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1.
Genes (Basel) ; 13(2)2022 01 19.
Artículo en Inglés | MEDLINE | ID: mdl-35205220

RESUMEN

In 2015 a mine dam with Mn-Fe-rich tailings collapsed releasing million tons of sediments over an estuary, in the Southwest of Brazil. The tailings have a high concentration of metals that contaminated soil until the present day. The high contaminant concentrations possibly caused a selection for microorganisms able to strive in such harsh conditions. Here, we isolated metal(loid) and anti-biotic resistance bacteria from the contaminated estuarine soil. After 16S rDNA sequencing to identify the strains, we selected the Mucilaginibacter sp. strain for a whole-genome sequence due to the bioprospective potential of the genus and the high resistance profile. We obtained a complete genome and a genome-guided characterization. Our finding suggests that the 21p strain is possibly a new species of the genus. The species presented genes for resistance for metals (i.e., As, Zn, Co, Cd, and Mn) beyond resistance and cross-resistance for antibiotics (i.e., quinolone, aminoglycoside, ß-lactamase, sulphonamide, tetracycline). The Mucilaginibacter sp. 21p description as new species should be further explored, as their extracellular polymeric substances and the potential of this strain as bioremediation and as a growth promoter in high met-al(loid) contaminated soil.


Asunto(s)
Contaminantes del Suelo , Suelo , Bacteroidetes , Farmacorresistencia Microbiana/genética , Monitoreo del Ambiente , Metales
2.
Microbiol Resour Announc ; 10(41): e0077921, 2021 Oct 14.
Artículo en Inglés | MEDLINE | ID: mdl-34647810

RESUMEN

We report the complete genome sequence of Mucilaginibacter strain 21P, which was isolated from estuarine soil contaminated with mine tailings from the Samarco disaster, which occurred in 2015 in Brazil. The genome sequence comprised 4,739,655 bp, with a G+C content of 43.2%, and harbors multiple antibiotic and metal resistance genes.

3.
Microbiol Resour Announc ; 10(16)2021 Apr 22.
Artículo en Inglés | MEDLINE | ID: mdl-33888506

RESUMEN

Bacillus safensis 3A was isolated from a contaminated estuarine sediment sample with mine tailing from the Samarco dam disaster, which occurred in 2015 in Minas Gerais State, Brazil. We report here a draft genome sequence (3.6 Mb) of this bacterial strain. B. safensis exhibited strong resistance to heavy metals.

4.
Environ Pollut ; 268(Pt A): 115757, 2021 Jan 01.
Artículo en Inglés | MEDLINE | ID: mdl-33168375

RESUMEN

Anthropogenic activities in coastal marine ecosystems can lead to an increase in the abundance of potentially harmful microorganisms in the marine environment. To understand anthropogenic impacts on the marine microbiome, we first used publicly available microbial phylogenetic and functional data to establish a dataset of bacterial genera potentially related to pathogens that cause diseases (BGPRD) in marine organisms. Representatives of low-, medium- and highly impacted marine coastal environments were selected, and the abundance and composition of their microbial communities were determined by quantitative PCR and 16 S rRNA gene sequencing. In total, 72 BGPRD were cataloged, and 11, 36 and 37 BGPRD were found in low-, medium- and highly human-impacted ecosystems, respectively. The absolute abundance of BGPRD and the co-occurrence of antibiotic resistance genes (AGR) increased with the degree of anthropogenic perturbation in these ecosystems. Anthropogenically impacted coastal microbiomes were compositionally and functionally distinct from those of less impacted sites, presenting features that may contribute to adverse outcomes for marine macrobiota in the Anthropocene era.


Asunto(s)
Microbiota , Organismos Acuáticos , Bacterias/genética , Farmacorresistencia Microbiana , Humanos , Filogenia
5.
An Acad Bras Cienc ; 91(suppl 1): e20180373, 2019.
Artículo en Inglés | MEDLINE | ID: mdl-30379272

RESUMEN

Mangroves are ecosystems located in the transition zone between land and sea, characterized by periodic flooding that confer to its unique characteristics. Little is known about the transformation of nutrients that occur during the organic matter degradation in this system. In this study, we monitor the nitrogen transformations in soils from three mangroves with distinct levels of contamination using labeled 15NO3-. We also screened the mangroves metagenomes for the presence of genes that encode enzymes involved in denitrification (nirS, nirK, nosZ, norB and narG), anaerobic oxidation of ammonia (anammox) (hh, hao and hzo) and dissimilatory nitrate reduction to ammonium (DNRA) (nrfA). The transformations of 15NO3- indicated the balance of denitrification over anammox and DNRA in all three mangroves, with lower rates of processes in the mangrove affected by oil contamination. The metagenomic analysis detected 56 sequences related to denitrification, 19 with anammox and 6 with DNRA. Genes related with denitrification were phylogenetically distributed among several groups of bacteria (mainly Gammaproteobacteria). Anammox and DNRA related sequences were affiliated with Planctomycetes and Gammaproteobacteria, respectively. Thus, metagenomic and functional approaches supported the description of denitrification, anammox and DNRA rates in mangrove soils, and identified the major bacterial groups involved in these processes.


Asunto(s)
Amoníaco/metabolismo , Anaerobiosis , Desnitrificación , Nitratos/metabolismo , Oxidación-Reducción , Humedales , Desnitrificación/genética , Metagenoma/genética , Ciclo del Nitrógeno , Plantas/metabolismo , Suelo
6.
Antonie Van Leeuwenhoek ; 98(4): 541-51, 2010 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-20563848

RESUMEN

The bacterial diversity present in sediments of a well-preserved mangrove in Ilha do Cardoso, located in the extreme south of São Paulo State coastline, Brazil, was assessed using culture-independent molecular approaches (denaturing gradient gel electrophoresis (DGGE) and analysis of 166 sequences from a clone library). The data revealed a bacterial community dominated by Alphaproteobacteria (40.36% of clones), Gammaproteobacteria (19.28% of clones) and Acidobacteria (27.71% of clones), while minor components of the assemblage were affiliated to Betaproteobacteria, Deltaproteobacteria, Firmicutes, Actinobacteria and Bacteroidetes. The clustering and redundancy analysis (RDA) based on DGGE were used to determine factors that modulate the diversity of bacterial communities in mangroves, such as depth, seasonal fluctuations, and locations over a transect area from the sea to the land. Profiles of specific DGGE gels showed that both dominant ('universal' Bacteria and Alphaproteobacteria) and low-density bacterial communities (Betaproteobacteria and Actinobacteria) are responsive to shifts in environmental factors. The location within the mangrove was determinant for all fractions of the community studied, whereas season was significant for Bacteria, Alphaproteobacteria, and Betaproteobacteria and sample depth determined the diversity of Alphaproteobacteria and Actinobacteria.


Asunto(s)
Bacterias/clasificación , Bacterias/crecimiento & desarrollo , Biodiversidad , Sedimentos Geológicos/microbiología , Rhizophoraceae/microbiología , Microbiología del Suelo , Actinobacteria/clasificación , Actinobacteria/genética , Actinobacteria/crecimiento & desarrollo , Alphaproteobacteria/clasificación , Alphaproteobacteria/genética , Alphaproteobacteria/crecimiento & desarrollo , Bacterias/genética , Bacteroidetes/clasificación , Bacteroidetes/genética , Bacteroidetes/crecimiento & desarrollo , Composición de Base , Betaproteobacteria/clasificación , Betaproteobacteria/genética , Betaproteobacteria/crecimiento & desarrollo , Brasil , ADN Bacteriano/análisis , ADN Bacteriano/genética , Deltaproteobacteria/clasificación , Deltaproteobacteria/genética , Deltaproteobacteria/crecimiento & desarrollo , Ecosistema , Gammaproteobacteria/clasificación , Gammaproteobacteria/genética , Gammaproteobacteria/crecimiento & desarrollo , Variación Genética , Sedimentos Geológicos/análisis , Reacción en Cadena de la Polimerasa , ARN Ribosómico 16S/análisis , ARN Ribosómico 16S/genética , Agua de Mar , Análisis de Secuencia de ADN , Temperatura
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