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添加苯唑西林的穆勒-欣顿琼脂用于体外抑制肠杆菌科细菌中的安布勒C类β-内酰胺酶

Oxacillin-Supplemented Mueller-Hinton Agar for In Vitro Inhibition of Ambler Class C β-Lactamases in Enterobacterales.

作者信息

Chelaru Edgar-Costin, Muntean Andrei-Alexandru, Muntean Mădălina-Maria, Hogea Mihai-Octav, Caracoti Costin-Ștefan, Ciomaga Bogdan-Florin, Naas Thierry, Popa Mircea Ioan

机构信息

Discipline of Microbiology II, Department 2, Faculty of Medicine, Carol Davila University of Medicine and Pharmacy, 020021 Bucharest, Romania.

Cantacuzino National Military Medical Institute for Research and Development, 050096 Bucharest, Romania.

出版信息

Antibiotics (Basel). 2025 Jun 18;14(6):616. doi: 10.3390/antibiotics14060616.

Abstract

: The increasing incidence of infection with Gram-negative bacilli (GNB) producing broad-spectrum β-lactamases, such as extended-spectrum β-lactamases (ESBLs), cephalosporinases (AmpCs), and carbapenemases, has become a great clinical concern. AmpCs are found in many clinically relevant Enterobacterales, where they may compromise the effectiveness of most β-lactams, including carbapenems when associated with an impaired outer membrane. Detection and distinction between these resistance mechanisms are crucial for antimicrobial therapy and for implementation of proper infection control procedures to prevent further spread. : The disk diffusion antibiogram using Mueller-Hinton agar (MHA) supplemented with cloxacillin (MHC), which inhibits AmpCs, was validated to identify AmpC-producing Enterobacterales (AmpC-PE). As cloxacillin is not available in several countries, we investigated the use of oxacillin as an alternative compound to inhibit AmpCs. The ability of MHA supplemented with oxacillin (MHO) to distinguish between carbapenem-resistant Enterobacterales (CREs) due to AmpC hyperproduction and the presence of a carbapenemase has particularly been investigated. : MHOs containing several concentrations of oxacillin were compared to MHA and MHC containing 250 mg/L cloxacillin (MHC250). A set of well-characterized Enterobacterales with different β-lactam resistance mechanisms were evaluated. MHO containing 300 mg/L of oxacillin (MHO300) gave similar results to MHC250. : The use of MHO300 proved to be efficient in inhibiting AmpCs, allowing differentiation between AmpC hyperproducers and carbapenemase producers. In addition, the use of MHO300 allowed detection of resistance mechanisms hidden by AmpCs, such as ESBLs.

摘要

产生超广谱β-内酰胺酶(ESBLs)、头孢菌素酶(AmpCs)和碳青霉烯酶等广谱β-内酰胺酶的革兰氏阴性杆菌(GNB)感染发生率不断上升,已成为临床上的一大关注点。在许多临床相关的肠杆菌科细菌中发现了AmpCs,当它们与外膜受损相关时,可能会削弱包括碳青霉烯类在内的大多数β-内酰胺类药物的有效性。检测和区分这些耐药机制对抗菌治疗以及实施适当的感染控制措施以防止进一步传播至关重要。使用补充有氯唑西林(MHC)的穆勒-欣顿琼脂(MHA)进行纸片扩散药敏试验,该试验可抑制AmpCs,已被验证用于鉴定产AmpC的肠杆菌科细菌(AmpC-PE)。由于氯唑西林在一些国家无法获得,我们研究了使用苯唑西林作为替代化合物来抑制AmpCs。特别研究了补充有苯唑西林(MHO)的MHA区分因AmpC过度产生和存在碳青霉烯酶而导致的耐碳青霉烯肠杆菌(CREs)的能力。将含有几种浓度苯唑西林的MHO与含有250 mg/L氯唑西林的MHA和MHC(MHC250)进行比较。评估了一组具有不同β-内酰胺耐药机制的特征明确的肠杆菌科细菌。含有300 mg/L苯唑西林的MHO(MHO300)给出了与MHC250相似的结果。事实证明,使用MHO300能有效抑制AmpCs,从而区分AmpC过度产生者和碳青霉烯酶产生者。此外,使用MHO300能够检测到被AmpCs掩盖的耐药机制,如ESBLs。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfa6/12189709/8850605db2b7/antibiotics-14-00616-g001.jpg

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