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Microbiomes associated with avian malaria survival differ between susceptible Hawaiian honeycreepers and sympatric malaria-resistant introduced birds

Authors: Navine, Amanda; Paxton, Kristina; Paxton, Eben; Hart, Patrick; Foster, Jeffrey; McInerney, Nancy; Fleischer, Robert; +1 Authors

Microbiomes associated with avian malaria survival differ between susceptible Hawaiian honeycreepers and sympatric malaria-resistant introduced birds

Abstract

Of the estimated 55 Hawaiian honeycreepers (subfamily Carduelinae) only 17 species remain, 9 of which the International Union for Conservation of Nature considers endangered. Among the most pressing threats to honeycreeper survival is avian malaria, caused by the introduced blood parasite Plasmodium relictum, which is increasing in distribution in Hawai`i as a result of climate change. Preventing further honeycreeper decline will require innovative conservation strategies that confront malaria from multiple angles. Research on mammals revealed strong connections between gut microbiome composition and malaria susceptibility, illuminating a potential novel approach to malaria control through the manipulation of gut microbiota. One honeycreeper species, Hawai`i `amakihi (Chlorodrepanis virens), persists in some areas of high malaria prevalence, indicating they have acquired some level of immunity. To investigate if avian host-specific microbes may be associated with malaria survival, we characterized cloacal microbiomes and malaria infection for 174 `amakihi and 172 malaria-resistant warbling white-eyes (Zosterops japonicus) from Hawai`i Island using 16S rRNA gene metabarcoding and qPCR. Neither microbial alpha nor beta diversity covaried with infection, but 149 microbes showed positive associations with malaria survivors. Among these were Escherichia and Lactobacillus spp., which appear to mitigate malaria severity in mammalian hosts, revealing promising candidates for future probiotic research for augmenting malaria immunity in sensitive endangered species.

Funding provided by: Smithsonian Conservation Biology Institute Center for Conservation Genomics*Crossref Funder Registry ID: Award Number: Scholarly Studies GrantFunding provided by: National Science FoundationCrossref Funder Registry ID: http://dx.doi.org/10.13039/100000001Award Number: Ecology and Evolution of Infectious Disease Grant 1717498Funding provided by: American Ornithological SocietyCrossref Funder Registry ID: http://dx.doi.org/10.13039/100012457Award Number: Mewaldt-King Research AwardFunding provided by: American Ornithological SocietyCrossref Funder Registry ID: http://dx.doi.org/10.13039/100012457Award Number: Postdoctoral Research AwardFunding provided by: Swedish Research CouncilCrossref Funder Registry ID: http://dx.doi.org/10.13039/501100004359Award Number: 2020-00259

Keywords

Conservation Biology, probiotics, Probiotics, 16S rRNA gene metabarcoding, Microbiota, Plasmodium relictum, Hawai'i 'Amakihi (Chlorodrepanis virens)

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selected citations
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This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
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popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
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