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Cappable-Seq Reveals Specific Patterns of Metabolism and Virulence for Salmonella Typhimurium Intracellular Survival within Acanthamoeba castellanii

The bacterial pathogen Salmonella enterica, which causes enteritis, has a broad host range and extensive environmental longevity. In water and soil, Salmonella interacts with protozoa and multiplies inside their phagosomes. Although this relationship resembles that between Salmonella and mammalian p...

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Autores principales: Balkin, Alexander S., Plotnikov, Andrey O., Gogoleva, Natalia E., Gogolev, Yuri V., Demchenko, Kirill N., Cherkasov, Sergey V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8396566/
https://www.ncbi.nlm.nih.gov/pubmed/34445780
http://dx.doi.org/10.3390/ijms22169077
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author Balkin, Alexander S.
Plotnikov, Andrey O.
Gogoleva, Natalia E.
Gogolev, Yuri V.
Demchenko, Kirill N.
Cherkasov, Sergey V.
author_facet Balkin, Alexander S.
Plotnikov, Andrey O.
Gogoleva, Natalia E.
Gogolev, Yuri V.
Demchenko, Kirill N.
Cherkasov, Sergey V.
author_sort Balkin, Alexander S.
collection PubMed
description The bacterial pathogen Salmonella enterica, which causes enteritis, has a broad host range and extensive environmental longevity. In water and soil, Salmonella interacts with protozoa and multiplies inside their phagosomes. Although this relationship resembles that between Salmonella and mammalian phagocytes, the interaction mechanisms and bacterial genes involved are unclear. Here, we characterized global gene expression patterns of S. enterica serovar Typhimurium within Acanthamoeba castellanii at the early stage of infection by Cappable-Seq. Gene expression features of S. Typhimurium within A. castellanii were presented with downregulation of glycolysis-related, and upregulation of glyoxylate cycle-related genes. Expression of Salmonella Pathogenicity Island-1 (SPI-1), chemotaxis system, and flagellar apparatus genes was upregulated. Furthermore, expression of genes mediating oxidative stress response and iron uptake was upregulated within A. castellanii as well as within mammalian phagocytes. Hence, global S. Typhimurium gene expression patterns within A. castellanii help better understand the molecular mechanisms of Salmonella adaptation to an amoeba cell and intracellular persistence in protozoa inhabiting water and soil ecosystems.
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spelling pubmed-83965662021-08-28 Cappable-Seq Reveals Specific Patterns of Metabolism and Virulence for Salmonella Typhimurium Intracellular Survival within Acanthamoeba castellanii Balkin, Alexander S. Plotnikov, Andrey O. Gogoleva, Natalia E. Gogolev, Yuri V. Demchenko, Kirill N. Cherkasov, Sergey V. Int J Mol Sci Article The bacterial pathogen Salmonella enterica, which causes enteritis, has a broad host range and extensive environmental longevity. In water and soil, Salmonella interacts with protozoa and multiplies inside their phagosomes. Although this relationship resembles that between Salmonella and mammalian phagocytes, the interaction mechanisms and bacterial genes involved are unclear. Here, we characterized global gene expression patterns of S. enterica serovar Typhimurium within Acanthamoeba castellanii at the early stage of infection by Cappable-Seq. Gene expression features of S. Typhimurium within A. castellanii were presented with downregulation of glycolysis-related, and upregulation of glyoxylate cycle-related genes. Expression of Salmonella Pathogenicity Island-1 (SPI-1), chemotaxis system, and flagellar apparatus genes was upregulated. Furthermore, expression of genes mediating oxidative stress response and iron uptake was upregulated within A. castellanii as well as within mammalian phagocytes. Hence, global S. Typhimurium gene expression patterns within A. castellanii help better understand the molecular mechanisms of Salmonella adaptation to an amoeba cell and intracellular persistence in protozoa inhabiting water and soil ecosystems. MDPI 2021-08-23 /pmc/articles/PMC8396566/ /pubmed/34445780 http://dx.doi.org/10.3390/ijms22169077 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Balkin, Alexander S.
Plotnikov, Andrey O.
Gogoleva, Natalia E.
Gogolev, Yuri V.
Demchenko, Kirill N.
Cherkasov, Sergey V.
Cappable-Seq Reveals Specific Patterns of Metabolism and Virulence for Salmonella Typhimurium Intracellular Survival within Acanthamoeba castellanii
title Cappable-Seq Reveals Specific Patterns of Metabolism and Virulence for Salmonella Typhimurium Intracellular Survival within Acanthamoeba castellanii
title_full Cappable-Seq Reveals Specific Patterns of Metabolism and Virulence for Salmonella Typhimurium Intracellular Survival within Acanthamoeba castellanii
title_fullStr Cappable-Seq Reveals Specific Patterns of Metabolism and Virulence for Salmonella Typhimurium Intracellular Survival within Acanthamoeba castellanii
title_full_unstemmed Cappable-Seq Reveals Specific Patterns of Metabolism and Virulence for Salmonella Typhimurium Intracellular Survival within Acanthamoeba castellanii
title_short Cappable-Seq Reveals Specific Patterns of Metabolism and Virulence for Salmonella Typhimurium Intracellular Survival within Acanthamoeba castellanii
title_sort cappable-seq reveals specific patterns of metabolism and virulence for salmonella typhimurium intracellular survival within acanthamoeba castellanii
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8396566/
https://www.ncbi.nlm.nih.gov/pubmed/34445780
http://dx.doi.org/10.3390/ijms22169077
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