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Daan R. Speth

University of Vienna

ORCID: 0000-0002-2361-5935

Publishes on Microbial Community Ecology and Physiology, Methane Hydrates and Related Phenomena, Wastewater Treatment and Nitrogen Removal. 93 papers and 6.4k citations.

93Publications
6.4kTotal Citations

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Top publicationsby citations

A highly abundant bacteriophage discovered in the unknown sequences of human faecal metagenomes
Bas E. Dutilh, Noriko A. Cassman, Katelyn McNair et al.|Nature Communications|2014
Cited by 863Open Access

Metagenomics, or sequencing of the genetic material from a complete microbial community, is a promising tool to discover novel microbes and viruses. Viral metagenomes typically contain many unknown sequences. Here we describe the discovery of a previously unidentified bacteriophage present in the majority of published human faecal metagenomes, which we refer to as crAssphage. Its ~97 kbp genome is six times more abundant in publicly available metagenomes than all other known phages together; it comprises up to 90% and 22% of all reads in virus-like particle (VLP)-derived metagenomes and total community metagenomes, respectively; and it totals 1.68% of all human faecal metagenomic sequencing reads in the public databases. The majority of crAssphage-encoded proteins match no known sequences in the database, which is why it was not detected before. Using a new co-occurrence profiling approach, we predict a Bacteroides host for this phage, consistent with Bacteroides-related protein homologues and a unique carbohydrate-binding domain encoded in the phage genome. Metagenomic studies of microbial communities often report DNA sequences from unidentified viruses. Here, Dutilh et al. analyse metagenomic data to reveal the complete genome of an abundant, ubiquitous virus from human faeces, and predict that the virus infects bacteria of the Bacteroides group.

Archaea catalyze iron-dependent anaerobic oxidation of methane
Katharina F. Ettwig, Baoli Zhu, Daan R. Speth et al.|Proceedings of the National Academy of Sciences|2016
Cited by 623Open Access

Significance Carbon and nitrogen cycles have been altered dramatically by human activities. Methane-producing (methanogenic) and methane-consuming (methanotrophic) microorganisms control the emission of methane, one of the most potent greenhouse gases, to the atmosphere. Earlier studies identified methanotrophic microorganisms that use methane as an electron donor and oxygen, sulfate, nitrite, and nitrate as electron acceptors. Previous research showed that methanotrophy coupled to the reduction of oxidized metals could be important in the environment. In the current paper, we identified archaea of the order Methanosarcinales , related to “ Candidatus Methanoperedens nitroreducens,” which couple the reduction of environmentally relevant particulate forms of iron and manganese to methane oxidation, filling one of the remaining lacunas in anaerobic methane oxidation.

Genome-based microbial ecology of anammox granules in a full-scale wastewater treatment system
Daan R. Speth, Michiel H. in ‘t Zandt, Simon Guerrero-Cruz et al.|Nature Communications|2016
Cited by 501Open Access

Partial-nitritation anammox (PNA) is a novel wastewater treatment procedure for energy-efficient ammonium removal. Here we use genome-resolved metagenomics to build a genome-based ecological model of the microbial community in a full-scale PNA reactor. Sludge from the bioreactor examined here is used to seed reactors in wastewater treatment plants around the world; however, the role of most of its microbial community in ammonium removal remains unknown. Our analysis yielded 23 near-complete draft genomes that together represent the majority of the microbial community. We assign these genomes to distinct anaerobic and aerobic microbial communities. In the aerobic community, nitrifying organisms and heterotrophs predominate. In the anaerobic community, widespread potential for partial denitrification suggests a nitrite loop increases treatment efficiency. Of our genomes, 19 have no previously cultivated or sequenced close relatives and six belong to bacterial phyla without any cultivated members, including the most complete Omnitrophica (formerly OP3) genome to date.

The metagenome of the marine anammox bacterium ‘ <i>Candidatus</i> Scalindua profunda’ illustrates the versatility of this globally important nitrogen cycle bacterium
Jack van de Vossenberg, Dagmar Woebken, Wouter J. Maalcke et al.|Environmental Microbiology|2012
Cited by 291Open Access

Summary Anaerobic ammonium‐oxidizing (anammox) bacteria are responsible for a significant portion of the loss of fixed nitrogen from the oceans, making them important players in the global nitrogen cycle. To date, marine anammox bacteria found in marine water columns and sediments worldwide belong almost exclusively to the ‘ Candidatus Scalindua’ species, but the molecular basis of their metabolism and competitive fitness is presently unknown. We applied community sequencing of a marine anammox enrichment culture dominated by ‘ Candidatus Scalindua profunda’ to construct a genome assembly, which was subsequently used to analyse the most abundant gene transcripts and proteins. In the S. profunda assembly, 4756 genes were annotated, and only about half of them showed the highest identity to the only other anammox bacterium of which a metagenome assembly had been constructed so far, the freshwater ‘ Candidatus Kuenenia stuttgartiensis’. In total, 2016 genes of S. profunda could not be matched to the K. stuttgartiensis metagenome assembly at all, and a similar number of genes in K. stuttgartiensis could not be found in S. profunda . Most of these genes did not have a known function but 98 expressed genes could be attributed to oligopeptide transport, amino acid metabolism, use of organic acids and electron transport. On the basis of the S. profunda metagenome, and environmental metagenome data, we observed pronounced differences in the gene organization and expression of important anammox enzymes, such as hydrazine synthase (HzsAB), nitrite reductase (NirS) and inorganic nitrogen transport proteins. Adaptations of Scalindua to the substrate limitation of the ocean may include highly expressed ammonium, nitrite and oligopeptide transport systems and pathways for the transport, oxidation, and assimilation of small organic compounds that may allow a more versatile lifestyle contributing to the competitive fitness of Scalindua in the marine realm.