Abundance of genes involved in mercury methylation in oceanic environments

Anthony V Palumbo1, Mircea Podar1, Cynthia C Gilmour2, Craig C Brandt1, Steven D Brown1, Bryan R Crable1, Deborah Weighill1,3, Daniel A Jacobson1, Anil C Somenahally4 and Dwayne A Elias1, (1)Oak Ridge National Laboratory, Biosciences Division, Oak Ridge, TN, United States, (2)Smithsonian Institution, Smithsonian Environmental Research Center, Edgewater, MD, United States, (3)The University of Tennessee, The Bredesen Center for Interdisciplinary Research and Graduate Education, Knoxville, TN, United States, (4)Texas Agrilife Research, Vernon, TX, United States
Abstract:
The distribution and diversity of genes involved in mercury methylation in oceanic environments is of interest in determining the source of mercury in ocean environments and may have predictive value for mercury methylation rates. The highly conserved hgcAB genes involved in mercury methylation provide an avenue for evaluating the genetic potential for mercury methylation. The genes are sporadically present in a few diverse groups of bacteria and Archaea including Deltaproteobacteria, Firmicutes and Archaea and of over 7000 sequenced species they are only present in about 100 genomes. Examination of sequence data from methylators and non-methylators indicates that these genes are associated with other genes involved in metal transformations and transport. We examined hgcAB presence in over 3500 microbial metagenomes (from all environments) and found the hgcAB genes were present in anaerobic oceanic environments but not in aerobic layers of the open ocean. The genes were common in sediments from marine, coastal and estuarine sources as well as polluted environments. The genes were rare, found in 7 of 138 samples, in metagenomes from the pelagic water column including profiles though the oxygen minimum zone. Other oxic and sub-oxic coastal waters also demonstrated a lack of hgcAB genes including the OMZ in the Eastern North Pacific Ocean. There were some unique hgcA like unique sequences found in metagenomes from depth in the Pacific and Southern Atlantic Ocean. Coastal “dead zone” waters may be important sources of MeHg as the hgcAB genes were abundant in the anoxic waters of a stratified fjord. The genes were absent in microbiomes from vertebrates but were in invertebrate microbiomes However, oceanic species were underrepresented in these samples. Climate change could provide an additional flux of MeHg to the oceans as we found the most abundant representation of hgcAB genes in arctic permafrost. Thus warming could increase flux of methyl mercury to arctic waters.