Müller Anja, Sakurai Keisuke, Seinige Diana, Nishino Kunihiko, Kehrenberg Corinna
Institute for Veterinary Food Science, Justus Liebig University Giessen, Giessen, Germany.
Institute for Protein Research, Osaka University, Osaka, Japan.
Front Microbiol. 2022 Jan 7;12:794435. doi: 10.3389/fmicb.2021.794435. eCollection 2021.
The prototype gene confers combined resistance to chloramphenicol and florfenicol. However, variants mediating resistance only to chloramphenicol have been identified, such as in the case of a isolate recovered from poultry meat illegally imported to Germany. The effects of the individual mutations detected in the sequence of this isolate were investigated in this study. A total of 11 variants, including prototype and variants containing the different previously described mutations either alone or in different combinations, were generated by on-chip gene synthesis and site-directed mutagenesis. The constructs were inserted into a shuttle vector and transformed into three recipient strains (, , and Typhimurium). Subsequently, minimal inhibitory concentrations (MIC) of florfenicol and chloramphenicol were determined. In addition, protein modeling was used to predict the structural effects of the mutations. The lack of florfenicol-resistance mediating properties of the variants could be attributed to the presence of a C110T and/or G98C mutation. Transformants carrying variants containing either of these mutations, or both, showed a reduction of florfenicol MICs compared to those transformants carrying prototype or any of the other variants. The significance of these mutations was supported by the generated protein models, indicating a substitution toward more voluminous amino-acids in the substrate-binding site of FexA. The remaining mutations, A391G and C961A, did not result in lower florfenicol-resistance compared to prototype .
原型基因赋予对氯霉素和氟苯尼考的联合抗性。然而,已鉴定出仅介导对氯霉素抗性的变体,例如从非法进口到德国的禽肉中分离出的一株菌。本研究调查了在该分离株序列中检测到的各个突变的影响。通过芯片上基因合成和定点诱变共产生了11种变体,包括原型变体以及单独或不同组合包含先前描述的不同突变的变体。将构建体插入穿梭载体并转化到三种受体菌株(大肠杆菌、枯草芽孢杆菌和鼠伤寒沙门氏菌)中。随后,测定了氟苯尼考和氯霉素的最低抑菌浓度(MIC)。此外,使用蛋白质建模来预测突变的结构效应。原型变体缺乏介导氟苯尼考抗性的特性可归因于存在C110T和/或G98C突变。与携带原型变体或任何其他变体的转化体相比,携带包含这些突变之一或两者的原型变体的转化体显示氟苯尼考MIC降低。生成的蛋白质模型支持了这些突变的重要性,表明在FexA的底物结合位点向更大体积的氨基酸发生了取代。与原型变体相比,其余突变A391G和C961A并未导致氟苯尼考抗性降低。