Preus H R, Sunday G J, Haraszthy V I, Zambon J J
Departments of Oral Biology and Periodontology, School of Dental Medicine, State University of New York at Buffalo.
Oral Microbiol Immunol. 1992 Dec;7(6):372-5. doi: 10.1111/j.1399-302x.1992.tb00639.x.
Actinobacillus actinomycetemcomitans is a key microorganism in the pathogenesis of several different forms of periodontal diseases. Identification of this bacterium from clinical specimens may often be complicated by the fact that the colony morphology on TSBV selective medium closely resembles that of Haemophilus aphrophilus and a key differentiating characteristic, catalase reaction, may be variable. Recent genetic studies have shown that the 23S ribosomal RNA molecule is split into two smaller forms in A. actinomycetemcomitans, but is intact in H. aphrophilus. Based on this finding, we describe a new, rapid method for identifying A. actinomycetemcomitans in which single colonies isolated from culture on TSBV agar in 5% CO2 in air are lysed, electrophoresed on 1.5% submarine agarose gels and visualized by staining with ethidium bromide. Using this assay, A. actinomycetemcomitans can be easily distinguished from morphologically similar colonies such as H. aphrophilus strains by differences in 23S rRNA within 2 h.
伴放线放线杆菌是多种不同形式牙周疾病发病机制中的关键微生物。从临床标本中鉴定这种细菌往往很复杂,因为在TSBV选择性培养基上的菌落形态与嗜沫嗜血杆菌非常相似,而一个关键的鉴别特征——过氧化氢酶反应可能会有所不同。最近的基因研究表明,伴放线放线杆菌中的23S核糖体RNA分子被分裂成两种较小的形式,但在嗜沫嗜血杆菌中是完整的。基于这一发现,我们描述了一种新的、快速鉴定伴放线放线杆菌的方法,即从在含5%二氧化碳的空气中于TSBV琼脂上培养分离得到的单菌落进行裂解,在1.5%的水下琼脂糖凝胶上进行电泳,并用溴化乙锭染色进行观察。使用这种检测方法,在2小时内就可以通过23S rRNA的差异轻松地将伴放线放线杆菌与形态相似的菌落(如嗜沫嗜血杆菌菌株)区分开来。