Genetic approaches to the identification of the mitis group within the genus Streptococcus

Department of Microbiology, Gifu University School of Medicine, 40 Tsukasa-machi, Gifu 500-8705, Japan 1 Department of Oral Microbiology, St. Bartholomew’s and the Royal London School of Medicine and Dentistry, Turner Street, London E1 2AD, UK 2 Author for correspondence: Yoshiaki Kawamura. Tel: +81...

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Veröffentlicht in:Microbiology (Society for General Microbiology) 1999-09, Vol.145 (9), p.2605-2613
Hauptverfasser: Kawamura, Yoshiaki, Whiley, Robert A, Shu, Shin-Ei, Ezaki, Takayuki, Hardie, Jeremy M
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container_end_page 2613
container_issue 9
container_start_page 2605
container_title Microbiology (Society for General Microbiology)
container_volume 145
creator Kawamura, Yoshiaki
Whiley, Robert A
Shu, Shin-Ei
Ezaki, Takayuki
Hardie, Jeremy M
description Department of Microbiology, Gifu University School of Medicine, 40 Tsukasa-machi, Gifu 500-8705, Japan 1 Department of Oral Microbiology, St. Bartholomew’s and the Royal London School of Medicine and Dentistry, Turner Street, London E1 2AD, UK 2 Author for correspondence: Yoshiaki Kawamura. Tel: +81 58 267 2240. Fax: +81 58 267 0156. e-mail: kawamura{at}cc.gifu-u.ac.jp The usefulness and reliability of partial sequence analysis of the manganese-dependent superoxide dismutase gene ( sodA ), autolysin ( lytA ) gene amplification and species-specific PCR based on the D-alanine:D-alanine ligase ( ddl ) gene for differentiating each member of the mitis group of the genus Streptococcus was investigated. On the phylogenetic tree based on sodA partial sequences (366 bp) from 96 strains, including all species currently within the mitis group isolated in different geographic areas (mainly Japan and the UK), eight well separated clusters were generated corresponding to recognized species, and all strains fell into those clusters to which they had also been assigned by DNA–DNA hybridization. The Streptococcus pneumoniae sub-cluster was located within the Streptococcus mitis cluster, but the sodA gene of S. pneumoniae was very conserved and therefore could be separated from all other species examined. Furthermore, the lytA gene amplification approach could also be used to differentiate S. pneumoniae from other species. The species-specific amplification product of the ddl gene was successfully detected in Streptococcus sanguinis and Streptococcus gordonii , but failed to be detected in some strains of Streptococcus oralis including the type strain and S. mitis . We conclude that the partial sequence analysis of the sodA gene could be applied globally as a reliable and easy method for the accurate identification of all species currently within the mitis group. View this table: [in this window] [in a new window]   Table 1. Strains used and identification results   Keywords: Superoxide dismutase gene, autolysin gene, d-alanine:d-alanine ligase gene, mitis group, Streptococcus The DDBJ accession numbers of the superoxide dismutase genes described in this paper are shown in Table 1.
doi_str_mv 10.1099/00221287-145-9-2605
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Tel: +81 58 267 2240. Fax: +81 58 267 0156. e-mail: kawamura{at}cc.gifu-u.ac.jp The usefulness and reliability of partial sequence analysis of the manganese-dependent superoxide dismutase gene ( sodA ), autolysin ( lytA ) gene amplification and species-specific PCR based on the D-alanine:D-alanine ligase ( ddl ) gene for differentiating each member of the mitis group of the genus Streptococcus was investigated. On the phylogenetic tree based on sodA partial sequences (366 bp) from 96 strains, including all species currently within the mitis group isolated in different geographic areas (mainly Japan and the UK), eight well separated clusters were generated corresponding to recognized species, and all strains fell into those clusters to which they had also been assigned by DNA–DNA hybridization. The Streptococcus pneumoniae sub-cluster was located within the Streptococcus mitis cluster, but the sodA gene of S. pneumoniae was very conserved and therefore could be separated from all other species examined. Furthermore, the lytA gene amplification approach could also be used to differentiate S. pneumoniae from other species. The species-specific amplification product of the ddl gene was successfully detected in Streptococcus sanguinis and Streptococcus gordonii , but failed to be detected in some strains of Streptococcus oralis including the type strain and S. mitis . We conclude that the partial sequence analysis of the sodA gene could be applied globally as a reliable and easy method for the accurate identification of all species currently within the mitis group. View this table: [in this window] [in a new window]   Table 1. 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Psychology ; Humans ; lytA gene ; Microbiology ; Molecular Sequence Data ; N-Acetylmuramoyl-L-alanine Amidase ; Nucleic Acid Hybridization ; Peptide Synthases - genetics ; Phylogeny ; Polymerase Chain Reaction - methods ; RNA, Ribosomal, 16S - genetics ; Sequence Analysis, DNA ; sodA gene ; Species Specificity ; Streptococcal Infections - microbiology ; Streptococcus - classification ; Streptococcus - genetics ; Streptococcus gordonii ; Streptococcus mitis ; Streptococcus oralis ; Streptococcus pneumoniae ; Streptococcus sanguinis ; Superoxide Dismutase - genetics ; Systematics</subject><ispartof>Microbiology (Society for General Microbiology), 1999-09, Vol.145 (9), p.2605-2613</ispartof><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27929,27930</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=1981798$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10517614$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kawamura, Yoshiaki</creatorcontrib><creatorcontrib>Whiley, Robert A</creatorcontrib><creatorcontrib>Shu, Shin-Ei</creatorcontrib><creatorcontrib>Ezaki, Takayuki</creatorcontrib><creatorcontrib>Hardie, Jeremy M</creatorcontrib><title>Genetic approaches to the identification of the mitis group within the genus Streptococcus</title><title>Microbiology (Society for General Microbiology)</title><addtitle>Microbiology</addtitle><description>Department of Microbiology, Gifu University School of Medicine, 40 Tsukasa-machi, Gifu 500-8705, Japan 1 Department of Oral Microbiology, St. Bartholomew’s and the Royal London School of Medicine and Dentistry, Turner Street, London E1 2AD, UK 2 Author for correspondence: Yoshiaki Kawamura. Tel: +81 58 267 2240. Fax: +81 58 267 0156. e-mail: kawamura{at}cc.gifu-u.ac.jp The usefulness and reliability of partial sequence analysis of the manganese-dependent superoxide dismutase gene ( sodA ), autolysin ( lytA ) gene amplification and species-specific PCR based on the D-alanine:D-alanine ligase ( ddl ) gene for differentiating each member of the mitis group of the genus Streptococcus was investigated. On the phylogenetic tree based on sodA partial sequences (366 bp) from 96 strains, including all species currently within the mitis group isolated in different geographic areas (mainly Japan and the UK), eight well separated clusters were generated corresponding to recognized species, and all strains fell into those clusters to which they had also been assigned by DNA–DNA hybridization. The Streptococcus pneumoniae sub-cluster was located within the Streptococcus mitis cluster, but the sodA gene of S. pneumoniae was very conserved and therefore could be separated from all other species examined. Furthermore, the lytA gene amplification approach could also be used to differentiate S. pneumoniae from other species. The species-specific amplification product of the ddl gene was successfully detected in Streptococcus sanguinis and Streptococcus gordonii , but failed to be detected in some strains of Streptococcus oralis including the type strain and S. mitis . We conclude that the partial sequence analysis of the sodA gene could be applied globally as a reliable and easy method for the accurate identification of all species currently within the mitis group. View this table: [in this window] [in a new window]   Table 1. Strains used and identification results   Keywords: Superoxide dismutase gene, autolysin gene, d-alanine:d-alanine ligase gene, mitis group, Streptococcus The DDBJ accession numbers of the superoxide dismutase genes described in this paper are shown in Table 1.</description><subject>Alanine</subject><subject>Bacterial Typing Techniques</subject><subject>Bacteriological methods and techniques used in bacteriology</subject><subject>Bacteriology</subject><subject>Biological and medical sciences</subject><subject>D-Alanine:D-alanine ligase</subject><subject>ddl gene</subject><subject>DNA, Bacterial - analysis</subject><subject>DNA, Bacterial - genetics</subject><subject>Enzymes - genetics</subject><subject>Fundamental and applied biological sciences. 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Tel: +81 58 267 2240. Fax: +81 58 267 0156. e-mail: kawamura{at}cc.gifu-u.ac.jp The usefulness and reliability of partial sequence analysis of the manganese-dependent superoxide dismutase gene ( sodA ), autolysin ( lytA ) gene amplification and species-specific PCR based on the D-alanine:D-alanine ligase ( ddl ) gene for differentiating each member of the mitis group of the genus Streptococcus was investigated. On the phylogenetic tree based on sodA partial sequences (366 bp) from 96 strains, including all species currently within the mitis group isolated in different geographic areas (mainly Japan and the UK), eight well separated clusters were generated corresponding to recognized species, and all strains fell into those clusters to which they had also been assigned by DNA–DNA hybridization. The Streptococcus pneumoniae sub-cluster was located within the Streptococcus mitis cluster, but the sodA gene of S. pneumoniae was very conserved and therefore could be separated from all other species examined. Furthermore, the lytA gene amplification approach could also be used to differentiate S. pneumoniae from other species. The species-specific amplification product of the ddl gene was successfully detected in Streptococcus sanguinis and Streptococcus gordonii , but failed to be detected in some strains of Streptococcus oralis including the type strain and S. mitis . We conclude that the partial sequence analysis of the sodA gene could be applied globally as a reliable and easy method for the accurate identification of all species currently within the mitis group. View this table: [in this window] [in a new window]   Table 1. Strains used and identification results   Keywords: Superoxide dismutase gene, autolysin gene, d-alanine:d-alanine ligase gene, mitis group, Streptococcus The DDBJ accession numbers of the superoxide dismutase genes described in this paper are shown in Table 1.</abstract><cop>Reading</cop><pub>Soc General Microbiol</pub><pmid>10517614</pmid><doi>10.1099/00221287-145-9-2605</doi><tpages>9</tpages></addata></record>
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subjects Alanine
Bacterial Typing Techniques
Bacteriological methods and techniques used in bacteriology
Bacteriology
Biological and medical sciences
D-Alanine:D-alanine ligase
ddl gene
DNA, Bacterial - analysis
DNA, Bacterial - genetics
Enzymes - genetics
Fundamental and applied biological sciences. Psychology
Humans
lytA gene
Microbiology
Molecular Sequence Data
N-Acetylmuramoyl-L-alanine Amidase
Nucleic Acid Hybridization
Peptide Synthases - genetics
Phylogeny
Polymerase Chain Reaction - methods
RNA, Ribosomal, 16S - genetics
Sequence Analysis, DNA
sodA gene
Species Specificity
Streptococcal Infections - microbiology
Streptococcus - classification
Streptococcus - genetics
Streptococcus gordonii
Streptococcus mitis
Streptococcus oralis
Streptococcus pneumoniae
Streptococcus sanguinis
Superoxide Dismutase - genetics
Systematics
title Genetic approaches to the identification of the mitis group within the genus Streptococcus
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