广泛耐药(XDR)铜绿假单胞菌在秘鲁利马共表达一种VIM-2金属β-内酰胺酶、OXA-1 β-内酰胺酶和GES-1广谱β-内酰胺酶。

JMM case reports Pub Date : 2018-06-21 eCollection Date: 2018-07-01 DOI:10.1099/jmmcr.0.005154
Paul Ríos, Claudio Rocha, William Castro, Maria Vidal, Enrique Canal, Manuela Bernal, Nathanael D Reynolds, Drake H Tilley, Mark P Simons
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引用次数: 9

摘要

铜绿假单胞菌有能力获得质粒和其他可移动的遗传元素,赋予抗生素耐药性。细菌基因编码不同的β-内酰胺酶(bla),如金属β-内酰胺酶(MBLs)和广谱β-内酰胺酶(ESBL),可赋予对多种β-内酰胺类抗生素的耐药性。病例介绍:一名83岁女性于2012年入住秘鲁利马的秘鲁海军医院(Cirujano Mayor Santiago Távara)。采集中游尿液样本,送往当地CEMENA实验室进行常规尿液培养。分离得到铜绿假单胞菌,初步药敏试验显示其对亚胺培南敏感。临床医生开始了一个疗程的美罗培南,但病人并没有好转。5天后,进行第二次尿液培养,再次分离出铜绿假单胞菌,但这次菌株对亚胺培南表现出耐药性。改用磷霉素治疗,病情好转。进行了表征抗生素耐药性的表型和分子实验室检测,证明存在MBL和ESBL基因。结论:据我们所知,这是秘鲁首次报道铜绿假单胞菌XDR临床分离株共表达MBL (VIM-2)、OXA-1 β -内酰胺酶和ESBL (GES-1)。这也是秘鲁首次报道VIM碳青霉烯酶。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Extensively drug-resistant (XDR) <i>Pseudomonas aeruginosa</i> identified in Lima, Peru co-expressing a VIM-2 metallo-β-lactamase, OXA-1 β-lactamase and GES-1 extended-spectrum β-lactamase.

Extensively drug-resistant (XDR) <i>Pseudomonas aeruginosa</i> identified in Lima, Peru co-expressing a VIM-2 metallo-β-lactamase, OXA-1 β-lactamase and GES-1 extended-spectrum β-lactamase.

Extensively drug-resistant (XDR) Pseudomonas aeruginosa identified in Lima, Peru co-expressing a VIM-2 metallo-β-lactamase, OXA-1 β-lactamase and GES-1 extended-spectrum β-lactamase.

Introduction: Pseudomonas aeruginosa has the ability to acquire plasmids and other mobile genetic elements that confer resistance to antibiotics. Bacterial genes encoding different β-lactamases (bla), such as metallo-β-lactamases (MBLs) and extended-spectrum β-lactamases (ESBL), can confer resistance to multiple classes of β-lactam antibiotics.

Case presentation: An 83 year old female was admitted in 2012 to the Peruvian Naval Hospital, Centro Médico Naval 'Cirujano Mayor Santiago Távara' (CEMENA), in Lima, Peru. A midstream urine sample was collected and sent to the local CEMENA laboratory for routine urine culture. P. aeruginosa was isolated and initial antibiotic susceptibility testing showed it to be sensitive to imipenem. The clinicians started a course of meropenem, but the patient did not improve. After 5 days, a second urine culture was performed and a P. aeruginosa was isolated again, but this time the strain showed resistance to imipenem. The treatment course was changed to fosfomycin and the patient improved. Phenotypic and molecular laboratory testing to characterize the antibiotic resistance were performed, demonstrating the presence of both MBL and ESBL genes.

Conclusion: To our knowledge, this is the first report of a P. aeruginosa XDR clinical isolate that co-expresses an MBL (VIM-2), OXA-1 beta-lactamase and the ESBL (GES-1) in Peru. It is also the first report of a VIM carbapenemase in Peru.

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