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Weak Organic Acids Decrease Borrelia burgdorferi Cytoplasmic pH, Eliciting an Acid Stress Response and Impacting RpoN- and RpoS-Dependent Gene Expression

The spirochete Borrelia burgdorferi survives in its tick vector, Ixodes scapularis, or within various hosts. To transition between and survive in these distinct niches, B. burgdorferi changes its gene expression in response to environmental cues, both biochemical and physiological. Exposure of B. bu...

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Autores principales: Dulebohn, Daniel P., Richards, Crystal L., Su, Hua, Lawrence, Kevin A., Gherardini, Frank C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5626856/
https://www.ncbi.nlm.nih.gov/pubmed/29033900
http://dx.doi.org/10.3389/fmicb.2017.01734
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author Dulebohn, Daniel P.
Richards, Crystal L.
Su, Hua
Lawrence, Kevin A.
Gherardini, Frank C.
author_facet Dulebohn, Daniel P.
Richards, Crystal L.
Su, Hua
Lawrence, Kevin A.
Gherardini, Frank C.
author_sort Dulebohn, Daniel P.
collection PubMed
description The spirochete Borrelia burgdorferi survives in its tick vector, Ixodes scapularis, or within various hosts. To transition between and survive in these distinct niches, B. burgdorferi changes its gene expression in response to environmental cues, both biochemical and physiological. Exposure of B. burgdorferi to weak monocarboxylic organic acids, including those detected in the blood meal of fed ticks, decreased the cytoplasmic pH of B. burgdorferi in vitro. A decrease in the cytoplasmic pH induced the expression of genes encoding enzymes that have been shown to restore pH homeostasis in other bacteria. These include putative coupled proton/cation exchangers, a putative Na(+)/H(+) antiporter, a neutralizing buffer transporter, an amino acid deaminase and a proton exporting vacuolar-type V(o)V(1) ATPase. Data presented in this report suggested that the acid stress response triggered the expression of RpoN- and RpoS-dependent genes including important virulence factors such as outer surface protein C (OspC), BBA66, and some BosR (Borrelia oxidative stress regulator)-dependent genes. Because the expression of virulence factors, like OspC, are so tightly connected by RpoS to general cellular stress responses and cell physiology, it is difficult to separate transmission-promoting conditions in what is clearly a multifactorial and complex regulatory web.
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spelling pubmed-56268562017-10-13 Weak Organic Acids Decrease Borrelia burgdorferi Cytoplasmic pH, Eliciting an Acid Stress Response and Impacting RpoN- and RpoS-Dependent Gene Expression Dulebohn, Daniel P. Richards, Crystal L. Su, Hua Lawrence, Kevin A. Gherardini, Frank C. Front Microbiol Microbiology The spirochete Borrelia burgdorferi survives in its tick vector, Ixodes scapularis, or within various hosts. To transition between and survive in these distinct niches, B. burgdorferi changes its gene expression in response to environmental cues, both biochemical and physiological. Exposure of B. burgdorferi to weak monocarboxylic organic acids, including those detected in the blood meal of fed ticks, decreased the cytoplasmic pH of B. burgdorferi in vitro. A decrease in the cytoplasmic pH induced the expression of genes encoding enzymes that have been shown to restore pH homeostasis in other bacteria. These include putative coupled proton/cation exchangers, a putative Na(+)/H(+) antiporter, a neutralizing buffer transporter, an amino acid deaminase and a proton exporting vacuolar-type V(o)V(1) ATPase. Data presented in this report suggested that the acid stress response triggered the expression of RpoN- and RpoS-dependent genes including important virulence factors such as outer surface protein C (OspC), BBA66, and some BosR (Borrelia oxidative stress regulator)-dependent genes. Because the expression of virulence factors, like OspC, are so tightly connected by RpoS to general cellular stress responses and cell physiology, it is difficult to separate transmission-promoting conditions in what is clearly a multifactorial and complex regulatory web. Frontiers Media S.A. 2017-09-29 /pmc/articles/PMC5626856/ /pubmed/29033900 http://dx.doi.org/10.3389/fmicb.2017.01734 Text en Copyright © 2017 Dulebohn, Richards, Su, Lawrence and Gherardini. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Dulebohn, Daniel P.
Richards, Crystal L.
Su, Hua
Lawrence, Kevin A.
Gherardini, Frank C.
Weak Organic Acids Decrease Borrelia burgdorferi Cytoplasmic pH, Eliciting an Acid Stress Response and Impacting RpoN- and RpoS-Dependent Gene Expression
title Weak Organic Acids Decrease Borrelia burgdorferi Cytoplasmic pH, Eliciting an Acid Stress Response and Impacting RpoN- and RpoS-Dependent Gene Expression
title_full Weak Organic Acids Decrease Borrelia burgdorferi Cytoplasmic pH, Eliciting an Acid Stress Response and Impacting RpoN- and RpoS-Dependent Gene Expression
title_fullStr Weak Organic Acids Decrease Borrelia burgdorferi Cytoplasmic pH, Eliciting an Acid Stress Response and Impacting RpoN- and RpoS-Dependent Gene Expression
title_full_unstemmed Weak Organic Acids Decrease Borrelia burgdorferi Cytoplasmic pH, Eliciting an Acid Stress Response and Impacting RpoN- and RpoS-Dependent Gene Expression
title_short Weak Organic Acids Decrease Borrelia burgdorferi Cytoplasmic pH, Eliciting an Acid Stress Response and Impacting RpoN- and RpoS-Dependent Gene Expression
title_sort weak organic acids decrease borrelia burgdorferi cytoplasmic ph, eliciting an acid stress response and impacting rpon- and rpos-dependent gene expression
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5626856/
https://www.ncbi.nlm.nih.gov/pubmed/29033900
http://dx.doi.org/10.3389/fmicb.2017.01734
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