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Select item 83175011.

Exploring the Microdiversity Within Marine Bacterial Taxa: Toward an Integrated Biogeography in the Southern Ocean

Guillaume Schwob, Nicolás I. Segovia, Claudio González-Wevar, Léa Cabrol, Julieta Orlando, Elie Poulin

Front Microbiol. 2021; 12: 703792. Published online 2021 Jul 14. doi: 10.3389/fmicb.2021.703792

PMCID:: PMC8317501

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Select item 26767182.

Phylogenetic diversity and temporal variation in the Spirochaeta populations from two Mediterranean microbial mats

Mercedes Berlanga, Jorn A. Aas, Bruce J. Paster, Tahani Boumenna, Floyd E. Dewhirst, Ricardo Guerrero

Int Microbiol. Author manuscript; available in PMC 2009 Dec 1.

Published in final edited form as: Int Microbiol. 2008 Dec; 11(4): 267–274. doi: 10.2436/20.1501.01.71

PMCID:: PMC2676718

Article PDF–937K

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Stability and Ligand Promiscuity of Type A Carbohydrate-binding Modules Are Illustrated by the Structure of Spirochaeta thermophila StCBM64C

Virgínia M. R. Pires, Pedro M. M. Pereira, Joana L. A. Brás, Márcia Correia, Vânia Cardoso, Pedro Bule, Victor D. Alves, Shabir Najmudin, Immacolata Venditto, Luís M. A. Ferreira, Maria João Romão, Ana Luísa Carvalho, Carlos M. G. A. Fontes, Duarte Miguel Prazeres

J Biol Chem. 2017 Mar 24; 292(12): 4847–4860. Published online 2017 Feb 8. doi: 10.1074/jbc.M116.767541

PMCID:: PMC5377800

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Spirochaeta coccoides sp. nov., a Novel Coccoid Spirochete from the Hindgut of the Termite Neotermes castaneus

Stefan Dröge, Jürgen Fröhlich, Renate Radek, Helmut König

Appl Environ Microbiol. 2006 Jan; 72(1): 392–397. doi: 10.1128/AEM.72.1.392-397.2006

PMCID:: PMC1352290

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Novel Family of Carbohydrate-Binding Modules Revealed by the Genome Sequence of Spirochaeta thermophila DSM 6192

Angel Angelov, Christoph Loderer, Susanne Pompei, Wolfgang Liebl

Appl Environ Microbiol. 2011 Aug; 77(15): 5483–5489. doi: 10.1128/AEM.00523-11

PMCID:: PMC3147429

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Spirochaeta aurantia Has Diacetyl Chloramphenicol Esterase Activity

Charles D. Sohaskey, Alan G. Barbour

J Bacteriol. 2000 Apr; 182(7): 1930–1934. doi: 10.1128/jb.182.7.1930-1934.2000

PMCID:: PMC101882

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Genome Sequence of the Polysaccharide-Degrading, Thermophilic Anaerobe Spirochaeta thermophila DSM 6192

Angel Angelov, Susanne Liebl, Meike Ballschmiter, Mechthild Bömeke, Rüdiger Lehmann, Heiko Liesegang, Rolf Daniel, Wolfgang Liebl

J Bacteriol. 2010 Dec; 192(24): 6492–6493. Published online 2010 Oct 8. doi: 10.1128/JB.01023-10

PMCID:: PMC3008529

Article PDF–40K

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Motility and Ultrastructure of Spirochaeta thermophila

Reinhard Wirth, Matthias Ugele, Gerhard Wanner

Front Microbiol. 2016; 7: 1609. Published online 2016 Oct 14. doi: 10.3389/fmicb.2016.01609

PMCID:: PMC5064287

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Inhibition of Spirochaeta aurantia chemotaxis by neurotoxins.

E A Goulbourne, Jr, E P Greenberg

J Bacteriol. 1983 Sep; 155(3): 1443–1445. doi: 10.1128/jb.155.3.1443-1445.1983

PMCID:: PMC217847

Summary Page Browse PDF–481K

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Antiserum to the 33,000-dalton periplasmic-flagellum protein of "Treponema phagedenis" reacts with other treponemes and Spirochaeta aurantia.

R J Limberger, N W Charon

J Bacteriol. 1986 Nov; 168(2): 1030–1032. doi: 10.1128/jb.168.2.1030-1032.1986

PMCID:: PMC213590

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Select item 24591011.

Lipids of the Spirochaetales: Comparison of the Lipids of Several Members of the Genera Spirochaeta, Treponema, and Leptospira

Brian P. Livermore, Russell C. Johnson

J Bacteriol. 1974 Dec; 120(3): 1268–1273. doi: 10.1128/jb.120.3.1268-1273.1974

PMCID:: PMC245910

Summary Page Browse PDF–907K

Select item 25145712.

Fatty Acid Composition of Spirochaeta stenostrepta

Ronald Joseph

J Bacteriol. 1972 Oct; 112(1): 629–631. doi: 10.1128/jb.112.1.629-631.1972

PMCID:: PMC251457

Summary Page Browse PDF–318K

Select item 25237813.

Fine Structure of Spirochaeta stenostrepta, a Free-living, Anaerobic Spirochete

S. C. Holt, E. Canale-Parola

J Bacteriol. 1968 Sep; 96(3): 822–835. doi: 10.1128/jb.96.3.822-835.1968

PMCID:: PMC252378

Summary Page Browse PDF–9.5M

Select item 21565514.

Uptake of D-xylose and D-glucose by Spirochaeta aurantia.

S Roberts, C A Paden, E P Greenberg

J Bacteriol. 1984 Jul; 159(1): 427–428. doi: 10.1128/jb.159.1.427-428.1984

PMCID:: PMC215655

Summary Page Browse PDF–411K

Select item 28546515.

Glucose and Pyruvate Metabolism of Spirochaeta litoralis, an Anaerobic Marine Spirochete

R. B. Hespell, E. Canale-Parola

J Bacteriol. 1973 Nov; 116(2): 931–937. doi: 10.1128/jb.116.2.931-937.1973

PMCID:: PMC285465

Summary Page Browse PDF–1005K

Select item 22171416.

A voltage clamp inhibits chemotaxis of Spirochaeta aurantia.

E A Goulbourne, Jr, E P Greenberg

J Bacteriol. 1983 Feb; 153(2): 916–920. doi: 10.1128/jb.153.2.916-920.1983

PMCID:: PMC221714

Summary Page Browse PDF–854K

Select item 20726517.

N-terminal amino acid sequences and amino acid compositions of the Spirochaeta aurantia flagellar filament polypeptides.

J Parales, Jr, E P Greenberg

J Bacteriol. 1991 Feb; 173(3): 1357–1359. doi: 10.1128/jb.173.3.1357-1359.1991

PMCID:: PMC207265

Summary Page Browse PDF–635K

Select item 20704418.

Nucleotide sequence and analysis of a gene encoding anthranilate synthase component I in Spirochaeta aurantia.

B Brahamsha, C Y Han, I P Crawford, E P Greenberg

J Bacteriol. 1991 Jan; 173(2): 541–548. doi: 10.1128/jb.173.2.541-548.1991

PMCID:: PMC207044

Summary Page Browse PDF–1.6M

Select item 24961719.

Spirochaeta aurantia, a Pigmented, Facultatively Anaerobic Spirochete

John A. Breznak, E. Canale-Parola

J Bacteriol. 1969 Jan; 97(1): 386–395. doi: 10.1128/jb.97.1.386-395.1969

PMCID:: PMC249617

Summary Page Browse PDF–3.7M

Select item 20963320.

Chemotaxis mutants of Spirochaeta aurantia.

K Fosnaugh, E P Greenberg

J Bacteriol. 1989 Jan; 171(1): 606–611. doi: 10.1128/jb.171.1.606-611.1989

PMCID:: PMC209633

Summary Page Browse PDF–1.2M

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Fig.2

Spirochaeta phylotypes detected from Ebro and Camargue microbial mats vs. Spirochaeta phylotypes from Guerrero Negro mats. Phylotypes from Guerrero Negro were named according to the layer they originated from (01 to 10), the time of collection (D for day, N for night), and the month of collection (1, June; 2, October).

Phylogenetic diversity and temporal variation in the Spirochaeta populations from two Mediterranean microbial mats

Int Microbiol. ;11(4):267-274.
Figure 6

Phylogenetic tree inferred from completely sequenced genomes of the Spirochaeta type strains. The tree was inferred from 11,131 gene-content characters under the maximum likelihood (ML) criterion and rooted with Leptospira. The branches are scaled in terms of the expected number of substitutions per site. Numbers above the branches are bootstrapping support values (if larger than 60%) from (i) maximum-likelihood gene-content analysis; (ii) maximum-parsimony gene-content analysis; (iii) maximum-likelihood supermatrix analysis; (iv) maximum-parsimony supermatrix analysis. For further details see [].

Genome sequence of the thermophilic fresh-water bacterium Spirochaeta caldaria type strain (H1T), reclassification of Spirochaeta caldaria, Spirochaeta stenostrepta, and Spirochaeta zuelzerae in the genus Treponema as Treponema caldaria comb. nov., Treponema stenostrepta comb. nov., and Treponema zuelzerae comb. nov., and emendation of the genus Treponema

Stand Genomic Sci. 2013 Apr 15;8(1):88-105.
Figure 6

Different morphological forms of Spirochaeta thermophila observed by scanning electron microscopy. Data were obtained by SEM. The cells indicated by [a], [b], and [c] have a wave-length of 0.88, 0.91, 0.56 μm and wave-amplitudes of 0.26, 0.22, 0.29 μm, respectively; [d] shows a linear cell.

Motility and Ultrastructure of Spirochaeta thermophila

Front Microbiol. 2016;7:1609.
Figure 1.

Borrelia spirochaeta in the Giemsa stain of the peripheral blood corrected at the febrile phase.

The First Case of Imported Relapsing Fever in Japan

Am J Trop Med Hyg. 2013 Sep 4;89(3):460-461.