Knapp Laura, Amézquita Alejandro, McClure Peter, Stewart Sara, Maillard Jean-Yves
Cardiff School of Pharmacy and Pharmaceutical Science, Cardiff, Wales, United Kingdom.
Unilever Safety and Environmental Assurance Centre, Colworth Science Park, Bedford, United Kingdom.
Appl Environ Microbiol. 2015 Apr;81(8):2652-9. doi: 10.1128/AEM.03843-14. Epub 2015 Jan 30.
Regulations dealing with microbicides in Europe and the United States are evolving and now require data on the risk of the development of resistance in organisms targeted by microbicidal products. There is no standard protocol to assess the risk of the development of resistance to microbicidal formulations. This study aimed to validate the use of changes in microbicide and antibiotic susceptibility as initial markers for predicting microbicide resistance and cross-resistance to antibiotics. Three industrial isolates (Pseudomonas aeruginosa, Burkholderia cepacia, and Klebsiella pneumoniae) and two Salmonella enterica serovar Typhimurium strains (SL1344 and 14028S) were exposed to a shampoo, a mouthwash, eye makeup remover, and the microbicides contained within these formulations (chlorhexidine digluconate [CHG] and benzalkonium chloride [BZC]) under realistic, in-use conditions. Baseline and postexposure data were compared. No significant increases in the MIC or the minimum bactericidal concentration (MBC) were observed for any strain after exposure to the three formulations. Increases as high as 100-fold in the MICs and MBCs of CHG and BZC for SL1344 and 14028S were observed but were unstable. Changes in antibiotic susceptibility were not clinically significant. The use of MICs and MBCs combined with antibiotic susceptibility profiling and stability testing generated reproducible data that allowed for an initial prediction of the development of resistance to microbicides. These approaches measure characteristics that are directly relevant to the concern over resistance and cross-resistance development following the use of microbicides. These are low-cost, high-throughput techniques, allowing manufacturers to provide to regulatory bodies, promptly and efficiently, data supporting an early assessment of the risk of resistance development.
欧美有关杀微生物剂的法规正在不断演变,现在要求提供关于杀微生物产品靶向生物产生耐药性风险的数据。目前尚无评估杀微生物剂配方耐药性发展风险的标准方案。本研究旨在验证将杀微生物剂和抗生素敏感性变化用作预测杀微生物剂耐药性及对抗生素交叉耐药性的初始标志物的可行性。在实际使用条件下,将三种工业分离株(铜绿假单胞菌、洋葱伯克霍尔德菌和肺炎克雷伯菌)以及两种鼠伤寒沙门氏菌菌株(SL1344和14028S)暴露于一种洗发水、一种漱口水、眼部卸妆液以及这些配方中所含的杀微生物剂(葡萄糖酸洗必泰[CHG]和苯扎氯铵[BZC])。比较了基线数据和暴露后的数据。暴露于这三种配方后,未观察到任何菌株的最低抑菌浓度(MIC)或最低杀菌浓度(MBC)有显著增加。观察到SL1344和14028S的CHG和BZC的MIC和MBC增加高达100倍,但不稳定。抗生素敏感性变化在临床上无显著意义。将MIC和MBC与抗生素敏感性分析及稳定性测试相结合,产生了可重复的数据,可对杀微生物剂耐药性的发展进行初步预测。这些方法测量的特征与使用杀微生物剂后对耐药性和交叉耐药性发展的担忧直接相关。这些是低成本、高通量的技术,可使制造商迅速、高效地向监管机构提供支持耐药性发展风险早期评估的数据。