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利用耐甲氧西林金黄色葡萄球菌(MRSA)作为模式生物,开发一种快速基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)的流行病学筛查方法。

Development of a rapid MALDI-TOF MS based epidemiological screening method using MRSA as a model organism.

机构信息

Department of Infectious Diseases, Institute of Biomedicine, Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden.

Centre for Antibiotic Resistance Research (CARe) at University of Gothenburg, Gothenburg, Sweden.

出版信息

Eur J Clin Microbiol Infect Dis. 2018 Jan;37(1):57-68. doi: 10.1007/s10096-017-3101-x. Epub 2017 Sep 18.

DOI:10.1007/s10096-017-3101-x
PMID:28924947
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5748427/
Abstract

In this study we present a method using whole cell MALDI-TOF MS and VITEK MS RUO/SARAMIS as a rapid epidemiological screening tool. MRSA was used as a model organism for setting up the screening strategy. A collection of well-characterised MRSA strains representing the 19 most common Pulsed-Field Gel Electrophoresis (PFGE)-types in the region of South-West Sweden for the past 20 years was analysed with MALDI-TOF MS. A total of 111 MRSA strains were used for creating 19 PFGE-specific Superspectra using VITEK MS RUO/SARAMIS. Prior to performing the final analysis, the 19 Superspectra were combined into ten groups displaying similar peak patterns, hereafter named "MALDI-types". Two-hundred fifty-five MRSA strains were analysed to test the constructed Superspectra/MALDI-type database. Matches to the Superspectra above a threshold of 65% (corresponding to the number of matched peaks in the Superspectrum) were considered as positive assignment of a strain to a MALDI-type. The median peak matching value for correct assignment of a strain to a MALDI-type was 78% (range 65.3-100%). In total, 172 strains (67.4%) were assigned to the correct MALDI-type and only 5.5% of the strains were incorrectly assigned to another MALDI-type than the expected based on the PFGE-type of the strain. We envision this methodology as a cost-efficient step to be used as a first screening strategy in the typing scheme of MRSA isolates, to exclude epidemiological relatedness of isolates or to identify the need for further typing.

摘要

在本研究中,我们提出了一种使用全细胞 MALDI-TOF MS 和 VITEK MS RUO/SARAMIS 的方法,作为一种快速的流行病学筛选工具。我们使用 MRSA 作为模型生物来建立筛选策略。我们分析了过去 20 年在瑞典西南部地区最常见的 19 种脉冲场凝胶电泳(PFGE)类型中的 19 种具有代表性的、特征良好的 MRSA 菌株,使用 MALDI-TOF MS。共使用了 111 株 MRSA 菌株,使用 VITEK MS RUO/SARAMIS 为 19 种 PFGE 特异性 Superspectrum 创建了 19 种。在进行最终分析之前,将这 19 种 Superspectrum 组合成 10 个显示相似峰模式的组,此后称为"MALDI 类型"。我们分析了 255 株 MRSA 菌株,以测试构建的 Superspectrum/MALDI-type 数据库。如果匹配的峰数量超过阈值(对应于 Superspectrum 中的匹配峰数量)的 65%,则认为该菌株与 MALDI-type 的匹配为阳性。将菌株正确分配到 MALDI-type 的中位数峰值匹配值为 78%(范围为 65.3-100%)。总共有 172 株(67.4%)被正确分配到 MALDI-type,只有 5.5%的菌株被错误地分配到与菌株的 PFGE-type 不符的另一个 MALDI-type。我们设想这种方法可以作为一种经济有效的步骤,作为 MRSA 分离株分型方案中的第一步筛选策略,以排除分离株的流行病学相关性,或识别进一步分型的需要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3dc/5748427/497a34d11ae0/10096_2017_3101_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3dc/5748427/707b998e2048/10096_2017_3101_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3dc/5748427/24d9b313f5f1/10096_2017_3101_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3dc/5748427/497a34d11ae0/10096_2017_3101_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3dc/5748427/707b998e2048/10096_2017_3101_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3dc/5748427/24d9b313f5f1/10096_2017_3101_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3dc/5748427/497a34d11ae0/10096_2017_3101_Fig3_HTML.jpg

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