Identification of a T-Cell Epitope That Is Globally Conserved among Outer Membrane Proteins (OMPs) OMP7, OMP8, and OMP9 of Anaplasma marginale Strains and with OMP7 from the A. marginale subsp. centrale Vaccine Strain

Author:

Deringer James R.1,Forero-Becerra Elkin G.2,Ueti Massaro W.3,Turse Joshua E.1,Futse James E.4,Noh Susan M.35,Palmer Guy H.15,Brown Wendy C.1

Affiliation:

1. Department of Veterinary Microbiology and Pathology, Washington State University, Pullman, Washington, USA

2. Department of Veterinary Medicine, Federal University of Viçosa, Viçosa, Minas Gerais, Brazil

3. Animal Diseases Research Unit, Agricultural Research Service, U.S. Department of Agriculture, Pullman, Washington, USA

4. Department of Animal Science, College of Basic and Applied Sciences, University of Ghana, Legon, Ghana

5. Paul G. Allen School for Global Animal Health, Washington State University, Pullman, Washington, USA

Abstract

ABSTRACT Within the protective outer membrane (OM) fraction of Anaplasma marginale , several vaccine candidates have emerged, including a family of OM proteins (OMPs) 7 to 9, which share sequence identity with each other and with the single protein OMP7 in the vaccine strain A. marginale subsp. centrale. A. marginale OMPs 7 to 9 are logical vaccine candidates because they are surface exposed, present in the OM immunogen and protective cross-linked OM proteins, recognized by immune serum IgG2 and T cells in cattle immunized with OM, and recognized by immune serum IgG2 from cattle immunized with the A. centrale vaccine strain. We report the identification of a globally conserved 9-amino-acid T-cell epitope FLLVDDAI/VV shared between A. centrale vaccine strain OMP7 and the related A. marginale OMPs 7 to 9, where position 8 of the peptide can be isoleucine or valine. The epitope is conserved in American A. marginale strains, in the Australia Gypsy Plains strain, and in multiple field isolates from Ghana. This epitope, together with additional T-cell epitopes that are present within these proteins, should be considered for inclusion in a multivalent vaccine for A. marginale that can provide protection against disease caused by globally distributed bacterial strains.

Funder

USDA ARS CRIS

NIH NIAID

Colombian Scholarship

Wellcome Trust

Publisher

American Society for Microbiology

Subject

Microbiology (medical),Clinical Biochemistry,Immunology,Immunology and Allergy

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