1887

Abstract

A strictly anaerobic bacterial strain, designated as PI-S10-A1B, was isolated from a sludge sample collected from an industrial effluent dump site at Hyderabad, India. Cells stained Gram-positive and contained terminal endospores. Optimal growth was observed at 30 °C and pH 7.0. It showed negative reactions to catalase and oxidase activities. Phylogenetic analysis of the 16S rRNA gene led to strain PI-S10-A1B being assigned to the genus Clostridium . It displayed high sequence similarity to species of cluster XIVa including Clostridium amygdalinum BR-10 (99.84 %), Clostridium saccharolyticum WM1 (98.93 %) and Clostridium indolis DSM 755 (98.31 %). It formed a coherent cluster with members of cluster XIVa. Despite high 16S rRNA gene sequence similarity, strain PI-S10-A1B displayed only 25.3 % identity in DNA–DNA hybridization tests with C. amygdalinum BR-10. A draft genome exhibited low values for average nucleotide identity and in silico DNA–DNA hybridization with strains of cluster XIVa. The DNA G+C content was 42.3 mol%. Major lipids were phosphatidylglycerol and diphosphatidylglycerol, with an abundance of phosphoglycolipids. Further, analysis of the draft genome revealed genomic insights against functional aspects. Considering the phenotypic differences and low genomic identity with phylogenetic relatives, strain PI-S10-A1B is concluded to represent a new species of the genus Clostridium , for which the name Clostridium indicum sp. nov. is proposed with type strain PI-S10-A1B (=MTCC 12282=DSM 24996=JCM 32788).

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2019-01-24
2024-04-26
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References

  1. Rainey FA, Hollen BJ SA. Bergey’s Manual of Systematic Bacteriology, 2nd ed. New York: Springer; 2009
    [Google Scholar]
  2. Wiegel J, Tanner R RF. The Prokaryotes: A Handbook on the Biology of Bacteria, 3rd ed. New York: Springer; 2006
    [Google Scholar]
  3. Parte AC. LPSN-list of prokaryotic names with standing in nomenclature. Nucleic Acids Res 2014; 42:D613–D616 [View Article][PubMed]
    [Google Scholar]
  4. Alam SI, Dixit A, Reddy GS, Dube S, Palit M et al. Clostridium schirmacherense sp. nov., an obligately anaerobic, proteolytic, psychrophilic bacterium isolated from lake sediment of Schirmacher Oasis, Antarctica. Int J Syst Evol Microbiol 2006; 56:715–720 [View Article][PubMed]
    [Google Scholar]
  5. Domingo MC, Huletsky A, Boissinot M, Hélie MC, Bernal A et al. Clostridium lavalense sp. nov., a glycopeptide-resistant species isolated from human faeces. Int J Syst Evol Microbiol 2009; 59:498–503 [View Article][PubMed]
    [Google Scholar]
  6. Kim S, Jeong H, Chun J. Clostridium aestuarii sp. nov., from tidal flat sediment. Int J Syst Evol Microbiol 2007; 57:1315–1317 [View Article][PubMed]
    [Google Scholar]
  7. Sakuma K, Kitahara M, Kibe R, Sakamoto M, Benno Y. Clostridium glycyrrhizinilyticum sp. nov., a glycyrrhizin-hydrolysing bacterium isolated from human faeces. Microbiol Immunol 2006; 50:481–485 [View Article][PubMed]
    [Google Scholar]
  8. Suresh K, Prakash D, Rastogi N, Jain RK. Clostridium nitrophenolicum sp. nov., a novel anaerobic p-nitrophenol-degrading bacterium, isolated from a subsurface soil sample. Int J Syst Evol Microbiol 2007; 57:1886–1890 [View Article][PubMed]
    [Google Scholar]
  9. Varel VH, Tanner RS, Woese CR. Clostridium herbivorans sp. nov., a cellulolytic anaerobe from the pig intestine. Int J Syst Bacteriol 1995; 45:490–494 [View Article][PubMed]
    [Google Scholar]
  10. Wilson M. Microbial Inhabitants of Humans New York, USA: Cambridge University Press; 2005
    [Google Scholar]
  11. Hippe H, Andreesen JR GG. The genus Clostridium-non-medical. In Balows A, Truper HG, Dworkin M, Harder W SK. (editors) The Prokaryotes, 2nd ed. New York: Springer; pp. 1800–1839
    [Google Scholar]
  12. Hughes JB, Wang CY, Zhang C. Anaerobic Biotransformation of 2,4-Dinitrotoluene and 2,6-Dinitrotoluene by Clostridium acetobutylicum: a pathway through dihydroxylamino intermediates. Environ Sci Technol 1999; 33:1065–1070 [View Article]
    [Google Scholar]
  13. Lewis TA, Goszczynski S, Crawford RL, Korus RA, Admassu W. Products of Anaerobic 2,4,6-Trinitrotoluene (TNT) Transformation by Clostridium bifermentans. Appl Environ Microbiol 1996; 62:4669–4674[PubMed]
    [Google Scholar]
  14. Mechichi T, Labat M, Patel BK, Woo TH, Thomas P et al. Clostridium methoxybenzovorans sp. nov., a new aromatic o-demethylating homoacetogen from an olive mill wastewater treatment digester. Int J Syst Bacteriol 1999; 49:1201–1209 [View Article][PubMed]
    [Google Scholar]
  15. Logan NA, De VP. Genus I. Clostridium Prazmowski 1880. In De VosP, Garrity G, Jones D, Kreig NR, Ludwig W et al. (editors) Bergey’s Manual of Systematic Bacteriology, 2nd ed. vol. 3, The Firmicutes New York: Springer; 2009 pp. 738–828
    [Google Scholar]
  16. Smith LDS HG, Prazmowski G. In Buchanan RE, Gibbons NE. (editors) Bergey’s Manual of Determinative Bacteriology, 8th ed. Baltimore: The Williams and Wilkins Company; 1974 pp. 551–572
    [Google Scholar]
  17. 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][PubMed]
    [Google Scholar]
  18. Lawson PA, Rainey FA. Proposal to restrict the genus Clostridium Prazmowski to Clostridium butyricum and related species. Int J Syst Evol Microbiol 2016; 66:1009–1016 [View Article][PubMed]
    [Google Scholar]
  19. Yutin N, Galperin MY. A genomic update on clostridial phylogeny: Gram-negative spore formers and other misplaced clostridia. Environ Microbiol 2013; 15:2631–2641 [View Article][PubMed]
    [Google Scholar]
  20. Kaur S, Yawar M, Kumar PA, Suresh K. Hungatella effluvii gen. nov., sp. nov., an obligately anaerobic bacterium isolated from an effluent treatment plant, and reclassification of Clostridium hathewayi as Hungatella hathewayi gen. nov., comb. nov. Int J Syst Evol Microbiol 2014; 64:710–718 [View Article][PubMed]
    [Google Scholar]
  21. Raje M, Dhiman R, Majumdar S, Dass T, Dikshit KL et al. Charged nylon membrane substrate for convenient and versatile high resolution microscopic analysis of Escherichia coli & mammalian cells in suspension culture. Cytotechnology 2006; 51:111–117 [View Article][PubMed]
    [Google Scholar]
  22. Gerhardt P, Murray RGE, Wood WA, Krieg NR. Methods for General and Molecular Bacteriology Washington, DC: American Society for Microbiology; 1994
    [Google Scholar]
  23. Cowan ST, Steel KJ. Manual for the identification of Medical Bacteria London: Cambridge University Press; 1965
    [Google Scholar]
  24. Lányi B. Classical and rapid identification methods for medically important bacteria. Methods Microbiol 1988; 19:1–67
    [Google Scholar]
  25. Smibert RM, Krieg NR. Phenotypic characterization. In Gerhardt P, Murray RGE, Wood WA, Krieg NR. (editors) Methods for General and Molecular Bacteriology Washington, DC: American Society for Microbiology; 1994 pp. 607–654
    [Google Scholar]
  26. Sasser M. Identification of Bacteria by Gas Chromatography of Cellular Fatty Acids, Tech. Note 101. pp. 1–6
    [Google Scholar]
  27. Minnikin DE, O'Donnell AG, Goodfellow M, Alderson G, Athalye M et al. An integrated procedure for the extraction of bacterial isoprenoid quinones and polar lipids. J Microbiol Methods 1984; 2:233–241 [View Article]
    [Google Scholar]
  28. Tamaoka J. Analysis of bacterial menaquinone mixtures by reverse-phase high-performance liquid chromatography. Methods Enzymol 1986; 123:31–36[PubMed]
    [Google Scholar]
  29. Schumann P. Peptidoglycan structure. Methods Microbiol 2011; 38:101–129
    [Google Scholar]
  30. Johnston NC, Baker JK, Goldfine H. Phospholipids of Clostridium perfringens: a reexamination. FEMS Microbiol Lett 2004; 233:65–68 [View Article][PubMed]
    [Google Scholar]
  31. Johnston NC, Goldfine H, Fischer W. Novel polar lipid composition of Clostridium innocuum as the basis for an assessment of its taxonomic status. Microbiology 1994; 140:105–111 [View Article][PubMed]
    [Google Scholar]
  32. Mandel M, Marmur J. Use of ultraviolet absorbance-temperature profile for determining the guanine plus cytosine content of DNA. Methods Enzymol 1967; 12:195–206
    [Google Scholar]
  33. Suresh K, Mayilraj S, Chakrabarti T. Effluviibacter roseus gen. nov., sp. nov., isolated from muddy water, belonging to the family "Flexibacteraceae". Int J Syst Evol Microbiol 2006; 56:1703–1707 [View Article][PubMed]
    [Google Scholar]
  34. Kumar S, Stecher G, Tamura K. MEGA7: Molecular Evolutionary Genetics Analysis Version 7.0 for bigger datasets. Mol Biol Evol 2016; 33:1870–1874 [View Article][PubMed]
    [Google Scholar]
  35. Tamura K, Nei M. Estimation of the number of nucleotide substitutions in the control region of mitochondrial DNA in humans and chimpanzees. Mol Biol Evol 1993; 10:512–526 [View Article][PubMed]
    [Google Scholar]
  36. Yoon SH, Ha SM, Kwon S, Lim J, Kim Y et al. Introducing EzBioCloud: a taxonomically united database of 16S rRNA gene sequences and whole-genome assemblies. Int J Syst Evol Microbiol 2017; 67:1613–1617 [View Article][PubMed]
    [Google Scholar]
  37. Meier-Kolthoff JP, Auch AF, Klenk HP, Göker M. Genome sequence-based species delimitation with confidence intervals and improved distance functions. BMC Bioinformatics 2013; 14:60 [View Article][PubMed]
    [Google Scholar]
  38. Na SI, Kim YO, Yoon SH, Ha SM, Baek I et al. UBCG: Up-to-date bacterial core gene set and pipeline for phylogenomic tree reconstruction. J Microbiol 2018; 56:280–285 [View Article][PubMed]
    [Google Scholar]
  39. Richter M, Rosselló-Móra R. Shifting the genomic gold standard for the prokaryotic species definition. Proc Natl Acad Sci USA 2009; 106:19126–19131 [View Article][PubMed]
    [Google Scholar]
  40. Wayne LG, Moore WEC, Stackebrandt E, Kandler O, Colwell RR et al. Report of the Ad Hoc Committee on reconciliation of approaches to bacterial systematics. Int J Syst Evol Microbiol 1987; 37:463–464 [View Article]
    [Google Scholar]
  41. Aziz RK, Bartels D, Best AA, Dejongh M, Disz T et al. The RAST Server: rapid annotations using subsystems technology. BMC Genomics 2008; 9:75 [View Article][PubMed]
    [Google Scholar]
  42. Alikhan NF, Petty NK, Ben Zakour NL, Beatson SA. BLAST Ring Image Generator (BRIG): simple prokaryote genome comparisons. BMC Genomics 2011; 12:402 [View Article][PubMed]
    [Google Scholar]
  43. Stothard P, Wishart DS. Circular genome visualization and exploration using CGView. Bioinformatics 2005; 21:537–539 [View Article][PubMed]
    [Google Scholar]
  44. Kalmokoff ML, Lu D, Whitford MF, Teather RM. Evidence for production of a new lantibiotic (butyrivibriocin OR79A) by the ruminal anaerobe Butyrivibrio fibrisolvens OR79: characterization of the structural gene encoding butyrivibriocin OR79A. Appl Environ Microbiol 1999; 65:2128–2135[PubMed]
    [Google Scholar]
  45. Wang S, Fleming RT, Westbrook EM, Matsumura P, McKay DB. Structure of the Escherichia coli FlhDC complex, a prokaryotic heteromeric regulator of transcription. J Mol Biol 2006; 355:798–808 [View Article][PubMed]
    [Google Scholar]
  46. Klemm P, Vejborg RM, Hancock V. Prevention of bacterial adhesion. Appl Microbiol Biotechnol 2010; 88:451–459 [View Article][PubMed]
    [Google Scholar]
  47. Parshina SN, Kleerebezem R, Sanz JL, Lettinga G, Nozhevnikova AN et al. Soehngenia saccharolytica gen. nov., sp. nov. and Clostridium amygdalinum sp. nov., two novel anaerobic, benzaldehyde-converting bacteria. Int J Syst Evol Microbiol 2003; 53:1791–1799 [View Article][PubMed]
    [Google Scholar]
  48. Murray WD, Khan AW, van den Berg L. Clostridium saccharolyticum sp. nov., asaccharolytic species from sewage sludge. Int J Syst Bacteriol 1982; 32:132–135 [View Article]
    [Google Scholar]
  49. Biddle AS, Leschine S, Huntemann M, Han J, Chen A et al. The complete genome sequence of Clostridium indolis DSM 755(T). Stand Genomic Sci 2014; 9:1089–1104 [View Article][PubMed]
    [Google Scholar]
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