ABSTRACT
The oral spirochete bacterium Treponema putidum inhabits human periodontal niches. The complete genome sequence of the OMZ 758T (ATCC 700334T) strain of this species was determined, revealing a 2,796,913-bp chromosome, with a G+C content of 37.30% and a single plasmid (pTPu1; 3,649 bp) identical to pTS1 from Treponema denticola.
GENOME ANNOUNCEMENT
More than 75 species or phylotypes of oral spirochetes inhabit the oral cavity (1, 2). All taxa belong to the genus Treponema and are classified into 10 phylogroups (3). Phylogroup 2 contains two formally described species, Treponema denticola (4) and Treponema putidum (5), which share ca. 98.5% 16S rRNA gene sequence homology. The genome sequence of T. denticola ATCC 35405T was published in 2004 (6). A large number of clinical studies have associated T. denticola with human periodontal diseases (reviewed in references 7–9). Unlike T. denticola, the ecology, distributions, and clinical disease associations of T. putidum are poorly understood. Here, we report the complete genome of the type strain of T. putidum (OMZ 758T, ATCC 700334T), which was originally isolated from a Swiss periodontitis patient (5).
The OMZ 758T strain was obtained directly from the original isolator and depositor (C. Wyss, University of Zurich) and was cultured anaerobically in supplemented tryptone-yeast extract-gelatin-volatile fatty acids-serum (TYGVS) medium, as previously described (10). Genomic DNA was extracted from a pure culture (QIAamp DNA mini extraction kit; Qiagen, Germany) and was sequenced using a 454 Life Sciences GS Junior platform at the Nanjing Agricultural University Bioinformatics Centre, Jiangsu, China. An initial shotgun library generated 245,625 reads, which was followed by an 8-kb span paired-end library yielding 119,479 reads, generating sequence data with 54× coverage. Using 454 Newbler version 2.7, the de novo assembly resulted in 40 large contigs, with an N50 contig size of 264,778 bp in two scaffolds. The single gap was closed by PCR and Sanger sequencing.
The T. putidum OMZ 758T chromosome is 2,796,913 bp, with a G+C content of 37.30%. Annotation was performed automatically using the PGAAP pipeline implemented in NCBI, following the best-placed reference protein set (GeneMarkS+ version 2.7). The genome contains 2,448 genes, 176 pseudogenes, 42 tRNAs, and two copies of an rRNA cluster (5S, 16S, and 23S). There is also a single plasmid of 3,649 bp (pTPu1), with a G+C content of 34.17%, which shares 100% sequence similarity with T. denticola plasmid pTS1 (accession no. AF112856) (11). The genome encodes homologues of virulence factors previously identified within T. denticola (7–9). These include the major surface protein (MSP) (locus tag JO40_03880) involved in cellular adhesion processes (12), factor H binding protein (FhbB, FHL-1) (locus tag JO40_03575), implicated in evading complement-mediated killing (13), and cystalysin (hemolysin [Hly]) (locus tag JO40_09085), involved in volatile sulfur compound production and erythrolysis (14).
The annotated full-genome sequence for T. putidum OMZ 758T (ATCC 700334T) reported here represents the first strain for this species. This significantly broadens the genomic data available for studying the biology, physiology, and phylogeny of oral treponemes associated with periodontal diseases. It will also facilitate efforts to systematically analyze genetically related species of treponemes that inhabit oral and nonoral niches in animals, many of which are implicated in polymicrobial tissue-destructive diseases (15, 16).
ACKNOWLEDGMENTS
This work was supported by the General Research Fund of the Research Grants Council (RGC) of Hong Kong (781911, to R.M.W.). Financial support from the Infection and Immunology Strategic Research Theme of the University of Hong Kong and the Bioinformatics Centre of Nanjing Agricultural University is also acknowledged.
We thank Manreet Brar from the School of Biological Sciences, the University of Hong Kong, for his technical assistance.
FOOTNOTES
- Received 11 September 2014.
- Accepted 16 September 2014.
- Published 23 October 2014.
- Copyright © 2014 Lacap-Bugler et al.
This is an open-access article distributed under the terms of the Creative Commons Attribution 3.0 Unported license.
