Martineau F, Picard F J, Roy P H, Ouellette M, Bergeron M G
Centre de Recherche en Infectiologie, Centre Hospitalier de l'Université Laval, Ste-Foy, Québec, Canada.
J Clin Microbiol. 1996 Dec;34(12):2888-93. doi: 10.1128/jcm.34.12.2888-2893.1996.
Staphylococcus epidermidis is an aerobic gram-positive coccus that is now recognized among the coagulase-negative staphylococci as an etiological agent with an important range of pathogenicity in humans. Several diagnostic kits based on biochemical or immunological reactions can efficiently identify Staphylococcus aureus. However, these tests are often unreliable for the identification of coagulase-negative staphylococcal species including S. epidermidis. Since DNA-based assays for the species-specific identification of S. epidermidis remain unavailable, we have developed such tests in order to improve the accuracy and the rapidity of tests for the diagnosis of S. epidermidis infections. On the basis of the results of hybridization assays with clones randomly selected from an S. epidermidis genomic library, we identified a chromosomal DNA fragment which is specific and 100% ubiquitous for the identification of S. epidermidis. This 705-bp fragment was sequenced and used to design PCR amplification primers. PCR assays with the selected primers were also highly specific and ubiquitous for the identification from bacterial cultures of clinical isolates of S. epidermidis from a variety of anatomic sites. While three strains of S. capitis were misidentified as S. epidermidis with the API Staph-Ident system and 2.5% of the S. epidermidis identifications were inconclusive with the MicroScan Autoscan-4 system, the PCR assay was highly specific and allowed for the correct identification of all 79 S. epidermidis strains tested. The PCR assays developed are simple and can be performed in about 1 h. The DNA-based tests provide novel diagnostic tools for improving the diagnosis of S. epidermidis infections.
表皮葡萄球菌是一种需氧革兰氏阳性球菌,目前在凝固酶阴性葡萄球菌中被认为是一种在人类中具有重要致病范围的病原体。几种基于生化或免疫反应的诊断试剂盒能够有效鉴定金黄色葡萄球菌。然而,这些检测方法对于包括表皮葡萄球菌在内的凝固酶阴性葡萄球菌的鉴定往往不可靠。由于目前尚无基于DNA的表皮葡萄球菌物种特异性鉴定方法,我们开发了此类检测方法,以提高表皮葡萄球菌感染诊断检测的准确性和速度。基于从表皮葡萄球菌基因组文库中随机选择的克隆进行杂交分析的结果,我们鉴定出一个染色体DNA片段,该片段对于表皮葡萄球菌的鉴定具有特异性且100%普遍存在。对这个705碱基对的片段进行了测序,并用于设计PCR扩增引物。使用所选引物进行的PCR分析对于从各种解剖部位的临床分离表皮葡萄球菌的细菌培养物中进行鉴定也具有高度特异性和普遍性。虽然有3株头状葡萄球菌被API Staph-Ident系统误鉴定为表皮葡萄球菌,并且2.5%的表皮葡萄球菌鉴定结果在MicroScan Autoscan-4系统中不确定,但PCR分析具有高度特异性,能够正确鉴定所有79株测试的表皮葡萄球菌菌株。所开发的PCR分析方法简单,大约1小时即可完成。基于DNA 的检测方法为改善表皮葡萄球菌感染的诊断提供了新的诊断工具。