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Tytuł pozycji:

Capsule expression in Streptococcus mitis modulates interaction with oral keratinocytes and alters susceptibility to human antimicrobial peptides.

Tytuł:
Capsule expression in Streptococcus mitis modulates interaction with oral keratinocytes and alters susceptibility to human antimicrobial peptides.
Autorzy:
Rukke HV; Department of Oral Biology, Faculty of Dentistry, University of Oslo, Norway.
Engen SA; Department of Oral Biology, Faculty of Dentistry, University of Oslo, Norway.
Schenck K; Department of Oral Biology, Faculty of Dentistry, University of Oslo, Norway.
Petersen FC; Department of Oral Biology, Faculty of Dentistry, University of Oslo, Norway.
Źródło:
Molecular oral microbiology [Mol Oral Microbiol] 2016 Aug; Vol. 31 (4), pp. 302-13. Date of Electronic Publication: 2015 Sep 22.
Typ publikacji:
Journal Article
Język:
English
Imprint Name(s):
Original Publication: Copenhagen : John Wiley & Sons
MeSH Terms:
Anti-Infective Agents/*pharmacology
Antimicrobial Cationic Peptides/*pharmacology
Bacterial Capsules/*drug effects
Bacterial Capsules/*metabolism
Keratinocytes/*microbiology
Mouth/*cytology
Streptococcus mitis/*cytology
Streptococcus mitis/*drug effects
alpha-Defensins/*pharmacology
Bacterial Adhesion ; Bacterial Capsules/genetics ; Bacterial Capsules/immunology ; Cathelicidins/pharmacology ; Cell Line, Tumor ; Epithelial Cells/immunology ; Epithelial Cells/microbiology ; Humans ; Interleukin-6/genetics ; Interleukin-8/genetics ; Keratinocytes/immunology ; Mouth/immunology ; Mouth/microbiology ; Mutation ; Streptococcus mitis/genetics ; Streptococcus mitis/immunology ; Streptococcus pneumoniae/cytology ; Streptococcus pneumoniae/genetics ; Streptococcus pneumoniae/immunology ; Streptococcus pneumoniae/physiology ; beta-Defensins/pharmacology
Contributed Indexing:
Keywords: Streptococcus; Streptococcus mitis; Streptococcus pneumoniae; capsule; human antimicrobial peptides
Substance Nomenclature:
0 (Anti-Infective Agents)
0 (Antimicrobial Cationic Peptides)
0 (CXCL8 protein, human)
0 (Cathelicidins)
0 (IL6 protein, human)
0 (Interleukin-6)
0 (Interleukin-8)
0 (alpha-Defensins)
0 (beta-Defensins)
0 (human neutrophil peptide 1)
0 (human neutrophil peptide 2)
0 (human neutrophil peptide 3)
Entry Date(s):
Date Created: 20150811 Date Completed: 20170525 Latest Revision: 20221207
Update Code:
20240104
DOI:
10.1111/omi.12123
PMID:
26255868
Czasopismo naukowe
Streptococcus mitis is a colonizer of the oral cavity and the nasopharynx, and is closely related to Streptococcus pneumoniae. Both species occur in encapsulated and unencapsulated forms, but in S. mitis the role of the capsule in host interactions is mostly unknown. Therefore, the aim of this study was to examine how capsule expression in S. mitis can modulate interactions with the host with relevance for colonization. The S. mitis type strain, as well as two mutants of the type strain, an isogenic capsule deletion mutant, and a capsule switch mutant expressing the serotype 4 capsule of S. pneumoniae TIGR4, were used. Wild-type and capsule deletion strains of S. pneumoniae TIGR4 were included for comparison. We found that capsule production in S. mitis reduced adhesion to oral and lung epithelial cells. Further, exposure of oral epithelial cells to encapsulated S. mitis resulted in higher interleukin-6 and CXCL-8 transcription levels relative to the unencapsulated mutant. Capsule expression in S. mitis increased the sensitivity to human neutrophil peptide 1-3 but reduced the sensitivity to human β-defensin-3 and cathelicidin. This was in contrast with S. pneumoniae in which capsule expression has been generally associated with increased sensitivity to human antimicrobial peptides (AMPs). Collectively, these findings indicate that capsule expression in S. mitis is important in modulating interactions with epithelial cells, and is associated with increased or reduced susceptibility to AMPs depending on the nature of the AMP.
(© 2015 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.)

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