Primary Structure and Antibacterial Activity of Chicken Bone Marrow-Derived β-Defensins

Author:

Derache Chrystelle1,Labas Valérie2,Aucagne Vincent3,Meudal Hervé3,Landon Céline3,Delmas Agnès F.3,Magallon Thierry2,Lalmanach Anne-Christine1

Affiliation:

1. INRA, UR 1282 Infectiologie Animale et Santé Publique

2. UMR INRA 85, CNRS 6175, Université François Rabelais, Physiologie de la Reproduction et des Comportements, Plate-forme de Protéomique Analytique et Fonctionnelle, F-37380 Nouzilly

3. Centre de Biophysique Moléculaire, CNRS UPR4301, affiliated to University of Orléans, rue Charles Sadron, 45071 Orléans Cedex 2, France

Abstract

ABSTRACT Three biologically active β-defensins were purified by chromatography from chicken bone marrow extract: avian β-defensin 1 (AvBD1), AvBD2, and the newly isolated β-defensin AvBD7. Mass spectrometry analyses showed that bone marrow-derived AvBD1, -2, and -7 peptides were present as mature peptides and revealed posttranslational modifications for AvBD1 and AvBD7 in comparison to their in silico-predicted amino acid sequences. Tandem mass spectrometry analysis using the nanoelectrospray-quadrupole time of flight method showed N-terminal glutaminyl cyclization of mature AvBD7 and C-terminal amidation of mature AvBD1 peptide, while posttranslational modifications were absent in bone marrow-derived mature AvBD2 peptide. Furthermore, mass spectrometry analysis performed on intact cells confirmed the presence of these three peptides in mature heterophils. In addition, the antibacterial activities of the three β-defensins against a large panel of gram-positive and -negative bacteria were assessed. While the three defensins displayed similar antibacterial spectra of activity against gram-positive strains, AvBD1 and AvBD7 exhibited the strongest activity against gram-negative strains in comparison to AvBD2.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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