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...
Autores principales: | , , , , , , , , , , |
---|---|
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 |