Gene Sequence Based Clustering Assists in Dereplication of <em>Pseudoalteromonas luteoviolacea</em> Strains with Identical Inhibitory Activity and Antibiotic Production

Some microbial species are chemically homogenous, and the same secondary metabolites are found in all strains. In contrast, we previously found that five strains of <em>P. luteoviolacea </em>were closely related by 16S rRNA gene sequence but produced two different antibio...

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Main Authors: Lone Gram, Nikolaj G. Vynne, Maria Mansson
Format: Article
Language:English
Published: MDPI AG 2012-08-01
Series:Marine Drugs
Subjects:
Online Access:http://www.mdpi.com/1660-3397/10/8/1729
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author Lone Gram
Nikolaj G. Vynne
Maria Mansson
author_facet Lone Gram
Nikolaj G. Vynne
Maria Mansson
author_sort Lone Gram
collection DOAJ
description Some microbial species are chemically homogenous, and the same secondary metabolites are found in all strains. In contrast, we previously found that five strains of <em>P. luteoviolacea </em>were closely related by 16S rRNA gene sequence but produced two different antibiotic profiles. The purpose of the present study was to determine whether such bioactivity differences could be linked to genotypes allowing methods from phylogenetic analysis to aid in selection of strains for biodiscovery. Thirteen <em>P. luteoviolacea </em>strains divided into three chemotypes based on production of known antibiotics and four antibacterial profiles based on inhibition assays against <em>Vibrio anguillarum </em>and <em>Staphylococcus aureus</em>. To determine whether chemotype and inhibition profile are reflected by phylogenetic clustering we sequenced 16S rRNA, <em>gyrB </em>and <em>recA </em>genes. Clustering based on 16S rRNA gene sequences alone showed little correlation to chemotypes and inhibition profiles, while clustering based on concatenated 16S rRNA, <em>gyrB</em>,<em> </em>and <em>recA </em>gene sequences resulted in three clusters, two of which uniformly consisted of strains of identical chemotype and inhibition profile. A major time sink in natural products discovery is the effort spent rediscovering known compounds, and this study indicates that phylogeny clustering of bioactive species has the potential to be a useful dereplication tool in biodiscovery efforts.
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spelling doaj.art-37da9a6c6db74fd3a2ab90c9c7af898f2022-12-22T04:24:37ZengMDPI AGMarine Drugs1660-33972012-08-011081729174010.3390/md10081729Gene Sequence Based Clustering Assists in Dereplication of <em>Pseudoalteromonas luteoviolacea</em> Strains with Identical Inhibitory Activity and Antibiotic ProductionLone GramNikolaj G. VynneMaria ManssonSome microbial species are chemically homogenous, and the same secondary metabolites are found in all strains. In contrast, we previously found that five strains of <em>P. luteoviolacea </em>were closely related by 16S rRNA gene sequence but produced two different antibiotic profiles. The purpose of the present study was to determine whether such bioactivity differences could be linked to genotypes allowing methods from phylogenetic analysis to aid in selection of strains for biodiscovery. Thirteen <em>P. luteoviolacea </em>strains divided into three chemotypes based on production of known antibiotics and four antibacterial profiles based on inhibition assays against <em>Vibrio anguillarum </em>and <em>Staphylococcus aureus</em>. To determine whether chemotype and inhibition profile are reflected by phylogenetic clustering we sequenced 16S rRNA, <em>gyrB </em>and <em>recA </em>genes. Clustering based on 16S rRNA gene sequences alone showed little correlation to chemotypes and inhibition profiles, while clustering based on concatenated 16S rRNA, <em>gyrB</em>,<em> </em>and <em>recA </em>gene sequences resulted in three clusters, two of which uniformly consisted of strains of identical chemotype and inhibition profile. A major time sink in natural products discovery is the effort spent rediscovering known compounds, and this study indicates that phylogeny clustering of bioactive species has the potential to be a useful dereplication tool in biodiscovery efforts.http://www.mdpi.com/1660-3397/10/8/1729<em>Pseudoalteromonas luteoviolacea</em>violaceinindolmycinpentabromopseudilinbiodiscovery
spellingShingle Lone Gram
Nikolaj G. Vynne
Maria Mansson
Gene Sequence Based Clustering Assists in Dereplication of <em>Pseudoalteromonas luteoviolacea</em> Strains with Identical Inhibitory Activity and Antibiotic Production
Marine Drugs
<em>Pseudoalteromonas luteoviolacea</em>
violacein
indolmycin
pentabromopseudilin
biodiscovery
title Gene Sequence Based Clustering Assists in Dereplication of <em>Pseudoalteromonas luteoviolacea</em> Strains with Identical Inhibitory Activity and Antibiotic Production
title_full Gene Sequence Based Clustering Assists in Dereplication of <em>Pseudoalteromonas luteoviolacea</em> Strains with Identical Inhibitory Activity and Antibiotic Production
title_fullStr Gene Sequence Based Clustering Assists in Dereplication of <em>Pseudoalteromonas luteoviolacea</em> Strains with Identical Inhibitory Activity and Antibiotic Production
title_full_unstemmed Gene Sequence Based Clustering Assists in Dereplication of <em>Pseudoalteromonas luteoviolacea</em> Strains with Identical Inhibitory Activity and Antibiotic Production
title_short Gene Sequence Based Clustering Assists in Dereplication of <em>Pseudoalteromonas luteoviolacea</em> Strains with Identical Inhibitory Activity and Antibiotic Production
title_sort gene sequence based clustering assists in dereplication of lt em gt pseudoalteromonas luteoviolacea lt em gt strains with identical inhibitory activity and antibiotic production
topic <em>Pseudoalteromonas luteoviolacea</em>
violacein
indolmycin
pentabromopseudilin
biodiscovery
url http://www.mdpi.com/1660-3397/10/8/1729
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AT nikolajgvynne genesequencebasedclusteringassistsindereplicationofltemgtpseudoalteromonasluteoviolacealtemgtstrainswithidenticalinhibitoryactivityandantibioticproduction
AT mariamansson genesequencebasedclusteringassistsindereplicationofltemgtpseudoalteromonasluteoviolacealtemgtstrainswithidenticalinhibitoryactivityandantibioticproduction