Nanopore Long-Read Metagenomics Reveals Pollution-Driven Antibiotic Resistance and Xenobiotic Degradation in Urban Beach Microbiomes

IF 3.1 4区 生物学 Q2 ENVIRONMENTAL SCIENCES
Angelo Felipe Barbosa de Oliveira, Bruno Santana Carneiro, Joelma Barbosa de Carvalho, Adan Rodrigues de Oliveira, Artur Luiz da Costa da Silva, Adonney Allan de Oliveira Veras, Rafael Azevedo Baraúna, Diego Assis das Graças
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Abstract

Coastal ecosystems are vital for biodiversity but are increasingly threatened by urbanisation and pollution, which significantly alter local microbial communities. This study assessed bacterial diversity and functional profiles in urban and island beaches in Belém, Brazil. Urban beaches showed significantly higher microbial diversity and evenness, alongside functional plasticity due to pollutant input, while island beaches hosted more specialised and stable communities. Taxonomic analysis revealed the significant enrichment of opportunistic genera such as Comamonas, Clostridium and Paenibacillus in urban areas, and the massive dominance of Prochlorococcus and Candidatus Pelagibacter in island sites. Furthermore, shotgun metagenomics identified a robust genomic potential for xenobiotic degradation and antibiotic resistance in urban microbiomes, whereas island microbiomes were significantly enriched in genes for energy production and biosynthesis. These results underscore the ecological divergence between anthropogenically impacted and natural coastal environments, highlighting the importance of microbiome monitoring for sustainable coastal management.

纳米孔长读宏基因组学揭示了污染驱动的抗生素耐药性和城市海滩微生物群落的外源降解。
沿海生态系统对生物多样性至关重要,但日益受到城市化和污染的威胁,这极大地改变了当地的微生物群落。本研究评估了巴西belsamim城市和岛屿海滩的细菌多样性和功能概况。城市海滩显示出更高的微生物多样性和均匀性,以及由于污染物输入而产生的功能可塑性,而岛屿海滩则拥有更专业和稳定的群落。分类学分析显示,城市地区Comamonas、Clostridium和Paenibacillus等机会性属显著富集,海岛地区原绿球藻(Prochlorococcus)和候选球藻(Candidatus Pelagibacter)大量富集。此外,霰弹枪宏基因组学发现,城市微生物群具有强大的外源降解和抗生素耐药性的基因组潜力,而岛屿微生物群则具有显著丰富的能源生产和生物合成基因。这些结果强调了人为影响与自然海岸环境之间的生态差异,强调了微生物组监测对可持续海岸管理的重要性。
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来源期刊
Environmental Microbiology Reports
Environmental Microbiology Reports ENVIRONMENTAL SCIENCES-MICROBIOLOGY
CiteScore
6.00
自引率
3.00%
发文量
91
审稿时长
3.0 months
期刊介绍: The journal is identical in scope to Environmental Microbiology, shares the same editorial team and submission site, and will apply the same high level acceptance criteria. The two journals will be mutually supportive and evolve side-by-side. Environmental Microbiology Reports provides a high profile vehicle for publication of the most innovative, original and rigorous research in the field. The scope of the Journal encompasses the diversity of current research on microbial processes in the environment, microbial communities, interactions and evolution and includes, but is not limited to, the following: the structure, activities and communal behaviour of microbial communities microbial community genetics and evolutionary processes microbial symbioses, microbial interactions and interactions with plants, animals and abiotic factors microbes in the tree of life, microbial diversification and evolution population biology and clonal structure microbial metabolic and structural diversity microbial physiology, growth and survival microbes and surfaces, adhesion and biofouling responses to environmental signals and stress factors modelling and theory development pollution microbiology extremophiles and life in extreme and unusual little-explored habitats element cycles and biogeochemical processes, primary and secondary production microbes in a changing world, microbially-influenced global changes evolution and diversity of archaeal and bacterial viruses new technological developments in microbial ecology and evolution, in particular for the study of activities of microbial communities, non-culturable microorganisms and emerging pathogens.
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