A SAFE-SITE FOR SALMONELLA-TYPHIMURIUM IS WITHIN SPLENIC POLYMORPHONUCLEAR CELLS

被引:50
作者
DUNLAP, NE
BENJAMIN, WH
BERRY, AK
ELDRIDGE, JH
BRILES, DE
机构
[1] UNIV ALABAMA,DEPT MICROBIOL,BIRMINGHAM,AL 35294
[2] UNIV ALABAMA,DEPT PEDIAT,BIRMINGHAM,AL 35294
[3] VET ADM MED CTR,BIRMINGHAM,AL 35294
关键词
SALMONELLA-TYPHIMURIUM; POLYMORPHONUCLEAR CELLS; INTRACELLULAR; SPLEEN; RETICULOENDOTHELIAL SYSTEM; MOUSE;
D O I
10.1016/0882-4010(92)90019-K
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Following oral or systemic infection with Salmonella typhimurium, the focus of infection is in the liver and spleen. The majority of Salmonella surviving in the liver and spleen by 4 h post infection are already in an environment where they are largely protected from subsequent killing. Previous studies have shown that the majority of surviving Salmonella are intracellular. In the present study we sought to determine the cell type containing most of the cell-associated Salmonella liberated from the spleen. We enriched for Salmonella-containing cells by Ficoll-Hypaque separation followed by fluorescence-activated cell sorting. Approximately 85% of the total intracellular Salmonella were found in Mac-1+/J-11d+ cell fractions of the Ficoll-Hypaque band and pellet. By microscopic examination of stained cells from the sorted cell populations, it was evident that virtually all of the Salmonella were in polymorphonuclear cells (PMN). The numbers of Salmonella observed microscopically were similar in numbers to Salmonella colony forming units detected by plating. Salmonella containing PMN in the Ficoll band generally contained a single bacterium, while those from the probably less healthy cells in the Ficoll pellet generally contained several Salmonella. © 1992.
引用
收藏
页码:181 / 190
页数:10
相关论文
共 35 条
[1]   GENETIC-MAPPING OF NOVEL VIRULENCE DETERMINANTS OF SALMONELLA-TYPHIMURIUM TO THE REGION BETWEEN TRPD AND SUPD [J].
BENJAMIN, WH ;
TURNBOUGH, CL ;
GOGUEN, JD ;
POSEY, BS ;
BRILES, DE .
MICROBIAL PATHOGENESIS, 1986, 1 (02) :115-124
[2]  
BENJAMIN WH, 1990, J IMMUNOL, V144, P3143
[3]   THE ABILITY OF SALMONELLA-TYPHIMURIUM TO PRODUCE THE SIDEROPHORE ENTEROBACTIN IS NOT A VIRULENCE FACTOR IN MOUSE TYPHOID [J].
BENJAMIN, WH ;
TURNBOUGH, CL ;
POSEY, BS ;
BRILES, DE .
INFECTION AND IMMUNITY, 1985, 50 (02) :392-397
[4]   THE SALMONELLA-TYPHIMURIUM LOCUS MVIA REGULATES VIRULENCE IN ITYS BUT NOT ITYR MICE - FUNCTIONAL MVIA RESULTS IN AVIRULENCE - MUTANT (NONFUNCTIONAL) MVIA RESULTS IN VIRULENCE [J].
BENJAMIN, WH ;
YOTHER, J ;
HALL, P ;
BRILES, DE .
JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 174 (05) :1073-1083
[5]  
BENJAMIN WH, 1986, J GEN MICROBIOL, V132, P183
[6]   PHAGOCYTOSIS AND KILLING OF SALMONELLA-TYPHIMURIUM BY PERITONEAL-EXUDATE CELLS [J].
BRILES, DE ;
LEHMEYER, J ;
FORMAN, C .
INFECTION AND IMMUNITY, 1981, 33 (02) :380-388
[7]  
BRUCE J, 1981, J IMMUNOL, V127, P2496
[8]   PHAGOLYSOSOME FORMATION, CYCLIC ADENOSINE 3'-5'-MONOPHOSPHATE AND THE FATE OF SALMONELLA-TYPHIMURIUM WITHIN MOUSE PERITONEAL MACROPHAGES [J].
CARROL, MEW ;
JACKETT, PS ;
ABER, VR ;
LOWRIE, DB .
JOURNAL OF GENERAL MICROBIOLOGY, 1979, 110 (FEB) :421-429
[9]   GROWTH OF TYPHOID AND PARATYPHOID BACILLI IN INTRAVENOUSLY INFECTED MICE [J].
CARTER, PB ;
COLLINS, FM .
INFECTION AND IMMUNITY, 1974, 10 (04) :816-822
[10]   SALMONELLOSIS IN ORALLY INFECTED SPECIFIC PATHOGEN-FREE C57B1 MICE [J].
COLLINS, FM .
INFECTION AND IMMUNITY, 1972, 5 (02) :191-&