Sialic acid permease system
This invention relates to purified sialic acid permease systems, and inhibitory agents of sialic acid permease systems.
1. A method of treating a mammal infected with a bacterium comprising a sialic acid permease, the method comprising administering a bacterial sialic acid permease inhibitory agent to the mammal, wherein the inhibitor is administered in an amount that reduces the transport of sialic acid by the bacterium, wherein the bacterium is Haernophilus influenzae, Haemophilus ducrevi, Vibrio cholera or Fusobacterium nucleatum , and wherein the inhibitor is 3-fluoro-N-acetylneuraminic acid (3FNA) or an N-alkano, d-derivative of sialic acid.
2. The method of claim 1 , wherein the mammal is diagnosed with otitis media, otitis media with effusion, pneumonia, or chronic bronchitis.
3. The method of claim 1 , wherein the bacterium is Haemophilus influenzae.
4. The method of claim 1 , wherein the transport of sialic acid by the bacterium is reduced by at least about 10%.
5. The method of claim 1 , wherein the agent is present in a physiologically-acceptable, non-toxic vehicle.
6. The method of claim 1 , wherein the viral neuraminidase inhibitor is 3-fluoro-N-acetylneuraminic acid (3FNA).
7. The method of claim 1 , wherein the inhibitory agent is an N-alkanoyl-derivative of sialic acid.
8. The method of claim 7 , wherein the N-alkanoyl-derivative of sialic acid is a 5-N-octanoyl derivative of sialic acid (SiaOct).
9. The method of any of the preceding claims, wherein the sialic acid permease is siaP or siaT.
10. The method of claim 1 , wherein the bacterium is Haemophilus ducreyi.
11. The method of claim 1 , wherein the bacterium is Vibrio cholerae or Fusobacterium nucleatum.
12. A method of treating a Haemophihis influenzae or Haemophilus ducreyi infection, comprising administering to a patient a sialic acid permease inhibitory agent, wherein the inhibitory agent is 3-fluoro-N-acetylneuraminic acid (3FNA) or an N-alkanoyl-derivative of sialic acid.
13. The method of claim 12 , wherein the inhibitory agent is 3-fluoro-N-acetylneuraminic acid (3FNA).
14. The method of claim 12 , wherein the inhibitory agent is an N-alkanoyl-derivative of sialic acid.
15. The method of claim 14 , wherein the N-alkanoyl-derivative of sialic acid is a 5-N-octanoyl derivative of sialic acid (SiaOct).