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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
-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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