Journal of Antimicrobial Chemotherapy (1983) 12, 435-449
© 1983 The British Society for Antimicrobial Chemotherapy
research-article |
The permeability barrier of Haemophilus influenzae type b against ß-lactam antibiotics
Department of Microbiology and Immunology, McGill University 3775 University Street, Montreal, Quebec, Canada H3A 2B4
accepted 18 May 1983
Reprint requests to: J. W. Coulton.
An evaluation was made of the role of the outer membrane of Haemophilus influenzae type b as a permeability barrier against ß-lactam antibiotics. Sonic extracts of H. influenzae containing ß-lactamase were assayed for the rates of hydrolysis of benzylpenicillin, ampicillin, cloxacillin, cephacetrile, cefazolin, cefamandole, cephalothin, cephaloridine, cephaloglycin, and cefaclor. Benzyl-penicillin was hydrolyzed most rapidly, whereas cephacetrile, cephaloridine, and cephaloglycin were the poorest substrates for the ß-lactamase. The hydrolysis of these ten ß-lactams by intact cells was also determined; it was necessary to stabilize the cells with MgCl2 to prevent lysis and thereby to maintain the ß-lactamase in the periplasm. Calculations were made of the concentration of the antibiotics which had accumulated in the periplasm. The transmembrane permeability coefficient, C, was determined for the ten ß-lactam antibiotics. All of the compounds tested were able to diffuse across the outer membrane of H. influenzae type b very efficiently. The values of the permeability coefficient were compared with the partition coefficients of the antibiotics in a two-phase isobutanol/water mixture. For a ten-fold increase in hydrophobicity, there was a ten-fold decrease in the permeability coefficient. The outer membrane of haemophilus was not an effective barrier against the penetration of penicillins or cephalosporins. The activity of these compounds could be attributed either to their low hydrolysis by ß-lactamase or to the high affinity of binding to their sensitive targets.
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