A role for the tfs3 ICE-encoded type IV secretion system in pro-inflammatory signalling by the Helicobacter pylori Ser/Thr kinase, CtkA

Two distinct type IV secretion systems (T4SSs) can be identified in certain Helicobacter pylori strains, encoded on mobile genetic elements termed tfs3 and tfs4. Although their function remains unknown, both have been implicated in clinical outcomes of H. pylori infection. Here we provide evidence t...

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Main Authors: Alandiyjany, Maher N., Croxall, Nicola J., Grove, Jane I., Delahay, Robin M.
Format: Article
Published: Public Library of Science 2017
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Online Access:https://eprints.nottingham.ac.uk/44568/
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author Alandiyjany, Maher N.
Croxall, Nicola J.
Grove, Jane I.
Delahay, Robin M.
author_facet Alandiyjany, Maher N.
Croxall, Nicola J.
Grove, Jane I.
Delahay, Robin M.
author_sort Alandiyjany, Maher N.
building Nottingham Research Data Repository
collection Online Access
description Two distinct type IV secretion systems (T4SSs) can be identified in certain Helicobacter pylori strains, encoded on mobile genetic elements termed tfs3 and tfs4. Although their function remains unknown, both have been implicated in clinical outcomes of H. pylori infection. Here we provide evidence that the Tfs3 T4SS is required for activity of the pro-inflammatory Ser/Thr kinase protein, CtkA, in a gastric epithelial cell infection model. Previously, purified recombinant CtkA protein has been shown to upregulate NF-kappaB signalling and induce TNF-alpha and IL-8 cytokine secretion from cultured macrophages suggesting that it may potentiate the H. pylori-mediated inflammatory response. In this study, we show that CtkA expressed from its native host, H. pylori has a similar capacity for stimulation of a pro-inflammatory response from gastric epithelial cells. CtkA interaction was found to be dependent upon a complement of tfs3 T4SS genes, but independent of the T4SSs encoded by either tfs4 or the cag pathogenicity island. Moreover, the availability of CtkA for host cell interaction was shown to be conditional upon the carboxyl-terminus of CtkA, encoding a putative conserved secretion signal common to other variably encoded Tfs3 proteins. Collectively, our observations indicate a role for the Tfs3 T4SS in CtkA-mediated pro-inflammatory signalling by H. pylori and identify CtkA as a likely Tfs3 T4SS secretion substrate.
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spelling nottingham-445682020-05-04T18:57:25Z https://eprints.nottingham.ac.uk/44568/ A role for the tfs3 ICE-encoded type IV secretion system in pro-inflammatory signalling by the Helicobacter pylori Ser/Thr kinase, CtkA Alandiyjany, Maher N. Croxall, Nicola J. Grove, Jane I. Delahay, Robin M. Two distinct type IV secretion systems (T4SSs) can be identified in certain Helicobacter pylori strains, encoded on mobile genetic elements termed tfs3 and tfs4. Although their function remains unknown, both have been implicated in clinical outcomes of H. pylori infection. Here we provide evidence that the Tfs3 T4SS is required for activity of the pro-inflammatory Ser/Thr kinase protein, CtkA, in a gastric epithelial cell infection model. Previously, purified recombinant CtkA protein has been shown to upregulate NF-kappaB signalling and induce TNF-alpha and IL-8 cytokine secretion from cultured macrophages suggesting that it may potentiate the H. pylori-mediated inflammatory response. In this study, we show that CtkA expressed from its native host, H. pylori has a similar capacity for stimulation of a pro-inflammatory response from gastric epithelial cells. CtkA interaction was found to be dependent upon a complement of tfs3 T4SS genes, but independent of the T4SSs encoded by either tfs4 or the cag pathogenicity island. Moreover, the availability of CtkA for host cell interaction was shown to be conditional upon the carboxyl-terminus of CtkA, encoding a putative conserved secretion signal common to other variably encoded Tfs3 proteins. Collectively, our observations indicate a role for the Tfs3 T4SS in CtkA-mediated pro-inflammatory signalling by H. pylori and identify CtkA as a likely Tfs3 T4SS secretion substrate. Public Library of Science 2017-07-28 Article PeerReviewed Alandiyjany, Maher N., Croxall, Nicola J., Grove, Jane I. and Delahay, Robin M. (2017) A role for the tfs3 ICE-encoded type IV secretion system in pro-inflammatory signalling by the Helicobacter pylori Ser/Thr kinase, CtkA. PLoS ONE, 12 (7). e0182144/1-e0182144/16. ISSN 1932-6203 Helicobacter pylori type IV secretion system Tfs3 CtkA JHP0940 integrative and conjugative element (ICE) http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0182144 10.1371/journal.pone.0182144 10.1371/journal.pone.0182144 10.1371/journal.pone.0182144
spellingShingle Helicobacter pylori
type IV secretion system
Tfs3
CtkA
JHP0940
integrative and conjugative element (ICE)
Alandiyjany, Maher N.
Croxall, Nicola J.
Grove, Jane I.
Delahay, Robin M.
A role for the tfs3 ICE-encoded type IV secretion system in pro-inflammatory signalling by the Helicobacter pylori Ser/Thr kinase, CtkA
title A role for the tfs3 ICE-encoded type IV secretion system in pro-inflammatory signalling by the Helicobacter pylori Ser/Thr kinase, CtkA
title_full A role for the tfs3 ICE-encoded type IV secretion system in pro-inflammatory signalling by the Helicobacter pylori Ser/Thr kinase, CtkA
title_fullStr A role for the tfs3 ICE-encoded type IV secretion system in pro-inflammatory signalling by the Helicobacter pylori Ser/Thr kinase, CtkA
title_full_unstemmed A role for the tfs3 ICE-encoded type IV secretion system in pro-inflammatory signalling by the Helicobacter pylori Ser/Thr kinase, CtkA
title_short A role for the tfs3 ICE-encoded type IV secretion system in pro-inflammatory signalling by the Helicobacter pylori Ser/Thr kinase, CtkA
title_sort role for the tfs3 ice-encoded type iv secretion system in pro-inflammatory signalling by the helicobacter pylori ser/thr kinase, ctka
topic Helicobacter pylori
type IV secretion system
Tfs3
CtkA
JHP0940
integrative and conjugative element (ICE)
url https://eprints.nottingham.ac.uk/44568/
https://eprints.nottingham.ac.uk/44568/
https://eprints.nottingham.ac.uk/44568/