Institute for Infectious Diseases, University of Bern, Bern, Switzerland.
PLoS One. 2013 Jul 2;8(7):e68298. doi: 10.1371/journal.pone.0068298. Print 2013.
Moraxella catarrhalis, a major nasopharyngeal pathogen of the human respiratory tract, is exposed to rapid downshifts of environmental temperature when humans breathe cold air. The prevalence of pharyngeal colonization and respiratory tract infections caused by M. catarrhalis is greatest in winter. We investigated how M. catarrhalis uses the physiologic exposure to cold air to regulate pivotal survival systems that may contribute to M. catarrhalis virulence.
In this study we used the RNA-seq techniques to quantitatively catalogue the transcriptome of M. catarrhalis exposed to a 26 °C cold shock or to continuous growth at 37 °C. Validation of RNA-seq data using quantitative RT-PCR analysis demonstrated the RNA-seq results to be highly reliable. We observed that a 26 °C cold shock induces the expression of genes that in other bacteria have been related to virulence a strong induction was observed for genes involved in high affinity phosphate transport and iron acquisition, indicating that M. catarrhalis makes a better use of both phosphate and iron resources after exposure to cold shock. We detected the induction of genes involved in nitrogen metabolism, as well as several outer membrane proteins, including ompA, m35-like porin and multidrug efflux pump (acrAB) indicating that M. catarrhalis remodels its membrane components in response to downshift of temperature. Furthermore, we demonstrate that a 26 °C cold shock enhances the induction of genes encoding the type IV pili that are essential for natural transformation, and increases the genetic competence of M. catarrhalis, which may facilitate the rapid spread and acquisition of novel virulence-associated genes.
Cold shock at a physiologically relevant temperature of 26 °C induces in M. catarrhalis a complex of adaptive mechanisms that could convey novel pathogenic functions and may contribute to enhanced colonization and virulence.
莫拉氏菌属,人类呼吸道的主要鼻咽病原体,当人类呼吸冷空气时,会迅速受到环境温度的急剧下降的影响。莫拉氏菌属引起的咽部分化和呼吸道感染的流行率在冬季最高。我们研究了莫拉氏菌属如何利用生理上对冷空气的暴露来调节可能有助于莫拉氏菌属毒力的关键生存系统。
在这项研究中,我们使用 RNA-seq 技术定量编目了暴露于 26°C 冷冲击或连续在 37°C 下生长的莫拉氏菌属的转录组。使用定量 RT-PCR 分析验证 RNA-seq 数据表明 RNA-seq 结果非常可靠。我们观察到 26°C 的冷冲击诱导了与毒力有关的基因的表达,在其他细菌中观察到与高亲和力磷酸盐转运和铁摄取有关的基因的强烈诱导,表明莫拉氏菌属在暴露于冷冲击后更好地利用磷酸盐和铁资源。我们检测到参与氮代谢的基因的诱导,以及几种外膜蛋白,包括 ompA、m35 样孔蛋白和多药外排泵(acrAB),表明莫拉氏菌属响应温度下降重塑其膜成分。此外,我们证明 26°C 的冷冲击增强了编码对自然转化至关重要的 IV 型菌毛的基因的诱导,并增加了莫拉氏菌属的遗传能力,这可能促进了新型毒力相关基因的快速传播和获得。
在生理相关的 26°C 冷冲击下,莫拉氏菌属诱导了一系列适应机制,这些机制可能赋予新的致病功能,并有助于增强定植和毒力。