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Using unique ORFan genes as strain-specific identifiers for Escherichia coli
BACKGROUND: Bacterial identification at the strain level is a much-needed, but arduous and challenging task. This study aimed to develop a method for identifying and differentiating individual strains among multiple strains of the same bacterial species. The set used for testing the method consisted...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9118744/ https://www.ncbi.nlm.nih.gov/pubmed/35585491 http://dx.doi.org/10.1186/s12866-022-02508-y |
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author | Ferrandis-Vila, Marta Tiwari, Sumeet K. Mamerow, Svenja Semmler, Torsten Menge, Christian Berens, Christian |
author_facet | Ferrandis-Vila, Marta Tiwari, Sumeet K. Mamerow, Svenja Semmler, Torsten Menge, Christian Berens, Christian |
author_sort | Ferrandis-Vila, Marta |
collection | PubMed |
description | BACKGROUND: Bacterial identification at the strain level is a much-needed, but arduous and challenging task. This study aimed to develop a method for identifying and differentiating individual strains among multiple strains of the same bacterial species. The set used for testing the method consisted of 17 Escherichia coli strains picked from a collection of strains isolated in Germany, Spain, the United Kingdom and Vietnam from humans, cattle, swine, wild boars, and chickens. We targeted unique or rare ORFan genes to address the problem of selective and specific strain identification. These ORFan genes, exclusive to each strain, served as templates for developing strain-specific primers. RESULTS: Most of the experimental strains (14 out of 17) possessed unique ORFan genes that were used to develop strain-specific primers. The remaining three strains were identified by combining a PCR for a rare gene with a selection step for isolating the experimental strains. Multiplex PCR allowed the successful identification of the strains both in vitro in spiked faecal material in addition to in vivo after experimental infections of pigs and recovery of bacteria from faecal material. In addition, primers for qPCR were also developed and quantitative readout from faecal samples after experimental infection was also possible. CONCLUSIONS: The method described in this manuscript using strain-specific unique genes to identify single strains in a mixture of strains proved itself efficient and reliable in detecting and following individual strains both in vitro and in vivo, representing a fast and inexpensive alternative to more costly methods. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-022-02508-y. |
format | Online Article Text |
id | pubmed-9118744 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-91187442022-05-20 Using unique ORFan genes as strain-specific identifiers for Escherichia coli Ferrandis-Vila, Marta Tiwari, Sumeet K. Mamerow, Svenja Semmler, Torsten Menge, Christian Berens, Christian BMC Microbiol Research BACKGROUND: Bacterial identification at the strain level is a much-needed, but arduous and challenging task. This study aimed to develop a method for identifying and differentiating individual strains among multiple strains of the same bacterial species. The set used for testing the method consisted of 17 Escherichia coli strains picked from a collection of strains isolated in Germany, Spain, the United Kingdom and Vietnam from humans, cattle, swine, wild boars, and chickens. We targeted unique or rare ORFan genes to address the problem of selective and specific strain identification. These ORFan genes, exclusive to each strain, served as templates for developing strain-specific primers. RESULTS: Most of the experimental strains (14 out of 17) possessed unique ORFan genes that were used to develop strain-specific primers. The remaining three strains were identified by combining a PCR for a rare gene with a selection step for isolating the experimental strains. Multiplex PCR allowed the successful identification of the strains both in vitro in spiked faecal material in addition to in vivo after experimental infections of pigs and recovery of bacteria from faecal material. In addition, primers for qPCR were also developed and quantitative readout from faecal samples after experimental infection was also possible. CONCLUSIONS: The method described in this manuscript using strain-specific unique genes to identify single strains in a mixture of strains proved itself efficient and reliable in detecting and following individual strains both in vitro and in vivo, representing a fast and inexpensive alternative to more costly methods. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-022-02508-y. BioMed Central 2022-05-18 /pmc/articles/PMC9118744/ /pubmed/35585491 http://dx.doi.org/10.1186/s12866-022-02508-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Ferrandis-Vila, Marta Tiwari, Sumeet K. Mamerow, Svenja Semmler, Torsten Menge, Christian Berens, Christian Using unique ORFan genes as strain-specific identifiers for Escherichia coli |
title | Using unique ORFan genes as strain-specific identifiers for Escherichia coli |
title_full | Using unique ORFan genes as strain-specific identifiers for Escherichia coli |
title_fullStr | Using unique ORFan genes as strain-specific identifiers for Escherichia coli |
title_full_unstemmed | Using unique ORFan genes as strain-specific identifiers for Escherichia coli |
title_short | Using unique ORFan genes as strain-specific identifiers for Escherichia coli |
title_sort | using unique orfan genes as strain-specific identifiers for escherichia coli |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9118744/ https://www.ncbi.nlm.nih.gov/pubmed/35585491 http://dx.doi.org/10.1186/s12866-022-02508-y |
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