GROWTH OF SALMONELLA-TYPHIMURIUM SL5319 AND ESCHERICHIA-COLI F-18 IN MOUSE CECAL MUCUS - ROLE OF PEPTIDES AND IRON

被引:5
作者
FRANKLIN, DP
LAUX, DC
WILLIAMS, TJ
FALK, MC
COHEN, PS
机构
[1] UNIV RHODE ISL,DEPT MICROBIOL,KINGSTON,RI 02881
[2] USN,MED RES INST,BETHESDA,MD 20814
关键词
INTESTINAL COLONIZATION; ENTEROCHELIN; AEROBACTIN; PEPTIDES;
D O I
10.1016/0378-1097(90)90557-7
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Escherichia coli F-18, a normal human fecal isolate, and Salmonella typhimurium SL5319, an avirulent strain, are known to colonize the streptomycin-treated CD-1 mouse large intestine by utilizing nutrients present in intestinal mucus for growth. Moreover, previous experiments suggested the possibility that E. coli F-18 and S. typhimurium SL5319 utilized different mucus nutrients. Therefore, mouse cecal mucus was fractionated into high and low molecular weight components, and each fraction was inoculated either simultaneously or separately with E. coli F-18 and S. typhimurium L5319. A 50 kd fraction was found in which the growth of S. typhimurium SL5319 suppressed growth of E. coli F-18. Evidence is presented that in this fraction S. typhimurium SL5319 utilizes peptides, presumably generated by mucus proteases, as a source of amino acids for growth. Furthermore, it is shown that S. typhimurium SL5319 grows in this 50 kd fraction with a generation time of 27 min in the presence of at most 7-mu-g of carbohydrate per ml and 22-mu-g of peptide per ml, and that S. typhimurium SL5319 suppresses E. coli F-18 growth in this fraction by sequestering iron. The data are discussed with respect to the role of peptide utilization and iron sequestration in the ability of S. typhimurium SL5319 to colonize the mouse large intestine.
引用
收藏
页码:229 / 239
页数:11
相关论文
共 22 条
[2]  
BROWN GM, 1987, ESCHERICHIA COLI SAL, P521
[3]   ADHESION OF A HUMAN FECAL ESCHERICHIA-COLI STRAIN TO MOUSE COLONIC MUCUS [J].
COHEN, PS ;
ARRUDA, JC ;
WILLIAMS, TJ ;
LAUX, DC .
INFECTION AND IMMUNITY, 1985, 48 (01) :139-145
[4]   NEW BIOTYPING SCHEME FOR SALMONELLA-TYPHIMURIUM AND ITS PHYLOGENETIC SIGNIFICANCE [J].
DUGUID, JP ;
ANDERSON, ES ;
ALFREDSSON, GA ;
BARKER, R ;
OLD, DC .
JOURNAL OF MEDICAL MICROBIOLOGY, 1975, 8 (01) :149-166
[5]   GENETIC-CHARACTERIZATION AND MOLECULAR-CLONING OF THE TRIPEPTIDE PERMEASE (TPP) GENES OF SALMONELLA-TYPHIMURIUM [J].
GIBSON, MM ;
PRICE, M ;
HIGGINS, CF .
JOURNAL OF BACTERIOLOGY, 1984, 160 (01) :122-130
[6]   COMPOUNDS WHICH SERVE AS SOLE SOURCE OF CARBON OR NITROGEN FOR SALMONELLA TYPHIMURIUM LT-2 [J].
GUTNICK, D ;
CALVO, JM ;
KLOPOTOWSKI, T ;
AMES, BN .
JOURNAL OF BACTERIOLOGY, 1969, 100 (01) :215-+
[7]   PERIPLASMIC PROTEIN ASSOCIATED WITH THE OLIGOPEPTIDE PERMEASES OF SALMONELLA-TYPHIMURIUM AND ESCHERICHIA-COLI [J].
HIGGINS, CF ;
HARDIE, MM .
JOURNAL OF BACTERIOLOGY, 1983, 155 (03) :1434-1438
[8]  
Kim YS, 1984, ATTACHMENT ORGANISMS, VII, P99
[9]   ROLES OF MOTILITY, CHEMOTAXIS, AND PENETRATION THROUGH AND GROWTH IN INTESTINAL MUCUS IN THE ABILITY OF AN AVIRULENT STRAIN OF SALMONELLA-TYPHIMURIUM TO COLONIZE THE LARGE-INTESTINE OF STREPTOMYCIN-TREATED MICE [J].
MCCORMICK, BA ;
STOCKER, BAD ;
LAUX, DC ;
COHEN, PS .
INFECTION AND IMMUNITY, 1988, 56 (09) :2209-2217
[10]   TYPE-1 PILI ARE NOT NECESSARY FOR COLONIZATION OF THE STREPTOMYCIN-TREATED MOUSE LARGE-INTESTINE BY TYPE-1-PILIATED ESCHERICHIA-COLI F-18 AND ESCHERICHIA-COLI K-12 [J].
MCCORMICK, BA ;
FRANKLIN, DP ;
LAUX, DC ;
COHEN, PS .
INFECTION AND IMMUNITY, 1989, 57 (10) :3022-3029