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嗜水气单胞菌中可诱导的β-内酰胺耐药性:抗菌治疗面临的挑战

Inducible beta-lactam resistance in Aeromonas hydrophila: therapeutic challenge for antimicrobial therapy.

作者信息

Ko W C, Wu H M, Chang T C, Yan J J, Wu J J

机构信息

Departments of Internal Medicine, National Cheng Kung University Hospital, National Cheng Kung University Medical College, Tainan, Taiwan.

出版信息

J Clin Microbiol. 1998 Nov;36(11):3188-92. doi: 10.1128/JCM.36.11.3188-3192.1998.

Abstract

Despite the abundant amount of knowledge about inducible chromosomally mediated beta-lactamases among Aeromonas species, extended-spectrum beta-lactam-resistant A. hydrophila strains selected in clinical practice were rarely reported. In the present study, two strains of A. hydrophila, A136 and A139, with markedly different susceptibilities to extended-spectrum cephalosporins were isolated from blood and the tip segment of an arterial catheter of a burn patient. Another strain (A136m) was selected in vitro by culturing A136 in a subinhibitory concentration of cefotaxime, the beta-lactam agent administered for the treatment of Aeromonas bacteremia in this patient. Typing studies by arbitrarily primed PCR and pulsed-field gel electrophoresis indicated a clonal relationship among strains A136, A136m, and A139. These strains were identified to be of DNA hybridization group 1. Wild-type strain A136 was resistant only to ampicillin and cephamycins, but A136m and A139 were highly resistant to the expanded- and broad-spectrum cephalosporins. The presence of increased beta-lactamase activity in A139 suggests that A139 is a derepressed mutant which overexpresses beta-lactamases. These results call attention to the use of beta-lactam agents for the treatment of invasive Aeromonas infections.

摘要

尽管关于气单胞菌属中可诱导的染色体介导的β-内酰胺酶已有大量知识,但临床实践中选择的对超广谱β-内酰胺耐药的嗜水气单胞菌菌株却鲜有报道。在本研究中,从一名烧伤患者的血液和动脉导管尖端分离出两株对超广谱头孢菌素敏感性明显不同的嗜水气单胞菌菌株A136和A139。通过在亚抑菌浓度的头孢噻肟(该患者用于治疗气单胞菌血症的β-内酰胺类药物)中培养A136,在体外筛选出另一株菌株(A136m)。通过任意引物PCR和脉冲场凝胶电泳进行的分型研究表明,菌株A136、A136m和A139之间存在克隆关系。这些菌株被鉴定为DNA杂交组1。野生型菌株A136仅对氨苄西林和头孢霉素耐药,但A136m和A139对超广谱和广谱头孢菌素高度耐药。A139中β-内酰胺酶活性增加表明A139是一个去阻遏突变体,其β-内酰胺酶过度表达。这些结果提醒人们注意β-内酰胺类药物在侵袭性气单胞菌感染治疗中的应用。

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