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感染新生儿肺炎克雷伯菌菌株中对氧亚氨基头孢菌素耐药性的转移及超广谱β-内酰胺酶的产生

Transfer of resistance to oxy-imino-cephalosporins and of extended-spectrum beta-lactamase productions in Klebsiella pneumoniae strains from infected neonates.

作者信息

Blahová J, Hupková M, Králiková K, Krcméry V, Lísková A, Kubonová K

机构信息

Institute of Preventive and Clinical Medicine, Bratislava, Slovak Republic.

出版信息

Zentralbl Bakteriol. 1998 Jul;288(1):75-86. doi: 10.1016/s0934-8840(98)80103-5.

Abstract

In this communication, we describe the occurrence of strains of Klebsiella pneumoniae resistant to cephalosporins of all generations and to aztreonam due to their production of Extended Spectrum beta-Lactamases (ESBLs), in two hospitals in Slovakia. They were found to transfer the genetic determinants of resistance of cefotaxime, ceftazidime and aztreonam and of ESBL production to suitable recipient strains of Escherichia coli K-12 No. 3110 and Proteus mirabilis P-38. Six donor K. pneumoniae strains were collected from six prematurely born babies gradually infected with strains of K. pneumoniae resistant to cefotaxime, ceftazidime and aztreonam. All six strains of K. pneumoniae gave an identical pattern in ESBL testing (double-disk diffusion test). The second cycle of transfers to nalidixin-resistant E. coli K-12 No. 185 nal+ also confirmed that all transconjugants were resistant to all beta-lactams tested. We conclude that a single gene was transferred from donor strains which confers 'en bloc' the resistance to the beta-lactams tested. Four strains of K. pneumoniae produced a uniform type of ESBI. Although with different quantitative expression. All transconjugants tested produced identical types of ESBL as did the donor strains of K. pneumoniae. This transfer of an identical pattern of ESBL production was confirmed also in the second cycle of transfers. Cefotaxime, ceftazidime and aztreonam were actively hydrolysed (as shown by the relative rate of hydrolysis [Vmax]) by strains of K. pneumoniae as well as by transconjugant colonies and clavulanate inhibited the hydrolysis of these beta-lactam antibiotics.

摘要

在本通讯中,我们描述了在斯洛伐克的两家医院中,肺炎克雷伯菌菌株对所有代头孢菌素及氨曲南耐药的情况,这些菌株因产生超广谱β-内酰胺酶(ESBLs)而耐药。发现它们能将头孢噻肟、头孢他啶和氨曲南的耐药基因决定簇以及ESBL产生相关基因转移至合适的大肠杆菌K-12 3110号受体菌株和奇异变形杆菌P-38。从六名早产婴儿中收集到六株供体肺炎克雷伯菌菌株,这些婴儿逐渐感染了对头孢噻肟、头孢他啶和氨曲南耐药的肺炎克雷伯菌菌株。所有六株肺炎克雷伯菌在ESBL检测(双纸片扩散试验)中呈现相同模式。将其转移至耐萘啶酸的大肠杆菌K-12 185 nal+的第二轮转移实验也证实,所有转接合子对所有测试的β-内酰胺类药物均耐药。我们得出结论,供体菌株转移了一个单一基因,该基因赋予对所测试的β-内酰胺类药物“整体”耐药性。四株肺炎克雷伯菌产生了一种统一类型的ESBI,尽管定量表达有所不同。所有测试的转接合子产生的ESBL类型与肺炎克雷伯菌供体菌株相同。在第二轮转移实验中也证实了这种相同ESBL产生模式的转移。肺炎克雷伯菌菌株以及转接合子菌落能积极水解头孢噻肟、头孢他啶和氨曲南(由相对水解速率[Vmax]显示),而克拉维酸抑制这些β-内酰胺类抗生素的水解。

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