MURINE MODEL OF CUTANEOUS INFECTION WITH GRAM-POSITIVE COCCI

被引:150
作者
BUNCE, C
WHEELER, L
REED, G
MUSSER, J
BARG, N
机构
[1] VANDERBILT UNIV,MED CTR,SCH MED,DEPT MED,DIV INFECT DIS,NASHVILLE,TN 37232
[2] VANDERBILT UNIV,MED CTR,SCH MED,DEPT PREVENT MED,NASHVILLE,TN 37232
[3] BAYLOR COLL MED,DEPT PATHOL,MOLEC PATHOBIOL SECT,HOUSTON,TX 77030
关键词
D O I
10.1128/IAI.60.7.2636-2640.1992
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
Staphylococcus aureus has remained an important cause of nosocomial wound infections, but standardized or reproducible systems for analyzing cutaneous infections caused by S. aureus do not exist. A variety of foreign materials, variable inocula, and skin traumas have been used to promote infection. To minimize these variables and ensure reproducibility, we chose a model using subcutaneous injections of a fixed quantity of dextran microbeads (Cytodex) as the foreign material added to standardized broth suspensions of S. aureus. Suspensions (0.2 ml) injected into an outbred strain of immunocompetent hairless mice generated reproducible, measurable lesions. With S. aureus Smith Diffuse, fluctuant, erythematous lesions with a peak diameter of 15 mm were observed; these lesions yielded purulent material containing gram-positive cocci and neutrophils and yielded growth of S. aureus on culture. Lesion size was proportional to the bacterial inoculum size. Histologic examination of excised lesions revealed typical abscesses. A second strain of S. aureus (SLC3) produced dermonecrosis instead of abscesses at an inoculum size of 10(7) CFU. Control injections with a sterile Cytodex suspension regularly produced nondraining, nonerythematous nodules with maximum diameters of less-than-or-equal-to 5 mm. Streptococcus pyogenes produced late-onset necrotic lesions and abscesses. Using a foreign substance, this model generates easily observed and reproducible cutaneous infection with S. aureus and streptococci that can potentially discriminate between inter- and intrastrain differences. Such a model could be used to test the pathogenicity of isogeneic strains of these bacterial species and to evaluate the efficacy of antimicrobial agents.
引用
收藏
页码:2636 / 2640
页数:5
相关论文
共 25 条
[1]
VIRULENCE OF STAPHYLOCOCCUS-AUREUS MUTANTS ALTERED IN TYPE-5 CAPSULE PRODUCTION [J].
ALBUS, A ;
ARBEIT, RD ;
LEE, JC .
INFECTION AND IMMUNITY, 1991, 59 (03) :1008-1014
[2]
BOR DH, 1983, REV INFECT DIS, V5, P885
[3]
ROLES OF ALPHA-TOXIN AND BETA-TOXIN IN VIRULENCE OF STAPHYLOCOCCUS-AUREUS FOR THE MOUSE MAMMARY-GLAND [J].
BRAMLEY, AJ ;
PATEL, AH ;
OREILLY, M ;
FOSTER, R ;
FOSTER, TJ .
INFECTION AND IMMUNITY, 1989, 57 (08) :2489-2494
[4]
CHARACTERIZATION OF A BACTERICIDAL LIPID DEVELOPING WITHIN STAPHYLOCOCCAL ABSCESSES [J].
DYE, ES ;
KAPRAL, FA .
INFECTION AND IMMUNITY, 1981, 32 (01) :98-104
[5]
ELEK SD, 1957, BRIT J EXP PATHOL, V38, P573
[6]
FORD CW, 1988, J MED MICROBIOL, V28, P259
[7]
CHEMOTHERAPEUTIC EFFICACY OF OFLOXACIN ON RENAL AND SUBCUTANEOUS INFECTION MODELS WITH STAPHYLOCOCCUS-AUREUS IN MICE [J].
FUJIMOTO, T ;
SATO, M ;
KATAMI, K ;
OSADA, Y ;
TSUMURA, M ;
TACHIZAWA, H ;
UNE, T .
CHEMOTHERAPY, 1986, 32 (03) :291-298
[8]
CEPHALOTHIN CLEARANCE OF STAPHYLOCOCCUS-AUREUS FROM 2 EXPERIMENTAL-INFECTION SITES IN THE PRESENCE AND ABSENCE OF LOCAL PHAGOCYTIC-CELLS [J].
GERDING, DN ;
BEAN, B ;
PETERSON, LR ;
MOODY, J ;
BETTIN, K .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1987, 20 (05) :685-695
[9]
IANDOLO JJ, 1989, ANNU REV MICROBIOL, V43, P375, DOI 10.1146/annurev.micro.43.1.375
[10]
VIRULENCE OF STAPHYLOCOCCUS-AUREUS IN A MOUSE MASTITIS MODEL - STUDIES OF ALPHA-HEMOLYSIN, COAGULASE, AND PROTEIN-A AS POSSIBLE VIRULENCE DETERMINANTS WITH PROTOPLAST FUSION AND GENE CLONING [J].
JONSSON, P ;
LINDBERG, M ;
HARALDSSON, I ;
WADSTROM, T .
INFECTION AND IMMUNITY, 1985, 49 (03) :765-769