transmission in Bornean foam-nesting frogs McGrath-Blaser, Sarah Steffen, Morgan Grafe, T. Ulmar Torres-Sánchez, María McLeod, David S. Muletz-Wolz, Carly R. Anim Microbiome Research Article BACKGROUND: The amphibian skin microbiome is an important mediator of host health and serves as a potential source of undiscovered scientifically significant compounds. However, the underlying modalities of how amphibian hosts obtain their initial skin-associated microbiome remains unclear. Here, we explore microbial transmission patterns in foam-nest breeding tree frogs from Southeast Asia (Genus: Polypedates) whose specialized breeding strategy allows for better delineation between vertically and environmentally derived microbes. To facilitate this, we analyzed samples associated with adult frog pairs taken after mating—including adults of each sex, their foam nests, environments, and tadpoles before and after environmental interaction—for the bacterial communities using DNA metabarcoding data (16S rRNA). Samples were collected from frogs in-situ in Brunei, Borneo, a previously unsampled region for amphibian-related microbial diversity. RESULTS: Adult frogs differed in skin bacterial communities among species, but tadpoles did not differ among species. Foam nests had varying bacterial community composition, most notably in the nests’ moist interior. Nest interior bacterial communities were discrete for each nest and overall displayed a narrower diversity compared to the nest exteriors. Tadpoles sampled directly from the foam nest displayed a bacterial composition less like the nest interior and more similar to that of the adults and nest exterior. After one week of pond water interaction the tadpole skin microbiome shifted towards the tadpole skin and pond water microbial communities being more tightly coupled than between tadpoles and the internal nest environment, but not to the extent that the skin microbiome mirrored the pond bacterial community. CONCLUSIONS: Both vertical influence and environmental interaction play a role in shaping the tadpole cutaneous microbiome. Interestingly, the interior of the foam nest had a distinct bacterial community from the tadpoles suggesting a limited environmental effect on tadpole cutaneous bacterial selection at initial stages of life. The shift in the tadpole microbiome after environmental interaction indicates an interplay between underlying host and ecological mechanisms that drive community formation. This survey serves as a baseline for further research into the ecology of microbial transmission in aquatic animals. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s42523-021-00147-8. BioMed Central 2021-12-20 /pmc/articles/PMC8686334/ /pubmed/34930504 http://dx.doi.org/10.1186/s42523-021-00147-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article McGrath-Blaser, Sarah Steffen, Morgan Grafe, T. Ulmar Torres-Sánchez, María McLeod, David S. Muletz-Wolz, Carly R. Early life skin microbial trajectory as a function of vertical and environmental transmission in Bornean foam-nesting frogs |
title | Early life skin microbial trajectory as a function of vertical and environmental transmission in Bornean foam-nesting frogs |
title_full | Early life skin microbial trajectory as a function of vertical and environmental transmission in Bornean foam-nesting frogs |
title_fullStr | Early life skin microbial trajectory as a function of vertical and environmental transmission in Bornean foam-nesting frogs |
title_full_unstemmed | Early life skin microbial trajectory as a function of vertical and environmental transmission in Bornean foam-nesting frogs |
title_short | Early life skin microbial trajectory as a function of vertical and environmental transmission in Bornean foam-nesting frogs |
title_sort | early life skin microbial trajectory as a function of vertical and environmental transmission in bornean foam-nesting frogs |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8686334/ https://www.ncbi.nlm.nih.gov/pubmed/34930504 http://dx.doi.org/10.1186/s42523-021-00147-8 |
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