OUTER-MEMBRANE PROTEINS AND LIPOPOLYSACCHARIDE CHANGES AFTER EXPOSURE OF PSEUDOMONAS-AERUGINOSA TO ANTIBACTERIAL DRUGS

被引:0
作者
GIORDANO, A
MAGNI, A
TRANSCASSINI, M
CIPRIANI, P
机构
来源
MICROBIOLOGICA | 1993年 / 16卷 / 03期
关键词
AZTREONAM; NETILMICIN; PD-131; 628; PSEUDOMONAS-AERUGINOSA; PORINS; LIPOPOLYSACCHARIDE;
D O I
暂无
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Many studies show the low sensitivity of P. aeruginosa to antimicrobial agents, due to the permeability degree of the outer membrane (OM). Since the alterations of porins and lipopolysaccharides (LPS) are responsible for permeability to antibacterial drugs, the aim of this study was to evaluate the sub-M.I.C. effects of different antibiotics on the OM components. The M.I.C.s of five P. aeruginosa strains were determined and sub-M.I.C.s. versus PD-131,628, a new difluoroquinolone, aztreonam and netilmicin were calculated. The OM components were extracted before and after contact with the antibacterial drugs. We noted a decrease in M.I.C. values in two strains, and simultaneously an increase in the 19 and 38 Kd bands after using aztreonam. The M.I.C.s tended to increase in three strains after using netilmicin. The electrophoresis profile showed a decrease in the 38, 41 and 45 Kd bands and in one strain also in the 19 Kd band. The use of the quinolone did not significantly modify the M.I.C. values, although an evident increase in 38 and 41 Kd bands occurred in three strains. LPS alterations were observed with aztreonam and netilmicin, but not when PD 131,628 was used.
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页码:281 / 286
页数:6
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共 49 条
[41]   ANION TRANSPORT THROUGH THE PHOSPHATE-SPECIFIC OPRP-CHANNEL OF THE PSEUDOMONAS-AERUGINOSA OUTER-MEMBRANE - EFFECTS OF PHOSPHATE, DI-BASIC AND TRIBASIC ANIONS AND OF NEGATIVELY-CHARGED LIPIDS [J].
BENZ, R ;
EGLI, C ;
HANCOCK, REW .
BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1149 (02) :224-230
[42]   In vivo incorporation of selenomethionine in proteins using Pseudomonas aeruginosa as expression host:: case study -: the outer membrane receptor FpvA [J].
Folschweiller, N ;
Pacaud, K ;
Celia, H ;
Potier, N ;
Cobessi, D ;
Van Dorsselaer, A ;
Pattus, F .
PROTEIN EXPRESSION AND PURIFICATION, 2004, 38 (01) :79-83
[43]   ANTIBODIES TO LIPOPOLYSACCHARIDE AND OUTER-MEMBRANE PROTEINS OF SALMONELLA-ENTERITIDIS PT4 ARE NOT INVOLVED IN PROTECTION FROM EXPERIMENTAL-INFECTION [J].
CHART, H ;
ROWE, B .
FEMS MICROBIOLOGY LETTERS, 1991, 84 (03) :345-350
[44]   Characterization of outer membrane efflux proteins OpmE, OpmD and OpmB of Pseudomonas aeruginosa:: molecular cloning and development of specific antisera [J].
Murata, T ;
Gotoh, N ;
Nishino, T .
FEMS MICROBIOLOGY LETTERS, 2002, 217 (01) :57-63
[45]   Intra-specific diversity and host specificity within Pasteurella haemolytica based on variation of capsular polysaccharide, lipopolysaccharide and outer-membrane proteins [J].
Davies, RL ;
Donachie, W .
MICROBIOLOGY-SGM, 1996, 142 :1895-1907
[46]   Heterogeneity in expression of lipopolysaccharide and major outer-membrane proteins by strains of Escherichia coli O157 with different H-serotypes [J].
Fujimoto, S ;
Meno, Y ;
Horikawa, K .
MICROBIOLOGY AND IMMUNOLOGY, 1998, 42 (08) :527-531
[47]   The interaction between Pseudomonas aeruginosa cells and cationic PC:Chol:DOTAP liposomal vesicles versus outer-membrane structure and envelope properties of bacterial cell [J].
Druis-Kawa, Zuzanna ;
Dorotkiewicz-Jach, Agata ;
Gubernator, Jerzy ;
Gula, Grzegorz ;
Bocer, Tomasz ;
Doroszkiewicz, Wlodzimierz .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2009, 367 (1-2) :211-219
[48]   Human anti-Pseudomonas aeruginosa outer membrane proteins IgG cross-protective against infection with heterologous immunotype strains of P-aeruginosa [J].
Lee, NG ;
Ahn, BY ;
Jung, SB ;
Kim, YG ;
Lee, Y ;
Kim, HS ;
Park, WJ .
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY, 1999, 25 (04) :339-347
[49]   Unchanged Antibiotic Susceptibility in Escherichia coli and Pseudomonas aeruginosa after Long-Term in vitro Exposure to Antineoplastic Drugs [J].
Kvakkestad, Kristin M. ;
Gammelsrud, Karianne W. ;
Brandtzaeg, Petter ;
Hoiby, E. Arne .
CHEMOTHERAPY, 2012, 58 (02) :118-122