ANALYSIS OF THE RNC LOCUS OF COXIELLA-BURNETII

A 3.2 kb EcoRI genomic DNA fragment of Coxiella burnetii was isolated by virtue of its ability to suppress mucoidy in Escherichia coli. Nucleotide sequence analysis revealed the presence of the genes homologous to me, era and recO of E. coli. Suppression of capsule synthesis, measured by beta-galactosidase expression in lon(-) cps-lac fusion strains of E. coli, is caused by gene-dosage effects of the plasmid-borne me genes of either C. burnetii or E. coli. The rnc gene of C. burnetii complemented rnc(-) E. coli hosts for lambda plaque morphology and stimulation of lambda N gene expression. We also demonstrated heterologous complementation of an E. coli strain defective for the expression of Era, an essential protein in E. coli, using the plasmid-borne C. burnetii era. Under the control of the bacteriophage lambda P-L promoter, this 3.2 kb EcoRI DNA fragment directed the synthesis in E. coli of three proteins with approximate molecular masses of 35, 27 and 25 kDa. Antibodies against purified E. coli Era protein cross-reacted with the 35 kDa protein of C. burnetii on Western blots.