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Antimicrobial Agents and Chemotherapy, July 1998, p. 1636-1640, Vol. 42, No. 7
0066-4804/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.

Outer Membrane Profiles of Clonally Related Klebsiella pneumoniae Isolates from Clinical Samples and Activities of Cephalosporins and Carbapenems

Carmen Ardanuy,1,* Josefina Liñares,1 María Angeles Domínguez,1 Santiago Hernández-Allés,2 Vicente J. Benedí,2 and Luis Martínez-Martínez3

Servicio de Microbiología, Hospital de Bellvitge, Universidad de Barcelona, Barcelona,1 Departamento de Biología Ambiental, Universidad de las Islas Baleares and IMEDEA (CSIC-UIB), Palma de Mallorca,2 and Departamento de Microbiología, Facultad de Medicina, Universidad de Sevilla, Seville,3 Spain

Received 19 November 1997/Returned for modification 11 February 1998/Accepted 16 April 1998

Fifteen isolates of Klebsiella pneumoniae producing extended-spectrum beta -lactamases (ESBLs) isolated during a nosocomial outbreak were studied. The strains belonged to the same clonal type, as shown by pulsed-field gel electrophoretic analysis of chromosomal DNA. All the isolates were resistant to extended-spectrum cephalosporins, aztreonam, gentamicin, and fluoroquinolones and were susceptible to carbapenems, tobramycin, netilmicin, and amikacin. None of the isolates expressed the OmpK36 porin. Eight isolates, for which the MICs of cefoxitin were >= 64 µg/ml, showed a diminished level or no expression of a 35-kDa porin. The MICs of meropenem, cefotaxime, and cefpirome were three to eight times higher for porin-deficient isolates than for isolates expressing the 35-kDa porin, but the MICs of imipenem increased two times for porin-deficient isolates compared to those for isolates expressing the porin. This MIC increase reverted to a level similar to that for the parental strain when porin-deficient isolates were transformed with the gene coding for the K. pneumoniae porin OmpK36. It is concluded that the high level of resistance to cefoxitin and the increase in the MICs of meropenem, cefotaxime, and cefpirome for the ESBL-producing K. pneumoniae isolates studied are associated with porin deficiency.


* Corresponding author. Mailing address: Servicio de Microbiología, Hospital de Bellvitge, Feixa Llarga s/n. 08907, L'Hospitalet, Barcelona, Spain. Phone: 34-3-3357011, ext. 2097. Fax: 34-93-2607547. E-mail: c.ardanuy{at}csub.scs.es.


Antimicrobial Agents and Chemotherapy, July 1998, p. 1636-1640, Vol. 42, No. 7
0066-4804/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.



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