Rams Thomas E, Sautter Jacqueline D, Getreu Adam, van Winkelhoff Arie J
Department of Periodontology and Oral Implantology, Oral Microbiology Testing Service Laboratory, Temple University School of Dentistry, Philadelphia, PA, 19140, USA; Department of Microbiology and Immunology, Temple University School of Medicine, Philadelphia, PA, 19140, USA.
Department of Periodontology and Oral Implantology, Oral Microbiology Testing Service Laboratory, Temple University School of Dentistry, Philadelphia, PA, 19140, USA.
Microb Pathog. 2016 May;94:112-6. doi: 10.1016/j.micpath.2016.01.021. Epub 2016 Feb 4.
Porphyromonas gingivalis is a major bacterial pathogen in human periodontitis. This study used matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry to assess the accuracy of a rapid phenotypic identification scheme for detection of cultivable P. gingivalis in human subgingival plaque biofilms.
A total of 314 fresh cultivable subgingival isolates from 38 adults with chronic periodontitis were presumptively identified on anaerobically-incubated enriched Brucella blood agar primary isolation plates as P. gingivalis based on dark-pigmented colony morphology, lack of a brick-red autofluorescence reaction under long-wave ultraviolet light, and a positive CAAM fluorescence test for trypsin-like enzyme activity. Each presumptive P. gingivalis isolate, and a panel of other human subgingival bacterial species, were subjected to MALDI-TOF mass spectrometry analysis using a benchtop mass spectrometer equipped with software containing mass spectra for P. gingivalis in its reference library of bacterial protein profiles. A MALDI-TOF mass spectrometry log score of ≥1.7 was required for species identification of the subgingival isolates.
All 314 (100%) presumptive P. gingivalis subgingival isolates were confirmed as P. gingivalis with MALDI-TOF mass spectrometry analysis (Cohen's kappa coefficient = 1.0). MALDI-TOF mass spectrometry log scores between 1.7 and 1.9, and ≥2.0, were found for 92 (29.3%) and 222 (70.7%), respectively, of the presumptive P. gingivalis clinical isolates. No other tested bacterial species was identified as P. gingivalis by MALDI-TOF mass spectrometry.
Rapid phenotypic identification of cultivable P. gingivalis in human subgingival biofilm specimens was found to be 100% accurate with MALDI-TOF mass spectrometry. These findings provide validation for the continued use of P. gingivalis research data based on this species identification methodology.
牙龈卟啉单胞菌是人类牙周炎的主要细菌病原体。本研究使用基质辅助激光解吸/电离飞行时间(MALDI-TOF)质谱法评估一种快速表型鉴定方案检测人类龈下菌斑生物膜中可培养牙龈卟啉单胞菌的准确性。
从38例慢性牙周炎成人患者中收集了314份新鲜的可培养龈下分离株,在厌氧培养的改良布氏血琼脂初代分离平板上,根据深色菌落形态、在长波紫外线下缺乏砖红色自发荧光反应以及胰蛋白酶样酶活性的CAAM荧光试验呈阳性,初步鉴定为牙龈卟啉单胞菌。使用配备有包含牙龈卟啉单胞菌质谱图谱的细菌蛋白质谱参考库软件的台式质谱仪,对每株初步鉴定为牙龈卟啉单胞菌的分离株以及一组其他人类龈下细菌进行MALDI-TOF质谱分析。龈下分离株的物种鉴定需要MALDI-TOF质谱对数分数≥1.7。
通过MALDI-TOF质谱分析,所有314株(100%)初步鉴定为牙龈卟啉单胞菌的龈下分离株均被确认为牙龈卟啉单胞菌(科恩kappa系数 = 1.0)。初步鉴定为牙龈卟啉单胞菌的临床分离株中,分别有92株(29.3%)和222株(70.7%)的MALDI-TOF质谱对数分数在1.7至1.9之间以及≥2.0。通过MALDI-TOF质谱未将其他测试细菌物种鉴定为牙龈卟啉单胞菌。
发现使用MALDI-TOF质谱法对人类龈下生物膜标本中可培养的牙龈卟啉单胞菌进行快速表型鉴定的准确率为100%。这些发现为基于该物种鉴定方法继续使用牙龈卟啉单胞菌研究数据提供了验证。