Turng B F, Guthmiller J M, Minah G E, Falkler W A
Department of Oral and Craniofacial Biological Sciences, School of Dentistry, University of Maryland at Baltimore 21201, USA.
Oral Microbiol Immunol. 1996 Oct;11(5):356-61. doi: 10.1111/j.1399-302x.1996.tb00194.x.
Peptostreptococcus micros, an anaerobic gram-positive coccus, has been associated with periodontal and endodontic lesions, including those refractory to treatment, as well as many human polymicrobial infections in other body locations. A selective and differential medium for the primary isolation of P. micros was developed and evaluated. Columbia CNA agar, a selective medium for gram-positive cocci, was supplemented with glutathione and lead acetate (P. micros medium: PMM). P. micros has a characteristic of rapidly utilizing the reduced form of glutathione to form hydrogen sulfide, which reacts with lead acetate producing a black precipitate in the medium. When grown on PMM, P. micros can be easily identified by its typical colonial morphology and the presence of a black precipitate directly under the colony. PMM was compared for the growth of P. micros with phenylethyl alcohol agar (PEA) and Columbia base medium (CBM) with 80 strains of P. micros and 30 strains of other gram-positive cocci. All P. micros isolates tested grew and showed the typical morphology of P. micros on PMM. Using colony counts on CBM as controls, there was an average 81.8% recovery in the number of P. micros colonies on PMM, in contrast to an average 6.1% recovery on PEA. Subgingival plaque and tongue samples from 12 adult periodontitis and 6 early-onset periodontitis patients were cultured onto PMM for the isolation of P. micros. P. micros was isolated on PMM and identified biochemically and enzymatically from both adult periodontitis and early-onset periodontitis patients with higher percentages isolated from the diseased periodontal pockets of adult periodontitis patients; furthermore, this is the first isolation of P. micros from tongue samples taken from periodontally diseased patients. This medium in cultural studies will further our understanding and assist future investigations of P. micros involved in disease processes.
微小消化链球菌是一种厌氧革兰氏阳性球菌,与牙周和牙髓病变(包括难治性病变)以及身体其他部位的许多人类混合感染有关。开发并评估了一种用于初次分离微小消化链球菌的选择性鉴别培养基。哥伦比亚CNA琼脂是一种革兰氏阳性球菌的选择性培养基,添加了谷胱甘肽和醋酸铅(微小消化链球菌培养基:PMM)。微小消化链球菌具有快速利用还原型谷胱甘肽形成硫化氢的特性,硫化氢与醋酸铅反应在培养基中产生黑色沉淀。当在PMM上生长时,微小消化链球菌可通过其典型的菌落形态以及菌落正下方黑色沉淀的存在而容易被识别。用80株微小消化链球菌菌株和30株其他革兰氏阳性球菌菌株,比较了PMM、苯乙醇琼脂(PEA)和哥伦比亚基础培养基(CBM)对微小消化链球菌生长的影响。所有测试的微小消化链球菌分离株均生长,并在PMM上呈现微小消化链球菌的典型形态。以CBM上的菌落计数为对照,PMM上微小消化链球菌菌落数量的平均回收率为81.8%,而PEA上的平均回收率为6.1%。将12例成人牙周炎患者和6例早发性牙周炎患者的龈下菌斑和舌样本接种到PMM上以分离微小消化链球菌。从成人牙周炎和早发性牙周炎患者中均在PMM上分离出微小消化链球菌,并进行了生化和酶学鉴定,从成人牙周炎患者患病牙周袋中分离出的比例更高;此外,这是首次从牙周病患者的舌样本中分离出微小消化链球菌。这种培养基在培养研究中将增进我们对参与疾病过程的微小消化链球菌的理解,并有助于未来的研究。