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Transferrin-mediated iron sequestration suggests a novel therapeutic strategy for controlling Nosema disease in the honey bee, Apis mellifera

Nosemosis C, a Nosema disease caused by microsporidia parasite Nosema ceranae, is a significant disease burden of the European honey bee Apis mellifera which is one of the most economically important insect pollinators. Nevertheless, there is no effective treatment currently available for Nosema dis...

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Autores principales: Rodríguez-García, Cristina, Heerman, Matthew C., Cook, Steven C., Evans, Jay D., DeGrandi-Hoffman, Gloria, Banmeke, Olubukola, Zhang, Yi, Huang, Shaokang, Hamilton, Michele, Chen, Yan Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7891791/
https://www.ncbi.nlm.nih.gov/pubmed/33600478
http://dx.doi.org/10.1371/journal.ppat.1009270
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author Rodríguez-García, Cristina
Heerman, Matthew C.
Cook, Steven C.
Evans, Jay D.
DeGrandi-Hoffman, Gloria
Banmeke, Olubukola
Zhang, Yi
Huang, Shaokang
Hamilton, Michele
Chen, Yan Ping
author_facet Rodríguez-García, Cristina
Heerman, Matthew C.
Cook, Steven C.
Evans, Jay D.
DeGrandi-Hoffman, Gloria
Banmeke, Olubukola
Zhang, Yi
Huang, Shaokang
Hamilton, Michele
Chen, Yan Ping
author_sort Rodríguez-García, Cristina
collection PubMed
description Nosemosis C, a Nosema disease caused by microsporidia parasite Nosema ceranae, is a significant disease burden of the European honey bee Apis mellifera which is one of the most economically important insect pollinators. Nevertheless, there is no effective treatment currently available for Nosema disease and the disease mechanisms underlying the pathological effects of N. ceranae infection in honey bees are poorly understood. Iron is an essential nutrient for growth and survival of hosts and pathogens alike. The iron tug-of-war between host and pathogen is a central battlefield at the host-pathogen interface which determines the outcome of an infection, however, has not been explored in honey bees. To fill the gap, we conducted a study to investigate the impact of N. ceranae infection on iron homeostasis in honey bees. The expression of transferrin, an iron binding and transporting protein that is one of the key players of iron homeostasis, in response to N. ceranae infection was analysed. Furthermore, the functional roles of transferrin in iron homeostasis and honey bee host immunity were characterized using an RNA interference (RNAi)-based method. The results showed that N. ceranae infection causes iron deficiency and upregulation of the A. mellifera transferrin (AmTsf) mRNA in honey bees, implying that higher expression of AmTsf allows N. ceranae to scavenge more iron from the host for its proliferation and survival. The suppressed expression levels of AmTsf via RNAi could lead to reduced N. ceranae transcription activity, alleviated iron loss, enhanced immunity, and improved survival of the infected bees. The intriguing multifunctionality of transferrin illustrated in this study is a significant contribution to the existing body of literature concerning iron homeostasis in insects. The uncovered functional role of transferrin on iron homeostasis, pathogen growth and honey bee’s ability to mount immune responses may hold the key for the development of novel strategies to treat or prevent diseases in honey bees.
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spelling pubmed-78917912021-03-01 Transferrin-mediated iron sequestration suggests a novel therapeutic strategy for controlling Nosema disease in the honey bee, Apis mellifera Rodríguez-García, Cristina Heerman, Matthew C. Cook, Steven C. Evans, Jay D. DeGrandi-Hoffman, Gloria Banmeke, Olubukola Zhang, Yi Huang, Shaokang Hamilton, Michele Chen, Yan Ping PLoS Pathog Research Article Nosemosis C, a Nosema disease caused by microsporidia parasite Nosema ceranae, is a significant disease burden of the European honey bee Apis mellifera which is one of the most economically important insect pollinators. Nevertheless, there is no effective treatment currently available for Nosema disease and the disease mechanisms underlying the pathological effects of N. ceranae infection in honey bees are poorly understood. Iron is an essential nutrient for growth and survival of hosts and pathogens alike. The iron tug-of-war between host and pathogen is a central battlefield at the host-pathogen interface which determines the outcome of an infection, however, has not been explored in honey bees. To fill the gap, we conducted a study to investigate the impact of N. ceranae infection on iron homeostasis in honey bees. The expression of transferrin, an iron binding and transporting protein that is one of the key players of iron homeostasis, in response to N. ceranae infection was analysed. Furthermore, the functional roles of transferrin in iron homeostasis and honey bee host immunity were characterized using an RNA interference (RNAi)-based method. The results showed that N. ceranae infection causes iron deficiency and upregulation of the A. mellifera transferrin (AmTsf) mRNA in honey bees, implying that higher expression of AmTsf allows N. ceranae to scavenge more iron from the host for its proliferation and survival. The suppressed expression levels of AmTsf via RNAi could lead to reduced N. ceranae transcription activity, alleviated iron loss, enhanced immunity, and improved survival of the infected bees. The intriguing multifunctionality of transferrin illustrated in this study is a significant contribution to the existing body of literature concerning iron homeostasis in insects. The uncovered functional role of transferrin on iron homeostasis, pathogen growth and honey bee’s ability to mount immune responses may hold the key for the development of novel strategies to treat or prevent diseases in honey bees. Public Library of Science 2021-02-18 /pmc/articles/PMC7891791/ /pubmed/33600478 http://dx.doi.org/10.1371/journal.ppat.1009270 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Rodríguez-García, Cristina
Heerman, Matthew C.
Cook, Steven C.
Evans, Jay D.
DeGrandi-Hoffman, Gloria
Banmeke, Olubukola
Zhang, Yi
Huang, Shaokang
Hamilton, Michele
Chen, Yan Ping
Transferrin-mediated iron sequestration suggests a novel therapeutic strategy for controlling Nosema disease in the honey bee, Apis mellifera
title Transferrin-mediated iron sequestration suggests a novel therapeutic strategy for controlling Nosema disease in the honey bee, Apis mellifera
title_full Transferrin-mediated iron sequestration suggests a novel therapeutic strategy for controlling Nosema disease in the honey bee, Apis mellifera
title_fullStr Transferrin-mediated iron sequestration suggests a novel therapeutic strategy for controlling Nosema disease in the honey bee, Apis mellifera
title_full_unstemmed Transferrin-mediated iron sequestration suggests a novel therapeutic strategy for controlling Nosema disease in the honey bee, Apis mellifera
title_short Transferrin-mediated iron sequestration suggests a novel therapeutic strategy for controlling Nosema disease in the honey bee, Apis mellifera
title_sort transferrin-mediated iron sequestration suggests a novel therapeutic strategy for controlling nosema disease in the honey bee, apis mellifera
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7891791/
https://www.ncbi.nlm.nih.gov/pubmed/33600478
http://dx.doi.org/10.1371/journal.ppat.1009270
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