Macrophages from mice with the restrictive Lgn1 allele exhibit multifactorial resistance to Legionella pneumophila

被引:61
作者
Derré, I
Isberg, RR
机构
[1] Tufts Univ, Sch Med, Dept Mol Biol & Microbiol, Boston, MA 02111 USA
[2] Tufts Univ, Sch Med, Howard Hughes Med Inst, Boston, MA 02111 USA
关键词
D O I
10.1128/IAI.72.11.6221-6229.2004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Although Legionella pneumophila can multiply in diverse cell types from a variety of species, macrophages from most inbred mouse strains are nonpermissive for intracellular replication and allow little or no growth of the bacteria. This phenomenon is likely genetically controlled by the mouse naip5 (birc1e) gene located within the Lgn1 locus. In this study, we have investigated the resistance of C57BL/6J macrophages to L. pneumophila infection by examining the fate of both the bacterium and the infected cells compared to that in macrophages from the permissive A/J strain. Our results indicate that although the trafficking of the L. pneumophila-containing vacuole is partially disrupted in C57BL/6J macrophages, this cannot account for the severity of the defect in intracellular growth observed in this strain. Infected macrophages are lost shortly after infection, and at later times a larger fraction of the C57BL/6J macrophages in which L. pneumophila undergoes replication are apoptotic compared to those derived from A/J mice. Finally, a loss of bacterial counts occurs after the first round of growth. Therefore, the resistance mechanism of C57BL/6J macrophages to L. pneumophila infection appears to be multifactorial, and we discuss how early and late responses result in clearing the infection.
引用
收藏
页码:6221 / 6229
页数:9
相关论文
共 56 条
  • [31] Legionella pneumophila suppresses macrophage interleukin-12 production by activating the p42/44 mitogen-activated protein kinase cascade
    Matsunaga, K
    Yamaguchi, H
    Klein, TW
    Friedman, H
    Yamamoto, Y
    [J]. INFECTION AND IMMUNITY, 2003, 71 (11) : 6672 - 6675
  • [32] Legionella pneumophila suppresses interleukin-12 production by macrophages
    Matsunaga, K
    Klein, TW
    Newton, C
    Friedman, H
    Yamamoto, Y
    [J]. INFECTION AND IMMUNITY, 2001, 69 (03) : 1929 - 1933
  • [33] PERIODATE-LYSINE-PARAFORMALDEHYDE FIXATIVE - NEW FIXATIVE FOR IMMUNOELECTRON MICROSCOPY
    MCLEAN, IW
    NAKANE, PK
    [J]. JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1974, 22 (12) : 1077 - 1083
  • [34] Apoptosis - Caspases find a new place to hide
    Mehmet, H
    [J]. NATURE, 2000, 403 (6765) : 29 - 30
  • [35] Activation of caspase-3 by the Dot/Icm virulence system is essential for arrested biogenesis of the Legionella-containing phagosome
    Molmeret, M
    Zink, SD
    Han, LH
    Abu-Zant, A
    Asari, R
    Bitar, DM
    Abu Kwaik, Y
    [J]. CELLULAR MICROBIOLOGY, 2004, 6 (01) : 33 - 48
  • [36] A bacterial guanine nucleotide exchange factor activates ARF on Legionella phagosomes
    Nagai, H
    Kagan, JC
    Zhu, XJ
    Kahn, RA
    Roy, CR
    [J]. SCIENCE, 2002, 295 (5555) : 679 - 682
  • [37] INTERACTION BETWEEN THE LEGIONNAIRES-DISEASE BACTERIUM (LEGIONELLA PNEUMOPHILA) AND HUMAN ALVEOLAR MACROPHAGES - INFLUENCE OF ANTIBODY, LYMPHOKINES, AND HYDROCORTISONE
    NASH, TW
    LIBBY, DM
    HORWITZ, MA
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1984, 74 (03) : 771 - 782
  • [38] Legionella pneumophila DotA protein is required for early phagosome trafficking decisions that occur within minutes of bacterial uptake
    Roy, CR
    Berger, KH
    Isberg, RR
    [J]. MOLECULAR MICROBIOLOGY, 1998, 28 (03) : 663 - 674
  • [39] IDENTIFICATION OF LEGIONELLA-PNEUMOPHILA GENES REQUIRED FOR GROWTH WITHIN AND KILLING OF HUMAN MACROPHAGES
    SADOSKY, AB
    WIATER, LA
    SHUMAN, HA
    [J]. INFECTION AND IMMUNITY, 1993, 61 (12) : 5361 - 5373
  • [40] Differential induction of gamma interferon in Legionella pneumophila-infected macrophages from BALB/c and A/J mice
    Salins, S
    Newton, C
    Widen, R
    Klein, TW
    Friedman, M
    [J]. INFECTION AND IMMUNITY, 2001, 69 (06) : 3605 - 3610