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. 2017 Apr 6;5(14):e00126-17. doi: 10.1128/genomeA.00126-17

Whole-Genome Sequences of Two Closely Related Bacteria, Actinomyces sp. Strain Chiba101 and Actinomyces denticolens DSM 20671T

Yu Kanesaki a,, Taichiro Ishige a, Yuriko Sekigawa b, Tomoko Kobayashi b, Yasushi Torii b, Eiji Yokoyama c, Hiroyuki Ishiwata d, Moriyuki Hamada e, Tomohiko Tamura e, Ryozo Azuma f,*, Satoshi Murakami b,
PMCID: PMC5383893  PMID: 28385845

ABSTRACT

Actinomyces sp. strain Chiba101, isolated from an arthritic leg joint of a pig raised in Japan, is a bacterium closely related to Actinomyces denticolens. Here, we deciphered the complete genome sequence of Actinomyces sp. Chiba101 and the high-quality draft genome sequence of A. denticolens DSM 20671T.

GENOME ANNOUNCEMENT

Cells of members of the genus Actinomyces are straight or slightly curved rods to filament with true branching. They are Gram-positive and facultative anaerobic actinobacteria, and are associated with a variety of infections in various animals. Several strains that were similar to “Actinomyces suis” Franke 1973 had been isolated from the tonsils, mammary gland, and an arthritic leg joint in pigs raised in Japan, and the representative strain was designated Chiba101 (1). These isolates have been found to be pathogenic in pigs (2, 3). However, since no type strain of A. suis Franke 1973 was extant (4), it is impossible to compare strain Chiba101 and A. suis Franke 1973. On the other hand, Actinomyces denticolens has been known as a commensal bacterium found in the oral cavity of cattle (5). Interestingly, we also found that strain Chiba101 had chemotaxonomical and serological characteristics which were identical to those of A. denticolens. Therefore, we carried out whole-genome sequencing of strain Chiba101 and A. denticolens DSM 20671T in order to clarify the taxonomic relationship between strain Chiba101 and A. denticolens.

Genomic DNA was extracted from a single colony from each strain. DNA detection was carried out using the Dr. GenTLE High Recovery (TaKaRa Bio, Inc., Kyoto, Japan), according to the manufacturer’s protocol. DNA libraries were sequenced through the massively parallel sequencing method using a PacBio RSII (Pacific Biosciences of California, Inc.), as described by the manufacturer. Approximately 380 Mbp and 113 Mbp of sequencing data were obtained for strains Chiba101 and A. denticolens DSM 20671T, respectively. Sequence reads from the PacBio RSII were assembled using Celera Assembler version 7.0. Only one supercontig was assembled for strain Chiba101. After checking the overhanging region at both ends, the supercontig can be circularized, with a total length of 2,877,864 bp in the case of strain Chiba101, with a G+C content of 71.28%. In the case of A. denticolens DSM 20671T, the eight contigs (>1 kb) were assembled with a total length of 2,904,857 bp, with a G+C content of 71.23%. An annotation of the complete genome of strain Chiba101 and the eight contigs of A. denticolens DSM 20671T was performed using the Microbial Genome Annotation Pipeline (MiGAP) (6), as well as manual curation. As a result, nine rRNAs, 51 tRNAs, and 2,364 coding sequences (CDSs) were identified for strain Chiba101. For A. denticolens DSM 20671T, 14 rRNAs, 51 tRNAs, and 2,510 CDSs were identified.

Our sequencing data will largely contribute to future studies for elucidating not only the taxonomic position of strain Chiba101 but also the epidemiological features and genetic variation among strains of A. denticolens.

Accession number(s).

The complete genome sequence of Actinomyces sp. Chiba101 (accession number AP017896) and draft genome sequence of A. denticolens DSM 20671T (accession numbers BDIO01000001 to BDIO01000008) have been deposited in DDBJ/ENA/GenBank.

ACKNOWLEDGMENT

This study was supported by the MEXT-Supported Program For the Strategic Research Foundation at Private Universities, 2013–2017 (grant S1311017).

Footnotes

Citation Kanesaki Y, Ishige T, Sekigawa Y, Kobayashi T, Torii Y, Yokoyama E, Ishiwata H, Hamada M, Tamura T, Azuma R, Murakami S. 2017. Whole-genome sequences of two closely related bacteria, Actinomyces sp. strain Chiba101 and Actinomyces denticolens DSM 20671T. Genome Announc 5:e00126-17. https://doi.org/10.1128/genomeA.00126-17.

REFERENCES

  • 1.Oomi H, Azuma Y, Ishiwata H, Asahara T, Watanabe T, Murakami S. 1994. Bacteriological study on another pathogenic agent “Actinomyces suis” Grässer 1957 in swine tonsils, 233 Proc Int Pig Vet Sci 13th Congress, 26 to 30 June 1994, Bangkok, Thailand. [Google Scholar]
  • 2.Murakami S, Azuma R, Koeda T, Oomi H, Watanabe T, Fujiwara H. 1998. Immunohistochemical detection for Actinomyces sp. in swine tonsillar abscess and granulomatous mastitis. Mycopathologia 141:15–19. doi: 10.1023/A:1006820611103. [DOI] [PubMed] [Google Scholar]
  • 3.Murakami S, Azuma R, Oomi H, Watanabe T, Suzuki S, Koeda T, Fujiwara H. 1999. Experimental actinomycosis caused by actinomyces-like bacteria in mice and sow. Zentralbl Veterinarmed A 46:533–543. doi: 10.1046/j.1439-0442.1999.00242.x. [DOI] [PubMed] [Google Scholar]
  • 4.Yassin AF, Spröer C, Pukall R, Sylvester M, Siering C, Schumann P. 2015. Dissection of the genus Actinobaculum: reclassification of Actinobaculum schaalii Lawson et al. 1997 and Actinobaculum urinale Hall et al. 2003 as Actinotignum schaalii gen. nov., comb. nov. and Actinotignum urinale comb. nov., description of Actinotignum sanguinis sp. nov. and emended descriptions of the genus Actinobaculum and Actinobaculum suis; and re-examination of the culture deposited as Actinobaculum massiliense CCUG 47753T ( = DSM 19118 T), revealing that it does not represent a strain of this species. Int J Syst Evol Microbiol 65:615–624. doi: 10.1099/ijs.0.069294-0. [DOI] [PubMed] [Google Scholar]
  • 5.Dent VE, Williams RA. 1984. Actinomyces denticolens Dent & W sp. nov: a new species from the dental plaque of cattle. J Appl Bacteriol 56:183–192. doi: 10.1111/j.1365-2672.1984.tb01338.x. [DOI] [PubMed] [Google Scholar]
  • 6.Sugawara H, Ohyama A, Mori H, Kurokawa K. 2009. Microbial Genome Annotation Pipeline (MiGAP) for diverse users S-001. Abstr 20th Int Conf Genome Informatics, Kanagawa, Japan. [Google Scholar]

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