International Journal of Systematic and Evolutionary Microbiology


Publications
250

Aristaeella hokkaidonensis gen. nov. sp. nov. and Aristaeella lactis sp. nov., two rumen bacterial species of a novel proposed family, Aristaeellaceae fam. nov

Citation
Mahoney-Kurpe et al. (2023). International Journal of Systematic and Evolutionary Microbiology 73 (5)
Names
Aristaeellaceae
Abstract
Two strains of Gram-negative, anaerobic, rod-shaped bacteria, from an abundant but uncharacterized rumen bacterial group of the order ‘Christensenellales’, were phylogenetically and phenotypically characterized. These strains, designated R-7T and WTE2008T, shared 98.6–99.0 % sequence identity between their 16S rRNA gene sequences. R-7T and WTE2008T clustered together on a distinct branch from other Christensenellaceae

Naming genera after geographical locations. Proposal to emend Appendix 9 of the International Code of Nomenclature of Prokaryotes

Citation
Oren, Chuvochina (2023). International Journal of Systematic and Evolutionary Microbiology 73 (5)
Names
Macondimonas Kapaibacterium
Abstract
Appendix 9, Section E of the International Code of Nomenclature of Prokaryotes provides guidelines on how to form adjectival specific and subspecific epithets that reflect the geographical location where the organism was found or studied. It does not mention ways of naming genera after geographical locations. We here propose emendation of Appendix 9 with the recommendations on how to form such names. Comments on the implementation of the current wording of Appendix 9, Section E are also made.

Candidatus List. Lists of names of prokaryotic Candidatus phyla

Citation
Oren, Göker (2023). International Journal of Systematic and Evolutionary Microbiology 73 (5)
Names
“Caldatribacteriota” “Caldipriscota” “Calescibacteriota” “Canglongiota” “Deferrimicrobiota” “Dormiibacterota” Eremiobacterota “Fermentibacterota” “Fervidibacterota” “Freyrarchaeota” “Geothermarchaeota” “Heilongiota” “Hermodarchaeota” “Hinthialibacterota” “Huberarchaeota” “Hydrogenedentota” “Hydrothermota” “Iainarchaeota” “Kapaibacteriota” “Krumholzibacteriota” “Kryptoniota” “Kerfeldiibacteriota” “Komeiliibacteriota” “Levyibacteriota” “Lindowiibacteriota” “Liptoniibacteriota” “Lloydiibacteriota” “Magasanikiibacteriota” “Margulisiibacteriota” “Martarchaeota” “Melainobacteriota” “Moissliibacteriota” “Montesoliibacteriota” “Nealsoniibacteriota” “Nezhaarchaeota” “Niyogiibacteriota” “Nomuraibacteriota” “Pacearchaeota” “Peregrinibacteriota” “Poribacteriota” “Portnoyibacteriota” “Ratteibacteriota” “Raymondiibacteriota” “Roizmaniibacteriota” “Rokuibacteriota” “Ryaniibacteriota” “Saganiibacteriota” “Schekmaniibacteriota” “Spechtiibacteriota” “Stahliibacteriota” “Staskawicziibacteriota” “Sungiibacteriota” “Tagaibacteriota” “Tayloriibacteriota” “Tectimicrobiota” “Terryibacteriota” “Torokiibacteriota” “Uhriibacteriota” “Vebleniibacteriota” “Wolfeibacteriota” “Woykeibacteriota” “Yanofskyibacteriota” “Yonathiibacteriota” “Zambryskiibacteriota” “Abawacaibacteriota” “Augarchaeota” “Lokiarchaeota” “Macinerneyibacteriota” “Methanomethylicota” “Moduliflexota” “Nanohalarchaeota” “Neomarinimicrobiota” “Odinarchaeota” “Paceibacterota” “Parcunitrobacterota” “Parvarchaeota” “Poseidoniota” “Qinglongiota” “Saccharimonadota” “Sifarchaeota” “Sumerlaeota” “Tianyaibacteriota” “Undinarchaeota” “Wukongarchaeota” “Babelota” “Wirthibacterota” “Rifleibacteriota” “Joergenseniibacteriota” “Kueneniibacteriota” “Jacksoniibacteriota” “Moraniibacteriota” “Shapirobacteriota” “Zixiibacteriota” Cloacimonadota Muiribacteriota “Latescibacterota” “Acetithermota” “Aenigmatarchaeota” “Aerophobota” “Altiarchaeota” “Altimarinota” “Aminicenantota”
Abstract

Aminithiophilus ramosus gen. nov., sp. nov., a sulphur-reducing bacterium isolated from a pyrite-forming enrichment culture, and taxonomic revision of the family Synergistaceae

Citation
Pradel et al. (2023). International Journal of Systematic and Evolutionary Microbiology 73 (2)
Names
Acetomicrobium Acetomicrobiaceae Aminiphilaceae Aminithiophilaceae Lactivibrio Aminobacteriaceae Rarimicrobium Jonquetella Dethiosulfovibrionaceae Thermovirga Thermovirgaceae
Abstract
A novel sulphur-reducing bacterium was isolated from a pyrite-forming enrichment culture inoculated with sewage sludge from a wastewater treatment plant. Based on phylogenetic data, strain J.5.4.2-T.3.5.2T could be affiliated with the phylum Synergistota . Among type strains of species with validly published names, the highest 16S rRNA gene sequence identity value was found with

Insights into the phylogenetic inconsistencies of the genus Amazonocrinis and description of epilithic Amazonocrinis malviyae sp. nov. (Cyanobacteria, Nostocales) from Jammu and Kashmir, India

Citation
Kumar et al. (2022). International Journal of Systematic and Evolutionary Microbiology 72 (12)
Names
Amazonocrinis malviyae
Abstract
A dark-coloured thin film of cyanobacteria growing on the bottom of a submerged stone was isolated from Basantgarh village in Udhampur district, Jammu and Kashmir, India. The isolated strain (designated 19C-PST) was characterized using a polyphasic approach. The strain exhibited typical Nostoc -like morphology with a characteristic feature of having heterocytes in series. The 16S rRNA gene phylogeny placed the

Filling the gaps: missing taxon names at the ranks of class, order and family

Citation
Göker (2022). International Journal of Systematic and Evolutionary Microbiology 72 (12)
Names
Kitasatosporales Nitrospiraceae Pseudobdellovibrionaceae Hydrogenophilia Bryobacterales Terriglobia Terriglobales Acidobacteriaceae Nitrospinales Nitrospinia Kiritimatiellia Chlorobiia Calditrichia Nitrospiria “Nitrobium” Nitrospirales Paracoccaceae
Abstract
The International Code of Nomenclature of Prokaryotes (ICNP) recently underwent some major modifications regarding the higher taxonomic ranks. On the one hand, the phylum category was introduced into the ICNP, which rapidly led to the valid publication of more than forty names of phyla. On the other hand, a decision on the retroactivity of Rule 8 regarding the names of classes was made, which removed most of the nomenclatural uncertainty that had affected those names during the last decade. Howe

Candidatus List No. 4: Lists of names of prokaryotic Candidatus taxa

Citation
Oren (2022). International Journal of Systematic and Evolutionary Microbiology 72 (11)
Names
“Vampirococcus archaeovorus” “Ventrenecus avicola” “Ventrenecus stercoripullorum” “Ventricola gallistercoris” “Ventricola intestinavium” “Ventrousia excrementavium” “Woodwardiibium gallinarum” “Woodwardiibium” “Wukongarchaeum yapense” “Xiphinematincola pachtaicus” “Yaniella excrementigallinarum” “Zophobacter franzmannii” “Zymogenus saltonensis” Aeolococcus gillhamiae Ts Nephthysia bennettiae Ts Nephthysia Dormibacter inghamiae Dormibacter spiritus Ts “Allochristensenella” “Allobutyricicoccus” “Alectryocaccomicrobium” “Alectryocaccobium” “Alangreenwoodia” Aeolococcus “Adamsella” “Acidoferrum” “Zymogenaceae” Xenobiaceae “Wukongarchaeaceae” “Uabimicrobiaceae” “Scalinduaceae” “Gimiplasmataceae” “Galloscillospiraceae” “Dormibacteraceae” “Borrarchaeaceae” “Anaeroferrophilaceae” Aeolococcaceae “Zymogenales” “Uabimicrobiales” “Kariarchaeales” “Gimiplasmatales” Eremiobacterales “Dormibacterales” “Borrarchaeales” Aeolococcales “Acidiferrales” “Zymogenia” “Wukongarchaeia” “Uabimicrobiia” “Kariarchaeia” Eremiobacteria “Dormibacteria” “Borrarchaeia” “Anaeropigmentatia” “Anaeroferrophilia” “Pleurinema perforans” “Phytoplasma cocoitanzaniae” “Phytoplasma cocoinigeriae” “Nardonella hylobii” “Mycoplasma haematosphigguri” “Methanoperedens ferrireducens” “Ichthyocystis spari” “Ichthyocystis hellenica” “Geobacter eutrophicus” “Erwinia haradaeae” “Blochmannia ulcerosa” “Blochmannia laevigata” “Acestibacter aggregatus” “Rubrimentiphilum” “Ichthyocystis” “Acestibacter” “Nitrosotaleaceae” “Rubrimentiphilales” “Brocadiia” “Neomicrothrix subdominans” “Allolimicola stercorigallinarum” “Allolimicola” Sulfomarinibacter kjeldsenii Ts Sulfomarinibacteraceae Sulfomarinibacter
Abstract

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