Cargando…

An inverse association between West Nile virus serostatus and avian malaria infection status

BACKGROUND: Various ecological and physiological mechanisms might influence the probability that two or more pathogens may simultaneously or sequentially infect a host individual. Concurrent infections can have important consequences for host condition and fitness, including elevated mortality risks...

Descripción completa

Detalles Bibliográficos
Autores principales: Medeiros, Matthew CI, Anderson, Tavis K, Higashiguchi, Jenni M, Kitron, Uriel D, Walker, Edward D, Brawn, Jeffrey D, Krebs, Bethany L, Ruiz, Marilyn O, Goldberg, Tony L, Ricklefs, Robert E, Hamer, Gabriel L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4262112/
https://www.ncbi.nlm.nih.gov/pubmed/25178911
http://dx.doi.org/10.1186/1756-3305-7-415
_version_ 1782348384591413248
author Medeiros, Matthew CI
Anderson, Tavis K
Higashiguchi, Jenni M
Kitron, Uriel D
Walker, Edward D
Brawn, Jeffrey D
Krebs, Bethany L
Ruiz, Marilyn O
Goldberg, Tony L
Ricklefs, Robert E
Hamer, Gabriel L
author_facet Medeiros, Matthew CI
Anderson, Tavis K
Higashiguchi, Jenni M
Kitron, Uriel D
Walker, Edward D
Brawn, Jeffrey D
Krebs, Bethany L
Ruiz, Marilyn O
Goldberg, Tony L
Ricklefs, Robert E
Hamer, Gabriel L
author_sort Medeiros, Matthew CI
collection PubMed
description BACKGROUND: Various ecological and physiological mechanisms might influence the probability that two or more pathogens may simultaneously or sequentially infect a host individual. Concurrent infections can have important consequences for host condition and fitness, including elevated mortality risks. In addition, interactions between coinfecting pathogens may have important implications for transmission dynamics. METHODS: Here, we explore patterns of association between two common avian pathogens (West Nile virus and avian malaria parasites) among a suburban bird community in Chicago, IL, USA that share mosquito vectors. We surveyed 1714 individual birds across 13 species for both pathogens through established molecular protocols. RESULTS: Field investigations of haemosporidian and West Nile virus (WNV) infections among sampled birds yielded an inverse association between WNV serostatus and Plasmodium infection status. This relationship occurred in adult birds but not in juveniles. There was no evidence for a relationship between Haemoproteus infection and WNV serostatus. We detected similar prevalence of Plasmodium among birds captured with active WNV infections and spatiotemporally paired WNV-naïve individuals of the same species, demonstrating that the two pathogens can co-infect hosts. CONCLUSIONS: Mechanisms explaining the negative association between WNV serostatus and Plasmodium infection status remain unclear and must be resolved through experimental infection procedures. However, our results highlight potential interactions between two common avian pathogens that may influence their transmission among hosts. This is especially relevant considering that West Nile virus is a common zoonotic pathogen with public health implications. Moreover, both pathogens are instructive models in infectious disease ecology, and infection with either has fitness consequences for their avian hosts. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1756-3305-7-415) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-4262112
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-42621122014-12-11 An inverse association between West Nile virus serostatus and avian malaria infection status Medeiros, Matthew CI Anderson, Tavis K Higashiguchi, Jenni M Kitron, Uriel D Walker, Edward D Brawn, Jeffrey D Krebs, Bethany L Ruiz, Marilyn O Goldberg, Tony L Ricklefs, Robert E Hamer, Gabriel L Parasit Vectors Research BACKGROUND: Various ecological and physiological mechanisms might influence the probability that two or more pathogens may simultaneously or sequentially infect a host individual. Concurrent infections can have important consequences for host condition and fitness, including elevated mortality risks. In addition, interactions between coinfecting pathogens may have important implications for transmission dynamics. METHODS: Here, we explore patterns of association between two common avian pathogens (West Nile virus and avian malaria parasites) among a suburban bird community in Chicago, IL, USA that share mosquito vectors. We surveyed 1714 individual birds across 13 species for both pathogens through established molecular protocols. RESULTS: Field investigations of haemosporidian and West Nile virus (WNV) infections among sampled birds yielded an inverse association between WNV serostatus and Plasmodium infection status. This relationship occurred in adult birds but not in juveniles. There was no evidence for a relationship between Haemoproteus infection and WNV serostatus. We detected similar prevalence of Plasmodium among birds captured with active WNV infections and spatiotemporally paired WNV-naïve individuals of the same species, demonstrating that the two pathogens can co-infect hosts. CONCLUSIONS: Mechanisms explaining the negative association between WNV serostatus and Plasmodium infection status remain unclear and must be resolved through experimental infection procedures. However, our results highlight potential interactions between two common avian pathogens that may influence their transmission among hosts. This is especially relevant considering that West Nile virus is a common zoonotic pathogen with public health implications. Moreover, both pathogens are instructive models in infectious disease ecology, and infection with either has fitness consequences for their avian hosts. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1756-3305-7-415) contains supplementary material, which is available to authorized users. BioMed Central 2014-09-01 /pmc/articles/PMC4262112/ /pubmed/25178911 http://dx.doi.org/10.1186/1756-3305-7-415 Text en © Medeiros et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Medeiros, Matthew CI
Anderson, Tavis K
Higashiguchi, Jenni M
Kitron, Uriel D
Walker, Edward D
Brawn, Jeffrey D
Krebs, Bethany L
Ruiz, Marilyn O
Goldberg, Tony L
Ricklefs, Robert E
Hamer, Gabriel L
An inverse association between West Nile virus serostatus and avian malaria infection status
title An inverse association between West Nile virus serostatus and avian malaria infection status
title_full An inverse association between West Nile virus serostatus and avian malaria infection status
title_fullStr An inverse association between West Nile virus serostatus and avian malaria infection status
title_full_unstemmed An inverse association between West Nile virus serostatus and avian malaria infection status
title_short An inverse association between West Nile virus serostatus and avian malaria infection status
title_sort inverse association between west nile virus serostatus and avian malaria infection status
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4262112/
https://www.ncbi.nlm.nih.gov/pubmed/25178911
http://dx.doi.org/10.1186/1756-3305-7-415
work_keys_str_mv AT medeirosmatthewci aninverseassociationbetweenwestnilevirusserostatusandavianmalariainfectionstatus
AT andersontavisk aninverseassociationbetweenwestnilevirusserostatusandavianmalariainfectionstatus
AT higashiguchijennim aninverseassociationbetweenwestnilevirusserostatusandavianmalariainfectionstatus
AT kitronurield aninverseassociationbetweenwestnilevirusserostatusandavianmalariainfectionstatus
AT walkeredwardd aninverseassociationbetweenwestnilevirusserostatusandavianmalariainfectionstatus
AT brawnjeffreyd aninverseassociationbetweenwestnilevirusserostatusandavianmalariainfectionstatus
AT krebsbethanyl aninverseassociationbetweenwestnilevirusserostatusandavianmalariainfectionstatus
AT ruizmarilyno aninverseassociationbetweenwestnilevirusserostatusandavianmalariainfectionstatus
AT goldbergtonyl aninverseassociationbetweenwestnilevirusserostatusandavianmalariainfectionstatus
AT ricklefsroberte aninverseassociationbetweenwestnilevirusserostatusandavianmalariainfectionstatus
AT hamergabriell aninverseassociationbetweenwestnilevirusserostatusandavianmalariainfectionstatus
AT medeirosmatthewci inverseassociationbetweenwestnilevirusserostatusandavianmalariainfectionstatus
AT andersontavisk inverseassociationbetweenwestnilevirusserostatusandavianmalariainfectionstatus
AT higashiguchijennim inverseassociationbetweenwestnilevirusserostatusandavianmalariainfectionstatus
AT kitronurield inverseassociationbetweenwestnilevirusserostatusandavianmalariainfectionstatus
AT walkeredwardd inverseassociationbetweenwestnilevirusserostatusandavianmalariainfectionstatus
AT brawnjeffreyd inverseassociationbetweenwestnilevirusserostatusandavianmalariainfectionstatus
AT krebsbethanyl inverseassociationbetweenwestnilevirusserostatusandavianmalariainfectionstatus
AT ruizmarilyno inverseassociationbetweenwestnilevirusserostatusandavianmalariainfectionstatus
AT goldbergtonyl inverseassociationbetweenwestnilevirusserostatusandavianmalariainfectionstatus
AT ricklefsroberte inverseassociationbetweenwestnilevirusserostatusandavianmalariainfectionstatus
AT hamergabriell inverseassociationbetweenwestnilevirusserostatusandavianmalariainfectionstatus