In silico analysis of 16S ribosomal RNA gene sequencing-based methods for identification of medically important anaerobic bacteria

This study is the first study that provides useful guidelines to clinical microbiologists and technicians on the usefulness of full 16S rRNA sequencing, 5′-end 527-bp 16S rRNA sequencing and the existing MicroSeq full and 500 16S rDNA bacterial identification system (MicroSeq, Perkin-Elmer Applied B...

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Published in:Journal of clinical pathology Vol. 60; no. 5; pp. 576 - 579
Main Authors: Woo, Patrick C Y, Chung, Liliane M W, Teng, Jade L L, Tse, Herman, Pang, Sherby S Y, Lau, Veronica Y T, Wong, Vanessa W K, Kam, Kwok-ling, Lau, Susanna K P, Yuen, Kwok-Yung
Format: Journal Article
Language:English
Published: London BMJ Publishing Group Ltd and Association of Clinical Pathologists 01-05-2007
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Summary:This study is the first study that provides useful guidelines to clinical microbiologists and technicians on the usefulness of full 16S rRNA sequencing, 5′-end 527-bp 16S rRNA sequencing and the existing MicroSeq full and 500 16S rDNA bacterial identification system (MicroSeq, Perkin-Elmer Applied Biosystems Division, Foster City, California, USA) databases for the identification of all existing medically important anaerobic bacteria. Full and 527-bp 16S rRNA sequencing are able to identify 52–63% of 130 Gram-positive anaerobic rods, 72–73% of 86 Gram-negative anaerobic rods and 78% of 23 anaerobic cocci. The existing MicroSeq databases are able to identify only 19–25% of 130 Gram-positive anaerobic rods, 38% of 86 Gram-negative anaerobic rods and 39% of 23 anaerobic cocci. These represent only 45–46% of those that should be confidently identified by full and 527-bp 16S rRNA sequencing. To improve the usefulness of MicroSeq, bacterial species that should be confidently identified by full and/or 527-bp 16S rRNA sequencing but not included in the existing MicroSeq databases should be included.
Bibliography:href:jclinpath-60-576.pdf
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PMID:17046845
Correspondence to:
 Dr K-Y Yuen
 Department of Microbiology, The University of Hong Kong, University Pathology Building, Queen Mary Hospital Compound, Pokfulam Road, Hong Kong; hkumicro@hkucc.hku.hk
local:0600576
ObjectType-Article-1
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content type line 23
ISSN:0021-9746
1472-4146
DOI:10.1136/jcp.2006.038653