Role of surfactant protein-A in nitric oxide production and mycoplasma killing in congenic C57BL/6 mice

Am J Respir Cell Mol Biol. 2004 Mar;30(3):319-25. doi: 10.1165/rcmb.2003-0246OC. Epub 2003 Sep 4.

Abstract

We generated congenic surfactant protein A (SP-A)-deficient (SP-A[-/-]) mice on the mycoplasma resistant C57BL/6 background (B6.SP-A[-/-]) and characterized their response to mycoplasma infection in comparison to C57BL/6 (B6) mice. B6.SP-A(-/-) mice infected with 10(6) colony-forming units (cfu) of Mycoplasma pulmonis had significantly higher bacterial lung loads than B6 mice at 72 h postinfection (p.i.). At the higher infection dose of 10(7), B6.SP-A(-/-) mice had significantly higher lung cfu at 24 h; however, no difference in mycoplasma cfu was observed between B6 and B6.SP-A(-/-) mice at 48 and 72 h p.i. We found that uninfected B6 mice had lower bronchoalveolar lavage nitrite (NO(2)(-)) and nitrate (NO(3)(-)) levels as compared with B6.SP-A(-/-) mice. On the other hand, infection of B6 mice with mycoplasmas resulted in significantly higher bronchoalveolar lavage NO(2)(-) and NO(3)(-) as compared with B6.SP-A(-/-) mice. These data indicate that SP-A may help regulate NO production in response to a specific stimulus, i.e., suppression of NO in the absence of bacteria and increased NO in the presence of bacteria. These data indicate that the contribution of SP-A to mycoplasma killing may be limited to lower doses of pathogens.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Bronchoalveolar Lavage
  • Cells, Cultured
  • Cytokines / metabolism
  • Genotype
  • Lung / microbiology
  • Mice
  • Mice, Congenic
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mycoplasma Infections / metabolism*
  • Mycoplasma pulmonis / physiology*
  • Nitrates / metabolism
  • Nitric Oxide / biosynthesis*
  • Nitrites / metabolism
  • Pulmonary Alveolar Proteinosis / metabolism
  • Pulmonary Surfactant-Associated Protein A / genetics
  • Pulmonary Surfactant-Associated Protein A / physiology*

Substances

  • Cytokines
  • Nitrates
  • Nitrites
  • Pulmonary Surfactant-Associated Protein A
  • Nitric Oxide