Kitagawa Haruaki, Izutani Naomi, Kitagawa Ranna, Maezono Hazuki, Yamaguchi Mikiyo, Imazato Satoshi
Department of Biomaterials Science, Osaka University Graduate School of Dentistry, Suita, Osaka, Japan.
Department of Restorative Dentistry and Endodontology, Osaka University Graduate School of Dentistry, Suita, Osaka, Japan.
J Dent. 2016 Apr;47:18-22. doi: 10.1016/j.jdent.2016.02.008. Epub 2016 Feb 22.
The aim of this study was to investigate whether Streptococcus mutans and Enterococcus faecalis develop resistance to the cationic biocides chlorhexidine (CHX), cetylpyridinium chloride (CPC), and 12-methacryloyloxydodecylpyridinium bromide (MDPB).
The minimum inhibitory concentrations (MICs) of CHX, CPC, and MDPB were assessed after repeated exposure of S. mutans and E. faecalis to these biocides. Cell-surface hydrophobicity and protein expression profiles of bacterial cells were examined to elucidate possible resistance mechanisms.
The MIC of CHX against E. faecalis showed constant increases up to 10 passages. No changes in the MICs of CPC and MDPB against E. faecalis were observed. The MICs of CHX, CPC, and MDPB against S. mutans did not increase. The surface hydrophobicity of E. faecalis significantly increased with increasing exposure to CHX and CPC. However, changes in protein expression profiles were only found in CHX-adapted E. faecalis, as evidenced by the emergence of a novel, approximately 19-kDa band following sodium dodecyl sulfate-polyacrylamide gel electrophoresis.
While E. faecalis and S. mutans did not exhibit increased resistance to CPC or MDPB, repeated exposure of E. faecalis to CHX led to resistance. It is likely that the acquisition of resistance is related to an altered protein composition.
Alkyl pyridinium compounds, such as CPC and MDPB, could have a lower risk to cause adaptation of E. faecalis, which is advantageous compared with CHX.
本研究旨在调查变形链球菌和粪肠球菌是否会对阳离子杀菌剂洗必泰(CHX)、西吡氯铵(CPC)和12-甲基丙烯酰氧十二烷基溴化吡啶(MDPB)产生耐药性。
在变形链球菌和粪肠球菌反复接触这些杀菌剂后,评估CHX、CPC和MDPB的最低抑菌浓度(MIC)。检测细菌细胞的表面疏水性和蛋白质表达谱,以阐明可能的耐药机制。
CHX对粪肠球菌的MIC在传代至第10代时持续升高。未观察到CPC和MDPB对粪肠球菌的MIC有变化。CHX、CPC和MDPB对变形链球菌的MIC未增加。随着接触CHX和CPC次数的增加,粪肠球菌的表面疏水性显著增加。然而,仅在适应CHX的粪肠球菌中发现了蛋白质表达谱的变化,十二烷基硫酸钠-聚丙烯酰胺凝胶电泳显示出现了一条新的约19 kDa的条带。
虽然粪肠球菌和变形链球菌对CPC或MDPB未表现出耐药性增加,但粪肠球菌反复接触CHX会导致耐药。获得耐药性可能与蛋白质组成改变有关。
烷基吡啶化合物,如CPC和MDPB,导致粪肠球菌产生适应性变化的风险可能较低,与CHX相比具有优势。