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Influence of the viscosity of healthy and diseased human mucins on the motility of Helicobacter pylori

We present particle tracking microrheology results on human mucins, isolated from normal surface and gland mucosa and one tumor sample, and examine the motility of Helicobacter pylori in these mucins. At 1.5% concentration human mucin solutions are purely viscous, with viscosity η (gland mucin) >...

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Autores principales: Su, Clover, Padra, Médea, Constantino, Maira Alves, Sharba, Sinan, Thorell, Anders, Lindén, Sara K., Bansil, Rama
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6018794/
https://www.ncbi.nlm.nih.gov/pubmed/29946149
http://dx.doi.org/10.1038/s41598-018-27732-3
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author Su, Clover
Padra, Médea
Constantino, Maira Alves
Sharba, Sinan
Thorell, Anders
Lindén, Sara K.
Bansil, Rama
author_facet Su, Clover
Padra, Médea
Constantino, Maira Alves
Sharba, Sinan
Thorell, Anders
Lindén, Sara K.
Bansil, Rama
author_sort Su, Clover
collection PubMed
description We present particle tracking microrheology results on human mucins, isolated from normal surface and gland mucosa and one tumor sample, and examine the motility of Helicobacter pylori in these mucins. At 1.5% concentration human mucin solutions are purely viscous, with viscosity η (gland mucin) > η (surface mucin) > η (tumor mucin). In the presence of motile H. pylori bacteria, particle diffusion is enhanced, with diffusivity D(+bac)(tumor mucin) > D(+bac)(gland mucin) > D(+bac)(surface mucin). The surface and tumor mucin solutions exhibit an elastic response in the presence of bacteria. Taken together these results imply that particle diffusion and active swimming are coupled and impact the rheology of mucin solutions. Both J99 wild type (WT) and its isogenic ΔbabA/ΔsabA mutant swam well in broth or PGM solutions. However, the human mucins affected their motility differently, rendering them immotile in certain instances. The distribution of swimming speeds in human mucin solutions was broader with a large fraction of fast swimmers compared to PGM and broth. The bacteria swam fastest in the tumor mucin solution correlating with it having the lowest viscosity of all mucin solutions. Overall, these results suggest that mucins from different tissue locations and disease status differ in their microrheological properties and their effect on H. pylori motility.
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spelling pubmed-60187942018-07-06 Influence of the viscosity of healthy and diseased human mucins on the motility of Helicobacter pylori Su, Clover Padra, Médea Constantino, Maira Alves Sharba, Sinan Thorell, Anders Lindén, Sara K. Bansil, Rama Sci Rep Article We present particle tracking microrheology results on human mucins, isolated from normal surface and gland mucosa and one tumor sample, and examine the motility of Helicobacter pylori in these mucins. At 1.5% concentration human mucin solutions are purely viscous, with viscosity η (gland mucin) > η (surface mucin) > η (tumor mucin). In the presence of motile H. pylori bacteria, particle diffusion is enhanced, with diffusivity D(+bac)(tumor mucin) > D(+bac)(gland mucin) > D(+bac)(surface mucin). The surface and tumor mucin solutions exhibit an elastic response in the presence of bacteria. Taken together these results imply that particle diffusion and active swimming are coupled and impact the rheology of mucin solutions. Both J99 wild type (WT) and its isogenic ΔbabA/ΔsabA mutant swam well in broth or PGM solutions. However, the human mucins affected their motility differently, rendering them immotile in certain instances. The distribution of swimming speeds in human mucin solutions was broader with a large fraction of fast swimmers compared to PGM and broth. The bacteria swam fastest in the tumor mucin solution correlating with it having the lowest viscosity of all mucin solutions. Overall, these results suggest that mucins from different tissue locations and disease status differ in their microrheological properties and their effect on H. pylori motility. Nature Publishing Group UK 2018-06-26 /pmc/articles/PMC6018794/ /pubmed/29946149 http://dx.doi.org/10.1038/s41598-018-27732-3 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Su, Clover
Padra, Médea
Constantino, Maira Alves
Sharba, Sinan
Thorell, Anders
Lindén, Sara K.
Bansil, Rama
Influence of the viscosity of healthy and diseased human mucins on the motility of Helicobacter pylori
title Influence of the viscosity of healthy and diseased human mucins on the motility of Helicobacter pylori
title_full Influence of the viscosity of healthy and diseased human mucins on the motility of Helicobacter pylori
title_fullStr Influence of the viscosity of healthy and diseased human mucins on the motility of Helicobacter pylori
title_full_unstemmed Influence of the viscosity of healthy and diseased human mucins on the motility of Helicobacter pylori
title_short Influence of the viscosity of healthy and diseased human mucins on the motility of Helicobacter pylori
title_sort influence of the viscosity of healthy and diseased human mucins on the motility of helicobacter pylori
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6018794/
https://www.ncbi.nlm.nih.gov/pubmed/29946149
http://dx.doi.org/10.1038/s41598-018-27732-3
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