Serap Süzük Yıldız, Sevgi Şahin, Esra Tavukcu, İpek Mumcuoğlu, Can Hüseyin Hekimoğlu, Ayşe Semra Güreser, Tuba Dal
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This process was repeated independently for three days and three times on each day for reproducibility. The mRAST test was performed on 50 samples with positive signals and gram-negative bacilli on Gram-stained samples (20 Klebsiella pneumoniae, 15 E. coli, 10 Acinetobacter baumannii, and five P. aeruginosa).Comparison of 90 mm MHA and 150 mm MHA showed that the categorical agreement of ATCC strains and 50 gram negative isolates was 100% and >95%, respectively, for all antibiotics. For K. pneumoniae, only 0.4 major error (ME) was detected at 4 h. For E. coli, 3.2, 1.6, and 1.5 ME were detected at 4, 8, and 20 h, respectively, whereas 1.6 very major error (VME) was detected at 4 h and 1.0 VME was detected at both 8, and 20 h, respectively. 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引用次数: 0
摘要
在这项研究中,我们评估了改良的快速抗生素敏感性试验(mRAST)的性能,该试验使用150 mm穆勒·辛顿琼脂(MHA)板,该板先前被EUCAST标准化为90 mm的MHA。制备了加入ATCC质控菌株的血培养瓶。以大肠埃希菌ATCC 25922、铜绿假单胞菌ATCC 27853、金黄色葡萄球菌ATCC 29213、粪肠球菌ATCC 29212为质量控制菌株。通过计算与90 mm板的比表面积,将350±50µL未稀释的血培养样品接种于150 mm MHA中,放置12个圆盘。该过程独立重复3天,每天重复3次。对50份阳性信号样本和革兰氏阴性杆菌(肺炎克雷伯菌20例、大肠杆菌15例、鲍曼不动杆菌10例、铜绿假单胞菌5例)进行mRAST检测。90 mm MHA和150 mm MHA的比较表明,ATCC菌株和50 g阴性菌株对所有抗生素的分类一致性分别为100%和95%。对于肺炎克雷伯菌,在4 h仅检测到0.4个主要误差(ME)。对于大肠杆菌,在4、8和20 h分别检测到3.2、1.6和1.5个ME,而在4 h检测到1.6个非常主要误差(VME),在8和20 h分别检测到1.0个VME。铜绿假单胞菌和鲍曼假单胞菌未检出错误。这些结果表明,350±50µL未稀释的血培养物在150 mm MHA中适合于体外mRAST试验。
Usage of 150 mm Mueller - Hinton Agar for the EUCAST rapid antimicrobial susceptibility test (RAST) directly from positive blood culture bottles.
In this study, we evaluated the performance of modified rapid antimicrobial susceptibility test (mRAST) with 150 mm Mueller Hinton Agar (MHA) plates which was earlier standardized for 90 mm MHA by EUCAST. Blood culture bottles spiked with ATCC quality control strains were prepared. For quality control Escherichia coli ATCC 25922, Pseudomonas aeruginosa ATCC 27853, Staphylococcus aureus ATCC 29213, and Enterococcus faecalis ATCC 29212 strains were used. By calculating and proportioning the surface areas of the plates comparing with 90 mm plates, 350 ± 50 µL undiluted blood culture samples were inoculated in 150 mm MHA, and 12 disks were placed. This process was repeated independently for three days and three times on each day for reproducibility. The mRAST test was performed on 50 samples with positive signals and gram-negative bacilli on Gram-stained samples (20 Klebsiella pneumoniae, 15 E. coli, 10 Acinetobacter baumannii, and five P. aeruginosa).Comparison of 90 mm MHA and 150 mm MHA showed that the categorical agreement of ATCC strains and 50 gram negative isolates was 100% and >95%, respectively, for all antibiotics. For K. pneumoniae, only 0.4 major error (ME) was detected at 4 h. For E. coli, 3.2, 1.6, and 1.5 ME were detected at 4, 8, and 20 h, respectively, whereas 1.6 very major error (VME) was detected at 4 h and 1.0 VME was detected at both 8, and 20 h, respectively. No errors were detected for P. aeruginosa or A. baumannii.These results indicated that 350 ± 50 µL of undiluted blood culture in 150 mm MHA was suitable for the mRAST test in vitro.
期刊介绍:
AMIH is devoted to the publication of research in all fields of medical microbiology (bacteriology, virology, parasitology, mycology); immunology of infectious diseases and study of the microbiome related to human diseases.