Literature DB >> 28034855

Genome Sequence of Actinomyces naeslundii Strain ATCC 27039, Isolated from an Abdominal Wound Abscess.

Chiho Mashimo1, Kazuyoshi Yamane2, Takeshi Yamanaka2, Hugo Maruyama2, Pao-Li Wang2, Satoshi Komasa3, Joji Okazaki3, Takayuki Nambu1.   

Abstract

Here, we present the complete genome sequence of Actinomyces naeslundii strain ATCC 27039, isolated from an abdominal wound abscess. This strain is genetically transformable and will thus provide valuable information related to its crucial role in oral multispecies biofilm development.
Copyright © 2016 Mashimo et al.

Entities:  

Year:  2016        PMID: 28034855      PMCID: PMC5201054          DOI: 10.1128/genomeA.01443-16

Source DB:  PubMed          Journal:  Genome Announc


GENOME ANNOUNCEMENT

It is well known that Actinomyces spp. are common bacteria in the normal flora of the mouth, and that they play an important role in the development of oral biofilm as one of the initial colonizers of tooth surfaces (1–3). Actinomyces spp. have been implicated in the dental caries process as acidogenic bacteria and could also be causative bacteria that make inroads to deeper tissues via traumatic wounds and surgical operations in both immunocompetent and immunocompromised individuals (4–6). Recently, the next-generation sequencing analysis of oral samples revealed that Actinomyces spp., especially A. naeslundii and A. oris, are core members of the healthy oral microbiome (7–12). Standard genetic engineering techniques are now applicable to A. oris (13, 14). On the other hand, there is no information regarding the gene modification system on A. naeslundii; therefore, we examined the transformability of several oral A. naeslundii strains and confirmed that strain ATCC 27039 was genetically tractable. The aim of the present study is to determine the full-genome sequence of A. naeslundii ATCC 27039. Total bacterial DNA of strain ATCC 27039 was extracted from an overnight culture using a Nucleo spin tissue kit (Macherey-Nagel). A 20-kb SMRTbell library was prepared, and the genome was sequenced using the PacBio RS II system (Pacific Biosciences) on a single-molecule real-time (SMRT) cell using PacBio P6-C4 chemistry. The de novo assembly of 153,093 reads with a mean length of 5,172 bp was completed using the hierarchical genome assembly process (HGAP) algorithm in SMRT Analysis software version 2.3 (15) and revealed a single contig approximately 3.04 Mb in length with an average coverage of 217.96×; the assembly was manually edited to circularize the overlapping ends of the genome. The final genome sequence is 3,040,449 bp in size and has a G+C content of 68.4%. The genome was then annotated using RAST version 2.0 (16), which successfully identified 3,229 coding sequences, as well as 60 RNA sequences. Of these, 43% of the annotated coding sequences fell within 318 subsystems available in the RAST database. The annotated data set presented here is expected to augment future study of this organism and provide resources for genetic manipulation.

Accession number(s).

The genome sequence of A. naeslundii ATCC 27039 has been deposited in the DDBJ/EMBL/GenBank database under accession number AP017894.
  16 in total

Review 1.  Oral multispecies biofilm development and the key role of cell-cell distance.

Authors:  Paul E Kolenbrander; Robert J Palmer; Saravanan Periasamy; Nicholas S Jakubovics
Journal:  Nat Rev Microbiol       Date:  2010-07       Impact factor: 60.633

2.  Allelic exchange in Actinomyces oris with mCherry fluorescence counterselection.

Authors:  Chenggang Wu; Hung Ton-That
Journal:  Appl Environ Microbiol       Date:  2010-07-02       Impact factor: 4.792

3.  Nonhybrid, finished microbial genome assemblies from long-read SMRT sequencing data.

Authors:  Chen-Shan Chin; David H Alexander; Patrick Marks; Aaron A Klammer; James Drake; Cheryl Heiner; Alicia Clum; Alex Copeland; John Huddleston; Evan E Eichler; Stephen W Turner; Jonas Korlach
Journal:  Nat Methods       Date:  2013-05-05       Impact factor: 28.547

Review 4.  Actinomyces and related organisms in human infections.

Authors:  Eija Könönen; William G Wade
Journal:  Clin Microbiol Rev       Date:  2015-04       Impact factor: 26.132

5.  The Actinomyces oris type 2 fimbrial shaft FimA mediates co-aggregation with oral streptococci, adherence to red blood cells and biofilm development.

Authors:  Arunima Mishra; Chenggang Wu; Jinghua Yang; John O Cisar; Asis Das; Hung Ton-That
Journal:  Mol Microbiol       Date:  2010-06-10       Impact factor: 3.501

6.  Beyond microbial community composition: functional activities of the oral microbiome in health and disease.

Authors:  Ana E Duran-Pinedo; Jorge Frias-Lopez
Journal:  Microbes Infect       Date:  2015-04-07       Impact factor: 2.700

7.  The human oral microbiome.

Authors:  Floyd E Dewhirst; Tuste Chen; Jacques Izard; Bruce J Paster; Anne C R Tanner; Wen-Han Yu; Abirami Lakshmanan; William G Wade
Journal:  J Bacteriol       Date:  2010-07-23       Impact factor: 3.490

8.  Bacterial diversity in the oral cavity of 10 healthy individuals.

Authors:  Elisabeth M Bik; Clara Davis Long; Gary C Armitage; Peter Loomer; Joanne Emerson; Emmanuel F Mongodin; Karen E Nelson; Steven R Gill; Claire M Fraser-Liggett; David A Relman
Journal:  ISME J       Date:  2010-03-25       Impact factor: 10.302

9.  Oral colonization with Actinomyces species in infants by two years of age.

Authors:  N Sarkonen; E Könönen; P Summanen; A Kanervo; A Takala; H Jousimies-Somer
Journal:  J Dent Res       Date:  2000-03       Impact factor: 6.116

10.  Defining the healthy "core microbiome" of oral microbial communities.

Authors:  Egija Zaura; Bart J F Keijser; Susan M Huse; Wim Crielaard
Journal:  BMC Microbiol       Date:  2009-12-15       Impact factor: 3.605

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