D. Jurgens et Fj. Fehrenbach, IDENTIFICATION OF LEGIONELLA SPECIES BY LIPOPOLYSACCHARIDE ANTIGEN PATTERN, Journal of clinical microbiology, 35(12), 1997, pp. 3054-3057
Electrophoretic analysis of lipopolysaccharide (LPS) er;tracts from 43
0 previously serotyped Legionella isolates and 28 American Type Cultur
e Collection (ATCC) non-Legionella pneumophila Legionella reference st
rains representing different Legionella species and serogroups has bee
n performed. LPS was prepared from Legionella suspensions by sonicatio
n and proteinase Ii digestion. Following sodium dodecyl sulfate-polyac
rylamide gel electrophoresis, LPS bands were either stained with silve
r nitrate or transferred onto a nitrocellulose membrane and detected w
ith rabbit antibodies raised against L. pneumophila serogroup 5, which
was known to cross-react with L. pneumophila serogroups 1 to 14. Silv
er staining revealed that each of the 28 ATCC non-L. pneumophila Legio
nella strains possessed an individual and characteristic LPS banding p
attern. The LPS profile was defined by the molecular weight of the vis
ualized bands and/or the individual ladder-like LPS pattern. It was de
monstrated by immunoblotting that non-L. pneumophila Legionella strain
s did not react with the serogroup 5 antiserum, thus allowing for the
differentiation between,een L. pneumophila and non-L. pneumophila spec
ies.