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Abstract

Taxon-specific conserved signature indels (CSIs) in genes/proteins provide reliable molecular markers (synapomorphies) for unambiguous demarcation of taxa of different ranks in molecular terms and for genetic, biochemical and diagnostic studies. Because of their predictive abilities, the shared presence of known taxon-specific CSIs in genome sequences has proven useful for taxonomic purposes. However, the lack of a convenient method for identifying the presence of known CSIs in genome sequences has limited their utility for taxonomic and other studies. We describe here a web-based tool/server (AppIndels.com) that identifies the presence of known and validated CSIs in genome sequences and uses this information for predicting taxonomic affiliation. The utility of this server was tested by using a database of 585 validated CSIs, which included 350 CSIs specific for ≈45 genera, with the remaining CSIs being specific for members of the orders , and , family , and some species/genera. Using this server, genome sequences were analysed for 721 strains of unknown taxonomic affiliation. Results obtained showed that 651 of these genomes contained significant numbers of CSIs specific for the following genera/families: , ’, , Cereus clade, Subtilis clade, , , , , , , , , , , , , , , , , , , , , , , and . Validity of the taxon assignment made by the server was examined by reconstructing phylogenomic trees. In these trees, all strains for which taxonomic predictions were made correctly branched with the indicated taxa. The unassigned strains likely correspond to taxa for which CSIs are lacking in our database. Results presented here show that the AppIndels server provides a useful new tool for predicting taxonomic affiliation based on shared presence of the taxon-specific CSIs. Some caveats in using this server are discussed.

Funding
This study was supported by the:
  • Natural Sciences and Engieering Research Council of Canada (Award RGPIN-2019-06397)
    • Principle Award Recipient: RadheyS. Gupta
  • This is an open-access article distributed under the terms of the Creative Commons Attribution NonCommercial License. This article was made open access via a Publish and Read agreement between the Microbiology Society and the corresponding author’s institution.
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2023-05-09
2024-04-26
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References

  1. Whitman WB. Genome sequences as the type material for taxonomic descriptions of prokaryotes. Syst Appl Microbiol 2015; 38:217–222 [View Article] [PubMed]
    [Google Scholar]
  2. Chun J, Oren A, Ventosa A, Christensen H, Arahal DR et al. Proposed minimal standards for the use of genome data for the taxonomy of prokaryotes. Int J Syst Evol Microbiol 2018; 68:461–466 [View Article] [PubMed]
    [Google Scholar]
  3. Hugenholtz P, Chuvochina M, Oren A, Parks DH, Soo RM. Prokaryotic taxonomy and nomenclature in the age of big sequence data. ISME J 2021; 15:1879–1892 [View Article]
    [Google Scholar]
  4. Parks DH, Chuvochina M, Waite DW, Rinke C, Skarshewski A et al. A standardized bacterial taxonomy based on genome phylogeny substantially revises the tree of life. Nat Biotechnol 2018; 36:996–1004 [View Article] [PubMed]
    [Google Scholar]
  5. Chun J, Rainey FA. Integrating genomics into the taxonomy and systematics of the Bacteria and Archaea. Int J Syst Evol Microbiol 2014; 64:316–324 [View Article] [PubMed]
    [Google Scholar]
  6. Meier-Kolthoff JP, Göker M. TYGS is an automated high-throughput platform for state-of-the-art genome-based taxonomy. Nat Commun 2019; 10:2182 [View Article]
    [Google Scholar]
  7. Gupta RS. Impact of genomics on the understanding of microbial evolution and classification: the importance of Darwin’s views on classification. FEMS Microbiol Rev 2016; 40:520–553 [View Article] [PubMed]
    [Google Scholar]
  8. Garrity GM. A new genomics-driven taxonomy of bacteria and archaea: are we there yet?. J Clin Microbiol 2016; 54:1956–1963 [View Article] [PubMed]
    [Google Scholar]
  9. Moore ERB, Mihaylova SA, Vandamme P, Krichevsky MI, Dijkshoorn L. Microbial systematics and taxonomy: relevance for a microbial commons. Res Microbiol 2010; 161:430–438 [View Article] [PubMed]
    [Google Scholar]
  10. Sangal V, Goodfellow M, Jones AL, Schwalbe EC, Blom J et al. Next-generation systematics: an innovative approach to resolve the structure of complex prokaryotic taxa. Sci Rep 2016; 6:38392 [View Article]
    [Google Scholar]
  11. Konstantinidis KT, Tiedje JM. Genomic insights that advance the species definition for prokaryotes. Proc Natl Acad Sci 2005; 102:2567–2572 [View Article]
    [Google Scholar]
  12. Kim M, Oh HS, Park SC, Chun J. Towards a taxonomic coherence between average nucleotide identity and 16S rRNA gene sequence similarity for species demarcation of prokaryotes. Int J Syst Evol Microbiol 2014; 64:346–351 [View Article] [PubMed]
    [Google Scholar]
  13. Richter M, Rosselló-Móra R. Shifting the genomic gold standard for the prokaryotic species definition. Proc Natl Acad Sci 2009; 106:19126–19131 [View Article]
    [Google Scholar]
  14. Varghese NJ, Mukherjee S, Ivanova N, Konstantinidis KT, Mavrommatis K et al. Microbial species delineation using whole genome sequences. Nucleic Acids Res 2015; 43:6761–6771 [View Article] [PubMed]
    [Google Scholar]
  15. Meier-Kolthoff JP, Auch AF, Klenk H-P, Göker M. Genome sequence-based species delimitation with confidence intervals and improved distance functions. BMC Bioinformatics 2013; 14:60 [View Article] [PubMed]
    [Google Scholar]
  16. Goris J, Konstantinidis KT, Klappenbach JA, Coenye T, Vandamme P et al. DNA–DNA hybridization values and their relationship to whole-genome sequence similarities. Int J Syst Evol Microbiol 2007; 57:81–91 [View Article] [PubMed]
    [Google Scholar]
  17. Stackebrandt E, Frederiksen W, Garrity GM, Grimont PA, Kampfer P. Report of the ad hoc committee for the re-evaluation of the species definition in bacteriology. Int J Syst Evol Microbiol 2002; 52:1043–1047 [View Article] [PubMed]
    [Google Scholar]
  18. Yarza P, Yilmaz P, Pruesse E, Glöckner FO, Ludwig W et al. Uniting the classification of cultured and uncultured bacteria and archaea using 16S rRNA gene sequences. Nat Rev Microbiol 2014; 12:635–645 [View Article] [PubMed]
    [Google Scholar]
  19. Gupta RS, Lo B, Son J. Phylogenomics and comparative genomic studies robustly support division of the genus Mycobacterium into an emended genus Mycobacterium and four novel genera. Front Microbiol 2018; 9:67 [View Article]
    [Google Scholar]
  20. Nouioui I, Carro L, García-López M, Meier-Kolthoff JP, Woyke T et al. Genome-based taxonomic classification of the Phylum Actinobacteria. Front Microbiol 2018; 9:2007 [View Article]
    [Google Scholar]
  21. Hördt A, López MG, Meier-Kolthoff JP, Schleuning M, Weinhold L-M et al. Analysis of 1,000+ type-strain genomes substantially improves taxonomic classification of Alphaproteobacteria. Front Microbiol 2020; 11:468 [View Article]
    [Google Scholar]
  22. Waite DW, Vanwonterghem I, Rinke C, Parks DH, Zhang Y et al. Comparative genomic analysis of the class Epsilonproteobacteria and proposed reclassification to Epsilonbacteraeota (phyl. nov.). Front Microbiol 2017; 8:682 [View Article]
    [Google Scholar]
  23. Parker CT, Tindall BJ, Garrity GM. International Code of Nomenclature of Prokaryotes. Int J Syst Evol Microbiol 2019; 69:S:1–S [View Article]
    [Google Scholar]
  24. Goodfellow M. Microbial systematics: background and uses. In Priest FG. eds Applied Microbial Systematics Dordrecht: Kluwer Academic Publishers; 2000 pp 1–18
    [Google Scholar]
  25. Gupta RS. Microbial taxonomy: how and why name changes occur and their significance for (clinical) microbiology. Clin Chem 2021; 68:134–137 [View Article]
    [Google Scholar]
  26. Oren A, Garrity GM. Then and now: a systematic review of the systematics of prokaryotes in the last 80 years. Antonie van Leeuwenhoek 2014; 106:43–56 [View Article]
    [Google Scholar]
  27. Ludwig W, Klenk H-P. Overview: A phylogenetic backbone and taxonomic framework for prokaryotic systamatics. In Brenner DJ, Krieg NR, Staley JT, Garrity GM. eds Bergey’s Manual of Systematic Bacteriology Berlin: Springer-Verlag; 2005 pp 49–65
    [Google Scholar]
  28. Gupta RS. Protein phylogenies and signature sequences: A reappraisal of evolutionary relationships among archaebacteria, eubacteria, and eukaryotes. Microbiol Mol Biol Rev 1998; 62:1435–1491 [View Article] [PubMed]
    [Google Scholar]
  29. Woese CR. How we do, don’t and should look at Bacteria and Bacteriology. In Mea D. eds The Prokaryotes: An Evolving Electronic Resource for the Microbiological Community New York: Springer-Verlag; 2003
    [Google Scholar]
  30. Baldauf SL. Phylogeny for the faint of heart: a tutorial. Trends Genet 2003; 19:345–351 [View Article] [PubMed]
    [Google Scholar]
  31. Felsenstein J. Inferring phylogenies from protein sequences by parsimony, distance, and likelihood methods. Methods Enzymol 1996; 266:418–427 [View Article]
    [Google Scholar]
  32. Lake JA. The order of sequence alignment can bias the selection of tree topology. Mol Biol Evol 1991; 8:378–385 [View Article] [PubMed]
    [Google Scholar]
  33. Konstantinidis KT, Tiedje JM. Prokaryotic taxonomy and phylogeny in the genomic era: advancements and challenges ahead. Curr Opin Microbiol 2007; 10:504–509 [View Article] [PubMed]
    [Google Scholar]
  34. Qin Q-L, Xie B-B, Zhang X-Y, Chen X-L, Zhou B-C et al. A proposed genus boundary for the prokaryotes based on genomic insights. J Bacteriol 2014; 196:2210–2215 [View Article] [PubMed]
    [Google Scholar]
  35. Barco RA, Garrity GM, Scott JJ, Amend JP, Nealson KH et al. A genus definition for bacteria and archaea based on a standard genome relatedness index. mBio 2020; 11: [View Article]
    [Google Scholar]
  36. Gupta RS. Distinction between Borrelia and Borreliella is more robustly supported by molecular and phenotypic characteristics than all other neighbouring prokaryotic genera: Response to Margos’ et al. “The genus Borrelia reloaded” (PLoS One 13(12): e0208432). PLoS One 2019; 14:e0221397 [View Article]
    [Google Scholar]
  37. Puigbò P, Wolf YI, Koonin EV. Seeing the Tree of Life behind the phylogenetic forest. BMC Biol 2013; 11:46 [View Article]
    [Google Scholar]
  38. Adeolu M, Alnajar S, Naushad S, S Gupta R. Genome-based phylogeny and taxonomy of the “Enterobacteriales”: proposal for Enterobacterales ord. nov. divided into the families Enterobacteriaceae, Erwiniaceae fam. nov., Pectobacteriaceae fam. nov., Yersiniaceae fam. nov., Hafniaceae fam. nov., Morganellaceae fam. nov., and Budviciaceae fam. nov. Int J Syst Evol Microbiol 2016; 66:5575–5599 [View Article]
    [Google Scholar]
  39. Sawana A, Adeolu M, Gupta RS. Molecular signatures and phylogenomic analysis of the genus Burkholderia: proposal for division of this genus into the emended genus Burkholderia containing pathogenic organisms and a new genus Paraburkholderia gen. nov. harboring environmental species. Front Genet 2014; 5:429 [View Article]
    [Google Scholar]
  40. Gupta RS, Griffiths E. Chlamydiae-specific proteins and indels: novel tools for studies. Trends Microbiol 2006; 14:527–535 [View Article] [PubMed]
    [Google Scholar]
  41. Griffiths E, Gupta RS. Identification of signature proteins that are distinctive of the Deinococcus-Thermus phylum. Int Microbiol 2007; 10:201–208
    [Google Scholar]
  42. Griffiths E, Petrich AK, Gupta RS. Conserved indels in essential proteins that are distinctive characteristics of Chlamydiales and provide novel means for their identification. Microbiology 2005; 151:2647–2657 [View Article]
    [Google Scholar]
  43. Naushad HS, Gupta RS. Phylogenomics and molecular signatures for species from the plant pathogen-containing order Xanthomonadales. PLoS ONE 2013; 8:e55216 [View Article]
    [Google Scholar]
  44. Gupta RS, Chander P, George S. Phylogenetic framework and molecular signatures for the class Chloroflexi and its different clades; proposal for division of the class Chloroflexia class. nov. [corrected] into the suborder Chloroflexineae subord. nov., consisting of the emended family Oscillochloridaceae and the family Chloroflexaceae fam. nov., and the suborder Roseiflexineae subord. nov., containing the family Roseiflexaceae fam. nov. Antonie van Leeuwenhoek 2013; 103:99–119 [View Article]
    [Google Scholar]
  45. Bhandari V, Gupta RS. Molecular signatures for the phylum Synergistetes and some of its subclades. Antonie van Leeuwenhoek 2012; 102:517–540 [View Article]
    [Google Scholar]
  46. Gao B, Gupta RS. Phylogenetic framework and molecular signatures for the main clades of the phylum Actinobacteria. Microbiol Mol Biol Rev 2012; 76:66–112 [View Article]
    [Google Scholar]
  47. Bhandari V, Gupta RS. Phylum Thermotogae. In Rosenberg E, DeLong E, Lory S, Stackebrandt E, Thompson F. eds The Prokaryotes- Other Major Lineages of Bacteria and the Archaea New York: Springer; 2014 pp 989–1015
    [Google Scholar]
  48. Gupta RS. Identification of conserved indels that are useful for classification and evolutionary studies. In Goodfellow M, Sutcliffe IC, Chun J. eds Bacterial Taxonomy, Methods in Microbiology vol 41 London: Elsevier; 2014 pp 153–182
    [Google Scholar]
  49. Naushad HS, Lee B, Gupta RS. Conserved signature indels and signature proteins as novel tools for understanding microbial phylogeny and systematics: identification of molecular signatures that are specific for the phytopathogenic genera Dickeya, Pectobacterium and Brenneria. Int J Syst Evol Microbiol 2014; 64:366–383 [View Article]
    [Google Scholar]
  50. Bhandari V, Gupta RS. Molecular signatures for the phylum (class) Thermotogae and a proposal for its division into three orders (Thermotogales, Kosmotogales ord. nov. and Petrotogales ord. nov.) containing four families (Thermotogaceae, Fervidobacteriaceae fam. nov., Kosmotogaceae fam. nov. and Petrotogaceae fam. nov.) and a new genus Pseudothermotoga gen. nov. with five new combinations. Antonie van Leeuwenhoek 2014; 105:143–168 [View Article]
    [Google Scholar]
  51. Gupta RS, Naushad S, Chokshi C, Griffiths E, Adeolu M. A phylogenomic and molecular markers based analysis of the phylum Chlamydiae: proposal to divide the class Chlamydiia into two orders, Chlamydiales and Parachlamydiales ord. nov., and emended description of the class Chlamydiia. Antonie van Leeuwenhoek 2015; 108:765–781 [View Article]
    [Google Scholar]
  52. Patel S, Gupta RS. A phylogenomic and comparative genomic framework for resolving the polyphyly of the genus Bacillus: Proposal for six new genera of Bacillus species, Peribacillus gen. nov., Cytobacillus gen. nov., Mesobacillus gen. nov., Neobacillus gen. nov., Metabacillus gen. nov. and Alkalihalobacillus gen. nov. Int J Syst Evol Microbiol 2020; 70:406–438 [View Article]
    [Google Scholar]
  53. Barbour AG, Adeolu M, Gupta RS. Division of the genus Borrelia into two genera (corresponding to Lyme disease and relapsing fever groups) reflects their genetic and phenotypic distinctiveness and will lead to a better understanding of these two groups of microbes (Margos et al. (2016) There is inadequate evidence to support the division of the genus Borrelia. Int. J. Syst. Evol. Microbiol. doi: 10.1099/ijsem.0.001717). Int J Syst Evol Microbiol 2017; 67:2058–2067 [View Article]
    [Google Scholar]
  54. Dobritsa AP, Samadpour M. Reclassification of Burkholderia insecticola as Caballeronia insecticola comb. nov. and reliability of conserved signature indels as molecular synapomorphies. Int J Syst Evol Microbiol 2019; 69:2057–2063 [View Article]
    [Google Scholar]
  55. Ma Y, Wu X, Li S, Tang L, Chen M et al. Proposal for reunification of the genus Raoultella with the genus Klebsiella and reclassification of Raoultella electrica as Klebsiella electrica comb. nov. Res Microbiol 2021; 172:103851 [View Article]
    [Google Scholar]
  56. Jiang L, Wang D, Kim J-S, Lee JH, Kim D-H et al. Reclassification of genus Izhakiella into the family Erwiniaceae based on phylogenetic and genomic analyses. Int J Syst Evol Microbiol 2020; 70:3541–3546 [View Article]
    [Google Scholar]
  57. Gupta RS. Protein signatures (molecular synapomorphies) that are distinctive characteristics of the major cyanobacterial clades. Int J Syst Evol Microbiol 2009; 59:2510–2526 [View Article] [PubMed]
    [Google Scholar]
  58. Gupta RS, Patel S, Saini N, Chen S. Erratum: Robust demarcation of seventeen distinct Bacillus species clades, proposed as novel Bacillaceae genera, by phylogenomics and comparative genomic analyses: description of Robertmurraya kyonggiensis sp. nov. and proposal for emended genus Bacillus limiting it only to the members of the Subtilis and Cereus clades of species. Int J Syst Evol Microbiol 2020; 70:6531–6533 [View Article]
    [Google Scholar]
  59. Campbell C, Adeolu M, Gupta RS. Genome-based taxonomic framework for the class Negativicutes: division of the class Negativicutes into the orders Selenomonadales emend., Acidaminococcales ord. nov. and Veillonellales ord. nov. Int J Syst Evol Microbiol 2015; 65:3203–3215 [View Article]
    [Google Scholar]
  60. Dobritsa AP, Linardopoulou EV, Samadpour M. Transfer of 13 species of the genus Burkholderia to the genus Caballeronia and reclassification of Burkholderia jirisanensis as Paraburkholderia jirisanensis comb. nov. Int J Syst Evol Microbiol 2017; 67:3846–3853 [View Article]
    [Google Scholar]
  61. Cutiño-Jiménez AM, Menck CFM, Cambas YT, Díaz-Pérez JC. Protein signatures to identify the different genera within the Xanthomonadaceae family. Braz J Microbiol 2020; 51:1515–1526 [View Article]
    [Google Scholar]
  62. Barbour AG. Borreliaceae. In Bergey Manual of Systematics of Bacteria and Archaea John Wiley & Sons, Inc. Bergey’s Trust; 2018
    [Google Scholar]
  63. Gupta RS, Sawnani S, Adeolu M, Alnajar S, Oren A. Phylogenetic framework for the phylum Tenericutes based on genome sequence data: proposal for the creation of a new order Mycoplasmoidales ord. nov., containing two new families Mycoplasmoidaceae fam. nov. and Metamycoplasmataceae fam. nov. harbouring Eperythrozoon, Ureaplasma and five novel genera. Antonie van Leeuwenhoek 2018; 111:1583–1630 [View Article]
    [Google Scholar]
  64. Saini N, Gupta RS. A robust phylogenetic framework for members of the order Legionellales and its main genera (Legionella, Aquicella, Coxiella and Rickettsiella) based on phylogenomic analyses and identification of molecular markers demarcating different clades. Antonie van Leeuwenhoek 2021; 114:957–982 [View Article]
    [Google Scholar]
  65. Gupta RS, Son J, Oren A. A phylogenomic and molecular markers based taxonomic framework for members of the order Entomoplasmatales: proposal for an emended order Mycoplasmatales containing the family Spiroplasmataceae and emended family Mycoplasmataceae comprised of six genera. Antonie van Leeuwenhoek 2019; 112:561–588 [View Article]
    [Google Scholar]
  66. Gupta RS, Patel S. Robust demarcation of the family Caryophanaceae (Planococcaceae) and its different genera including three novel genera based on phylogenomics and highly specific molecular signatures. Front Microbiol 2019; 10:2821 [View Article]
    [Google Scholar]
  67. Kämpfer P, Glaeser SP, Busse H-J, McInroy JA, Clermont D et al. Pseudoneobacillus rhizosphaerae gen. nov., sp. nov., isolated from maize root rhizosphere. Int J Syst Evol Microbiol 2022; 72: [View Article]
    [Google Scholar]
  68. Jiang L, Lee MH, Jeong JC, Kim D-H, Kim CY et al. Neobacillus endophyticus sp. nov., an endophytic bacterium isolated from Selaginella involvens roots. Int J Syst Evol Microbiol 2019; 71: [View Article]
    [Google Scholar]
  69. Montecillo JAV, Bae H. Reclassification of Brevibacterium frigoritolerans as Peribacillus frigoritolerans comb. nov. based on phylogenomics and multiple molecular synapomorphies. Int J Syst Evol Microbiol 2022; 72: [View Article] [PubMed]
    [Google Scholar]
  70. Jiang L, Jung WY, Li Z, Lee M-K, Park S-H et al. Peribacillus faecalis sp. nov., a moderately halophilic bacterium isolated from the faeces of a cow. Int J Syst Evol Microbiol 2019; 71: [View Article] [PubMed]
    [Google Scholar]
  71. Rai A, Smita N, Shabbir A, Jagadeeshwari U, Keertana T et al. Mesobacillus aurantius sp. nov., isolated from an orange-colored pond near a solar saltern. Arch Microbiol 2021; 203:1499–1507 [View Article]
    [Google Scholar]
  72. Jeong JW, Kim YS, Kim SB. Metabacillus bambusae sp. nov., isolated from bamboo grove soil. Int J Syst Evol Microbiol 2022; 72: [View Article] [PubMed]
    [Google Scholar]
  73. Lee SY, Son JS, Hwang YJ, Shin JH, Ghim SY. Metabacillus elymi sp. nov., isolated from the Rhizosphere of Elymus tsukushiensis, a plant native to the Dokdo Islands, Republic of Korea. Antonie van Leeuwenhoek 2021; 114:1709–1719 [View Article]
    [Google Scholar]
  74. Montecillo JAV. Phylogenomics and comparative genomic analyses support the creation of the novel family Ignatzschineriaceae fam. nov. comprising the genera Ignatzschineria and Wohlfahrtiimonas within the order Cardiobacteriales. Res Microbiol 2023; 174:103988 [View Article]
    [Google Scholar]
  75. Bello S, Rudra B, Gupta RS. Phylogenomic and comparative genomic analyses of Leuconostocaceae species: identification of molecular signatures specific for the genera Leuconostoc, Fructobacillus and Oenococcus and proposal for a novel genus Periweissella gen. nov. Int J Syst Evol Microbiol 2022; 72: [View Article]
    [Google Scholar]
  76. Chen S, Rudra B, Gupta RS. Phylogenomics and molecular signatures support division of the order Neisseriales into emended families Neisseriaceae and Chromobacteriaceae and three new families Aquaspirillaceae fam. nov., Chitinibacteraceae fam. nov., and Leeiaceae fam. nov. Syst Appl Microbiol 2021; 44:126251 [View Article]
    [Google Scholar]
  77. Bello S, Howard-Azzeh M, Schellhorn HE, Gupta RS. Phylogenomic analyses and molecular signatures elucidating the evolutionary relationships amongst the Chlorobia and Ignavibacteria species: Robust demarcation of two family-level clades within the order Chlorobiales and proposal for the family Chloroherpetonaceae fam. nov. Microorganisms 2022; 10:1312 [View Article]
    [Google Scholar]
  78. Adeolu M, Gupta RS. A phylogenomic and molecular marker based proposal for the division of the genus Borrelia into two genera: the emended genus Borrelia containing only the members of the relapsing fever Borrelia, and the genus Borreliella gen. nov. containing the members of the Lyme disease Borrelia (Borrelia burgdorferi sensu lato complex). Antonie van Leeuwenhoek 2014; 105:1049–1072 [View Article]
    [Google Scholar]
  79. Rudra B, Duncan L, Shah AJ, Shah HN, Gupta RS. Phylogenomic and comparative genomic studies robustly demarcate two distinct clades of Pseudomonas aeruginosa strains: proposal to transfer the strains from an outlier clade to a novel species Pseudomonas paraeruginosa sp. nov. Int J Syst Evol Microbiol 2022; 72:11 [View Article]
    [Google Scholar]
  80. Rudra B, Gupta RS. Phylogenomic and comparative genomic analyses of species of the family Pseudomonadaceae: Proposals for the genera Halopseudomonas gen. nov. and Atopomonas gen. nov., merger of the genus Oblitimonas with the genus Thiopseudomonas, and transfer of some misclassified species of the genus Pseudomonas into other genera. Int J Syst Evol Microbiol 2021; 71: [View Article]
    [Google Scholar]
  81. Gupta RS, Mahmood S, Adeolu M. A phylogenomic and molecular signature based approach for characterization of the phylum Spirochaetes and its major clades: proposal for a taxonomic revision of the phylum. Front Microbiol 2013; 4:217 [View Article]
    [Google Scholar]
  82. Sayers EW, Agarwala R, Bolton EE, Brister JR, Canese K et al. Database resources of the National Center for Biotechnology Information. Nucleic Acids Res 2019; 47:D23–D28 [View Article] [PubMed]
    [Google Scholar]
  83. Parte AC. LPSN - the List of Prokaryotic Names with Standing in Nomenclature. Int J Syst Evol Microbiol 2018; 68:1825–1829
    [Google Scholar]
  84. Parks DH, Imelfort M, Skennerton CT, Hugenholtz P, Tyson GW. CheckM: assessing the quality of microbial genomes recovered from isolates, single cells, and metagenomes. Genome Res 2015; 25:1043–1055 [View Article] [PubMed]
    [Google Scholar]
  85. Altschul SF, Madden TL, Schäffer AA, Zhang J, Zhang Z et al. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res 1997; 25:3389–3402 [View Article] [PubMed]
    [Google Scholar]
  86. Wu D, Jospin G, Eisen JA, Brochier-Armanet C. Systematic identification of gene families for use as “markers” for phylogenetic and phylogeny-driven ecological studies of bacteria and archaea and their major subgroups. PLoS One 2013; 8:e77033 [View Article]
    [Google Scholar]
  87. Price MN, Dehal PS, Arkin AP. FastTree 2--approximately maximum-likelihood trees for large alignments. PLoS One 2010; 5:e9490 [View Article]
    [Google Scholar]
  88. Stamatakis A. RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies. Bioinformatics 2014; 30:1312–1313 [View Article] [PubMed]
    [Google Scholar]
  89. Tamura K, Stecher G, Peterson D, Filipski A, Kumar S. MEGA6: Molecular Evolutionary Genetics Analysis version 6.0. Mol Biol Evol 2013; 30:2725–2729 [View Article] [PubMed]
    [Google Scholar]
  90. Bhandari V, Ahmod NZ, Shah HN, Gupta RS. Molecular signatures for Bacillus species: demarcation of the Bacillus subtilis and Bacillus cereus clades in molecular terms and proposal to limit the placement of new species into the genus Bacillus. Int J Syst Evol Microbiol 2013; 63:2712–2726 [View Article]
    [Google Scholar]
  91. Joshi A, Thite S, Karodi P, Joseph N, Lodha T. Alkalihalobacterium elongatum gen. nov. sp. nov.: an antibiotic-producing bacterium isolated from Lonar Lake and reclassification of the genus Alkalihalobacillus into seven novel genera. Front Microbiol 2021; 12:722369 [View Article]
    [Google Scholar]
  92. Heyrman J, Balcaen A, Rodriguez-Diaz M, Logan NA, Swings J et al. Bacillus decolorationis sp. nov., isolated from biodeteriorated parts of the mural paintings at the Servilia tomb (Roman necropolis of Carmona, Spain) and the Saint-Catherine chapel (Castle Herberstein, Austria). Int J Syst Evol Microbiol 2003; 53:459–463 [View Article]
    [Google Scholar]
  93. Gupta RS, Shami A. Molecular signatures for the Crenarchaeota and the Thaumarchaeota. Antonie van Leeuwenhoek 2011; 99:133–157 [View Article]
    [Google Scholar]
  94. Gupta RS, Lali R. Molecular signatures for the phylum Aquificae and its different clades: proposal for division of the phylum Aquificae into the emended order Aquificales, containing the families Aquificaceae and Hydrogenothermaceae, and a new order Desulfurobacteriales ord. nov., containing the family Desulfurobacteriaceae. Antonie van Leeuwenhoek 2013; 104:349–368 [View Article]
    [Google Scholar]
  95. Collins MD, Lawson PA, Willems A, Cordoba JJ, Fernandez-Garayzabal J et al. The phylogeny of the genus Clostridium: proposal of five new genera and eleven new species combinations. Int J Syst Bacteriol 1994; 44:812–826 [View Article]
    [Google Scholar]
  96. Collins MD. The genus Brevibacterium. In Dworkin M, Falkow S, Rosenberg E, Schleifer KH, Stackebrandt E. eds The Prokaryotes: An Evolving Electronic Resource for the Microbiological Community New York: Springer-Verlag; 2006 pp 1013–1019
    [Google Scholar]
  97. Patel S, Gupta RS. Robust demarcation of fourteen different species groups within the genus Streptococcus based on genome-based phylogenies and molecular signatures. Infect Genet Evol 2018; 66:130–151 [View Article]
    [Google Scholar]
  98. Alnajar S, Gupta RS. Phylogenomics and comparative genomic studies delineate six main clades within the family Enterobacteriaceae and support the reclassification of several polyphyletic members of the family. Infect Genet Evol 2017; 54:108–127 [View Article]
    [Google Scholar]
  99. Gupta RS, Naushad S, Fabros R, Adeolu M. Erratum to: a phylogenomic reappraisal of family-level divisions within the class Halobacteria: proposal to divide the order Halobacteriales into the families Halobacteriaceae, Haloarculaceae fam. nov., and Halococcaceae fam. nov., and the order Haloferacales into the families, Haloferacaceae and Halorubraceae fam nov. Antonie van Leeuwenhoek 2016; 109:1521–1523 [View Article]
    [Google Scholar]
  100. Zhang G, Gao B, Adeolu M, Khadka B, Gupta RS. Phylogenomic analyses and comparative studies on genomes of the Bifidobacteriales: identification of molecular signatures specific for the order Bifidobacteriales and its different subclades. Front Microbiol 2016; 7:978 [View Article]
    [Google Scholar]
  101. Ho J, Adeolu M, Khadka B, Gupta RS. Identification of distinctive molecular traits that are characteristic of the phylum “Deinococcus-Thermus” and distinguish its main constituent groups. Syst Appl Microbiol 2016; 39:453–463 [View Article] [PubMed]
    [Google Scholar]
  102. Gupta RS, Naushad S, Baker S. Phylogenomic analyses and molecular signatures for the class Halobacteria and its two major clades: a proposal for division of the class Halobacteria into an emended order Halobacteriales and two new orders, Haloferacales ord. nov. and Natrialbales ord. nov., containing the novel families Haloferacaceae fam. nov. and Natrialbaceae fam. nov. Int J Syst Evol Microbiol 2015; 65:1050–1069 [View Article]
    [Google Scholar]
  103. Naushad S, Adeolu M, Wong S, Sohail M, Schellhorn HE et al. A phylogenomic and molecular marker based taxonomic framework for the order Xanthomonadales: proposal to transfer the families Algiphilaceae and Solimonadaceae to the order Nevskiales ord. nov. and to create a new family within the order Xanthomonadales, the family Rhodanobacteraceae fam. nov., containing the genus Rhodanobacter and its closest relatives. Antonie van Leeuwenhoek 2015; 107:467–485 [View Article]
    [Google Scholar]
  104. Ravinesan DA, Gupta RS. Molecular signatures for members of the genus Dehalococcoides and the class Dehalococcoidia. Int J Syst Evol Microbiol 2014; 64:2176–2181 [View Article]
    [Google Scholar]
  105. Kim O-S, Cho Y-J, Lee K, Yoon S-H, Kim M et al. Introducing EzTaxon-e: a prokaryotic 16S rRNA gene sequence database with phylotypes that represent uncultured species. Int J Syst Evol Microbiol 2012; 62:716–721 [View Article] [PubMed]
    [Google Scholar]
  106. Wong SY, Paschos A, Gupta RS, Schellhorn HE. Insertion/deletion-based approach for the detection of Escherichia coli O157:H7 in freshwater environments. Environ Sci Technol 2014; 48:11462–11470 [View Article]
    [Google Scholar]
  107. Ahmod NZ, Gupta RS, Shah HN. Identification of a Bacillus anthracis specific indel in the yeaC gene and development of a rapid pyrosequencing assay for distinguishing B. anthracis from the B. cereus group. J Microbiol Methods 2011; 87:278–285 [View Article]
    [Google Scholar]
  108. Chun J, Lee J-H, Jung Y, Kim M, Kim S et al. EzTaxon: a web-based tool for the identification of prokaryotes based on 16S ribosomal RNA gene sequences. Int J Syst Evol Microbiol 2007; 57:2259–2261 [View Article]
    [Google Scholar]
  109. Meier-Kolthoff JP, Carbasse JS, Peinado-Olarte RL, Göker M. TYGS and LPSN: a database tandem for fast and reliable genome-based classification and nomenclature of prokaryotes. Nucleic Acids Res 2022; 50:D801–D807 [View Article]
    [Google Scholar]
  110. Gao B, Gupta RS. Conserved indels in protein sequences that are characteristic of the phylum Actinobacteria. Int J Syst Evol Microbiol 2005; 55:2401–2412 [View Article]
    [Google Scholar]
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