Experimental assessment of interactions between marine bacteria and model protists: from predator-prey relationships to bacterial-mediated lysis.

IF 3.9 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Applied and Environmental Microbiology Pub Date : 2025-06-18 Epub Date: 2025-05-30 DOI:10.1128/aem.00929-25
Diana Axelsson-Olsson, Nikolaj Gubonin, Stina Israelsson, Jarone Pinhassi
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引用次数: 0

Abstract

Bacteria in aquatic environments are a principal food source for predatory protists. Whereas interactions between bacteria and protists are recognized to determine the pathogenesis and epidemiology of several human pathogens, few studies have systematically characterized the interactions between specific aquatic bacteria and protists beyond the prey-predator relation. We, therefore, surveyed individual co-cultures between 18 different genome-sequenced marine bacteria with known virulence gene repertoires and three model protist species widely used for assessing bacteria-protist interactions. Strikingly, 10, 5, and 3 bacterial isolates were capable of lysing the protists Acanthamoeba polyphaga, Tetrahymena pyriformis, and Euglena gracilis, respectively. A majority of the bacteria were able to grow and/or maintain viable populations in the presence of viable protists. Some bacteria survived longer with viable protists but not heat-killed protists and were observed in protist vacuoles. In this respect, marine bacteria are similar to several protist-dependent human pathogens, including Legionella. Analyses of growth patterns in low-nutrient media showed that co-cultivation with A. polyphaga allowed one bacterial strain to overcome nutritional stress and obtain active growth. Five isolates depended on viable amoebae to grow, notwithstanding nutrient media status. The remarkable capability of these marine bacteria to survive encounters with, and even actively kill, model predatory protists under laboratory conditions suggests that diverse bacterial defense strategies and virulence mechanisms to access nutrients may be important in shaping microbial interactions. If verified with native marine and freshwater populations, the diversity of interactions uncovered here has implications for understanding ecological and evolutionary consequences of population dynamics in bacteria and protists.IMPORTANCEThe microbiome constitutes the base of food webs in aquatic environments. Its composition partly reflects biotic interactions, where bacteria primarily are considered prey of predatory protists. However, studies that focus on one or a few species have shown that some bacteria have abilities to escape grazing and may even be capable of lysing their protist predators. In this study, we substantially extend these findings by systematically investigating interactions among multiple taxa of both bacteria and protists. Our results show that marine bacteria display a wider and more complex range of interactions with their predators than generally recognized-from growth dependency to protist lysis. Given that such interactions play key roles in the pathogenesis and epidemiology of several human pathogens, our findings imply that bacterial virulence traits can contribute to defining the structure and ecology of aquatic microbiomes.

海洋细菌和模式原生生物之间相互作用的实验评估:从捕食者-猎物关系到细菌介导的裂解。
水生环境中的细菌是掠食性原生生物的主要食物来源。虽然细菌和原生生物之间的相互作用被认为决定了几种人类病原体的发病机制和流行病学,但很少有研究系统地描述了特定水生细菌和原生生物之间的相互作用。因此,我们调查了18种不同基因组测序的具有已知毒力基因库的海洋细菌和三种被广泛用于评估细菌-原生生物相互作用的模式原生生物物种之间的个体共培养。值得注意的是,分别有10株、5株和3株细菌分离株能够裂解原生生物棘阿米巴多食虫、梨状四膜虫和细叶藻。大多数细菌能够在有活性原生生物存在的情况下生长和/或维持有活力的种群。一些细菌在有活力的原生生物中存活时间更长,而在热杀死的原生生物中却没有,并且在原生生物液泡中观察到。在这方面,海洋细菌类似于一些依赖原生生物的人类病原体,包括军团菌。对低营养培养基中生长模式的分析表明,与多食单胞菌共培养可使一株细菌克服营养胁迫,获得积极生长。5个分离株依赖活的变形虫生长,尽管营养介质状态。这些海洋细菌在实验室条件下与模范掠食性原生生物相遇时生存甚至主动杀死的卓越能力表明,不同的细菌防御策略和获取营养物质的毒力机制可能在形成微生物相互作用中很重要。如果在本地海洋和淡水种群中得到验证,这里发现的相互作用的多样性对理解细菌和原生生物种群动态的生态和进化后果具有重要意义。微生物群构成了水生环境中食物网的基础。它的组成部分反映了生物相互作用,细菌主要被认为是掠食性原生生物的猎物。然而,对一种或几种细菌的研究表明,一些细菌有能力逃避放牧,甚至可能有能力溶解它们的原生捕食者。在这项研究中,我们通过系统地研究细菌和原生生物的多个分类群之间的相互作用,大大扩展了这些发现。我们的研究结果表明,海洋细菌与捕食者的相互作用比通常认为的更广泛、更复杂——从生长依赖到原生生物裂解。鉴于这种相互作用在几种人类病原体的发病机制和流行病学中起着关键作用,我们的研究结果表明,细菌的毒力特征可以有助于定义水生微生物群的结构和生态。
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来源期刊
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
期刊介绍: Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.
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