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Antimicrobial properties of Pseudomonas strains producing the antibiotic mupirocin
Sandra Matthijs1, Corinne Vander Wauven1, Bertrand Cornu1
1Institut de Recherches Microbiologiques - Wiame, Campus du CERIA, 1 avenue Emile Gryson, bât 4B, B-1070 Bruxelles, Belgium.
Abstract:
Mupirocin is a polyketide antibiotic with broad antibacterial activity. It was isolated and characterized about 40 years ago from Pseudomonas fluorescens NCIMB 10586. To study the phylogenetic distribution of mupirocin producing strains in the genus Pseudomonas a large collection of Pseudomonas strains of worldwide origin, consisting of 117 Pseudomonas type strains and 461 strains isolated from different biological origins, was screened by PCR for the mmpD gene of the mupirocin gene cluster. Five mmpD(+) strains from different geographic and biological origin were identified. They all produced mupirocin and were strongly antagonistic against Staphylococcus aureus. Phylogenetic analysis showed that mupirocin production is limited to a single species. Inactivation of mupirocin production leads to complete loss of in vitro antagonism against S. aureus, except on certain iron-reduced media where the siderophore pyoverdine is responsible for the in vitro antagonism of a mupirocin-negative mutant. In addition to mupirocin some of the strains produced lipopeptides of the massetolide group. These lipopeptides do not play a role in the observed in vitro antagonism of the mupirocin producing strains against S. aureus.
Insights
Mupirocin antibiotic production is confined to a single Pseudomonas species. This antibiotic is crucial for antagonism against Staphylococcus aureus, though pyoverdine plays a role in specific conditions.
Area of Science:
- Microbiology
- Molecular Biology
- Biochemistry
Background:
- Mupirocin is a potent polyketide antibiotic with extensive antibacterial properties.
- It was first isolated from Pseudomonas fluorescens approximately 40 years ago.
- Understanding the distribution of mupirocin-producing strains is vital for antibiotic research.
Purpose of the Study:
- To investigate the phylogenetic distribution of mupirocin-producing Pseudomonas strains globally.
- To identify specific Pseudomonas species responsible for mupirocin biosynthesis.
- To elucidate the role of mupirocin and other metabolites in antagonism against Staphylococcus aureus.
Main Methods:
- Screening of a large collection of Pseudomonas strains (117 type strains, 461 isolates) using PCR for the mupirocin gene cluster component, mmpD.
- Identification of mupirocin-producing strains through molecular and phenotypic analyses.
- Phylogenetic analysis to determine the taxonomic distribution of mupirocin producers.
- In vitro antagonism assays against Staphylococcus aureus, including experiments with mupirocin-negative mutants and on iron-reduced media.
Main Results:
- Five mupirocin-producing strains were identified across diverse geographic and biological origins, all positive for the mmpD gene.
- Phylogenetic analysis revealed that mupirocin production is restricted to a single Pseudomonas species.
- Mupirocin production was essential for in vitro antagonism against Staphylococcus aureus, except on iron-reduced media where pyoverdine mediated antagonism.
- Some identified strains also produced massetolide lipopeptides, but these did not contribute to the observed antagonism against S. aureus.
Conclusions:
- Mupirocin production in Pseudomonas is taxonomically restricted to a single species.
- Mupirocin is the primary agent for in vitro antagonism against Staphylococcus aureus in these strains.
- Pyoverdine can mediate antagonism under specific iron-limited conditions, highlighting the complexity of microbial interactions.
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