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Testing the Role of Multicopy Plasmids in the Evolution of Antibiotic Resistance
Published on: May 2, 2018
Genome evolution and plasticity of Serratia marcescens, an important multidrug-resistant nosocomial pathogen
Atsushi Iguchi1, Yutaka Nagaya2, Elizabeth Pradel3
1Interdisciplinary Research Organization, University of Miyazaki, JapanPresent address: Department of Animal and Grassland Sciences, Faculty of Agriculture, University of Miyazaki, Japan.
Abstract:
Serratia marcescens is an important nosocomial pathogen that can cause an array of infections, most notably of the urinary tract and bloodstream. Naturally, it is found in many environmental niches, and is capable of infecting plants and animals. The emergence and spread of multidrug-resistant strains producing extended-spectrum or metallo beta-lactamases now pose a threat to public health worldwide. Here we report the complete genome sequences of two carefully selected S. marcescens strains, a multidrug-resistant clinical isolate (strain SM39) and an insect isolate (strain Db11). Our comparative analyses reveal the core genome of S. marcescens and define the potential metabolic capacity, virulence, and multidrug resistance of this species. We show a remarkable intraspecies genetic diversity, both at the sequence level and with regards genome flexibility, which may reflect the diversity of niches inhabited by members of this species. A broader analysis with other Serratia species identifies a set of approximately 3,000 genes that characterize the genus. Within this apparent genetic diversity, we identified many genes implicated in the high virulence potential and antibiotic resistance of SM39, including the metallo beta-lactamase and multiple other drug resistance determinants carried on plasmid pSMC1. We further show that pSMC1 is most closely related to plasmids circulating in Pseudomonas species. Our data will provide a valuable basis for future studies on S. marcescens and new insights into the genetic mechanisms that underlie the emergence of pathogens highly resistant to multiple antimicrobial agents.
Insights
Serratia marcescens, a multidrug-resistant pathogen, shows significant genetic diversity. Its genome sequencing reveals key virulence and resistance genes, offering insights into emerging infectious threats.
Area of Science:
- Microbiology
- Genomics
- Pathogen Research
Background:
- Serratia marcescens is a significant nosocomial pathogen causing urinary tract and bloodstream infections.
- Multidrug-resistant strains producing extended-spectrum or metallo beta-lactamases are a global public health concern.
- The species naturally inhabits diverse environmental niches, infecting plants and animals.
Purpose of the Study:
- To determine the complete genome sequences of a multidrug-resistant clinical isolate (SM39) and an insect isolate (Db11) of Serratia marcescens.
- To conduct comparative genomic analyses to understand the core genome, metabolic capacity, virulence, and multidrug resistance of S. marcescens.
- To identify genetic factors contributing to the emergence of multidrug-resistant pathogens.
Main Methods:
- Whole-genome sequencing of two S. marcescens strains (SM39 and Db11).
- Comparative genomic analysis of S. marcescens strains and other Serratia species.
- Plasmid analysis to identify genetic determinants of antibiotic resistance.
Main Results:
- Remarkable intraspecies genetic diversity in S. marcescens, including sequence variation and genome flexibility.
- Identification of approximately 3,000 core genes characterizing the Serratia genus.
- Discovery of virulence and antibiotic resistance genes in strain SM39, including metallo beta-lactamase on plasmid pSMC1, which is related to Pseudomonas plasmids.
Conclusions:
- The genetic diversity of S. marcescens may reflect its adaptation to various ecological niches.
- The study provides a foundation for future research on S. marcescens.
- Genomic insights into multidrug resistance mechanisms are crucial for combating emerging infectious diseases.
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