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Vancomycin-resistant enterococci in a Chinese hospital
1Department of Clinical Laboratory Medicine, People's Hospital of Peking University, No. 11 Xizhimen South Street, Xicheng District, Beijing 100044, China.
Abstract:
In investigating the prevalence of vancomycin-resistant enterococci (VREs) in a hospital in China, 338 enterococci were detected by using multiplex polymerase chain reaction. Eleven VREs were found, including one VanA E. faecalis, one VanB E. faecium, three VanB E. faecalis, five VanC(1) E. gallinarum, and one VanC(2 ) E. flavescens. VITEK 2, microbroth dilution, and E-test were used to determine the susceptibilities of the VREs to certain antimicrobial agents; multiple-drug resistance of the 11 VREs was distinct. Compared with phenotypic methods, multiplex PCR rapidly detected 11 VREs and provided van genotype information. This is the first study that sequenced van genes of VRE isolates in China to date and found type VanB in China. Because of the relatively low isolating rate, early detection of VRE is vital.
Insights
This study identified vancomycin-resistant enterococci (VREs) in a Chinese hospital using multiplex PCR. Early detection methods are crucial for managing VRE infections and their associated antimicrobial resistance.
Area of Science:
- Clinical microbiology
- Infectious diseases
- Molecular diagnostics
Background:
- Vancomycin-resistant enterococci (VRE) pose a significant threat in healthcare settings.
- Understanding the prevalence and genetic characteristics of VRE is essential for infection control.
Purpose of the Study:
- To investigate the prevalence of VRE in a Chinese hospital.
- To characterize the vancomycin resistance genotypes of detected VRE isolates.
- To evaluate the utility of multiplex PCR for rapid VRE detection and genotyping.
Main Methods:
- Multiplex polymerase chain reaction (PCR) for VRE detection.
- VITEK 2, microbroth dilution, and E-test for antimicrobial susceptibility testing.
- Sequencing of van genes for genotypic identification.
Main Results:
- Eleven VRE isolates were detected, including various species and van genotypes (VanA, VanB, VanC1, VanC2).
- Multiplex PCR provided rapid detection and van genotype information, outperforming phenotypic methods.
- This study is the first to sequence van genes of VRE isolates in China, identifying VanB type.
Conclusions:
- Multiplex PCR is a valuable tool for rapid VRE detection and genotypic characterization.
- The presence of diverse VRE strains, including VanB type, highlights the need for vigilant surveillance in China.
- Early detection of VRE is vital to mitigate the spread of antimicrobial resistance.
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