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Dastgheib, S. M. M.

Publications and source records attributed to Dastgheib, S. M. M..

3 recordsLinked to original sources

Genome-resolved analyses show an extensive diversification in key aerobic hydrocarbon-degrading enzymes across bacteria and archaea

Hydrocarbons (HCs) are organic compounds composed solely of carbon and hydrogen. They mainly accumulate in oil reservoirs, but aromatic HCs can also have other sources and are widely distributed in the biosphere. Our perception of pathways for biotic degradation of major HCs and genetic information of key enzymes in these bioconversion processes have mainly been based on cultured microbes and are biased by uneven taxonomic representation. Here we use Annotree to provide a gene-centric view of aerobic degradation of aliphatic and aromatic HCs in a total of 23446 genomes from 123 bacterial and 14 archaeal phyla. Apart from the widespread genetic potential for HC degradation in Proteobacteria, Actinobacteriota, Bacteroidota, and Firmicutes, genomes from an additional 18 bacterial and 3 archaeal phyla also hosted key HC degrading enzymes. Among these, such degradation potential has not been previously reported for representatives in the phyla UBA8248, Tectomicrobia, SAR324, and Eremiobacterota. While genomes containing full pathways for complete degradation of HCs were only detected in Proteobacteria and Actinobacteriota, other lineages capable of mediating such key steps could partner with representatives with truncated HC degradation pathways and collaboratively drive the process. Phylogeny reconstruction shows that the reservoir of key aerobic hydrocarbon-degrading enzymes in Bacteria and Archaea undergoes extensive diversification via gene duplication and horizontal gene transfer. This diversification could potentially enable microbes to rapidly adapt to novel and manufactured HCs that reach the environment.

microbiology↗

Distinct microbial communities along the chronic oil pollution continuum of the Persian Gulf converge with oil spill accidents

Persian Gulf hosting ca. 48% of the worlds oil reserves; has been chronically exposed to natural oil seepage. Oil spill events have been studied over the last decade; however, the influence of chronic oil exposure on the microbial community of the Persian Gulf has remained unknown. We performed genome-resolved comparative analyses of the water and sediments prokaryotic community along the Gulfs pollution continuum (Strait of Hormuz, Asalouyeh and Khark Island). The continuous exposure to trace amounts of pollution has shifted the microbial profile toward the dominance of Oceanospirillales, Flavobacteriales, Alteromonadales, and Rhodobacterales in Asalouyeh and Khark samples. Intrinsic oil-degrading microbes present in low abundances in marine habitats; experience a bloom in response to oil pollution. Comparative analysis of the Persian Gulf samples with 106 oil-polluted marine samples reveals the pollutants hydrocarbon content, exposure time and sediment depth as main determinants of microbial response to pollution. High aliphatic content enriches for Oceanospirillales, Alteromonadales and Pseudomonadales whereas, Alteromonadales, Cellvibrionales, Flavobacteriales and Rhodobacterales dominate polyaromatic polluted samples. In sediment samples, Deltaproteobacteria and Gammaproteobacteria had the highest abundance. In chronic exposure and oil spill events, the community composition converges towards higher dominance of oil-degrading constituents while promoting the division of labor for successful bioremediation. Originality-Significance StatementThe impact of anthropogenic oil pollution on the microbial community has been studied for oil spill events; while the influence of long-term chronic exposure to oil derivatives on The microbes has remained unknown. Persian Gulf hosts ca. 48% of the worlds oil reserves and has been chronically exposed to natural and accidental oil pollutions. Different pollutant profilesin different locations and the recurrent pollution events; make Persian Gulf an ideal model system to analyse the impact of oil hydrocarbon on the microbial community and the recovery potential of marine ecosystems after pollution. In this study we perform an extensive analysis of thhe Persian Gulfs water and sediment samples along the water circulation and pollution continuum for the first time. Our results show that these long-standing trace exposure to oil has imposed a consistent selection pressure on the Gulfs microbes; developing unique and distinct communities along the pollution continuum. Our extensive genome-resolved analysis of the metabolic capabilities of the reconstructed MAGs shows an intricate division of labor among different microbes for oil degradation and determine the major drivers of each degradation step. Intrinsic oil-degrading microbes (e.g., Immundisolibacter, Roseovarius and Lutimaribacter) bloom along the Persian Gulfs pollution continuum and function as the main oil degraders. Comparative study of PG datasets with 106 oil-polluted marine samples (water and sediment) reveals similar community compositions in the Persian Gulfs water and sediment samples to those of oil spill events and suggests hydrocarbon type and exposure time as the main determinants of the microbial response to oil pollution.

microbiology↗

Phylogenomic analysis reveals the basis of adaptation of Pseudorhizobium species to extreme environments

The family Rhizobiaceae includes many genera of soil bacteria, often isolated for their association with plants. Herein, we investigate the genomic diversity of a group of Rhizobium species and unclassified strains isolated from atypical environments, including seawater, rock matrix or polluted soil. Based on whole-genome similarity and core genome phylogeny, we show that this group corresponds to the genus Pseudorhizobium. We thus reclassify Rhizobium halotolerans, R. marinum, R. flavum and R. endolithicum as P. halotolerans comb. nov., P. marinum comb. nov., P. flavum comb. nov. and R. endolithicum comb. nov., respectively, and show that P. pelagicum is a synonym of P. marinum. We also delineate a new chemolithoautotroph species, P. banfieldiae sp. nov., whose type strain is NT-26T (= DSM 106348T = CFBP 8663T). This genome-based classification was supported by a chemotaxonomic comparison, with gradual taxonomic resolution provided by fatty acid, protein and metabolic profiles. In addition, we used a phylogenetic approach to infer scenarios of duplication, horizontal transfer and loss for all genes in the Pseudorhizobium pangenome. We thus identify the key functions associated with the diversification of each species and higher clades, shedding light on the mechanisms of adaptation to their respective ecological niches. Respiratory proteins acquired at the origin of Pseudorhizobium are combined with clade-specific genes to encode different strategies for detoxification and nutrition in harsh, nutrient-poor environments. Finally, we predict diagnostic phenotypes for the distinction of P. banfieldiae from other Pseudorhizobium species, including autotrophy and sensitivity to the azo dye Congo Red, which we experimentally validated.

microbiology↗