Skip to main content
Antimicrobial Agents and Chemotherapy logoLink to Antimicrobial Agents and Chemotherapy
. 1978 Apr;13(4):669–675. doi: 10.1128/aac.13.4.669

Use of a Heavy Inoculum in the In Vitro Evaluation of the Anti-Staphylococcal Activity of 19 Cephalosporins

Michel Laverdiere 1, Diane Welter 1, L D Sabath 1
PMCID: PMC352308  PMID: 352261

Abstract

The in vitro activity of 19 cephalosporins against 105 clinical isolates of Staphylococcus aureus and S. epidermidis was determined by using a heavy inoculum, i.e., 108 to 109 organisms per ml, to maximally challenge the antibiotics. The anti-staphylococcal activities of cephaloridine and 87/312 were consistently decreased by the use of a heavy inoculum when compared with the activity obtained with two less-concentrated inocula. The activity of most of the other compounds was also decreased with the use of a heavy inoculum, but this was observed only with selected isolates. Cephapirin, cephalothin, and cefazaflur were the most active drugs against the methicillin-susceptible isolates. Cephaloridine, cefamandole, cefazaflur, and 87/312 had substantial activity against methicillin-resistant staphylococci even with heavy inocula. With the exception of cefaclor against S. aureus, the orally absorbed cephalosporins were generally one-half to one-sixteenth as active as the parenterally administered cephalosporins. The median minimal inhibitory concentrations of five of the 12 parenteral cephalosporins were lower with the methicillin-susceptible S. aureus than with the methicillin-susceptible S. epidermidis strains.

Full text

PDF
674

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Chabbert Y. A. Behaviour of "methicillin hetero-resistant" staphylococci to cephaloridine. Postgrad Med J. 1967 Aug;43(Suppl):40–42. [PubMed] [Google Scholar]
  2. Farrar W. E., Jr, Gramling P. K. Antistaphylococcal activity and beta-lactamase resistance of newer cephalosporins. J Infect Dis. 1976 Jun;133(6):691–695. doi: 10.1093/infdis/133.6.691. [DOI] [PubMed] [Google Scholar]
  3. Fong I. W., Engelking E. R., Kirby W. M. Relative inactivation by Staphylococcus aureus of eight cephalosporin antibiotics. Antimicrob Agents Chemother. 1976 Jun;9(6):939–944. doi: 10.1128/aac.9.6.939. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Kisch A. L., Bartholomew L. Comparison of the in vitro activity of several cephalosporin antibiotics against gram-negative and gram-positive bacteria resistant to cephaloridine. Antimicrob Agents Chemother. 1976 Sep;10(3):507–510. doi: 10.1128/aac.10.3.507. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Klimek J. J., Marsik F. J., Bartlett R. C., Weir B., Shea P., Quintiliani R. Clinical, epidemiologic and bacteriologic observations of an outbreak of methicillin-resistant Staphylococcus aureus at a large community hospital. Am J Med. 1976 Sep;61(3):340–345. doi: 10.1016/0002-9343(76)90370-3. [DOI] [PubMed] [Google Scholar]
  6. Leitner F., Misiek M., Pursiano T. A., Buck R. E., Chisholm D. R., DeRegis R. G., Tsai Y. H., Price K. E. Laboratory evaluation of BL-S786, a cephalosporin with broad-spectrum antibacterial activity. Antimicrob Agents Chemother. 1976 Sep;10(3):426–435. doi: 10.1128/aac.10.3.426. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Nishida M., Murakawa T., Kamimura T., Okada N., Sakamoto H. Laboratory evaluation of FR10612, a new oral cephalosporin derivative. J Antibiot (Tokyo) 1976 Apr;29(4):444–459. doi: 10.7164/antibiotics.29.444. [DOI] [PubMed] [Google Scholar]
  8. O'Callaghan C. H. Classification of cephalosporins by their antibacterial activity and pharmacokinetic properties. J Antimicrob Chemother. 1975;1(3 Suppl):1–12. doi: 10.1093/jac/1.suppl_3.1. [DOI] [PubMed] [Google Scholar]
  9. O'Callaghan C. H., Morris A., Kirby S. M., Shingler A. H. Novel method for detection of beta-lactamases by using a chromogenic cephalosporin substrate. Antimicrob Agents Chemother. 1972 Apr;1(4):283–288. doi: 10.1128/aac.1.4.283. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. RICHMOND M. H. WILD-TYPE VARIANTS OF EXOPENICILLINASE FROM STAPHYLOCOCCUS AUREUS. Biochem J. 1965 Mar;94:584–593. doi: 10.1042/bj0940584. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Sabath L. D., Garner C., Wilcox C., Finland M. Effect of inoculum and of beta-lactamase on the anti-staphylococcal activity of thirteen penicillins and cephalosporins. Antimicrob Agents Chemother. 1975 Sep;8(3):344–349. doi: 10.1128/aac.8.3.344. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Sabath L. D., Garner C., Wilcox C., Finland M. Susceptibility of Staphylococcus aureus and Staphylococcus epidermidis to 65 antibiotics. Antimicrob Agents Chemother. 1976 Jun;9(6):962–969. doi: 10.1128/aac.9.6.962. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Stewart D., Bodey G. P. Comparative in vitro activity of cephalosporins. J Antibiot (Tokyo) 1976 Feb;29(2):181–186. doi: 10.7164/antibiotics.29.181. [DOI] [PubMed] [Google Scholar]

Articles from Antimicrobial Agents and Chemotherapy are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES