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Mangrove crab intestine and habitat sediment microbiomes cooperatively work on carbon and nitrogen cycling
Mangrove ecosystems, where litter and organic components are degraded and converted into detrital materials, support rich coastal fisheries resources. Sesarmid (Grapsidae) crabs, which feed on mangrove litter, play a crucial role in material flow in carbon-rich and nitrogen-limited mangrove ecosyste...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8719709/ https://www.ncbi.nlm.nih.gov/pubmed/34972143 http://dx.doi.org/10.1371/journal.pone.0261654 |
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author | Tongununui, Prasert Kuriya, Yuki Murata, Masahiro Sawada, Hideki Araki, Michihiro Nomura, Mika Morioka, Katsuji Ichie, Tomoaki Ikejima, Kou Adachi, Kohsuke |
author_facet | Tongununui, Prasert Kuriya, Yuki Murata, Masahiro Sawada, Hideki Araki, Michihiro Nomura, Mika Morioka, Katsuji Ichie, Tomoaki Ikejima, Kou Adachi, Kohsuke |
author_sort | Tongununui, Prasert |
collection | PubMed |
description | Mangrove ecosystems, where litter and organic components are degraded and converted into detrital materials, support rich coastal fisheries resources. Sesarmid (Grapsidae) crabs, which feed on mangrove litter, play a crucial role in material flow in carbon-rich and nitrogen-limited mangrove ecosystems; however, the process of assimilation and conversion into detritus has not been well studied. In this study, we performed microbiome analyses of intestinal bacteria from three species of mangrove crab and five sediment positions in the mud lobster mounds, including the crab burrow wall, to study the interactive roles of crabs and sediment in metabolism. Metagenome analysis revealed species-dependent intestinal profiles, especially in Neosarmatium smithi, while the sediment microbiome was similar in all positions, albeit with some regional dependency. The microbiome profiles of crab intestines and sediments were significantly different in the MDS analysis based on OTU similarity; however, 579 OTUs (about 70% of reads in the crab intestinal microbiome) were identical between the intestinal and sediment bacteria. In the phenotype prediction, cellulose degradation was observed in the crab intestine. Cellulase activity was detected in both crab intestine and sediment. This could be mainly ascribed to Demequinaceae, which was predominantly found in the crab intestines and burrow walls. Nitrogen fixation was also enriched in both the crab intestines and sediments, and was supported by the nitrogenase assay. Similar to earlier reports, sulfur-related families were highly enriched in the sediment, presumably degrading organic compounds as terminal electron acceptors under anaerobic conditions. These results suggest that mangrove crabs and habitat sediment both contribute to carbon and nitrogen cycling in the mangrove ecosystem via these two key reactions. |
format | Online Article Text |
id | pubmed-8719709 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-87197092022-01-01 Mangrove crab intestine and habitat sediment microbiomes cooperatively work on carbon and nitrogen cycling Tongununui, Prasert Kuriya, Yuki Murata, Masahiro Sawada, Hideki Araki, Michihiro Nomura, Mika Morioka, Katsuji Ichie, Tomoaki Ikejima, Kou Adachi, Kohsuke PLoS One Research Article Mangrove ecosystems, where litter and organic components are degraded and converted into detrital materials, support rich coastal fisheries resources. Sesarmid (Grapsidae) crabs, which feed on mangrove litter, play a crucial role in material flow in carbon-rich and nitrogen-limited mangrove ecosystems; however, the process of assimilation and conversion into detritus has not been well studied. In this study, we performed microbiome analyses of intestinal bacteria from three species of mangrove crab and five sediment positions in the mud lobster mounds, including the crab burrow wall, to study the interactive roles of crabs and sediment in metabolism. Metagenome analysis revealed species-dependent intestinal profiles, especially in Neosarmatium smithi, while the sediment microbiome was similar in all positions, albeit with some regional dependency. The microbiome profiles of crab intestines and sediments were significantly different in the MDS analysis based on OTU similarity; however, 579 OTUs (about 70% of reads in the crab intestinal microbiome) were identical between the intestinal and sediment bacteria. In the phenotype prediction, cellulose degradation was observed in the crab intestine. Cellulase activity was detected in both crab intestine and sediment. This could be mainly ascribed to Demequinaceae, which was predominantly found in the crab intestines and burrow walls. Nitrogen fixation was also enriched in both the crab intestines and sediments, and was supported by the nitrogenase assay. Similar to earlier reports, sulfur-related families were highly enriched in the sediment, presumably degrading organic compounds as terminal electron acceptors under anaerobic conditions. These results suggest that mangrove crabs and habitat sediment both contribute to carbon and nitrogen cycling in the mangrove ecosystem via these two key reactions. Public Library of Science 2021-12-31 /pmc/articles/PMC8719709/ /pubmed/34972143 http://dx.doi.org/10.1371/journal.pone.0261654 Text en © 2021 Tongununui et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Tongununui, Prasert Kuriya, Yuki Murata, Masahiro Sawada, Hideki Araki, Michihiro Nomura, Mika Morioka, Katsuji Ichie, Tomoaki Ikejima, Kou Adachi, Kohsuke Mangrove crab intestine and habitat sediment microbiomes cooperatively work on carbon and nitrogen cycling |
title | Mangrove crab intestine and habitat sediment microbiomes cooperatively work on carbon and nitrogen cycling |
title_full | Mangrove crab intestine and habitat sediment microbiomes cooperatively work on carbon and nitrogen cycling |
title_fullStr | Mangrove crab intestine and habitat sediment microbiomes cooperatively work on carbon and nitrogen cycling |
title_full_unstemmed | Mangrove crab intestine and habitat sediment microbiomes cooperatively work on carbon and nitrogen cycling |
title_short | Mangrove crab intestine and habitat sediment microbiomes cooperatively work on carbon and nitrogen cycling |
title_sort | mangrove crab intestine and habitat sediment microbiomes cooperatively work on carbon and nitrogen cycling |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8719709/ https://www.ncbi.nlm.nih.gov/pubmed/34972143 http://dx.doi.org/10.1371/journal.pone.0261654 |
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