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Published on: June 29, 2017
The Capsule Regulatory Network of Klebsiella pneumoniae Defined by density-TraDISort
Matthew J Dorman1, Theresa Feltwell1, David A Goulding1
1Wellcome Sanger Institute, Hinxton, Cambridgeshire, United Kingdom.
Insights
We developed density-TraDISort to identify genes regulating Klebsiella pneumoniae capsule production. This method revealed a complex network of regulators essential for virulence and provides a tool for studying capsule synthesis in other bacteria.
Area of Science:
- Microbiology
- Genetics
- Bacterial Pathogenesis
Background:
- Klebsiella pneumoniae infections pose a significant threat, particularly to infants and immunocompromised individuals.
- Emergence of hypervirulent and multidrug-resistant K. pneumoniae strains heightens healthcare concerns.
- Capsule overproduction is a key factor in K. pneumoniae hypervirulence, but its regulation and synthesis pathways remain incompletely understood.
Purpose of the Study:
- To develop and apply a novel method for genome-wide identification of genes influencing Klebsiella pneumoniae capsule production.
- To elucidate the regulatory network governing capsule biosynthesis in clinically relevant K. pneumoniae strains.
- To investigate the impact of identified capsule regulators on bacterial virulence and serum resistance.
Main Methods:
- Development of density-TraDISort, a high-throughput screening method combining density gradient centrifugation with transposon insertion sequencing.
- Application of density-TraDISort to identify genes affecting capsule production in K. pneumoniae NTUH-K2044 (K1) and ATCC 43816 (K2).
- Validation of screen results through targeted knockout mutants and investigation of specific regulatory genes (ArgR, MprA/KvrB, SlyA/KvrA, Sap transporter).
Main Results:
- Identification of multiple genes essential for K. pneumoniae capsule production and putative capsule suppressors.
- Demonstration that regulators like ArgR, MprA/KvrB, SlyA/KvrA, and Sap transporter influence capsule amount, architecture, serum resistance, and virulence.
- Characterization of capsule production as a central node in a complex regulatory network involving global regulators and environmental cues.
- Finding that most capsule regulatory genes reside within the core genome.
Conclusions:
- Capsule regulation in K. pneumoniae is intricate, involving numerous global regulators and environmental signals.
- The identified regulators play crucial roles in modulating capsule synthesis, serum resistance, and overall virulence.
- The developed density-TraDISort method is a valuable tool for studying capsule regulation in K. pneumoniae and can be adapted for other capsulated bacteria.
- Findings expand the understanding of K. pneumoniae pathogenesis and offer potential targets for therapeutic intervention.
Abstract:
Klebsiella pneumoniae infections affect infants and the immunocompromised, and the recent emergence of hypervirulent and multidrug-resistant K. pneumoniae lineages is a critical health care concern. Hypervirulence in K. pneumoniae is mediated by several factors, including the overproduction of extracellular capsule. However, the full details of how K. pneumoniae capsule biosynthesis is achieved or regulated are not known. We have developed a robust and sensitive procedure to identify genes influencing capsule production, density-TraDISort, which combines density gradient centrifugation with transposon insertion sequencing. We have used this method to explore capsule regulation in two clinically relevant Klebsiella strains, K. pneumoniae NTUH-K2044 (capsule type K1) and K. pneumoniae ATCC 43816 (capsule type K2). We identified multiple genes required for full capsule production in K. pneumoniae, as well as putative suppressors of capsule in NTUH-K2044, and have validated the results of our screen with targeted knockout mutants. Further investigation of several of the K. pneumoniae capsule regulators identified-ArgR, MprA/KvrB, SlyA/KvrA, and the Sap ABC transporter-revealed effects on capsule amount and architecture, serum resistance, and virulence. We show that capsule production in K. pneumoniae is at the center of a complex regulatory network involving multiple global regulators and environmental cues and that the majority of capsule regulatory genes are located in the core genome. Overall, our findings expand our understanding of how capsule is regulated in this medically important pathogen and provide a technology that can be easily implemented to study capsule regulation in other bacterial species.IMPORTANCE Capsule production is essential for K. pneumoniae to cause infections, but its regulation and mechanism of synthesis are not fully understood in this organism. We have developed and applied a new method for genome-wide identification of capsule regulators. Using this method, many genes that positively or negatively affect capsule production in K. pneumoniae were identified, and we use these data to propose an integrated model for capsule regulation in this species. Several of the genes and biological processes identified have not previously been linked to capsule synthesis. We also show that the methods presented here can be applied to other species of capsulated bacteria, providing the opportunity to explore and compare capsule regulatory networks in other bacterial strains and species.
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