Ecology, Evolution, Behavior and Systematics


Publications
589

Verrucomicrobiota are specialist consumers of sulfated methyl pentoses during diatom blooms

Citation
Orellana et al. (2022). The ISME Journal 16 (3)
Names
“Fucivorax forsetii” “Fucivorax” “Mariakkermansia forsetii” “Mariakkermansia” “Chordibacter forsetii”
Abstract
AbstractMarine algae annually sequester petagrams of carbon dioxide into polysaccharides, which are a central metabolic fuel for marine carbon cycling. Diatom microalgae produce sulfated polysaccharides containing methyl pentoses that are challenging to degrade for bacteria compared to other monomers, implicating these sugars as a potential carbon sink. Free-living bacteria occurring in phytoplankton blooms that specialise on consuming microalgal sugars, containing fucose and rhamnose remain unk

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

16S rRNA gene sequences of Candidatus Methylumidiphilus (Methylococcales), a putative methanotrophic genus in lakes and ponds

Citation
Rissanen et al. (2022). Aquatic Microbial Ecology 88
Names
Ca. Methylumidiphilus Ca. Methylumidiphilus alinenensis
Abstract
A putative novel methanotrophic genus, Candidatus Methylumidiphilus (Methylococcales), was recently shown to be ubiquitous and one of the most abundant methanotrophic genera in water columns of oxygen-stratified lakes and ponds in boreal and subarctic areas. However, it has probably escaped detection in many previous studies that used 16S rRNA gene amplicon sequencing due to insufficient database coverage, as previously analysed metagenome-assembled genomes (MAGs) affiliated with Ca. Methylumidi

Beetle–Bacterial Symbioses: Endless Forms Most Functional

Citation
Salem, Kaltenpoth (2022). Annual Review of Entomology 67 (1)
Names
Shikimatogenerans silvanidophilus Ts
Abstract
Beetles are hosts to a remarkable diversity of bacterial symbionts. In this article, we review the role of these partnerships in promoting beetle fitness following a surge of recent studies characterizing symbiont localization and function across the Coleoptera. Symbiont contributions range from the supplementation of essential nutrients and digestive or detoxifying enzymes to the production of bioactive compounds providing defense against natural enemies. Insights on this functional diversity