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Adela Straskova

Researcher at University of Defence

Publications -  11
Citations -  271

Adela Straskova is an academic researcher from University of Defence. The author has contributed to research in topics: Francisella tularensis & Virulence. The author has an hindex of 6, co-authored 11 publications receiving 241 citations. Previous affiliations of Adela Straskova include Swedish Defence Research Agency & Academy of Sciences of the Czech Republic.

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Tetratricopeptide repeat motifs in the world of bacterial pathogens: role in virulence mechanisms.

TL;DR: The current knowledge of the TPR-containing proteins involved in virulence mechanisms of bacterial pathogens are summarized while highlighting the importance of TPR motifs for the proper functioning of class II chaperones of a type III secretion system in the pathogenesis of Yersinia, Pseudomonas, and Shigella.
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Proteome analysis of an attenuated Francisella tularensis dsbA mutant: identification of potential DsbA substrate proteins.

TL;DR: Using a combination of classical and shotgun proteome analyses, several proteins that accumulated in fractions enriched for membrane-associated proteins in the dsbA mutant are identified as substrate candidates for the DsbA disulfide oxidoreductase as well as being responsible for the virulence attenuation of the dSBA mutant.
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Deletion of IglH in virulent Francisella tularensis subsp. holarctica FSC200 strain results in attenuation and provides protection against the challenge with the parental strain.

TL;DR: It is shown that the iglH gene is necessary for intracellular growth and escape of F. tularensis from phagosomes and is avirulent in a mouse model of infection and persists in the organs for about three weeks after infection.
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Francisella tularensis subsp. holarctica DsbA homologue: a thioredoxin-like protein with chaperone function.

TL;DR: Recombinant protein analysis revealed that the active site CXXC as well as the cis-proline residue and the FKBP_N domain are necessary for correct thiol/disulphide oxidoreductase activity.
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Francisella tularensis type B ΔdsbA mutant protects against type A strain and induces strong inflammatory cytokine and Th1-like antibody response in vivo.

TL;DR: Results show that vaccination with ΔdsbA/F SC200 mutant, but not ΔiglH/FSC200 mutants, induces an early innate inflammatory response leading to strong Th1-like antibody response, and elicited protection against the subsequent challenge with type A SCHU S4 strain in mice.