Journal of Antimicrobial Chemotherapy, Vol 39, 79-84, Copyright © 1997 by The British Society for Antimicrobial Chemotherapy
PC Braga, M Dal Sasso and S Maci
Exposure of Staphylococcus aureus and Escherichia coli strains to different
subMICs of cefodizime, cefotaxime and ceftriaxone significantly reduced the
bacterial attachment to human buccal cells, but the resultant patterns of
inhibition were different for S. aureus and E. coli and for the behaviour
of the three cephalosporins. Morphological anomalies such as clusters of
enlarged S. aureus cells and filamentation with spheroplast-like structures
and bulge formations in E. coli were also present. Analogies between the
different patterns of inhibition of adhesiveness and the corresponding
degree of morphological changes were observed. Cefodizime behaved
differently from cefotaxime and ceftriaxone and this could be attributed to
the presence in the cefodizime molecule of an additional substituent, a 3-
methyl-5-carboxymethyl-1,3-thiazole-2-thio group in the 3' position, not
present in cefotaxime or ceftriaxone.
JOURNAL ARTICLE
Cefodizime: effects of sub-inhibitory concentrations on adhesiveness and bacterial morphology of Staphylococcus aureus and Escherichia coli: comparison with cefotaxime and ceftriaxone
Centre for Respiratory Pharmacology, School of Medicine, University of Milan, Italy.
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