Characterization of Pseudomonas aeruginosa isolates from patients with urinary tract infections during antibiotic therapy

被引:10
作者
Horii, T
Muramatsu, H
Morita, M
Maekawa, M
机构
[1] Hamamatsu Univ Sch Med, Dept Lab Med, Hamamatsu, Shizuoka 4313192, Japan
[2] Hamamatsu Univ Sch Med, Grp Infect Control Res, Hamamatsu, Shizuoka 4313192, Japan
[3] Hamamatsu Univ Sch Med, Grp Infect Control Res, Hamamatsu, Shizuoka 4313192, Japan
[4] Hamamatsu Univ Sch Med, Div Pharm, Hamamatsu, Shizuoka 4313192, Japan
[5] Daiichi Pure Chem, Ryugasaki 3010852, Japan
关键词
D O I
10.1089/107662903765826831
中图分类号
R51 [传染病];
学科分类号
100401 [流行病与卫生统计学];
摘要
We characterized susceptibilities and genotypes in a series of Pseudomonas aeruginosa isolates from five cases of urinary tract infections (UTIs) to evaluate clonal shifts of carbapenem resistance. In one case, a series of isolates showed different susceptibility patterns for carbapenems but an identical genotype. In another case, genotypes varied among 4 P. aeruginosa isolates from recurrent UTIs over 9 months. Although the patient had been treated with no antibiotic immediately before isolation, the susceptibility patterns for carbapenems and ceftazidime varied. Further analysis in these two cases of outer membrane protein profiles showed that loss of OprD production resulted in reduced susceptibilities to carbapenems in all of the carbapenem-resistant isolates. Loss of OprD production was likely due to oprD gene inactivation in both of cases, since the carbapenem-resistant isolates showed no cross resistance to levofloxacin and chloramphenicol compared with the carbapenem-susceptible isolates. There was another case in which all isolates showed similar susceptibility patterns for carbapenems and ceftazidime, and an identical genotype during the intermittent use of antibiotics over 5 months. In two cases, a single course of antibiotic therapy resulted in eradication of P. aeruginosa. Our results suggest that clonal shifts of carbapenem resistance in P. aeruginosa may result from loss of OprD during antibiotic treatment. Therefore, it is important for clinicians to monitor susceptibilities to antibiotics, especially carbapenems, in P. aeruginosa isolated during therapy.
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收藏
页码:223 / 229
页数:7
相关论文
共 23 条
[1]
Involvement of an active efflux system in the natural resistance of Pseudomonas aeruginosa to aminoglycosides [J].
Aires, JR ;
Köhler, T ;
Nikaido, H ;
Plésiat, P .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1999, 43 (11) :2624-2628
[2]
Arakawa Y, 2000, J CLIN MICROBIOL, V38, P40
[3]
Emergence of antibiotic-resistant Pseudomonas aeruginosa:: Comparison of risks associated with different antipseudomonal agents [J].
Carmeli, Y ;
Troillet, N ;
Eliopoulos, GM ;
Samore, MH .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1999, 43 (06) :1379-1382
[4]
Nosocomial outbreak due to a multiresistant strain of Pseudomonas aeruginosa P12:: Efficacy of cefepime-amikacin therapy and analysis of β-lactam resistance [J].
Dubois, V ;
Arpin, C ;
Melon, M ;
Melon, B ;
Andre, C ;
Frigo, CC ;
Quentin, C .
JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (06) :2072-2078
[5]
El Amari EB, 2001, CLIN INFECT DIS, V33, P1859, DOI 10.1086/324346
[6]
Resistance mechanisms in Pseudomonas aeruginosa and other nonfermentative gram-negative bacteria [J].
Hancock, REW .
CLINICAL INFECTIOUS DISEASES, 1998, 27 :S93-S99
[7]
Risk factors for imipenem-resistant Pseudomonas aeruginosa among hospitalized patients [J].
Harris, AD ;
Smith, D ;
Johnson, JA ;
Bradham, DD ;
Roghmann, MC .
CLINICAL INFECTIOUS DISEASES, 2002, 34 (03) :340-345
[8]
HOMMA JY, 1982, JPN J EXP MED, V52, P317
[9]
Emergence of fosfomycin-resistant isolates of shiga-like toxin-producing Escherichia coli O26 [J].
Horii, T ;
Kimura, T ;
Sato, K ;
Shibayama, K ;
Ohta, M .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1999, 43 (04) :789-793
[10]
Persistence of a multidrug-resistant Pseudomonas aeruginosa clone in an intensive care burn unit [J].
Hsueh, PR ;
Teng, LJ ;
Yang, PC ;
Chen, YC ;
Ho, SW ;
Luh, KT .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (05) :1347-1351