微生物群落结构受到与噬菌体抗性相关的宿主密度增加的影响。

IF 4.1 3区 生物学 Q2 MICROBIOLOGY FEMS microbiology ecology Pub Date : 2025-03-18 DOI:10.1093/femsec/fiaf027
Meaghan Castledine, Daniel Padfield, Rai Lewis, Angus Buckling
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引用次数: 0

摘要

裂解噬菌体(“噬菌体”)可以限制细菌密度和塑造群落结构,直接通过裂解或间接通过抗性成本。然而,也有报道称噬菌体对宿主密度没有影响,在某些情况下甚至是积极的影响。在这里,我们研究了在噬菌体灭绝后维持抗性固定后,varovorax种群中宿主密度增加的机制。我们的结果表明,密度增加是一种与抗性出现相一致的遗传性状。生长曲线显示,噬菌体抗性使种群生长曲线发生位移,在死亡期密度较高。这种抗性的密度增加效应对群落结构具有重要意义,因为抗噬菌体的变异螟降低了同种的密度。对裂解噬菌体的抗性可以增加宿主密度,这对更广泛的生态学和噬菌体治疗有影响,其中裂解噬菌体被认为对其宿主有负面影响。
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Microbial community structure is affected by phage-resistance associated increases in host density.

Lytic bacteriophages ('phages') can limit bacterial densities and shape community structure, either directly through lysis or indirectly through costs to resistance. However, phages have also been reported to have no, and in some cases even positive, effects on host densities. Here, we investigate the mechanisms behind an increase in host density in Variovorax sp. populations following a fixation of resistance that was maintained after phage extinction. Our results demonstrate that the density increase was a genetic trait coinciding with resistance emergence. Growth curves showed that phage resistance shifted population growth curves such that density was higher in the death phase. This density-increasing effect of resistance had important implications for community structure with phage-resistant Variovorax decreasing the density of a conspecific. That resistance to lytic phage can increase host densities has implications for wider ecology and phage therapy, where lytic phages are presumed to have negative effects on their 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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