Sphaerotilus uruguayifluvii sp. nov., a novel filamentous bacterium isolated from river water.


Journal

Antonie van Leeuwenhoek
ISSN: 1572-9699
Titre abrégé: Antonie Van Leeuwenhoek
Pays: Netherlands
ID NLM: 0372625

Informations de publication

Date de publication:
09 Jul 2024
Historique:
received: 02 05 2024
accepted: 29 06 2024
medline: 9 7 2024
pubmed: 9 7 2024
entrez: 9 7 2024
Statut: epublish

Résumé

Strain C29

Identifiants

pubmed: 38980405
doi: 10.1007/s10482-024-01996-4
pii: 10.1007/s10482-024-01996-4
doi:

Substances chimiques

RNA, Ribosomal, 16S 0
DNA, Bacterial 0
Fatty Acids 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

96

Informations de copyright

© 2024. The Author(s), under exclusive licence to Springer Nature Switzerland AG.

Références

Andrews S (2010) FastQC: a quality control tool for high throughput sequence data. Available online at http://www.bioinformatics.babraham.ac.uk/projects/fastqc
Aramaki T, Blanc-Mathieu R, Endo H, Ohkubo K, Kanehisa M, Goto S, Ogata H (2020) KofamKOALA: KEGG ortholog assignment based on profile HMM and adaptive score threshold. Bioinformatics 34:2251–2252. https://doi.org/10.1093/bioinformatics/btz859
doi: 10.1093/bioinformatics/btz859
Arkin AP, Cottingham RW, Henry CS et al (2018) KBase: the United States department of energy systems biology knowledgebase. Nat Biotechnol 36:566–569. https://doi.org/10.1038/nbt.4163
doi: 10.1038/nbt.4163 pubmed: 29979655 pmcid: 6870991
Aziz RK, Bartels D, Best AA et al (2008) The RAST server: rapid annotations using subsystems technology. BMC Genomics 9:75. https://doi.org/10.1186/1471-2164-9-75
doi: 10.1186/1471-2164-9-75 pubmed: 18261238 pmcid: 2265698
Bankevich A, Nurk S, Antipov D et al (2012) SPAdes: a new genome assembly algorithm and its applications to single-cell sequencing. J Comput Biol 19:455–477. https://doi.org/10.1089/cmb.2012.0021
doi: 10.1089/cmb.2012.0021 pubmed: 22506599 pmcid: 3342519
Barrow GI, Feltham RKA (2003) Cowan and Steel’s Manual for the identification of medical bacteria, 3rd edn. Cambridge University
Bennett S (2004) Solexa Ltd. Pharmacogenomics 5:433–438. https://doi.org/10.1517/14622416.5.4.433
doi: 10.1517/14622416.5.4.433 pubmed: 15165179
Blin K, Shaw S, Augustijn HE et al (2023) antiSMASH 7.0: new and improved predictions for detection, regulation, chemical structures and visualisation. Nucleic Acids Res 51(W1):W46–W50. https://doi.org/10.1093/nar/gkad344
doi: 10.1093/nar/gkad344 pubmed: 37140036 pmcid: 10320115
Bolger AM, Lohse M, Usadel B (2014) Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics 30:2114–2120. https://doi.org/10.1093/bioinformatics/btu170
doi: 10.1093/bioinformatics/btu170 pubmed: 24695404 pmcid: 4103590
Brettin T, Davis JJ, Disz T et al (2015) RASTtk: a modular and extensible implementation of the RAST algorithm for building custom annotation pipelines and annotating batches of genomes. Sci Rep 5:8365. https://doi.org/10.1038/srep08365
doi: 10.1038/srep08365 pubmed: 25666585 pmcid: 4322359
Chaumeil P-A, Mussig AJ, Hugenholtz P, Parks DH (2019) GTDB-Tk: a toolkit to classify genomes with the Genome Taxonomy Database. Bioinformatics 36:1925–1927. https://doi.org/10.1093/bioinformatics/btz848
doi: 10.1093/bioinformatics/btz848 pubmed: 31730192 pmcid: 7703759
Dondero NC (1961) Sphaerotilus, Its nature and economic significance. Adv Appl Microbiol 3:77–107. https://doi.org/10.1016/s0065-2164(08)70507-0
doi: 10.1016/s0065-2164(08)70507-0 pubmed: 13887196
Exton B, Hassard F, Medina-Vaya A, Grabowski RC (2024) Undesirable river biofilms: the composition, environmental drivers, and occurrence of sewage fungus. Ecol Ind 161:111949. https://doi.org/10.1016/j.ecolind.2024.111949
doi: 10.1016/j.ecolind.2024.111949
Francke C, Groot Kormelink T, Hagemeijer Y, Overmars L, Sluijter V, Moezelaar R et al (2011) Comparative analyses imply that the enigmatic Sigma factor 54 is a central controller of the bacterial exterior. BMC Genomics 12:385. https://doi.org/10.1186/1471-2164-12-385
doi: 10.1186/1471-2164-12-385 pubmed: 21806785 pmcid: 3162934
Goris J, Konstantinidis KT, Klappenbach JA et al (2007) DNA-DNA hybridization values and their relationship to whole-genome sequence similarities. Int J Syst Evol Microbiol 57:81–91. https://doi.org/10.1099/ijs.0.64483-0
doi: 10.1099/ijs.0.64483-0 pubmed: 17220447
Grabovich MY, Smolyakov DD, Beletsky AV et al (2021) Reclassification of Sphaerotilus natans subsp. sulfidivorans Gridneva et al. 2011 as Sphaerotilus sulfidivorans sp. Nov. and comparative genome analysis of the genus Sphaerotilus. Arch Microbiol 203:1595–1599. https://doi.org/10.1007/s00203-020-02158-6
doi: 10.1007/s00203-020-02158-6 pubmed: 33399897
Gridneva E, Chernousova E, Dubinina G et al (2011) Taxonomic investigation of representatives of the genus Sphaerotilus: descriptions of Sphaerotilus montanus sp. nov., Sphaerotilus hippei sp. nov., Sphaerotilus natans subsp. natans subsp. nov. and Sphaerotilus natans subsp. sulfidivorans subsp. nov., and an emended description of the genus Sphaerotilus. Int J Syst Evol Microbiol 61:916–925. https://doi.org/10.1099/ijs.0.023887-0
doi: 10.1099/ijs.0.023887-0 pubmed: 20495027
Kämpfer P, Spring S (2015) Incertae Sedis VI. Sphaerotilus. In: Trujillo ME, Dedysh S, DeVos P, Hedlund B, Kämpfer P, Rainey FA, Whitman WB (eds) Bergey’s manual of systematics of archaea and bacteria. Wiley, New York, pp 1–11
Kämpfer P, Weltin D, Hoffmeister D, Dott W (1995) Growth requirements of filamentous bacteria isolated from bulking and scumming sludge. Water Res 29:1585–1588. https://doi.org/10.1016/0043-1354(94)00275-c
doi: 10.1016/0043-1354(94)00275-c
Kimura M (1980) A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences. J Mol Evol 16:111–120. https://doi.org/10.1007/BF01731581
doi: 10.1007/BF01731581 pubmed: 7463489
Konstantinidis KT, Rosselló-Mora R, Amann R (2017) Uncultivated microbes in need of their own taxonomy. ISME J 11:2399–2406. https://doi.org/10.1038/ismej.2017.113
doi: 10.1038/ismej.2017.113 pubmed: 28731467 pmcid: 5649169
Larkin MA, Blackshields G, Brown NP et al (2007) Clustal W and Clustal X version 2.0. Bioinformatics 23:2947–2948. https://doi.org/10.1093/bioinformatics/btm404
doi: 10.1093/bioinformatics/btm404 pubmed: 17846036
Liu Y, Du J, Pei T et al (2022) Genome-based taxonomic classification of the closest-to-Comamonadaceae group supports a new family Sphaerotilaceae fam. Nov. and taxonomic revisions. Syst Appl Microbiol 45:126352. https://doi.org/10.1016/j.syapm.2022.126352
doi: 10.1016/j.syapm.2022.126352 pubmed: 36063784
Ludwig W, Viver T, Westram R et al (2021) Release LTP_12_2020, featuring a new ARB alignment and improved 16S rRNA tree for prokaryotic type strains. Syst Appl Microbiol 44:126218. https://doi.org/10.1016/j.syapm.2021.126218
doi: 10.1016/j.syapm.2021.126218 pubmed: 34111737
Machin EV, Asem MD, Salam N et al (2019) Nesterenkonia natronophila sp. nov., an alkaliphilic actinobacterium isolated from a soda lake, and emended description of the genus Nesterenkonia. Int J Syst Evol Microbiol 69:1960–1966. https://doi.org/10.1099/ijsem.0.003409
doi: 10.1099/ijsem.0.003409 pubmed: 31046899
Meier-Kolthoff JP, Carbasse JS, Peinado-Olarte RL, Göker M (2022) TYGS and LPSN: a database tandem for fast and reliable genome-based classification and nomenclature of prokaryotes. Nucleic Acids Res 50:D801–D807. https://doi.org/10.1093/nar/gkab902
doi: 10.1093/nar/gkab902 pubmed: 34634793
Menes RJ, Machin EV, Roldán DM, Kyrpides N, Woyke T, Whitman WB, Busse HJ (2021) Frigoriflavimonas asaccharolytica gen. nov., sp. nov., a novel psychrophilic esterase and protease producing bacterium isolated from Antarctica. Antonie Van Leeuwenhoek 114:1991–2002. https://doi.org/10.1007/s10482-021-01656-x
doi: 10.1007/s10482-021-01656-x pubmed: 34541621
Mulder EG, Veen V (1963) Investigations on the Sphaerotilus-Leptothrix Group. Antonie Van Leeuwenhoek 29:121–153. https://doi.org/10.1007/BF02046045
doi: 10.1007/BF02046045 pubmed: 14047145
Ostle AG, Holt JG (1982) Nile blue A as a fluorescent stain for poly-beta-hydroxybutyrate. Appl Environ Microbiol 44:238–241. https://doi.org/10.1128/aem.44.1.238-241.1982
doi: 10.1128/aem.44.1.238-241.1982 pubmed: 6181737 pmcid: 241995
Overbeek R, Olson R, Pusch GD et al (2014) The SEED and the Rapid Annotation of microbial genomes using Subsystems Technology (RAST). Nucleic Acids Res 42:D206–D214. https://doi.org/10.1093/nar/gkt1226
doi: 10.1093/nar/gkt1226 pubmed: 24293654
Parks DH, Imelfort M, Skennerton CT et al (2015) CheckM: assessing the quality of microbial genomes recovered from isolates, single cells, and metagenomes. Genome Res 25:1043–1055. https://doi.org/10.1101/gr.186072.114
doi: 10.1101/gr.186072.114 pubmed: 25977477 pmcid: 4484387
Parks DH, Chuvochina M, Waite DW et al (2018) A standardized bacterial taxonomy based on genome phylogeny substantially revises the tree of life. Nat Biotechnol 36:996–1004. https://doi.org/10.1038/nbt.4229
doi: 10.1038/nbt.4229 pubmed: 30148503
Pellegrin V, Juretschko S, Wagner M, Cottenceau G (1999) Morphological and biochemical properties of a Sphaerotilus sp. isolated from paper mill slimes. Appl Environ Microbiol 65:156–162. https://doi.org/10.1128/AEM.65.1.156-162.1999
doi: 10.1128/AEM.65.1.156-162.1999 pubmed: 9872774 pmcid: 90997
Phégnon L, Pérochon J, Uttenweiler-Joseph S, Cahoreau E, Millard P, Létisse F (2023) 6-Phosphogluconolactonase is critical for the efficient functioning of the pentose phosphate pathway. bioRxiv. https://doi.org/10.1101/2023.11.29.569206
doi: 10.1101/2023.11.29.569206
Quast C, Pruesse E, Yilmaz P et al (2013) The SILVA ribosomal RNA gene database project: improved data processing and web-based tools. Nucleic Acids Res 41:D590–D596. https://doi.org/10.1093/nar/gks1219
doi: 10.1093/nar/gks1219 pubmed: 23193283
Richter M, Rosselló-Mora R (2009) Shifting the genomic gold standard for the prokaryotic species definition. Proc Natl Acad Sci U S A 106:19126–19131. https://doi.org/10.1073/pnas.0906412106
doi: 10.1073/pnas.0906412106 pubmed: 19855009 pmcid: 2776425
Rodriguez-R LM, Konstantinidis KT (2016) The enveomics collection: a toolbox for specialized analyses of microbial genomes and metagenomes. Peer J Preprints 4:e19000v1. https://doi.org/10.7287/peerj.preprints.1900v1
doi: 10.7287/peerj.preprints.1900v1
Seder-Colomina M, Morin G, Benzerara K et al (2014) Sphaerotilus natans, a neutrophilic iron-related sheath-forming bacterium: perspectives for metal remediation strategies. Geomicrobiol J 31:64–75. https://doi.org/10.1080/01490451.2013.806611
doi: 10.1080/01490451.2013.806611
Siering PL, Ghiorse WC (1996) Phylogeny of the Sphaerotilus-Leptothrix group inferred from morphological comparisons, genomic fingerprinting, and 16S ribosomal DNA sequence analyses. Int J Syst Bacteriol 46:173–182. https://doi.org/10.1099/00207713-46-1-173
doi: 10.1099/00207713-46-1-173 pubmed: 8573492
Smibert RM, Krieg NR (1994) Phenotypic characterization. In: Gerhardt P, Murray RGE, Wood WA, Krieg NR (eds) Methods for general and molecular bacteriology. American Society for Microbiology, Washington D.C., pp 607–654
Spring S (2006) The genera Leptothrix and Sphaerotilus. In: Dworkin M, Falkow S, Rosenberg E et al (eds) The prokaryotes: volume 5: proteobacteria: alpha and beta subclasses. Springer, New York, pp 758–777
Spring S, Kampfer P, Ludwig W, Schleifer K-H (1996) Polyphasic characterization of the genus Leptothrix: new descriptions of Leptothrix mobilis sp. nov. and Leptothrix discophora sp. nov. nom. rev. and emended description of Leptothrix cholodnii emend. Syst Appl Microbiol 19:634–643. https://doi.org/10.1016/S0723-2020(96)80036-1
doi: 10.1016/S0723-2020(96)80036-1
Stokes JL (1954) Studies on the filamentous sheathed iron bacterium Sphaerotilus natans. J Bacteriol 67:278–291. https://doi.org/10.1128/jb.67.3.278-291.1954
doi: 10.1128/jb.67.3.278-291.1954 pubmed: 13142992 pmcid: 357221
Tamura K, Stecher G, Kumar S (2021) MEGA11: molecular evolutionary genetics analysis version 11. Mol Biol Evol 38:3022–3027. https://doi.org/10.1093/molbev/msab120
doi: 10.1093/molbev/msab120 pubmed: 33892491 pmcid: 8233496
van Veen WL, Mulder EG, Deinema MH (1978) The Sphaerotilus-Leptothrix group of bacteria. Microbiol Rev 42:329–356. https://doi.org/10.1128/mr.42.2.329-356.1978
doi: 10.1128/mr.42.2.329-356.1978 pubmed: 353479 pmcid: 281433
Yoon S-H, Ha S-M, Kwon S et al (2017) Introducing EzBioCloud: a taxonomically united database of 16S rRNA gene sequences and whole-genome assemblies. Int J Syst Evol Microbiol 67:1613–1617. https://doi.org/10.1099/ijsem.0.001755
doi: 10.1099/ijsem.0.001755 pubmed: 28005526 pmcid: 5563544

Auteurs

Eliana V Machin (EV)

Laboratorio de Ecología Microbiana Medioambiental, Facultad de Química y Unidad Asociada del Instituto de Química Biológica, Facultad de Ciencias, Universidad de la República, Montevideo, Uruguay.

Diego M Roldán (DM)

Laboratorio de Ecología Microbiana Medioambiental, Facultad de Química y Unidad Asociada del Instituto de Química Biológica, Facultad de Ciencias, Universidad de la República, Montevideo, Uruguay.

Rodolfo Javier Menes (RJ)

Laboratorio de Ecología Microbiana Medioambiental, Facultad de Química y Unidad Asociada del Instituto de Química Biológica, Facultad de Ciencias, Universidad de la República, Montevideo, Uruguay. jmenes@fq.edu.uy.

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Classifications MeSH