Abram F, Starr E, Karatzas K A G, Matlawska-Wasowska K, Boyd A, Wiedmann M, Boor K J, Connally D, O'Byrne C P
Department of Microbiology, National University of Ireland-Galway, Galway, Ireland.
Appl Environ Microbiol. 2008 Nov;74(22):6848-58. doi: 10.1128/AEM.00442-08. Epub 2008 Sep 19.
Sigma B (sigma(B)) is an alternative sigma factor that controls the transcriptional response to stress in Listeria monocytogenes and is also known to play a role in the virulence of this human pathogen. In the present study we investigated the impact of a sigB deletion on the proteome of L. monocytogenes grown in a chemically defined medium both in the presence and in the absence of osmotic stress (0.5 M NaCl). Two new phenotypes associated with the sigB deletion were identified using this medium. (i) Unexpectedly, the strain with the DeltasigB deletion was found to grow faster than the parent strain in the growth medium, but only when 0.5 M NaCl was present. This phenomenon was independent of the carbon source provided in the medium. (ii) The DeltasigB mutant was found to have unusual Gram staining properties compared to the parent, suggesting that sigma(B) contributes to the maintenance of an intact cell wall. A proteomic analysis was performed by two-dimensional gel electrophoresis, using cells growing in the exponential and stationary phases. Overall, 11 proteins were found to be differentially expressed in the wild type and the DeltasigB mutant; 10 of these proteins were expressed at lower levels in the mutant, and 1 was overexpressed in the mutant. All 11 proteins were identified by tandem mass spectrometry, and putative functions were assigned based on homology to proteins from other bacteria. Five proteins had putative functions related to carbon utilization (Lmo0539, Lmo0783, Lmo0913, Lmo1830, and Lmo2696), while three proteins were similar to proteins whose functions are unknown but that are known to be stress inducible (Lmo0796, Lmo2391, and Lmo2748). To gain further insight into the role of sigma(B) in L. monocytogenes, we deleted the genes encoding four of the proteins, lmo0796, lmo0913, lmo2391, and lmo2748. Phenotypic characterization of the mutants revealed that Lmo2748 plays a role in osmotolerance, while Lmo0796, Lmo0913, and Lmo2391 were all implicated in acid stress tolerance to various degrees. Invasion assays performed with Caco-2 cells indicated that none of the four genes was required for mammalian cell invasion. Microscopic analysis suggested that loss of Lmo2748 might contribute to the cell wall defect observed in the DeltasigB mutant. Overall, this study highlighted two new phenotypes associated with the loss of sigma(B). It also demonstrated clear roles for sigma(B) in both osmotic and low-pH stress tolerance and identified specific components of the sigma(B) regulon that contribute to the responses observed.
Sigma B(σ(B))是一种替代的σ因子,它控制着单核细胞增生李斯特菌对压力的转录反应,并且已知在这种人类病原体的毒力中发挥作用。在本研究中,我们调查了sigB缺失对在化学限定培养基中生长的单核细胞增生李斯特菌蛋白质组的影响,该培养基中存在和不存在渗透胁迫(0.5 M NaCl)。使用这种培养基鉴定出了两种与sigB缺失相关的新表型。(i)出乎意料的是,发现缺失DeltasigB的菌株在生长培养基中比亲本菌株生长得更快,但仅当存在0.5 M NaCl时才如此。这种现象与培养基中提供的碳源无关。(ii)与亲本相比,发现DeltasigB突变体具有异常的革兰氏染色特性,这表明σ(B)有助于维持完整的细胞壁。通过二维凝胶电泳对处于指数生长期和稳定期的细胞进行了蛋白质组分析。总体而言,发现11种蛋白质在野生型和DeltasigB突变体中差异表达;其中10种蛋白质在突变体中的表达水平较低,1种在突变体中过表达。通过串联质谱法鉴定了所有11种蛋白质,并根据与其他细菌蛋白质的同源性赋予了推定功能。5种蛋白质具有与碳利用相关的推定功能(Lmo0539、Lmo0783、Lmo0913、Lmo1830和Lmo2696),而3种蛋白质与功能未知但已知受胁迫诱导的蛋白质相似(Lmo0796、Lmo2391和Lmo2748)。为了进一步深入了解σ(B)在单核细胞增生李斯特菌中的作用,我们删除了编码其中4种蛋白质(lmo0796、lmo0913、lmo2391和lmo2748)的基因。对突变体的表型特征分析表明,Lmo2748在渗透压耐受性中起作用,而Lmo0796、Lmo0913和Lmo2391在不同程度上都与酸胁迫耐受性有关。用Caco - 2细胞进行的侵袭试验表明,这4个基因中没有一个是哺乳动物细胞侵袭所必需的。显微镜分析表明,Lmo2748的缺失可能导致在DeltasigB突变体中观察到的细胞壁缺陷。总体而言,这项研究突出了与σ(B)缺失相关的两种新表型。它还证明了σ(B)在渗透压和低pH胁迫耐受性中的明确作用,并确定了σ(B)调控子中有助于观察到的反应的特定成分。