首页> 外文期刊>Journal of AOAC International >Confirmation and Identification of Listeria monocytogenes, Listeria spp. and Other Gram-Positive Organisms by the Bruker MALDI Biotyper Method: Collaborative Study, First Action 2017.10
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Confirmation and Identification of Listeria monocytogenes, Listeria spp. and Other Gram-Positive Organisms by the Bruker MALDI Biotyper Method: Collaborative Study, First Action 2017.10

机译:Histeria单核细胞增生李斯特菌的确认和鉴定。 和Bruker Maldi Biotyper方法的其他革兰氏阳性生物:合作研究,第一行动2017.10

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摘要

The Bruker MALDI Biotyper? method utilizes matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) MS for the rapid and accurate confirmation and identification of Gram-positive bacteria from select media types. This alternative method was evaluated using nonselectiveand selective agar plates to identify and confirm Listeria monocytogenes, Listeria species, and select Gram-positive bacteria. Results obtained by the Bruker MALDI Biotyper were compared with the traditional biochemical methods as prescribed in the appropriate reference method standards.Sixteen collaborators from 16 different laboratories located within the European Union participated in the collaborative study. A total of 36 blind-coded isolates were evaluated by each collaborator. In each set of 36 organisms, there were 16 L. monocytogenes strains, 12 non-monocytogenesListeria species strains, and 8 additional Gram-positive exclusivity strains. After testing was completed, the total percentage of correct identifications (to both genus and species level) and confirmation from each agar type for each strain was determined at a percentage of 99.9% to thegenus level and 98.8% to the species level. The results indicated that the alternative method produced equivalent results when compared with the confirmatory procedures specified by each reference method.
机译:Bruker Maldi Biotyper?方法利用基质辅助激光解吸/电离飞行时间(MALDI-TOF)MS,用于从选择培养基类型的快速准确确认和鉴定革兰氏阳性细菌。使用Nonselectiveand选择性琼脂平板评估该替代方法,以鉴定和确认李斯特菌单核细胞增生,李斯特里亚物种,并选择革兰氏阳性细菌。将Bruker Maldi Biotyper获得的结果与在适当的参考方法标准中规定的传统生化方法进行了比较。在欧洲联盟内的16个不同实验室的共同合作者参加了合作研究。每个合作员评估总共36个盲编分离株。在每组36个生物中,16升单核细胞增生菌株,12种非单核细胞增生菌株,和8种额外的革兰氏阳性排除菌株。测试完成后,将正确鉴定的总百分比(对本周和种类水平)和每个菌株的每个琼脂型的确认以99.9%至TheGANUS水平的百分比和物种水平的98.8%。结果表明,与每个参考方法规定的确认程序相比,替代方法产生了等效结果。

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