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Artificial Diets Modulate Infection Rates by Nosema ceranae in Bumblebees
Parasites alter the physiology and behaviour of their hosts. In domestic honey bees, the microsporidia Nosema ceranae induces energetic stress that impairs the behaviour of foragers, potentially leading to colony collapse. Whether this parasite similarly affects wild pollinators is little understood...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7827189/ https://www.ncbi.nlm.nih.gov/pubmed/33445614 http://dx.doi.org/10.3390/microorganisms9010158 |
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author | Gómez-Moracho, Tamara Durand, Tristan Pasquaretta, Cristian Heeb, Philipp Lihoreau, Mathieu |
author_facet | Gómez-Moracho, Tamara Durand, Tristan Pasquaretta, Cristian Heeb, Philipp Lihoreau, Mathieu |
author_sort | Gómez-Moracho, Tamara |
collection | PubMed |
description | Parasites alter the physiology and behaviour of their hosts. In domestic honey bees, the microsporidia Nosema ceranae induces energetic stress that impairs the behaviour of foragers, potentially leading to colony collapse. Whether this parasite similarly affects wild pollinators is little understood because of the low success rates of experimental infection protocols. Here, we present a new approach for infecting bumblebees (Bombus terrestris) with controlled amounts of N. ceranae by briefly exposing individual bumblebees to parasite spores before feeding them with artificial diets. We validated our protocol by testing the effect of two spore dosages and two diets varying in their protein to carbohydrate ratio on the prevalence of the parasite (proportion of PCR-positive bumblebees), the intensity of parasites (spore count in the gut and the faeces), and the survival of bumblebees. Overall, insects fed a low-protein, high-carbohydrate diet showed the highest parasite prevalence (up to 70%) but lived the longest, suggesting that immunity and survival are maximised at different protein to carbohydrate ratios. Spore dosage did not affect parasite infection rate and host survival. The identification of experimental conditions for successfully infecting bumblebees with N. ceranae in the lab will facilitate future investigations of the sub-lethal effects of this parasite on the behaviour and cognition of wild pollinators. |
format | Online Article Text |
id | pubmed-7827189 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-78271892021-01-25 Artificial Diets Modulate Infection Rates by Nosema ceranae in Bumblebees Gómez-Moracho, Tamara Durand, Tristan Pasquaretta, Cristian Heeb, Philipp Lihoreau, Mathieu Microorganisms Article Parasites alter the physiology and behaviour of their hosts. In domestic honey bees, the microsporidia Nosema ceranae induces energetic stress that impairs the behaviour of foragers, potentially leading to colony collapse. Whether this parasite similarly affects wild pollinators is little understood because of the low success rates of experimental infection protocols. Here, we present a new approach for infecting bumblebees (Bombus terrestris) with controlled amounts of N. ceranae by briefly exposing individual bumblebees to parasite spores before feeding them with artificial diets. We validated our protocol by testing the effect of two spore dosages and two diets varying in their protein to carbohydrate ratio on the prevalence of the parasite (proportion of PCR-positive bumblebees), the intensity of parasites (spore count in the gut and the faeces), and the survival of bumblebees. Overall, insects fed a low-protein, high-carbohydrate diet showed the highest parasite prevalence (up to 70%) but lived the longest, suggesting that immunity and survival are maximised at different protein to carbohydrate ratios. Spore dosage did not affect parasite infection rate and host survival. The identification of experimental conditions for successfully infecting bumblebees with N. ceranae in the lab will facilitate future investigations of the sub-lethal effects of this parasite on the behaviour and cognition of wild pollinators. MDPI 2021-01-12 /pmc/articles/PMC7827189/ /pubmed/33445614 http://dx.doi.org/10.3390/microorganisms9010158 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Gómez-Moracho, Tamara Durand, Tristan Pasquaretta, Cristian Heeb, Philipp Lihoreau, Mathieu Artificial Diets Modulate Infection Rates by Nosema ceranae in Bumblebees |
title | Artificial Diets Modulate Infection Rates by Nosema ceranae in Bumblebees |
title_full | Artificial Diets Modulate Infection Rates by Nosema ceranae in Bumblebees |
title_fullStr | Artificial Diets Modulate Infection Rates by Nosema ceranae in Bumblebees |
title_full_unstemmed | Artificial Diets Modulate Infection Rates by Nosema ceranae in Bumblebees |
title_short | Artificial Diets Modulate Infection Rates by Nosema ceranae in Bumblebees |
title_sort | artificial diets modulate infection rates by nosema ceranae in bumblebees |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7827189/ https://www.ncbi.nlm.nih.gov/pubmed/33445614 http://dx.doi.org/10.3390/microorganisms9010158 |
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