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206


Zarconia navalis gen. nov., sp. nov., Romeriopsis navalis gen. nov., sp. nov. and Romeriopsis marina sp. nov., isolated from inter- and subtidal environments from northern Portugal

Citation
Hentschke et al. (2022). International Journal of Systematic and Evolutionary Microbiology 72 (10)
Names
Romeriopsis Zarconia Romeriopsis marina Romeriopsis navalis T Zarconia navalis T
Abstract
The morphology, 16S rRNA gene phylogeny and 16S–23S rRNA gene ITS secondary structures of three strains of marine Cyanobacteria, isolated from inter- and subtidal environments from north Portugal were studied, resulting in the description of Zarconia navalis gen. nov., sp. nov. (Oscillatoriales incertae sedis), Romeriopsis navalis gen. nov., sp. nov. (Leptolyngbyaceae) and Romeriopsis marina sp. nov., named under the International Code of Nomenclature for algae, fungi, and plants. No diacritical

Validation of the names Cyanobacterium and Cyanobacterium stanieri, and proposal of Cyanobacteriota phyl. nov

Citation
Oren et al. (2022). International Journal of Systematic and Evolutionary Microbiology 72 (10)
Names
Cyanobacterium Cyanobacterium stanieri T Cyanobacteriota Cyanophyceae
Abstract
The decision by the International Committee on Systematics of Prokaryotes (ICSP) to place the rank of phylum under the rules of the International Code of Nomenclature of Prokaryotes (ICNP), with phylum names ending in –ota based on the name of a type genus, enables the valid publication of the phylum name Cyanobacteriota with Cyanobacterium as the type genus. The names

Naming the unnamed: over 65,000 Candidatus names for unnamed Archaea and Bacteria in the Genome Taxonomy Database

Citation
Pallen et al. (2022). International Journal of Systematic and Evolutionary Microbiology 72 (9)
Names
“Afabia udivosa” “Afabia” “Afabiaceae” “Afabiales” “Afabiia” “Afabiota” “Paenistieleria bergensis”
Abstract
Thousands of new bacterial and archaeal species and higher-level taxa are discovered each year through the analysis of genomes and metagenomes. The Genome Taxonomy Database (GTDB) provides hierarchical sequence-based descriptions and classifications for new and as-yet-unnamed taxa. However, bacterial nomenclature, as currently configured, cannot keep up with the need for new well-formed names. Instead, microbiologists have been forced to use hard-to-remember alphanumeric placeholder labels. Here

Nanobdella aerobiophila gen. nov., sp. nov., a thermoacidophilic, obligate ectosymbiotic archaeon, and proposal of Nanobdellaceae fam. nov., Nanobdellales ord. nov. and Nanobdellia class. nov

Citation
Kato et al. (2022). International Journal of Systematic and Evolutionary Microbiology 72 (8)
Names
Nanobdella aerobiophila T Nanobdella Nanobdellaceae Nanobdellales Nanobdellia
Abstract
A co-culture of a novel thermoacidophilic, obligate symbiotic archaeon, designated as strain MJ1T, with its specific host archaeon Metallosphaera sedula strain MJ1HA was obtained from a terrestrial hot spring in Japan. Strain MJ1T grew in the co-culture under aerobic conditions. Coccoid cells of strain MJ1T were 200–500 nm in diameter, and attached to the MJ1HA cells in the co-culture. The ranges and optima o

Revision of the ‘Candidatus Phytoplasma’ species description guidelines

Citation
Bertaccini et al. (2022). International Journal of Systematic and Evolutionary Microbiology 72 (4)
Names
Ca. Phytoplasma
Abstract
The genus ‘Candidatus Phytoplasma’ was proposed to accommodate cell wall-less bacteria that are molecularly and biochemically incompletely characterized, and colonize plant phloem and insect vector tissues. This provisional classification is highly relevant due to its application in epidemiological and ecological studies, mainly aimed at keeping the severe phytoplasma plant diseases under control worldwide. Given the increasing discovery of molecular diversity within the genus ‘Ca. Phytoplasma’,

CANDIDATUS LIST No. 3. Lists of names of prokaryotic Candidatus taxa

Citation
Oren, Garrity (2022). International Journal of Systematic and Evolutionary Microbiology 72 (1)
Names
Elulimicrobiia “Saccharimonadia” “Ozemibacteria” “Caenarcanales” “Fibrimonadales” “Methanoflorentales” “Ozemibacterales” “Fibrimonadaceae” “Ozemibacteraceae” “Acidiflorens” “Annandiella” “Aramenus” “Arocatia” “Changshengia” “Cibionibacter” “Cuticulibacterium” “Didemniditutus” “Endohaliclona” “Euplotella” “Fibrimonas” “Forterrea” “Ischnodemia” “Neowolbachia” “Nitrobium” “Ozemibacter” “Paracaedimonas” “Parafinniella” “Pleuronema” “Reconciliibacillus” “Roseilinea” “Rubidus” “Stammera” “Theodorhartigia” “Acidiflorens stordalenmirensis” “Anadelfobacter sociabilis” “Anaerococcus massiliensis” “Anaerococcus phoceensis” “Anaerococcus timonensis” “Annandiella adelgistsugae” “Annandiella pinicola” “Aramenus sulfurataquae” “Arocatia carayonii” “Azospirillum massiliense” “Bandiella numerosa” “Desulfofervidia” “Macinerneyibacteriia” “Nanohalobiia” “Nanoperiodontomorbia” “Nanosyncoccia” “Syntrophaliphaticia” “Undinarchaeia” “Bartonella gerbillinarum” “Bartonella khokhlovae” “Bartonella negevensis” “Bartonella rudakovii” “Borrelia africana” “Borrelia ivorensis” “Borrelia fainii” “Brocadia braziliensis” “Cibionibacter quicibialis” “Clostridium massiliense” “Clostridium timonense” “Cuticulibacterium kirbyi” “Cytophaga massiliensis” “Desulfopertinax cowenii” Desulfosporosinus infrequens “Didemniditutus mandelae” “Ehrlichia regneryi” “Ehrlichia shimanensis” “Endohaliclona renieramycinifaciens” “Adiutricales” “Desulfofervidales” “Fermentimicrarchaeales” “Entotheonella gemina” “Euplotella sexta” “Finniella dimorpha” “Fibrimonas termitidis” “Forterrea multitransposorum” “Halobeggiatoa borealis” “Ischnodemia utriculi” “Liberibacter brunswickensis” “Mastigocoleus perforans” “Methanoflorens crillii” “Mycoplasma erythrocervae” “Guanabaribacteriales” “Hakubellales” “Macinerneyibacteriales” “Methylospongiales” “Naiadarchaeales” “Nanogingivalales” “Nanohalobiales” “Tepidaquicellales” “Adiutricaceae” “Aminobacteroidaceae” “Chazhemtonibacteriaceae” “Fermentimicrarchaeaceae” “Hakubellaceae” “Macinerneyibacteriaceae” “Magnetomoraceae” “Nanogingivalaceae” “Nanohalobiaceae” “Tepidaquicellaceae” “Thiobarbaceae” “Undinarchaeaceae” “Abditibacter” “Acidifodinimicrobium” “Aminobacteroides” “Anthektikosiphon” “Vallotia laricis” “Vallotia japonica” “Typhincola belonochilicola” “Treponema suis” “Mycoplasma haematomelis” “Nardonella dryophthoridicola” “Nardonella hylobii” “Neoehrlichia tanzaniensis” “Neowolbachia serbiensis” “Tokpelaia hoelldobleri” “Ozemibacter sibiricus” “Paracaedimonas acanthamoebae” “Parafinniella ignota” “Peptoniphilus massiliensis” “Piscichlamydia cyprini” “Pleuronema perforans” “Pleuronema testarum” “Profftia japonica” “Profftia laricis” “Pseudomonas adelgistsugae” “Reconciliibacillus cellulosivorans” “Rickettsia laoensis” “Rickettsia mahosoti” “Roseilinea gracilis” “Sedimenticola endophacoides” “Spiroplasma holothuriicola” “Stammera capsulata” “Synechococcus calcipolaris” “Theodorhartigia pinicola” “Thiosymbium robbeae” “Weimeria bifida”
Abstract

Taxonomic note on the family Pseudonocardiaceae based on phylogenomic analysis and descriptions of Allosaccharopolyspora gen. nov. and Halosaccharopolyspora gen. nov

Citation
Teo et al. (2021). International Journal of Systematic and Evolutionary Microbiology 71 (10)
Names
Pseudonocardiaceae Amycolatopsis Actinoalloteichus cyanogriseus T Actinoalloteichus Actinoalloteichus caeruleus
Abstract
The taxonomic positions of members within the family Pseudonocardiaceae were assessed based on phylogenomic trees reconstructed using core-proteome and genome blast distance phylogeny approaches. The closely clustered genome sequences from the type strains of validly published names within the family Pseudonocardiaceae wer

Valid publication of the names of forty-two phyla of prokaryotes

Citation
Oren, Garrity (2021). International Journal of Systematic and Evolutionary Microbiology 71 (10)
Names
Acidobacterium Actinomyces Aquifex Armatimonas Atribacterota Atribacter Bacillus Actinomycetota Myxococcota Bacillota Chloroflexota Pseudomonadota Acidobacteriota Chlamydiota Planctomycetota “Thermofontia” Verrucomicrobiota Elusimicrobiota Nitrososphaerota Cenarchaeales
Abstract
After the International Committee on Systematics of Prokaryotes (ICSP) had voted to include the rank of phylum in the rules of the International Code of Nomenclature of Prokaryotes (ICNP), and following publication of the decision in the IJSEM, we here present names and formal descriptions of 42 phyla to effect valid publication of their names, based on genera as the nomenclatural types.