Distinguishing Clinical Enterococcus faecium Strains and Resistance to Vancomycin Using a Simple In-House Screening Test

被引:5
作者
Saenhom, Natkamon [1 ]
Boueroy, Parichart [1 ]
Chopjitt, Peechanika [1 ]
Hatrongjit, Rujirat [2 ]
Kerdsin, Anusak [1 ]
机构
[1] Kasetsart Univ Chalermphrakiat Sakon Nakhon Prov, Fac Publ Hlth, Sakon Nakhon 47000, Thailand
[2] Kasetsart Univ Chalermphrakiat Sakon Nakhon Prov, Fac Sci & Engn, Sakon Nakhon 47000, Thailand
来源
ANTIBIOTICS-BASEL | 2022年 / 11卷 / 03期
关键词
Enterococci; Enterococcus faecium; screening test; vancomycin; RAPID DETECTION; EPIDEMIOLOGY; PCR;
D O I
10.3390/antibiotics11030286
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Vancomycin-resistant enterococci (VRE) are a major concern as microorganisms with antimicrobial resistance and as a public health threat contributing significantly to morbidity, mortality, and socio-economic costs. Among VREs, vancomycin-resistant Enterococcus faecium (VREfm) is frequently isolated and is resistant to many antibiotics used to treat patients with hospital-acquired infection. Accurate and rapid detection of VREfm results in effective antimicrobial therapy, immediate patient isolation, dissemination control, and appropriate disinfection measures. An in-house VREfm screening broth was developed and compared to the broth microdilution method and multiplex polymerase chain reaction for the detection of 105 enterococci, including 81 VRE isolates (61 E. faecium, 5 E. faecalis, 10 E. gallinarum, and 5 E. casseliflavus). Verification of this screening broth on 61 VREfm, 20 other VRE, and 24 non-VRE revealed greater validity for VREfm detection. The accuracy of this broth was 100% in distinguishing E. faecium from other enterococcal species. Our test revealed 93.3% accuracy, 97.5% sensitivity, and 79.2% specificity compared with broth microdilution and PCR detecting van genes. The kappa statistic to test interrater reliability was 0.8, revealing substantial agreement for this screening test to the broth microdilution method. In addition, the in-house VREfm screening broth produced rapid positivity after at least 8 h of incubation. Application of this assay to screen VREfm should be useful in clinical laboratories and hospital infection control units.
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页数:10
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