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Updated: May 23, 2026

Nanomechanics of Drug-target Interactions and Antibacterial Resistance Detection
Published on: October 25, 2013
Unmet needs and prospects for oritavancin in the management of vancomycin-resistant enterococcal infections
Cesar A Arias1, Rodrigo E Mendes, Matthew G Stilwell
1Department of Internal Medicine, Division of Infectious Diseases, University of Texas Medical School, 6431 Fannin St, Houston, TX 77030, USA.
Abstract:
The treatment of infections caused by vancomycin-resistant enterococci (VRE) has become an important clinical challenge and compromises the care of critically ill patients. A striking increase in the frequency of nosocomial isolation of multidrug-resistant Enterococcus faecium has dramatically reduced the therapeutic alternatives because the majority of E. faecium isolates are resistant to ampicillin and vancomycin. Only 2 agents have US Food and Drug Administration approval for the treatment of VRE (E. faecium) infections, namely, linezolid and quinupristin/dalfopristin (Q/D). However, the use of these compounds in severe VRE infections is hampered by the lack of in vivo bactericidal activity, reports of therapeutic failures with monotherapy, a requirement for central venous access for administration (Q/D), and adverse-effect profile. The lipopeptide antimicrobial daptomycin has in vitro bactericidal activity against VRE; however, clinical use of this compound for VRE has not been well studied, and the reports of resistance emerging during therapy at the approved doses are worrisome. Tigecycline has in vitro bacteriostatic activity against VRE, but its clinical use for serious enterococcal infections is unclear due to low serum levels and static effect. Thus, current reliable therapies for VRE appear to be limited, and clinical data that use the above compounds are certainly scant. Oritavancin is an investigational semisynthetic glycopeptide with potent in vitro activity against VRE (both VanA and VanB phenotypes). Although review of the available preclinical data indicates that this compound used as a single agent is likely to have important limitations for the treatment of a severe VRE infection (ie, endocarditis), combination of oritavancin with other agents such as aminoglycosides may offer promise and deserves further investigation, as does use of oritavancin for less serious infections as monotherapy for vancomycin-susceptible and multidrug-resistant enterococci.
Insights
Vancomycin-resistant enterococci (VRE) infections pose a significant challenge. Oritavancin shows promise, particularly in combination therapy, for treating these difficult-to-treat Gram-positive bacterial infections.
Area of Science:
- Infectious Diseases
- Microbiology
- Pharmacology
Background:
- Vancomycin-resistant enterococci (VRE) infections are a growing clinical concern, especially in critically ill patients.
- Multidrug-resistant Enterococcus faecium strains limit therapeutic options, with few FDA-approved agents available.
- Existing treatments like linezolid and quinupristin/dalfopristin have limitations, including lack of bactericidal activity and adverse effects.
Purpose of the Study:
- To evaluate the potential of oritavancin, an investigational glycopeptide, for treating VRE infections.
- To assess the in vitro activity of oritavancin against VRE with VanA and VanB phenotypes.
- To explore the limitations and potential applications of oritavancin, including combination therapy.
Main Methods:
- Review of preclinical data for oritavancin.
- Assessment of in vitro activity against VRE phenotypes (VanA and VanB).
- Evaluation of existing therapeutic options and their limitations.
Main Results:
- Oritavancin demonstrates potent in vitro activity against VRE.
- Preclinical data suggest limitations for oritavancin monotherapy in severe VRE infections like endocarditis.
- Emerging resistance to daptomycin and static activity of tigecycline highlight the need for new agents.
Conclusions:
- Oritavancin shows promise for VRE treatment, especially in combination with other agents like aminoglycosides.
- Further investigation is warranted for oritavancin's use in less severe infections and as monotherapy for susceptible strains.
- Current therapeutic options for VRE infections remain limited, emphasizing the need for novel treatment strategies.
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