Macrophages from Mice with the Restrictive Lgn1 Allele Exhibit Multifactorial Resistance to Legionella pneumophila

I Derré, RR Isberg - Infection and immunity, 2004 - Am Soc Microbiol
I Derré, RR Isberg
Infection and immunity, 2004Am Soc Microbiol
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 …
Abstract
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.
American Society for Microbiology