Legionella pneumophila can invade and grow within explanted alveolar e
pithelial cells. Given its potential clinical significance, an examina
tion of the molecular basis of epithelial cell infection was initiated
. The mip gene encodes a 24-kilodalton surface protein that promotes m
acrophage infection and virulence. To determine whether this gene is r
equired for pneumocyte infection, we tested a strain bearing a mip nul
l mutation for its ability to infect both explanted type II cells and
type I-like cell lines. For infection of type II cells, the infective
dose 50% for the Mip(-) strain was 25-fold higher than an isogenic Mip
(+) strain. Type I cell monolayers infected with the mutant for 3 days
yielded similar to 50-fold fewer bacteria than did monolayers infecte
d with the parental strain. These data indicate that Mip enhances infe
ction of pneumocytes and that L, pneumophila employs some of the same
genes (mechanisms) to infect epithelial cells and macrophages.