铜绿假单胞菌与六种机会性病原体之间的相互作用涵盖了从互作到拮抗的广泛范围。

IF 3.6 4区 生物学 Q2 ENVIRONMENTAL SCIENCES
Clémentine Laffont, Tobias Wechsler, Rolf Kümmerli
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引用次数: 0

摘要

细菌感染通常涉及不止一种病原体。虽然多微生物感染会影响疾病的预后已是公认的事实,但我们对病原体如何相互作用并影响彼此的行为和健康状况却知之甚少。在这里,我们使用显微镜方法来探索铜绿假单胞菌与六种人类机会性病原体之间的相互作用,这些病原体经常同时出现在多微生物感染中:这些病原体包括:鲍曼不动杆菌(Acinetobacter baumannii)、伯克霍尔德氏球菌(Burkholderia cenocepacia)、大肠杆菌(Escherichia coli)、粪肠球菌(Enterococcus faecium)、肺炎克雷伯菌(Klebsiella pneumoniae)和金黄色葡萄球菌(Staphylococcus aureus)。在对琼脂糖垫上生长的微菌落进行长期跟踪时,我们观察到了从互生到拮抗的广泛的物种特异性生态相互作用。例如,铜绿假单胞菌与粪肠球菌之间存在互利的相互作用,但与大肠杆菌之间存在拮抗作用。虽然我们几乎没有发现向或不向同居者主动定向生长的证据,但我们观察到,一些病原体在竞争中增加了双层生长,而菌落快速扩张所产生的物理力对适应性产生了重大影响。总之,我们的工作提供了病原体相互作用的图谱,突出了多微生物感染中可能出现的潜在物种动态的多样性。我们讨论了驱动病原体相互作用的可能机制,并对不同的生态相互作用如何影响毒力进行了预测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Interactions between Pseudomonas aeruginosa and six opportunistic pathogens cover a broad spectrum from mutualism to antagonism

Interactions between Pseudomonas aeruginosa and six opportunistic pathogens cover a broad spectrum from mutualism to antagonism

Bacterial infections often involve more than one pathogen. While it is well established that polymicrobial infections can impact disease outcomes, we know little about how pathogens interact and affect each other's behaviour and fitness. Here, we used a microscopy approach to explore interactions between Pseudomonas aeruginosa and six human opportunistic pathogens that often co-occur in polymicrobial infections: Acinetobacter baumannii, Burkholderia cenocepacia, Escherichia coli, Enterococcus faecium, Klebsiella pneumoniae, and Staphylococcus aureus. When following growing microcolonies on agarose pads over time, we observed a broad spectrum of species-specific ecological interactions, ranging from mutualism to antagonism. For example, P. aeruginosa engaged in a mutually beneficial interaction with E. faecium but suffered from antagonism by E. coli. While we found little evidence for active directional growth towards or away from cohabitants, we observed that some pathogens increased growth in double layers in response to competition and that physical forces due to fast colony expansion had a major impact on fitness. Overall, our work provides an atlas of pathogen interactions, highlighting the diversity of potential species dynamics that may occur in polymicrobial infections. We discuss possible mechanisms driving pathogen interactions and offer predictions of how the different ecological interactions could affect virulence.

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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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