Reproducible experimental surgical-wound infections in mice for use in the evaluation of topical antibacterial agents are described. The experimental wound was created on the backs of mice by means of a midline incision and was infected by means of cotton sutures monocontaminated with Staphylococcus aureus or Pseudomonas aeruginosa. The course of these wound infections was followed by quantitation of surface bacteria through use of a surface rinse technique. Surface wound counts of the infecting organisms thus obtained appeared to reflect the dynamics of the total wound count, as determined by homogenization of biopsied tissue. Treatment of infected wounds with a placebo cream had only a slight effect on surface wound counts and on mortality in the case of the S. aureus infection but enhanced markedly the lethality of the P. aeruginosa infection.The search for new drugs effective as topical antibacterial agents requires the careful and systematic evaluation of drugs not only in vitro but also in vivo, i.e., in the control and management of experimental infections. Several model infections for evaluating topical antibacterial agents have been developed in laboratory animals (5-7, 9, 18, 19, 21) and in humans (3,14,15,20). Although many of the models have proved to be effective in assessing topical agents, most of them do not lend themselves easily to a mass screening of potential agents. This paper describes and characterizes a relatively simple surgical-wound model in mice in which potential topical antibacterial drugs can be evaluated easily and expeditiously against Staphylococcus aureus and Pseudomonas aeruginosa wound infections.MATERIALS AND METHODS Animals. Female CF-1 mice, 18 to 20 g, purchased from a commercial source (Carworth Farms, New City, N.Y.) were used in all experiments. Mice were maintained, 10 to a cage, on wire, in temperatureand humidity-controlled quarters and were allowed food and water ad libitum.Test organisms. S. aureus SC 2406 (phage type 53/77/84/85) and P. aeruginosa SC 8822, clinical isolates from the departmental culture collection, were used as test organisms. The two organisms were maintained on brain heart infusion (BHI) agar (BBL) slants stored at 4 C, with transfers to fresh slants made monthly. For each experiment, a fresh slant was inoculated from the appropriate stock culture and incubated at 37 C for 18 h. After incubation, the growth was removed from the slant by washing with 0.1 M phosphate buffer, pH 7.2, and the resulting suspension was adjusted to a concentration of 2.0 x 109 cells/ml by use of a Klett-Summerson colorimeter with a 540-nm filter and a previously prepared standard curve. The suspension was then appropriately diluted and used for the contamination of sutures or the direct seeding of the experimental wounds. Preparation of contaminated sutures. Commercial cotton thread (Coats and Clark's, mercerized, size 8) monocontaminated with S. aureus or P. aeruginosa was used as the suture material to initiate and potentiate the experimental infection. The thread ...