Systemic Administration of Avian Defensin 7: Distribution, Cellular Target, and Antibacterial Potential in Mice

Defensins are natural antimicrobial peptides. The avian beta-defensin AvBD7 isolated from the chicken bone marrow possess broad antibacterial spectrum and strong resistance to proteolysis. However, its ability to fight systemic infections of major concern for public health, such as salmonellosis, is...

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Main Authors: Geoffrey Bailleul, Rodrigo Guabiraba, Isabelle Virlogeux-Payant, Isabelle Lantier, Jérôme Trotereau, Florence B. Gilbert, Agnès Wiedemann, Angélina Trotereau, Philippe Velge, Catherine Schouler, Anne-Christine Lalmanach
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-03-01
Series:Frontiers in Microbiology
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Online Access:https://www.frontiersin.org/article/10.3389/fmicb.2019.00541/full
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author Geoffrey Bailleul
Rodrigo Guabiraba
Isabelle Virlogeux-Payant
Isabelle Lantier
Jérôme Trotereau
Florence B. Gilbert
Agnès Wiedemann
Angélina Trotereau
Philippe Velge
Catherine Schouler
Anne-Christine Lalmanach
author_facet Geoffrey Bailleul
Rodrigo Guabiraba
Isabelle Virlogeux-Payant
Isabelle Lantier
Jérôme Trotereau
Florence B. Gilbert
Agnès Wiedemann
Angélina Trotereau
Philippe Velge
Catherine Schouler
Anne-Christine Lalmanach
author_sort Geoffrey Bailleul
collection DOAJ
description Defensins are natural antimicrobial peptides. The avian beta-defensin AvBD7 isolated from the chicken bone marrow possess broad antibacterial spectrum and strong resistance to proteolysis. However, its ability to fight systemic infections of major concern for public health, such as salmonellosis, is unknown. As a first approach, fluorescence labeling of AvBD7 allowed to track its systemic distribution after intraperitoneal injection in mice using whole body live imaging. It was associated to peritoneal cells and to deeper organs such as the liver. In the next step, the use of labeled AvBD7 allowed to observe its interaction with murine macrophages in culture. After incubation, it was able to penetrate inside the cells through an endocytosis-like mechanism. Furthermore, natural AvBD7 contributed to the control of intracellular multiplication of a multidrug resistant Salmonella strain, after incubation with infected macrophages. Finally, administration in a model of systemic lethal Salmonella infection in mice led to significant improvement of mouse survival, consistently with significant reduction of the liver bacterial load. In conclusion, the results reveal a hitherto unknown intracellular antibacterial effect of AvBD7 in Salmonella target cells and support AvBD7 as a candidate of interest for the treatment of infectious diseases caused by multidrug-resistant pathogenic Enterobacteriaceae.
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spelling doaj.art-4d733d2e88ce431fb9dfb708ea6ff7ea2022-12-21T20:03:21ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2019-03-011010.3389/fmicb.2019.00541425438Systemic Administration of Avian Defensin 7: Distribution, Cellular Target, and Antibacterial Potential in MiceGeoffrey BailleulRodrigo GuabirabaIsabelle Virlogeux-PayantIsabelle LantierJérôme TrotereauFlorence B. GilbertAgnès WiedemannAngélina TrotereauPhilippe VelgeCatherine SchoulerAnne-Christine LalmanachDefensins are natural antimicrobial peptides. The avian beta-defensin AvBD7 isolated from the chicken bone marrow possess broad antibacterial spectrum and strong resistance to proteolysis. However, its ability to fight systemic infections of major concern for public health, such as salmonellosis, is unknown. As a first approach, fluorescence labeling of AvBD7 allowed to track its systemic distribution after intraperitoneal injection in mice using whole body live imaging. It was associated to peritoneal cells and to deeper organs such as the liver. In the next step, the use of labeled AvBD7 allowed to observe its interaction with murine macrophages in culture. After incubation, it was able to penetrate inside the cells through an endocytosis-like mechanism. Furthermore, natural AvBD7 contributed to the control of intracellular multiplication of a multidrug resistant Salmonella strain, after incubation with infected macrophages. Finally, administration in a model of systemic lethal Salmonella infection in mice led to significant improvement of mouse survival, consistently with significant reduction of the liver bacterial load. In conclusion, the results reveal a hitherto unknown intracellular antibacterial effect of AvBD7 in Salmonella target cells and support AvBD7 as a candidate of interest for the treatment of infectious diseases caused by multidrug-resistant pathogenic Enterobacteriaceae.https://www.frontiersin.org/article/10.3389/fmicb.2019.00541/fullchickendefensinsmousemacrophagesSalmonella Typhimurium
spellingShingle Geoffrey Bailleul
Rodrigo Guabiraba
Isabelle Virlogeux-Payant
Isabelle Lantier
Jérôme Trotereau
Florence B. Gilbert
Agnès Wiedemann
Angélina Trotereau
Philippe Velge
Catherine Schouler
Anne-Christine Lalmanach
Systemic Administration of Avian Defensin 7: Distribution, Cellular Target, and Antibacterial Potential in Mice
Frontiers in Microbiology
chicken
defensins
mouse
macrophages
Salmonella Typhimurium
title Systemic Administration of Avian Defensin 7: Distribution, Cellular Target, and Antibacterial Potential in Mice
title_full Systemic Administration of Avian Defensin 7: Distribution, Cellular Target, and Antibacterial Potential in Mice
title_fullStr Systemic Administration of Avian Defensin 7: Distribution, Cellular Target, and Antibacterial Potential in Mice
title_full_unstemmed Systemic Administration of Avian Defensin 7: Distribution, Cellular Target, and Antibacterial Potential in Mice
title_short Systemic Administration of Avian Defensin 7: Distribution, Cellular Target, and Antibacterial Potential in Mice
title_sort systemic administration of avian defensin 7 distribution cellular target and antibacterial potential in mice
topic chicken
defensins
mouse
macrophages
Salmonella Typhimurium
url https://www.frontiersin.org/article/10.3389/fmicb.2019.00541/full
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