Type VI secretion is a major virulence determinant in Burkholderia mallei

@article{Schell2007TypeVS,
  title={Type VI secretion is a major virulence determinant in Burkholderia mallei},
  author={Mark A. Schell and Ricky L. Ulrich and Wilson J. Ribot and Ernst E. Brueggemann and Harry B. Hines and Dan Chen and Lyla Lipscomb and H. Stanley Kim and Jan Mr{\'a}zek and William C. Nierman and David DeShazer},
  journal={Molecular Microbiology},
  year={2007},
  volume={64},
  url={https://api.semanticscholar.org/CorpusID:25690886}
}
It is shown with expression profiling that overexpression of virAG resulted in transcriptional activation of ∼60 genes, including some involved in capsule production, actin‐based intracellular motility, and type VI secretion (T6S) in hamsters, and BMAA0742 was secreted by the T6S system when virAG was overexpressed.

Burkholderia mallei and Burkholderia pseudomallei Cluster 1 Type VI Secretion System Gene Expression Is Negatively Regulated by Iron and Zinc

Findings indicate that in addition to being positively regulated by VirAG, B. mallei and B. pseudomallei T6SS-1 gene expression is negatively regulated by iron and zinc.

Regulation of Type VI Secretion System during Burkholderia pseudomallei Infection

Novel evidence is provided that virAG, bprC, and tssAB are critical for T6SS-1 function in macrophages, and virAG and bPRC regulator mutants were avirulent in mice, demonstrating the absolute dependence of T6 SS-1 expression on these regulators in vivo.

The Cluster 1 Type VI Secretion System Is a Major Virulence Determinant in Burkholderia pseudomallei

The results suggest that the cluster 1 T6SS is essential for virulence and plays an important role in the intracellular lifestyle of B. pseudomallei.

Burkholderia cenocepacia utilizes a type VI secretion system for bacterial competition

It is concluded that B. cenocepacia T6SS‐1 plays an important role in bacterial competition for this organism, and probably in all Burkholderia species that possess this system, thereby broadening the range of species that utilize the T 6SS for this purpose.

VgrG-5 Is a Burkholderia Type VI Secretion System-Exported Protein Required for Multinucleated Giant Cell Formation and Virulence

ABSTRACT The type VI secretion system (T6SS) has emerged as a critical virulence factor for the group of closely related Burkholderia spp. that includes Burkholderia pseudomallei, B. mallei, and B.

A Type VI Secretion System Encoding Locus Is Required for Bordetella bronchiseptica Immunomodulation and Persistence In Vivo

D disruption of a gene within locus encoding a putative T6SS in Bordetella bronchiseptica strain RB50 is described, revealing a natural host infection system in which to interrogate T 6SS contributions to immunomodulation and pathogenesis.

Novel Burkholderia mallei Virulence Factors Linked to Specific Host-Pathogen Protein Interactions

Results point to the importance of these pathogen proteins in modulating host ubiquitination pathways, phagosomal escape, and actin-cytoskeleton rearrangement processes.

The Burkholderia Type VI Secretion System 5: Composition, Regulation and Role in Virulence

Disruption of the T6SS-5 in B. thailandensis causes a drastic attenuation of virulence in wildtype but not in mice lacking the central innate immune adapter protein MyD88, suggesting that the T 6SS- 5 is deployed by the bacteria to overcome innate immune responses.

Identification of a regulatory cascade controlling Type III Secretion System 3 gene expression in Burkholderia pseudomallei

The complete delineation of the bspR initiated T3SS regulatory cascade not only contributes to the understanding of B. pseudomallei pathogenesis but also provides an important example of how bacterial pathogens could co‐opt and integrate various regulatory motifs to form a new regulatory network adapted for its own purposes.

Comparative Genomics and an Insect Model Rapidly Identify Novel Virulence Genes of Burkholderia mallei

In silico genomic subtraction is used to generate their virulome, a set of 650 putative virulence-related genes shared by B. pseudomallei and B. mallei but not present in five closely related nonpathogenic Burkholderia species and identified three new potential virulence genes.
...

Identification of a Burkholderia mallei polysaccharide gene cluster by subtractive hybridization and demonstration that the encoded capsule is an essential virulence determinant.

The results presented here demonstrate that the capsular polysaccharide of B. mallei is required for production of disease in two animal models of glanders infection and is a major virulence factor.

Quorum Sensing: a Transcriptional Regulatory System Involved in the Pathogenicity of Burkholderia mallei

Findings demonstrate that B. mallei carries multiple luxIR homologues that either directly or indirectly regulate the biosynthesis of an essential virulence factor(s) that contributes to the pathogenicity of B.mallei in vivo.

The Animal Pathogen-Like Type III Secretion System Is Required for the Intracellular Survival of Burkholderia mallei within J774.2 Macrophages

It is demonstrated that this bacterial protein delivery system is required for intracellular growth of B. mallei in J774.2 cells, formation of macrophage membrane protrusions, actin polymerization, and phagosomal escape.

Identification of a bacterial factor required for actin‐based motility of Burkholderia pseudomallei

It is reported that purified truncated BimA protein binds monomeric actin in a concentration‐dependent manner in cosedimentation assays and that BIMA stimulates actin polymerization in vitro in a manner independent of the cellular Arp2/3 complex.

Type III Secretion: a Virulence Factor Delivery System Essential for the Pathogenicity of Burkholderia mallei

Mutagenesis demonstrated that a functional TTSS was required for the full pathogenicity of ATCC 23344 in the BALB/c mouse and Syrian hamster models of infection, however, vaccination with each mutant failed to elicit a protective immunity against challenge with wild-type AT CC 23344.

Proteomic and microarray characterization of the AggR regulon identifies a pheU pathogenicity island in enteroaggregative Escherichia coli

Using proteomic and microarray analysis, it is identified for the first time that AggR activates the expression of chromosomal genes, including 25 contiguous genes (aaiA–Y), which are localized to a 117 kb pathogenicity island (PAI) inserted at pheU.

CmeABC Functions as a Multidrug Efflux System in Campylobacter jejuni

It is formally established that CmeABC functions as a tripartite multidrug efflux pump that contributes to the intrinsic resistance of C. jejuni to a broad range of structurally unrelated antimicrobial agents.

Bacterial genome adaptation to niches: Divergence of the potential virulence genes in three Burkholderia species of different survival strategies

The data suggest that divergent evolution of a small set of genes, rather than acquisition or loss of pathogenic islands, is associated with the development of different life styles in these bacteria of similar genomic contents.

Identification of a conserved bacterial protein secretion system in Vibrio cholerae using the Dictyostelium host model system

It is shown that vas genes are required for cytotoxicity of V. cholerae cells toward Dictyostelium amoebae and mammalian J774 macrophages by a contact-dependent mechanism, and it is proposed that these genes encode a prototypic “type VI” secretion system.

Use of proteomics to identify novel virulence determinants that are required for Edwardsiella tarda pathogenesis

Two possible secretion systems (TTSS and Evp) that are vital for E. tarda pathogenesis are identified and similar gene clusters are widely distributed in other pathogens such as Escherichia, Salmonella, Vibrio and Yersinia species with unknown functions.
...