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Updated: May 25, 2026

Biosensor for Detection of Antibiotic Resistant Staphylococcus Bacteria
Published on: May 8, 2013
Selection of antibiotics for meticillin-resistant Staphylococcus pseudintermedius: time to revisit some old drugs?
1College of Veterinary Medicine, North Carolina State University, Raleigh, NC 27607, USA. mark_papich@ncsu.edu
Abstract:
The aim of this review is to consider systemic therapy options for meticillin-resistant Staphylococcus pseudintermedius (MRSP). Infections caused by MRSP in small animals--particularly dogs--have been frustrating veterinarians in recent years. After a susceptibility test is performed, veterinarians are left to select from drugs that have not been frequently encountered on a susceptibility report. Some of these are old drugs that have not been used regularly by veterinary dermatologists. As MRSP is, by definition, resistant to all β-lactam antibiotics, including cephalosporins, penicillins and amoxicillin-clavulanate combinations, the β-lactam drugs are not an option for systemic treatment. As most MRSPs are multidrug resistant, familiar drugs, such as trimethoprim-sulfonamides, fluoroquinolones, macrolides and lincosamides (clindamycin), are also not usually an option for treatment. Therefore, veterinarians are left with drugs such as rifampicin, chloramphenicol, tetracyclines, aminoglycosides and vancomycin to choose from on the basis of an in vitro susceptibility test. Some of these drugs were originally approved over 50 years ago and may not be familiar to some veterinarians. Each of these drugs possesses unique properties and has particular advantages and disadvantages. Veterinarians should be particularly aware of the adverse effects, limitations and precautions when using these drugs. New drugs also have been developed for meticillin-resistant Staphylococcus aureus in humans. These include linezolid, ceftaroline, daptomycin and tigecycline. Although these drugs are very infrequently--if ever--considered for veterinary use, the properties of these drugs should also be known to veterinary dermatologists.
Insights
Veterinarians face challenges treating meticillin-resistant Staphylococcus pseudintermedius (MRSP) infections in pets. This review details systemic therapy options, including older and newer drugs, for effective MRSP treatment.
Area of Science:
- Veterinary Dermatology
- Infectious Diseases
- Pharmacology
Background:
- Meticillin-resistant Staphylococcus pseudintermedius (MRSP) infections are increasingly problematic in small animals, especially dogs.
- Standard antibiotic susceptibility testing often yields limited treatment options due to widespread resistance.
- MRSP resistance extends to beta-lactam antibiotics and commonly used antimicrobials like fluoroquinolones and macrolides.
Purpose of the Study:
- To review available systemic antimicrobial therapies for MRSP infections in veterinary medicine.
- To highlight the properties, advantages, and disadvantages of less commonly used antibiotics for MRSP.
- To inform veterinarians about potential treatment options and considerations for MRSP.
Main Methods:
- Literature review of systemic therapy options for MRSP.
- Analysis of antibiotic classes effective against MRSP based on susceptibility data.
- Consideration of established and emerging antimicrobial agents.
Main Results:
- Systemic treatment options for MRSP are limited, often requiring older drugs like rifampicin, chloramphenicol, tetracyclines, aminoglycosides, and vancomycin.
- These drugs require careful consideration of adverse effects, limitations, and specific usage guidelines.
- Newer human-approved drugs for MRSA, such as linezolid and daptomycin, may offer future possibilities but are rarely used in veterinary practice.
Conclusions:
- Veterinarians must be knowledgeable about a range of systemic drugs for MRSP, including those not routinely encountered.
- Careful interpretation of susceptibility testing and understanding drug-specific profiles are crucial for successful MRSP treatment.
- Awareness of emerging antimicrobial agents is important for future therapeutic strategies against resistant bacteria.
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