Mercury is a redox-active heavy metal that reacts with active thiols and depletes cellular antioxidants. Active resistance to the mercuric ion is a widely distributed trait among bacteria and results from the action of mercuric reductase (MerA). Protein phylogenetic analysis of MerA in bacteria indicated the occurrence of a second distinctive form of MerA among the archaea, which lacked an N-terminal metal recruitment domain and a C-terminal active tyrosine. To assess the distribution of the forms of MerA in an interacting community comprising members of both prokaryotic domains, studies were conducted at a naturally occurring mercuryrich geothermal environment. Geochemical analyses of Coso Hot Springs indicated that mercury ore (cinnabar) was present at concentrations of parts per thousand. Under high-temperature and acid conditions, cinnabar may be oxidized to the toxic form Hg 2؉ , necessitating mercury resistance in resident prokaryotes. Culture-independent analysis combined with culture-based methods indicated the presence of thermophilic crenarchaeal and gram-positive bacterial taxa. Fluorescence in situ hybridization analysis provided quantitative data for community composition. DNA sequence analysis of archaeal and bacterial merA sequences derived from cultured pool isolates and from community DNA supported the hypothesis that both forms of MerA were present. Competition experiments were performed to assess the role of archaeal merA in biological fitness. An essential role for this protein was evident during growth in a mercury-contaminated environment. Despite environmental selection for mercury resistance and the proximity of community members, MerA retains the two distinct prokaryotic forms and avoids genetic homogenization.The separation of prokaryotes into bacterial and archaeal domains (or superkingdoms) has gained considerable support from the ongoing input of genome sequencing efforts and their identification of proteins separately categorized in this organizational structure. The exchange of genes between domains, however, means that this finding is not absolute because it can result in genomes having mixed compositions. Lateral gene transfer (LGT) has been reported within the archaeal domain (22) and between the bacterial and archaeal domains (4,12,13,23). In addition, some authors have noted that there is preferential gene transfer of housekeeping genes, also called operational genes, rather than genes concerned with information processing (16).LGT also plays a role in the evolution of mercury resistance encoded in the mer operon, which makes it suitable for analysis of evolutionary processes. Recent studies of microbes residing at marine hydrothermal vents support such efforts (38). The mer genes have been well studied in bacteria and usually are plasmid encoded and therefore mobile (5). This may explain why some bacteria possess mer genes even if they do not live in environments rich in mercury. However, mer genes appear to be absent in anaerobic organisms, which perhaps reflects a reduced n...