首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Identification of Rare Pathogenic Bacteria in a Clinical Microbiology Laboratory: Impact of Matrix-Assisted Laser Desorption Ionization–Time of Flight Mass Spectrometry
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Identification of Rare Pathogenic Bacteria in a Clinical Microbiology Laboratory: Impact of Matrix-Assisted Laser Desorption Ionization–Time of Flight Mass Spectrometry

机译:在临床微生物学实验室中鉴定罕见病原细菌:基质辅助激光解吸电离的影响–飞行时间质谱

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摘要

During the past 5 years, matrix-assisted laser desorption ionization–time of flight (MALDI-TOF) mass spectrometry (MS) has become a powerful tool for routine identification in many clinical laboratories. We analyzed our 11-year experience in routine identification of clinical isolates (40 months using MALDI-TOF MS and 91 months using conventional phenotypic identification [CPI]). Among the 286,842 clonal isolates, 284,899 isolates of 459 species were identified. The remaining 1,951 isolates were misidentified and required confirmation using a second phenotypic identification for 670 isolates and using a molecular technique for 1,273 isolates of 339 species. MALDI-TOF MS annually identified 112 species, i.e., 36 species/10,000 isolates, compared to 44 species, i.e., 19 species/10,000 isolates, for CPI. Only 50 isolates required second phenotypic identifications during the MALDI-TOF MS period (i.e., 4.5 reidentifications/10,000 isolates) compared with 620 isolates during the CPI period (i.e., 35.2/10,000 isolates). We identified 128 bacterial species rarely reported as human pathogens, including 48 using phenotypic techniques (22 using CPI and 37 using MALDI-TOF MS). Another 75 rare species were identified using molecular methods. MALDI-TOF MS reduced the time required for identification by 55-fold and 169-fold and the cost by 5-fold and 96-fold compared with CPI and gene sequencing, respectively. MALDI-TOF MS was a powerful tool not only for routine bacterial identification but also for identification of rare bacterial species implicated in human infectious diseases. The ability to rapidly identify bacterial species rarely described as pathogens in specific clinical specimens will help us to study the clinical burden resulting from the emergence of these species as human pathogens, and MALDI-TOF MS may be considered an alternative to molecular methods in clinical laboratories.
机译:在过去的5年中,基质辅助激光解吸电离飞行时间(MALDI-TOF)质谱(MS)已成为许多临床实验室常规鉴定的强大工具。我们分析了11年常规鉴定临床分离株的经验(使用MALDI-TOF MS鉴定40个月,使用常规表型鉴定[CPI]鉴定91个月)。在286,842个克隆分离株中,鉴定出459种的284,899个分离株。剩余的1,951个分离物被错误鉴定,需要使用第二个表型鉴定法对670个分离物进行确认,并使用分子技术对339个物种的1,273个分离物进行确认。 MALDI-TOF MS每年确定CPI的112种,即36种/ 10,000菌种,而44种,即19种/ 10,000菌种。在MALDI-TOF MS期间,只有50个分离株需要第二个表型鉴定(即4.5个重新鉴定/ 10,000个分离株),而在CPI期间,只有620个分离株(即35.2 / 10,000个分离株)。我们鉴定了128种极少报道为人类病原体的细菌,包括使用表型技术的48种(使用CPI的22种和使用MALDI-TOF MS的37种)。使用分子方法鉴定了另外75种稀有物种。与CPI和基因测序相比,MALDI-TOF MS分别将鉴定所需的时间减少了55倍和169倍,并将成本减少了5倍和96倍。 MALDI-TOF MS是强大的工具,不仅可用于常规细菌鉴定,而且可用于鉴定与人类传染病有关的稀有细菌。快速鉴定在特定临床标本中很少被描述为病原体的细菌种类的能力将帮助我们研究由于这些菌种作为人类病原体而引起的临床负担,而MALDI-TOF MS在临床实验室中可能被视为分子方法的替代方法。

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