Escherichia coli O157:H7 gene expression in the presence of catecholamine norepinephrine

被引:42
作者
Dowd, Scot E. [1 ]
机构
[1] USDA ARS, Livestock Issues Res Unit, Lubbock, TX 79403 USA
关键词
pathogenesis; neuroendocrine; virulence; norepinephrine; Escherichia coli;
D O I
10.1111/j.1574-6968.2007.00800.x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Various forms of host stresses (e.g. physiological, psychological) are thought to influence susceptibility to pathogenic microorganisms. Catecholamines such as norepinephrine are released into the GI environment during acute stress and may influence the infective process of bacterial pathogens associated with the GI tract. To examine the effects of norepinephrine on expression of virulence factors in Escherichia coli O157:H7, the clinical-type isolate EDL933 (ATCC 43895) was grown in serum-Standard American Petroleum Institute media in the presence or absence of norepinephrine. After 5 h of exposure to norepinephrine, treatment and control cultures (not exposed to norepinephrine) were harvested, their RNA isolated, and gene expression evaluated. There was a dramatic increase in the expression of virulence factor transcripts including stx1, stx2, and eae. Also induced were transcripts involved in iron metabolism. Conversely, there was comparative repression of iron acquisition and phage shock protein-related transcripts in the presence of norepinephrine. Novel observations from these data suggested that exposure to norepinephrine induced glutamate decarboxylase acid resistance as well as an SOS response in E. coli 0 157:H7. The results corroborate many of the previous findings detailed in the literature and provide new observations that could expand the scope of microbial endocrinology.
引用
收藏
页码:214 / 223
页数:10
相关论文
共 66 条
[1]   Sympathetic discharge to mesenteric organs and the liver - Evidence for substantial mesenteric organ norepinephrine spillover [J].
Aneman, A ;
Eisenhofer, G ;
Olbe, L ;
Dalenback, J ;
Nitescu, P ;
Fandriks, L ;
Friberg, P .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (07) :1640-1646
[2]   CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING [J].
BENJAMINI, Y ;
HOCHBERG, Y .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) :289-300
[3]   Stress-induced mutagenesis in bacteria [J].
Bjedov, I ;
Tenaillon, O ;
Gérard, B ;
Souza, V ;
Denamur, E ;
Radman, M ;
Taddei, F ;
Matic, I .
SCIENCE, 2003, 300 (5624) :1404-1409
[4]   STIMULATORY EFFECT OF DIHYDROXYPHENYL COMPOUNDS ON AEROTOLERANCE OF SPIRILLUM-VOLUTANS AND CAMPYLOBACTER-FETUS SUBSPECIES JEJUNI [J].
BOWDRE, JH ;
KRIEG, NR ;
HOFFMAN, PS ;
SMIBERT, RM .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1976, 31 (01) :127-133
[5]   New horizons for (p)ppGpp in bacterial and plant physiology [J].
Braeken, K ;
Moris, M ;
Daniels, R ;
Vanderleyden, J ;
Michiels, J .
TRENDS IN MICROBIOLOGY, 2006, 14 (01) :45-54
[6]   The glutamate-dependent acid resistance system in Escherichia coli:: essential and dual role of the His-Asp phosphorelay RcsCDB/AF [J].
Castanie-Cornet, Marie-Pierre ;
Treffandier, Helene ;
Francez-Charlot, Anne ;
Gutierrez, Claude ;
Cam, Kaymeuang .
MICROBIOLOGY-SGM, 2007, 153 :238-246
[7]   A generic approach for the design of whole-genome oligoarrays, validated for genomotyping, deletion mapping and gene expression analysis on Staphylococcus aureus -: art. no. 95 [J].
Charbonnier, Y ;
Gettler, B ;
Francois, P ;
Bento, M ;
Renzoni, A ;
Vaudaux, P ;
Schlegel, W ;
Schrenzel, J .
BMC GENOMICS, 2005, 6 (1)
[8]   Mucosally-directed adrenergic nerves and sympathomimetic drugs enhance non-intimate adherence of Escherichia coli O157:H7 to porcine cecum and colon [J].
Chen, Chunsheng ;
Lyte, Mark ;
Stevens, Mark P. ;
Vulchanova, Lucy ;
Brown, David R. .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2006, 539 (1-2) :116-124
[9]   Catecholamines, modulate Escherichia coli O157:H7 adherence to murine cecal mucosa [J].
Chen, CS ;
Brown, DR ;
Xie, YH ;
Green, BT ;
Lyte, M .
SHOCK, 2003, 20 (02) :183-188
[10]   Enteropathogenic Escherichia coli virulence genes encoding secreted signalling proteins are essential for modulation of Caco-2 cell electrolyte transport [J].
Collington, GK ;
Booth, IW ;
Donnenberg, MS ;
Kaper, JB ;
Knutton, S .
INFECTION AND IMMUNITY, 1998, 66 (12) :6049-6053