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Staphylococcus aureus Interferes with Streptococci Spatial Distribution and with Protein Expression of Species within a Polymicrobial Oral Biofilm.
Schnurr, Etyene; Paqué, Pune N; Attin, Thomas; Nanni, Paolo; Grossmann, Jonas; Holtfreter, Silva; Bröker, Barbara M; Kohler, Christian; Diep, Binh An; Ribeiro, Apoena de Aguiar; Thurnheer, Thomas.
Affiliation
  • Schnurr E; Instituto de Saúde de Nova Friburgo, Federal Fluminense University, 28625-650 Nova Friburgo, Brazil.
  • Paqué PN; Clinic of Conservative and Preventive Dentistry, Center of Dental Medicine, University of Zurich, 8032 Zurich, Switzerland.
  • Attin T; Clinic of Conservative and Preventive Dentistry, Center of Dental Medicine, University of Zurich, 8032 Zurich, Switzerland.
  • Nanni P; Functional Genomics Center, ETH Zürich and University of Zurich, 8057 Zurich, Switzerland.
  • Grossmann J; Functional Genomics Center, ETH Zürich and University of Zurich, 8057 Zurich, Switzerland.
  • Holtfreter S; SIB Swiss Institute of Bioinformatics, 1015 Lausanne, Switzerland.
  • Bröker BM; Department of Immunology, University Medicine Greifswald, 17475 Greifswald, Germany.
  • Kohler C; Department of Immunology, University Medicine Greifswald, 17475 Greifswald, Germany.
  • Diep BA; Friedrich-Loeffler Institute for Medical Microbiology, University Medicine Greifswald, 17475 Greifswald, Germany.
  • Ribeiro AA; Division of HIV, Infectious Diseases, and Global Medicine, Department of Medicine, University of California San Francisco, San Francisco, CA 94143, USA.
  • Thurnheer T; Division of Diagnostic Sciences, University of North Carolina, Chapel Hill, NC 27599, USA.
Antibiotics (Basel) ; 10(2)2021 Jan 26.
Article in En | MEDLINE | ID: mdl-33530340
ABSTRACT
We asked whether transient Staphylococcus aureus in the oral environment synergistically interacts with orally associated bacterial species such as Actinomyces oris, Candida albicans, Fusobacterium nucleatum, Streptococcus oralis, Streptococcus mutans, and Veillonella dispar (six-species control biofilm 6S). For this purpose, four modified biofilms with seven species that contain either the wild type strain of the S. aureus genotype (USA300-MRSA WT), its isogenic mutant with MSCRAMM deficiency (USA300-MRSA ΔMSCRAMM), a methicillin-sensitive S. aureus (ST72-MSSA-) or a methicillin-resistant S. aureus (USA800-MRSA) grown on hydroxyapatite disks were examined. Culture analyses, confocal-laser-scanning microscopy and proteome analyses were performed. S. aureus strains affected the amount of supragingival biofilm-associated species differently. The deletion of MSCRAMM genes disrupted the growth of S. aureus and the distribution of S. mutans and S. oralis within the biofilms. In addition, S. aureus caused shifts in the number of detectable proteins of other species in the 6S biofilm. S. aureus (USA300-MRSA WT), aggregated together with early colonizers such as Actinomyces and streptococci, influenced the number of secondary colonizers such as Fusobacterium nucleatum and was involved in structuring the biofilm architecture that triggered the change from a homeostatic biofilm to a dysbiotic biofilm to the development of oral diseases.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Antibiotics (Basel) Year: 2021 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Antibiotics (Basel) Year: 2021 Document type: Article