Response of Streptococcus pyogenes to therapy with amoxicillin or amoxicillin-clavulanic acid in a mouse model of mixed infection caused by Staphylococcus aureus and Streptococcus pyogenes
- PMID: 3307617
- PMCID: PMC174904
- DOI: 10.1128/AAC.31.8.1204
Response of Streptococcus pyogenes to therapy with amoxicillin or amoxicillin-clavulanic acid in a mouse model of mixed infection caused by Staphylococcus aureus and Streptococcus pyogenes
Abstract
The response of Streptococcus pyogenes to amoxicillin or amoxicillin-clavulanic acid (Augmentin; Beecham Group) therapy of a mixed streptococcal-staphylococcal infection was studied in a surgical wound in mice. A superficial wound was produced on the backs of anesthetized mice, and a suture infected with S. pyogenes, Staphylococcus aureus, or a mixed inoculum of both organisms was inserted. Oral therapy was started 4 h after infection and continued for 3 days. Both amoxicillin and amoxicillin-clavulanic acid were effective in eliminating the streptococci from the pure wound infection. In contrast, amoxicillin failed to eliminate the streptococci from a mixed infection in which a beta-lactamase-producing strain of S. aureus was also present, wound counts reaching 10(7) streptococci per wound by 80 h, whereas amoxicillin-clavulanic acid reduced the count to less than 33 streptococci per wound by 24 h. Numbers of S. aureus were also reduced by amoxicillin-clavulanic acid therapy, controlling the infection, whereas amoxicillin was ineffective. Also of significance was the fact that successful therapy was achieved with blood and tissue concentrations of amoxicillin and clavulanic acid of the same order as those measured in humans. These results show that amoxicillin therapy failed to eliminate S. pyogenes from a wound infection in the presence of a beta-lactamase-producing strain of S. aureus and suggest the potential of amoxicillin-clavulanic acid in the treatment of mixed bacterial skin infections involving beta-lactamase-producing organisms.
Similar articles
-
Lack of influence of beta-lactamase-producing flora on recovery of group A streptococci after treatment of acute pharyngitis.J Pediatr. 1990 Dec;117(6):859-63. doi: 10.1016/s0022-3476(05)80122-2. J Pediatr. 1990. PMID: 2123240 Clinical Trial.
-
Efficacy of amoxycillin/clavulanic acid in experimental Staphylococcus aureus endocarditis in the rat.J Antimicrob Chemother. 1991 Jan;27(1):117-26. doi: 10.1093/jac/27.1.117. J Antimicrob Chemother. 1991. PMID: 2050588
-
Influence of clavulanic acid on the activity of amoxicillin against an experimental Streptococcus pneumoniae-Staphylococcus aureus mixed respiratory infection.Antimicrob Agents Chemother. 1990 Feb;34(2):210-4. doi: 10.1128/AAC.34.2.210. Antimicrob Agents Chemother. 1990. PMID: 2327767 Free PMC article.
-
Amoxicillin-potassium clavulanate, a beta-lactamase-resistant antibiotic combination.Clin Pharm. 1984 Nov-Dec;3(6):591-9. Clin Pharm. 1984. PMID: 6391783 Review.
-
Beta-lactamase inhibitors: another approach to overcoming antimicrobial resistance.Infect Control. 1987 Jan;8(1):36-40. doi: 10.1017/s0195941700066972. Infect Control. 1987. PMID: 3028975 Review.
Cited by
-
Mouse model for evaluation of antibiotic treatment of acute and chronic infections.Eur J Clin Microbiol Infect Dis. 1988 Dec;7(6):753-7. doi: 10.1007/BF01975042. Eur J Clin Microbiol Infect Dis. 1988. PMID: 3145857
-
Artificial intelligence enabled parabolic response surface platform identifies ultra-rapid near-universal TB drug treatment regimens comprising approved drugs.PLoS One. 2019 May 10;14(5):e0215607. doi: 10.1371/journal.pone.0215607. eCollection 2019. PLoS One. 2019. PMID: 31075149 Free PMC article.
-
In vivo bioluminescence imaging to evaluate systemic and topical antibiotics against community-acquired methicillin-resistant Staphylococcus aureus-infected skin wounds in mice.Antimicrob Agents Chemother. 2013 Feb;57(2):855-63. doi: 10.1128/AAC.01003-12. Epub 2012 Dec 3. Antimicrob Agents Chemother. 2013. PMID: 23208713 Free PMC article.
-
Direct and indirect pathogenicity of beta-lactamase-producing bacteria in respiratory tract infection in children. Role of cephalosporins resistant to enzymatic hydrolysis.Drugs. 1991;42 Suppl 4:14-8. doi: 10.2165/00003495-199100424-00006. Drugs. 1991. PMID: 1725149
-
Development of an experimental model of infected skin ulcer.Int Wound J. 2004 Apr;1(1):49-55. doi: 10.1111/j.1742-481x.2004.00006.x. Int Wound J. 2004. PMID: 16722897 Free PMC article.
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Molecular Biology Databases