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Host circadian rhythms are disrupted during malaria infection in parasite genotype-specific manners

Infection can dramatically alter behavioural and physiological traits as hosts become sick and subsequently return to health. Such “sickness behaviours” include disrupted circadian rhythms in both locomotor activity and body temperature. Host sickness behaviours vary in pathogen species-specific man...

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Autores principales: Prior, Kimberley F., O’Donnell, Aidan J., Rund, Samuel S. C., Savill, Nicholas J., van der Veen, Daan R., Reece, Sarah E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6662749/
https://www.ncbi.nlm.nih.gov/pubmed/31358780
http://dx.doi.org/10.1038/s41598-019-47191-8
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author Prior, Kimberley F.
O’Donnell, Aidan J.
Rund, Samuel S. C.
Savill, Nicholas J.
van der Veen, Daan R.
Reece, Sarah E.
author_facet Prior, Kimberley F.
O’Donnell, Aidan J.
Rund, Samuel S. C.
Savill, Nicholas J.
van der Veen, Daan R.
Reece, Sarah E.
author_sort Prior, Kimberley F.
collection PubMed
description Infection can dramatically alter behavioural and physiological traits as hosts become sick and subsequently return to health. Such “sickness behaviours” include disrupted circadian rhythms in both locomotor activity and body temperature. Host sickness behaviours vary in pathogen species-specific manners but the influence of pathogen intraspecific variation is rarely studied. We examine how infection with the murine malaria parasite, Plasmodium chabaudi, shapes sickness in terms of parasite genotype-specific effects on host circadian rhythms. We reveal that circadian rhythms in host locomotor activity patterns and body temperature become differentially disrupted and in parasite genotype-specific manners. Locomotor activity and body temperature in combination provide more sensitive measures of health than commonly used virulence metrics for malaria (e.g. anaemia). Moreover, patterns of host disruption cannot be explained simply by variation in replication rate across parasite genotypes or the severity of anaemia each parasite genotype causes. It is well known that disruption to circadian rhythms is associated with non-infectious diseases, including cancer, type 2 diabetes, and obesity. Our results reveal that disruption of host circadian rhythms is a genetically variable virulence trait of pathogens with implications for host health and disease tolerance.
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spelling pubmed-66627492019-08-02 Host circadian rhythms are disrupted during malaria infection in parasite genotype-specific manners Prior, Kimberley F. O’Donnell, Aidan J. Rund, Samuel S. C. Savill, Nicholas J. van der Veen, Daan R. Reece, Sarah E. Sci Rep Article Infection can dramatically alter behavioural and physiological traits as hosts become sick and subsequently return to health. Such “sickness behaviours” include disrupted circadian rhythms in both locomotor activity and body temperature. Host sickness behaviours vary in pathogen species-specific manners but the influence of pathogen intraspecific variation is rarely studied. We examine how infection with the murine malaria parasite, Plasmodium chabaudi, shapes sickness in terms of parasite genotype-specific effects on host circadian rhythms. We reveal that circadian rhythms in host locomotor activity patterns and body temperature become differentially disrupted and in parasite genotype-specific manners. Locomotor activity and body temperature in combination provide more sensitive measures of health than commonly used virulence metrics for malaria (e.g. anaemia). Moreover, patterns of host disruption cannot be explained simply by variation in replication rate across parasite genotypes or the severity of anaemia each parasite genotype causes. It is well known that disruption to circadian rhythms is associated with non-infectious diseases, including cancer, type 2 diabetes, and obesity. Our results reveal that disruption of host circadian rhythms is a genetically variable virulence trait of pathogens with implications for host health and disease tolerance. Nature Publishing Group UK 2019-07-29 /pmc/articles/PMC6662749/ /pubmed/31358780 http://dx.doi.org/10.1038/s41598-019-47191-8 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Prior, Kimberley F.
O’Donnell, Aidan J.
Rund, Samuel S. C.
Savill, Nicholas J.
van der Veen, Daan R.
Reece, Sarah E.
Host circadian rhythms are disrupted during malaria infection in parasite genotype-specific manners
title Host circadian rhythms are disrupted during malaria infection in parasite genotype-specific manners
title_full Host circadian rhythms are disrupted during malaria infection in parasite genotype-specific manners
title_fullStr Host circadian rhythms are disrupted during malaria infection in parasite genotype-specific manners
title_full_unstemmed Host circadian rhythms are disrupted during malaria infection in parasite genotype-specific manners
title_short Host circadian rhythms are disrupted during malaria infection in parasite genotype-specific manners
title_sort host circadian rhythms are disrupted during malaria infection in parasite genotype-specific manners
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6662749/
https://www.ncbi.nlm.nih.gov/pubmed/31358780
http://dx.doi.org/10.1038/s41598-019-47191-8
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