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基质辅助激光解吸电离飞行时间质谱分析直接鉴定液体培养物中的临床病原体。

Direct identification of clinical pathogens from liquid culture media by MALDI-TOF MS analysis.

机构信息

Servicio de Microbiología, Complejo Hospitalario Universitario A Coruña, La Coruña, Spain.

Servicio de Microbiología, Hospital General Universitario Gregorio Marañón, Instituto de Investigación Sanitaria Gregorio Marañón, Madrid, Spain.

出版信息

Clin Microbiol Infect. 2018 Jun;24(6):624-629. doi: 10.1016/j.cmi.2017.09.010. Epub 2017 Sep 27.

DOI:10.1016/j.cmi.2017.09.010
PMID:28962998
Abstract

OBJECTIVES

We propose using MALDI-TOF MS as a tool for identifying microorganisms directly from liquid cultures after enrichment of the clinical sample in the media, to obtain a rapid microbiological diagnosis and an adequate administration of the antibiotic therapy in a clinical setting.

METHODS

To evaluate this approach, a series of quality control isolates were grown in thioglycollate (TG) broth and brain heart infusion (BHI) broth and extracted under four different protocols before finally being identified by MALDI-TOF MS. After establishing the best extraction protocol, we validated the method in a total of 300 liquid cultures (150 in TG broth and 150 in BHI broth) of different types of clinical samples obtained from two tertiary Spanish hospitals.

RESULTS

The initial evaluation showed that the extraction protocol including a 5 minute sonication step yielded 100% valid identifications, with an average score value of 2.305. In the clinical validation of the procedure, 98% of the microorganisms identified from the TG broth were correctly identified relative to 97% of those identified from the BHI broth. In 24% of the samples analysed, growth by direct sowing was only successful in the liquid medium, and no growth was observed in the direct solid agar cultures.

CONCLUSIONS

Use of MALDI-TOF MS plus the sonication-based extraction method enabled direct and accurate identification of microorganisms in liquid culture media in 15 minutes, in contrast to the 24 hours of subculture required for conventional identification, allowing the administration of a targeted antimicrobial therapy.

摘要

目的

我们建议使用 MALDI-TOF MS 作为一种工具,直接从液体培养物中识别经过培养基富集的临床样本中的微生物,以在临床环境中获得快速微生物诊断和适当的抗生素治疗。

方法

为了评估这种方法,一系列质控分离株在硫代甘油(TG)肉汤和脑心浸液(BHI)肉汤中生长,并在最终通过 MALDI-TOF MS 鉴定之前根据四种不同的方案进行提取。在建立最佳提取方案后,我们共验证了来自西班牙两家三级医院的 300 种不同类型临床样本的 300 种液体培养物(150 种在 TG 肉汤中,150 种在 BHI 肉汤中)。

结果

初步评估表明,包括 5 分钟超声处理步骤的提取方案可实现 100%有效的鉴定,平均得分值为 2.305。在该程序的临床验证中,相对于从 BHI 肉汤中鉴定的微生物,从 TG 肉汤中鉴定的 98%的微生物得到了正确鉴定。在分析的 24%的样本中,直接播种仅在液体培养基中成功生长,而直接固体琼脂培养物中未观察到生长。

结论

使用 MALDI-TOF MS 加上基于超声的提取方法,可在 15 分钟内直接准确地鉴定液体培养物中的微生物,而传统鉴定需要 24 小时的传代培养,从而可以进行靶向抗菌治疗。

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