MODES OF ACTION AND INHIBITORY ACTIVITIES OF NEW SIDEROPHORE BETA-LACTAM CONJUGATES THAT USE SPECIFIC IRON UPTAKE PATHWAYS FOR ENTRY INTO BACTERIA

被引:50
作者
BROCHU, A
BROCHU, N
NICAS, TI
PARR, TR
MINNICK, AA
DOLENCE, EK
MCKEE, JA
MILLER, MJ
LAVOIE, MC
MALOUIN, F
机构
[1] CHU LAVAL,CTR RECH,DEPT MICROBIOL,QUEBEC CITY G1V 4G2,QUEBEC,CANADA
[2] CHU LAVAL,CTR RECH,INFECTIOL LAB,QUEBEC CITY G1V 4G2,QUEBEC,CANADA
[3] CHU LAVAL,CTR RECH,SERV INFECTIOL,QUEBEC CITY G1V 4G2,QUEBEC,CANADA
[4] ELI LILLY & CO,LILLY RES LAB,INDIANAPOLIS,IN 46285
[5] UNIV NOTRE DAME,DEPT CHEM & BIOCHEM,NOTRE DAME,IN 46556
[6] UNIV LAVAL,ECOLE MED DENT,GREB,QUEBEC CITY G1K 7P4,QUEBEC,CANADA
关键词
D O I
10.1128/AAC.36.10.2166
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We describe here the mechanism of inhibition of two new siderophore-beta-lactam conjugates against Escherichia coli X580. One conjugate is a spermidine-based catechol siderophore-carbacephalosporin (JAM-2-263), and the other is an N5-acetyl-N5-hydroxy-L-Ornithine tripeptide hydroxamate siderophore-carbacephalosporin (EKD-3-88). In an agar diffusion test, both conjugates produced large inhibitory zones against strain X580. Resistant strains (i.e., JAM(R) and EKD(R)) could be isolated after exposure of X580 to the conjugates JAM-2-263 and EKD-3-88, respectively. No cross-resistance was observed in these individual isolates. JAM(R) and EKD(R) were studied further to elucidate the mechanism of inhibition of each conjugated drug. The affinities of JAM-2-263 and EKD-3-88 for penicillin-binding proteins (PBPs) of isolated inner membranes were determined by a competition assay with I-125-penicillin V. JAM-2-263 targeted primarily PBPs 1A/B and 5/6, while EKD-3-88 targeted PBPs 1A/B and 3. Strains X580, JAM(R), and EKD(R) showed similar PBP affinities for the conjugates. However, marked changes were observed in the iron-regulated outer membrane proteins of resistant isolates grown on agar plates depleted of iron. EKD(R) lost the expression of FhuA (78 kDa) and its sensitivity to phages T1 and T5, whereas JAM(R) lost the expression of Cir (74 kDa) and its sensitivity to colicin Ia. These results revealed the requirement of FhuA and Cir for the inhibitory activities of EKD-3-88 and JAM-2-263, respectively. In an antibiotic diffusion assay, ferrichrome (1 muM) strongly antagonized the activities of both conjugates against X580 and JAM(R), including the residual activity of JAM-2-263 against JAM(R). However, the susceptibility of strain EKD(R) lacking the ferrichrome receptor (FhuA-) to the two conjugates remained the same in the presence of ferrichrome. The antagonistic effect of ferrichrome on the activity of JAM-2-263 may also indicate a role for FhuA in the activity of this beta-lactam conjugate. A FhuA- Cir- double mutant confirmed this hypothesis, since it showed a higher level of resistance to JAM-2-263. To reproduce iron-restricted in vivo growth conditions, we grew X580 and EKD(R) cells in diffusion chambers implanted in the peritoneal cavities of rats. Strain EKD(R) showed impaired growth in such a cultivation system. This is the first report of beta-lactam drug transport into E. coli cells that involves the FhuA outer membrane protein.
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页码:2166 / 2175
页数:10
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