Lawhon Sara D, Frye Jonathan G, Suyemoto Mitsu, Porwollik Steffen, McClelland Michael, Altier Craig
College of Veterinary Medicine, North Carolina State University, 4700 Hillsborough Street, Raleigh 27606, USA.
Mol Microbiol. 2003 Jun;48(6):1633-45. doi: 10.1046/j.1365-2958.2003.03535.x.
CsrA is a regulator of invasion genes in Salmonella enterica serovar Typhimurium. To investigate the wider role of CsrA in gene regulation, we compared the expression of Salmonella genes in a csrA mutant with those in the wild type using a DNA microarray. As expected, we found that expression of Salmonella pathogenicity island 1 (SPI-1) invasion genes was greatly reduced in the csrA mutant, as were genes outside the island that encode proteins translocated into eukaryotic cells by the SPI-1 type III secretion apparatus. The flagellar synthesis operons, flg and fli, were also poorly expressed, and the csrA mutant was aflagellate and non-motile. The genes of two metabolic pathways likely to be used by Salmonella in the intestinal milieu also showed reduced expression: the pdu operon for utilization of 1,2-propanediol and the eut operon for ethanolamine catabolism. Reduced expression of reporter fusions in these two operons confirmed the microarray data. Moreover, csrA was found to regulate co-ordinately the cob operon for synthesis of vitamin B12, required for the metabolism of either 1,2-propanediol or ethanolamine. Additionally, the csrA mutant poorly expressed the genes of the mal operon, required for transport and use of maltose and maltodextrins, and had reduced amounts of maltoporin, normally a dominant protein of the outer membrane. These results show that csrA controls a number of gene classes in addition to those required for invasion, some of them unique to Salmonella, and suggests a co-ordinated bacterial response to conditions that exist at the site of bacterial invasion, the intestinal tract of a host animal.
CsrA是鼠伤寒沙门氏菌中侵袭基因的调控因子。为了研究CsrA在基因调控中的更广泛作用,我们使用DNA微阵列比较了csrA突变体和野生型沙门氏菌基因的表达情况。正如预期的那样,我们发现沙门氏菌致病岛1(SPI-1)侵袭基因在csrA突变体中的表达大幅降低,该致病岛外那些编码由SPI-1 III型分泌装置转运到真核细胞中的蛋白质的基因表达也降低了。鞭毛合成操纵子flg和fli的表达也很差,并且csrA突变体无鞭毛且不运动。沙门氏菌在肠道环境中可能使用的两条代谢途径的基因表达也降低了:用于利用1,2-丙二醇的pdu操纵子和用于乙醇胺分解代谢的eut操纵子。这两个操纵子中报告基因融合体表达的降低证实了微阵列数据。此外,发现csrA协同调节维生素B12合成的cob操纵子,维生素B12是1,2-丙二醇或乙醇胺代谢所必需的。此外,csrA突变体中麦芽糖操纵子的基因表达很差,麦芽糖操纵子是转运和利用麦芽糖及麦芽糊精所必需的,并且其麦芽糖孔蛋白的量减少,麦芽糖孔蛋白通常是外膜的主要蛋白质。这些结果表明,CsrA除了控制侵袭所需的基因类别外,还控制许多其他基因类别,其中一些是沙门氏菌特有的,并表明细菌对细菌侵袭部位(宿主动物肠道)存在的条件有协同反应。