Galactose‐α‐1,3‐galactose‐presenting bacterial families are associated with resistance to experimental avian malaria infection

The gut microbiome can contribute to host health through defense against pathogens. However, links between the host gut microbiome and resistance to infection have been primarily investigated in humans and lab‐bred rodents, so we do not know to what extent this relationship exists in wild animals. T...

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Main Authors: R. K. Noble, T. R. Kelly, C. R. Lattin
Format: Article
Language:English
Published: Wiley 2025-05-01
Series:Journal of Avian Biology
Subjects:
Online Access:https://doi.org/10.1111/jav.03330
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author R. K. Noble
T. R. Kelly
C. R. Lattin
author_facet R. K. Noble
T. R. Kelly
C. R. Lattin
author_sort R. K. Noble
collection DOAJ
description The gut microbiome can contribute to host health through defense against pathogens. However, links between the host gut microbiome and resistance to infection have been primarily investigated in humans and lab‐bred rodents, so we do not know to what extent this relationship exists in wild animals. To fill this knowledge gap, we used an experimental malaria inoculation with Plasmodium relictum in wild‐caught house sparrows Passer domesticus (n = 18) to examine interactions of the host gut microbiome and resistance to avian malaria infection. Before and after inoculation, we collected blood samples to quantify circulating parasitemia and fecal samples to evaluate the gut microbiome through amplification and sequencing of the V4 region of the bacterial 16S rRNA gene. We found that gut microbiome alpha diversity (species richness and evenness) and beta diversity (community composition) were not significantly different between infected and resistant sparrows prior to or during malaria infection. However, we identified several indicator ASVs that occurred at higher prevalence and proportional abundance in malaria‐resistant sparrows, most of which were from the family Lactobacillaceae that is hypothesized to confer resistance to malaria through inducing the production of anti‐α‐Gal antibodies. Future studies should experimentally manipulate the composition of the avian gut microbiome to causally investigate the relationship between specific bacterial taxa in the host gut microbiome and resistance to avian malaria infection.
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spelling doaj-art-87b9deaf94094fe39feb1143932a7d4b2025-08-20T03:27:48ZengWileyJournal of Avian Biology0908-88571600-048X2025-05-0120253n/an/a10.1111/jav.03330Galactose‐α‐1,3‐galactose‐presenting bacterial families are associated with resistance to experimental avian malaria infectionR. K. Noble0T. R. Kelly1C. R. Lattin2Department of Biological Sciences, Louisiana State University Baton Rouge LA USADepartment of Biological Sciences, Louisiana State University Baton Rouge LA USADepartment of Biological Sciences, Louisiana State University Baton Rouge LA USAThe gut microbiome can contribute to host health through defense against pathogens. However, links between the host gut microbiome and resistance to infection have been primarily investigated in humans and lab‐bred rodents, so we do not know to what extent this relationship exists in wild animals. To fill this knowledge gap, we used an experimental malaria inoculation with Plasmodium relictum in wild‐caught house sparrows Passer domesticus (n = 18) to examine interactions of the host gut microbiome and resistance to avian malaria infection. Before and after inoculation, we collected blood samples to quantify circulating parasitemia and fecal samples to evaluate the gut microbiome through amplification and sequencing of the V4 region of the bacterial 16S rRNA gene. We found that gut microbiome alpha diversity (species richness and evenness) and beta diversity (community composition) were not significantly different between infected and resistant sparrows prior to or during malaria infection. However, we identified several indicator ASVs that occurred at higher prevalence and proportional abundance in malaria‐resistant sparrows, most of which were from the family Lactobacillaceae that is hypothesized to confer resistance to malaria through inducing the production of anti‐α‐Gal antibodies. Future studies should experimentally manipulate the composition of the avian gut microbiome to causally investigate the relationship between specific bacterial taxa in the host gut microbiome and resistance to avian malaria infection.https://doi.org/10.1111/jav.03330gut microbiomehost–pathogen dynamicshouse sparrowPasser domesticusPlasmodium relictum.
spellingShingle R. K. Noble
T. R. Kelly
C. R. Lattin
Galactose‐α‐1,3‐galactose‐presenting bacterial families are associated with resistance to experimental avian malaria infection
Journal of Avian Biology
gut microbiome
host–pathogen dynamics
house sparrow
Passer domesticus
Plasmodium relictum.
title Galactose‐α‐1,3‐galactose‐presenting bacterial families are associated with resistance to experimental avian malaria infection
title_full Galactose‐α‐1,3‐galactose‐presenting bacterial families are associated with resistance to experimental avian malaria infection
title_fullStr Galactose‐α‐1,3‐galactose‐presenting bacterial families are associated with resistance to experimental avian malaria infection
title_full_unstemmed Galactose‐α‐1,3‐galactose‐presenting bacterial families are associated with resistance to experimental avian malaria infection
title_short Galactose‐α‐1,3‐galactose‐presenting bacterial families are associated with resistance to experimental avian malaria infection
title_sort galactose α 1 3 galactose presenting bacterial families are associated with resistance to experimental avian malaria infection
topic gut microbiome
host–pathogen dynamics
house sparrow
Passer domesticus
Plasmodium relictum.
url https://doi.org/10.1111/jav.03330
work_keys_str_mv AT rknoble galactosea13galactosepresentingbacterialfamiliesareassociatedwithresistancetoexperimentalavianmalariainfection
AT trkelly galactosea13galactosepresentingbacterialfamiliesareassociatedwithresistancetoexperimentalavianmalariainfection
AT crlattin galactosea13galactosepresentingbacterialfamiliesareassociatedwithresistancetoexperimentalavianmalariainfection