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A 组链球菌的氧依赖性表型变异。

Oxygen-dependent phenotypic variation in group A streptococcus.

机构信息

Department of Microbiology and Immunology, College of Medicine, Chang Gung University, Tao-Yuan, Taiwan.

Department of Microbiology and Immunology, College of Medicine, Chang Gung University, Tao-Yuan, Taiwan.

出版信息

J Microbiol Immunol Infect. 2016 Dec;49(6):837-842. doi: 10.1016/j.jmii.2014.11.010. Epub 2014 Nov 22.

Abstract

BACKGROUND

The phenotypic heterogeneity of the human pathogen Streptococcus pyogenes [group A streptococcus (GAS)] is associated with bacterial virulence variation. During invasive GAS infection, mutations in the two-component regulatory system covR/covS leads to increases in hyaluronic acid capsule production, virulence genes expression, and lethality in the mouse infection model. Phenotypic variation of GAS is also found under in vitro culture conditions. However, whether a specific environmental factor is important for phenotypic variation is still unknown.

METHODS

GAS968 is an emm12-type clinical isolate that converts from mucoid to hypermucoid morphology under in vitro culture conditions. To clarify whether morphology variation can be triggered by specific environmental signals, or whether different morphology variants would be selected under specific environmental stresses, GAS968 was cultured under different conditions, and the changes in the number of mucoid and hypermucoid colonies in the total bacterial population were analyzed.

RESULTS

The ratio of mucoid and hypermucoid colonies of GAS968 in the total bacterial population changes dramatically under aerobic and anaerobic conditions. The decrease in the number of hypermucoid colonies in the total bacterial population under aerobic conditions is not caused by growth repression, suggesting that the morphology conversion of GAS968 is inhibited by oxygen.

CONCLUSION

Phenotypic heterogeneity has been shown to contribute to invasive GAS infection. Our results suggest that oxygen-dependent morphology variation in GAS968 may have important roles in bacterial pathogenesis.

摘要

背景

人类病原体化脓链球菌(A 组链球菌(GAS))的表型异质性与细菌毒力变化有关。在侵袭性 GAS 感染期间,双组分调节系统 covR/covS 的突变导致透明质酸荚膜产生、毒力基因表达增加,并在小鼠感染模型中导致致死性。GAS 的表型变异也在体外培养条件下发现。然而,特定的环境因素是否对表型变异很重要仍然未知。

方法

GAS968 是一种 emm12 型临床分离株,在体外培养条件下从粘液型转变为超粘液型形态。为了阐明形态变异是否可以由特定的环境信号触发,或者不同的形态变异是否会在特定的环境压力下被选择,GAS968 在不同的条件下培养,并分析总细菌群体中粘液型和超粘液型菌落数量的变化。

结果

GAS968 在总细菌群体中粘液型和超粘液型菌落的比例在需氧和厌氧条件下发生剧烈变化。需氧条件下总细菌群体中超粘液型菌落数量的减少不是由于生长抑制引起的,这表明 GAS968 的形态转换受到氧气的抑制。

结论

表型异质性已被证明有助于侵袭性 GAS 感染。我们的结果表明,GAS968 中依赖于氧气的形态变化可能在细菌发病机制中具有重要作用。

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