Campylobacter coli VC167, which undergoes an antigenic flagellar variation, contains two full-length flagellin genes, flaA and flaB, that are located adjacent to one another in a tandem orientation and are 91.5%homologous. The gene product offlaB, which has an Mr of 58,946, has 93% sequence homology to the gene product of flaA, which has an M, of 58,916 (S. M. Logan, T. J. Trust, and P. Guerry, J. Bacteriol. 171:3031-3038, 1989). Mutational analyses and primer extension experiments indicated that the two genes are transcribed under the control of distinct promoters but that they are expressed concomitantly in the same cell, regardless of the antigenic phase of flagella being produced. TheflaA gene, which was expressed at higher levels than theflaB gene in both phases, was transcribed from a typical 2.8-type promoter, whereas theflaB promoter was unusual. A mutant producing only the flaB gene product did not synthesize a flagellar filament and was nonmotile. Southern blot analysis indicated that flagellar antigenic variation involves a rearrangement of flagellin sequence information rather than the alternate expression of the two distinct genes.Campylobacterjejuni and Campylobacter coli are important gastrointestinal pathogens of humans, most commonly producing an acute enteritis (6,8,39). An essential step in the establishment of Campylobacter enteritis is the colonization of the viscous mucous blanket covering the epithelium of the small intestine. The motility imparted by the polar flagellum of the Campylobacter cell appears to play a significant role in the colonization of this mucous niche (23,30,31), since nonmotile variants appear unable to colonize the gastrointestinal tract of experimental animals or human volunteers (4, 7). Flagellin is also the immunodominant protein antigen recognized during infection, so flagella are clearly important virulence determinants of the thermophilic campylobacters.Flagellar expression in Campylobacter spp. is subject to both phase and antigenic variation (7,12). Phase variation refers to ability of some Campylobacter strains to exhibit a bidirectional transition between flagellated and nonflagellated phenotypes (7). Antigenic variation refers to the ability of other strains to reversibly express flagella of different antigenic specificities (12). In the case of C. coli VC167, the reversible variation corresponds to the production of flagellar filaments containing antigenically distinguishable flagellin monomers of apparent subunit molecular weight 61,500 in antigenic phase 1 (P1) cells and 59,500 in antigenic phase 2 (P2) cells. Importantly, recent studies with C. coli VC167 have demonstrated an in vivo preference for one flagellar phase, P2, during colonization in an animal model (19), further emphasizing the functional importance of this locomotory organelle in gastrointestinal colonization by Campylobacter spp.Phase and antigenic variation of surface antigens has been described for other pathogenic bacteria, including fimbrialphase variation in Escherichia coli (1), Mor...