Institute for Infectious Diseases, University of Bern, CH-3010 Bern, Switzerland.
J Antimicrob Chemother. 2010 Oct;65(10):2089-96. doi: 10.1093/jac/dkq312. Epub 2010 Aug 27.
The outer membrane protein M35 of Moraxella catarrhalis is an antigenically conserved porin. Knocking out M35 significantly increases the MICs of aminopenicillins. The aim of this study was to determine the biological mechanism of this potentially new antimicrobial resistance mechanism of M. catarrhalis and the behaviour of M35 in general stress situations.
PCR using m35-specific primers was used to detect the m35 gene in clinical isolates. The m35 mRNA expression of strains 300, O35E and 415 after exposure to amoxicillin and different stress conditions was measured by real-time PCR and normalized in relation to their 16S rRNA expression. The expression of M35 protein was analysed by SDS-PAGE and western blotting.
Screening of 52 middle ear isolates resulted in positive PCR products for all tested strains. The analysis of m35 mRNA expression after amoxicillin treatment showed 24%-85% down-regulation compared with the respective amoxicillin-free controls in all three strains tested. Also, analysis of protein concentrations revealed lower M35 expression after growth with amoxicillin. Investigation of M35 during general stress responses showed down-regulation of the porin with growth at 26°C and 42°C, under hyperosmolar stress and under iron restriction.
The reduced expression of M35 after aminopenicillin exposure indicates a novel resistance mechanism against aminopenicillins in M. catarrhalis, which may be relevant in vivo. The differences in expression after different stress treatments demonstrate that M35 is involved in general stress responses.
卡他莫拉菌的外膜蛋白 M35 是一种抗原保守的孔蛋白。敲除 M35 会显著增加氨苄西林类抗生素的 MIC 值。本研究旨在确定 M. catarrhalis 这种潜在新的抗生素耐药机制的生物学机制以及 M35 在一般应激情况下的行为。
使用 m35 特异性引物的 PCR 用于检测临床分离株中的 m35 基因。通过实时 PCR 测量菌株 300、O35E 和 415 在暴露于阿莫西林和不同应激条件后的 m35 mRNA 表达,并相对于其 16S rRNA 表达进行归一化。通过 SDS-PAGE 和 Western blot 分析 M35 蛋白的表达。
对 52 个中耳分离株进行筛选,所有测试菌株的 PCR 产物均为阳性。在所有三种测试菌株中,阿莫西林处理后 m35 mRNA 表达的分析显示与相应的无阿莫西林对照相比,下调了 24%-85%。此外,蛋白浓度分析显示,在阿莫西林生长后 M35 表达降低。对一般应激反应期间的 M35 进行研究表明,在 26°C 和 42°C 生长、高渗透压应激和铁限制下,孔蛋白下调。
氨苄西林暴露后 M35 的表达减少表明 M. catarrhalis 对氨苄西林类抗生素有新的耐药机制,这在体内可能是相关的。不同应激处理后的表达差异表明 M35 参与一般应激反应。