A new phylum of Archaea represented by a nanosized hyperthermophilic symbiont

By H. Huber, Michael J. Hohn, R. Rachel, T. Fuchs, Verena C. Wimmer, K. Stetter. Nature, 2002

818 citations recorded by the source corpus.

View Paper: https://www.semanticscholar.org/paper/fd816f4be627035b0a530bdd80cb18a1be168c9d

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Citations in the corpus

Atomic force microscopy reveals microscale networks and possible symbioses among pelagic marine bacteria (2009, background): “The symbionts’ genome sizes could be reduced where metabolic potentials are shared (Boetius et al. 2000, Huber et al. 2002).”
Review and re-analysis of domain-specific 16S primers. (2003, background): “The Nanoarchaea exhibit uncharacteristically small cell size and were first documented as exosymbionts of the Crenarchaeote, Ignicoccus at 70—98 °C (Huber et al., 2002).”
The Biocatalytic Potential of Extremophiles and Extremozymes (2004, background): “It grows only in co-culture with a new chemolithoautotrophic Ignicoccus species (31,32).”
Genomics of bacteria and archaea: the emerging dynamic view of the prokaryotic world (2008, background): “equitans that parasitizes on another archaeon, Ignicoccus hospitalis (14,16).”
Varieties of Living Things: Life at the Intersection of Lineage and Metabolism (2009, background): “One example is Nanoarchaeum equitans, an exceedingly tiny archaeon, which is always described as an organism despite its extremely reduced genome and consequent inability to metabolize, grow and reproduce independently of another archaeon, Ignicoccus hospitalis (Huber et al. 2002).”
Iron corrosion by novel anaerobic microorganisms (2004, methodology): “A partial (about 1,000 bp) 16S rRNA gene sequence of the methanogenic isolate was amplified with archaeal primer”
Microbial Diversity in Soils (2005, background): “Their rRNA nucleotides are quite different from those of other organisms (DeLong and Pace 2001; Huber et al. 2002).”
Major New Microbial Groups Expand Diversity and Alter our Understanding of the Tree of Life. (2018, neutral): “equitans cells attached to host Ignicoccus hospitalis archaea in a co-culture of these organisms (Huber et al., 2002).”
Phylogenetic analysis of epiphytic marine bacteria on Hole-Rotten diseased sporophytes of Laminaria japonica (2008, methodology): “2002) and thermophilic Nanoarchaeota (Huber et al. 2002).”
Evaluation of general 16S ribosomal RNA gene PCR primers for classical and next-generation sequencing-based diversity studies (2012, neutral): “Addition of Nanoarchaeota-specific primers (43) is recommended.”
Mesophilic crenarchaeota: proposal for a third archaeal phylum, the Thaumarchaeota (2008, methodology): “gov/sites/entrez?db=genomeprj&cmd=search&term=Nanoarchaeum equitans"> Nanoarchaeum equitans was originally proposed to represent a third (and basal) archaeal phylum based on trees that were produced using SSU rRN”
Dynamic Energy Budget Theory for Metabolic Organisation (2005, background): “5 Mbp [532], but it lives symbiotically with the H2-producing and sulphur-reducing archaean Ignicoccus , which complicates the comparison.”
Genomic studies of uncultivated archaea (2005, background): “From an evolutionary viewpoint, it might be justified to give priority to the extremists: archaea from hot environments are phylogenetically diverse and some of them branch close to the root of the archaeal tre”
Comparative genomics, minimal gene-sets and the last universal common ancestor (2003, background): “Smaller genomes will probably be found; for example, a tiny, symbiotic archaeal organism (tentatively assigned to a new phylum, Nanoarchaeota), seems to have a genome of only ∼300 kilobase”
Simultaneous Assessment of Soil Microbial Community Structure and Function through Analysis of the Meta-Transcriptome (2008, neutral): “the Nanoarchaeota [27].”