Growth of ammonia-oxidizing archaea in soil microcosms is inhibited by acetylene
Pierre Offre
Institute of Biological and Environmental Sciences, University of Aberdeen, Aberdeen, UK
Search for more papers by this authorJames I. Prosser
Institute of Biological and Environmental Sciences, University of Aberdeen, Aberdeen, UK
Search for more papers by this authorGraeme W. Nicol
Institute of Biological and Environmental Sciences, University of Aberdeen, Aberdeen, UK
Search for more papers by this authorPierre Offre
Institute of Biological and Environmental Sciences, University of Aberdeen, Aberdeen, UK
Search for more papers by this authorJames I. Prosser
Institute of Biological and Environmental Sciences, University of Aberdeen, Aberdeen, UK
Search for more papers by this authorGraeme W. Nicol
Institute of Biological and Environmental Sciences, University of Aberdeen, Aberdeen, UK
Search for more papers by this authorEditor: Christoph Tebbe
Abstract
Autotrophic ammonia-oxidizing bacteria were considered to be responsible for the majority of ammonia oxidation in soil until the recent discovery of the autotrophic ammonia-oxidizing archaea. To assess the relative contributions of bacterial and archaeal ammonia oxidizers to soil ammonia oxidation, their growth was analysed during active nitrification in soil microcosms incubated for 30 days at 30 °C, and the effect of an inhibitor of ammonia oxidation (acetylene) on their growth and soil nitrification kinetics was determined. Denaturing gradient gel electrophoresis (DGGE) analysis of bacterial ammonia oxidizer 16S rRNA genes did not detect any change in their community composition during incubation, and quantitative PCR (qPCR) analysis of bacterial amoA genes indicated a small decrease in abundance in control and acetylene-containing microcosms. DGGE fingerprints of archaeal amoA and 16S rRNA genes demonstrated changes in the relative abundance of specific crenarchaeal phylotypes during active nitrification. Growth was also indicated by increases in crenarchaeal amoA gene copy number, determined by qPCR. In microcosms containing acetylene, nitrification and growth of the crenarchaeal phylotypes were suppressed, suggesting that these crenarchaea are ammonia oxidizers. Growth of only archaeal but not bacterial ammonia oxidizers occurred in microcosms with active nitrification, indicating that ammonia oxidation was mostly due to archaea in the conditions of the present study.
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