Pathology North Hunter Laboratory, Newcastle, NSW, Australia.
Pathology North Hunter Laboratory, Newcastle, NSW, Australia.
Pathology. 2018 Jun;50(4):437-441. doi: 10.1016/j.pathol.2017.10.020. Epub 2018 Apr 17.
Gram negative anaerobic organisms are important pathogens in a range of clinical infections, and susceptibility testing is not commonly performed in the microbiology laboratory. We performed anaerobic susceptibility testing on 70 clinically relevant Gram negative anaerobes isolated from routine cultures in a busy diagnostic laboratory which were identified by MALDI-TOF mass spectrometry (MALDI-TOF MS). The susceptibility testing was performed by two methods: Sensititre trays (ThermoFisher Scientific) against 15 different antibiotics, and Etests (bioMérieux) against five clinically relevant antibiotics (metronidazole, piperacillin-tazobactam, amoxicillin-clavulanate, meropenem and clindamycin). We found that all isolates were susceptible to metronidazole, and overall susceptibility to commonly used antibiotics such as piperacillin-tazobactam and amoxicillin-clavulanate was high (93-100% and 89-100%, respectively). Two isolates of Bacteroides fragilis were resistant to both broad spectrum β-lactams and carbapenems. Comparing the two methods, using Sensititre broth microdilution as gold standard, there was high categorical agreement (92-100%). Antibiograms provide useful information for clinicians when choosing antimicrobials for infections caused by anaerobic organisms. This study has shown that in our area, use of metronidazole as a broad spectrum anti-anaerobic agent remains appropriate. Anaerobic susceptibility testing is also important to perform in individual clinical isolates, especially from sterile sites or in pure culture. The emergence of broad spectrum β-lactam and carbapenem resistance in clinical isolates of Bacteroides fragilis is of concern and will require further monitoring. The Etest method was considered superior to Sensititre trays given that the higher inoculum used may allow demonstration of heteroresistance, anaerobiasis can be maintained during setup, lower failure rates, and the ability to select only the antibiotics required.
革兰氏阴性厌氧菌是一系列临床感染中的重要病原体,微生物实验室通常不进行药敏试验。我们对从繁忙的诊断实验室常规培养中分离出的 70 种临床相关革兰氏阴性厌氧菌进行了厌氧药敏试验,这些菌通过基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)进行了鉴定。药敏试验采用两种方法进行:ThermoFisher Scientific 的 Sensititre 药敏板(Sensititre trays)检测 15 种不同抗生素,bioMérieux 的 Etest(Etests)检测五种临床相关抗生素(甲硝唑、哌拉西林他唑巴坦、阿莫西林克拉维酸、美罗培南和克林霉素)。我们发现所有分离株均对甲硝唑敏感,对哌拉西林他唑巴坦和阿莫西林克拉维酸等常用抗生素的总体敏感性较高(分别为 93-100%和 89-100%)。两株脆弱拟杆菌对广谱β-内酰胺类抗生素和碳青霉烯类抗生素均耐药。与两种方法相比,以 Sensititre 肉汤微量稀释法为金标准,分类一致性很高(92-100%)。药敏谱图为临床医生在选择抗厌氧微生物药物治疗由厌氧菌引起的感染时提供了有用的信息。本研究表明,在我们所在地区,将甲硝唑作为广谱抗厌氧菌药物仍然适用。在个体临床分离株中进行厌氧药敏试验也很重要,特别是在无菌部位或纯培养中。临床分离的脆弱拟杆菌对广谱β-内酰胺类抗生素和碳青霉烯类抗生素的耐药性的出现令人担忧,需要进一步监测。Etest 法优于 Sensititre 药敏板,因为较高的接种量可能可以显示异质性耐药性,可以在设置过程中保持厌氧菌的活性,降低失败率,并且可以只选择所需的抗生素。