Matrix-assisted Laser Desorption Ionization–Time of Flight Mass Spectrometry (MALDI-TOF MS) for subgingival bacteriome identification in a group of treated periodontitis patients: a case series

Author:

Lupșe Irina1,Flonta Mirela2,Ciurea Andreea34,Micu Iulia Cristina3,Roman Alexandra34,Pall Emoke5,Popescu Dora Maria6,Soancă Andrada34

Affiliation:

1. Department of Paediatric Dentistry, Faculty of Dental Medicine , Iuliu Hațieganu University of Medicine and Pharmacy Cluj-Napoca , Avram Iancu St., no.31 , , Cluj-Napoca , Romania .

2. Clinical Hospital of Infectious Diseases , Cluj-Napoca, Romania .

3. Department of Periodontology, Faculty of Dental Medicine , Iuliu Haţieganu University of Medicine and Pharmacy Cluj-Napoca , Victor Babeş St., no.15 , Cluj-Napoca , Romania .

4. Emegency County Clinical Hospital , Cluj-Napoca , Romania

5. Department of Infectious Disease, Faculty of Veterinary Medicine , University of Agricultural Sciences and Veterinary Medicine , Calea Mănăștur St., no.3-5 , Cluj-Napoca , Romania .

6. Faculty of Dentistry , University of Medicine and Pharmacy from Craiova , 2 Petru Rares St ., Craiova , Romania

Abstract

Abstract Periodontitis is a chronic multifactorial polymicrobial infection, characterized by profound modifications of the composition and proportion of the subgingival microbiota. Microbiological laboratory tests are sometimes used in periodontal diagnosis and monitoring of treatment, but both conventional cultivation methods and molecular techniques have some major drawbacks. Therefore, other performant bacterial identification methods must be considered. The aim of the current study was to use Matrix-assisted Laser Desorption Ionization–Time of Flight Mass Spectrometry (MALTI-TOF MS) analysis in association with bacterial culture method to evaluate the modifications of the subgingival bacterial composition in periodontitis patients, before and after cause-related subgingival therapy. Subgingival plaque samples were collected from periodontal pockets before and after subgingival mechanical instrumentation and adjunctive local antimicrobial applications and were cultured in aerobic and anaerobic conditions. Microbial colonies were further assessed using MALDI-TOF-MS. A total of 36 bacterial strains were isolated from a group of 16 patients. All species from the orange complex were identified by MALDI-TOF MS. A marked reduction of detection frequency was observed in most bacterial strains, including the orange complex after cause-related periodontal treatment. The results of this study indicate that MALDI-TOF MS could be considered an accurate method for oral microbial identification and the cause-related periodontal treatment is useful for reducing the microbial burden.

Publisher

Walter de Gruyter GmbH

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