In vitro activity of thiamphenicol against multiresistant Streptococcus pneumoniae, Haemophilus influenzae and
A Marchese1, E A Debbia, E Tonoli
1Institute of Microbiology, University of Genoa, Italy. anna.marchese@unige.it
Abstract:
Thiamphenicol is a derivative of chloramphenicol characterized by a spectrum comparable to that of the parent compound against multiresistant pathogens but showing satisfactory tolerability. The in vitro activity of thiamphenicol and of 11 comparative drugs against 397 recently isolated antibiotic-resistant and/or invasive pneumococci and 52 multiply-resistant MRSA including 2 VISA strains was determined. Bactericidal activity against Haemophilus influenzae and the post-antibiotic effect on Streptococcus pneumoniae, H. influenzae, Staphylococcus aureus and Escherichia coli were also assessed. Against invasive pneumococci, thiamphenicol and chloramphenicol were the most potent non-beta-lactam molecules together with vancomycin and rifampin. Against high-level penicillin-resistant strains phenicol activities were superior to those of cefotaxime, ceftriaxone and imipenem. Against MRSA thiamphenicol and chloramphenicol were second only to the glycopetides and also inhibited the VISA strains. Thiamphenicol showed a significant PAE (0.33 to 2.9h) on all pathogens studied and a powerful bactericidal effect against beta-lactamase-positive and -negative H. influenzae. These results indicate a good in vitro activity of thiamphenicol against difficult-to-treat multiply resistant pathogens.
Insights
Thiamphenicol demonstrates potent in vitro activity against antibiotic-resistant bacteria, including pneumococci and MRSA. This chloramphenicol derivative shows efficacy comparable to other key antibiotics, offering a viable option for treating difficult-to-treat infections.
Area of Science:
- Microbiology
- Infectious Diseases
- Pharmacology
Background:
- Thiamphenicol, a chloramphenicol derivative, exhibits a comparable spectrum of activity against multiresistant pathogens with improved tolerability.
- Antibiotic resistance in pathogens like Streptococcus pneumoniae and Methicillin-resistant Staphylococcus aureus (MRSA) poses a significant clinical challenge.
Purpose of the Study:
- To evaluate the in vitro activity of thiamphenicol against antibiotic-resistant and invasive strains of Streptococcus pneumoniae and MRSA.
- To assess the bactericidal activity and post-antibiotic effect (PAE) of thiamphenicol on key bacterial pathogens.
Main Methods:
- In vitro susceptibility testing of thiamphenicol and 11 comparator drugs against 397 pneumococcal and 52 MRSA isolates.
- Determination of bactericidal activity against Haemophilus influenzae.
- Assessment of the post-antibiotic effect on Streptococcus pneumoniae, H. influenzae, Staphylococcus aureus, and Escherichia coli.
Main Results:
- Thiamphenicol and chloramphenicol were potent non-beta-lactam agents against invasive pneumococci, comparable to vancomycin and rifampin.
- Phenicol activity surpassed cefotaxime, ceftriaxone, and imipenem against high-level penicillin-resistant pneumococci.
- Thiamphenicol and chloramphenicol showed significant activity against MRSA, including vancomycin-intermediate S. aureus (VISA) strains, and demonstrated a notable PAE on all tested pathogens.
Conclusions:
- Thiamphenicol exhibits significant in vitro activity against challenging, multiply resistant bacterial pathogens.
- The findings support thiamphenicol's potential as a therapeutic option for infections caused by antibiotic-resistant bacteria.
- Further clinical investigation is warranted to confirm the efficacy and safety of thiamphenicol in treating resistant infections.
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