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首页> 外文期刊>Revista do Instituto de Medicina Tropical de So Paulo >COMPARISON BETWEEN AUTOMATED SYSTEM AND PCR-BASED METHOD FOR IDENTIFICATION AND ANTIMICROBIAL SUSCEPTIBILITY PROFILE OF CLINICAL Enterococcus spp
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COMPARISON BETWEEN AUTOMATED SYSTEM AND PCR-BASED METHOD FOR IDENTIFICATION AND ANTIMICROBIAL SUSCEPTIBILITY PROFILE OF CLINICAL Enterococcus spp

机译:自动化系统与基于PCR的临床肠球菌属种的鉴定和抗菌谱的比较

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Enterococci are increasingly responsible for nosocomial infections worldwide. This study was undertaken to compare the identification and susceptibility profile using an automated MicrosScan system, PCR-based assay and disk diffusion assay of Enterococcus spp. We evaluated 30 clinical isolates of Enterococcus spp. Isolates were identified by MicrosScan system and PCR-based assay. The detection of antibiotic resistance genes (vancomycin, gentamicin, tetracycline and erythromycin) was also determined by PCR. Antimicrobial susceptibilities to vancomycin (30 μg), gentamicin (120 μg), tetracycline (30 μg) and erythromycin (15 μg) were tested by the automated system and disk diffusion method, and were interpreted according to the criteria recommended in CLSI guidelines. Concerning Enterococcus identification the general agreement between data obtained by the PCR method and by the automatic system was 90.0% (27/30). For all isolates of E. faecium and E. faecalis we observed 100% agreement. Resistance frequencies were higher in E. faecium than E. faecalis. The resistance rates obtained were higher for erythromycin (86.7%), vancomycin (80.0%), tetracycline (43.35) and gentamicin (33.3%). The correlation between disk diffusion and automation revealed an agreement for the majority of the antibiotics with category agreement rates of 80%. The PCR-based assay, the van(A) gene was detected in 100% of vancomycin resistant enterococci. This assay is simple to conduct and reliable in the identification of clinically relevant enterococci. The data obtained reinforced the need for an improvement of the automated system to identify some enterococci.
机译:肠球菌在全球范围内日益引起医院感染。进行了这项研究,以比较使用自动MicrosScan系统,基于PCR的测定和肠球菌属菌种的圆片扩散测定法的鉴定和药敏曲线。我们评估了30种肠球菌的临床分离株。分离物通过MicrosScan系统和基于PCR的测定进行鉴定。还通过PCR确定了抗生素抗性基因(万古霉素,庆大霉素,四环素和红霉素)的检测。通过自动系统和磁盘扩散法测试了对万古霉素(30μg),庆大霉素(120μg),四环素(30μg)和红霉素(15μg)的抗菌敏感性,并根据CLSI指南中推荐的标准进行了解释。关于肠球菌鉴定,通过PCR方法获得的数据和通过自动系统获得的数据之间的总体一致性为90.0%(27/30)。对于粪肠球菌和粪肠球菌的所有分离株,我们观察到100%一致。粪肠球菌的抵抗频率高于粪肠球菌。红霉素(86.7%),万古霉素(80.0%),四环素(43.35)和庆大霉素(33.3%)的耐药率更高。磁盘扩散与自动化之间的相关性表明,大多数抗生素的协议达成,其类别协议率> 80%。基于PCR的检测方法在100%耐万古霉素的肠球菌中检测到van(A)基因。该测定法操作简便,在临床相关肠球菌的鉴定中可靠。获得的数据加强了对自动化系统的识别,以识别某些肠球菌的需求。

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