Use of the 16S–23S ribosomal genes spacer region for the molecular typing of sphingomonads

The ability of sphingomonads in drinking water to cause community- and hospital-acquired opportunistic infections has raised the need to establish reproducible identification assays. In this study, a total of 129 isolates recovered from drinking water with yellow- to orange-pigmented colonies were d...

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Main Author: Tokajian, Sima (author)
Other Authors: Hashwa, Fuad (author), El-Medawar, Siba (author)
Format: article
Published: 2008
Online Access:http://hdl.handle.net/10725/3390
http://dx.doi.org/10.1139/W08-054
http://www.nrcresearchpress.com/doi/abs/10.1139/W08-054#.V6MQG7h97y0
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author Tokajian, Sima
author2 Hashwa, Fuad
El-Medawar, Siba
author2_role author
author
author_facet Tokajian, Sima
Hashwa, Fuad
El-Medawar, Siba
author_role author
dc.creator.none.fl_str_mv Tokajian, Sima
Hashwa, Fuad
El-Medawar, Siba
dc.date.none.fl_str_mv 2008
2016-03-23T09:18:16Z
2016-03-23T09:18:16Z
2016-03-23
dc.identifier.none.fl_str_mv 0008-4166
http://hdl.handle.net/10725/3390
http://dx.doi.org/10.1139/W08-054
Tokajian, S., Al-Medawar, S., & Hashwa, F. (2008). Use of the 16S-23S ribosomal genes spacer region for the molecular typing of sphingomonads. Canadian journal of microbiology, 54(8), 668-676.
http://www.nrcresearchpress.com/doi/abs/10.1139/W08-054#.V6MQG7h97y0
dc.language.none.fl_str_mv en
dc.relation.none.fl_str_mv Canadian Journal of Microbiology
dc.rights.*.fl_str_mv info:eu-repo/semantics/openAccess
dc.title.none.fl_str_mv Use of the 16S–23S ribosomal genes spacer region for the molecular typing of sphingomonads
dc.type.none.fl_str_mv Article
info:eu-repo/semantics/publishedVersion
info:eu-repo/semantics/article
description The ability of sphingomonads in drinking water to cause community- and hospital-acquired opportunistic infections has raised the need to establish reproducible identification assays. In this study, a total of 129 isolates recovered from drinking water with yellow- to orange-pigmented colonies were distributed among 10 biotypes on the basis of colony morphology. Polymorphisms, based on the amplification and restriction digestion of the intergenic transcribed spacer (ITS) region within the 10 assigned biotypes and 18 ATCC reference strains, were used to investigate the ability of this approach to differentiate closely related sphingomonads. ITS size, which ranged between 400 and 1100 bp, did not vary enough among the different genera. However, 16 distinct banding patterns within the ATCC reference strains and 9 within the 10 biotypes were obtained through ITS restriction digestion, and the majority of the tested biotypes produced patterns similar to those generated by the ATCC strains. To our knowledge, this study is not only the first comprehensive record of the size of the ITS region in sphingomonads, it is also the first study that describes the use of ITS restriction digestion to subtype those isolates.
eu_rights_str_mv openAccess
format article
id LAURepo_f2d6ec62b71cb3a2ba4ec44c4d252e69
identifier_str_mv 0008-4166
Tokajian, S., Al-Medawar, S., & Hashwa, F. (2008). Use of the 16S-23S ribosomal genes spacer region for the molecular typing of sphingomonads. Canadian journal of microbiology, 54(8), 668-676.
language_invalid_str_mv en
network_acronym_str LAURepo
network_name_str Lebanese American University repository
oai_identifier_str oai:laur.lau.edu.lb:10725/3390
publishDate 2008
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spelling Use of the 16S–23S ribosomal genes spacer region for the molecular typing of sphingomonadsTokajian, SimaHashwa, FuadEl-Medawar, SibaThe ability of sphingomonads in drinking water to cause community- and hospital-acquired opportunistic infections has raised the need to establish reproducible identification assays. In this study, a total of 129 isolates recovered from drinking water with yellow- to orange-pigmented colonies were distributed among 10 biotypes on the basis of colony morphology. Polymorphisms, based on the amplification and restriction digestion of the intergenic transcribed spacer (ITS) region within the 10 assigned biotypes and 18 ATCC reference strains, were used to investigate the ability of this approach to differentiate closely related sphingomonads. ITS size, which ranged between 400 and 1100 bp, did not vary enough among the different genera. However, 16 distinct banding patterns within the ATCC reference strains and 9 within the 10 biotypes were obtained through ITS restriction digestion, and the majority of the tested biotypes produced patterns similar to those generated by the ATCC strains. To our knowledge, this study is not only the first comprehensive record of the size of the ITS region in sphingomonads, it is also the first study that describes the use of ITS restriction digestion to subtype those isolates.PublishedN/A2016-03-23T09:18:16Z2016-03-23T09:18:16Z20082016-03-23Articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article0008-4166http://hdl.handle.net/10725/3390http://dx.doi.org/10.1139/W08-054Tokajian, S., Al-Medawar, S., & Hashwa, F. (2008). Use of the 16S-23S ribosomal genes spacer region for the molecular typing of sphingomonads. Canadian journal of microbiology, 54(8), 668-676.http://www.nrcresearchpress.com/doi/abs/10.1139/W08-054#.V6MQG7h97y0enCanadian Journal of Microbiologyinfo:eu-repo/semantics/openAccessoai:laur.lau.edu.lb:10725/33902016-12-20T12:25:20Z
spellingShingle Use of the 16S–23S ribosomal genes spacer region for the molecular typing of sphingomonads
Tokajian, Sima
status_str publishedVersion
title Use of the 16S–23S ribosomal genes spacer region for the molecular typing of sphingomonads
title_full Use of the 16S–23S ribosomal genes spacer region for the molecular typing of sphingomonads
title_fullStr Use of the 16S–23S ribosomal genes spacer region for the molecular typing of sphingomonads
title_full_unstemmed Use of the 16S–23S ribosomal genes spacer region for the molecular typing of sphingomonads
title_short Use of the 16S–23S ribosomal genes spacer region for the molecular typing of sphingomonads
title_sort Use of the 16S–23S ribosomal genes spacer region for the molecular typing of sphingomonads
url http://hdl.handle.net/10725/3390
http://dx.doi.org/10.1139/W08-054
http://www.nrcresearchpress.com/doi/abs/10.1139/W08-054#.V6MQG7h97y0