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Systems analysis of multiple regulator perturbations allows discovery of virulence factors in Salmonella.

ABSTRACT: Systemic bacterial infections are highly regulated and complex processes that are orchestrated by numerous virulence factors. Genes that are coordinately controlled by the set of regulators required for systemic infection are potentially required for pathogenicity.In this study we present a systems biology approach in which sample-matched multi-omic measurements of fourteen virulence-essential regulator mutants were coupled with computational network analysis to efficiently identify Salmonella virulence factors. Immunoblot experiments verified network-predicted virulence factors and a subset was determined to be secreted into the host cytoplasm, suggesting that they are virulence factors directly interacting with host cellular components. Two of these, SrfN and PagK2, were required for full mouse virulence and were shown to be translocated independent of either of the type III secretion systems in Salmonella or the type III injectisome-related flagellar mechanism.Integrating multi-omic datasets from Salmonella mutants lacking virulence regulators not only identified novel virulence factors but also defined a new class of translocated effectors involved in pathogenesis. The success of this strategy at discovery of known and novel virulence factors suggests that the approach may have applicability for other bacterial pathogens.

SUBMITTER: Yoon H

PROVIDER: S-EPMC3213010 | biostudies-literature | 2011 Jun

REPOSITORIES: biostudies-literature

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Systems analysis of multiple regulator perturbations allows discovery of virulence factors in Salmonella.

Yoon Hyunjin H Ansong Charles C McDermott Jason E JE Gritsenko Marina M Smith Richard D RD Heffron Fred F Adkins Joshua N JN

BMC systems biology 20110628

<h4>Background</h4>Systemic bacterial infections are highly regulated and complex processes that are orchestrated by numerous virulence factors. Genes that are coordinately controlled by the set of regulators required for systemic infection are potentially required for pathogenicity.<h4>Results</h4>In this study we present a systems biology approach in which sample-matched multi-omic measurements of fourteen virulence-essential regulator mutants were coupled with computational network analysis t ...[more]

PMID: 21711513

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Project description:As one of the most notorious and successful phytopathogenic bacteria, Ralstonia solanacearum controls the transition between long-term survival and pathogenic modes through an intricate regulatory network, the understanding of which remains incomplete despite years of effort. In this study, we identified PhcX, a previously uncharacterized response regulator in R. solanacearum, and uncovered its essential functions in modulating virulence and metabolism. The phcX deletion mutant exhibited substantial phenotypic alterations, including slower initial growth, altered response to host extract, reduced motilities, polygalacturonase activity, and exopolysaccharide production, elevated biofilm formation, delayed hypersensitive response, and impaired virulence. Moreover, ~16% of all genes were differentially expressed in the mutant, among which the genes associated with virulence, nitrogen metabolism, and regulation were overrepresented (e.g., most T3SS/T3Es genes). Many of these traits and genes were regulated by PhcX and the global virulence regulator PhcA, but 81.4% of the genes were regulated in opposite directions. The functions of PhcX were largely conserved in R. solanacearum EP1 and GMI1000 strains. Apparent orthologs of PhcX are widely distributed in Proteobacteria, including the LqsR quorum sensing (QS) response regulator in Legionella pneumophilia. Notably, our data suggest that phcX was originally part of the Lqs QS system but was decoupled from Lqs in Ralstonia/Cupriavidus, physically linked to the phc QS genes, and connected with the virulence regulatory network in Ralstonia during its evolution. The findings of this study contribute to a better understanding of the virulence and metabolism regulation mechanisms in R. solanacearum and shed light on the evolution of its complex regulatory network. IMPORTANCE The bacterial wilt caused by the soil-borne phytopathogen Ralstonia solanacearum is one of the most destructive crop diseases. To achieve a successful infection, R. solanacearum has evolved an intricate regulatory network to orchestrate the expression of an arsenal of virulence factors and fine-tune the allocation of energy. However, despite the wealth of knowledge gained in the past decades, many players and connections are still missing from the network. The importance of our study lies in the identification of PhcX, a novel conserved global regulator with critical roles in modulating the virulence and metabolism of R. solanacearum. PhcX affects many well-characterized regulators and exhibits contrasting modes of regulation from the central regulator PhcA on a variety of virulence-associated traits and genes. Our findings add a valuable piece to the puzzle of how the pathogen regulates its proliferation and infection, which is critical for understanding its pathogenesis and developing disease control strategies.

Dataset Information

Systems analysis of multiple regulator perturbations allows discovery of virulence factors in Salmonella.

Publications

Systems analysis of multiple regulator perturbations allows discovery of virulence factors in Salmonella.

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