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Rapid identification of oral Actinomyces species cultivated from subgingival biofilm by MALDI-TOF-MS
BACKGROUND: Actinomyces are a common part of the residential flora of the human intestinal tract, genitourinary system and skin. Isolation and identification of Actinomyces by conventional methods is often difficult and time consuming. In recent years, matrix-assisted laser desorption/ionization tim...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Co-Action Publishing
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4297926/ https://www.ncbi.nlm.nih.gov/pubmed/25597306 http://dx.doi.org/10.3402/jom.v7.26110 |
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author | Stingu, Catalina S. Borgmann, Toralf Rodloff, Arne C. Vielkind, Paul Jentsch, Holger Schellenberger, Wolfgang Eschrich, Klaus |
author_facet | Stingu, Catalina S. Borgmann, Toralf Rodloff, Arne C. Vielkind, Paul Jentsch, Holger Schellenberger, Wolfgang Eschrich, Klaus |
author_sort | Stingu, Catalina S. |
collection | PubMed |
description | BACKGROUND: Actinomyces are a common part of the residential flora of the human intestinal tract, genitourinary system and skin. Isolation and identification of Actinomyces by conventional methods is often difficult and time consuming. In recent years, matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS) has become a rapid and simple method to identify bacteria. OBJECTIVE: The present study evaluated a new in-house algorithm using MALDI-TOF-MS for rapid identification of different species of oral Actinomyces cultivated from subgingival biofilm. DESIGN: Eleven reference strains and 674 clinical strains were used in this study. All the strains were preliminarily identified using biochemical methods and then subjected to MALDI-TOF-MS analysis using both similarity-based analysis and classification methods (support vector machine [SVM]). The genotype of the reference strains and of 232 clinical strains was identified by sequence analysis of the 16S ribosomal RNA (rRNA). RESULTS: The sequence analysis of the 16S rRNA gene of all references strains confirmed their previous identification. The MALDI-TOF-MS spectra obtained from the reference strains and the other clinical strains undoubtedly identified as Actinomyces by 16S rRNA sequencing were used to create the mass spectra reference database. Already a visual inspection of the mass spectra of different species reveals both similarities and differences. However, the differences between them are not large enough to allow a reliable differentiation by similarity analysis. Therefore, classification methods were applied as an alternative approach for differentiation and identification of Actinomyces at the species level. A cross-validation of the reference database representing 14 Actinomyces species yielded correct results for all species which were represented by more than two strains in the database. CONCLUSIONS: Our results suggest that a combination of MALDI-TOF-MS with powerful classification algorithms, such as SVMs, provide a useful tool for the differentiation and identification of oral Actinomyces. |
format | Online Article Text |
id | pubmed-4297926 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Co-Action Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-42979262015-02-12 Rapid identification of oral Actinomyces species cultivated from subgingival biofilm by MALDI-TOF-MS Stingu, Catalina S. Borgmann, Toralf Rodloff, Arne C. Vielkind, Paul Jentsch, Holger Schellenberger, Wolfgang Eschrich, Klaus J Oral Microbiol Original Article BACKGROUND: Actinomyces are a common part of the residential flora of the human intestinal tract, genitourinary system and skin. Isolation and identification of Actinomyces by conventional methods is often difficult and time consuming. In recent years, matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS) has become a rapid and simple method to identify bacteria. OBJECTIVE: The present study evaluated a new in-house algorithm using MALDI-TOF-MS for rapid identification of different species of oral Actinomyces cultivated from subgingival biofilm. DESIGN: Eleven reference strains and 674 clinical strains were used in this study. All the strains were preliminarily identified using biochemical methods and then subjected to MALDI-TOF-MS analysis using both similarity-based analysis and classification methods (support vector machine [SVM]). The genotype of the reference strains and of 232 clinical strains was identified by sequence analysis of the 16S ribosomal RNA (rRNA). RESULTS: The sequence analysis of the 16S rRNA gene of all references strains confirmed their previous identification. The MALDI-TOF-MS spectra obtained from the reference strains and the other clinical strains undoubtedly identified as Actinomyces by 16S rRNA sequencing were used to create the mass spectra reference database. Already a visual inspection of the mass spectra of different species reveals both similarities and differences. However, the differences between them are not large enough to allow a reliable differentiation by similarity analysis. Therefore, classification methods were applied as an alternative approach for differentiation and identification of Actinomyces at the species level. A cross-validation of the reference database representing 14 Actinomyces species yielded correct results for all species which were represented by more than two strains in the database. CONCLUSIONS: Our results suggest that a combination of MALDI-TOF-MS with powerful classification algorithms, such as SVMs, provide a useful tool for the differentiation and identification of oral Actinomyces. Co-Action Publishing 2015-01-16 /pmc/articles/PMC4297926/ /pubmed/25597306 http://dx.doi.org/10.3402/jom.v7.26110 Text en © 2015 Catalina S. Stingu et al. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Stingu, Catalina S. Borgmann, Toralf Rodloff, Arne C. Vielkind, Paul Jentsch, Holger Schellenberger, Wolfgang Eschrich, Klaus Rapid identification of oral Actinomyces species cultivated from subgingival biofilm by MALDI-TOF-MS |
title | Rapid identification of oral Actinomyces species cultivated from subgingival biofilm by MALDI-TOF-MS |
title_full | Rapid identification of oral Actinomyces species cultivated from subgingival biofilm by MALDI-TOF-MS |
title_fullStr | Rapid identification of oral Actinomyces species cultivated from subgingival biofilm by MALDI-TOF-MS |
title_full_unstemmed | Rapid identification of oral Actinomyces species cultivated from subgingival biofilm by MALDI-TOF-MS |
title_short | Rapid identification of oral Actinomyces species cultivated from subgingival biofilm by MALDI-TOF-MS |
title_sort | rapid identification of oral actinomyces species cultivated from subgingival biofilm by maldi-tof-ms |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4297926/ https://www.ncbi.nlm.nih.gov/pubmed/25597306 http://dx.doi.org/10.3402/jom.v7.26110 |
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