Abstract
A novel actinobacterium, designated strain CMAA 1533T, was isolated from the rhizosphere of Deschampsia antarctica collected at King George Island, Antarctic Peninsula. Strain CMAA 1533T was found to grow over a wide range of temperatures (4–28 °C) and pH (4–10). Macroscopically, the colonies were observed to be circular shaped, smooth, brittle and opaque-cream on most of the culture media tested. Phylogenetic analysis based on 16S rRNA gene sequences revealed that strain CMAA 1533T belongs to the family Nocardiaceae and forms a distinct phyletic line within the genus Rhodococcus. Sequence similarity calculations indicated that the novel strain is closely related to Rhodococcus degradans CCM 4446T, Rhodococcus erythropolis NBRC 15567T and Rhodococcus triatomae DSM 44892T (≤ 96.9%). The organism was found to contain meso-diaminopimelic acid, galactose and arabinose in whole cell hydrolysates. Its predominant isoprenologue was identified as MK-8(H2) and the polar lipids as diphosphatidylglycerol, phosphatidylglycerol, phosphatidylethanolamine, phosphatidylinositol and phosphatidylinositol mannosides. The major fatty acids were identified as Summed feature (C16:1 ω6c and/or C16:1 ω7c), C16:0, C18:1 ω9c and 10-methyl C18:0. The G+C content of genomic DNA was determined to be 65.5 mol%. Unlike the closely related type strains, CMAA 1533T can grow at 4 °C but not at 37 °C and was able to utilise adonitol and galactose as sole carbon sources. Based on phylogenetic, chemotaxonomic and physiological data, it is concluded that strain CMAA 1533T (= NRRL B-65465T = DSM 104532T) represents a new species of the genus Rhodococcus, for which the name Rhodococcus psychrotolerans sp. nov. is proposed.
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References
Adachi K, Katsuta A, Matsuda S, Peng X, Misawa N, Shizuri Y, Kroppenstedt RM, Yokota A, Kasai H (2007) Smaragdicoccus niigatensis gen. nov., sp. nov., a novel member of the suborder Corynebacterineae. Int J Syst Evolut Microbiol 57:297–301
Anastasi E, MacArthur I, Scortti M, Alvarez S, Giguère S, Vázquez-Boland JA (2016) Pangenome and phylogenomic analysis of the pathogenic actinobacterium Rhodococcus equi. Genome Biol Evol 8:3140–3148
Collins MD, Goodfellow M (1979) Isoprenoid Quinones in the classification of Coryneform and related bacteria. J Gen Microbiol 110:127–136
Creason AL, Davis EW, Putnam ML II, Vandeputte OM, Chang JH (2014) Use of whole genome sequences to develop a molecular phylogenetic framework for Rhodococcus fascians and the Rhodococcus genus. Front Plant Sci 5:406
Felsenstein J (1981) Evolutionary trees from DNA sequences: a maximum likelihood approach. J Mol Evol 17:368–376
Felsenstein J (1985) Phylogenies and the comparative method. Am Soc Nat 125:1–15
Fitch WM (1971) Toward defining the course of evolution: minimum change for a specific tree topology. Soc Syst Biol 20:406–416
Gonzalez JM, Saiz-Jimenez C (2005) A simple fluorimetric method for the estimation of DNA–DNA relatedness between closely related microorganisms by thermal denaturation temperatures. Extremophiles 9:75–79
Goodfellow M, Sangal V, Jones AL, Sutcliffe IC (2015) Charting stormy waters: a commentary on the nomenclature of the equine pathogen variously named Prescottella equi, Rhodococcus equi and Rhodococcus hoagii. Equine Vet J 47:508–509
Gordon RE, Mihm JM (1962) Identification of Nocardia caviae (Erikson) nov. comb. Ann N Y Acad Sci 98:628–636
Guo QQ, Ming H, Meng XL, Duan YY, Gao R, Zhang JX, Huang JR, Li WJ, Nie GX (2015) Rhodococcus agglutinans sp. nov., an actinobacterium isolated from a soil sample. Antonie Van Leeuwenhoek 107:1271–1280
Hasegawa T, Takaziwa M, Tanida S (1983) A rapid analysis for chemical grouping of aerobic actinomycetes. J Gen Appl Microbiol 29:319–322
Hwang CY, Lee I, Cho Y, Lee YM, Baek K, Jung YJ, Yang YY, Lee T, Rhee TS, Lee HK (2015) Rhodococcus aerolatus sp. nov., isolated from subarctic rainwater. Int J Syst Evolut Microbiol 65:465–471
Jones AL, Goodfellow M (2015) Rhodococcus Bergey´s manual of systematics bacteriology. Springer, Berlin
Jones AL, Sutcliffe IC, Goodfellow M (2013) Proposal to replace the illegitimate genus name Prescottia Jones et al. 2013 with the genus name Prescottella gen. nov. and to replace the illegitimate combination Prescottia equi Jones et al. 2013 with Prescottella equi comb. nov. Antonie Van Leeuwenhoek 103:1405–1407
Kumar S, Stecher G, Tamura K (2016) MEGA7: molecular evolutionary genetics analysis version 7.0 for bigger datasets. Mol Biol Evol 33:1870–1874
Kuster E, Williams S (1964) Selection of media for isolation of Streptomycetes. Nat Microbiol 3:928–929
Lechevalier MP, Lechevalier H (1970) Chemical composition as a criterion in the classification of aerobic actinomycetes. Int J Syst Bacteriol 20:435–443
Lechevalier MP, De Bievre C, Lechevalier H (1977) Chemotaxonomy of aerobic Actinomycetes: phospholipid composition. Biochem Syst Ecol 5:249–260
Li J, Zhao GZ, Long LJ, Wang FZ, Tian XP, Zhang S, Li WJ (2012) Rhodococcus nanhaiensis ap. nov., an actinobacterium isolated from marine sediment. Int J Syst Evolut Microbiol 62:2517–2521
Martínková L, Uhnáková B, Pátek M, Nesvera J, Kren V (2009) Biodegradation potential of the genus Rhodococcus. Environ Int 35:162–177
Meier-Kolthoff JP, Goker M, Sproer C, Klenk HP (2013) When should a DDH experiment be mandatory in microbial taxonomy? Arch Microbiol 195:413–418
Minnikin D, Hutchinson I, Caldicott A, Goodfellow M (1980) Thin-layer chromatography of methanolysates of mycolic acid-containing bacteria. J Chromatogr 188:221–233
Minnikin DE, O`donnell AG, Goodfellow M, Alderson G, Athalye M, Schaal A, Parlett JH (1984) An integrated procedure for the extraction of bacterial isoprenoid quinones and polar lipids. J Microbiol Methods 2:233–241
Rosselló-Móra R, Trujillo ME, Sutcliffe IC (2017) Introducing a digital protologue: a timely move towards a database-driven systematic of archaea and bacteria. Antonie Van Leeuwenhoek 110:455–456
Saitou N, Nei M (1987) The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol Biol Evol 4:406–425
Sangal V, Goodfellow M, Jones AL, Schwalbe EC, Blom J, Hoskisson PA, Sutcliffe IC (2016) Next-generation systematics: an innovative approach to resolve the structure of complex prokaryotic taxa. Sci Rep 6:38392
Sasser M (1990) Identification of bacteria by gas chromatography of cellular fatty acids. MIDI—Tech Note 101:1–6
Shirling EB, Gottlieb D (1966) Methods for characterization of Streptomyces species. Int J Syst Bacteriol 16:313–340
Silva LJ, Taketani RG, Melo IS, Goodfellow M, Zucchi TD (2013) Streptomyces araujoniae sp. nov.: an actinomycete isolated from a potato tubercle. Antonie Van Leeuwenhoek 103:1235–1244
Souza DT, da Silva FSP, da Silva LJ, Crevelin EJ, Moraes LAB, Zucchi TD, Melo IS (2017) Saccharopolyspora spongiae sp. nov., a novel actinomycete isolated from the marine sponge Scopalina ruetzleri (Wiedenmayer, 1977). Int J Syst Evolut Microbiol 67:2019–2025
Stackebrandt E, Rainey FA, Ward-Rainey NL (1997) Proposal for a new hierarchic classification system, Actinobacteria classis nov. Int J Syst Bacteriol 47:479–491
Staneck J, Roberts GD (1974) Simplified approach to identification of aerobic actinomycetes by thin-layer chromatography. Appl Microbiol 28:226–231
Taketani RG, Zucchi TD, Melo IS, Mendes R (2013) Whole-genome shotgun sequencing of Rhodococcus erythropolis strain P27, a highly radiation-resistant actinomycete from Antarctica. Genome Announc 1:e00763
Tamura K (1992) Estimation of the number of nucleotide substitutions when there are strong transition- transversion and G+C content biases. Mol Biol Evol 9:678–687
Wang Z, Xu J, Li Y, Wang K, Wang Y, Hong Q, Li WJ, Li SP (2010) Rhodococcus jialingiae sp. nov., an actinobacterium isolated from sludge of a carbendazim wastewater treatment facility. Int J Syst Evolut Microbiol 60:378–381
Yoon SH, Ha SM, Kwon S, Lim J, Kim Y, Seo H, Chun J (2017) Introducing EzBioCloud: a taxonomically united database of 16S rRNA and whole genome assemblies. Int J Syst Evolut Microbiol 67:1613–1617
Zhi XY, Li WJ, Stackebrandt E (2009) An update of the structure and 16S rRNA gene sequence-based definition of higher ranks of the class Actinobacteria, with the proposal of two new suborders and four new families and emended descriptions of the existing higher taxa. Int J Syst Evolut Microbiol 59:589–608
Zopf W (1981) Uber Ausscheidung von Fettfarbstoffen (Lipochromen) seitens gewisser Spaltpilze. Berichte der Deutschen Botanischen Gesellschaft 9:22–28
Acknowledgements
Silva, L.J. thanks the support from National Council for Scientific and Technological Development [CNPq 141705/2014-0] and [CNPq PROANTAR 407230/2013-0, INCT Criosfera]. Genuario, D. B. and Souza, D.T were supported by FAPESP graduate scholarships 2014/26131-7 and 2013/25505-8, respectively. The authors are grateful to Marcia Maria Parma Leme, João Luiz da Silva, Renato Barbosa Salaroli and Roseli dos Santos Nascimento by their contributions with the laboratory techniques. Finally, thanks are due to the PROANTAR Research Program and Brazilian Navy for logistical support during the OPERANTAR EXPEDITION.
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Silva, L.J., Souza, D.T., Genuario, D.B. et al. Rhodococcus psychrotolerans sp. nov., isolated from rhizosphere of Deschampsia antarctica . Antonie van Leeuwenhoek 111, 629–636 (2018). https://doi.org/10.1007/s10482-017-0983-7
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DOI: https://doi.org/10.1007/s10482-017-0983-7