VITEK 2系统在血小板浓缩物常规细菌筛选过程中,将痤疮表皮杆菌误诊为阴道托波菌的多相方法研究

Dilini Kumaran, Carmelie Laflamme, Sandra Ramirez-Arcos
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引用次数: 0

摘要

皮肤菌群细菌,如痤疮角质杆菌,是用于输血的血液制品的主要污染物。血小板浓缩物(PCs)是一种用于治疗血小板缺乏患者的治疗产品,在室温下搅拌储存,为细菌增殖提供理想的条件。在加拿大血液服务中心,使用自动BACT/ALERT培养系统对pc进行微生物污染筛选。使用VITEK 2系统处理阳性培养物并鉴定污染生物体。在大约2年的时间里,几个PC分离株被确定为阴道托托菌,具有很高的可信度。然而,由于阴道芽胞杆菌与细菌性阴道病有关,而不是常见的PC污染物,回顾性调查显示,在所有病例中,痤疮芽胞杆菌都被误认为阴道芽胞杆菌。我们的研究表明,用于培养PC细菌分离物的培养基类型对VITEK 2系统上获得的结果有显著影响。此外,其他鉴定方法,如基质辅助激光解吸/电离飞行时间质谱(MALD-TOF MS)和PCR扩增16S RNA基因仅部分成功鉴定痤疮C.。因此,我们的研究结果支持多相方法,当PC分离物被VITEK 2系统鉴定为阴道芽胞杆菌时,可以通过宏观、微观和其他生化分析来正确鉴定痤疮芽胞杆菌。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A multiphasic approach to solve misidentification of <i>Cutibacterium acnes</i> as <i>Atopobium vaginae</i> during routine bacterial screening of platelet concentrates using the VITEK 2 system.

A multiphasic approach to solve misidentification of Cutibacterium acnes as Atopobium vaginae during routine bacterial screening of platelet concentrates using the VITEK 2 system.

Skin flora bacteria, such as Cutibacterium acnes , are the predominant contaminants of blood products used for transfusion. Platelet concentrates (PCs), a therapeutic product used to treat patients with platelet deficiencies, are stored at ambient temperature under agitation, providing ideal conditions for bacterial proliferation. At Canadian Blood Services, PCs are screened for microbial contamination using the automated BACT/ALERT culture system. Positive cultures are processed and contaminating organisms are identified using the VITEK 2 system. Over a period of approximately 2 years, several PC isolates were identified as Atopobium vaginae to a high level of confidence. However, since A. vaginae is associated with bacterial vaginosis and is not a common PC contaminant, a retrospective investigation revealed that in all cases C. acnes was misidentified as A. vaginae . Our investigation demonstrated that the media type used to grow PC bacterial isolates can have a significant impact on the results obtained on the VITEK 2 system. Furthermore, other identification methods such as matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALD-TOF MS) and PCR amplification of the 16S RNA gene were only partially successful in the identification of C. acnes . Therefore, our findings support a multiphasic approach when PC isolates are identified as A. vaginae by the VITEK 2 system for proper identification of C. acnes using macroscopic, microscopic and other biochemical analyses.

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