Adriana Vallesi

Prof. Adriana Vallesi

University of Camerino
orcid

Research Focus & Metrics

Academic Career Length

41Years (1986-Present)

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

Representative Publications

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6 January 2017 in Journal of Eukaryotic Microbiology
Verified
Journal Article
Open access
PDF file
AWAlan Warren
Alan Warren
DPDavid J. Patterson
David J. Patterson
MDMicah Dunthorn
Micah Dunthorn
JCJohn C. Clamp
John C. Clamp
UAUndine E.M. Achilles‐Day
Undine E.M. Achilles‐Day
SASabine Agatha
Sabine Agatha
Recent advances in molecular technology have revolutionized research on all aspects of the biology of organisms, including ciliates, and created unprecedented opportunities for pursuing a more integrative approach to investigations of biodiversity. However, this goal is complicated by large gaps and inconsistencies that still exist in the foundation of basic information about biodiversity of ciliates. The present paper reviews issues relating to the taxonomy of ciliates and presents specific recommendations for best practice in the observation and documentation of their biodiversity. This effort stems from a workshop that explored ways to implement six Grand Challenges proposed by the International Research Coordination Network for Biodiversity of Ciliates (IRCN‐BC). As part of its commitment to strengthening the knowledge base that supports research on biodiversity of ciliates, the IRCN‐BC proposes to populate The Ciliate Guide, an online database, with biodiversity‐related data and metadata to create a resource that will facilitate accurate taxonomic identifications and promote sharing of data.

1 August 1995 in Nature
Verified
Journal Article
Closed access
Adriana VallesiAdriana Vallesi
Adriana Vallesi
GGGiovanna Giuli
Giovanna Giuli
RBRalph A. Bradshaw
Ralph A. Bradshaw
PLPierangelo Luporini
Pierangelo Luporini

26 November 2010 in Microbial Ecology
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Journal Article
Closed access
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Martina SchrallhammerMartina Schrallhammer
Martina Schrallhammer
MSMichael Schweikert
Michael Schweikert
Adriana VallesiAdriana Vallesi
Adriana Vallesi
FVFranco Verni
Franco Verni
GPGiulio Petroni
Giulio Petroni

1 May 1995 in Journal of Eukaryotic Microbiology
Verified
Journal Article
Closed access
PDF file
PLPierangelo Luporini
Pierangelo Luporini
Adriana VallesiAdriana Vallesi
Adriana Vallesi
CMCristina Miceli
Cristina Miceli
RBRalph A. Bradshaw
Ralph A. Bradshaw

7 February 2011 in Proceedings of the National Academy of Sciences
Verified
Journal Article
Closed access
GGGraziano Di Giuseppe
Graziano Di Giuseppe
FEFabrizio Erra
Fabrizio Erra
FDFernando Dini
Fernando Dini
CAClaudio Alimenti
Claudio Alimenti
Adriana VallesiAdriana Vallesi
Adriana Vallesi
Pierangelo LuporiniPierangelo Luporini
Pierangelo Luporini
Wild-type strains of the protozoan ciliate Euplotes collected from different locations on the coasts of Antarctica, Tierra del Fuego and the Arctic were taxonomically identified as the morpho-species Euplotes nobilii , based on morphometric and phylogenetic analyses. Subsequent studies of their sexual interactions revealed that mating combinations of Antarctic and Arctic strains form stable pairs of conjugant cells. These conjugant pairs were isolated and shown to complete mutual gene exchange and cross-fertilization. The biological significance of this finding was further substantiated by demonstrating that close homology exists among the three-dimensional structures determined by NMR of the water-borne signaling pheromones that are constitutively secreted into the extracellular space by these interbreeding strains, in which these molecules trigger the switch between the growth stage and the sexual stage of the life cycle. The fact that Antarctic and Arctic E. nobilii populations share the same gene pool and belong to the same biological species provides new support to the biogeographic model of global distribution of eukaryotic microorganisms, which had so far been based exclusively on studies of morphological and phylogenetic taxonomy.

1 July 2005 in Eukaryotic Cell
Verified
Journal Article
Open access
PDF file
Adriana VallesiAdriana Vallesi
Adriana Vallesi
PBPatrizia Ballarini
Patrizia Ballarini
BPBarbara Di Pretoro
Barbara Di Pretoro
CAClaudio Alimenti
Claudio Alimenti
CMCristina Miceli
Cristina Miceli
Pierangelo LuporiniPierangelo Luporini
Pierangelo Luporini
The ciliate Euplotes raikovi produces a family of diffusible signal proteins (pheromones) that function as prototypic growth factors. They may either promote cell growth, by binding to pheromone receptors synthesized by the same cells from which they are secreted (autocrine activity), or induce a temporary cell shift from the growth stage to a mating (sexual) one by binding to pheromone receptors of other, conspecific cells (paracrine activity). In cells constitutively secreting the pheromone E r -1, it was first observed that the expression of the E r -1 receptor “p15,” a type II membrane protein of 130 amino acids, is quantitatively correlated with the extracellular concentration of secreted pheromone. p15 expression on the cell surface rapidly and markedly increased after the removal of secreted E r -1 and gradually decreased in parallel with new E r -1 secretion. It was then shown that p15 is internalized through endocytic vesicles following E r -1 binding and that the internalization of p15/E r -1 complexes is specifically blocked by the paracrine p15 binding of E r -2, a pheromone structurally homologous to, and thus capable of fully antagonizing, E r -1. Based on previous findings that the p15 pheromone-binding site is structurally equivalent to E r -1 and that E r -1 molecules polymerize in crystals following a pattern of cooperative interaction, it was proposed that p15/E r -1 complexes are internalized as a consequence of their unique property (not shared by p15/E r -2 complexes) of undergoing clustering.