Suppression of toxin production in Clostridium difficile VPI 10463 by amino acids

被引:108
作者
Karlsson, S
Burman, LG
Åkerlund, T [1 ]
机构
[1] Swedish Inst Infect Dis Control, Dept Bacteriol, S-17182 Solna, Sweden
[2] Karolinska Inst, Microbiol & Tumourbiol Ctr, S-17177 Stockholm, Sweden
来源
MICROBIOLOGY-UK | 1999年 / 145卷
关键词
amino acids; bicarbonate; biotin; Clostridium difficile; toxin production;
D O I
10.1099/13500872-145-7-1683
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The impact of various growth conditions on the expression of toxins and other proteins by Clostridium difficile VPI 10463 was studied. During non-starved conditions, the rate of toxin synthesis paralleled that of total protein during both exponential growth and stationary phase, and in both defined and complex media. Biotin limitation reduced growth rate and bulk protein synthesis, whereas toxin expression continued, leading to a 50- to 200-fold increase in intracellular toxin levels. Concomitantly, several 22 kDa proteins were up-regulated as revealed by two-dimensional PACE analysis. The toxin yield was 30-fold higher in peptone yeast extract (PY) than in PY containing glucose (PYG). By contrast, glucose limitation reduced toxin yields by 20- to 100-fold in defined media. By elevating the buffering capacity and bicarbonate concentration, toxin yields were Increased by 10-fold in PY and PYC. The high toxin production by C. difficile during growth in PY was lowered 100-fold by adding a blend of nine amino acids and several 60-100 kDa proteins were concomitantly down-regulated. It was concluded that toxin expression in C. difficile VPI 10463 was not affected by growth rate, growth phase, catabolite repression or the stringent response. Instead the Eo-expression of toxins and a few specific additional proteins appeared to be influenced by metabolic pathways involving CO2 assimilation, carboxylation reactions end metabolism of certain amino acids.
引用
收藏
页码:1683 / 1693
页数:11
相关论文
共 29 条
[11]   Intestinal flora in new-borin infants - With a description of a new pathogenic anaerobe, Bacillus difficilis [J].
Hall, IC ;
O'Toole, E .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1935, 49 (02) :390-402
[12]   Transcriptional analysis of the toxigenic element of Clostridium difficile [J].
Hammond, GA ;
Lyerly, DM ;
Johnson, JL .
MICROBIAL PATHOGENESIS, 1997, 22 (03) :143-154
[13]   Transcription analysis of the genes tcdA-E of the pathogenicity locus of Clostridium difficile [J].
Hundsberger, T ;
Braun, V ;
Weidmann, M ;
Leukel, P ;
Sauerborn, M ;
vonEichelStreiber, C .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1997, 244 (03) :735-742
[14]   THE ENTEROTOXIN FROM CLOSTRIDIUM-DIFFICILE (TOXA) MONOGLUCOSYLATES THE RHO-PROTEINS [J].
JUST, I ;
WILM, M ;
SELZER, J ;
REX, G ;
VONEICHELSTREIBER, C ;
MANN, M ;
AKTORIES, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (23) :13932-13936
[15]   GLUCOSYLATION OF RHO-PROTEINS BY CLOSTRIDIUM-DIFFICILE TOXIN-B [J].
JUST, I ;
SELZER, J ;
WILM, M ;
VONEICHELSTREIBER, C ;
MANN, M ;
AKTORIES, K .
NATURE, 1995, 375 (6531) :500-503
[16]   A DEFINED GROWTH-MEDIUM FOR CLOSTRIDIUM-DIFFICILE [J].
KARASAWA, T ;
IKOMA, S ;
YAMAKAWA, K ;
NAKAMURA, S .
MICROBIOLOGY-UK, 1995, 141 :371-375
[17]   SPOROGENESIS AND TOXIN-A PRODUCTION BY CLOSTRIDIUM-DIFFICILE [J].
KETLEY, JM ;
MITCHELL, TJ ;
HASLAM, SC ;
STEPHEN, J ;
CANDY, DCA ;
BURDON, DW .
JOURNAL OF MEDICAL MICROBIOLOGY, 1986, 22 (01) :33-38
[18]   PRODUCTION AND RELEASE OF TOXINS A AND B BY CLOSTRIDIUM-DIFFICILE [J].
KETLEY, JM ;
HASLAM, SC ;
MITCHELL, TJ ;
STEPHEN, J ;
CANDY, DCA ;
BURDON, DW .
JOURNAL OF MEDICAL MICROBIOLOGY, 1984, 18 (03) :385-391
[19]  
Lyerly David M., 1995, P867
[20]   COMMERCIAL LATEX TEST FOR CLOSTRIDIUM-DIFFICILE TOXIN-A DOES NOT DETECT TOXIN-A [J].
LYERLY, DM ;
WILKINS, TD .
JOURNAL OF CLINICAL MICROBIOLOGY, 1986, 23 (03) :622-623