C. Ardanuy et al., OUTER-MEMBRANE PROFILES OF CLONALLY RELATED KLEBSIELLA-PNEUMONIAE ISOLATES FROM CLINICAL-SAMPLES AND ACTIVITIES OF CEPHALOSPORINS AND CARBAPENEMS, Antimicrobial agents and chemotherapy, 42(7), 1998, pp. 1636-1640
Fifteen isolates of Klebsiella pneumoniae producing extended-spectrum
beta-lactamases (ESBLs) isolated during a nosocomial outbreak were stu
died. The strains belonged to the same clonal type, as shown by pulsed
-field gel electrophoretic analysis of chromosomal DNA. All the isolat
es were resistant to extended-spectrum cephalosporins, aztreonam, gent
amicin, and fluoroquinolones and mere susceptible to carbapenems, tobr
amycin, netilmicin, and amikacin, None of the isolates expressed the O
mpK36 porin, Eight isolates, for which the MICs of cefoxitin were grea
ter than or equal to 64 mu g/ml, showed a diminished level or no expre
ssion of a 35-kDa porin, The MICs of meropenem, cefotaxime, and cefpir
ome mere three to eight times higher for porin-deficient isolates than
for isolates expressing the 35-kDa porin, but the MICs of imipenem in
creased two times for porin-deficient isolates compared to those for i
solates expressing the porin, This MIC increase reverted to a level si
milar to that for the parental strain when porin-deficient isolates we
re transformed with the gene coding for the K. pneumoniae porin OmpK36
, It is concluded that the high level of resistance to cefoxitin and t
he increase in the MICs of meropenem, cefotaxime, and cefpirome for th
e ESBL-producing K. pneumoniae isolates studied are associated with po
rin deficiency.