Bowman John P, Bittencourt Claudio R, Ross Tom
Australian Food Safety Centre of Excellence, Tasmanian Institute of Agricultural Research, School of Agricultural Science, University of Tasmania, Private Bag 54, Hobart, Tasmania, 7001, Australia.
Microbiology (Reading). 2008 Feb;154(Pt 2):462-475. doi: 10.1099/mic.0.2007/010314-0.
High hydrostatic pressure processing (HPP) is currently being used as a treatment for certain foods to control the presence of food-borne pathogens, such as Listeria monocytogenes. Genomic microarray analysis was performed to determine the effects of HPP on L. monocytogenes in order to understand how it responds to mechanical stress injury. Reverse transcriptase PCR analysis of tufA and rpoC indicated that the reduction of mRNA expression in HPP-treated cells was dependent on intensity and time of the treatment. Treatments of 400 and 600 MPa for 5 min on cells in the exponential growth phase, though leading to partial or complete cellular inactivation, still resulted in measurable relative differential gene expression. Gene set enrichment analysis indicated that HPP induced increased expression of genes associated with DNA repair mechanisms, transcription and translation protein complexes, the septal ring, the general protein translocase system, flagella assemblage and chemotaxis, and lipid and peptidoglycan biosynthetic pathways. On the other hand, HPP appears to suppress a wide range of energy production and conversion, carbohydrate metabolism and virulence-associated genes accompanied by strong suppression of the SigB and PrfA regulons. HPP also affected genes controlled by the pleotrophic regulator CodY. HPP-induced cellular damage appears to lead to increased expression of genes linked to sections of the cell previously shown in bacteria to be damaged or altered during HPP exposure and suppression of gene expression associated with cellular growth processes and virulence.
高静水压处理(HPP)目前被用作某些食品的一种处理方法,以控制食源性病原体的存在,如单核细胞增生李斯特菌。进行了基因组微阵列分析,以确定HPP对单核细胞增生李斯特菌的影响,从而了解它如何应对机械应激损伤。对tufA和rpoC的逆转录酶PCR分析表明,HPP处理细胞中mRNA表达的降低取决于处理的强度和时间。在指数生长期对细胞施加400和600 MPa处理5分钟,尽管导致部分或完全细胞失活,但仍导致可测量的相对差异基因表达。基因集富集分析表明,HPP诱导了与DNA修复机制、转录和翻译蛋白复合物、隔膜环、一般蛋白转位酶系统、鞭毛组装和趋化作用以及脂质和肽聚糖生物合成途径相关的基因表达增加。另一方面,HPP似乎抑制了广泛的能量产生和转换、碳水化合物代谢以及与毒力相关的基因,同时强烈抑制了SigB和PrfA调控子。HPP还影响了由多效性调节因子CodY控制的基因。HPP诱导的细胞损伤似乎导致与细胞先前在HPP暴露期间显示受损或改变的部分相关的基因表达增加,并抑制了与细胞生长过程和毒力相关的基因表达。