Long‐term nitrogen enrichment mediates the effects of nitrogen supply and co‐inoculation on a viral pathogen

Abstract Host nutrient supply can mediate host–pathogen and pathogen–pathogen interactions. In terrestrial systems, plant nutrient supply is mediated by soil microbes, suggesting a potential role of soil microbes in plant diseases beyond soil‐borne pathogens and induced plant defenses. Long‐term nit...

Full description

Bibliographic Details
Main Authors: Casey A. Easterday, Amy E. Kendig, Christelle Lacroix, Eric W. Seabloom, Elizabeth T. Borer
Format: Article
Language:English
Published: Wiley 2022-01-01
Series:Ecology and Evolution
Subjects:
Online Access:https://doi.org/10.1002/ece3.8450
_version_ 1797924561222631424
author Casey A. Easterday
Amy E. Kendig
Christelle Lacroix
Eric W. Seabloom
Elizabeth T. Borer
author_facet Casey A. Easterday
Amy E. Kendig
Christelle Lacroix
Eric W. Seabloom
Elizabeth T. Borer
author_sort Casey A. Easterday
collection DOAJ
description Abstract Host nutrient supply can mediate host–pathogen and pathogen–pathogen interactions. In terrestrial systems, plant nutrient supply is mediated by soil microbes, suggesting a potential role of soil microbes in plant diseases beyond soil‐borne pathogens and induced plant defenses. Long‐term nitrogen (N) enrichment can shift pathogenic and nonpathogenic soil microbial community composition and function, but it is unclear if these shifts affect plant–pathogen and pathogen–pathogen interactions. In a growth chamber experiment, we tested the effect of long‐term N enrichment on infection by Barley Yellow Dwarf Virus (BYDV‐PAV) and Cereal Yellow Dwarf Virus (CYDV‐RPV), aphid‐vectored RNA viruses, in a grass host. We inoculated sterilized growing medium with soil collected from a long‐term N enrichment experiment (ambient, low, and high N soil treatments) to isolate effects mediated by the soil microbial community. We crossed soil treatments with a N supply treatment (low, high) and virus inoculation treatment (mock‐, singly‐, and co‐inoculated) to evaluate the effects of long‐term N enrichment on plant–pathogen and pathogen–pathogen interactions, as mediated by N availability. We measured the proportion of plants infected (i.e., incidence), plant biomass, and leaf chlorophyll content. BYDV‐PAV incidence (0.96) declined with low N soil (to 0.46), high N supply (to 0.61), and co‐inoculation (to 0.32). Low N soil mediated the effect of N supply on BYDV‐PAV: instead of N supply reducing BYDV‐PAV incidence, the incidence increased. Additionally, ambient and low N soil ameliorated the negative effect of co‐inoculation on BYDV‐PAV incidence. BYDV‐PAV infection only reduced chlorophyll when plants were grown with low N supply and ambient N soil. There were no significant effects of long‐term N soil on CYDV‐RPV incidence. Soil inoculant with different levels of long‐term N enrichment had different effects on host–pathogen and pathogen–pathogen interactions, suggesting that shifts in soil microbial communities with long‐term N enrichment may mediate disease dynamics.
first_indexed 2024-04-10T15:02:56Z
format Article
id doaj.art-485ff42b8fcb47be9e8573a36a886c36
institution Directory Open Access Journal
issn 2045-7758
language English
last_indexed 2024-04-10T15:02:56Z
publishDate 2022-01-01
publisher Wiley
record_format Article
series Ecology and Evolution
spelling doaj.art-485ff42b8fcb47be9e8573a36a886c362023-02-15T09:06:07ZengWileyEcology and Evolution2045-77582022-01-01121n/an/a10.1002/ece3.8450Long‐term nitrogen enrichment mediates the effects of nitrogen supply and co‐inoculation on a viral pathogenCasey A. Easterday0Amy E. Kendig1Christelle Lacroix2Eric W. Seabloom3Elizabeth T. Borer4Department of Ecology, Evolution, and Behavior University of Minnesota St. Paul Minnesota USADepartment of Ecology, Evolution, and Behavior University of Minnesota St. Paul Minnesota USADepartment of Ecology, Evolution, and Behavior University of Minnesota St. Paul Minnesota USADepartment of Ecology, Evolution, and Behavior University of Minnesota St. Paul Minnesota USADepartment of Ecology, Evolution, and Behavior University of Minnesota St. Paul Minnesota USAAbstract Host nutrient supply can mediate host–pathogen and pathogen–pathogen interactions. In terrestrial systems, plant nutrient supply is mediated by soil microbes, suggesting a potential role of soil microbes in plant diseases beyond soil‐borne pathogens and induced plant defenses. Long‐term nitrogen (N) enrichment can shift pathogenic and nonpathogenic soil microbial community composition and function, but it is unclear if these shifts affect plant–pathogen and pathogen–pathogen interactions. In a growth chamber experiment, we tested the effect of long‐term N enrichment on infection by Barley Yellow Dwarf Virus (BYDV‐PAV) and Cereal Yellow Dwarf Virus (CYDV‐RPV), aphid‐vectored RNA viruses, in a grass host. We inoculated sterilized growing medium with soil collected from a long‐term N enrichment experiment (ambient, low, and high N soil treatments) to isolate effects mediated by the soil microbial community. We crossed soil treatments with a N supply treatment (low, high) and virus inoculation treatment (mock‐, singly‐, and co‐inoculated) to evaluate the effects of long‐term N enrichment on plant–pathogen and pathogen–pathogen interactions, as mediated by N availability. We measured the proportion of plants infected (i.e., incidence), plant biomass, and leaf chlorophyll content. BYDV‐PAV incidence (0.96) declined with low N soil (to 0.46), high N supply (to 0.61), and co‐inoculation (to 0.32). Low N soil mediated the effect of N supply on BYDV‐PAV: instead of N supply reducing BYDV‐PAV incidence, the incidence increased. Additionally, ambient and low N soil ameliorated the negative effect of co‐inoculation on BYDV‐PAV incidence. BYDV‐PAV infection only reduced chlorophyll when plants were grown with low N supply and ambient N soil. There were no significant effects of long‐term N soil on CYDV‐RPV incidence. Soil inoculant with different levels of long‐term N enrichment had different effects on host–pathogen and pathogen–pathogen interactions, suggesting that shifts in soil microbial communities with long‐term N enrichment may mediate disease dynamics.https://doi.org/10.1002/ece3.8450Avena sativaBarley and Cereal Yellow Dwarf Viruseslong‐term N enrichmentplant–pathogen interactionssoil microbesvectored plant pathogen
spellingShingle Casey A. Easterday
Amy E. Kendig
Christelle Lacroix
Eric W. Seabloom
Elizabeth T. Borer
Long‐term nitrogen enrichment mediates the effects of nitrogen supply and co‐inoculation on a viral pathogen
Ecology and Evolution
Avena sativa
Barley and Cereal Yellow Dwarf Viruses
long‐term N enrichment
plant–pathogen interactions
soil microbes
vectored plant pathogen
title Long‐term nitrogen enrichment mediates the effects of nitrogen supply and co‐inoculation on a viral pathogen
title_full Long‐term nitrogen enrichment mediates the effects of nitrogen supply and co‐inoculation on a viral pathogen
title_fullStr Long‐term nitrogen enrichment mediates the effects of nitrogen supply and co‐inoculation on a viral pathogen
title_full_unstemmed Long‐term nitrogen enrichment mediates the effects of nitrogen supply and co‐inoculation on a viral pathogen
title_short Long‐term nitrogen enrichment mediates the effects of nitrogen supply and co‐inoculation on a viral pathogen
title_sort long term nitrogen enrichment mediates the effects of nitrogen supply and co inoculation on a viral pathogen
topic Avena sativa
Barley and Cereal Yellow Dwarf Viruses
long‐term N enrichment
plant–pathogen interactions
soil microbes
vectored plant pathogen
url https://doi.org/10.1002/ece3.8450
work_keys_str_mv AT caseyaeasterday longtermnitrogenenrichmentmediatestheeffectsofnitrogensupplyandcoinoculationonaviralpathogen
AT amyekendig longtermnitrogenenrichmentmediatestheeffectsofnitrogensupplyandcoinoculationonaviralpathogen
AT christellelacroix longtermnitrogenenrichmentmediatestheeffectsofnitrogensupplyandcoinoculationonaviralpathogen
AT ericwseabloom longtermnitrogenenrichmentmediatestheeffectsofnitrogensupplyandcoinoculationonaviralpathogen
AT elizabethtborer longtermnitrogenenrichmentmediatestheeffectsofnitrogensupplyandcoinoculationonaviralpathogen