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改变的青霉素结合蛋白(PBPs)与克隆的超广谱β-内酰胺酶的表达相结合,赋予流感嗜血杆菌对头孢噻肟的耐药性。

Combination of altered PBPs and expression of cloned extended-spectrum beta-lactamases confers cefotaxime resistance in Haemophilus influenzae.

作者信息

Bozdogan Bülent, Tristram Stephen, Appelbaum Peter C

机构信息

Mikrobiyoloji ve Klinik Mikrobiyoloji, Adnan Menderes Universitesi Hastanesi, Aydin, Turkey.

出版信息

J Antimicrob Chemother. 2006 Apr;57(4):747-9. doi: 10.1093/jac/dkl039. Epub 2006 Feb 21.

Abstract

BACKGROUND

Resistance to beta-lactams in Haemophilus influenzae is mostly due to the presence of TEM beta-lactamases. beta-Lactamase-negative ampicillin resistance (BLNAR) also occurs as a result of PBP3 modifications. BLNAR strains are particularly common in Japan and France, and strains with combined mechanisms of altered PBP3 and beta-lactamase (BLPACR) are emerging. Although the prevalence of beta-lactamase-positive strains is high, TEM-derived extended-spectrum beta-lactamase (ESBL)-mediated cephalosporin resistance, which is common in Enterobacteriaceae, has not been reported in H. influenzae. In this study, the ability of ESBLs TEM-3, -4 and -5 to confer beta-lactam resistance in H. influenzae strains with or without modified PBP3 was tested.

METHODS

The genes encoding TEM-1, -3, -4 and -5 were cloned into plasmid pLS88 and were used to transform H. influenzae Rd and BLNAR H. influenzae Rd strains with PBP3 modifications. MICs were determined using CLSI macrobroth dilution. The ability of amoxicillin/clavulanate pre-diffusion disc tests to discriminate between ESBL-producing strains and other strains was also tested.

RESULTS

The presence of ESBLs in BLNAR strains conferred cefotaxime resistance, but H. influenzae Rd strains expressing ESBLs and BLNAR strains expressing TEM-1 remained cefotaxime susceptible. The amoxicillin/clavulanate pre-diffusion tests were able to discriminate the ESBL-producing strains from the other strains.

CONCLUSIONS

The presence of altered PBP3 increases the effect of ESBLs in recombinant H. influenzae strains to produce cefotaxime resistance. Amoxicillin/clavulanate pre-diffusion disc tests can discriminate ESBL-producing strains from other strains.

摘要

背景

流感嗜血杆菌对β-内酰胺类药物的耐药性主要归因于TEMβ-内酰胺酶的存在。β-内酰胺酶阴性氨苄西林耐药性(BLNAR)也因青霉素结合蛋白3(PBP3)修饰而出现。BLNAR菌株在日本和法国尤为常见,同时具有PBP3改变和β-内酰胺酶(BLPACR)联合机制的菌株也在不断出现。尽管β-内酰胺酶阳性菌株的流行率很高,但在肠杆菌科中常见的由TEM衍生的超广谱β-内酰胺酶(ESBL)介导的头孢菌素耐药性在流感嗜血杆菌中尚未见报道。在本研究中,测试了ESBLs TEM-3、-4和-5在有或无PBP3修饰的流感嗜血杆菌菌株中赋予β-内酰胺耐药性的能力。

方法

将编码TEM-1、-3、-4和-5的基因克隆到质粒pLS88中,并用于转化带有PBP3修饰的流感嗜血杆菌Rd和BLNAR流感嗜血杆菌Rd菌株。使用美国临床和实验室标准协会(CLSI)的常量肉汤稀释法测定最低抑菌浓度(MIC)。还测试了阿莫西林/克拉维酸预扩散纸片法区分产ESBL菌株和其他菌株的能力。

结果

BLNAR菌株中ESBL的存在赋予了头孢噻肟耐药性,但表达ESBL的流感嗜血杆菌Rd菌株和表达TEM-1的BLNAR菌株对头孢噻肟仍敏感。阿莫西林/克拉维酸预扩散试验能够区分产ESBL菌株和其他菌株。

结论

PBP3改变的存在增加了重组流感嗜血杆菌菌株中ESBL产生头孢噻肟耐药性的作用。阿莫西林/克拉维酸预扩散纸片法可以区分产ESBL菌株和其他菌株。

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