scholarly journals Distribution of antiseptic resistance genes in Staphylococcus spp. from bovine mastitis

2017 ◽  
Vol 62 (No. 4) ◽  
pp. 200-203
Author(s):  
Y. Ergun ◽  
Z. Cantekin ◽  
K. Gurturk ◽  
H. Solmaz ◽  
IH Ekin ◽  
...  
Keyword(s):  
Public Health ◽  
Resistance Genes ◽  
Quaternary Ammonium ◽  
Bovine Mastitis ◽  
Quaternary Ammonium Compounds ◽  
Staphylococcus Spp ◽  
Ammonium Compounds

The purpose of this study was the determination of antiseptic resistance genes (qacA/B and qacC) from staphylococcal mastitis in cattle in various regions of Turkey. In total, 283 isolates (Burdur: 36, Hatay: 47 and Van: 200) were studied, and the antiseptic resistance genes were detected using simplex PCR. The distribution of the qacA/B and qacC genes, mediating resistance against quaternary ammonium compounds, was found to vary among the different isolates. The qacA/B genes were found in three of the Burdur isolates, six of the Hatay isolates and seven of the Van isolates. The qacC gene was found in two of the Burdur isolates, none of the Hatay isolates and two of the Van isolates. The presence of these genes and transmission among Staphylococcus spp. strains may pose risks in the control of mastitis, as well as to public health.

Determination of quaternary ammonium compounds in food products by the method of ultra-performance liquid chromatography/high resolution mass-spectrometry

2020 ◽  
Vol 86 (8) ◽  
pp. 23-31
Author(s):  
V. G. Amelin ◽  
D. S. Bolshakov
Keyword(s):  
Mass Spectrometry ◽  
High Resolution ◽  
Quaternary Ammonium ◽  
High Resolution Mass Spectrometry ◽  
Food Products ◽  
Quaternary Ammonium Compounds ◽  
High Resolution Mass ◽  
Ammonium Compounds ◽  
Resolution Mass

The goal of the study is developing a methodology for determination of the residual amounts of quaternary ammonium compounds (QAC) in food products by UHPLC/high-resolution mass spectrometry after water-acetonitrile extraction of the determined components from the analyzed samples. The identification and determination of QAC was carried out on an «UltiMate 3000» ultra-high-performance liquid chromatograph (Thermo Scientific, USA) equipped with a «maXis 4G» high-resolution quadrupole-time-of-flight mass spectrometric detector and an ion spray «ionBooster» source (Bruker Daltonics, Germany). Samples of milk, cheese (upper cortical layer), dumplings, pork, chicken skin and ground beef were used as working samples. Optimal conditions are specified for chromatographic separation of the mixture of five QAC, two of them being a mixture of homologues with a linear structure (including isomeric forms). The identification of QAC is carried out by the retention time, exact mass of the ions, and coincidence of the mSigma isotopic distribution. The limits for QAC detection are 0.1 – 0.5 ng/ml, the determination limits are 1 ng/ml for aqueous standard solutions. The determinable content of QAC in food products ranges within 1 – 100 ng/g. The results of analysis revealed the residual amount of QAC present in all samples, which confirms data of numerous sources of information about active use of QAC-based disinfectants in the meat and dairy industry. The correctness of the obtained results is verified by introduction of the additives in food products at a level of 10 ng/g for each QAC. The relative standard deviation of the analysis results does not exceed 0.18. The duration of the analysis is 30 – 40 min.

scholarly journals Minimal inhibitory concentration (MIC) determination of disinfectant and/or sterilizing agents

2009 ◽  
Vol 45 (2) ◽  
pp. 241-248 ◽  
Author(s):  
Priscila Gava Mazzola ◽  
Angela Faustino Jozala ◽  
Letícia Célia de Lencastre Novaes ◽  
Patricia Moriel ◽  
Thereza Christina Vessoni Penna
Keyword(s):  
Hydrogen Peroxide ◽  
Minimal Inhibitory Concentration ◽  
Quaternary Ammonium ◽  
Inhibitory Activity ◽  
Inhibitory Concentration ◽  
Quaternary Ammonium Compounds ◽  
Chemical Agent ◽  
Set Up ◽  
Ammonium Compounds

Due to the growing number of outbreaks of infection in hospital and nurseries, it becomes essential to set up a sanitation program that indicates that the appropriate chemical agent was chosen for application in the most effective way. Validating the effectiveness of decontamination and disinfection is an important and often challenging task. In order to study and compare the behavior of selected microorganisms, they were submitted to minimal inhibitory concentration (MIC). The MIC intervals, which reduced bacteria populations over 6 log10, were: 59 to 156 mg/L of quaternary ammonium compounds (QACs); 63 to 10000 mg/L of chlorhexidine; 1375 to 3250 mg/L of glutaraldehyde; 39 to 246 mg/L of formaldehyde; 43750 to 87500 mg/L of ethanol; 1250 to 6250 mg/L of iodine in polyvinyl-pyrolidone complexes, 150 to 4491 mg/L of chlorine-releasing-agents (CRAs) and 469 to 2500 mg/L of hydrogen peroxide. Chlorhexidine showed non inhibitory activity over germinating spores. A. calcoaceticus showed resistance to the majority of the agents tested, followed by E. cloacae and S. marcescens.

Determination of Quaternary Ammonium Compounds in Oranges and Cucumbers Using QuEChERS Extraction and Ultra-Performance Liquid Chromatography/Tandem Mass Spectrometry

2014 ◽  
Vol 97 (4) ◽  
pp. 1021-1026 ◽  
Author(s):  
Francisco Javier Arrebola-Liébanas ◽  
María Angeles Herrera Abdo ◽  
José Luis Fernandez Moreno ◽  
José L Martínez-Vidal ◽  
Antonia Garrido Frenich
Keyword(s):  
Quaternary Ammonium ◽  
Ultra Performance Liquid Chromatography ◽  
Quaternary Ammonium Compounds ◽  
Fast Method ◽  
Benzethonium Chloride ◽  
Liquid Chromatography Tandem Mass ◽  
Didecyldimethylammonium Chloride ◽  
Accredited Laboratory ◽  
Ammonium Compounds

Abstract A simple and fast method has been developed for determining relevant quaternary ammonium compounds in cucumber and orange samples. The target compounds were benzoalkonium chloride (BAC-10, BAC-12, BAC-14, and BAC-16), didecyldimethylammonium chloride, and benzethonium chloride, all frequently used biocides in the agrifood industry. An extraction based on the buffered Quick, Easy, Cheap, Effective, Rugged, and Safe method and determination by ultra-performance LC/MS/MS that eluted the biocides in less than 5 min were used. The method was fully validated and implemented in a UNE-EN-ISO/IEC 17025 accredited laboratory for its application to the analysis of real samples. Performance characteristics of the method are reported, including an estimation of measurement uncertainty. Calibration curves were set between 0.01 and 0.150 mg/kg, LOD values were always between 0.4 and 1.0 μg/kg, LOQ values were in the range 1–4 μg/kg, recovery was between 81 and 115%, intraday and interday precision were always lower than 17% (expressed as RSD), and expanded uncertainty was always lower than 40%. The validation was accomplished for the two studied matrixes at spiking concentrations of 0.011 and 0.050 mg/kg. The method has been applied to the analysis of 30 cucumber and orange samples that were found to contain concentrations of BAC-12 that ranged between 0.015 and 0.210 mg/kg and of BAC-14 between 0.018 and 0.081 mg/kg.

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