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Very Early Blood Diffusion of the Active Lethal and Edema Factors of Bacillus anthracis After Intranasal Infection

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  • معلومة اضافية
    • Contributors:
      Unité de Biothérapies anti-Infectieuses et Immunité Brétigny-sur-Orge; Institut de Recherche Biomédicale des Armées Brétigny-sur-Orge (IRBA); Pathogénie des Toxi-infections bactériennes; Institut Pasteur Paris (IP); Service de Pharmacologie et Immunoanalyse (SPI); Médicaments et Technologies pour la Santé (MTS); Université Paris-Saclay-Institut des Sciences du Vivant Frédéric JOLIOT (JOLIOT); Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)-Université Paris-Saclay-Institut des Sciences du Vivant Frédéric JOLIOT (JOLIOT); Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE); École du Val de Grâce (EVDG); Service de Santé des Armées; National Reference Center for Anthrax Brétigny-sur-Orge (CNR-LE Charbon); This work was funded by the Joint Ministerial Program of R&D against CBRNE risks (NRBC H1.11).
    • بيانات النشر:
      HAL CCSD
      Oxford University Press
    • الموضوع:
      2020
    • Collection:
      Institut National de la Recherche Agronomique: ProdINRA
    • نبذة مختصرة :
      International audience ; Background: Lethal and edema toxins are critical virulence factors of Bacillus anthracis. Few data are available on their presence in the early stage of intranasal infection. Methods: To investigate the diffusion of edema factor (EF) and lethal factor (LF), we use sensitive quantitative methods to measure their enzymatic activities in mice intranasally challenged with a wild-type B anthracis strain or with an isogenic mutant deficient for the protective antigen. Results: One hour after mouse challenge, although only 7% of mice presented bacteremia, LF and EF were detected in the blood of 100% and 42% of mice, respectively. Protective antigen facilitated the diffusion of LF and EF into the blood compartment. Toxins played a significant role in the systemic dissemination of B anthracis in the blood, spleen, and liver. A mouse model of intoxination further confirmed that LT and ET could diffuse rapidly in the circulation, independently of bacteria. Conclusions: In this inhalational model, toxins have disseminated rapidly in the blood, playing a significant and novel role in the early systemic diffusion of bacteria, demonstrating that they may represent a very early target for the diagnosis and the treatment of anthrax.
    • ISBN:
      978-0-00-518533-9
      0-00-518533-5
    • Relation:
      info:eu-repo/semantics/altIdentifier/pmid/31574153; pasteur-03293185; https://pasteur.hal.science/pasteur-03293185; https://pasteur.hal.science/pasteur-03293185/document; https://pasteur.hal.science/pasteur-03293185/file/jiz497.pdf; PUBMED: 31574153; PUBMEDCENTRAL: PMC6996859; WOS: 000518533500022
    • الرقم المعرف:
      10.1093/infdis/jiz497
    • Rights:
      http://creativecommons.org/licenses/by-nc-nd/ ; info:eu-repo/semantics/OpenAccess
    • الرقم المعرف:
      edsbas.1AC2064C