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Published on: March 17, 2014
Pseudomonas aeruginosa Alters Peptidoglycan Composition under Nutrient Conditions Resembling Cystic Fibrosis Lung
Erin M Anderson1, Neethu Shaji Saji1, Alexander C Anderson1
1Department of Molecular and Cellular Biology, University of Guelphgrid.34429.38, Guelph, Ontario, Canada.
Abstract:
Epidemic strains of Pseudomonas aeruginosa are highly virulent opportunistic pathogens with increased transmissibility and enhanced antimicrobial resistance. Understanding the cellular mechanisms behind this heightened virulence and resistance is critical. Peptidoglycan (PG) is an integral component of P. aeruginosa cells that is essential to its survival and a target for antimicrobials. Here, we examined the global PG composition of two P. aeruginosa epidemic strains, LESB58 and LESlike1, and compared them to the common laboratory strains PAO1 and PA14. We also examined changes in PG composition when the strains were cultured under nutrient conditions that resembled cystic fibrosis lung infections. We identified 448 unique muropeptides and provide the first evidence for stem peptides modified with O-methylation, meso-diaminopimelic acid (mDAP) deamination, and novel substitutions of mDAP residues within P. aeruginosa PG. Our results also present the first evidence for both d,l- and l,d-endopeptidase activity on the PG sacculus of a Gram-negative organism. The PG composition of the epidemic strains varied significantly when grown under conditions resembling cystic fibrosis (CF) lung infections, showing increases in O-methylated stem peptides and decreases in l,d-endopeptidase activity as well as an increased abundance of de-N-acetylated sugars and l,d-transpeptidase activity, which are related to bacterial virulence and antibiotic resistance, respectively. We also identified strain-specific changes where LESlike1 increased the addition of unique amino acids to the terminus of the stem peptide and LESB58 increased amidase activity. Overall, this study demonstrates that P. aeruginosa PG composition is primarily influenced by nutrient conditions that mimic the CF lung; however, inherent strain-to-strain differences also exist. IMPORTANCE Using peptidoglycomics to examine the global composition of the peptidoglycan (PG) allows insights into the enzymatic activity that functions on this important biopolymer. Changes within the PG structure have implications for numerous physiological processes, including virulence and antimicrobial resistance. The identification of highly unique PG modifications illustrates the complexity of this biopolymer in Pseudomonas aeruginosa. Analyzing the PG composition of clinical P. aeruginosa epidemic strains provides insights into the increased virulence and antimicrobial resistance of these difficult-to-eradicate infections.
Insights
Pseudomonas aeruginosa epidemic strains show significant changes in peptidoglycan (PG) composition under cystic fibrosis conditions, revealing novel modifications linked to increased virulence and antibiotic resistance.
Area of Science:
- Microbiology
- Biochemistry
- Molecular Biology
Background:
- Pseudomonas aeruginosa epidemic strains exhibit high virulence, transmissibility, and antimicrobial resistance.
- Peptidoglycan (PG) is crucial for bacterial survival and a target for antimicrobials.
- Understanding PG composition is key to addressing P. aeruginosa virulence and resistance.
Purpose of the Study:
- To analyze the global peptidoglycan (PG) composition of P. aeruginosa epidemic strains (LESB58, LESlike1) and laboratory strains (PAO1, PA14).
- To investigate how PG composition changes under nutrient conditions mimicking cystic fibrosis (CF) lung infections.
- To identify novel PG modifications and enzymatic activities related to P. aeruginosa virulence and resistance.
Main Methods:
- Peptidoglycomics analysis to determine global PG composition.
- Comparison of PG composition between epidemic and laboratory strains.
- Culturing strains under simulated CF lung infection conditions.
Main Results:
- Identified 448 unique muropeptides, including novel O-methylation, meso-diaminopimelic acid (mDAP) deamination, and mDAP substitutions.
- First evidence of both d,l- and l,d-endopeptidase activity on Gram-negative PG.
- Significant PG compositional changes in epidemic strains under CF conditions: increased O-methylated stem peptides, decreased l,d-endopeptidase activity, increased de-N-acetylated sugars, and enhanced l,d-transpeptidase activity.
- Strain-specific modifications observed: LESlike1 added unique amino acids, LESB58 increased amidase activity.
Conclusions:
- P. aeruginosa PG composition is primarily shaped by CF lung-mimicking nutrient conditions, with strain-specific variations also present.
- Novel PG modifications and enzymatic activities identified contribute to the heightened virulence and antimicrobial resistance of epidemic strains.
- This peptidoglycomics approach provides crucial insights into the complex PG structure and its role in P. aeruginosa pathogenesis and treatment resistance.
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