Life Science and Technology News

Role of Hydrogen Sulfide in the Expression of Iron Uptake Genes in Escherichia coli

Researchers establish the role of YgaV, a hydrogen sulfide dependent transcription factor in regulating iron uptake dynamics in Escherichia coli

October 22, 2024

Hydrogen sulfide (H₂S) plays an important role in various cellular activities such as oxidative stress response through activation of iron uptake in bacteria. However, the underlying mechanism by which intracellular H₂S regulates iron uptake remains unknown. The H₂S-/supersulfides-responsive transcription factor, YgaV is crucial for activating iron uptake in Escherichia coli report researchers from Institute of Science Tokyo, Japan, providing insights into the intracellular dynamics that guides oxidative stress response and antibiotic resistance.

Impact of Hyperaccumulation of Intracellular Hydrogen Sulfide on Iron Uptake in Escherichia coli

Increased Intracellular H₂S Levels Enhances Iron Uptake in Escherichia coli
Nonoyama et al. (2024) | mBio

Antibiotic resistance and oxidative stress response are important biological mechanisms that help bacteria thrive, especially pathogenic bacteria like Escherichia coli. Hydrogen sulfide (H₂S), a chemical messenger molecule, regulates several intracellular activities in bacteria such as responses to oxidative stress and antibiotics. Increased iron uptake triggered by intracellular H₂S levels has been identified in the pathogenic bacterium Vibrio cholerae, contributing to its oxidative stress response. However, the precise mechanism behind H₂S dependent cellular responses of E. coli remains unclear.

In this light, a team of researchers led by Professor Shinji Masuda from the Department of Life Science & Technology, Institute of Science Tokyo, Japan have attempted to unravel the underlying mechanism and relationship between intracellular H₂S and iron uptake in E. coli. They utilized a genetically manipulated wild-type (WT) E. coli strain overexpressing mstA, which encodes 3-mercaptopyruvate sulfur transferase enzyme responsible for the production of H₂S. Additionally, they employed advanced genetic sequencing techniques and assays to identify the molecular pathways involved in the overall regulation of iron uptake in response to H₂S availability. Their findings were published in the mBio journal.

Sharing the motivation and rationale behind the present research, Masuda states, “Our research group had previously identified and characterized the arsenic repressor-type H₂S-/supersulfide-responsive transcription factor SqrR in the purple photosynthetic bacterium Rhodobacter capsulatus, where SqrR regulated gene expression in response to H₂S availability. YgaV, the SqrR homolog in E. coli, has also been reported for repressing the transcription of anaerobic respiratory genes in the absence of extracellular sulfide. This motivated our team to further investigate the relationship between intracellular H₂S, YgaV dependent transcription, and iron uptake in E. coli.”

Initially, the researchers observed that the WT strain overexpressing mstA produced elevated levels of intracellular H₂S which resulted in significantly higher antibiotic resistance. Subsequently, they conducted RNA sequencing analysis and found that certain genes were upregulated in response to the overproduction of H₂S. They noted a 10-fold increase in the genetic transcript levels of tcyP, which encodes the L-cysteine (a sulphur containing amino acid) transporter. In addition, they found that cysteinyl-tRNA synthase gene, which catalyzes the synthesis of supersulfides-molecules with self-linked sulphur atoms, was particularly upregulated. Supersulfides can directly inactivate β-lactam antibiotics and contribute to the overall antibiotic resistance in E. coli with mstA overexpression. Moreover, genes associated with antibiotic efflux pumps were upregulated and dipeptide/heme transporter genes were downregulated in the WT strain overexpressing mstA, indicative of the influence of H₂S hyperaccumulation on iron uptake.

Furthermore, the researchers confirmed the role of YgaV, a H₂S-/supersulfide-responsive transcription factor, in the upregulation of iron uptake genes in E. coli. By utilizing a ΔygaV mutant strain of E. coli where ygaV is not expressed but mstA is overexpressed, they discovered that the expression of iron uptake genes, namely, fes, fepA, fhuE, fhuF, nfeF, and cirA was dependent on the presence of YgaV, which in turn is dependent on intracellular H₂S levels.

"Our study provides valuable insights into the iron uptake dynamics in E. coli and substantiates the role of H₂S-dependent YgaV in regulating the overall oxidative stress response and antibiotic resistance,” concludes Masuda.

Reference

Authors:	Shouta Nonoyama¹, Shintaro Maeno², Yasuhiro Gotoh³, Ryota Sugimoto^1,4, Kan Tanaka⁴, Tetsuya Hayashi³, and Shinji Masuda¹* *Corresponding author
Title:	Increased intracellular H₂S levels enhance iron uptake in Escherichia coli
Journal:	mBio
Affiliations:	¹ Department of Life Science & Technology, Tokyo Institute of Technology, Japan ² Department of Biological Chemistry, Yamaguchi University, Japan ³ Department of Bacteriology, Kyushu University, Japan ⁴ Laboratory for Chemistry and Life Science, Tokyo Institute of Technology, Japan
DOI:	10.1128/mbio.01991-24