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首页> 外文期刊>Journal of Clinical Microbiology >Evaluation of the Hodge Test and the Imipenem-EDTA Double-Disk Synergy Test for Differentiating Metallo-β-Lactamase-Producing Isolates of Pseudomonas spp. and Acinetobacter spp.
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Evaluation of the Hodge Test and the Imipenem-EDTA Double-Disk Synergy Test for Differentiating Metallo-β-Lactamase-Producing Isolates of Pseudomonas spp. and Acinetobacter spp.

机译:霍奇测试和亚胺培南-EDTA双盘协同测试用于鉴定产假单胞菌的产金属β-内酰胺酶分离株的评价。和不动杆菌属。

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Gram-negative bacilli with acquired metallo-β-lactamase (MBL) production have been increasingly reported in some countries, necessitating their detection. The aim of this study was to evaluate the performance of the Hodge test and those of the imipenem (IPM)-EDTA, ceftazidime (CAZ)-mercaptopropionic acid (MPA), and CAZ-sodium mercaptoacetic acid (SMA) double-disk synergy tests (DDSTs). The efficiencies of testing CAZ-resistant and IPM-nonsusceptible isolates were also compared. Strains used for the evaluation were known IMP-1 and VIM-2 MBL-producing isolates and consecutive and CAZ-nonsusceptible isolates of pseudomonads and acinetobacters. The performance of the Hodge test was improved by addition of zinc sulfate (140 μg/disk) to an IPM disk. In DDSTs, EDTA (ca. 1,900 μg) disks were better at detecting MBL-producing strains among pseudomonads, while MPA (3 μl) and SMA (3 mg) disks performed better for acinetobacters. EDTA (ca. 750 μg)-plus-SMA (ca. 2 mg) disks performed better than EDTA, MPA, or SMA disks with both organisms. CAZ-SMA DDSTs failed to detect 22 of 80 (28%) MBL-producing acinetobacters. In conclusion, use of an IPM disk and an EDTA (750 μg)-plus-SMA (2 mg) disk improves performance, and testing IPM-nonsusceptible isolates rather than CAZ-resistant isolates could reduce screening work. Further evaluation of the test is required for the detection of other types of MBL-producing gram-negative bacilli.
机译:在某些国家,越来越多的报道了革兰氏阴性杆菌与金属β-内酰胺酶(MBL)的生产,因此有必要对其进行检测。这项研究的目的是评估Hodge试验和亚胺培南(IPM)-EDTA,头孢他啶(CAZ)-巯基丙酸(MPA)和CAZ-巯基乙酸钠(SMA)双盘协同试验的性能(DDST)。还比较了测试抗CAZ和IPM不敏感的分离株的效率。用于评估的菌株是已知的产生IMP-1和VIM-2 MBL的分离株以及假单胞菌和不动杆菌的连续和CAZ不敏感的分离株。通过向IPM磁盘添加硫酸锌(140μg/磁盘),改善了Hodge测试的性能。在DDSTs中,EDTA(约1,900μg)盘在检测假单胞菌中产生MBL的菌株方面更好,而MPA(3μl)和SMA(3 mg)盘在不动杆菌中表现更好。 EDTA(约750μg)加SMA(约2 mg)盘的效果优于两种生物的EDTA,MPA或SMA盘。 CAZ-SMA DDST无法检测出80种(28%)MBL产生的不动细菌中的22种。总之,使用IPM盘和EDTA(750μg)加SMA(2 mg)盘可以提高性能,测试IPM敏感分离株而不是耐CAZ分离株可以减少筛选工作。检测其他类型的产生MBL的革兰氏阴性杆菌需要对测试进行进一步评估。

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