Cargando…

Role of amoebae for survival and recovery of ‘non-culturable’ Helicobacter pylori cells in aquatic environments

Helicobacter pylori is a fastidious Gram-negative bacterium that infects over half of the world's population, causing chronic gastritis and is a risk factor for stomach cancer. In developing and rural regions where prevalence rate exceeds 60%, persistence and waterborne transmission are often l...

Descripción completa

Detalles Bibliográficos
Autores principales: Dey, Rafik, Rieger, Aja, Banting, Graham, Ashbolt, Nicholas J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7494403/
https://www.ncbi.nlm.nih.gov/pubmed/32897313
http://dx.doi.org/10.1093/femsec/fiaa182
_version_ 1783582743608688640
author Dey, Rafik
Rieger, Aja
Banting, Graham
Ashbolt, Nicholas J
author_facet Dey, Rafik
Rieger, Aja
Banting, Graham
Ashbolt, Nicholas J
author_sort Dey, Rafik
collection PubMed
description Helicobacter pylori is a fastidious Gram-negative bacterium that infects over half of the world's population, causing chronic gastritis and is a risk factor for stomach cancer. In developing and rural regions where prevalence rate exceeds 60%, persistence and waterborne transmission are often linked to poor sanitation conditions. Here we demonstrate that H. pylori not only survives but also replicates within acidified free-living amoebal phagosomes. Bacterial counts of the clinical isolate H. pylori G27 increased over 50-fold after three days in co-culture with amoebae. In contrast, a H. pylori mutant deficient in a cagPAI gene (cagE) showed little growth within amoebae, demonstrating the likely importance of a type IV secretion system in H. pylori for amoebal infection. We also demonstrate that H. pylori can be packaged by amoebae and released in extracellular vesicles. Furthermore, and for the first time, we successfully demonstrate the ability of two free-living amoebae to revert and recover viable but non-cultivable coccoid (VBNC)-H. pylori to a culturable state. Our studies provide evidence to support the hypothesis that amoebae and perhaps other free-living protozoa contribute to the replication and persistence of human-pathogenic H. pylori by providing a protected intracellular microenvironment for this pathogen to persist in natural aquatic environments and engineered water systems, thereby H. pylori potentially uses amoeba as a carrier and a vector of transmission.
format Online
Article
Text
id pubmed-7494403
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-74944032020-09-22 Role of amoebae for survival and recovery of ‘non-culturable’ Helicobacter pylori cells in aquatic environments Dey, Rafik Rieger, Aja Banting, Graham Ashbolt, Nicholas J FEMS Microbiol Ecol Research Article Helicobacter pylori is a fastidious Gram-negative bacterium that infects over half of the world's population, causing chronic gastritis and is a risk factor for stomach cancer. In developing and rural regions where prevalence rate exceeds 60%, persistence and waterborne transmission are often linked to poor sanitation conditions. Here we demonstrate that H. pylori not only survives but also replicates within acidified free-living amoebal phagosomes. Bacterial counts of the clinical isolate H. pylori G27 increased over 50-fold after three days in co-culture with amoebae. In contrast, a H. pylori mutant deficient in a cagPAI gene (cagE) showed little growth within amoebae, demonstrating the likely importance of a type IV secretion system in H. pylori for amoebal infection. We also demonstrate that H. pylori can be packaged by amoebae and released in extracellular vesicles. Furthermore, and for the first time, we successfully demonstrate the ability of two free-living amoebae to revert and recover viable but non-cultivable coccoid (VBNC)-H. pylori to a culturable state. Our studies provide evidence to support the hypothesis that amoebae and perhaps other free-living protozoa contribute to the replication and persistence of human-pathogenic H. pylori by providing a protected intracellular microenvironment for this pathogen to persist in natural aquatic environments and engineered water systems, thereby H. pylori potentially uses amoeba as a carrier and a vector of transmission. Oxford University Press 2020-09-08 /pmc/articles/PMC7494403/ /pubmed/32897313 http://dx.doi.org/10.1093/femsec/fiaa182 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of FEMS. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Dey, Rafik
Rieger, Aja
Banting, Graham
Ashbolt, Nicholas J
Role of amoebae for survival and recovery of ‘non-culturable’ Helicobacter pylori cells in aquatic environments
title Role of amoebae for survival and recovery of ‘non-culturable’ Helicobacter pylori cells in aquatic environments
title_full Role of amoebae for survival and recovery of ‘non-culturable’ Helicobacter pylori cells in aquatic environments
title_fullStr Role of amoebae for survival and recovery of ‘non-culturable’ Helicobacter pylori cells in aquatic environments
title_full_unstemmed Role of amoebae for survival and recovery of ‘non-culturable’ Helicobacter pylori cells in aquatic environments
title_short Role of amoebae for survival and recovery of ‘non-culturable’ Helicobacter pylori cells in aquatic environments
title_sort role of amoebae for survival and recovery of ‘non-culturable’ helicobacter pylori cells in aquatic environments
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7494403/
https://www.ncbi.nlm.nih.gov/pubmed/32897313
http://dx.doi.org/10.1093/femsec/fiaa182
work_keys_str_mv AT deyrafik roleofamoebaeforsurvivalandrecoveryofnonculturablehelicobacterpyloricellsinaquaticenvironments
AT riegeraja roleofamoebaeforsurvivalandrecoveryofnonculturablehelicobacterpyloricellsinaquaticenvironments
AT bantinggraham roleofamoebaeforsurvivalandrecoveryofnonculturablehelicobacterpyloricellsinaquaticenvironments
AT ashboltnicholasj roleofamoebaeforsurvivalandrecoveryofnonculturablehelicobacterpyloricellsinaquaticenvironments