Acid-shock responses in Staphylococcus aureus investigated by global gene expression analysis

被引:138
作者
Bore, Erlend
Langsrud, Solveig
Langsrud, Oyvind
Rode, Tone Mari
Holck, Askild
机构
[1] Norwegian Food Res Inst, N-1430 As, Norway
[2] Norwegian Univ Life Sci, N-1432 As, Norway
来源
MICROBIOLOGY-SGM | 2007年 / 153卷
关键词
D O I
10.1099/mic.0.2007/005942-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A general overview is presented of the changes in the genetic expression along a time curve through the first 20 min after acidification to pH 4.5 of exponentially growing cultures of the food pathogenic strain Staphylococcus aureus 50583. A newly developed method for statistical significance testing was used to detect significant gene expression responses. Most responses showed an increase or decrease from time zero to 10 min after acidification, and then generally a stabilization in expression level from 10 to 20 min. Increased urease activity appeared to be an important factor in the acid defence, along with proton excretion by NADH dehydrogenase and macromolecule repair mechanisms. Oxidative-stress responses, such as increased expression of thioredoxin genes and upregulation of pentose phosphate pathway genes to generate more reducing power, were also induced. A general reduction in the expression of genes encoding ribosomal proteins and genes involved in nucleotide synthesis, as well as fatty acid and lipoprotein metabolism, reflected the lowered growth rate after acidification. The pH shock did not appear to trigger major virulence responses or biofilm formation. Metal ion regulation and transport were affected by the acid shock, and production of several cofactors such as molybdopterin was increased. Many of the presented observations could be explained, while some represent still-unknown mechanisms. The patterns of regulation were confirmed by quantitive reverse transcriptase PCR (ORT-PCR). Together, these results showed the main responses of S. aureus and will be a good starting point for future, more specific, in-depth studies of specific gene responses that occur in conjunction with the acid-stress defence of S. aureus.
引用
收藏
页码:2289 / 2303
页数:15
相关论文
共 54 条
[1]   Enzyme level of enterococcal F1F0-ATPase is regulated by pH at the step of assembly [J].
Arikado, E ;
Ishihara, H ;
Ehara, T ;
Shibata, C ;
Saito, H ;
Kakegawa, T ;
Igarashi, K ;
Kobayashi, H .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1999, 259 (1-2) :262-268
[2]   A HOMOLOG TO THE ESCHERICHIA-COLI ALKYL HYDROPEROXIDE REDUCTASE AHPC IS INDUCED BY OSMOTIC UPSHOCK IN STAPHYLOCOCCUS-AUREUS [J].
ARMSTRONGBUISSERET, L ;
COLE, MB ;
STEWART, GSAB .
MICROBIOLOGY-SGM, 1995, 141 :1655-1661
[3]   Allelic exchange mutagenesis of nixA in Helicobacter pylori results in reduced nickel transport and urease activity [J].
Bauerfeind, P ;
Garner, RM ;
Mobley, HLT .
INFECTION AND IMMUNITY, 1996, 64 (07) :2877-2880
[4]   Global gene expression in Staphylococcus aureus biofilms [J].
Beenken, KE ;
Dunman, PM ;
McAleese, F ;
Macapagal, D ;
Murphy, E ;
Projan, SJ ;
Blevins, JS ;
Smeltzer, MS .
JOURNAL OF BACTERIOLOGY, 2004, 186 (14) :4665-4684
[5]   The MerR family of transcriptional regulators [J].
Brown, NL ;
Stoyanov, JV ;
Kidd, SP ;
Hobman, JL .
FEMS MICROBIOLOGY REVIEWS, 2003, 27 (2-3) :145-163
[6]   2-oxo acid dehydrogenase complexes in redox regulation - Role of the lipoate residues and thioredoxin [J].
Bunik, VI .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2003, 270 (06) :1036-1042
[7]   Bacterial ureases in infectious diseases [J].
Burne, RA ;
Chen, YYM .
MICROBES AND INFECTION, 2000, 2 (05) :533-542
[8]  
Chan PF, 1998, J BACTERIOL, V180, P6232
[9]   Toxicogenomic response of Staphylococcus aureus to peracetic acid [J].
Chang, Wook ;
Toghrol, Freshteh ;
Bentley, William E. .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2006, 40 (16) :5124-5131
[10]   clpB, a novel member of the Listeria monocytogenes CtsR regulon, is involved in virulence but not in general stress tolerance [J].
Chastanet, A ;
Derre, I ;
Nair, S ;
Msadek, T .
JOURNAL OF BACTERIOLOGY, 2004, 186 (04) :1165-1174