Project: Gene content, gene expression, and physiology in mesopelagic ammonia-oxidizing archaea

Acronym/Short Name:AmoA Archaea
Project Duration:2013-04 - 2018-03
Geolocation:Epipelagic and mesopelagic, Equatorial Pacific

Description

NSF award abstract:

Intellectual Merit. How organisms respond to their physical and chemical and environment is a central question in marine ecology. For microbes living in the mesopelagic - the ocean's "twilight zone" - an efficient response is particularly important to capitalize on the intermittent delivery of organic and inorganic compounds sinking from the surface ocean. These organisms must have a suite of metabolic and regulatory strategies used to cope with environmental variability, but these strategies are largely unknown. Understanding when and why metabolic genes are expressed is critical to our understanding of nutrient remineralization in the ocean. Marine group 1 (MG1) archaea are ubiquitous, abundant microbes in the meso- and bathypelagic and promising model organisms for investigating these questions. MG1 archaea are chemolithoautotrophs that oxidize ammonia for energy and fix carbon for biomass, and as such, play a central role in the ocean's coupled carbon and nitrogen cycles. Though MG1 have historically eluded cultivation, recent efforts have been successful at bringing representative MG1 archaea from the open ocean into culture and demonstrating their importance in the production of the greenhouse gas nitrous oxide. This project takes advantage of unique MG1 cultures and the recently sequenced draft genome of one of the organisms - strain CN25 - to investigate the physiological and transcriptional responses of MG1 archaea to variations in their chemical environment, specifically:

1. Comparative transcriptomics of CN25 cells grown under a range of energy availability and nitrosative stress will identify select genes that can be used to diagnose the physiological state of natural populations

2. Improvements in the genomic and transcriptomic knowledge of MG1 archaea will facilitate a thorough reinterpretation of existing metagenomic and metatranscriptomic datasets, as well as provide a better contextual understanding in future studies

The investigators will conduct comparative transcriptomics of CN25 cells harvested in mid-exponential growth and stationary phase versus starved cells. Transcriptomes of cells grown at high nitrate concentrations and low pO2 with those grown in standard conditions will be characterized. A strand-specific, high-density RNAseq approach will be used to examine the expression of putative ORFs, polycistronic operons, and small RNAs, which, in addition to gene expression profiling, has the ancillary benefit of improving genome annotation. Finally, the investigators will sequence the genomes of two additional MG1 strains isolated from the open ocean, as well as single cells from environmental surveys, and leverage the combination with the CN25 genome to reanalyze available metagenomic and metatranscriptomic datasets. The results will define the transcriptional response of a model mesopelagic microbe to a range of chemical environments, and show how the physicochemical environment induces changes in gene expression and gene content that result in greenhouse gas production. This work will rapidly generate new knowledge of how some of the most ubiquitous, yet heretofore elusive, microorganisms respond to geochemical variability and shape our evolving understanding of the marine nitrogen cycle.

Broader Impacts. The scientific and societal impact of the project will be to elucidate the mechanisms of greenhouse gas production in a model marine organism that is of broad interest to biological and chemical oceanographers. Transcriptome sequencing will improve the assembly of the CN25 genome, the first genome of an MG1 archaeon from the open ocean. Both the genome and transcriptomes will be important references for researchers using metagenomics, metatranscriptomics, and metaproteomics in the ocean, as these techniques are reliant on a knowledgebase composed of both DNA sequence and physiology. Thus, the results add value to both existing and future studies. The proposed research will advance education, teaching, and training for the next generation of marine scientists by providing support for two early-career investigators, one postdoctoral researcher, and a secondary school teacher.


DatasetLatest Version DateCurrent State
Coastal eastern subtropical pacific2018-09-06Preliminary and in progress
Nitrosopelagicus brevis CN25 and U25 grown in nitrogen replete and deplete conditions, with subsequent transcriptome sequencing and identification.2018-07-10Final no updates expected
Nitrous oxide concentrations from CTD bottle samples collected during R/V Hugh R. Sharp cruises HRS1316 and HRS1317 in Chesapeake Bay from August to September of 20132018-06-15Final no updates expected
Nitrate concentrations from CTD bottle samples collected during R/V Hugh R. Sharp cruises HRS1316 and HRS1317 in the Chesapeake Bay from August to September of 20132018-06-15Final no updates expected
Dinitrogen to argon ratios (N2:Ar) from CTD bottle samples collected during R/V Hugh R. Sharp cruise HRS1317 in Chesapeake Bay in September of 20132018-06-15Final no updates expected
Ammonium concentrations from CTD bottle samples collected during R/V Hugh R. Sharp cruises HRS1316 and HRS1317 in Chesapeake Bay from August to September of 20132018-06-15Final no updates expected
Ammonia oxidation rates from CTD bottle samples collected during R/V Hugh R. Sharp cruises HRS1316 and HRS1317 in Chesapeake Bay from August to September of 20132018-06-15Final no updates expected
Nitrite concentrations from CTD bottle samples collected during R/V Hugh R. Sharp cruises HRS1316 and HRS1317 in Chesapeake Bay from August to September of 20132018-06-15Final no updates expected
NCBI Accession number link to the closed genome of Nitrosopelagicus brevis CN25 (AmoA Archaea project)2016-10-13Final with updates expected
Rates of water column nitrification determined from bottle incubations with 15N tracers (15NH4Cl); samples collected on METZYME cruise.2016-05-27Final no updates expected
qPCR data for archaeal amoA ecotypes; samples collected on METZYME cruise.2016-05-24Final no updates expected

People

Principal Investigator: Christopher Dupont
J. Craig Venter Institute (JCVI)

Principal Investigator: Alyson E. Santoro
University of California-Santa Barbara (UCSB)

Contact: Alyson E. Santoro
University of California-Santa Barbara (UCSB)


Data Management Plan

DMP_Dupont_Santoro_OCE-1259994_OCE-1260006.pdf (250.81 KB)
02/09/2025