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在急性伯克霍尔德氏菌病感染中头孢他啶耐药性的发展。

Development of ceftazidime resistance in an acute Burkholderia pseudomallei infection.

机构信息

Center for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff, AZ, USA.

出版信息

Infect Drug Resist. 2012;5:129-32. doi: 10.2147/IDR.S35529. Epub 2012 Aug 22.

DOI:10.2147/IDR.S35529
PMID:22977307
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3430440/
Abstract

Burkholderia pseudomallei, a bacterium that causes the disease melioidosis, is intrinsically resistant to many antibiotics. First-line antibiotic therapy for treating melioidosis is usually the synthetic β-lactam, ceftazidime (CAZ), as almost all B. pseudomallei strains are susceptible to this drug. However, acquired CAZ resistance can develop in vivo during treatment with CAZ, which can lead to mortality if therapy is not switched to a different drug in a timely manner. Serial B. pseudomallei isolates obtained from an acute Thai melioidosis patient infected by a CAZ susceptible strain, who ultimately succumbed to infection despite being on CAZ therapy for the duration of their infection, were analyzed. Isolates that developed CAZ resistance due to a proline to serine change at position 167 in the β-lactamase PenA were identified. Importantly, these CAZ resistant isolates remained sensitive to the alternative melioidosis treatments; namely, amoxicillin-clavulanate, imipenem, and meropenem. Lastly, real-time polymerase chain reaction-based assays capable of rapidly identifying CAZ resistance in B. pseudomallei isolates at the position 167 mutation site were developed. The ability to rapidly identify the emergence of CAZ resistant B. pseudomallei populations in melioidosis patients will allow timely alterations in treatment strategies, thereby improving patient outcomes for this serious disease.

摘要

类鼻疽伯克霍尔德菌是一种引起类鼻疽病的细菌,对许多抗生素具有内在耐药性。治疗类鼻疽病的一线抗生素治疗通常是合成的β-内酰胺类药物头孢他啶(CAZ),因为几乎所有的类鼻疽伯克霍尔德菌菌株都对这种药物敏感。然而,在使用 CAZ 治疗期间,体内可能会产生获得性 CAZ 耐药性,如果不及时将治疗方案切换为其他药物,可能会导致死亡率。从一名急性泰国类鼻疽病患者身上分离出的类鼻疽伯克霍尔德菌连续分离株进行了分析,该患者感染了对 CAZ 敏感的菌株,但尽管在感染期间一直接受 CAZ 治疗,最终还是死于感染。鉴定出由于β-内酰胺酶 PenA 位置 167 处脯氨酸到丝氨酸的变化而产生 CAZ 耐药的分离株。重要的是,这些对 CAZ 耐药的分离株对替代类鼻疽病治疗方法仍保持敏感;即阿莫西林-克拉维酸、亚胺培南和美罗培南。最后,开发了能够快速鉴定位于 167 位突变点的 CAZ 耐药类鼻疽伯克霍尔德菌分离株的实时聚合酶链反应检测方法。能够快速鉴定出类鼻疽病患者中出现 CAZ 耐药的类鼻疽伯克霍尔德菌群体的能力,将使治疗策略能够及时改变,从而改善这种严重疾病患者的预后。

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