M. Saunier et al., DISTRIBUTION OF PSEUDOMONAS-SYRINGAE PATHOVARS INTO 23 O-SEROGROUPS, Applied and environmental microbiology, 62(7), 1996, pp. 2360-2374
Serological reactions of Pseudomonas syringae and Pseudomonas viridifl
ava were studied by Ouchterlony double diffusion, A total of 55 polycl
onal antisera, containing anti-lipopolysaccharide (anti-LPS) precipita
ting antibodies, were cross-tested against antigenic suspensions of 51
strains. Twenty-three O serogroups were defined, primarily on the rea
ction of the type strains, Two families of O serogroups showed antigen
ic crossreactivities (PHA, MOP1, MOP2, MOP3, HEL1, HEL2, and SYR1; PER
SAVTOM1, PERSAVTOM2, DEL, POR, and SYR2), Ten O serogroups showed a cl
earcut specificity: APTPIS, TAB, VIR1, VIR2, VIR3, SYR3, SYR4, SYR5, H
US, and LAC. The last serogroup (RIB) contained strains with rough col
ony morphology and side chain-deficient LPSs, as evidenced by sodium d
odecyl sulfate-polyacrylamide gel electrophoresis. The LPS basis of th
e O serogroups was demonstrated by immunoblotting, Serological referen
ce strains were designated for all of the O serogroups, and correspond
ence was established between the O serogroups studied and seven previo
us serogroups (L, T, Pastushenko and I, D. Simonovich, Mikrobiol, Zh,
41:222-229 and 330-339, 1979). A total of 355 strains of P. syringae (
sensu late) belonging to 15 pathovars, not including pathovar syringae
, were typed into the 23 described O serogroups, O serogroups were ass
igned after double-diffusion reactions, with each strain compared with
serological references, The utility of O serogrouping to study P. syr
ingae pathovar structure and diversity is discussed.