Cystic fibrosis (CF) patients develop chronic airway infections with Pseudo
monas aeruginosa (PA), Pseudomonas aeruginosa synthesized lipopolysaccharid
e (LPS) with a variety of penta- and hexa-acylated lipid A structures under
different environmental conditions. CF patient PA synthesized LPS with spe
cific Lipid A structures indicating unique recognition of the CF airway env
ironment. CF-specific Lipid A forms containing palmitate and aminoarabinose
were associated with resistance to cationic antimicrobial peptides and inc
reased inflammatory responses, indicating that they are likely to be involv
ed in airway disease.