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RNA Isolation of Pseudomonas aeruginosa Colonizing the Murine Gastrointestinal Tract
Published on: September 28, 2011
The Pseudomonas aeruginosa PrrF Small RNAs Regulate Iron Homeostasis during Acute Murine Lung Infection
Alexandria A Reinhart1, Angela T Nguyen2, Luke K Brewer2
1University of Maryland, School of Medicine, Department of Microbiology and Immunology, Baltimore, Maryland, USA.
Abstract:
Pseudomonas aeruginosa is a Gram-negative opportunistic pathogen that requires iron for virulence. Iron homeostasis is maintained in part by the PrrF1 and PrrF2 small RNAs (sRNAs), which block the expression of iron-containing proteins under iron-depleted conditions. The PrrF sRNAs also promote the production of the Pseudomonas quinolone signal (PQS), a quorum sensing molecule that activates the expression of several virulence genes. The tandem arrangement of the prrF genes allows for expression of a third sRNA, PrrH, which is predicted to regulate gene expression through its unique sequence derived from the prrF1-prrF2 intergenic (IG) sequence (the PrrHIG sequence). Previous studies showed that the prrF locus is required for acute lung infection. However, the individual functions of the PrrF and PrrH sRNAs were not determined. Here, we describe a system for differentiating PrrF and PrrH functions by deleting the PrrHIG sequence [prrF(ΔHIG)]. Our analyses of this construct indicate that the PrrF sRNAs, but not PrrH, are required for acute lung infection by P. aeruginosa Moreover, we show that the virulence defect of the ΔprrF1-prrF2 mutant is due to decreased bacterial burden during acute lung infection. In vivo analysis of gene expression in lung homogenates shows that PrrF-mediated regulation of genes for iron-containing proteins is disrupted in the ΔprrF1-prrF2 mutant during infection, while the expression of genes that mediate PrrF-regulated PQS production are not affected by prrF deletion in vivo Combined, these studies demonstrate that regulation of iron utilization plays a critical role in P. aeruginosa's ability to survive during infection.
Insights
Pseudomonas aeruginosa requires iron for virulence, regulated by PrrF small RNAs (sRNAs). PrrF sRNAs, not PrrH, are essential for acute lung infection by controlling bacterial burden and iron utilization.
Area of Science:
- Microbiology
- Molecular Biology
- Infectious Diseases
Background:
- Pseudomonas aeruginosa is an opportunistic pathogen requiring iron for virulence.
- Iron homeostasis is partly regulated by PrrF1 and PrrF2 small RNAs (sRNAs), which inhibit iron-containing protein expression under iron deficiency.
- PrrF sRNAs also influence Pseudomonas quinolone signal (PQS) production, a quorum sensing molecule impacting virulence genes.
Purpose of the Study:
- To differentiate the functions of PrrF and PrrH sRNAs in Pseudomonas aeruginosa virulence.
- To investigate the role of the PrrF locus in acute lung infection.
- To elucidate the specific contributions of PrrF sRNAs and PrrH to P. aeruginosa pathogenesis.
Main Methods:
- Development of a system to differentiate PrrF and PrrH functions by deleting the PrrH intergenic (IG) sequence [prrF(ΔH_IG)].
- Analysis of the virulence of P. aeruginosa mutants in acute lung infection models.
- In vivo gene expression analysis in lung homogenates to assess PrrF-mediated regulation.
Main Results:
- PrrF sRNAs, but not PrrH, are essential for acute lung infection in P. aeruginosa.
- The virulence defect in ΔprrF1-prrF2 mutants is attributed to reduced bacterial burden during infection.
- PrrF-mediated regulation of iron-utilizing genes is impaired in ΔprrF1-prrF2 mutants during infection, while PQS production genes remain unaffected.
Conclusions:
- PrrF sRNAs play a critical role in P. aeruginosa virulence during acute lung infection.
- Regulation of iron utilization by PrrF sRNAs is crucial for P. aeruginosa survival in vivo.
- PrrH does not appear to be required for acute lung infection, suggesting specialized roles for PrrF sRNAs.
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