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Immunization against Anaplasma phagocytophilum Adhesin Binding Domains Confers Protection against Infection in the Mouse Model.
- Source :
-
Infection and immunity [Infect Immun] 2020 Sep 18; Vol. 88 (10). Date of Electronic Publication: 2020 Sep 18 (Print Publication: 2020). - Publication Year :
- 2020
-
Abstract
- Anaplasma phagocytophilum causes granulocytic anaplasmosis, a debilitating infection that can be fatal in the immunocompromised. It also afflicts animals, including dogs, horses, and sheep. No granulocytic anaplasmosis vaccine exists. Because A. phagocytophilum is an obligate intracellular bacterium, inhibiting microbe-host cell interactions that facilitate invasion can disrupt infection. The binding domains of A. phagocytophilum adhesins A. phagocytophilum invasion protein A (AipA), A. phagocytophilum surface protein (Asp14), and outer membrane protein A (OmpA) are essential for optimal bacterial entry into host cells, but their relevance to infection in vivo is undefined. In this study, C57BL/6 mice were immunized with a cocktail of keyhole limpet hemocyanin-conjugated peptides corresponding to the AipA, Asp14, and OmpA binding domains in alum followed by challenge with A. phagocytophilum The bacterial peripheral blood burden was pronouncedly reduced in immunized mice compared to controls. Examination of pre- and postchallenge sera from these mice revealed that immunization elicited antibodies against AipA and Asp14 peptides but not OmpA peptide. Nonetheless, pooled sera from pre- and postchallenge groups, but not from control groups, inhibited A. phagocytophilum infection of HL-60 cells. Adhesin domain immunization also elicited interferon gamma (IFN-γ)-producing CD8-positive (CD8 <superscript>+</superscript> ) T cells. A follow-up study confirmed that immunization against only the AipA or Asp14 binding domain was sufficient to reduce the bacterial peripheral blood load in mice following challenge and elicit antibodies that inhibit A. phagocytophilum cellular infection in vitro These data demonstrate that AipA and Asp14 are critical for A. phagocytophilum to productively infect mice, and immunization against their binding domains elicits a protective immune response.<br /> (Copyright © 2020 American Society for Microbiology.)
- Subjects :
- Adhesins, Bacterial chemistry
Animals
Antibodies, Bacterial blood
Antibodies, Bacterial immunology
Antibodies, Blocking blood
Antibodies, Blocking immunology
Bacterial Load
Bacterial Vaccines administration & dosage
CD8-Positive T-Lymphocytes immunology
Disease Models, Animal
HL-60 Cells
Humans
Immunization
Interferon-gamma immunology
Mice
Mice, Inbred C57BL
Protein Binding
Protein Domains immunology
Vaccines, Conjugate administration & dosage
Vaccines, Conjugate immunology
Vaccines, Subunit administration & dosage
Vaccines, Subunit immunology
Adhesins, Bacterial immunology
Anaplasma phagocytophilum immunology
Bacterial Vaccines immunology
Ehrlichiosis prevention & control
Subjects
Details
- Language :
- English
- ISSN :
- 1098-5522
- Volume :
- 88
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- Infection and immunity
- Publication Type :
- Academic Journal
- Accession number :
- 32661123
- Full Text :
- https://doi.org/10.1128/IAI.00106-20