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Prediction of the origin of French Legionella pneumophila strains using a mixed-genome microarray

BACKGROUND: Legionella is a water and soil bacterium that can infect humans, causing a pneumonia known as Legionnaires’ disease. The pneumonia is almost exclusively caused by the species L. pneumophila, of which serogroup 1 is responsible for 90% of patients. Within serogroup 1, large differences in...

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Autores principales: Den Boer, Jeroen W, Euser, Sjoerd M, Nagelkerke, Nico J, Schuren, Frank, Jarraud, Sophie, Etienne, Jerome
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3701591/
https://www.ncbi.nlm.nih.gov/pubmed/23815549
http://dx.doi.org/10.1186/1471-2164-14-435
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author Den Boer, Jeroen W
Euser, Sjoerd M
Nagelkerke, Nico J
Schuren, Frank
Jarraud, Sophie
Etienne, Jerome
author_facet Den Boer, Jeroen W
Euser, Sjoerd M
Nagelkerke, Nico J
Schuren, Frank
Jarraud, Sophie
Etienne, Jerome
author_sort Den Boer, Jeroen W
collection PubMed
description BACKGROUND: Legionella is a water and soil bacterium that can infect humans, causing a pneumonia known as Legionnaires’ disease. The pneumonia is almost exclusively caused by the species L. pneumophila, of which serogroup 1 is responsible for 90% of patients. Within serogroup 1, large differences in prevalence in clinical isolates have been described. A recent study, using a Dutch Legionella strain collection, identified five virulence associated markers. In our study, we verify whether these five Dutch markers can predict the patient or environmental origin of a French Legionella strain collection. In addition, we identify new potential virulence markers and verify whether these can predict better. A total of 219 French patient isolates and environmental strains were compared using a mixed-genome micro-array. The micro-array data were analysed to identify predictive markers, using a Random Forest algorithm combined with a logistic regression model. The sequences of the identified markers were compared with eleven known Legionella genomes, using BlastN and BlastX; the functionality for each of the predictive markers was checked in the literature. RESULTS: The five Dutch markers insufficiently predicted the patient or environmental origin of the French Legionella strains. Subsequent analyses identified four predictive markers for the French collection that were used for the logistic regression model. This model showed a negative predictive value of 91%. Three of the French markers differed from the Dutch markers, one showed considerable overlap and was found in one of the Legionella genomes (Lorraine strain). This marker encodes for a structural toxin protein RtxA, described for L. pneumophila as a factor involved in virulence and entry in both human cells and amoebae. CONCLUSIONS: The combination of a mixed-genome micro-array and statistical analysis using a Random Forest algorithm has identified virulence markers in a consistent way. The Lorraine strain and related Dutch and French Legionella strains contain a marker that encodes a RtxA protein which probably is involved in the increased prevalence in clinical isolates. The current set of predictive markers is insufficient to justify its use as a reliable test in the public health field in France. Our results suggest that genetic differences in Legionella strains exist between geographically distinct entities. It may be necessary to develop region-specific mixed-genome microarrays that are constantly adapted and updated.
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spelling pubmed-37015912013-07-05 Prediction of the origin of French Legionella pneumophila strains using a mixed-genome microarray Den Boer, Jeroen W Euser, Sjoerd M Nagelkerke, Nico J Schuren, Frank Jarraud, Sophie Etienne, Jerome BMC Genomics Research Article BACKGROUND: Legionella is a water and soil bacterium that can infect humans, causing a pneumonia known as Legionnaires’ disease. The pneumonia is almost exclusively caused by the species L. pneumophila, of which serogroup 1 is responsible for 90% of patients. Within serogroup 1, large differences in prevalence in clinical isolates have been described. A recent study, using a Dutch Legionella strain collection, identified five virulence associated markers. In our study, we verify whether these five Dutch markers can predict the patient or environmental origin of a French Legionella strain collection. In addition, we identify new potential virulence markers and verify whether these can predict better. A total of 219 French patient isolates and environmental strains were compared using a mixed-genome micro-array. The micro-array data were analysed to identify predictive markers, using a Random Forest algorithm combined with a logistic regression model. The sequences of the identified markers were compared with eleven known Legionella genomes, using BlastN and BlastX; the functionality for each of the predictive markers was checked in the literature. RESULTS: The five Dutch markers insufficiently predicted the patient or environmental origin of the French Legionella strains. Subsequent analyses identified four predictive markers for the French collection that were used for the logistic regression model. This model showed a negative predictive value of 91%. Three of the French markers differed from the Dutch markers, one showed considerable overlap and was found in one of the Legionella genomes (Lorraine strain). This marker encodes for a structural toxin protein RtxA, described for L. pneumophila as a factor involved in virulence and entry in both human cells and amoebae. CONCLUSIONS: The combination of a mixed-genome micro-array and statistical analysis using a Random Forest algorithm has identified virulence markers in a consistent way. The Lorraine strain and related Dutch and French Legionella strains contain a marker that encodes a RtxA protein which probably is involved in the increased prevalence in clinical isolates. The current set of predictive markers is insufficient to justify its use as a reliable test in the public health field in France. Our results suggest that genetic differences in Legionella strains exist between geographically distinct entities. It may be necessary to develop region-specific mixed-genome microarrays that are constantly adapted and updated. BioMed Central 2013-07-01 /pmc/articles/PMC3701591/ /pubmed/23815549 http://dx.doi.org/10.1186/1471-2164-14-435 Text en Copyright © 2013 Den Boer et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Den Boer, Jeroen W
Euser, Sjoerd M
Nagelkerke, Nico J
Schuren, Frank
Jarraud, Sophie
Etienne, Jerome
Prediction of the origin of French Legionella pneumophila strains using a mixed-genome microarray
title Prediction of the origin of French Legionella pneumophila strains using a mixed-genome microarray
title_full Prediction of the origin of French Legionella pneumophila strains using a mixed-genome microarray
title_fullStr Prediction of the origin of French Legionella pneumophila strains using a mixed-genome microarray
title_full_unstemmed Prediction of the origin of French Legionella pneumophila strains using a mixed-genome microarray
title_short Prediction of the origin of French Legionella pneumophila strains using a mixed-genome microarray
title_sort prediction of the origin of french legionella pneumophila strains using a mixed-genome microarray
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3701591/
https://www.ncbi.nlm.nih.gov/pubmed/23815549
http://dx.doi.org/10.1186/1471-2164-14-435
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