MAVS regulates the quality of the antibody response to West-Nile Virus.

A key difference that distinguishes viral infections from protein immunizations is the recognition of viral nucleic acids by cytosolic pattern recognition receptors (PRRs). Insights into the functions of cytosolic PRRs such as the RNA-sensing Rig-I-like receptors (RLRs) in the instruction of adaptiv...

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Main Authors: Marvin O'Ketch, Spencer Williams, Cameron Larson, Jennifer L Uhrlaub, Rachel Wong, Brenna Hall, Neha R Deshpande, Dominik Schenten
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2020-10-01
Series:PLoS Pathogens
Online Access:https://doi.org/10.1371/journal.ppat.1009009
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author Marvin O'Ketch
Spencer Williams
Cameron Larson
Jennifer L Uhrlaub
Rachel Wong
Brenna Hall
Neha R Deshpande
Dominik Schenten
author_facet Marvin O'Ketch
Spencer Williams
Cameron Larson
Jennifer L Uhrlaub
Rachel Wong
Brenna Hall
Neha R Deshpande
Dominik Schenten
author_sort Marvin O'Ketch
collection DOAJ
description A key difference that distinguishes viral infections from protein immunizations is the recognition of viral nucleic acids by cytosolic pattern recognition receptors (PRRs). Insights into the functions of cytosolic PRRs such as the RNA-sensing Rig-I-like receptors (RLRs) in the instruction of adaptive immunity are therefore critical to understand protective immunity to infections. West Nile virus (WNV) infection of mice deficent of RLR-signaling adaptor MAVS results in a defective adaptive immune response. While this finding suggests a role for RLRs in the instruction of adaptive immunity to WNV, it is difficult to interpret due to the high WNV viremia, associated exessive antigen loads, and pathology in the absence of a MAVS-dependent innate immune response. To overcome these limitations, we have infected MAVS-deficient (MAVSKO) mice with a single-round-of-infection mutant of West Nile virus. We show that MAVSKO mice failed to produce an effective neutralizing antibody response to WNV despite normal antibody titers against the viral WNV-E protein. This defect occurred independently of antigen loads or overt pathology. The specificity of the antibody response in infected MAVSKO mice remained unchanged and was still dominated by antibodies that bound the neutralizing lateral ridge (LR) epitope in the DIII domain of WNV-E. Instead, MAVSKO mice produced IgM antibodies, the dominant isotype controlling primary WNV infection, with lower affinity for the DIII domain. Our findings suggest that RLR-dependent signals are important for the quality of the humoral immune response to WNV.
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spelling doaj.art-2f0e120c8794480ca6ac2709aa4a958a2022-12-21T22:00:34ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742020-10-011610e100900910.1371/journal.ppat.1009009MAVS regulates the quality of the antibody response to West-Nile Virus.Marvin O'KetchSpencer WilliamsCameron LarsonJennifer L UhrlaubRachel WongBrenna HallNeha R DeshpandeDominik SchentenA key difference that distinguishes viral infections from protein immunizations is the recognition of viral nucleic acids by cytosolic pattern recognition receptors (PRRs). Insights into the functions of cytosolic PRRs such as the RNA-sensing Rig-I-like receptors (RLRs) in the instruction of adaptive immunity are therefore critical to understand protective immunity to infections. West Nile virus (WNV) infection of mice deficent of RLR-signaling adaptor MAVS results in a defective adaptive immune response. While this finding suggests a role for RLRs in the instruction of adaptive immunity to WNV, it is difficult to interpret due to the high WNV viremia, associated exessive antigen loads, and pathology in the absence of a MAVS-dependent innate immune response. To overcome these limitations, we have infected MAVS-deficient (MAVSKO) mice with a single-round-of-infection mutant of West Nile virus. We show that MAVSKO mice failed to produce an effective neutralizing antibody response to WNV despite normal antibody titers against the viral WNV-E protein. This defect occurred independently of antigen loads or overt pathology. The specificity of the antibody response in infected MAVSKO mice remained unchanged and was still dominated by antibodies that bound the neutralizing lateral ridge (LR) epitope in the DIII domain of WNV-E. Instead, MAVSKO mice produced IgM antibodies, the dominant isotype controlling primary WNV infection, with lower affinity for the DIII domain. Our findings suggest that RLR-dependent signals are important for the quality of the humoral immune response to WNV.https://doi.org/10.1371/journal.ppat.1009009
spellingShingle Marvin O'Ketch
Spencer Williams
Cameron Larson
Jennifer L Uhrlaub
Rachel Wong
Brenna Hall
Neha R Deshpande
Dominik Schenten
MAVS regulates the quality of the antibody response to West-Nile Virus.
PLoS Pathogens
title MAVS regulates the quality of the antibody response to West-Nile Virus.
title_full MAVS regulates the quality of the antibody response to West-Nile Virus.
title_fullStr MAVS regulates the quality of the antibody response to West-Nile Virus.
title_full_unstemmed MAVS regulates the quality of the antibody response to West-Nile Virus.
title_short MAVS regulates the quality of the antibody response to West-Nile Virus.
title_sort mavs regulates the quality of the antibody response to west nile virus
url https://doi.org/10.1371/journal.ppat.1009009
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