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Isolation and Identification of Waterborne Antibiotic-Resistant Bacteria and Molecular Characterization of their Antibiotic Resistance Genes
Published on: March 3, 2023
New antibiotic agents: problems and prospects
David J Weber1, William A Rutala
1University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599-7030, USA. dweber@unch.unc.edu
Background:
Surgical site infections are the third most common healthcare-associated infection, often leading to prolonged hospital stay and excessive expenditures. Management of these infections has become more challenging due to rising rates of multi-drug-resistant organisms and few new antibiotic options.
Methods:
This paper reviews the literature, summarizes the epidemiology of surgical site infections and the threat of antibiotic-resistant bacteria, and provides an insight into new treatment options for this condition.
Results:
Patients with surgical site infections are at greater risk of acquiring healthcare-associated antibiotic-resistant pathogens, including methicillin-resistant Staphylococcus aureus (MRSA), vancomycin-resistant Enterococcus (VRE) sp., and extended-spectrum beta-lactamase-(ESBL)-producing Escherichia coli and Klebsiella pneumoniae. Multi-drug-resistant Pseudomonas aeruginosa and Bacteroides fragilis are also a growing problem. Several useful drugs have recently become available for the management of serious, gram-positive infections (e.g., daptomycin, linezolid, telithromycin). Tigecycline, the first-in-class glycylcycline, has broad-spectrum in vitro activity, including against MRSA, VRE, resistant enteric gram-negative bacilli (e.g., Acinetobacter sp.), "atypical" pathogens, and anaerobes. Phase 3 clinical trials suggest that tigecycline will be an excellent option for antibiotic monotherapy for complicated skin and soft tissue infections (cSSSI) and intra-abdominal infections. Oritavancin and dalbavacin, two novel glycopeptide antibiotics that are also in late-stage clinical development, appear that they, too, will be useful for cSSSI due to resistant, gram-positive bacteria.
Conclusions:
Multi-drug-resistant pathogens are threatening the success of available antibiotic therapy. Many new options are useful for infections due to multi-drug-resistant, gram-positive bacteria. Tigecycline is a promising new agent that provides coverage against a broad spectrum of gram-positive and gram-negative, aerobic, facultative, and anaerobic strains, including resistant isolates, and may make broad-spectrum, single-agent therapy possible.
Insights
New antibiotics offer hope against challenging surgical site infections caused by multi-drug-resistant bacteria. Tigecycline shows promise for broad-spectrum therapy against resistant gram-positive and gram-negative pathogens.
Area of Science:
- Infectious Diseases
- Microbiology
- Pharmacology
Background:
- Surgical site infections (SSIs) are a major healthcare-associated infection, increasing hospital stays and costs.
- Rising multi-drug-resistant organisms (MDROs) complicate SSI management due to limited new antibiotic options.
Purpose of the Study:
- To review the epidemiology of SSIs and the threat of antibiotic resistance.
- To provide insights into emerging treatment options for SSIs.
Main Methods:
- Literature review
- Epidemiological summary of SSIs and antibiotic resistance
- Analysis of new treatment options
Main Results:
- Patients with SSIs face higher risks from healthcare-associated MDROs like MRSA, VRE, ESBL-producing E. coli, and K. pneumoniae.
- Emerging drugs include daptomycin, linezolid, and tigecycline for gram-positive infections. Tigecycline demonstrates broad-spectrum activity against gram-positive, gram-negative, and anaerobic pathogens.
- Oritavancin and dalbavacin are novel glycopeptides in development for resistant gram-positive bacterial infections.
Conclusions:
- MDROs pose a significant threat to current antibiotic therapies for SSIs.
- New antibiotics are available for treating infections caused by resistant gram-positive bacteria.
- Tigecycline offers broad-spectrum coverage against resistant strains, potentially enabling single-agent therapy.
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