Accession Number : ADA453733


Title :   Anthrax Lethal Toxin Impairs Innate Immune Functions of Alveolar Macrophages and Facilitates Bacillus anthracis Survival


Descriptive Note : Journal article


Corporate Author : ARMY MEDICAL RESEARCH INST OF INFECTIOUS DISEASES FORT DETRICK MD


Personal Author(s) : Ribot, Wilson J. ; Panchal, Rekha G. ; Brittingham, Katherine C. ; Ruthel, Gordon ; Kenny, Tara A. ; Lane, Douglas ; Curry, Bob ; Hoover, Timothy A. ; Friedlander, Arthur M. ; Bavari, Sina


Full Text : http://www.dtic.mil/get-tr-doc/pdf?AD=ADA453733


Report Date : 14 JUN 2006


Pagination or Media Count : 7


Abstract : Alveolar macrophages (AM) are very important for pulmonary innate immune responses against invading inhaled pathogens because they directly kill the organisms and initiate a cascade of innate and adaptive immune responses. Although several factors contribute to inhalational anthrax, we hypothesized that unimpeded infection of Bacillus anthracis is directly linked to disabling the innate immune functions contributed by AM. Here, we investigated the effects of lethal toxin (LT), one of the binary complex virulence factors produced by B. anthracis, on freshly isolated nonhuman primate AM. Exposure of AM to doses of LT that killed susceptible macrophages had no effect on the viability of AM, despite complete MEK1 cleavage. Intoxicated AM remained fully capable of B. anthracis spore phagocytosis. However, pretreatment of AM with LT resulted in a significant decrease in the clearance of both the Sterne strain and the fully virulent Ames strain of B. anthracis, which may have been a result of impaired AM secretion of proinflammatory cytokines. Our data imply that cytolysis does not correlate with MEK1 cleavage, and this is the first report of LT-mediated impairment of nonhuman primate AM bactericidal activity against B. anthracis.


Descriptors :   *ANTHRAX , *IMMUNITY , REPRINTS , LETHALITY , MACROPHAGES , ALVEOLI , BACILLUS ANTHRACIS , RETICULOENDOTHELIAL SYSTEM , BACTERIAL TOXINS , PATHOGENIC MICROORGANISMS , PRIMATES , RESPONSE(BIOLOGY)


Subject Categories : BIOCHEMISRTY
      MEDICINE AND MEDICAL RESEARCH


Distribution Statement : APPROVED FOR PUBLIC RELEASE