Bats generate lower affinity but higher diversity antibody responses than those of mice, but pathogen-binding capacity increases if protein is restricted in their diet.

Publication date: Sep 01, 2024

Bats are reservoirs of many zoonotic viruses that are fatal in humans but do not cause disease in bats. Moreover, bats generate low neutralizing antibody titers in response to experimental viral infection, although more robust antibody responses have been observed in wild-caught bats during times of food stress. Here, we compared the antibody titers and B cell receptor (BCR) diversity of Jamaican fruit bats (Artibeus jamaicensis; JFBs) and BALB/c mice generated in response to T-dependent and T-independent antigens. We then manipulated the diet of JFBs and challenged them with H18N11 influenza A-like virus or a replication incompetent Nipah virus VSV (Nipah-riVSV). Under standard housing conditions, JFBs generated a lower avidity antibody response and possessed more BCR mRNA diversity compared to BALB/c mice. However, withholding protein from JFBs improved serum neutralization in response to Nipah-riVSV and improved serum antibody titers specific to H18 but reduced BCR mRNA diversity.

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Concepts Keywords
Fatal Animals
Fruit Antibodies, Neutralizing
H18n11 Antibodies, Neutralizing
Mice Antibodies, Viral
Viral Antibodies, Viral
Antibody Affinity
Antibody Diversity
Antibody Formation
Chiroptera
Diet, Protein-Restricted
Female
Influenza A virus
Mice
Nipah Virus
Receptors, Antigen, B-Cell
Receptors, Antigen, B-Cell

Semantics

Type Source Name
disease MESH Infectious Diseases
disease IDO replication
pathway KEGG Influenza A
disease IDO cell
disease MESH viral infection
disease IDO protein
disease IDO pathogen
drug DRUGBANK Tacrine
disease IDO host
disease IDO immune response
disease IDO history
disease IDO process
pathway REACTOME Reproduction
disease MESH infections
disease MESH persistent infections
disease IDO infection
disease MESH causality
pathway KEGG Metabolic pathways
drug DRUGBANK Sirolimus
disease MESH nutritional status
drug DRUGBANK Cytidine
disease MESH influenza
drug DRUGBANK Indoleacetic acid
disease IDO reagent
disease IDO blood
disease MESH bleeding
disease MESH starvation
drug DRUGBANK Coenzyme M
pathway REACTOME Immune System
disease IDO assay
disease MESH malnutrition
disease MESH reinfection
disease IDO colony
drug DRUGBANK Water
drug DRUGBANK Sucrose
disease MESH viral shedding
drug DRUGBANK Tenoxicam
drug DRUGBANK Methionine
drug DRUGBANK Influenza A virus

Original Article

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