Cargando…
Gut microbiota of the threatened takahē: biogeographic patterns and conservation implications
BACKGROUND: The Aotearoa New Zealand takahē (Porphyrio hochstetteri), once thought to be extinct, is a nationally threatened flightless rail under intensive conservation management. While there has been previous research into disease-related microbes in takahē, little is known about the microbes pre...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8790836/ https://www.ncbi.nlm.nih.gov/pubmed/35078539 http://dx.doi.org/10.1186/s42523-021-00158-5 |
_version_ | 1784640102479167488 |
---|---|
author | West, Annie G. DeLaunay, Anne Marsh, Phil Perry, Elena K. Jolly, Megan Gartrell, Brett D. Pas, An Digby, Andrew Taylor, Michael W. |
author_facet | West, Annie G. DeLaunay, Anne Marsh, Phil Perry, Elena K. Jolly, Megan Gartrell, Brett D. Pas, An Digby, Andrew Taylor, Michael W. |
author_sort | West, Annie G. |
collection | PubMed |
description | BACKGROUND: The Aotearoa New Zealand takahē (Porphyrio hochstetteri), once thought to be extinct, is a nationally threatened flightless rail under intensive conservation management. While there has been previous research into disease-related microbes in takahē, little is known about the microbes present in the gastrointestinal tract. Given the importance of gut-associated microbes to herbivore nutrition and immunity, knowledge of these communities is likely to be of considerable conservation value. Here we examined the gut microbiotas of 57 takahē at eight separate locations across Aotearoa New Zealand. RESULTS: Faecal samples, taken as a proxy for the hindgut bacterial community, were subjected to 16S rRNA gene amplicon sequencing using Illumina MiSeq. Phylogenetic analysis of > 2200 amplicon sequence variants (ASVs) revealed nine main bacterial phyla (Acidobacteriota, Actinobacteriota, Bacteroidota, Campilobacterota, Firmicutes, Fusobacteriota, Planctomycetota, Proteobacteria, and Verrucomicrobiota) that accounted for the majority of sequence reads. Location was a significant effect (p value < 0.001, 9999 permutations) that accounted for 32% of the observed microbiota variation. One ASV, classified as Lactobacillus aviarius, was present in all samples at an average relative abundance of 17% (SD = 23.20). There was strong evidence (p = 0.002) for a difference in the abundance of the genus Lactobacillus between locations. A common commensal bacterium previously described in takahē, Campylobacter spp., was also detected in most faecal samples. CONCLUSIONS: Location plays a pivotal role in the observed variation among takahē gut bacterial communities and is potentially due to factors such as supplemental feeding and medical treatment experienced by birds housed in captivity at one of the eight sampled sites. These data present a first glimpse of the previously unexplored takahē gut microbiota and provide a baseline for future microbiological studies and conservation efforts. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s42523-021-00158-5. |
format | Online Article Text |
id | pubmed-8790836 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-87908362022-01-26 Gut microbiota of the threatened takahē: biogeographic patterns and conservation implications West, Annie G. DeLaunay, Anne Marsh, Phil Perry, Elena K. Jolly, Megan Gartrell, Brett D. Pas, An Digby, Andrew Taylor, Michael W. Anim Microbiome Research Article BACKGROUND: The Aotearoa New Zealand takahē (Porphyrio hochstetteri), once thought to be extinct, is a nationally threatened flightless rail under intensive conservation management. While there has been previous research into disease-related microbes in takahē, little is known about the microbes present in the gastrointestinal tract. Given the importance of gut-associated microbes to herbivore nutrition and immunity, knowledge of these communities is likely to be of considerable conservation value. Here we examined the gut microbiotas of 57 takahē at eight separate locations across Aotearoa New Zealand. RESULTS: Faecal samples, taken as a proxy for the hindgut bacterial community, were subjected to 16S rRNA gene amplicon sequencing using Illumina MiSeq. Phylogenetic analysis of > 2200 amplicon sequence variants (ASVs) revealed nine main bacterial phyla (Acidobacteriota, Actinobacteriota, Bacteroidota, Campilobacterota, Firmicutes, Fusobacteriota, Planctomycetota, Proteobacteria, and Verrucomicrobiota) that accounted for the majority of sequence reads. Location was a significant effect (p value < 0.001, 9999 permutations) that accounted for 32% of the observed microbiota variation. One ASV, classified as Lactobacillus aviarius, was present in all samples at an average relative abundance of 17% (SD = 23.20). There was strong evidence (p = 0.002) for a difference in the abundance of the genus Lactobacillus between locations. A common commensal bacterium previously described in takahē, Campylobacter spp., was also detected in most faecal samples. CONCLUSIONS: Location plays a pivotal role in the observed variation among takahē gut bacterial communities and is potentially due to factors such as supplemental feeding and medical treatment experienced by birds housed in captivity at one of the eight sampled sites. These data present a first glimpse of the previously unexplored takahē gut microbiota and provide a baseline for future microbiological studies and conservation efforts. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s42523-021-00158-5. BioMed Central 2022-01-25 /pmc/articles/PMC8790836/ /pubmed/35078539 http://dx.doi.org/10.1186/s42523-021-00158-5 Text en © The Author(s) 2022 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 West, Annie G. DeLaunay, Anne Marsh, Phil Perry, Elena K. Jolly, Megan Gartrell, Brett D. Pas, An Digby, Andrew Taylor, Michael W. Gut microbiota of the threatened takahē: biogeographic patterns and conservation implications |
title | Gut microbiota of the threatened takahē: biogeographic patterns and conservation implications |
title_full | Gut microbiota of the threatened takahē: biogeographic patterns and conservation implications |
title_fullStr | Gut microbiota of the threatened takahē: biogeographic patterns and conservation implications |
title_full_unstemmed | Gut microbiota of the threatened takahē: biogeographic patterns and conservation implications |
title_short | Gut microbiota of the threatened takahē: biogeographic patterns and conservation implications |
title_sort | gut microbiota of the threatened takahē: biogeographic patterns and conservation implications |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8790836/ https://www.ncbi.nlm.nih.gov/pubmed/35078539 http://dx.doi.org/10.1186/s42523-021-00158-5 |
work_keys_str_mv | AT westannieg gutmicrobiotaofthethreatenedtakahebiogeographicpatternsandconservationimplications AT delaunayanne gutmicrobiotaofthethreatenedtakahebiogeographicpatternsandconservationimplications AT marshphil gutmicrobiotaofthethreatenedtakahebiogeographicpatternsandconservationimplications AT perryelenak gutmicrobiotaofthethreatenedtakahebiogeographicpatternsandconservationimplications AT jollymegan gutmicrobiotaofthethreatenedtakahebiogeographicpatternsandconservationimplications AT gartrellbrettd gutmicrobiotaofthethreatenedtakahebiogeographicpatternsandconservationimplications AT pasan gutmicrobiotaofthethreatenedtakahebiogeographicpatternsandconservationimplications AT digbyandrew gutmicrobiotaofthethreatenedtakahebiogeographicpatternsandconservationimplications AT taylormichaelw gutmicrobiotaofthethreatenedtakahebiogeographicpatternsandconservationimplications |