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Defining the Species Micromonospora saelicesensis and Micromonospora noduli Under the Framework of Genomics
The type isolates of species Micromonospora saelicesensis and Micromonospora noduli are Gram-stain positive actinobacteria that were originally isolated from nitrogen fixing nodules of the legumes Lupinus angustifolius and Pisum sativum, respectively. These two species are very closely related and q...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6026663/ https://www.ncbi.nlm.nih.gov/pubmed/29988535 http://dx.doi.org/10.3389/fmicb.2018.01360 |
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author | Riesco, Raúl Carro, Lorena Román-Ponce, Brenda Prieto, Carlos Blom, Jochen Klenk, Hans-Peter Normand, Philippe Trujillo, Martha E. |
author_facet | Riesco, Raúl Carro, Lorena Román-Ponce, Brenda Prieto, Carlos Blom, Jochen Klenk, Hans-Peter Normand, Philippe Trujillo, Martha E. |
author_sort | Riesco, Raúl |
collection | PubMed |
description | The type isolates of species Micromonospora saelicesensis and Micromonospora noduli are Gram-stain positive actinobacteria that were originally isolated from nitrogen fixing nodules of the legumes Lupinus angustifolius and Pisum sativum, respectively. These two species are very closely related and questions arise as to whether they should be merged into a single species. To better delineate the relationship of M. saelicesensis and M. noduli, 10 strains isolated from plant tissue (nodules and leaves) and identified by their 16S rRNA gene sequences as either M. saelicensesis or M. noduli, based on a cut-off value of ≥99.5% were selected for whole-genome sequencing and compared with the type strains of M. saelicesensis Lupac 09(T) and M. noduli GUI43(T) using overall genome relatedness indices (OGRI) which included ANI, OrthoANI and digital DNA-DNA hybridization. Whole- and core-genome phylogenomic analyses were also carried out. These results were compared with the topologies of the 16S rRNA and gyrB gene phylogenies. Good correlation was found between all trees except for the 16S rRNA gene. Overall results also supported the current classification of M. saelicesensis and M. noduli as separate species. Especially useful was the core-genome phylogenetic analyses based on 92 genes and the dDDH results which were highly correlated. The importance of using more than one strain for a better definition of a species was also shown. A series of in vitro phenotypic assays performed at different times were compared with in silico predictions based on genomic data. In vitro phenotypic tests showed discrepancies among the independent studies, confirming the lack of reproducibility even when tests were performed in the same laboratory. On the other hand, the use of in silico predictions proved useful for defining a stable phenotype profile among the strains analyzed. These results provide a working framework for defining Micromonospora species at the genomic and phenotypic level. |
format | Online Article Text |
id | pubmed-6026663 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-60266632018-07-09 Defining the Species Micromonospora saelicesensis and Micromonospora noduli Under the Framework of Genomics Riesco, Raúl Carro, Lorena Román-Ponce, Brenda Prieto, Carlos Blom, Jochen Klenk, Hans-Peter Normand, Philippe Trujillo, Martha E. Front Microbiol Microbiology The type isolates of species Micromonospora saelicesensis and Micromonospora noduli are Gram-stain positive actinobacteria that were originally isolated from nitrogen fixing nodules of the legumes Lupinus angustifolius and Pisum sativum, respectively. These two species are very closely related and questions arise as to whether they should be merged into a single species. To better delineate the relationship of M. saelicesensis and M. noduli, 10 strains isolated from plant tissue (nodules and leaves) and identified by their 16S rRNA gene sequences as either M. saelicensesis or M. noduli, based on a cut-off value of ≥99.5% were selected for whole-genome sequencing and compared with the type strains of M. saelicesensis Lupac 09(T) and M. noduli GUI43(T) using overall genome relatedness indices (OGRI) which included ANI, OrthoANI and digital DNA-DNA hybridization. Whole- and core-genome phylogenomic analyses were also carried out. These results were compared with the topologies of the 16S rRNA and gyrB gene phylogenies. Good correlation was found between all trees except for the 16S rRNA gene. Overall results also supported the current classification of M. saelicesensis and M. noduli as separate species. Especially useful was the core-genome phylogenetic analyses based on 92 genes and the dDDH results which were highly correlated. The importance of using more than one strain for a better definition of a species was also shown. A series of in vitro phenotypic assays performed at different times were compared with in silico predictions based on genomic data. In vitro phenotypic tests showed discrepancies among the independent studies, confirming the lack of reproducibility even when tests were performed in the same laboratory. On the other hand, the use of in silico predictions proved useful for defining a stable phenotype profile among the strains analyzed. These results provide a working framework for defining Micromonospora species at the genomic and phenotypic level. Frontiers Media S.A. 2018-06-25 /pmc/articles/PMC6026663/ /pubmed/29988535 http://dx.doi.org/10.3389/fmicb.2018.01360 Text en Copyright © 2018 Riesco, Carro, Román-Ponce, Prieto, Blom, Klenk, Normand and Trujillo. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Riesco, Raúl Carro, Lorena Román-Ponce, Brenda Prieto, Carlos Blom, Jochen Klenk, Hans-Peter Normand, Philippe Trujillo, Martha E. Defining the Species Micromonospora saelicesensis and Micromonospora noduli Under the Framework of Genomics |
title | Defining the Species Micromonospora saelicesensis and Micromonospora noduli Under the Framework of Genomics |
title_full | Defining the Species Micromonospora saelicesensis and Micromonospora noduli Under the Framework of Genomics |
title_fullStr | Defining the Species Micromonospora saelicesensis and Micromonospora noduli Under the Framework of Genomics |
title_full_unstemmed | Defining the Species Micromonospora saelicesensis and Micromonospora noduli Under the Framework of Genomics |
title_short | Defining the Species Micromonospora saelicesensis and Micromonospora noduli Under the Framework of Genomics |
title_sort | defining the species micromonospora saelicesensis and micromonospora noduli under the framework of genomics |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6026663/ https://www.ncbi.nlm.nih.gov/pubmed/29988535 http://dx.doi.org/10.3389/fmicb.2018.01360 |
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