Marianna Pauletto

Prof. Marianna Pauletto

Comparative Biomedicine and Food Science, University of Padua, Padua, Italy
orcid

Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

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

Representative Publications

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1 March 2015 in Environmental Pollution
Verified
Journal Article
Closed access
CACarlo Giacomo Avio
Carlo Giacomo Avio
SGStefania Gorbi
Stefania Gorbi
MMMassimo Milan
Massimo Milan
MBMaura Benedetti
Maura Benedetti
Daniele FattoriniDaniele Fattorini
Daniele Fattorini
FRFrancesco Regoli
Francesco Regoli

1 January 2013 in Aquatic Toxicology
Verified
Journal Article
Closed access
MMMassimo Milan
Massimo Milan
Marianna PaulettoMarianna Pauletto
Marianna Pauletto
TPTomaso Patarnello
Tomaso Patarnello
LBLuca Bargelloni
Luca Bargelloni
Maria Gabriella MarinMaria Gabriella Marin
Maria Gabriella Marin
Valerio MatozzoValerio Matozzo
Valerio Matozzo

13 October 2017 in Scientific Reports
Verified
Journal Article
Open access
PDF file
MLMaxime Lafont
Maxime Lafont
BPBruno Petton
Bruno Petton
AVAgnès Vergnes
Agnès Vergnes
Marianna PaulettoMarianna Pauletto
Marianna Pauletto
ASAmélie Segarra
Amélie Segarra
CMCaroline Montagnani
Caroline Montagnani
In the last decade, a paradigm shift has emerged in comparative immunology. Invertebrates can no longer be considered to be devoid of specific recognition and immune memory. However, we still lack a comprehensive view of these phenomena and their molecular mechanisms across phyla, especially in terms of duration, specificity, and efficiency in a natural context. In this study, we focused on a Lophotrochozoan/virus interaction, as antiviral priming is mostly overlooked in molluscs. Juvenile Crassostrea gigas oysters experience reoccurring mass mortalities events from Ostreid herpes virus 1 with no existing therapeutic treatment. Our results showed that various nucleic acid injections can prime oysters to trigger an antiviral state ultimately protecting them against a subsequent viral infection. Focusing on poly(I:C) as elicitor, we evidenced that it protected from an environmental infection, by mitigating viral replication. That protection seemed to induce a specific antiviral response as poly(I:C) fails to protect against a pathogenic bacteria. Finally, we showed that this phenomenon was long-lasting, persisting for at least 5 months thus suggesting for the first time the existence of innate immune memory in this invertebrate species. This study strengthens the emerging hypotheses about the broad conservation of innate immune priming and memory mechanisms in Lophotrochozoans.

1 March 2014 in Fish & Shellfish Immunology
Verified
Journal Article
Closed access
Marianna PaulettoMarianna Pauletto
Marianna Pauletto
MMMassimo Milan
Massimo Milan
RMRebeca Moreira
Rebeca Moreira
BNBeatriz Novoa
Beatriz Novoa
AFAntonio Figueras
Antonio Figueras
LBLuca Bargelloni
Luca Bargelloni

22 June 2017 in Scientific Reports
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Journal Article
Open access
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ABAndrea Basso
Andrea Basso
MBMassimiliano Babbucci
Massimiliano Babbucci
Marianna PaulettoMarianna Pauletto
Marianna Pauletto
EREmilio Riginella
Emilio Riginella
TPTomaso Patarnello
Tomaso Patarnello
ENEnrico Negrisolo
Enrico Negrisolo
We sequenced the mitochondrial genomes of the spider crabsMaja crispataandMaja squinado(Majidae, Brachyura). Both genomes contain the whole set of 37 genes characteristic of Bilaterian genomes, encoded on both α- and β-strands. Both species exhibit the same gene order, which is unique among known animal genomes. In particular, all the genes located on the β-strand form a single block. This gene order was analysed together with the other nine gene orders known for the Brachyura. Our study confirms that the most widespread gene order (BraGO) represents the plesiomorphic condition for Brachyura and was established at the onset of this clade. All other gene orders are the result of transformational pathways originating from BraGO. The different gene orders exhibit variable levels of genes rearrangements, which involve only tRNAs or all types of genes. Local homoplastic arrangements were identified, while complete gene orders remain unique and represent signatures that can have a diagnostic value. Brachyura appear to be a hot-spot of gene order diversity within the phylum Arthropoda. Our analysis, allowed to track, for the first time, the fully evolutionary pathways producing the Brachyuran gene orders. This goal was achieved by coupling sophisticated bioinformatic tools with phylogenetic analysis.

17 August 2018 in Communications Biology
Verified
Journal Article
Open access
PDF file
Marianna PaulettoMarianna Pauletto
Marianna Pauletto
TMTereza Manousaki
Tereza Manousaki
SFSerena Ferraresso
Serena Ferraresso
MBMassimiliano Babbucci
Massimiliano Babbucci
ATAlexandros Tsakogiannis
Alexandros Tsakogiannis
LBLuca Bargelloni
Luca Bargelloni
Sexual dimorphism is a fascinating subject in evolutionary biology and mostly results from sex-biased expression of genes, which have been shown to evolve faster in gonochoristic species. We report here genome and sex-specific transcriptome sequencing ofSparus aurata, a sequential hermaphrodite fish. Evolutionary comparative analysis reveals that sex-biased genes inS. aurataare similar in number and function, but evolved following strikingly divergent patterns compared with gonochoristic species, showing overall slower rates because of stronger functional constraints. Fast evolution is observed only for highly ovary-biased genes due to female-specific patterns of selection that are related to the peculiar reproduction mode ofS. aurata, first maturing as male, then as female. To our knowledge, these findings represent the first genome-wide analysis on sex-biased loci in a hermaphrodite vertebrate species, demonstrating how having two sexes in the same individual profoundly affects the fate of a large set of evolutionarily relevant genes.