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Title: Development and validation of broad-range qualitative and clade-specific quantitative molecular probes for assessing mercury methylation in the environment

Journal Article · · Applied and Environmental Microbiology
DOI:https://doi.org/10.1128/AEM.01271-16· OSTI ID:1326544

Two genes, hgcA and hgcB, are essential for microbial mercury (Hg)-methylation. Detection and estimation of their abundance, in conjunction with Hg concentration, bioavailability and biogeochemistry is critical in determining potential hot spots of methylmercury (MeHg) generation in at-risk environments. We developed broad-range degenerate PCR primers spanning known hgcAB genes to determine the presence of both genes in diverse environments. These primers were tested against an extensive set of pure cultures with published genomes, including 13 Deltaproteobacteria, nine Firmicutes, and nine methanogenic Archaea. A distinct PCR product at the expected size was confirmed for all hgcAB+ strains tested via Sanger sequencing. Additionally, we developed clade-specific degenerate quantitative primers (qPCR) that targeted hgcA for each of the three dominant Hg-methylating clades. The clade-specific qPCR primers amplified hgcA from 64%, 88% and 86% of tested pure cultures of Deltaproteobacteria, Firmicutes and Archaea, respectively, and were highly specific for each clade. Amplification efficiencies and detection limits were quantified for each organism. Primer sensitivity varied among species based on sequence conservation. Finally, to begin to evaluate the utility of our primer sets in nature, we tested hgcA and hgcAB recovery from pure cultures spiked into sand and soil. These novel quantitative molecular tools designed in this study will allow for more accurate identification and quantification of the individual Hg-methylating groups of microorganisms in the environment. Here, the resulting data will be essential in developing accurate and robust predictive models of Hg-methylation potential, ideally integrating the geochemistry of Hg methylation to the microbiology and genetics of hgcAB.

Research Organization:
Oak Ridge National Laboratory (ORNL), Oak Ridge, TN (United States)
Sponsoring Organization:
USDOE Office of Science (SC)
Grant/Contract Number:
AC05-00OR22725
OSTI ID:
1326544
Journal Information:
Applied and Environmental Microbiology, Vol. 82, Issue 19; ISSN 0099-2240
Publisher:
American Society for MicrobiologyCopyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 53 works
Citation information provided by
Web of Science

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Cited By (11)

Biotic formation of methylmercury: A bio–physico–chemical conundrum journal November 2019
Microbial community structure with trends in methylation gene diversity and abundance in mercury-contaminated rice paddy soils in Guizhou, China journal January 2018
Robust Mercury Methylation across Diverse Methanogenic Archaea journal April 2018
A review of global environmental mercury processes in response to human and natural perturbations: Changes of emissions, climate, and land use journal January 2018
Challenges and opportunities for managing aquatic mercury pollution in altered landscapes journal January 2018
Recent advances in the study of mercury methylation in aquatic systems journal May 2017
Molecular evidence for novel mercury methylating microorganisms in sulfate-impacted lakes journal February 2019
Mercury methylating microbial communities of boreal forest soils journal January 2019
Distribution of mercury‐cycling genes in the Arctic and equatorial Pacific Oceans and their relationship to mercury speciation journal January 2020
A review of global environmental mercury processes in response to human and natural perturbations: Changes of emissions, climate, and land use text January 2018
Methanogens and Iron-Reducing Bacteria: the Overlooked Members of Mercury-Methylating Microbial Communities in Boreal Lakes text January 2018