Legionella pneumophila and related species were examined by sodium dodecyl sulfate-polyacrylamide gel electrophoresis for outer membrane proteins. Of the 10 species examined, 9 contained a 24-kilodalton (kDa) major outer membrane protein (MOMP) that was resolvable only when outer membrane material was heated in the presence of 2-mercaptoethanol. Labeling studies with [35S]cysteine indicated that the protein contained cysteine, and disulfide cross-linking of the unreduced complex was demonstrated by labeling with iodoacetamide. The unreduced outer membrane preparation contained peptidoglycan, and after treatment with lysozyme to remove peptidoglycan, a protein complex of 95 kDa was observed by sodium dodecyl sulfate polyacrylamide gel electrophoresis in the absence of 2-mercaptoethanol. Reduction of the 95-kDa complex yielded 24-kDa monomers, suggesting that the 95-kDa complex was composed of four subunits. The 24-kDa MOMP from L. pneumophila was purified, and antibody produced to this protein cross-reacted with all species of Legionella as determined from an immunoblot of a sodium dodecyl sulfate gel. Only serogroup 1 strains of L. bozemanii lacked the 24-kDa MOMP and showed no cross-reactivity. These results suggest that the 24-kDa MOMP common to most species of Legionella contains a genus-specific epitope.
Transposon TnS was introduced into Legionella pneumophila on plasmid pRK340, which is temperature sensitive for plasmid maintenance. The presence of plasmid DNA was confirmed by agarose gel electrophoresis and by coijugal transfer of the plasmid to Escherichia coli. TnS insertions were obtaied by culturing L. pneumophia at the nonpermissive temperature (43°C) on buffered charcoal-yeast extract agar containing kanamycin. Of the 260 kanamycin-resistant colonies picked, 220 failed to conjugate pRK340 to E. coli. Plasmid DNA was not visualized from eight randomly picked TnS-containing strains, and Southern hybridizations indicated that TnS, but not pRK340, inserted into multiple sites in the Legioneila chromosome. In addition, the streptomycin resistance determinant on TnS was expressed in L. pneumophila.Legionella pneumophila and related species are fastidious facultative intracellular parasites for which determinants of virulence have not been clearly established. Continued propagation of virulent strains on laboratory media leads to a loss of virulence (15), which can be restored by passage of the avirulent strains in cell culture (24). Despite transitions between virulence and avirulence, no phenotypic markers have been found which correlate with loss of virulence. Although plasmid-encoded virulence factors have been reported for other gram-negative bacteria (18,19), no correlation between plasmids and virulence has been made for the legionellae (1, 5). Genetic regulation of the transition from virulence to avirulence in the legionellae may be under control mechanisms similar to those recently described for Bordetella pertussis (23). Weiss and Falkow (23) demonstrated that the phase change (reversible conversion from virulence to avirulence) of B. pertussis was controlled by a chromosomal trans-acting gene product. However, before progress can be made towards resolving mechanisms of pathogenesis for the legionellae, it will be necessary both to develop a workable genetic system and to identify specific markers associated with virulence.Since transposon mutagenesis has proved to be an effective tool in studies of pathogenesis, we set out to develop a means for delivering transposons into the chromosome of L. pneumophila. It has recently been reported that Pseudomonas plasmids of the IncP-1 incompatibility group can be transferred to several Legionella species via conjugation (8). Chen et al. (6) have introduced TnS into several Legionella species on the broad-host-range suicide plasmid pJB4JI, but they did not demonstrate transposition. In this study we show that pRK340, a temperature-sensitive derivative of the IncP-1 plasmid RK2, can effectively deliver Tn5 to the chromosome of L. pneumophila.All strains and plasmids used in this study are listed in Table 1. L. pneumophila strains were maintained on ACES (N-(2-acetamido)-2-aminoethanesulfonic acid)-buffered charcoal-yeast extract (BCYE) agar (17), and batch cultures were grown in BYE medium (without charcoal) and harvested as previously described (12). All cultu...
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