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Françoise Laval

Researcher at University of Toulouse

Publications -  52
Citations -  3414

Françoise Laval is an academic researcher from University of Toulouse. The author has contributed to research in topics: Mycobacterium tuberculosis & Mycobacterium smegmatis. The author has an hindex of 30, co-authored 52 publications receiving 3107 citations. Previous affiliations of Françoise Laval include Centre national de la recherche scientifique & Paul Sabatier University.

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Reductive evolution and niche adaptation inferred from the genome of Mycobacterium ulcerans, the causative agent of Buruli ulcer

TL;DR: The complete 5.8-Mb genome sequence of M. ulcerans is reported and indicates that it has recently evolved via lateral gene transfer and reductive evolution from the generalist, more rapid-growing environmental species M. marinum to become a niche-adapted specialist.
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The Mycobacterium tuberculosis PhoPR two‐component system regulates genes essential for virulence and complex lipid biosynthesis

TL;DR: Functional evidence is provided for the PhoPR 2‐CS involvement in Mtb pathogenesis and it is suggested that a major reason for the attenuation observed in the phoP mutant is the absence of certain complex lipids that are known to be important for virulence.
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The virulence-associated two-component PhoP-PhoR system controls the biosynthesis of polyketide-derived lipids in Mycobacterium tuberculosis.

TL;DR: The results indicate that PhoP coordinately and positively regulates the synthesis of methyl-branched fatty acid-containing acyltrehaloses known to be restricted to pathogenic species of the M. tuberculosis complex, namely diacylt rehaloses, polyacyltre Haloses, and sulfolipids.
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Requirement for kasB in Mycobacterium mycolic acid biosynthesis, cell wall impermeability and intracellular survival: implications for therapy

TL;DR: The kasB mutants exhibited strikingly altered cell wall permeability, leading to a marked increase in susceptibility to lipophilic antibiotics and the host antimicrobial molecules defensin and lysozyme, and are identified as a novel target for therapeutic intervention in mycobacterial diseases.
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Evolutionary history of tuberculosis shaped by conserved mutations in the PhoPR virulence regulator

TL;DR: It is shown by genetic transfer and virulence experiments that specific mutations in a virulence regulator contribute to lower fitness and virosity of M. bovis and related strains for the human host, likely obstructing the capacity of causing overt disease needed for efficient human-to-human transmission.