Interactions between the Aggregatibacter actinomycetemcomitans secretin HofQ and host cytokines indicate a link between natural competence and interleukin-8 uptake

Naturally competent bacteria acquire DNA from their surroundings to survive in nutrient-poor environments and incorporate DNA into their genomes as new genes for improved survival. The secretin HofQ from the oral pathogen Aggregatibacter actinomycetemcomitans has been associated with DNA uptake. Cyt...

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Main Authors: Tuuli Ahlstrand, Annamari Torittu, Heli Elovaara, Hannamari Välimaa, Marja T. Pöllänen, Sergo Kasvandik, Martin Högbom, Riikka Ihalin
Format: Article
Language:English
Published: Taylor & Francis Group 2018-12-01
Series:Virulence
Subjects:
Online Access:http://dx.doi.org/10.1080/21505594.2018.1499378
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spelling doaj-7059331c049f4841a0b578684e6bc7af2020-11-24T23:05:59ZengTaylor & Francis GroupVirulence2150-55942150-56082018-12-01911205122310.1080/21505594.2018.14993781499378Interactions between the Aggregatibacter actinomycetemcomitans secretin HofQ and host cytokines indicate a link between natural competence and interleukin-8 uptakeTuuli Ahlstrand0Annamari Torittu1Heli Elovaara2Hannamari Välimaa3Marja T. Pöllänen4Sergo Kasvandik5Martin Högbom6Riikka Ihalin7University of TurkuUniversity of TurkuUniversity of TurkuUniversity of HelsinkiUniversity of TurkuUniversity of TartuStockholm UniversityUniversity of TurkuNaturally competent bacteria acquire DNA from their surroundings to survive in nutrient-poor environments and incorporate DNA into their genomes as new genes for improved survival. The secretin HofQ from the oral pathogen Aggregatibacter actinomycetemcomitans has been associated with DNA uptake. Cytokine sequestering is a potential virulence mechanism in various bacteria and may modulate both host defense and bacterial physiology. The objective of this study was to elucidate a possible connection between natural competence and cytokine uptake in A. actinomycetemcomitans. The extramembranous domain of HofQ (emHofQ) was shown to interact with various cytokines, of which IL-8 exhibited the strongest interaction. The dissociation constant between emHofQ and IL-8 was 43 nM in static settings and 2.4 μM in dynamic settings. The moderate binding affinity is consistent with the hypothesis that emHofQ recognizes cytokines before transporting them into the cells. The interaction site was identified via crosslinking and mutational analysis. By structural comparison, relateda type I KH domain with a similar interaction site was detected in the Neisseria meningitidis secretin PilQ, which has been shown to participate in IL-8 uptake. Deletion of hofQ from the A. actinomycetemcomitans genome decreased the overall biofilm formation of this organism, abolished the response to cytokines, i.e., decreased eDNA levels in the presence of cytokines, and increased the susceptibility of the biofilm to tested β-lactams. Moreover, we showed that recombinant IL-8 interacted with DNA. These results can be used in further studies on the specific role of cytokine uptake in bacterial virulence without interfering with natural-competence-related DNA uptake.http://dx.doi.org/10.1080/21505594.2018.1499378Aggregatibacter actinomycetemcomitansperiodontitisbacterial outer membrane proteinschemotactic cytokinesinterleukin-8protein interaction domains and motifsDNA-binding proteins
collection DOAJ
language English
format Article
sources DOAJ
author Tuuli Ahlstrand
Annamari Torittu
Heli Elovaara
Hannamari Välimaa
Marja T. Pöllänen
Sergo Kasvandik
Martin Högbom
Riikka Ihalin
spellingShingle Tuuli Ahlstrand
Annamari Torittu
Heli Elovaara
Hannamari Välimaa
Marja T. Pöllänen
Sergo Kasvandik
Martin Högbom
Riikka Ihalin
Interactions between the Aggregatibacter actinomycetemcomitans secretin HofQ and host cytokines indicate a link between natural competence and interleukin-8 uptake
Virulence
Aggregatibacter actinomycetemcomitans
periodontitis
bacterial outer membrane proteins
chemotactic cytokines
interleukin-8
protein interaction domains and motifs
DNA-binding proteins
author_facet Tuuli Ahlstrand
Annamari Torittu
Heli Elovaara
Hannamari Välimaa
Marja T. Pöllänen
Sergo Kasvandik
Martin Högbom
Riikka Ihalin
author_sort Tuuli Ahlstrand
title Interactions between the Aggregatibacter actinomycetemcomitans secretin HofQ and host cytokines indicate a link between natural competence and interleukin-8 uptake
title_short Interactions between the Aggregatibacter actinomycetemcomitans secretin HofQ and host cytokines indicate a link between natural competence and interleukin-8 uptake
title_full Interactions between the Aggregatibacter actinomycetemcomitans secretin HofQ and host cytokines indicate a link between natural competence and interleukin-8 uptake
title_fullStr Interactions between the Aggregatibacter actinomycetemcomitans secretin HofQ and host cytokines indicate a link between natural competence and interleukin-8 uptake
title_full_unstemmed Interactions between the Aggregatibacter actinomycetemcomitans secretin HofQ and host cytokines indicate a link between natural competence and interleukin-8 uptake
title_sort interactions between the aggregatibacter actinomycetemcomitans secretin hofq and host cytokines indicate a link between natural competence and interleukin-8 uptake
publisher Taylor & Francis Group
series Virulence
issn 2150-5594
2150-5608
publishDate 2018-12-01
description Naturally competent bacteria acquire DNA from their surroundings to survive in nutrient-poor environments and incorporate DNA into their genomes as new genes for improved survival. The secretin HofQ from the oral pathogen Aggregatibacter actinomycetemcomitans has been associated with DNA uptake. Cytokine sequestering is a potential virulence mechanism in various bacteria and may modulate both host defense and bacterial physiology. The objective of this study was to elucidate a possible connection between natural competence and cytokine uptake in A. actinomycetemcomitans. The extramembranous domain of HofQ (emHofQ) was shown to interact with various cytokines, of which IL-8 exhibited the strongest interaction. The dissociation constant between emHofQ and IL-8 was 43 nM in static settings and 2.4 μM in dynamic settings. The moderate binding affinity is consistent with the hypothesis that emHofQ recognizes cytokines before transporting them into the cells. The interaction site was identified via crosslinking and mutational analysis. By structural comparison, relateda type I KH domain with a similar interaction site was detected in the Neisseria meningitidis secretin PilQ, which has been shown to participate in IL-8 uptake. Deletion of hofQ from the A. actinomycetemcomitans genome decreased the overall biofilm formation of this organism, abolished the response to cytokines, i.e., decreased eDNA levels in the presence of cytokines, and increased the susceptibility of the biofilm to tested β-lactams. Moreover, we showed that recombinant IL-8 interacted with DNA. These results can be used in further studies on the specific role of cytokine uptake in bacterial virulence without interfering with natural-competence-related DNA uptake.
topic Aggregatibacter actinomycetemcomitans
periodontitis
bacterial outer membrane proteins
chemotactic cytokines
interleukin-8
protein interaction domains and motifs
DNA-binding proteins
url http://dx.doi.org/10.1080/21505594.2018.1499378
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