Cited by 14Bacterial Genetics and BiotechnologyEscherichia coli research studiesEnterobacteriaceae and Cronobacter Research

Conserved metabolic regulator ArcA responds to oxygen availability, iron limitation, and cell envelope perturbations during bacteremia

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Brown, Aric N., Anderson, Mark T., Smith, Sara N., Bachman, Michael A., Mobley, Harry L. T.·2023·mBio

Published version of a preprint

Abstract

Gram-negative facultative anaerobes often cause bacteremia, a systemic infection associated with severe clinical outcomes. ArcAB, a two-component regulatory system that represses aerobic respiration, is a key mediator of metabolic adaptation for such bacteria. Using targeted mutational analysis informed by global genetic screens, we identified the arcA gene as promoting fitness of Citrobacter freundii , Klebsiella pneumoniae , and Serratia marcescens but not Escherichia coli in a murine model of bacteremia. arcA mutants exhibit a dysregulated response to changes in oxygen availability, iron limitation, and membrane perturbations, which bacterial cells experience during infection. The genetic response of the arcA mutants to the cationic antimicrobial peptide polymyxin B supports an expanded role for ArcA as an activator in response to membrane damage. ArcA function is linked to electron transport chain activity based on its response to proton motive force uncoupling by carbonylcyanide- m -chlorophenylhydrazone (CCCP). Differences in lactate, acetate, and lactate dehydrogenase activity between arcA mutant and wild-type cells following CCCP treatment support an ArcA-mediated shift to fermentation independent of oxygen availability. This study highlights the semi-conserved role of ArcA during bacteremia and consolidates infection phenotypes into a comprehensive model based on respiratory activity. IMPORTANCE: Infections of the bloodstream are life-threatening and can result in sepsis. Gram-negative bacteria cause a significant portion of bloodstream infections, which is also referred to as bacteremia. The long-term goal of our work is to understand how such bacteria establish and maintain infection during bacteremia. We have previously identified the transcription factor ArcA, which promotes fermentation in bacteria, as a likely contributor to the growth and survival of bacteria in this environment. Here, we study ArcA in the Gram-negative species Citrobacter freundii , Klebsiella pneumoniae, and Serratia marcescens . Our findings aid in determining how these bacteria sense their environment, utilize nutrients, and generate energy while countering the host immune system. This information is critical for developing better models of infection to inform future therapeutic development.

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Authors
Brown, A. N., Anderson, M. T., Smith, S. N., Bachman, M. A., & Mobley, H. L. T.
Affiliations
University of Michigan (US)
Corresponding author
Mobley, Harry L. T.
Venue
mBio
Published
2023-10-31
Volume
14
Issue
5
Pages
e0144823-e0144823
ISSN
2150-7511 (ISSN-L)
OpenAlex
W4386529760
Cited by
14
References
90
Citations by year
2026: 7 · 2025: 3 · 2024: 4
FWCI
2.32
Type
journal article
Language
en
Open access
Locations
  • mBio (publishedVersion, cc-by)
  • bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
  • American Heart Association (828854)
  • HHS | National Institutes of Health (AI134731)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Endocrinology › Escherichia coli research studies
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Endocrinology › Enterobacteriaceae and Cronobacter Research
Keywords
Arca, bacteremia, oxygen availability, iron limitation, polymyxin B, membrane damage, electron transport chain, fermentation, lactate dehydrogenase, Citrobacter freundii, Klebsiella pneumoniae, Serratia marcescens, bacterial metabolism, sepsis
MeSH terms
Gram-Negative Bacteria, Humans, Iron, Klebsiella pneumoniae, Bacteremia, Sepsis

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