Cargando…
The fecal bacterial microbiome of the Kuhl’s pipistrelle bat (Pipistrellus kuhlii) reflects landscape anthropogenic pressure
BACKGROUND: Anthropogenic disturbance has the potential to negatively affect wildlife health by altering food availability and diet composition, increasing the exposure to agrochemicals, and intensifying the contact with humans, domestic animals, and their pathogens. However, the impact of these fac...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9898988/ https://www.ncbi.nlm.nih.gov/pubmed/36739423 http://dx.doi.org/10.1186/s42523-023-00229-9 |
_version_ | 1784882548041580544 |
---|---|
author | Lobato-Bailón, Lourdes García-Ulloa, Manuel Santos, Andrés Guixé, David Camprodon, Jordi Florensa-Rius, Xavier Molleda, Raúl Manzano, Robert P. Ribas, Maria Espunyes, Johan Dias-Alves, Andrea Marco, Ignasi Migura-Garcia, Lourdes Martínez-Urtaza, Jaime Cabezón, Oscar |
author_facet | Lobato-Bailón, Lourdes García-Ulloa, Manuel Santos, Andrés Guixé, David Camprodon, Jordi Florensa-Rius, Xavier Molleda, Raúl Manzano, Robert P. Ribas, Maria Espunyes, Johan Dias-Alves, Andrea Marco, Ignasi Migura-Garcia, Lourdes Martínez-Urtaza, Jaime Cabezón, Oscar |
author_sort | Lobato-Bailón, Lourdes |
collection | PubMed |
description | BACKGROUND: Anthropogenic disturbance has the potential to negatively affect wildlife health by altering food availability and diet composition, increasing the exposure to agrochemicals, and intensifying the contact with humans, domestic animals, and their pathogens. However, the impact of these factors on the fecal microbiome composition of wildlife hosts and its link to host health modulation remains barely explored. Here we investigated the composition of the fecal bacterial microbiome of the insectivorous bat Kuhl’s pipistrelle (Pipistrellus kuhlii) dwelling in four environmental contexts with different levels of anthropogenic pressure. We analyzed their microbiome composition, structure and diversity through full-length 16S rRNA metabarcoding using the nanopore long-read sequencer MinION™. We hypothesized that the bacterial community structure of fecal samples would vary across the different scenarios, showing a decreased diversity and richness in samples from disturbed ecosystems. RESULTS: The fecal microbiomes of 31 bats from 4 scenarios were sequenced. A total of 4,829,302 reads were obtained with a taxonomic assignment percentage of 99.9% at genus level. Most abundant genera across all scenarios were Enterococcus, Escherichia/Shigella, Bacillus and Enterobacter. Alpha diversity varied significantly between the four scenarios (p < 0.05), showing the lowest Shannon index in bats from urban and intensive agriculture landscapes, while the highest alpha diversity value was found in near pristine landscapes. Beta diversity obtained by Bray–Curtis distance showed weak statistical differentiation of bacterial taxonomic profiles among scenarios. Furthermore, core community analysis showed that 1,293 genera were shared among localities. Differential abundance analyses showed that the highest differentially abundant taxa were found in near pristine landscapes, with the exception of the family Alcaligenaceae, which was also overrepresented in urban and intensive agriculture landscapes. CONCLUSIONS: This study suggests that near pristine and undisturbed landscapes could promote a more resilient gut microbiome in wild populations of P. kuhlii. These results highlight the potential of the fecal microbiome as a non-invasive bioindicator to assess insectivorous bats’ health and as a key element of landscape conservation strategies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s42523-023-00229-9. |
format | Online Article Text |
id | pubmed-9898988 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-98989882023-02-05 The fecal bacterial microbiome of the Kuhl’s pipistrelle bat (Pipistrellus kuhlii) reflects landscape anthropogenic pressure Lobato-Bailón, Lourdes García-Ulloa, Manuel Santos, Andrés Guixé, David Camprodon, Jordi Florensa-Rius, Xavier Molleda, Raúl Manzano, Robert P. Ribas, Maria Espunyes, Johan Dias-Alves, Andrea Marco, Ignasi Migura-Garcia, Lourdes Martínez-Urtaza, Jaime Cabezón, Oscar Anim Microbiome Research BACKGROUND: Anthropogenic disturbance has the potential to negatively affect wildlife health by altering food availability and diet composition, increasing the exposure to agrochemicals, and intensifying the contact with humans, domestic animals, and their pathogens. However, the impact of these factors on the fecal microbiome composition of wildlife hosts and its link to host health modulation remains barely explored. Here we investigated the composition of the fecal bacterial microbiome of the insectivorous bat Kuhl’s pipistrelle (Pipistrellus kuhlii) dwelling in four environmental contexts with different levels of anthropogenic pressure. We analyzed their microbiome composition, structure and diversity through full-length 16S rRNA metabarcoding using the nanopore long-read sequencer MinION™. We hypothesized that the bacterial community structure of fecal samples would vary across the different scenarios, showing a decreased diversity and richness in samples from disturbed ecosystems. RESULTS: The fecal microbiomes of 31 bats from 4 scenarios were sequenced. A total of 4,829,302 reads were obtained with a taxonomic assignment percentage of 99.9% at genus level. Most abundant genera across all scenarios were Enterococcus, Escherichia/Shigella, Bacillus and Enterobacter. Alpha diversity varied significantly between the four scenarios (p < 0.05), showing the lowest Shannon index in bats from urban and intensive agriculture landscapes, while the highest alpha diversity value was found in near pristine landscapes. Beta diversity obtained by Bray–Curtis distance showed weak statistical differentiation of bacterial taxonomic profiles among scenarios. Furthermore, core community analysis showed that 1,293 genera were shared among localities. Differential abundance analyses showed that the highest differentially abundant taxa were found in near pristine landscapes, with the exception of the family Alcaligenaceae, which was also overrepresented in urban and intensive agriculture landscapes. CONCLUSIONS: This study suggests that near pristine and undisturbed landscapes could promote a more resilient gut microbiome in wild populations of P. kuhlii. These results highlight the potential of the fecal microbiome as a non-invasive bioindicator to assess insectivorous bats’ health and as a key element of landscape conservation strategies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s42523-023-00229-9. BioMed Central 2023-02-04 /pmc/articles/PMC9898988/ /pubmed/36739423 http://dx.doi.org/10.1186/s42523-023-00229-9 Text en © The Author(s) 2023 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 Lobato-Bailón, Lourdes García-Ulloa, Manuel Santos, Andrés Guixé, David Camprodon, Jordi Florensa-Rius, Xavier Molleda, Raúl Manzano, Robert P. Ribas, Maria Espunyes, Johan Dias-Alves, Andrea Marco, Ignasi Migura-Garcia, Lourdes Martínez-Urtaza, Jaime Cabezón, Oscar The fecal bacterial microbiome of the Kuhl’s pipistrelle bat (Pipistrellus kuhlii) reflects landscape anthropogenic pressure |
title | The fecal bacterial microbiome of the Kuhl’s pipistrelle bat (Pipistrellus kuhlii) reflects landscape anthropogenic pressure |
title_full | The fecal bacterial microbiome of the Kuhl’s pipistrelle bat (Pipistrellus kuhlii) reflects landscape anthropogenic pressure |
title_fullStr | The fecal bacterial microbiome of the Kuhl’s pipistrelle bat (Pipistrellus kuhlii) reflects landscape anthropogenic pressure |
title_full_unstemmed | The fecal bacterial microbiome of the Kuhl’s pipistrelle bat (Pipistrellus kuhlii) reflects landscape anthropogenic pressure |
title_short | The fecal bacterial microbiome of the Kuhl’s pipistrelle bat (Pipistrellus kuhlii) reflects landscape anthropogenic pressure |
title_sort | fecal bacterial microbiome of the kuhl’s pipistrelle bat (pipistrellus kuhlii) reflects landscape anthropogenic pressure |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9898988/ https://www.ncbi.nlm.nih.gov/pubmed/36739423 http://dx.doi.org/10.1186/s42523-023-00229-9 |
work_keys_str_mv | AT lobatobailonlourdes thefecalbacterialmicrobiomeofthekuhlspipistrellebatpipistrelluskuhliireflectslandscapeanthropogenicpressure AT garciaulloamanuel thefecalbacterialmicrobiomeofthekuhlspipistrellebatpipistrelluskuhliireflectslandscapeanthropogenicpressure AT santosandres thefecalbacterialmicrobiomeofthekuhlspipistrellebatpipistrelluskuhliireflectslandscapeanthropogenicpressure AT guixedavid thefecalbacterialmicrobiomeofthekuhlspipistrellebatpipistrelluskuhliireflectslandscapeanthropogenicpressure AT camprodonjordi thefecalbacterialmicrobiomeofthekuhlspipistrellebatpipistrelluskuhliireflectslandscapeanthropogenicpressure AT florensariusxavier thefecalbacterialmicrobiomeofthekuhlspipistrellebatpipistrelluskuhliireflectslandscapeanthropogenicpressure AT molledaraul thefecalbacterialmicrobiomeofthekuhlspipistrellebatpipistrelluskuhliireflectslandscapeanthropogenicpressure AT manzanorobert thefecalbacterialmicrobiomeofthekuhlspipistrellebatpipistrelluskuhliireflectslandscapeanthropogenicpressure AT pribasmaria thefecalbacterialmicrobiomeofthekuhlspipistrellebatpipistrelluskuhliireflectslandscapeanthropogenicpressure AT espunyesjohan thefecalbacterialmicrobiomeofthekuhlspipistrellebatpipistrelluskuhliireflectslandscapeanthropogenicpressure AT diasalvesandrea thefecalbacterialmicrobiomeofthekuhlspipistrellebatpipistrelluskuhliireflectslandscapeanthropogenicpressure AT marcoignasi thefecalbacterialmicrobiomeofthekuhlspipistrellebatpipistrelluskuhliireflectslandscapeanthropogenicpressure AT miguragarcialourdes thefecalbacterialmicrobiomeofthekuhlspipistrellebatpipistrelluskuhliireflectslandscapeanthropogenicpressure AT martinezurtazajaime thefecalbacterialmicrobiomeofthekuhlspipistrellebatpipistrelluskuhliireflectslandscapeanthropogenicpressure AT cabezonoscar thefecalbacterialmicrobiomeofthekuhlspipistrellebatpipistrelluskuhliireflectslandscapeanthropogenicpressure AT lobatobailonlourdes fecalbacterialmicrobiomeofthekuhlspipistrellebatpipistrelluskuhliireflectslandscapeanthropogenicpressure AT garciaulloamanuel fecalbacterialmicrobiomeofthekuhlspipistrellebatpipistrelluskuhliireflectslandscapeanthropogenicpressure AT santosandres fecalbacterialmicrobiomeofthekuhlspipistrellebatpipistrelluskuhliireflectslandscapeanthropogenicpressure AT guixedavid fecalbacterialmicrobiomeofthekuhlspipistrellebatpipistrelluskuhliireflectslandscapeanthropogenicpressure AT camprodonjordi fecalbacterialmicrobiomeofthekuhlspipistrellebatpipistrelluskuhliireflectslandscapeanthropogenicpressure AT florensariusxavier fecalbacterialmicrobiomeofthekuhlspipistrellebatpipistrelluskuhliireflectslandscapeanthropogenicpressure AT molledaraul fecalbacterialmicrobiomeofthekuhlspipistrellebatpipistrelluskuhliireflectslandscapeanthropogenicpressure AT manzanorobert fecalbacterialmicrobiomeofthekuhlspipistrellebatpipistrelluskuhliireflectslandscapeanthropogenicpressure AT pribasmaria fecalbacterialmicrobiomeofthekuhlspipistrellebatpipistrelluskuhliireflectslandscapeanthropogenicpressure AT espunyesjohan fecalbacterialmicrobiomeofthekuhlspipistrellebatpipistrelluskuhliireflectslandscapeanthropogenicpressure AT diasalvesandrea fecalbacterialmicrobiomeofthekuhlspipistrellebatpipistrelluskuhliireflectslandscapeanthropogenicpressure AT marcoignasi fecalbacterialmicrobiomeofthekuhlspipistrellebatpipistrelluskuhliireflectslandscapeanthropogenicpressure AT miguragarcialourdes fecalbacterialmicrobiomeofthekuhlspipistrellebatpipistrelluskuhliireflectslandscapeanthropogenicpressure AT martinezurtazajaime fecalbacterialmicrobiomeofthekuhlspipistrellebatpipistrelluskuhliireflectslandscapeanthropogenicpressure AT cabezonoscar fecalbacterialmicrobiomeofthekuhlspipistrellebatpipistrelluskuhliireflectslandscapeanthropogenicpressure |