Giuseppe D'auria

Dr. Giuseppe D'auria

orcid

Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 June 2006 in FEMS Microbiology Ecology
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Journal Article
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MZMilagros Zaballos
Milagros Zaballos
ALArantxa Lã³Pez-Lã³Pez
Arantxa Lã³Pez-Lã³Pez
LOLise Ovreas
Lise Ovreas
SBSergio Galã¡N Bartual
Sergio Galã¡N Bartual
GDGiuseppe D'auria
Giuseppe D'auria
ALArantxa López-López
Arantxa López-López
The bacterial and archaeal assemblages at two offshore sites located in polar (Greenland Sea; depth: 50 and 2000 m) and Mediterranean (Ionian Sea; de

12 January 2007 in Environmental Microbiology
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Journal Article
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JHJohn Hallsworth
John Hallsworth
Michail M. YakimovMichail M. Yakimov
Michail M. Yakimov
PGPeter Golyshin
Peter Golyshin
JGJenny L. M. Gillion
Jenny L. M. Gillion
GDGiuseppe D'auria
Giuseppe D'auria
TMTerry McGenity
Terry McGenity

3 October 2018 in Frontiers in Microbiology
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Journal Article
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EMEveliina Munukka
Eveliina Munukka
JAJuha P. Ahtiainen
Juha P. Ahtiainen
Pere PuigboPere Puigbo
Pere Puigbo
SJSirpa Jalkanen
Sirpa Jalkanen
KPKatja Pahkala
Katja Pahkala
Satu PekkalaSatu Pekkala
Satu Pekkala
Recent studies suggest that exercise alters the gut microbiome. We determined whether six-weeks endurance exercise, without changing diet, affected the gut metagenome and systemic metabolites of overweight women. Previously sedentary overweight women (n = 19) underwent a six-weeks endurance exercise intervention, but two were excluded due to antibiotic therapy. The gut microbiota composition and functions were analyzed by 16S rRNA gene amplicon sequencing and metagenomics. Body composition was analyzed with DXA X-ray densitometer and serum metabolomics with NMR metabolomics. Total energy and energy-yielding nutrient intakes were analyzed from food records using Micro-Nutrica software. Serum clinical variables were determined with KONELAB instrument. Soluble Vascular Adhesion Protein 1 (VAP-1) was measured with ELISA and its' enzymatic activity as produced hydrogen peroxide. The exercise intervention was effective, as maximal power and maximum rate of oxygen consumption increased while android fat mass decreased. No changes in diet were observed. Metagenomic analysis revealed taxonomic shifts including an increase in Akkermansia and a decrease in Proteobacteria. These changes were independent of age, weight, fat % as well as energy and fiber intake. Training slightly increased Jaccard distance of genus level β-diversity. Training did not alter the enriched metagenomic pathways, which, according to Bray Curtis dissimilarity analysis, may have been due to that only half of the subjects' microbiomes responded considerably to exercise. Nevertheless, tranining decreased the abundance of several genes including those related to fructose and amino acid metabolism. These metagenomic changes, however, were not translated into major systemic metabolic changes as only two metabolites, phospholipids and cholesterol in large VLDL particles, decreased after exercise. Training also decreased the amine oxidase activity of pro-inflammatory VAP-1, whereas no changes in CRP were detected. All clinical blood variables were within normal range, yet exercise slightly increased glucose and decreased LDL and HDL. In conclusion, exercise training modified the gut microbiome without greatly affecting systemic metabolites or body composition. Based on our data and existing literature, we propose that especially Akkermansia and Proteobacteria are exercise-responsive taxa. Our results warrant the need for further studies in larger cohorts to determine whether exercise types other than endurance exercise also modify the gut metagenome.

7 January 2005 in Science
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PWPaul W. J. J. Van Der Wielen
Paul W. J. J. Van Der Wielen
HBHenk Bolhuis
Henk Bolhuis
SBSara Borin
Sara Borin
DDDaniele Daffonchio
Daniele Daffonchio
CCCesare Corselli
Cesare Corselli
BPBioDeep Scientific Party
BioDeep Scientific Party
Deep hypersaline anoxic basins in the Mediterranean Sea are a legacy of dissolution of ancient subterranean salt deposits from the Miocene period. Our study revealed that these hypersaline basins are not biogeochemical dead ends, but support in situ sulfate reduction, methanogenesis, and heterotrophic activity. A wide diversity of prokaryotes was observed, including a new, abundant, deeply branching order within the Euryarchaeota . Furthermore, we demonstrated the presence of a unique, metabolically active microbial community in the Discovery basin, which is one of the most extreme terrestrial saline environments known, as it is almost saturated with MgCl 2 (5 M).

31 July 2008 in The ISME Journal
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Journal Article
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EIElena Ivars-Martinez
Elena Ivars-Martinez
AMAna-Belen Martin-Cuadrado
Ana-Belen Martin-Cuadrado
GDGiuseppe D'auria
Giuseppe D'auria
Alex MiraAlex Mira
Alex Mira
SFSteve Ferriera
Steve Ferriera
FRFrancisco Rodriguez-Valera
Francisco Rodriguez-Valera
Alteromonas macleodii is a common marine heterotrophic γ-proteobacterium. Isolates from this microbe cluster by molecular analysis into two major genotypic groups or ecotypes, one found in temperate latitudes in the upper water column and another that is for the most part found in the deep water column of the Mediterranean. Here, we describe the genome of one strain of the ‘deep ecotype’ (AltDE) isolated from 1000 m in the Eastern Mediterranean and compare this genome with that of the type strain ATCC 27126, a representative of the global ‘surface’ ecotype. The genomes are substantially different with DNA sequence similarity values that are borderline for microbes belonging to the same species, and a large differential gene content, mainly found in islands larger than 20 kbp, that also recruit poorly to the Global Ocean Sampling project (GOS). These genomic differences indicate that AltDE is probably better suited to microaerophilic conditions and for the degradation of recalcitrant compounds such as urea. These, together with other features, and the distribution of this genotypic group, indicate that this microbe colonizes relatively large particles that sink rapidly to meso and bathypelagic depths. The genome of ATCC 27126 on the other hand has more potential for regulation (two component systems) and degrades more sugars and amino acids, which is consistent with a more transient particle attachment, as would be expected for lineages specialized in colonizing smaller particulate organic matter with much slower sinking rates. The genomic data are also consistent with a picture of incipient speciation driven by niche specialization.

1 January 2010 in BMC Genomics
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GDGiuseppe D'auria
Giuseppe D'auria
NJNuria Jiménez-Hernández
Nuria Jiménez-Hernández
FPFrancesc Peris-Bondia
Francesc Peris-Bondia
Andrés MoyaAndrés Moya
Andrés Moya
ALAmparo Latorre
Amparo Latorre
Legionella pneumophila subsp. pneumophila is a gram-negative γ-Proteobacterium and the causative agent of Legionnaires' disease, a form of epidemic pneumonia. It has a water-related life cycle. In industrialized cities L. pneumophila is commonly encountered in refrigeration towers and water pipes. Infection is always via infected aerosols to humans. Although many efforts have been made to eradicate Legionella from buildings, it still contaminates the water systems. The town of Alcoy (Valencian Region, Spain) has had recurrent outbreaks since 1999. The strain "Alcoy 2300/99" is a particularly persistent and recurrent strain that was isolated during one of the most significant outbreaks between the years 1999-2000. We have sequenced the genome of the particularly persistent L. pneumophila strain Alcoy 2300/99 and have compared it with four previously sequenced strains known as Philadelphia (USA), Lens (France), Paris (France) and Corby (England). Pangenome analysis facilitated the identification of strain-specific features, as well as some that are shared by two or more strains. We identified: (1) three islands related to anti-drug resistance systems; (2) a system for transport and secretion of heavy metals; (3) three systems related to DNA transfer; (4) two CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) systems, known to provide resistance against phage infections, one similar in the Lens and Alcoy strains, and another specific to the Paris strain; and (5) seven islands of phage-related proteins, five of which seem to be strain-specific and two shared. The dispensable genome disclosed by the pangenomic analysis seems to be a reservoir of new traits that have mainly been acquired by horizontal gene transfer and could confer evolutionary advantages over strains lacking them.