LACK OF COMPLETE CORRELATION BETWEEN EMETIC AND T-CELL-STIMULATORY ACTIVITIES OF STAPHYLOCOCCAL ENTEROTOXINS

被引:96
作者
HARRIS, TO
GROSSMAN, D
KAPPLER, JW
MARRACK, P
RICH, RR
BETLEY, MJ
机构
[1] UNIV WISCONSIN,DEPT BACTERIOL,MADISON,WI 53706
[2] BAYLOR COLL MED,DEPT MED,HOUSTON,TX 77030
[3] BAYLOR COLL MED,DEPT MICROBIOL & IMMUNOL,HOUSTON,TX 77030
[4] UNIV COLORADO,NATL JEWISH CTR IMMUNOL & RESP MED,DEPT MED,HOWARD HUGHES MED INST,DENVER,CO 80207
[5] UNIV COLORADO,DEPT MED,DENVER,CO 80202
[6] UNIV COLORADO,DEPT MICROBIOL & IMMUNOL,DENVER,CO 80202
[7] UNIV COLORADO,HLTH SCI CTR,DEPT BIOCHEM,DENVER,CO 80262
[8] UNIV COLORADO,HLTH SCI CTR,DEPT BIOPHYS,DENVER,CO 80262
[9] UNIV COLORADO,HLTH SCI CTR,DEPT GENET,DENVER,CO 80262
关键词
D O I
10.1128/IAI.61.8.3175-3183.1993
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
This study examined the emetic activity of several staphylococcal enterotoxin type A and B (SEA and SEB, respectively) mutants that had either one or two amino acid residue substitutions. New sea gene mutations were constructed by site-directed mutagenesis; gene products were obtained with glycine residues at position 25, 47, 48, 81, 85, or 86 of mature SEA. Culture supernatants from Staphylococcus aureus RN4220, or derivatives containing either sea or a sea mutation, were analyzed for the ability to stimulate proliferation of murine splenocytes, as determined by incorporation of [H-3]thymidine. Culture supernatants containing SEA-N25G (a SEA mutant with a substitution of glycine for the asparagine residue at position 25), SEA-F47G, or SEA-L48G did not stimulate T-cell proliferation, unlike supernatants containing the other substitution mutants. Purified preparations of SEA-N25G had weak activity and those of SEA-F47G and SEA-LA8G had essentially no activity in the T-cell proliferation assay. All mutants except SEA-V85G, which was degraded by monkey stomach lavage fluid in vitro, were tested for emetic activity. SEA-C106A and two SEB mutants, SEB-D9N/N23D and SEB-F44S (previously referred to as BR-257 and BR-358, respectively), whose construction and altered immunological properties have been reported previously, were also tested in the emetic assay. Each mutant was initially administered intragastrically at doses of 75 to 100 mug per animal; if none of the animals responded, the dose was increased four- to fivefold. SEA-F47G, SEA-C106A, and SEB-D9N/N23D were the only mutants that did not induce vomiting at either dose tested; these three mutants had reduced immunological activity. However, there was not a perfect correlation between immunological and emetic activities; SEA-L48G and SEB-F44S retained emetic activity, although they had essentially no T-cell-stimulatory activity. These studies suggest that these two activities can be dissociated.
引用
收藏
页码:3175 / 3183
页数:9
相关论文
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