Antidiabetic “gliptins” affect biofilm formation by Streptococcus mutans

De, Arpan, Pompilio, Arianna, Francis, Jenifer, Sutcliffe, Iain, Black, Gary, Lupidi, Giulio, Petrelli, Dezemona and Vitali, Luca A. (2018) Antidiabetic “gliptins” affect biofilm formation by Streptococcus mutans. Microbiological Research, 209. pp. 79-85. ISSN 0944-5013

[img] Text (Full text)
De et al - Antidiabetic “gliptins” affect biofilm formation by Streptococcus mutans.pdf - Accepted Version
Restricted to Repository staff only until 19 February 2019.

Download (3MB)
Official URL: https://doi.org/10.1016/j.micres.2018.02.005

Abstract

Streptococcus mutans, a dental caries causing odontopathogen, produces X-prolyl dipeptidyl peptidase (Sm-XPDAP, encoded by pepX), a serine protease known to have a nutritional role. Considering the potential of proteases as therapeutic targets in pathogens, this study was primarily aimed at investigating the role of Sm-XPDAP in contributing to virulence-related traits. Dipeptidyl peptidase (DPP IV), an XPDAP analogous enzyme found in mammalian tissues,is a well known therapeutic target in Type II diabetes. Based on the hypothesis that gliptins, commonly used as anti-human-DPP IV drugs, may affect bacterial growth upon inhibition of Sm-XPDAP, we have determined their ex vivo antimicrobial and anti-biofilm activity towards S. mutans. All three DPP IV drugs tested reduced biofilm formation as determined by crystal violet staining. To link the observed biofilm inhibition to the human-DPP IV analogue present in S. mutans UA159, a pepX isogenic mutant was generated. In addition to reduced biofilm formation, CLSM studies of the biofilm formed by the pepX isogenic mutant showed these were comparable to those formed in the presence of saxagliptin, suggesting a probable role of this enzyme in biofilm formation by S. mutans UA159. The effects of both pepX deletion and DPP IV drugs on the proteome were studied using LC–MS/MS. Overall, this study highlights the potential of Sm-XPDAP as a novel anti-biofilm target and suggests a template molecule to synthesize lead compounds effective against this enzyme.

Item Type: Article
Uncontrolled Keywords: Streptococcus mutans; Biofilm; X-prolyl dipeptidyl peptidase; Saxagliptin; Shot-gun proteomics
Subjects: A200 Pre-clinical Dentistry
B900 Others in Subjects allied to Medicine
C500 Microbiology
Department: Faculties > Health and Life Sciences > Applied Sciences
Related URLs:
Depositing User: Iain Sutcliffe
Date Deposited: 28 Feb 2018 10:27
Last Modified: 28 Feb 2018 19:00
URI: http://nrl.northumbria.ac.uk/id/eprint/33512

Actions (login required)

View Item View Item

Downloads

Downloads per month over past year

View more statistics


Policies: NRL Policies | NRL University Deposit Policy | NRL Deposit Licence