Valerio Iebba

Dr. Valerio Iebba

1. Department of Medical, Surgical, and Health Sciences, University of Trieste, Trieste, Italy
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orcid

Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

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

Representative Publications

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8 May 2010 in Proceedings of the National Academy of Sciences
Verified
Journal Article
Closed access
RLR. Di Leonardo
R. Di Leonardo
LALuca Angelani
Luca Angelani
DDD. Dell’aRciprete
D. Dell’aRciprete
Giancarlo RuoccoGiancarlo Ruocco
Giancarlo Ruocco
Valerio IebbaValerio Iebba
Valerio Iebba
EFE. Di Fabrizio
E. Di Fabrizio
Self-propelling bacteria are a nanotechnology dream. These unicellular organisms are not just capable of living and reproducing, but they can swim very efficiently, sense the environment, and look for food, all packaged in a body measuring a few microns. Before such perfect machines can be artificially assembled, researchers are beginning to explore new ways to harness bacteria as propelling units for microdevices. Proposed strategies require the careful task of aligning and binding bacterial cells on synthetic surfaces in order to have them work cooperatively. Here we show that asymmetric environments can produce a spontaneous and unidirectional rotation of nanofabricated objects immersed in an active bacterial bath. The propulsion mechanism is provided by the self-assembly of motile Escherichia coli cells along the rotor boundaries. Our results highlight the technological implications of active matter’s ability to overcome the restrictions imposed by the second law of thermodynamics on equilibrium passive fluids.

3 February 2022 in Nature Medicine
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Journal Article
Closed access
PDF file
LDLisa Derosa
Lisa Derosa
BRBertrand Routy
Bertrand Routy
ATAndrew Thomas
Andrew Thomas
Valerio IebbaValerio Iebba
Valerio Iebba
GZGérard Zalcman
Gérard Zalcman
BBBenjamin Besse
Benjamin Besse

8 July 2021 in Nature Medicine
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Journal Article
Closed access
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MAMiles C. Andrews
Miles C. Andrews
CDConnie P. M. Duong
Connie P. M. Duong
VGVancheswaran Gopalakrishnan
Vancheswaran Gopalakrishnan
Valerio IebbaValerio Iebba
Valerio Iebba
WCWei-Shen Chen
Wei-Shen Chen
JWJennifer A. Wargo
Jennifer A. Wargo

1 August 2020 in European Urology
Verified
Journal Article
Closed access
LDLisa Derosa
Lisa Derosa
BRBertrand Routy
Bertrand Routy
MFMarine Fidelle
Marine Fidelle
Valerio IebbaValerio Iebba
Valerio Iebba
LALaurie Alla
Laurie Alla
LZLaurence Zitvogel
Laurence Zitvogel

21 August 2020 in Science
Verified
Journal Article
Closed access
AFAurélie Fluckiger
Aurélie Fluckiger
RDRomain Daillère
Romain Daillère
MSMohamed Sassi
Mohamed Sassi
BSBarbara Susanne Sixt
Barbara Susanne Sixt
PLPeng Liu
Peng Liu
LZLaurence Zitvogel
Laurence Zitvogel
Phages and cancer immunity: Gut bacteria are involved in the education of T cell immune responses, and the intestinal ecosystem influences anticancer immunity. Fluckiger et al. report microbial antigens that might cross-react with antigens associated with tumor cells. They found that a type of intestinal bacteria called enterococci harbor a bacteriophage that modulates immune responses. In mouse models, administration of enterococci containing the bacteriophage boosted T cell responses after treatment with chemotherapy or programmed cell death protein 1 (PD-1) blockade. In humans, the presence of the bacteriophage was associated with improved survival after PD-1 immunotherapy. A fraction of human T cells specific for naturally processed melanoma epitopes appeared to be able to recognize microbial peptides. This “molecular mimicry” may represent cross-reactivity between tumors and microbial antigens. Science , this issue p. 936

19 January 2011 in Physical Review Letters
Verified
Journal Article
Closed access
RLR. Di Leonardo
R. Di Leonardo
DDD. Dell’arciprete
D. Dell’arciprete
LALuca Angelani
Luca Angelani
Valerio IebbaValerio Iebba
Valerio Iebba
The hydrodynamic interactions of a swimming bacterium with a neighboring surface can cause it to swim in circles. For example, when E.~coli is above a solid surface it had been observed to swim in a clockwise direction. By contrast we observe that, when swimming near a liquid-air interface, the sense of rotation is reversed. We quantitatively account for this through the hydrodynamic interaction of the bacterium with its own mirror image swimming on the opposite side of a perfect-slip boundary. The strength of the coupling is reduced for longer cells, where the torque is spread over a larger length, resulting in longer bacteria swimming in larger circles. We confirm this through precise video measurements of bacterial trajectories and orientations.