Carloni G H, Bentancor L D, De Torres R A
Microbiología, Facultad de Ciencias Veterinarias, UBA, Chorroarín 280, (1427) Bs. As.
Rev Argent Microbiol. 2005 Apr-Jun;37(2):87-8.
Beta toxin of C. chauvoei has desoxiribonuclease (DNase) activity which is regarded as one of its virulence factors. The production of DNase was detected in strains isolated from bovines, using as controls C. chauvoei ATCC 10092, and C. perfringens Type A and C. septicum, both laboratory isolates. The enzyme activity was made evident on a DNA substrate observing the macroscopic degradation. A simple methodology was developed using a commercial medium for DNase test, with the incorporation of sterile horse serum. Each strain was streaked on the surface of the medium, incubated in anaerobic atmosphere at 37 degrees C for 48 hours. The plates were revealed with HCI 1 N. The appearance of a clear and transparent zone around and under the microbial growing was considered a positive reaction. Enzyme activity was detected in 10 of 12 strains and also in the controls. The serum addition to the commercial basal medium allows the optimum development of the microorganism showing the enzymatic digestion zone.
产气荚膜梭菌β毒素具有脱氧核糖核酸酶(DNase)活性,该活性被视为其毒力因子之一。在从牛身上分离出的菌株中检测到了DNase的产生,使用产气荚膜梭菌ATCC 10092以及A型产气荚膜梭菌和腐败梭菌(均为实验室分离株)作为对照。通过观察宏观降解情况,在DNA底物上证实了该酶的活性。开发了一种简单的方法,使用用于DNase检测的商业培养基,并加入无菌马血清。将每个菌株划线接种在培养基表面,在37℃厌氧环境中培养48小时。用1N盐酸对平板进行显色。在微生物生长周围和下方出现清晰透明的区域被视为阳性反应。在12株菌株中的10株以及对照中均检测到了酶活性。向商业基础培养基中添加血清可使微生物得到最佳生长,并显示出酶消化区域。