DEAD SALMONELLAE OR THEIR ENDOTOXIN ACCELERATE THE EARLY COURSE OF A SALMONELLA INFECTION IN MICE

被引:11
作者
HORMAECHE, CE
机构
[1] Division of Microbiology and Parasitology, University Department of Pathology, Cambridge, CB2 1QP, Tennis Court Road
关键词
lipopolysaccharide; macrophage; mouse; Salmonella;
D O I
10.1016/0882-4010(90)90023-J
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The course of a Salmonella infection following a low intravenous dose of virulent organisms was studied in mice. Simultaneous administration of 104 S. typhimurium C5 together with c. 108 dead salmonellae caused a marked acceleration of early net bacterial growth in the liver and spleen, leading to a rapidly overwhelming infection. Administration of similar numbers of either Staphylococcus albus or Bacillus cereus had no effect, whereas 20 μg of S. typhimurium Boivin-type lipopolysaccharide (B-LPS) produced an effect similar to dead organisms; 1 μg B-LPS had a significant infection-accelerating effect. Both B-LPS and Westphal-type endotoxin (W-LPS) could enhance a salmonella infection in LPS-responsive C3H/HeMg mice, whereas only B-LPS was effective in LPS non-responder C3H/HeJ mice, implying that the infectionenhancing effect of a large bolus of dead organisms may be due in part to its LPS content. The results show that the course of a Salmonella infection following administration of large numbers of salmonellae in mice is different from that of Salmonella infections arising from small inocula. The relevance of these results to studies on the possible intracellular location of salmonellae in vivo is discussed. © 1990.
引用
收藏
页码:213 / 218
页数:6
相关论文
共 16 条
[1]   CACHECTIN AND TUMOR-NECROSIS-FACTOR AS 2 SIDES OF THE SAME BIOLOGICAL COIN [J].
BEUTLER, B ;
CERAMI, A .
NATURE, 1986, 320 (6063) :584-588
[2]  
BIOZZI G, 1955, BRIT J EXP PATHOL, V36, P226
[3]  
COLLINS FM, 1977, CORNELL VET, V67, P103
[4]   VACCINES AND CELL-MEDIATED-IMMUNITY [J].
COLLINS, FM .
BACTERIOLOGICAL REVIEWS, 1974, 38 (04) :371-402
[5]   MUTANTS OF SALMONELLA-TYPHIMURIUM THAT CANNOT SURVIVE WITHIN THE MACROPHAGE ARE AVIRULENT [J].
FIELDS, PI ;
SWANSON, RV ;
HAIDARIS, CG ;
HEFFRON, F .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (14) :5189-5193
[6]  
FINLAY BB, 1989, MOL MICROBIOL, V3, P1833, DOI 10.1111/j.1365-2958.1989.tb00170.x
[7]   COMMON THEMES IN MICROBIAL PATHOGENICITY [J].
FINLAY, BB ;
FALKOW, S .
MICROBIOLOGICAL REVIEWS, 1989, 53 (02) :210-230
[8]   HEPATIC CLEARANCE OF SALMONELLA-TYPHIMURIUM IN SILICA-TREATED MICE [J].
FRIEDMAN, RL ;
MOON, RJ .
INFECTION AND IMMUNITY, 1977, 16 (03) :1005-1012
[9]   EXPRESSION OF THE INNATE RESISTANCE GENE ITY IN MOUSE KUPFFER CELLS INFECTED WITH SALMONELLA-TYPHIMURIUM INVITRO [J].
HARRINGTON, KA ;
HORMAECHE, CE .
MICROBIAL PATHOGENESIS, 1986, 1 (03) :269-274
[10]  
HORMAECHE CE, 1979, IMMUNOLOGY, V37, P311