Lynch T, Gregson D, Church D L
Division of Microbiology, Calgary Laboratory Services (CLS), University of Calgary, Calgary, Alberta, Canada Department of Pathology & Laboratory Medicine, University of Calgary, Calgary, Alberta, Canada
Division of Microbiology, Calgary Laboratory Services (CLS), University of Calgary, Calgary, Alberta, Canada Department of Pathology & Laboratory Medicine, University of Calgary, Calgary, Alberta, Canada Department of Medicine, University of Calgary, Calgary, Alberta, Canada.
J Clin Microbiol. 2016 Mar;54(3):712-7. doi: 10.1128/JCM.02872-15. Epub 2016 Jan 6.
Actinomyces species are uncommon but important causes of invasive infections. The ability of our regional clinical microbiology laboratory to report species-level identification of Actinomyces relied on molecular identification by partial sequencing of the 16S ribosomal gene prior to the implementation of the Vitek MS (matrix-assisted laser desorption ionization-time of flight mass spectrometry [MALDI-TOF MS]) system. We compared the use of the Vitek MS to that of 16S rRNA gene sequencing for reliable species-level identification of invasive infections caused by Actinomyces spp. because limited data had been published for this important genera. A total of 115 cases of Actinomyces spp., either alone or as part of a polymicrobial infection, were diagnosed between 2011 and 2014. Actinomyces spp. were considered the principal pathogen in bloodstream infections (n = 17, 15%), in skin and soft tissue abscesses (n = 25, 22%), and in pulmonary (n = 26, 23%), bone (n = 27, 23%), intraabdominal (n = 16, 14%), and central nervous system (n = 4, 3%) infections. Compared to sequencing and identification from the SmartGene Integrated Database Network System (IDNS), Vitek MS identified 47/115 (41%) isolates to the correct species and 10 (9%) isolates to the correct genus. However, the Vitek MS was unable to provide identification for 43 (37%) isolates while 15 (13%) had discordant results. Phylogenetic analyses of the 16S rRNA sequences demonstrate high diversity in recovered Actinomyces spp. and provide additional information to compare/confirm discordant identifications between MALDI-TOF and 16S rRNA gene sequences. This study highlights the diversity of clinically relevant Actinomyces spp. and provides an important typing comparison. Based on our analysis, 16S rRNA gene sequencing should be used to rapidly identify Actinomyces spp. until MALDI-TOF databases are optimized.
放线菌属是侵袭性感染的罕见但重要的病因。在Vitek MS(基质辅助激光解吸电离飞行时间质谱 [MALDI-TOF MS])系统实施之前,我们地区临床微生物实验室报告放线菌属物种水平鉴定的能力依赖于通过16S核糖体基因部分测序进行分子鉴定。由于关于这个重要属的公开数据有限,我们比较了Vitek MS与16S rRNA基因测序在可靠鉴定由放线菌属引起的侵袭性感染物种水平方面的应用。2011年至2014年期间共诊断出115例放线菌属感染病例,这些病例单独存在或作为混合微生物感染的一部分。放线菌属被认为是血流感染(n = 17,15%)、皮肤和软组织脓肿(n = 25,22%)以及肺部(n = 26,23%)、骨骼(n = 27,23%)、腹腔内(n = 16,14%)和中枢神经系统(n = 4,3%)感染的主要病原体。与来自SmartGene综合数据库网络系统(IDNS)的测序和鉴定相比,Vitek MS将47/115(41%)株分离菌鉴定到正确的物种,10(9%)株分离菌鉴定到正确的属。然而,Vitek MS无法对43(37%)株分离菌进行鉴定,同时有15(13%)株结果不一致。对16S rRNA序列的系统发育分析表明,回收的放线菌属具有高度多样性,并提供了额外信息以比较/确认MALDI-TOF和16S rRNA基因序列之间不一致的鉴定结果。本研究突出了临床相关放线菌属的多样性,并提供了重要的分型比较。基于我们的分析,在MALDI-TOF数据库得到优化之前,应使用16S rRNA基因测序来快速鉴定放线菌属。