Votava M, Skalka B, Ondrovcík P, Růzicka F, Svoboda J, Woznicová V
Mikrobiologický ústav Lékarské fakulty Masarykovy univerzity, Brnĕ.
Epidemiol Mikrobiol Imunol. 2000 Aug;49(3):123-9.
Colonies of Arcanobacterium haemolyticum on common blood agar can be easily overlooked. Therefore a diagnostic medium was developed, on which A. haemolyticum colonies produce a conspicuous zone of complete hemolysis. The medium under question is blood agar prepared from the Columbia Blood Agar Base and 5% washed sheep erythrocytes sensitised with equi factor (EF) of Rhodococcus equi. Optimally, 10 activity units (AU) of EF per 1 ml were used. EF was titrated on a non-nutrient medium consisting of agar Purified (Difco) and 5% washed sheep erythrocytes sensitized with beta-haemolysin (BL) of Staphylococcus aureus, 10 AU/ml. On the same medium, staphylococcal BL was titrated on the basis of its direct haemolytic effect. Despite the very distinct haemolytic reaction of the control strains evident on the diagnostic medium with EF, A. haemolyticum failed to grow from 2.597 throat swabs examined especially for the particular microbe during the a period of two years. However, A. haemolyticum was isolated on this medium twice from 223 swabs from wounds and skin lesions. The proposed medium makes also the rapid diagnosis of species Corynebacterium ulcerans, Dermatophilus congolensis and Listeria monocytogenes on the basis of haemolytic synergism possible.
溶血隐秘杆菌在普通血琼脂上的菌落很容易被忽视。因此,开发了一种诊断培养基,在该培养基上溶血隐秘杆菌菌落会产生明显的完全溶血区。所述培养基是由哥伦比亚血琼脂基础培养基和用马红球菌的equi因子(EF)致敏的5%洗涤过的绵羊红细胞制备的血琼脂。最佳情况下,每1 ml使用10活性单位(AU)的EF。EF在由纯化琼脂(Difco)和用金黄色葡萄球菌的β-溶血素(BL)致敏的5%洗涤过的绵羊红细胞组成的非营养培养基上进行滴定,10 AU/ml。在同一培养基上,根据其直接溶血作用对葡萄球菌BL进行滴定。尽管对照菌株在含有EF的诊断培养基上有非常明显的溶血反应,但在两年期间对2597份专门检测该特定微生物的咽喉拭子进行检测时,溶血隐秘杆菌未能生长。然而,在该培养基上从223份伤口和皮肤病变拭子中两次分离出溶血隐秘杆菌。所提出的培养基还使得基于溶血协同作用对溃疡棒状杆菌、刚果嗜皮菌和单核细胞增生李斯特菌进行快速诊断成为可能。