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Comparative genomics of lactic acid bacteria reveals a niche-specific gene set
BACKGROUND: The recently sequenced genome of Lactobacillus helveticus DPC4571 [1] revealed a dairy organism with significant homology (75% of genes are homologous) to a probiotic bacteria Lb. acidophilus NCFM [2]. This led us to hypothesise that a group of genes could be determined which could defin...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2660350/ https://www.ncbi.nlm.nih.gov/pubmed/19265535 http://dx.doi.org/10.1186/1471-2180-9-50 |
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author | O'Sullivan, Orla O'Callaghan, John Sangrador-Vegas, Amaia McAuliffe, Olivia Slattery, Lydia Kaleta, Pawel Callanan, Michael Fitzgerald, Gerald F Ross, R Paul Beresford, Tom |
author_facet | O'Sullivan, Orla O'Callaghan, John Sangrador-Vegas, Amaia McAuliffe, Olivia Slattery, Lydia Kaleta, Pawel Callanan, Michael Fitzgerald, Gerald F Ross, R Paul Beresford, Tom |
author_sort | O'Sullivan, Orla |
collection | PubMed |
description | BACKGROUND: The recently sequenced genome of Lactobacillus helveticus DPC4571 [1] revealed a dairy organism with significant homology (75% of genes are homologous) to a probiotic bacteria Lb. acidophilus NCFM [2]. This led us to hypothesise that a group of genes could be determined which could define an organism's niche. RESULTS: Taking 11 fully sequenced lactic acid bacteria (LAB) as our target, (3 dairy LAB, 5 gut LAB and 3 multi-niche LAB), we demonstrated that the presence or absence of certain genes involved in sugar metabolism, the proteolytic system, and restriction modification enzymes were pivotal in suggesting the niche of a strain. We identified 9 niche specific genes, of which 6 are dairy specific and 3 are gut specific. The dairy specific genes identified in Lactobacillus helveticus DPC4571 were lhv_1161 and lhv_1171, encoding components of the proteolytic system, lhv_1031 lhv_1152, lhv_1978 and lhv_0028 encoding restriction endonuclease genes, while bile salt hydrolase genes lba_0892 and lba_1078, and the sugar metabolism gene lba_1689 from Lb. acidophilus NCFM were identified as gut specific genes. CONCLUSION: Comparative analysis revealed that if an organism had homologs to the dairy specific geneset, it probably came from a dairy environment, whilst if it had homologs to gut specific genes, it was highly likely to be of intestinal origin. We propose that this "barcode" of 9 genes will be a useful initial guide to researchers in the LAB field to indicate an organism's ability to occupy a specific niche. |
format | Text |
id | pubmed-2660350 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26603502009-03-25 Comparative genomics of lactic acid bacteria reveals a niche-specific gene set O'Sullivan, Orla O'Callaghan, John Sangrador-Vegas, Amaia McAuliffe, Olivia Slattery, Lydia Kaleta, Pawel Callanan, Michael Fitzgerald, Gerald F Ross, R Paul Beresford, Tom BMC Microbiol Research article BACKGROUND: The recently sequenced genome of Lactobacillus helveticus DPC4571 [1] revealed a dairy organism with significant homology (75% of genes are homologous) to a probiotic bacteria Lb. acidophilus NCFM [2]. This led us to hypothesise that a group of genes could be determined which could define an organism's niche. RESULTS: Taking 11 fully sequenced lactic acid bacteria (LAB) as our target, (3 dairy LAB, 5 gut LAB and 3 multi-niche LAB), we demonstrated that the presence or absence of certain genes involved in sugar metabolism, the proteolytic system, and restriction modification enzymes were pivotal in suggesting the niche of a strain. We identified 9 niche specific genes, of which 6 are dairy specific and 3 are gut specific. The dairy specific genes identified in Lactobacillus helveticus DPC4571 were lhv_1161 and lhv_1171, encoding components of the proteolytic system, lhv_1031 lhv_1152, lhv_1978 and lhv_0028 encoding restriction endonuclease genes, while bile salt hydrolase genes lba_0892 and lba_1078, and the sugar metabolism gene lba_1689 from Lb. acidophilus NCFM were identified as gut specific genes. CONCLUSION: Comparative analysis revealed that if an organism had homologs to the dairy specific geneset, it probably came from a dairy environment, whilst if it had homologs to gut specific genes, it was highly likely to be of intestinal origin. We propose that this "barcode" of 9 genes will be a useful initial guide to researchers in the LAB field to indicate an organism's ability to occupy a specific niche. BioMed Central 2009-03-05 /pmc/articles/PMC2660350/ /pubmed/19265535 http://dx.doi.org/10.1186/1471-2180-9-50 Text en Copyright ©2009 O'Sullivan 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 O'Sullivan, Orla O'Callaghan, John Sangrador-Vegas, Amaia McAuliffe, Olivia Slattery, Lydia Kaleta, Pawel Callanan, Michael Fitzgerald, Gerald F Ross, R Paul Beresford, Tom Comparative genomics of lactic acid bacteria reveals a niche-specific gene set |
title | Comparative genomics of lactic acid bacteria reveals a niche-specific gene set |
title_full | Comparative genomics of lactic acid bacteria reveals a niche-specific gene set |
title_fullStr | Comparative genomics of lactic acid bacteria reveals a niche-specific gene set |
title_full_unstemmed | Comparative genomics of lactic acid bacteria reveals a niche-specific gene set |
title_short | Comparative genomics of lactic acid bacteria reveals a niche-specific gene set |
title_sort | comparative genomics of lactic acid bacteria reveals a niche-specific gene set |
topic | Research article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2660350/ https://www.ncbi.nlm.nih.gov/pubmed/19265535 http://dx.doi.org/10.1186/1471-2180-9-50 |
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