Superantigen profile of Staphylococcus aureus isolates from patients with steroid-resistant atopic dermatitis

被引:93
作者
Schlievert, Patrick M. [1 ]
Case, Laura C. [1 ]
Strandberg, Kristi L. [1 ]
Abrams, Bea B. [2 ]
Leung, Donald Y. M.
机构
[1] Univ Minnesota, Sch Med, Dept Microbiol, Minneapolis, MN 55455 USA
[2] Nova Pharmaceut Corp, E Hanover, NJ USA
关键词
D O I
10.1086/586746
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Background. Superantigens induce skin inflammatory responses in atopic dermatitis, which is commonly associated with Staphylococcus aureus infection. T cells activated in vitro by superantigens become steroid resistant. The objective was to assess the superantigen profiles of S. aureus isolates from patients with steroid-resistant atopic dermatitis. Methods. We compared the superantigen-production capability of S. aureus isolates from 78 patients with steroid-resistant atopic dermatitis (group 1) with that of 30 vaginal isolates from healthy women (group 2) and 22 isolates from a general population of patients with atopic dermatitis (group 3). Polymerase chain reaction with primers for superantigens, combined with selected antibody testing, was used to analyze the presence of toxic shock syndrome toxin 1, staphylococcal enterotoxins, and enterotoxin-like superantigens. Results. S. aureus isolates from group 1 had a statistically significant difference in superantigen profile, compared with the profiles of group 2 and group 3 isolates. Group 2 isolates were similar in profile to group 3 isolates, with 4 and 5 superantigens per isolate, respectively. In contrast, group 1 isolates produced a mean of 8 superantigens each (P<<.001) for comparison with group 2 or group 3). These group 1 isolates were more likely to produce the 3 major toxic shock syndrome-associated superantigens (toxic shock syndrome toxin 1, staphylococcal enterotoxin B, and staphylococcal enterotoxin C) and to produce unusual combinations of superantigens (e.g., toxic shock syndrome toxin 1 and staphylococcal enterotoxin B). Conclusions. S. aureus isolates from patients with steroid-resistant atopic dermatitis appear to be selected on the basis of greater production of superantigens, compared with that of isolates from control groups. Superantigens may offer selective advantages for colonization of patients.
引用
收藏
页码:1562 / 1567
页数:6
相关论文
共 38 条
[1]
[Anonymous], 1999, MMWR-MORBID MORTAL W, V48, P707
[2]
[Anonymous], IMAGEJ IMAGE PROCESS
[3]
BETLEY MJ, 1984, P NATL ACAD SCI-BIOL, V81, P5179, DOI 10.1073/pnas.81.16.5179
[4]
A RAPID, SENSITIVE METHOD FOR DETECTION OF ALKALINE-PHOSPHATASE CONJUGATED ANTI-ANTIBODY ON WESTERN BLOTS [J].
BLAKE, MS ;
JOHNSTON, KH ;
RUSSELLJONES, GJ ;
GOTSCHLICH, EC .
ANALYTICAL BIOCHEMISTRY, 1984, 136 (01) :175-179
[5]
Atopic dermatitis [J].
Boguniewicz, Mark ;
Schmid-Grendelmeier, Peter ;
Leung, Donald Y. M. .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2006, 118 (01) :40-43
[6]
BOHACH GA, 1989, REV INFECT DIS, V11, pS75
[7]
SELECTIVE EXPANSION OF T-CELLS EXPRESSING V-BETA-2 IN TOXIC SHOCK SYNDROME [J].
CHOI, YW ;
LAFFERTY, JA ;
CLEMENTS, JR ;
TODD, JK ;
GELFAND, EW ;
KAPPLER, J ;
MARRACK, P ;
KOTZIN, BL .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 172 (03) :981-984
[8]
A novel methicillin-resistance cassette in community- acquired Methicillin-resistant Staphylococcus aureus isolates of diverse genetic backgrounds [J].
Daum, RS ;
Ito, T ;
Hiramatsu, K ;
Hussain, F ;
Mongkolrattanothai, K ;
Jamklang, M ;
Boyle-Wang, S .
JOURNAL OF INFECTIOUS DISEASES, 2002, 186 (09) :1344-1347
[9]
TOXIC SHOCK SYNDROME TOXIN 1-PRODUCING STAPHYLOCOCCUS-AUREUS ISOLATES CONTAIN THE STAPHYLOCOCCAL-ENTEROTOXIN-B GENETIC ELEMENT BUT DO NOT EXPRESS STAPHYLOCOCCAL-ENTEROTOXIN-B [J].
DEBOER, ML ;
CHOW, AW .
JOURNAL OF INFECTIOUS DISEASES, 1994, 170 (04) :818-827
[10]
Community-acquired methicillin-resistant Staphylococcus aureus infections in France:: Emergence of a single clone that produces Panton-Valentine leukocidin [J].
Dufour, P ;
Gillet, Y ;
Bes, M ;
Lina, G ;
Vandenesch, F ;
Floret, D ;
Etienne, J ;
Richet, H .
CLINICAL INFECTIOUS DISEASES, 2002, 35 (07) :819-824