铜绿假单胞菌菌株分类与IR生物分型的相关性及分子流行病学方法。

Megumi Oho, Zenzo Nagasawa, Yumiko Funashima, Osamu Ueda, Shinya Watamabe, Longzhu Cui, Hiroshi Miyamoto, Eisaburo Sueoka
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引用次数: 0

摘要

自2018年起,IR Biotyper (IRBT;Bruker Daltonik GmbH, Germany)基于傅里叶变换红外分光光度计的方法已经开始作为一种新的菌株分类方法被引入临床微生物检查领域。我们将其与分子流行病学方法进行比较,评价IRBT菌株分类的有效性。方法:采用分子流行病学方法(多位点测序分型;基于MLST和pcr的ORF分型研究比较不同机构对48株铜绿假单胞菌不同检测次数的IRBT的准确性。结果:IRBT采用“KBM”SCD琼脂培养基进行预培养,按cut - cut值0.181划分为12种类型,MLST划分为8种类型,POT划分为13种类型。IRBT与分子流行病学方法的Adjusted Wallace, MLST为0.458 (95% CI;0.295 ~ 0.620), POT为0.330 (95% CI;0.135 ~ 0.525),说明菌株分类存在差异。结论:IRBT与分子流行病学分类结果无相关性。在分子流行病学方法中,菌株仅通过匹配特定的基因区域进行分类,而IRBT是用红外激光照射样品,根据分子结构根据吸收光谱的差异对菌株进行分类,因此测量原理是不同的。利用IRBT对菌株进行分类时,应掌握检出菌株的临床信息,同时针对同一设施分离的多株菌株进行分类。
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Correlation of Strain Classification with IR Biotyper and Molecular Epidemiological Method of Pseudomonas aeruginosa.

Introduction: From 2018, IR Biotyper (IRBT; Bruker Daltonik GmbH, Germany) based on the Fourier transform infrared spectrophotometer has begun to be introduced as a new strain classification method in the field of clinical microbiological examination. We compared it with molecular epidemiology method to evaluate the usefulness of strain classification by IRBT.

Method: Homology of strain classification with molecular epidemiology method (Multilocus Sequencing Typing; MLST and PCR-based ORF Typing; POT) for 48 strains of Pseudomonas aeruginosa with different detection times from multiple institutions to evaluate the accuracy of IRBT was compared.

Results: IRBT used "KBM" SCD agar medium for preculture and was classified into 12 types when classified by Cut-off value 0.181, 8 types by MLST, and 13 types by POT. In the Adjusted Wallace between IRBT and molecular epidemiology method, MLST was 0.458 (95% CI; 0.295 to 0.620) and POT was 0.330 (95% CI; 0.135 to 0.525), indicating a discrepancy in strain classification.

Conclusion: No correlation was found between IRBT and the classification results by the molecular epidemiology method. In the molecular epidemiology method, strains are classified by matching only specific gene regions, but IRBT irradiates a sample with an infrared laser and classifies the strains according to the difference in absorption spectrum according to the molecular structure, so the measurement principle is different. When classifying strains by IRBT, it is desirable to grasp the clinical information of the detected strains and to target multiple strains isolated at the same facility at the same time.

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