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Updated: Feb 16, 2026

A 1.5 Hour Procedure for Identification of Enterococcus Species Directly from Blood Cultures
Published on: February 10, 2011
Immunological responses against vancomycin-resistant Enterococcus faecium and Enterococcus faecalis by mice
Yun Sang Cho1, Mun Han Lee2, Jong Man Kim1
1a Bacterial Disease Division, Animal and Plant Disease Research Department , Animal and Plant Quarantine Agency , Gimcheon , Gyeongsangbuk-do , Republic of Korea.
Abstract:
Methicillin-resistant Staphylococcus aureus (MRSA) infections in humans can currently only be treated with vancomycin. Consequently, vancomycin-resistant Enterococcus spp. pose a serious public health hazard because MRSA can acquire their vancomycin resistance. While the microbiological and genetic characteristics of vancomycin-resistant enterococci (VRE) have been extensively studied, serological diagnostic tools for these organisms are lacking. The VanA and VanB classes of VRE show marked resistance. Here, we identified the VanA and VanB proteins that are immunogenic in mice. To do so, mice were orally infected with a VanA strain of E. faecium or a VanB strain of E. faecalis and the serologically immunogenic proteins were identified by SDS-PAGE and Western blot analysis. The mice reacted to the 27 and 65 kDa cell envelope (CE) proteins of VanA at 1 week post-infection (wpi) and then reacted to the 100 kDa cytoplasmic protein (CP) at 2-4 wpi. With regard to VanB, the mice responded at 1-4 wpi, 3-4 wpi, and 4 wpi to the 70 kDa, 25 and 35 kDa, and 79 kDa CE proteins, respectively, and at 3 wpi to the 39 kDa CP. The identification of these immunogenic proteins may be useful for diagnosing and for producing immunotherapeutic VRE antibodies.
Insights
Researchers identified specific proteins from vancomycin-resistant Enterococcus (VRE) strains that trigger an immune response in mice. These immunogenic VRE proteins could aid in developing new diagnostic tools and treatments for VRE infections.
Area of Science:
- Microbiology
- Immunology
- Infectious Diseases
Background:
- Methicillin-resistant Staphylococcus aureus (MRSA) treatment relies solely on vancomycin.
- Vancomycin-resistant Enterococcus (VRE) poses a significant public health threat as MRSA can acquire vancomycin resistance.
- Current diagnostic tools for VRE are limited, despite extensive research on their microbiology and genetics.
Purpose of the Study:
- To identify immunogenic proteins from VanA and VanB classes of VRE.
- To explore potential targets for serological diagnostic tools and immunotherapeutic VRE antibodies.
Main Methods:
- Mice were orally infected with VanA (E. faecium) or VanB (E. faecalis) strains.
- Proteins were separated using SDS-PAGE and identified via Western blot analysis.
- Serological immune responses to specific VRE proteins were analyzed post-infection.
Main Results:
- VanA infection elicited immune responses to 27 and 65 kDa cell envelope (CE) proteins at 1 week post-infection (wpi), and a 100 kDa cytoplasmic protein (CP) at 2-4 wpi.
- VanB infection induced responses to 70 kDa CE protein (1-4 wpi), 25 and 35 kDa CE proteins (3-4 wpi), 79 kDa CE protein (4 wpi), and a 39 kDa CP (3 wpi).
Conclusions:
- Specific immunogenic proteins from VanA and VanB VRE strains have been identified.
- These identified proteins show potential for developing novel serological diagnostic methods for VRE.
- The findings may facilitate the production of VRE-specific immunotherapeutic antibodies.
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