Cargando…
Metagenomics reveals global-scale contrasts in nitrogen cycling and cyanobacterial light-harvesting mechanisms in glacier cryoconite
BACKGROUND: Cryoconite granules are mineral–microbial aggregates found on glacier surfaces worldwide and are hotspots of biogeochemical reactions in glacier ecosystems. However, despite their importance within glacier ecosystems, the geographical diversity of taxonomic assemblages and metabolic pote...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8941735/ https://www.ncbi.nlm.nih.gov/pubmed/35317857 http://dx.doi.org/10.1186/s40168-022-01238-7 |
_version_ | 1784673163706105856 |
---|---|
author | Murakami, Takumi Takeuchi, Nozomu Mori, Hiroshi Hirose, Yuu Edwards, Arwyn Irvine-Fynn, Tristram Li, Zhongqin Ishii, Satoshi Segawa, Takahiro |
author_facet | Murakami, Takumi Takeuchi, Nozomu Mori, Hiroshi Hirose, Yuu Edwards, Arwyn Irvine-Fynn, Tristram Li, Zhongqin Ishii, Satoshi Segawa, Takahiro |
author_sort | Murakami, Takumi |
collection | PubMed |
description | BACKGROUND: Cryoconite granules are mineral–microbial aggregates found on glacier surfaces worldwide and are hotspots of biogeochemical reactions in glacier ecosystems. However, despite their importance within glacier ecosystems, the geographical diversity of taxonomic assemblages and metabolic potential of cryoconite communities around the globe remain unclear. In particular, the genomic content of cryoconite communities on Asia’s high mountain glaciers, which represent a substantial portion of Earth’s ice masses, has rarely been reported. Therefore, in this study, to elucidate the taxonomic and ecological diversities of cryoconite bacterial consortia on a global scale, we conducted shotgun metagenomic sequencing of cryoconite acquired from a range of geographical areas comprising Polar (Arctic and Antarctic) and Asian alpine regions. RESULTS: Our metagenomic data indicate that compositions of both bacterial taxa and functional genes are particularly distinctive for Asian cryoconite. Read abundance of the genes responsible for denitrification was significantly more abundant in Asian cryoconite than the Polar cryoconite, implying that denitrification is more enhanced in Asian glaciers. The taxonomic composition of Cyanobacteria, the key primary producers in cryoconite communities, also differs between the Polar and Asian samples. Analyses on the metagenome-assembled genomes and fluorescence emission spectra reveal that Asian cryoconite is dominated by multiple cyanobacterial lineages possessing phycoerythrin, a green light-harvesting component for photosynthesis. In contrast, Polar cryoconite is dominated by a single cyanobacterial species Phormidesmis priestleyi that does not possess phycoerythrin. These findings suggest that the assemblage of cryoconite bacterial communities respond to regional- or glacier-specific physicochemical conditions, such as the availability of nutrients (e.g., nitrate and dissolved organic carbon) and light (i.e., incident shortwave radiation). CONCLUSIONS: Our genome-resolved metagenomics provides the first characterization of the taxonomic and metabolic diversities of cryoconite from contrasting geographical areas, highlighted by the distinct light-harvesting approaches of Cyanobacteria and nitrogen utilization between Polar and Asian cryoconite, and implies the existence of environmental controls on the assemblage of cryoconite communities. These findings deepen our understanding of the biodiversity and biogeochemical cycles of glacier ecosystems, which are susceptible to ongoing climate change and glacier decline, on a global scale. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01238-7. |
format | Online Article Text |
id | pubmed-8941735 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-89417352022-03-24 Metagenomics reveals global-scale contrasts in nitrogen cycling and cyanobacterial light-harvesting mechanisms in glacier cryoconite Murakami, Takumi Takeuchi, Nozomu Mori, Hiroshi Hirose, Yuu Edwards, Arwyn Irvine-Fynn, Tristram Li, Zhongqin Ishii, Satoshi Segawa, Takahiro Microbiome Research BACKGROUND: Cryoconite granules are mineral–microbial aggregates found on glacier surfaces worldwide and are hotspots of biogeochemical reactions in glacier ecosystems. However, despite their importance within glacier ecosystems, the geographical diversity of taxonomic assemblages and metabolic potential of cryoconite communities around the globe remain unclear. In particular, the genomic content of cryoconite communities on Asia’s high mountain glaciers, which represent a substantial portion of Earth’s ice masses, has rarely been reported. Therefore, in this study, to elucidate the taxonomic and ecological diversities of cryoconite bacterial consortia on a global scale, we conducted shotgun metagenomic sequencing of cryoconite acquired from a range of geographical areas comprising Polar (Arctic and Antarctic) and Asian alpine regions. RESULTS: Our metagenomic data indicate that compositions of both bacterial taxa and functional genes are particularly distinctive for Asian cryoconite. Read abundance of the genes responsible for denitrification was significantly more abundant in Asian cryoconite than the Polar cryoconite, implying that denitrification is more enhanced in Asian glaciers. The taxonomic composition of Cyanobacteria, the key primary producers in cryoconite communities, also differs between the Polar and Asian samples. Analyses on the metagenome-assembled genomes and fluorescence emission spectra reveal that Asian cryoconite is dominated by multiple cyanobacterial lineages possessing phycoerythrin, a green light-harvesting component for photosynthesis. In contrast, Polar cryoconite is dominated by a single cyanobacterial species Phormidesmis priestleyi that does not possess phycoerythrin. These findings suggest that the assemblage of cryoconite bacterial communities respond to regional- or glacier-specific physicochemical conditions, such as the availability of nutrients (e.g., nitrate and dissolved organic carbon) and light (i.e., incident shortwave radiation). CONCLUSIONS: Our genome-resolved metagenomics provides the first characterization of the taxonomic and metabolic diversities of cryoconite from contrasting geographical areas, highlighted by the distinct light-harvesting approaches of Cyanobacteria and nitrogen utilization between Polar and Asian cryoconite, and implies the existence of environmental controls on the assemblage of cryoconite communities. These findings deepen our understanding of the biodiversity and biogeochemical cycles of glacier ecosystems, which are susceptible to ongoing climate change and glacier decline, on a global scale. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01238-7. BioMed Central 2022-03-23 /pmc/articles/PMC8941735/ /pubmed/35317857 http://dx.doi.org/10.1186/s40168-022-01238-7 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Murakami, Takumi Takeuchi, Nozomu Mori, Hiroshi Hirose, Yuu Edwards, Arwyn Irvine-Fynn, Tristram Li, Zhongqin Ishii, Satoshi Segawa, Takahiro Metagenomics reveals global-scale contrasts in nitrogen cycling and cyanobacterial light-harvesting mechanisms in glacier cryoconite |
title | Metagenomics reveals global-scale contrasts in nitrogen cycling and cyanobacterial light-harvesting mechanisms in glacier cryoconite |
title_full | Metagenomics reveals global-scale contrasts in nitrogen cycling and cyanobacterial light-harvesting mechanisms in glacier cryoconite |
title_fullStr | Metagenomics reveals global-scale contrasts in nitrogen cycling and cyanobacterial light-harvesting mechanisms in glacier cryoconite |
title_full_unstemmed | Metagenomics reveals global-scale contrasts in nitrogen cycling and cyanobacterial light-harvesting mechanisms in glacier cryoconite |
title_short | Metagenomics reveals global-scale contrasts in nitrogen cycling and cyanobacterial light-harvesting mechanisms in glacier cryoconite |
title_sort | metagenomics reveals global-scale contrasts in nitrogen cycling and cyanobacterial light-harvesting mechanisms in glacier cryoconite |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8941735/ https://www.ncbi.nlm.nih.gov/pubmed/35317857 http://dx.doi.org/10.1186/s40168-022-01238-7 |
work_keys_str_mv | AT murakamitakumi metagenomicsrevealsglobalscalecontrastsinnitrogencyclingandcyanobacteriallightharvestingmechanismsinglaciercryoconite AT takeuchinozomu metagenomicsrevealsglobalscalecontrastsinnitrogencyclingandcyanobacteriallightharvestingmechanismsinglaciercryoconite AT morihiroshi metagenomicsrevealsglobalscalecontrastsinnitrogencyclingandcyanobacteriallightharvestingmechanismsinglaciercryoconite AT hiroseyuu metagenomicsrevealsglobalscalecontrastsinnitrogencyclingandcyanobacteriallightharvestingmechanismsinglaciercryoconite AT edwardsarwyn metagenomicsrevealsglobalscalecontrastsinnitrogencyclingandcyanobacteriallightharvestingmechanismsinglaciercryoconite AT irvinefynntristram metagenomicsrevealsglobalscalecontrastsinnitrogencyclingandcyanobacteriallightharvestingmechanismsinglaciercryoconite AT lizhongqin metagenomicsrevealsglobalscalecontrastsinnitrogencyclingandcyanobacteriallightharvestingmechanismsinglaciercryoconite AT ishiisatoshi metagenomicsrevealsglobalscalecontrastsinnitrogencyclingandcyanobacteriallightharvestingmechanismsinglaciercryoconite AT segawatakahiro metagenomicsrevealsglobalscalecontrastsinnitrogencyclingandcyanobacteriallightharvestingmechanismsinglaciercryoconite |