In vitro and in vivo activity of meropenem and sulbactam against a multidrug-resistant Acinetobacter baumannii strain

被引:67
作者
Ko, WC
Lee, HC
Chiang, SR
Yan, JJ
Wu, JJ
Lu, CL
Chuang, YC
机构
[1] Natl Cheng Kung Univ, Coll Med, Dept Med, Tainan 70101, Taiwan
[2] Natl Cheng Kung Univ, Coll Med, Dept Med Technol, Tainan 70101, Taiwan
[3] Chi Mei Med Ctr, Dept Med, Tainan, Taiwan
[4] Chi Mei Med Ctr, Dept Med Res, Tainan, Taiwan
[5] Natl Cheng Kung Univ Hosp, Dept Internal Med, Tainan 70428, Taiwan
关键词
synergy; combination therapy; time-kill curves;
D O I
10.1093/jac/dkh080
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: The potential therapeutic role of meropenem combined with sulbactam against a clinical endemic isolate of multidrug-resistant Acinetobacter baumannii, Ab-153, was investigated. Methods: The antimicrobial susceptibility of Ab-153 to various drugs was studied by the agar dilution method and Etest strips. The antibacterial activity of meropenem and sulbactam were investigated by a time-kill study in vitro and further examined for therapeutic efficacy in vivo in a murine model. Results: In the time-kill study, at a concentration of 0.5 x MIC (4 mg/L) of meropenem, 1 x MIC (8 mg/L) of sulbactam and both in combination, only the combination demonstrated bactericidal effects and there was at least a 5 log(10) reduction in bacterial colony counts after 48 h, compared with either drug alone. BALB/c mice infected with 2.1-2.6 x 10(7) cfu of Ab-153 were treated with 20 mg/kg meropenem every 8 h, 40 mg/kg sulbactam every 8 h or both in combination. The survival rate of mice in the combination group was significantly higher than that in the meropenem-treated or sulbactam-treated group (87% versus 35%, P = 0.0004; 87% versus 30%, P = 0.0002). Conclusions: Meropenem in conjunction with sulbactam can exhibit more potent antimicrobial activity against Ab-153 than meropenem or sulbactam alone.
引用
收藏
页码:393 / 395
页数:3
相关论文
共 12 条
[1]  
ALPHONSUS U, 1994, AM J HOSP PHARM, V51, P2671
[2]   Epidemiological significance of cutaneous, pharyngeal, and digestive tract colonization by multiresistant Acinetobacter baumannii in ICU patients [J].
Ayats, J ;
Corbella, X ;
Ardanuy, C ;
Dominguez, MA ;
Ricart, A ;
Ariza, J ;
Martin, R ;
Linares, J .
JOURNAL OF HOSPITAL INFECTION, 1997, 37 (04) :287-295
[3]   Efficacy of sulbactam alone and in combination with ampicillin in nosocomial infections caused by multiresistant Acinetobacter baumannii [J].
Corbella, X ;
Ariza, J ;
Ardanuy, C ;
Vuelta, M ;
Tubau, F ;
Sora, M ;
Pujol, M ;
Gudiol, F .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1998, 42 (06) :793-802
[4]   Influence of relative humidity and suspending menstrua on survival of Acinetobacter spp on dry surfaces [J].
Jawad, A ;
Heritage, J ;
Snelling, AM ;
GascoyneBinzi, DM ;
Hawkey, PM .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (12) :2881-2887
[5]   Successful treatment of multidrug-resistant Acinetobacter baumannii meningitis with intravenous colistin sulfomethate sodium [J].
Jiménez-Mejías, ME ;
Becerril, B ;
Márquez-Rivas, FJ ;
Pichardo, C ;
Cuberos, L ;
Pachón, J .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2000, 19 (12) :970-971
[6]   Multiresistant Acinetobacter infections:: a role for sulbactam combinations in overcoming an emerging worldwide problem [J].
Levin, AS .
CLINICAL MICROBIOLOGY AND INFECTION, 2002, 8 (03) :144-153
[7]   In vitro and in vivo activities of meropenem and comparable antimicrobial agents against Haemophilus influenzae, including β-lactamase-negative ampicillin-resistant strains [J].
Miyazaki, S ;
Fujikawa, T ;
Kanazawa, K ;
Yamaguchi, K .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2001, 48 (05) :723-726
[8]  
National Committee for Clinical Laboratory Standards, 2000, M7A5 NCCLS, VM100-S10
[9]  
SABALLS M, 2003, 43 INT C ANT AG CHEM, P360
[10]   Surveillance of an adult intensive care unit for long-term persistence of a multi-resistant strain of Acinetobacter baumannii [J].
Webster, CA ;
Crowe, M ;
Humphreys, H ;
Towner, KJ .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 1998, 17 (03) :171-176