In the United States, mycoplasmas account for up to 20 to 30% of the 4 million cases of pneumonia reported annually and cause significant morbidity and mortality. Murine respiratory infection with Mycoplasma pulmonis reproduces the essential features of human respiratory mycoplasmosis. This model has revealed that reactive oxygen and nitrogen species (RONS) produced by the alveolar macrophage (AM) and surfactant protein A, secreted by the alveolar type II (ATII) cells, are essential for early clearance of respiratory mycoplasmas in vivo and in vitro (1, 2). However, even with significant production of RONS in response to mycoplasma infection, susceptible individuals may develop serious illness. In this context, adherence of mycoplasma species to the respiratory epithelium is necessary for effective coloniza-