The longitudinal expression of P. aeruginosa reference genes in infection-mimicking media

Quantitative reverse transcription PCR (RT-qPCR) is a popular and reliable tool for monitoring fluctuations in functional bacterial gene expression. A necessary step of the qRT-qPCR process is the use of a reference gene, which acts to distinguish between technical bias and true biological variation. Many reference genes have been defined for bacterial species; however, few studies have validated their stability across strain types and environmental test conditions. In this study of <i>Pseudomonas aeruginosa</i>, the expression consistency of seven commonly used reference genes (<i>rpoD</i>, <i>proC</i>, <i>rpoS</i>, <i>16S</i>, <i>algD</i>, <i>gyrA</i> and <i>ampC</i>) was assessed in <i>P. aeruginosa</i> laboratory (PAO1) and clinical (LESB65) isolates grown in Lysogeny broth, synthetic cystic fibrosis (CF) media 2 (SCFM2) and CF lung media (CFLM) at various growth time points (2, 6, 24 and 72 h). The stability of the reference genes was then ranked using the RefFinder programme, and three differentially ranked (<i>rpoS</i>, <i>16S</i> and <i>ampC</i>) were used to interpret the expression of a <i>Pseudomonas</i> virulence-related gene (<i>exoS</i>). The results showed that <i>16S</i> was the only reference gene that was quantifiably expressed by both <i>P. aeruginosa</i> strains grown in all media types at all growth times. Furthermore, analysing the expression of <i>exoS</i> with different reference genes significantly influenced the calculated expression of <i>exoS</i> in SCFM2 and CFLM. This study has identified a suitable reference gene for RT-qPCR with <i>P. aeruginosa</i> grown in complex respiratory-mimicking media. The results presented here also highlight the importance of validating reference gene expression under the chosen experimental conditions and increase our understanding of how pathogen biology can fluctuate across diverse conditions. Such knowledge is paramount for the development of novel therapeutics, including antimicrobials and anti-virulence agents.

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Journal
Microbiology
Published
2026-01-12
DOI
https://doi.org/10.1099/mic.0.001627
Primary Topic
Molecular Biology Techniques and Applications
Type
article
Field-Weighted Citation Impact
0.00

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article

The longitudinal expression of P. aeruginosa reference genes in infection-mimicking media

Daniel R. Neill, Sian Pottenger, Hollie Leighton, T. Hibbert et al.
Microbiology
Molecular Biology Techniques and Applications
article

The longitudinal expression of P. aeruginosa reference genes in infection-mimicking media

Daniel R. Neill, Sian Pottenger, Hollie Leighton, T. Hibbert, Joanne L. Fothergill
article en

Abstract

Quantitative reverse transcription PCR (RT-qPCR) is a popular and reliable tool for monitoring fluctuations in functional bacterial gene expression. A necessary step of the qRT-qPCR process is the use of a reference gene, which acts to distinguish between technical bias and true biological variation. Many reference genes have been defined for bacterial species; however, few studies have validated their stability across strain types and environmental test conditions. In this study of <i>Pseudomonas aeruginosa</i>, the expression consistency of seven commonly used reference genes (<i>rpoD</i>, <i>proC</i>, <i>rpoS</i>, <i>16S</i>, <i>algD</i>, <i>gyrA</i> and <i>ampC</i>) was assessed in <i>P. aeruginosa</i> laboratory (PAO1) and clinical (LESB65) isolates grown in Lysogeny broth, synthetic cystic fibrosis (CF) media 2 (SCFM2) and CF lung media (CFLM) at various growth time points (2, 6, 24 and 72 h). The stability of the reference genes was then ranked using the RefFinder programme, and three differentially ranked (<i>rpoS</i>, <i>16S</i> and <i>ampC</i>) were used to interpret the expression of a <i>Pseudomonas</i> virulence-related gene (<i>exoS</i>). The results showed that <i>16S</i> was the only reference gene that was quantifiably expressed by both <i>P. aeruginosa</i> strains grown in all media types at all growth times. Furthermore, analysing the expression of <i>exoS</i> with different reference genes significantly influenced the calculated expression of <i>exoS</i> in SCFM2 and CFLM. This study has identified a suitable reference gene for RT-qPCR with <i>P. aeruginosa</i> grown in complex respiratory-mimicking media. The results presented here also highlight the importance of validating reference gene expression under the chosen experimental conditions and increase our understanding of how pathogen biology can fluctuate across diverse conditions. Such knowledge is paramount for the development of novel therapeutics, including antimicrobials and anti-virulence agents.

MicrobiologyVol. 172(1)
University of Liverpool (GB), University of Dundee (GB)
Cystic Fibrosis Foundation, University of Dundee, Medical Research Council
Life in Land
Openalex Percentile: Top 89%
Molecular Biology Techniques and Applications
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