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1.
Genes (Basel) ; 12(3)2021 03 09.
Article de Anglais | MEDLINE | ID: mdl-33803363

RÉSUMÉ

A phylogenomic and functional analysis of the first two Crenarchaeota MAGs belonging to El Tatio geysers fields in Chile is reported. A soil sample contiguous to a geothermal activity exposed lagoon of El Tatio was used for shotgun sequencing. Afterwards, contigs were binned into individual population-specific genomes data. A phylogenetic placement was carried out for both MAG 9-5TAT and MAG 47-5TAT. Then functional comparisons and metabolic reconstruction were carried out. Results showed that both MAG 9-5TAT and MAG 47-5TAT likely represent new species in the genus Thermoproteus and the genus Sulfolobus, respectively. These findings provide new insights into the phylogenetic and genomic diversity for archaea species that inhabit the El Tatio geysers field and expand the understanding of the Crenarchaeota phylum diversity.


Sujet(s)
Archéobactéries/génétique , Crenarchaeota/génétique , Génome d'archéobactérie/génétique , Métagénome/génétique , Métagénomique/méthodes , Phylogenèse
2.
Microb Ecol ; 69(2): 372-82, 2015 Feb.
Article de Anglais | MEDLINE | ID: mdl-25219446

RÉSUMÉ

Podzols frequently show bleached mottles depleted in organic matter, most readily visible in the Bh horizons. Even though the process of bleached mottles development is not understood, it has been suggested that the selective degradation of organic matter by soil microorganisms has a major contribution. In this study, we examined the bacterial and archaeal communities along three Brazilian coastal podzol profiles, as well as in bleached mottles and their immediate vicinity, using 16S rRNA gene profiling. Our results showed that the bacterial and archaeal community structures in the studied podzols varied with depth and that the bacterial communities in the bleached mottles were significantly different from that in their immediate vicinity. In contrast, the archaeal communities in bleached mottles were significantly different from their vicinity only in the Bertioga (BT) profile, based on sequencing of amplicons of the 16S rRNA gene. Redundancy analyses showed that the bacterial community structures in the bleached mottles of BT were negatively associated mostly with the levels of organic carbon, exchangeable-aluminum (Al), exchangeable potassium, and Al-saturation, whereas in the surrounding soil, the opposite was observed. In the Ilha Comprida (IC) profiles, no such relationships were observed, suggesting distinct drivers of the bacterial community structures in bleached mottles of different podzols. In the bleached mottles of the BT profile, operational taxonomic units (OTUs) phylogenetically related to Pseudomonas were the most abundant Bacteria, whereas in the IC profiles, OTUs related to Acidobacteria were predominant. Thermoprotei (Crenarchaeota) were the most abundant Archaea in the bleached mottles and in their immediate vicinity. Based on the diverse metabolic capabilities of Pseudomonas and Acidobacteria, our data suggest that these groups of bacteria may be involved in the development of bleached mottles in the podzols studied and that the selection of specific bacterial populations in the bleached mottles may depend on the local edaphic conditions.


Sujet(s)
Archéobactéries/classification , Bactéries/classification , Phylogenèse , Microbiologie du sol , Archéobactéries/génétique , Archéobactéries/isolement et purification , Bactéries/génétique , Bactéries/isolement et purification , Brésil , Phénomènes chimiques , Crenarchaeota/classification , Crenarchaeota/génétique , Crenarchaeota/isolement et purification , ADN des archées/génétique , ADN bactérien/génétique , Phylogéographie , ARN ribosomique 16S/génétique , Analyse de séquence d'ADN
3.
ISME J ; 5(2): 209-19, 2011 Feb.
Article de Anglais | MEDLINE | ID: mdl-20703318

RÉSUMÉ

The presence and role of Archaea in artificial, human-controlled environments is still unclear. The search for Archaea has been focused on natural biotopes where they have been found in overwhelming numbers, and with amazing properties. However, they are considered as one of the major group of microorganisms that might be able to survive a space flight, or even to thrive on other planets. Although still concentrating on aerobic, bacterial spores as a proxy for spacecraft cleanliness, space agencies are beginning to consider Archaea as a possible contamination source that could affect future searches for life on other planets. This study reports on the discovery of archaeal 16S rRNA gene signatures not only in US American spacecraft assembly clean rooms but also in facilities in Europe and South America. Molecular methods revealed the presence of Crenarchaeota in all clean rooms sampled, while signatures derived from methanogens and a halophile appeared only sporadically. Although no Archaeon was successfully enriched in our multiassay cultivation approach thus far, samples from a European clean room revealed positive archaeal fluorescence in situ hybridization (FISH) signals of rod-shaped microorganisms, representing the first visualization of Archaea in clean room environments. The molecular and visual detection of Archaea was supported by the first quantitative PCR studies of clean rooms, estimating the overall quantity of Archaea therein. The significant presence of Archaea in these extreme environments in distinct geographical locations suggests a larger role for these microorganisms not only in natural biotopes, but also in human controlled and rigorously cleaned environments.


Sujet(s)
Archéobactéries/physiologie , Environnement contrôlé , Microbiologie de l'environnement , Archéobactéries/classification , Archéobactéries/génétique , Archéobactéries/isolement et purification , Biodiversité , Crenarchaeota/classification , Crenarchaeota/génétique , Crenarchaeota/isolement et purification , Crenarchaeota/physiologie , Europe , Gènes d'archée/génétique , Hybridation fluorescente in situ , Phylogenèse , Réaction de polymérisation en chaîne , ARN ribosomique 16S/génétique , Amérique du Sud , Vaisseaux spatiaux
4.
ISME J ; 5(5): 908-17, 2011 May.
Article de Anglais | MEDLINE | ID: mdl-21085198

RÉSUMÉ

Archaea, primarily Crenarchaeota, are common in soil; however, the structure of soil archaeal communities and the factors regulating their diversity and abundance remain poorly understood. Here, we used barcoded pyrosequencing to comprehensively survey archaeal and bacterial communities in 146 soils, representing a multitude of soil and ecosystem types from across the globe. Relative archaeal abundance, the percentage of all 16S rRNA gene sequences recovered that were archaeal, averaged 2% across all soils and ranged from 0% to >10% in individual soils. Soil C:N ratio was the only factor consistently correlated with archaeal relative abundances, being higher in soils with lower C:N ratios. Soil archaea communities were dominated by just two phylotypes from a constrained clade within the Crenarchaeota, which together accounted for >70% of all archaeal sequences obtained in the survey. As one of these phylotypes was closely related to a previously identified putative ammonia oxidizer, we sampled from two long-term nitrogen (N) addition experiments to determine if this taxon responds to experimental manipulations of N availability. Contrary to expectations, the abundance of this dominant taxon, as well as archaea overall, tended to decline with increasing N. This trend was coupled with a concurrent increase in known N-oxidizing bacteria, suggesting competitive interactions between these groups.


Sujet(s)
Crenarchaeota/classification , Écosystème , Microbiologie du sol , Régions antarctiques , Bactéries/classification , Bactéries/génétique , Bactéries/isolement et purification , Crenarchaeota/génétique , Crenarchaeota/isolement et purification , Banque de gènes , Gènes d'archée , Gènes bactériens , Gènes d'ARN ribosomique , Azote/métabolisme , Amérique du Nord , Phylogenèse , ARN ribosomique 16S/génétique , Analyse de séquence d'ADN , Sol/analyse , Amérique du Sud
5.
Curr Microbiol ; 60(6): 439-45, 2010 Jun.
Article de Anglais | MEDLINE | ID: mdl-20024655

RÉSUMÉ

Archaeal 16S rRNA gene clone libraries using PCR amplicons from eight different layers of the MD06-3051 core were obtained from the tropical Western Pacific sediments. A total of 768 clones were randomly selected, and 264 representative clones were sequenced by restriction fragment length polymorphism. Finally, 719 valid clones and 104 operational taxonomic units were identified after chimera-check and > or =97% similarity analysis. The phylogenetic analysis of 16S rDNA sequences obtained from sediment samples were very diverse and showed stratification with depth. Majority of the members were most closely related to uncultivated groups and physiologically uncharacterized assemblages. All phylotypes were affiliated with Crenarchaeota (76%) and Euryarchaeota (24%), respectively. Deep-sea archaeal group (DSAG, 41% of total clones) and miscellaneous crenarchaeotic group (MCG, 29% of total clones) belonging to Crenarchaeota were the most predominant archaeal 16S rDNA phylotypes in clone libraries. Phylotypes in this study shared high similarity with those in subsurface sediments from Peru Margin sites, which indicated that different geographical zones might host similar members of archaeal populations based on similar sedimentary environments. In our study, members of DSAG and MCG seemed to dominate certain layers of the nonhydrate sediments, suggesting a wide ecophysiological adaptation than previously appreciated. The spatial distribution and community structure of these groups might vary with the different geochemical gradients of the environment.


Sujet(s)
Crenarchaeota/classification , Euryarchaeota/classification , Sédiments géologiques/microbiologie , Séquence nucléotidique , Biodiversité , Crenarchaeota/génétique , ADN des archées/génétique , ADN ribosomique/génétique , Euryarchaeota/génétique , Banque de gènes , Océan Pacifique , Pérou , Phylogenèse , Réaction de polymérisation en chaîne , Polymorphisme de restriction , ARN ribosomique 16S/génétique , Climat tropical
6.
J Microbiol ; 46(1): 34-9, 2008 Feb.
Article de Anglais | MEDLINE | ID: mdl-18337690

RÉSUMÉ

Archaea have been found in many more diverse habitats than previously believed due in part to modern molecular approaches to discovering microbial diversity. We report here an unexpected expansion of the habitat diversity of the Archaea in the Cariaco Basin we found using a primer set designed for 18S eukaryotic rDNA sequence analysis. The results presented here expand the originally identified 9 archaeal clones reported in this environment using bacterial/archaeal primers to 152 archaeal clones: 67 (18 OTU) of these clones were found at a depth of 900 m of station A while 71 (9 OTU) of them were at a depth of between 300 approximately 335 m of station B&C depending upon which location the samples were taken. We used three phylogenetic analysis methods and detected 20 phylotypes belonging to a single previously unreported group distantly related to the Crenarchaeota. Also, we determined that the original nine sequences did not fall into any of the known phyla of the Archaea suggesting that they may represent a novel group within the Kingdom Archaea. Thus, from these two studies, we suggest that Archaea in the Cariaco Basin could be unique; however, further studies using archaeal-specific primers and the design of new primers as well as the systematic use of several different primer combinations may improve the chances of understanding the archeal diversity in the Cariaco Basin.


Sujet(s)
Crenarchaeota/classification , Crenarchaeota/isolement et purification , Eau de mer/microbiologie , Archéobactéries/classification , Archéobactéries/génétique , Archéobactéries/isolement et purification , Clonage moléculaire , Crenarchaeota/génétique , Amorces ADN/génétique , ADN des archées/génétique , ADN ribosomique/génétique , Données de séquences moléculaires , Réaction de polymérisation en chaîne , ARN ribosomique 16S/génétique , Analyse de séquence d'ADN , Venezuela
7.
Appl Environ Microbiol ; 72(12): 7767-77, 2006 Dec.
Article de Anglais | MEDLINE | ID: mdl-17012598

RÉSUMÉ

Nitrification within estuarine sediments plays an important role in the nitrogen cycle, both at the global scale and in individual estuaries. Although bacteria were once thought to be solely responsible for catalyzing the first and rate-limiting step of this process, several recent studies have suggested that mesophilic Crenarchaeota are capable of performing ammonia oxidation. Here we examine the diversity (richness and community composition) of ammonia-oxidizing archaea (AOA) and bacteria (AOB) within sediments of Bahía del Tóbari, a hypernutrified estuary receiving substantial amounts of ammonium in agricultural runoff. Using PCR primers designed to specifically target the archaeal ammonia monooxygenase alpha-subunit (amoA) gene, we found AOA to be present at five sampling sites within this estuary and at two sampling time points (January and October 2004). In contrast, the bacterial amoA gene was PCR amplifiable from only 40% of samples. Bacterial amoA libraries were dominated by a few widely distributed Nitrosomonas-like sequence types, whereas AOA diversity showed significant variation in both richness and community composition. AOA communities nevertheless exhibited consistent spatial structuring, with two distinct end member assemblages recovered from the interior and the mouths of the estuary and a mixed assemblage from an intermediate site. These findings represent the first detailed examination of archaeal amoA diversity in estuarine sediments and demonstrate that diverse communities of Crenarchaeota capable of ammonia oxidation are present within estuaries, where they may be actively involved in nitrification.


Sujet(s)
Ammoniac/métabolisme , Crenarchaeota , Écosystème , Sédiments géologiques/microbiologie , Nitrosomonas , Eau de mer/microbiologie , Crenarchaeota/classification , Crenarchaeota/génétique , Crenarchaeota/isolement et purification , Mexique , Données de séquences moléculaires , Nitrosomonas/classification , Nitrosomonas/génétique , Nitrosomonas/isolement et purification , Oxydoréduction , Oxidoreductases/génétique , Oxidoreductases/métabolisme , Phylogenèse , Analyse de séquence d'ADN
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