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Development of a Novel Test for Simultaneous Bacterial Identification and Antibiotic Susceptibility

机译:同时细菌鉴定和抗生素敏感性的新型测试方法的开发

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摘要

Background. Elucidation of a pathogen's antimicrobial susceptibility requires subculture after the organism is first isolated. This takes several days, requiring patients to be treated with broad-spectrum antibiotics. This approach contributes to the development of bacterial resistance. Methods. Microtiter wells were coated with a polyclonal antibody targeting the pathogen of interest. Bacterial suspensions were added in the presence/absence of selected antibiotics. After washing, captured bacteria were detected. Findings. Group B streptococcus (GBS), Enterococcus faecalis, and Neisseria gonorrhoeae were each detected at 105 bacteria/mL following a 20-minute incubation period. Susceptibility to select antibiotics was discernable following a 6-hour incubation period (GBS and Enterococcus). Sensitivity was increased to 10−2 bacteria/mL for GBS, 10−1 bacteria/mL for E. faecalis, and 101 bacteria/mL for N. gonorrhoeae following 18–24-hour culture. Conclusion. This novel assay allows for the highly sensitive and specific identification of a pathogen and simultaneous determination of its antimicrobial susceptibility in a reduced time.
机译:背景。要阐明病原体的抗菌敏感性,需要在首次分离出生物后进行传代培养。这需要几天的时间,要求患者接受广谱抗生素治疗。这种方法有助于细菌抗性的发展。方法。用针对目标病原体的多克隆抗体包被微量滴定孔。在存在/不存在选定抗生素的情况下添加细菌悬液。洗涤后,检测到捕获的细菌。发现。孵育20分钟后,分别以10 5 细菌/ mL检出B组链球菌(GBS),粪肠球菌和淋病奈瑟菌。经过6小时的潜伏期(GBS和肠球菌),可以看出选择抗生素的敏感性。对GBS的敏感度增加到10 −2 细菌/ mL,对粪肠球菌的敏感度增加到10 -1 细菌/ mL,对10 1 细菌/培养18–24小时后,淋病奈瑟氏球菌的毫升数为2。结论。这种新颖的测定方法可对病原体进行高度灵敏和特异的鉴定,并在较短的时间内同时测定其抗药性。

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