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Characterization of heterotrophic prokaryote subgroups in the Sfax coastal solar salterns by combining flow cytometry cell sorting and phylogenetic analysis

Here, we combined flow cytometry (FCM) and phylogenetic analyses after cell sorting to characterize the dominant groups of the prokaryotic assemblages inhabiting two ponds of increasing salinity: a crystallizer pond (TS) with a salinity of 390 g/L, and the non-crystallizer pond (M1) with a salinity...

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Autores principales: Trigui, Hana, Masmoudi, Salma, Brochier-Armanet, Céline, Barani, Aude, Grégori, Gérald, Denis, Michel, Dukan, Sam, Maalej, Sami
Formato: Texto
Lenguaje:English
Publicado: Springer Japan 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3084946/
https://www.ncbi.nlm.nih.gov/pubmed/21424516
http://dx.doi.org/10.1007/s00792-011-0364-5
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author Trigui, Hana
Masmoudi, Salma
Brochier-Armanet, Céline
Barani, Aude
Grégori, Gérald
Denis, Michel
Dukan, Sam
Maalej, Sami
author_facet Trigui, Hana
Masmoudi, Salma
Brochier-Armanet, Céline
Barani, Aude
Grégori, Gérald
Denis, Michel
Dukan, Sam
Maalej, Sami
author_sort Trigui, Hana
collection PubMed
description Here, we combined flow cytometry (FCM) and phylogenetic analyses after cell sorting to characterize the dominant groups of the prokaryotic assemblages inhabiting two ponds of increasing salinity: a crystallizer pond (TS) with a salinity of 390 g/L, and the non-crystallizer pond (M1) with a salinity of 200 g/L retrieved from the solar saltern of Sfax in Tunisia. As expected, FCM analysis enabled the resolution of high nucleic acid content (HNA) and low nucleic acid content (LNA) prokaryotes. Next, we performed a taxonomic analysis of the bacterial and archaeal communities comprising the two most populated clusters by phylogenetic analyses of 16S rRNA gene clone library. We show for the first time that the presence of HNA and LNA content cells could also be extended to the archaeal populations. Archaea were detected in all M1 and TS samples, whereas representatives of Bacteria were detected only in LNA for M1 and HNA for TS. Although most of the archaeal sequences remained undetermined, other clones were most frequently affiliated to Haloquadratum and Halorubrum. In contrast, most bacterial clones belonged to the Alphaproteobacteria class (Phyllobacterium genus) in M1 samples and to the Bacteroidetes phylum (Sphingobacteria and Salinibacter genus) in TS samples. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00792-011-0364-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-30849462011-06-06 Characterization of heterotrophic prokaryote subgroups in the Sfax coastal solar salterns by combining flow cytometry cell sorting and phylogenetic analysis Trigui, Hana Masmoudi, Salma Brochier-Armanet, Céline Barani, Aude Grégori, Gérald Denis, Michel Dukan, Sam Maalej, Sami Extremophiles Original Paper Here, we combined flow cytometry (FCM) and phylogenetic analyses after cell sorting to characterize the dominant groups of the prokaryotic assemblages inhabiting two ponds of increasing salinity: a crystallizer pond (TS) with a salinity of 390 g/L, and the non-crystallizer pond (M1) with a salinity of 200 g/L retrieved from the solar saltern of Sfax in Tunisia. As expected, FCM analysis enabled the resolution of high nucleic acid content (HNA) and low nucleic acid content (LNA) prokaryotes. Next, we performed a taxonomic analysis of the bacterial and archaeal communities comprising the two most populated clusters by phylogenetic analyses of 16S rRNA gene clone library. We show for the first time that the presence of HNA and LNA content cells could also be extended to the archaeal populations. Archaea were detected in all M1 and TS samples, whereas representatives of Bacteria were detected only in LNA for M1 and HNA for TS. Although most of the archaeal sequences remained undetermined, other clones were most frequently affiliated to Haloquadratum and Halorubrum. In contrast, most bacterial clones belonged to the Alphaproteobacteria class (Phyllobacterium genus) in M1 samples and to the Bacteroidetes phylum (Sphingobacteria and Salinibacter genus) in TS samples. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00792-011-0364-5) contains supplementary material, which is available to authorized users. Springer Japan 2011-03-20 2011 /pmc/articles/PMC3084946/ /pubmed/21424516 http://dx.doi.org/10.1007/s00792-011-0364-5 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Original Paper
Trigui, Hana
Masmoudi, Salma
Brochier-Armanet, Céline
Barani, Aude
Grégori, Gérald
Denis, Michel
Dukan, Sam
Maalej, Sami
Characterization of heterotrophic prokaryote subgroups in the Sfax coastal solar salterns by combining flow cytometry cell sorting and phylogenetic analysis
title Characterization of heterotrophic prokaryote subgroups in the Sfax coastal solar salterns by combining flow cytometry cell sorting and phylogenetic analysis
title_full Characterization of heterotrophic prokaryote subgroups in the Sfax coastal solar salterns by combining flow cytometry cell sorting and phylogenetic analysis
title_fullStr Characterization of heterotrophic prokaryote subgroups in the Sfax coastal solar salterns by combining flow cytometry cell sorting and phylogenetic analysis
title_full_unstemmed Characterization of heterotrophic prokaryote subgroups in the Sfax coastal solar salterns by combining flow cytometry cell sorting and phylogenetic analysis
title_short Characterization of heterotrophic prokaryote subgroups in the Sfax coastal solar salterns by combining flow cytometry cell sorting and phylogenetic analysis
title_sort characterization of heterotrophic prokaryote subgroups in the sfax coastal solar salterns by combining flow cytometry cell sorting and phylogenetic analysis
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3084946/
https://www.ncbi.nlm.nih.gov/pubmed/21424516
http://dx.doi.org/10.1007/s00792-011-0364-5
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