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Free-living psychrophilic bacteria of the genus Psychrobacter are descendants of pathobionts

https://doi.org/10.1101/2020.10.23.352302

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Outgoing claims: the papers this work cites, builds on, or argues with.

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Bergey's Manual of Systematics of Archaea and Bacteria

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Some like it cold: understanding the survival strategies of psychrophiles

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A clinical and bacteriological study of diplo‐bacillary conjunctivitis

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Über das Vorkommen von Neisserien bei einigen Tieren

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Psychrophilic lifestyles: mechanisms of adaptation and biotechnological tools

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Isolated faecal bacterial communities found for Weddell seals, Leptonychotes weddellii, at White Island, McMurdo Sound, Antarctica

inferredcites →https://doi.org/10.1007/s00792-013-0521-0openalex-snapshot

Plasmid diversity in arctic strains of Psychrobacter spp.

inferredcites →https://doi.org/10.1016/0022-2836(82)90515-0openalex-snapshot

A simple method for displaying the hydropathic character of a protein

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Iron availability and infection

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Human Genetics Shape the Gut Microbiome

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Arabidopsis thaliana and Pseudomonas Pathogens Exhibit Stable Associations over Evolutionary Timescales

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Characterisation of the microbiota of Atlantic mackerel (Scomber scombrus)

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Tracing the evolution of gene loss in obligate bacterial symbionts

inferredcites →https://doi.org/10.1016/j.mib.2017.11.021openalex-snapshot

Evolution of virulence in the Mycobacterium tuberculosis complex

inferredcites →https://doi.org/10.1016/j.mib.2019.12.004openalex-snapshot

Virulence from the rhizosphere: ecology and evolution of Burkholderia pseudomallei-complex species

inferredcites →https://doi.org/10.1016/s0723-2020(97)80067-7openalex-snapshot

Psychrobacter glacincola sp. nov., a Halotolerant, Psychrophilic Bacterium Isolated from Antarctic Sea Ice

inferredcites →https://doi.org/10.1038/nrmicro.2018.8openalex-snapshot

Ecology and evolution of Mycobacterium tuberculosis

inferredcites →https://doi.org/10.1038/nrmicro1008openalex-snapshot

Invertebrates as a source of emerging human pathogens

inferredcites →https://doi.org/10.1038/nrmicro1978openalex-snapshot

Worlds within worlds: evolution of the vertebrate gut microbiota

inferredcites →https://doi.org/10.1038/nrmicro730openalex-snapshot

The Yersiniae — a model genus to study the rapid evolution of bacterial pathogens

inferredcites →https://doi.org/10.1038/s41396-018-0231-9openalex-snapshot

Low spatial structure and selection against secreted virulence factors attenuates pathogenicity in Pseudomonas aeruginosa

inferredcites →https://doi.org/10.1046/j.1365-2958.1998.01010.xopenalex-snapshot

Type IV pili are involved in plant–microbe and fungus–microbe interactions

inferredcites →https://doi.org/10.1073/pnas.0832438100openalex-snapshot

Conservation of genome content and virulence determinants among clinical and environmental isolates of Pseudomonas aeruginosa

inferredcites →https://doi.org/10.1073/pnas.1000080107openalex-snapshot

Global patterns of 16S rRNA diversity at a depth of millions of sequences per sample

inferredcites →https://doi.org/10.1078/0723-2020-00099openalex-snapshot

Psychrobacter faecalis sp. nov., a New Species from a Bioaerosol Originating from Pigeon Faeces

inferredcites →https://doi.org/10.1093/femsec/fiy102openalex-snapshot

Adaptations to marine versus terrestrial low temperature environments as revealed by comparative genomic analyses of the genus Psychrobacter

inferredcites →https://doi.org/10.1093/gbe/evp016openalex-snapshot

Deletional Bias across the Three Domains of Life

inferredcites →https://doi.org/10.1093/gbe/evt209openalex-snapshot

Extensive Gene Acquisition in the Extremely Psychrophilic Bacterial Species Psychroflexus torquis and the Link to Sea-Ice Ecosystem Specialism

inferredcites →https://doi.org/10.1093/infdis/106.2.162openalex-snapshot

A Neisseria Species Associated with Infectious Keratoconjunctivitis of Sheep Neisseria Ovis Nov. Spec.

inferredcites →https://doi.org/10.1097/qco.0b013e3283298e4eopenalex-snapshot

Virulence mechanisms of Moraxella in the pathogenesis of infection

inferredcites →https://doi.org/10.1099/00207713-17-2-127openalex-snapshot

A new Moraxella species, Moraxella osloensis, and a revised description of Moraxella nonliquefaciens

inferredcites →https://doi.org/10.1099/00207713-20-2-155openalex-snapshot

Transfer of the Organism Named Neisseria Catarrhalis to Branhamella Gen. Nov

inferredcites →https://doi.org/10.1099/00207713-21-1-28openalex-snapshot

Designation of a Neotype Strain for Moraxella bovis (Hauduroy et al.) Murray

inferredcites →https://doi.org/10.1099/00207713-26-4-511openalex-snapshot

Moraxella atlantae sp. nov. and Its Distinction from Moraxella phenylpyrouvica

inferredcites →https://doi.org/10.1099/00207713-36-2-228openalex-snapshot

Taxonomy of the Genus Acinetobacter with the Recognition of Acinetobacter baumannii sp. nov., Acinetobacter haemolyticus sp. nov., Acinetobacter johnsonii sp. nov., and Acinetobacter junii sp. nov. and Emended Descriptions of Acinetobacter calcoaceticus and Acinetobacter lwoffii

inferredcites →https://doi.org/10.1099/00207713-36-3-388openalex-snapshot

Psychrobacter immobilis gen. nov., sp. nov.: Genospecies Composed of Gram-Negative, Aerobic, Oxidase-Positive Coccobacilli

inferredcites →https://doi.org/10.1099/00207713-38-2-209openalex-snapshot

Acinetobacter radioresistens sp. nov. Isolated from Cotton and Soil

inferredcites →https://doi.org/10.1099/00207713-43-3-438openalex-snapshot

Polyphasic Taxonomy Leading to the Proposal of Moraxella canis sp. nov. for Moraxella catarrhalis-Like Strains

inferredcites →https://doi.org/10.1099/00207713-43-3-474openalex-snapshot

Moraxella lincolnii sp. nov., Isolated from the Human Respiratory Tract, and Reevaluation of the Taxonomic Position of Moraxella osloensis

inferredcites →https://doi.org/10.1099/00207713-45-3-467openalex-snapshot

Moraxella caprae sp. nov., a New Member of the Classical Moraxellae with Very Close Affinity to Moraxella bovis

inferredcites →https://doi.org/10.1099/00207713-46-4-841openalex-snapshot

Novel Psychrobacter Species from Antarctic Ornithogenic Soils

inferredcites →https://doi.org/10.1099/00207713-47-1-115openalex-snapshot

Moraxella boevrei sp. nov., a New Moraxella Species Found in Goats

inferredcites →https://doi.org/10.1099/00207713-50-2-835openalex-snapshot

Phylogenetic analysis of psychrophilic bacteria isolated from the Japan Trench, including a description of the deep-sea species Psychrobacter pacificensis sp. nov.

inferredcites →https://doi.org/10.1099/00207713-51-5-1891openalex-snapshot

Acinetobacter ursingii sp. nov. and Acinetobacter schindleri sp. nov., isolated from human clinical specimens.

inferredcites →https://doi.org/10.1099/ijs.0.000013openalex-snapshot

Psychrobacter ciconiae sp. nov., isolated from white storks (Ciconia ciconia)

inferredcites →https://doi.org/10.1099/ijs.0.000118openalex-snapshot

Psychrobacter oceani sp. nov., isolated from marine sediment

inferredcites →https://doi.org/10.1099/ijs.0.001230-0openalex-snapshot

Acinetobacter beijerinckii sp. nov. and Acinetobacter gyllenbergii sp. nov., haemolytic organisms isolated from humans

inferredcites →https://doi.org/10.1099/ijs.0.003541-0openalex-snapshot

Description of Acinetobacter venetianus ex Di Cello et al. 1997 sp. nov.

inferredcites →https://doi.org/10.1099/ijs.0.006205-0openalex-snapshot

Moraxella pluranimalium sp. nov., isolated from animal specimens

inferredcites →https://doi.org/10.1099/ijs.0.008706-0openalex-snapshot

Psychrobacter lutiphocae sp. nov., isolated from the faeces of a seal

inferredcites →https://doi.org/10.1099/ijs.0.010959-0openalex-snapshot

Psychrobacter piscatorii sp. nov., a psychrotolerant bacterium exhibiting high catalase activity isolated from an oxidative environment

inferredcites →https://doi.org/10.1099/ijs.0.016626-0openalex-snapshot

Moraxella porci sp. nov., isolated from pigs

inferredcites →https://doi.org/10.1099/ijs.0.016782-0openalex-snapshot

Psychrobacter aestuarii sp. nov., isolated from a tidal flat sediment

inferredcites →https://doi.org/10.1099/ijs.0.02686-0openalex-snapshot

Psychrobacter okhotskensis sp. nov., a lipase-producing facultative psychrophile isolated from the coast of the Okhotsk Sea

inferredcites →https://doi.org/10.1099/ijs.0.029058-0openalex-snapshot

Psychrobacter sanguinis sp. nov., recovered from four clinical specimens over a 4-year period

inferredcites →https://doi.org/10.1099/ijs.0.032631-0openalex-snapshot

Psychrobacter isolates of human origin, other than P. phenylpyruvicus, do not belong to P. immobilis, but are predominantly P. faecalis and P. pulmonis

inferredcites →https://doi.org/10.1099/ijs.0.037721-0openalex-snapshot

Acinetobacter indicus sp. nov., isolated from a hexachlorocyclohexane dump site

inferredcites →https://doi.org/10.1099/ijs.0.043489-0openalex-snapshot

Acinetobacter nectaris sp. nov. and Acinetobacter boissieri sp. nov., isolated from floral nectar of wild Mediterranean insect-pollinated plants

inferredcites →https://doi.org/10.1099/ijs.0.047274-0openalex-snapshot

Acinetobacter puyangensis sp. nov., isolated from the healthy and diseased part of Populus ×euramericana canker bark

inferredcites →https://doi.org/10.1099/ijs.0.047969-0openalex-snapshot

Acinetobacter kookii sp. nov., isolated from soil

inferredcites →https://doi.org/10.1099/ijs.0.068791-0openalex-snapshot

Acinetobacter gandensis sp. nov. isolated from horse and cattle

inferredcites →https://doi.org/10.1099/ijs.0.63096-0openalex-snapshot

Psychrobacter maritimus sp. nov. and Psychrobacter arenosus sp. nov., isolated from coastal sea ice and sediments of the Sea of Japan

inferredcites →https://doi.org/10.1099/ijs.0.63250-0openalex-snapshot

Transfer of the misnamed [Alysiella] sp. IAM 14971 (=ATCC 29468) to the genus Moraxella as Moraxella oblonga sp. nov.

inferredcites →https://doi.org/10.1099/ijs.0.63464-0openalex-snapshot

Psychrobacter aquimaris sp. nov. and Psychrobacter namhaensis sp. nov., isolated from sea water of the South Sea in Korea

inferredcites →https://doi.org/10.1099/ijs.0.63682-0openalex-snapshot

Psychrobacter celer sp. nov., isolated from sea water of the South Sea in Korea

inferredcites →https://doi.org/10.1099/ijs.0.64043-0openalex-snapshot

Psychrobacter cryohalolentis sp. nov. and Psychrobacter arcticus sp. nov., isolated from Siberian permafrost

inferredcites →https://doi.org/10.1099/ijs.0.64333-0openalex-snapshot

Moraxella bovoculi sp. nov., isolated from calves with infectious bovine keratoconjunctivitis

inferredcites →https://doi.org/10.1099/ijsem.0.000806openalex-snapshot

Acinetobacter equi sp. nov., isolated from horse faeces

inferredcites →https://doi.org/10.1099/ijsem.0.000932openalex-snapshot

Taxonomy of haemolytic and/or proteolytic strains of the genus Acinetobacter with the proposal of Acinetobacter courvalinii sp. nov. (genomic species 14 sensu Bouvet & Jeanjean), Acinetobacter dispersus sp. nov. (genomic species 17), Acinetobacter modestus sp. nov., Acinetobacter proteolyticus sp.…

inferredcites →https://doi.org/10.1099/ijsem.0.000939openalex-snapshot

Psychrobacter glaciei sp. nov., isolated from the ice core of an Arctic glacier

inferredcites →https://doi.org/10.1099/ijsem.0.001526openalex-snapshot

Acinetobacter celticus sp. nov., a psychrotolerant species widespread in natural soil and water ecosystems

inferredcites →https://doi.org/10.1099/ijsem.0.001903openalex-snapshot

Acinetobacter colistiniresistens sp. nov. (formerly genomic species 13 sensu Bouvet and Jeanjean and genomic species 14 sensu Tjernberg and Ursing), isolated from human infections and characterized by intrinsic resistance to polymyxins

inferredcites →https://doi.org/10.1099/ijsem.0.002608openalex-snapshot

Acinetobacter piscicola sp. nov., isolated from diseased farmed Murray cod (Maccullochella peelii peelii)

inferredcites →https://doi.org/10.1099/ijsem.0.003739openalex-snapshot

Psychrobacter pygoscelis sp. nov. isolated from the penguin Pygoscelis papua

inferredcites →https://doi.org/10.1099/mgen.0.000301openalex-snapshot

Genus-wide Yersinia core-genome multilocus sequence typing for species identification and strain characterization

inferredcites →https://doi.org/10.1111/1574-6968.12024openalex-snapshot

The role ofrpoSinEscherichia coliO157 manure-amended soil survival and distribution of allelic variations among bovine, food and clinical isolates

inferredcites →https://doi.org/10.1111/j.1574-6976.2008.00153.xopenalex-snapshot

Colonization outwith the colon: plants as an alternative environmental reservoir for human pathogenic enterobacteria

inferredcites →https://doi.org/10.1111/j.1751-0813.1987.tb09647.xopenalex-snapshot

Isolation of a Moraxella sp from horses with conjunctivitis

inferredcites →https://doi.org/10.1111/j.2041-210x.2011.00169.xopenalex-snapshot

phytools: an R package for phylogenetic comparative biology (and other things)

inferredcites →https://doi.org/10.1126/science.1104816openalex-snapshot

Host-Bacterial Mutualism in the Human Intestine

inferredcites →https://doi.org/10.1128/genomea.00280-14openalex-snapshot

Draft Genome Sequences of Psychrobacter Strains JCM 18900, JCM 18901, JCM 18902, and JCM 18903, Isolated Preferentially from Frozen Aquatic Organisms

inferredcites →https://doi.org/10.1128/jb.00795-17openalex-snapshot

Environmental Role of Pathogenic Traits in Vibrio cholerae

inferredcites →https://doi.org/10.1128/jb.01377-08openalex-snapshot

Psychrobacter arcticus 273-4 Uses Resource Efficiency and Molecular Motion Adaptations for Subzero Temperature Growth

inferredcites →https://doi.org/10.1128/jb.65.6.744-744.1953openalex-snapshot

NEISSERIA CAVIAE NOV SPEC

inferredcites →https://doi.org/10.1128/jcm.01197-14openalex-snapshot

Psychrobacter sanguinis: an Unusual Bacterium for Nosocomial Meningitis

inferredcites →https://doi.org/10.1128/mbio.01033-18openalex-snapshot

Ongoing Transposon-Mediated Genome Reduction in the Luminous Bacterial Symbionts of Deep-Sea Ceratioid Anglerfishes

inferredcites →https://doi.org/10.1128/msystems.00119-17openalex-snapshot

Extensive Core Microbiome in Drone-Captured Whale Blow Supports a Framework for Health Monitoring

inferredcites →https://doi.org/10.1128/msystems.01045-20openalex-snapshot

Large-Scale Metagenome Assembly Reveals Novel Animal-Associated Microbial Genomes, Biosynthetic Gene Clusters, and Other Genetic Diversity

inferredcites →https://doi.org/10.1155/2013/512840openalex-snapshot

Psychrophilic Enzymes: From Folding to Function and Biotechnology

inferredcites →https://doi.org/10.1186/gb-2004-5-9-r64openalex-snapshot

Comprehensive analysis of pseudogenes in prokaryotes: widespread gene decay and failure of putative horizontally transferred genes

inferredcites →https://doi.org/10.1242/jeb.114298openalex-snapshot

Adaptations of protein structure and function to temperature: there is more than one way to ‘skin a cat’

inferredcites →https://doi.org/10.1371/journal.pcbi.1005958openalex-snapshot

A phylogenetic method to perform genome-wide association studies in microbes that accounts for population structure and recombination

inferredcites →https://doi.org/10.1371/journal.pone.0043801openalex-snapshot

Life History Trade-Offs and Relaxed Selection Can Decrease Bacterial Virulence in Environmental Reservoirs

inferredcites →https://doi.org/10.1371/journal.pone.0048374openalex-snapshot

Next-Generation Sequencing for Rodent Barcoding: Species Identification from Fresh, Degraded and Environmental Samples

inferredcites →https://doi.org/10.1371/journal.pone.0090785openalex-snapshot

Humpback Whale Populations Share a Core Skin Bacterial Community: Towards a Health Index for Marine Mammals?

inferredcites →https://doi.org/10.2460/ajvr.1970.31.03.457openalex-snapshot

Isolation and Description of a Moraxella from Horses with Conjunctivitis

inferredcites →https://doi.org/10.3389/fcimb.2016.00100openalex-snapshot

Two Glycosyltransferase Genes of Haemophilus parasuis SC096 Implicated in Lipooligosaccharide Biosynthesis, Serum Resistance, Adherence, and Invasion

inferredcites →https://doi.org/10.3389/fgene.2017.00072openalex-snapshot

The Evolution of Bacterial Genome Architecture

inferredcites →https://doi.org/10.3389/fmicb.2017.00369openalex-snapshot

Genotypes Associated with Listeria monocytogenes Isolates Displaying Impaired or Enhanced Tolerances to Cold, Salt, Acid, or Desiccation Stress

inferredcites →https://doi.org/10.3390/biology2020719openalex-snapshot

Psychrophily and Catalysis

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