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J Hosp Infect. 2014 Aug;87(4):194-202. doi: 10.1016/j.jhin.2014.04.012. Epub 2014 Jun 5.
2
The effect of cationic microbicide exposure against Burkholderia cepacia complex (Bcc); the use of Burkholderia lata strain 383 as a model bacterium.暴露于阳离子杀微生物剂对伯克霍尔德氏菌复合群(Bcc)的影响;使用伯克霍尔德氏菌亚种 383 作为模式细菌。
J Appl Microbiol. 2013 Nov;115(5):1117-26. doi: 10.1111/jam.12320. Epub 2013 Sep 3.
3
Does microbicide use in consumer products promote antimicrobial resistance? A critical review and recommendations for a cohesive approach to risk assessment.消费者产品中使用杀菌剂是否会促进抗菌药物耐药性? 批判性评价及建立协调一致的风险评估方法的建议。
Microb Drug Resist. 2013 Oct;19(5):344-54. doi: 10.1089/mdr.2013.0039. Epub 2013 Jun 14.
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Evaluation of reduced susceptibility to quaternary ammonium compounds and bisbiguanides in clinical isolates and laboratory-generated mutants of Staphylococcus aureus.评估金黄色葡萄球菌临床分离株和实验室产生的突变株对季铵化合物和双胍类的耐药性降低情况。
Antimicrob Agents Chemother. 2013 Aug;57(8):3488-97. doi: 10.1128/AAC.00498-13. Epub 2013 May 13.
5
Development of antimicrobial resistance in Campylobacter jejuni and Campylobacter coli adapted to biocides.适应消毒剂的空肠弯曲菌和结肠弯曲菌中抗菌耐药性的发展。
Int J Food Microbiol. 2013 Jan 1;160(3):304-12. doi: 10.1016/j.ijfoodmicro.2012.11.006. Epub 2012 Nov 17.
6
Genome-wide enrichment screening reveals multiple targets and resistance genes for triclosan in Escherichia coli.全基因组富集筛选揭示了大肠杆菌中三氯生的多个靶标和抗性基因。
J Microbiol. 2012 Oct;50(5):785-91. doi: 10.1007/s12275-012-2439-0. Epub 2012 Nov 4.
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Sublethal triclosan exposure decreases susceptibility to gentamicin and other aminoglycosides in Listeria monocytogenes.亚致死浓度三氯生暴露降低单核细胞增生李斯特菌对庆大霉素和其他氨基糖苷类药物的敏感性。
Antimicrob Agents Chemother. 2011 Sep;55(9):4064-71. doi: 10.1128/AAC.00460-11. Epub 2011 Jul 11.
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Exposure of Escherichia coli and Salmonella enterica serovar Typhimurium to triclosan induces a species-specific response, including drug detoxification.大肠杆菌和肠炎沙门氏菌血清型鼠伤寒对三氯生的暴露会引起物种特异性反应,包括药物解毒。
J Antimicrob Chemother. 2009 Nov;64(5):973-85. doi: 10.1093/jac/dkp320. Epub 2009 Sep 16.
9
Variations in MIC value caused by differences in experimental protocol.
J Microbiol Methods. 2009 Oct;79(1):44-7. doi: 10.1016/j.mimet.2009.07.017. Epub 2009 Jul 25.
10
BSAC standardized disc susceptibility testing method (version 8).英国抗菌化疗学会标准化纸片药敏试验方法(第8版)
J Antimicrob Chemother. 2009 Sep;64(3):454-89. doi: 10.1093/jac/dkp244. Epub 2009 Jul 8.

一种预测细菌对杀菌剂耐药性的方案的制定。

Development of a protocol for predicting bacterial resistance to microbicides.

作者信息

Knapp Laura, Amézquita Alejandro, McClure Peter, Stewart Sara, Maillard Jean-Yves

机构信息

Cardiff School of Pharmacy and Pharmaceutical Science, Cardiff, Wales, United Kingdom.

Unilever Safety and Environmental Assurance Centre, Colworth Science Park, Bedford, United Kingdom.

出版信息

Appl Environ Microbiol. 2015 Apr;81(8):2652-9. doi: 10.1128/AEM.03843-14. Epub 2015 Jan 30.

DOI:10.1128/AEM.03843-14
PMID:25636848
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4375328/
Abstract

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.

摘要

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。