乳糖琼脂生长培养基选择性添加剂的研制

Владимир Ермаков, V. V. Ermakov, Оксана Датченко, O. Datchenko, Юлия Курлыкова, Yuliya Kurlykova
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引用次数: 0

摘要

本研究的目的是改进选择性培养基的选择性补充,以产生肠杆菌。该研究的任务是确定获得的肠杆菌菌株对抗生素的敏感性;开发了一种新的选择性添加抗生素的营养培养基乳糖琼脂。培养基的内容应尽可能以最佳方式确保某些物种或科微生物的生长和繁殖。密集的生物技术发展和微生物学允许今天开发新的营养培养基和修改已经存在的培养基内容。本研究以一种新的抗生素选择性添加剂添加到Drigalski乳糖琼脂营养培养基中,以不同动物肠道微生物群分离的253株细菌为研究材料。该研究在2010年至2017年期间进行。卡比西林和哌拉西林的抗菌活性分别为:卡那霉素组(30±2.3)、卡那霉素组(24±1.5)、阿米卡霉素组(26±1.7)和庆大霉素组(25±0,8)、头孢吡肟组(38±3.2)、四环素组(28±1.6)、强力霉素组(34±2.3)和氯霉素组(31±2.5)、萘啶酸37±2.8、甲氧苄啶35±3,4。肠杆菌对天然青霉素类的苄青霉素、链霉素、第一代头孢菌素类的头孢菌素、多粘菌素B、氧氟沙星(tarivid)和甲硝唑具有高耐药性。选择对伴随的革兰氏阳性和革兰氏阴性菌群有效的抗菌药物作为选择性组分的样品。从糖肽类中选择万古霉素,从恶唑烷酮类中选择利奈唑胺,从酮类中选择泰利霉素。选择万古霉素和特利霉素为0.008 g/dm3,利奈唑胺为0.004 g/dm3的抗生素作为Drigalski乳糖琼脂培养基的选择性添加剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
THE PRODUCTION OF SELECTIVE ADDITIVES TO GROWING MEDIUM DRIGALSKI LACTOSE AGAR
The purpose of the study is to improve the selective supplement for selective media with the purpose to produce enterobacteria. Tasks of the study are to identify the sensitivity of strains obtained of enterobacteria in regard to an-tibiotics; develop a new selective supplement with antibiotics to the nutrient medium Drigalski Lactose Agar. Media should have a content that in the best way possible ensures the growth and reproduction of microorganisms of cer-tain species or family. Intensive biotechnology development and Microbiology allows today to develop new nutrient media and modify the already existing content of media. The object of the study was a new selective additive with antibiotics to the nutrient medium Drigalski Lactose Agar. 253 isolates of bacteria produced from the intestinal mi-crobiotope of different animal species have been the Material for research. The study was conducted in the period from 2010 to 2017. Carbenicillin 30±2.3 from the group of carboxypenicillins and piperacillin 37±2.5 from the group of ureidopenicillins, kanamycin 24±1.5, amikacin 26±1.7 and gentamicin 25±0,8, cefepime 38±3.2 from the group of IV generation cephalosporins, tetracycline 28±1.6, doxycycline 34±2.3 and chloramphenicol 31±2.5, nalidixic acid 37±2.8, trimethoprim 35±3,4 demonstrated the greatest antimicrobial activity against all cultures of enterobac-teria that has been achieved. The high resistance of enterobacteria was shown to benzylpenicillin from the group of natural penicillins, to streptomycin, cephalotine from the group of cephalosporins of the first generation, to polymyx-in B, to ofloxacin (tarivid) and metronidazole. Antibacterial drugs effective against the accompanying gram-positive and gram-negative microflora were considered as the samples of the selective components. Vancomycin from the group of glycopeptides, linezolid from the group of oxazolidinones, and telithromycin from the group of ketolides were chosen. Antibiotics vancomycin and telithromycin in a dose of 0.008 g/dm3, linezolid 0.004 g/dm3 were cho-sen as the selective additive to Drigalski Lactose Agar medium.
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