微生物保管:关键微生物群居民鞘氨单胞菌减轻银纳米颗粒对大水蚤的毒性。

IF 3.5 3区 生物学 Q2 MICROBIOLOGY
Jesse Ouwehand, Bregje W Brinkmann, Willie J G M Peijnenburg, Martina G Vijver
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引用次数: 0

摘要

纳米技术应用的增加不可避免地导致宿主及其相关微生物群暴露于金属纳米颗粒。微生物群中的各种细菌都有保护自己免受金属毒性侵害的机制。在没有宿主的情况下,这些机制已被广泛描述。在这里,我们研究了从大水蚤微生物群中分离出的抗银离子细菌如何影响宿主对银纳米颗粒的暴露。在无菌新生儿和单相关新生儿中,研究了这些微生物对D. magna对纳米银的敏感性的影响。通过这种方法,鉴定出D. magna微生物组Sphingomonas yanokuyae的核心成员是耐银的。单一关联的新生儿与自然定植的新生儿一样对银纳米颗粒敏感,而单一关联的微细菌和无菌新生儿对银纳米颗粒的敏感性增加。银离子是对无细菌和微细菌相关的新生儿的毒性的主要原因,而颗粒对自然定植的和鞘单胞菌定植的新生儿的毒性更大。鞘氨单胞菌在体内从局部环境中积累的银离子比其他大蠊菌株多。目前的研究表明,细菌可以在塑造纳米材料的形态从而改变对宿主的毒性方面发挥至关重要的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Microbial custody: key microbiome inhabitant Sphingomonas alleviates silver nanoparticle toxicity in Daphnia magna.

Increased usage of nanotechnological applications inevitably leads to exposure of hosts and their associated microbiomes to metallic nanoparticles. Various bacteria within the microbiome harbour mechanisms to protect themselves against metal-related toxicity. These mechanisms have broadly been described in the absence of a host. Here, we studied how silver ion-resistant bacteria isolated from the Daphnia magna microbiome shape the host's exposure to silver nanoparticles. With germfree and mono-associated neonates, the effects of these microbes on the sensitivity of D. magna to silver nanoparticles were studied. By using this approach, a core member of the D. magna microbiome Sphingomonas yanoikuyae was identified to be silver-resistant. Neonates mono-associated with S. yanoikuyae were as sensitive to silver nanoparticles as naturally colonized neonates, whereas mono-association with Microbacterium and germfree neonates had increased sensitivity. Silver ions are the major attribution to toxicity in germfree and Microbacterium-associated neonates, whereas particles contribute more to the toxicity for the naturally- and Sphingomonas-colonized neonates. Sphingomonas accumulated in vivo more silver ions from its local environment than the other D. magna bacterial isolates. The current study shows that bacteria can play a vital role in shaping the speciation of nanomaterials and thereby modifying the toxicity to hosts.

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来源期刊
FEMS microbiology ecology
FEMS microbiology ecology 生物-微生物学
CiteScore
7.50
自引率
2.40%
发文量
132
审稿时长
3 months
期刊介绍: FEMS Microbiology Ecology aims to ensure efficient publication of high-quality papers that are original and provide a significant contribution to the understanding of microbial ecology. The journal contains Research Articles and MiniReviews on fundamental aspects of the ecology of microorganisms in natural soil, aquatic and atmospheric habitats, including extreme environments, and in artificial or managed environments. Research papers on pure cultures and in the areas of plant pathology and medical, food or veterinary microbiology will be published where they provide valuable generic information on microbial ecology. Papers can deal with culturable and non-culturable forms of any type of microorganism: bacteria, archaea, filamentous fungi, yeasts, protozoa, cyanobacteria, algae or viruses. In addition, the journal will publish Perspectives, Current Opinion and Controversy Articles, Commentaries and Letters to the Editor on topical issues in microbial ecology. - Application of ecological theory to microbial ecology - Interactions and signalling between microorganisms and with plants and animals - Interactions between microorganisms and their physicochemical enviornment - Microbial aspects of biogeochemical cycles and processes - Microbial community ecology - Phylogenetic and functional diversity of microbial communities - Evolutionary biology of microorganisms
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