Abstract

Aggregatibacter actinomycetemcomitans is a Gram-negative organism, strongly associated with aggressive forms of periodontitis. An important virulence property of A. actinomycetemcomitans is its ability to form tenacious biofilms that can attach to abiotic as well as biotic surfaces. The histone-like (H-NS) family of nucleoid-structuring proteins act as transcriptional silencers in many Gram-negative bacteria. To evaluate the role of H-NS in A. actinomycetemcomitans, hns mutant derivatives of serotype a strain D7S were generated. Characteristics of the hns mutant phenotype included shorter and fewer pili, and substantially lower monospecies biofilm formation relative to the wild type. Furthermore, the D7S hns mutant exhibited significantly reduced growth within a seven-species oral biofilm model. However, no apparent difference was observed regarding the numbers and proportions of the remaining six species regardless of being co-cultivated with D7S hns or its parental strain. Proteomics analysis of the strains grown in monocultures confirmed the role of H-NS as a repressor of gene expression in A. actinomycetemcomitans. Interestingly, proteomics analysis of the multispecies biofilms indicated that the A. actinomycetemcomitans wild type and hns mutant imposed different regulatory effects on the pattern of protein expression in the other species, i.e., mainly Streptococcus spp., Fusobacterium nucleatum, and Veillonella dispar. Gene ontology analysis revealed that a large portion of the differentially regulated proteins was related to translational activity. Taken together, our data suggest that, apart from being a negative regulator of protein expression in A. actinomycetemcomitans, H-NS promotes biofilm formation and may be an important factor for survival of this species within a multispecies biofilm.

Details

Title
Aggregatibacter actinomycetemcomitans H-NS promotes biofilm formation and alters protein dynamics of other species within a polymicrobial oral biofilm
Author
Bao, Kai 1 ; Bostanci, Nagihan 2 ; Thurnheer, Thomas 3 ; Grossmann, Jonas 4 ; Wolski, Witold E 4 ; Thay, Bernard 5 ; Belibasakis, Georgios N 2 ; Oscarsson, Jan 5   VIAFID ORCID Logo 

 Division of Oral Diseases, Department of Dental Medicine, Karolinska Institutet, Solnavägen, Sweden; Division of Oral Microbiology and Immunology, Center of Dental Medicine, University of Zürich, Zürich, Switzerland 
 Division of Oral Diseases, Department of Dental Medicine, Karolinska Institutet, Solnavägen, Sweden 
 Division of Oral Microbiology and Immunology, Center of Dental Medicine, University of Zürich, Zürich, Switzerland 
 Functional Genomics Center, ETH Zürich and University of Zürich, Zürich, Switzerland 
 Oral Microbiology, Department of Odontology, Umeå University, Umeå, Sweden 
Pages
1-11
Publication year
2018
Publication date
May 2018
Publisher
Nature Publishing Group
e-ISSN
20555008
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2042728664
Copyright
© 2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.