Prüller Sandra, Frömke Cornelia, Kaspar Heike, Klein Günter, Kreienbrock Lothar, Kehrenberg Corinna
Institute for Food Quality and Food Safety, University of Veterinary Medicine Hannover, Foundation, Bischofsholer Damm 15, D-30173, Hannover, Germany.
Department of Biometry, Epidemiology and Information Processing, WHO Collaborating Centre for Research and Training in Veterinary Public Health, University of Veterinary Medicine Hannover, Foundation, Hannover, Germany.
PLoS One. 2015 Apr 24;10(4):e0123883. doi: 10.1371/journal.pone.0123883. eCollection 2015.
The objective was to establish and standardise a broth microdilution susceptibility testing method for porcine Bordetella (B.) bronchiseptica. B. bronchiseptica isolates from different geographical regions and farms were genotyped by macrorestriction analysis and subsequent pulsed-field gel electrophoresis. One reference and one type strain plus two field isolates of B. bronchiseptica were chosen to analyse growth curves in four different media: cation-adjusted Mueller-Hinton broth (CAMHB) with and without 2% lysed horse blood, Brain-Heart-Infusion (BHI), and Caso broth. The growth rate of each test strain in each medium was determined by culture enumeration and the suitability of CAMHB was confirmed by comparative statistical analysis. Thereafter, reference and type strain and eight epidemiologically unrelated field isolates of B. bronchiseptica were used to test the suitability of a broth microdilution susceptibility testing method following CLSI-approved performance standards given in document VET01-A4. Susceptibility tests, using 20 antimicrobial agents, were performed in five replicates, and data were collected after 20 and 24 hours incubation and statistically analysed. Due to the low growth rate of B. bronchiseptica, an incubation time of 24 hours resulted in significantly more homogeneous minimum inhibitory concentrations after five replications compared to a 20-hour incubation. An interlaboratory comparison trial including susceptibility testing of 24 antimicrobial agents revealed a high mean level of reproducibility (97.9%) of the modified method. Hence, in a harmonization for broth microdilution susceptibility testing of B. bronchiseptica, an incubation time of 24 hours in CAMHB medium with an incubation temperature of 35°C and an inoculum concentration of approximately 5 x 10(5) cfu/ml was proposed.
目的是建立并标准化一种用于猪支气管败血波氏杆菌的肉汤微量稀释药敏试验方法。通过宏观限制性分析及随后的脉冲场凝胶电泳对来自不同地理区域和养殖场的支气管败血波氏杆菌分离株进行基因分型。选择一株参考菌株、一株模式菌株以及两株支气管败血波氏杆菌的田间分离株,分析它们在四种不同培养基中的生长曲线:添加和不添加2%裂解马血的阳离子调整型穆勒-欣顿肉汤(CAMHB)、脑心浸液(BHI)和酪蛋白胨肉汤。通过培养计数确定每个测试菌株在每种培养基中的生长速率,并通过比较统计分析确认CAMHB的适用性。此后,使用支气管败血波氏杆菌的参考菌株、模式菌株以及八株流行病学上不相关的田间分离株,按照CLSI文件VET01 - A4中批准的性能标准,测试肉汤微量稀释药敏试验方法的适用性。使用20种抗菌药物进行药敏试验,一式五份重复进行,在孵育20小时和24小时后收集数据并进行统计分析。由于支气管败血波氏杆菌生长速率较低,与20小时孵育相比,24小时孵育在五次重复后产生的最低抑菌浓度显著更均匀。一项包括对24种抗菌药物进行药敏试验的实验室间比较试验显示,改良方法具有较高的平均再现性水平(97.9%)。因此,在支气管败血波氏杆菌肉汤微量稀释药敏试验的协调中,建议在CAMHB培养基中于35°C孵育温度和接种浓度约为5×10(5) cfu/ml的条件下孵育24小时。