Synergistic parasite-pathogen interactions mediated by host immunity can drive the collapse of honeybee colonies
The health of the honeybee and, indirectly, global crop production are threatened by several biotic and abiotic factors, which play a poorly defined role in the induction of widespread colony losses. Recent descriptive studies suggest that colony losses are often related to the interaction between p...
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creator | Nazzi, Francesco Brown, Sam P Annoscia, Desiderato Del Piccolo, Fabio Di Prisco, Gennaro Varricchio, Paola Della Vedova, Giorgio Cattonaro, Federica Caprio, Emilio Pennacchio, Francesco |
description | The health of the honeybee and, indirectly, global crop production are threatened by several biotic and abiotic factors, which play a poorly defined role in the induction of widespread colony losses. Recent descriptive studies suggest that colony losses are often related to the interaction between pathogens and other stress factors, including parasites. Through an integrated analysis of the population and molecular changes associated with the collapse of honeybee colonies infested by the parasitic mite Varroa destructor, we show that this parasite can de-stabilise the within-host dynamics of Deformed wing virus (DWV), transforming a cryptic and vertically transmitted virus into a rapidly replicating killer, which attains lethal levels late in the season. The de-stabilisation of DWV infection is associated with an immunosuppression syndrome, characterized by a strong down-regulation of the transcription factor NF-κB. The centrality of NF-κB in host responses to a range of environmental challenges suggests that this transcription factor can act as a common currency underlying colony collapse that may be triggered by different causes. Our results offer an integrated account for the multifactorial origin of honeybee losses and a new framework for assessing, and possibly mitigating, the impact of environmental challenges on honeybee health. |
doi_str_mv | 10.1371/journal.ppat.1002735 |
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Recent descriptive studies suggest that colony losses are often related to the interaction between pathogens and other stress factors, including parasites. Through an integrated analysis of the population and molecular changes associated with the collapse of honeybee colonies infested by the parasitic mite Varroa destructor, we show that this parasite can de-stabilise the within-host dynamics of Deformed wing virus (DWV), transforming a cryptic and vertically transmitted virus into a rapidly replicating killer, which attains lethal levels late in the season. The de-stabilisation of DWV infection is associated with an immunosuppression syndrome, characterized by a strong down-regulation of the transcription factor NF-κB. The centrality of NF-κB in host responses to a range of environmental challenges suggests that this transcription factor can act as a common currency underlying colony collapse that may be triggered by different causes. Our results offer an integrated account for the multifactorial origin of honeybee losses and a new framework for assessing, and possibly mitigating, the impact of environmental challenges on honeybee health.</description><identifier>ISSN: 1553-7374</identifier><identifier>ISSN: 1553-7366</identifier><identifier>EISSN: 1553-7374</identifier><identifier>DOI: 10.1371/journal.ppat.1002735</identifier><identifier>PMID: 22719246</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Agriculture ; Animals ; Bees ; Bees - immunology ; Bees - parasitology ; Biology ; Coinfection - immunology ; Coinfection - veterinary ; Health aspects ; Host-Parasite Interactions - immunology ; Host-parasite relationships ; Immunology ; Infections ; Insect Viruses - immunology ; Mite Infestations - complications ; Mite Infestations - immunology ; Mite Infestations - veterinary ; NF-kappa B - immunology ; Parasites ; Pathogenic microorganisms ; Physiological aspects ; Plant reproduction ; Real-Time Polymerase Chain Reaction ; RNA Virus Infections - complications ; RNA Virus Infections - immunology ; RNA Virus Infections - veterinary ; RNA Viruses - immunology ; Statistical methods ; Varroidae - immunology ; Veterinary Science ; Viral infections ; Virulence (Microbiology)</subject><ispartof>PLoS pathogens, 2012-06, Vol.8 (6), p.e1002735</ispartof><rights>COPYRIGHT 2012 Public Library of Science</rights><rights>2012 Nazzi et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Nazzi F, Brown SP, Annoscia D, Del Piccolo F, Di Prisco G, et al. (2012) Synergistic Parasite-Pathogen Interactions Mediated by Host Immunity Can Drive the Collapse of Honeybee Colonies. PLoS Pathog 8(6): e1002735. doi:10.1371/journal.ppat.1002735</rights><rights>Nazzi et al. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c727t-dc3c82f577d71bed59fbba9e18f8c77a95dd867b775150dc3e476fd268298a703</citedby><cites>FETCH-LOGICAL-c727t-dc3c82f577d71bed59fbba9e18f8c77a95dd867b775150dc3e476fd268298a703</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3375299/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3375299/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23847,27903,27904,53769,53771,79346,79347</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22719246$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Schneider, David S.</contributor><creatorcontrib>Nazzi, Francesco</creatorcontrib><creatorcontrib>Brown, Sam P</creatorcontrib><creatorcontrib>Annoscia, Desiderato</creatorcontrib><creatorcontrib>Del Piccolo, Fabio</creatorcontrib><creatorcontrib>Di Prisco, Gennaro</creatorcontrib><creatorcontrib>Varricchio, Paola</creatorcontrib><creatorcontrib>Della Vedova, Giorgio</creatorcontrib><creatorcontrib>Cattonaro, Federica</creatorcontrib><creatorcontrib>Caprio, Emilio</creatorcontrib><creatorcontrib>Pennacchio, Francesco</creatorcontrib><title>Synergistic parasite-pathogen interactions mediated by host immunity can drive the collapse of honeybee colonies</title><title>PLoS pathogens</title><addtitle>PLoS Pathog</addtitle><description>The health of the honeybee and, indirectly, global crop production are threatened by several biotic and abiotic factors, which play a poorly defined role in the induction of widespread colony losses. Recent descriptive studies suggest that colony losses are often related to the interaction between pathogens and other stress factors, including parasites. Through an integrated analysis of the population and molecular changes associated with the collapse of honeybee colonies infested by the parasitic mite Varroa destructor, we show that this parasite can de-stabilise the within-host dynamics of Deformed wing virus (DWV), transforming a cryptic and vertically transmitted virus into a rapidly replicating killer, which attains lethal levels late in the season. The de-stabilisation of DWV infection is associated with an immunosuppression syndrome, characterized by a strong down-regulation of the transcription factor NF-κB. The centrality of NF-κB in host responses to a range of environmental challenges suggests that this transcription factor can act as a common currency underlying colony collapse that may be triggered by different causes. Our results offer an integrated account for the multifactorial origin of honeybee losses and a new framework for assessing, and possibly mitigating, the impact of environmental challenges on honeybee health.</description><subject>Agriculture</subject><subject>Animals</subject><subject>Bees</subject><subject>Bees - immunology</subject><subject>Bees - parasitology</subject><subject>Biology</subject><subject>Coinfection - immunology</subject><subject>Coinfection - veterinary</subject><subject>Health aspects</subject><subject>Host-Parasite Interactions - immunology</subject><subject>Host-parasite relationships</subject><subject>Immunology</subject><subject>Infections</subject><subject>Insect Viruses - immunology</subject><subject>Mite Infestations - complications</subject><subject>Mite Infestations - immunology</subject><subject>Mite Infestations - veterinary</subject><subject>NF-kappa B - immunology</subject><subject>Parasites</subject><subject>Pathogenic microorganisms</subject><subject>Physiological aspects</subject><subject>Plant reproduction</subject><subject>Real-Time Polymerase Chain Reaction</subject><subject>RNA Virus Infections - complications</subject><subject>RNA Virus Infections - immunology</subject><subject>RNA Virus Infections - veterinary</subject><subject>RNA Viruses - immunology</subject><subject>Statistical methods</subject><subject>Varroidae - immunology</subject><subject>Veterinary Science</subject><subject>Viral infections</subject><subject>Virulence 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parasite-pathogen interactions mediated by host immunity can drive the collapse of honeybee colonies</title><author>Nazzi, Francesco ; Brown, Sam P ; Annoscia, Desiderato ; Del Piccolo, Fabio ; Di Prisco, Gennaro ; Varricchio, Paola ; Della Vedova, Giorgio ; Cattonaro, Federica ; Caprio, Emilio ; Pennacchio, Francesco</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c727t-dc3c82f577d71bed59fbba9e18f8c77a95dd867b775150dc3e476fd268298a703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Agriculture</topic><topic>Animals</topic><topic>Bees</topic><topic>Bees - immunology</topic><topic>Bees - parasitology</topic><topic>Biology</topic><topic>Coinfection - immunology</topic><topic>Coinfection - veterinary</topic><topic>Health aspects</topic><topic>Host-Parasite Interactions - immunology</topic><topic>Host-parasite relationships</topic><topic>Immunology</topic><topic>Infections</topic><topic>Insect Viruses - immunology</topic><topic>Mite Infestations - complications</topic><topic>Mite Infestations - immunology</topic><topic>Mite Infestations - veterinary</topic><topic>NF-kappa B - immunology</topic><topic>Parasites</topic><topic>Pathogenic microorganisms</topic><topic>Physiological aspects</topic><topic>Plant reproduction</topic><topic>Real-Time Polymerase Chain Reaction</topic><topic>RNA Virus Infections - complications</topic><topic>RNA Virus Infections - immunology</topic><topic>RNA Virus Infections - veterinary</topic><topic>RNA Viruses - immunology</topic><topic>Statistical methods</topic><topic>Varroidae - immunology</topic><topic>Veterinary Science</topic><topic>Viral infections</topic><topic>Virulence (Microbiology)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nazzi, Francesco</creatorcontrib><creatorcontrib>Brown, Sam 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abiotic factors, which play a poorly defined role in the induction of widespread colony losses. Recent descriptive studies suggest that colony losses are often related to the interaction between pathogens and other stress factors, including parasites. Through an integrated analysis of the population and molecular changes associated with the collapse of honeybee colonies infested by the parasitic mite Varroa destructor, we show that this parasite can de-stabilise the within-host dynamics of Deformed wing virus (DWV), transforming a cryptic and vertically transmitted virus into a rapidly replicating killer, which attains lethal levels late in the season. The de-stabilisation of DWV infection is associated with an immunosuppression syndrome, characterized by a strong down-regulation of the transcription factor NF-κB. The centrality of NF-κB in host responses to a range of environmental challenges suggests that this transcription factor can act as a common currency underlying colony collapse that may be triggered by different causes. Our results offer an integrated account for the multifactorial origin of honeybee losses and a new framework for assessing, and possibly mitigating, the impact of environmental challenges on honeybee health.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>22719246</pmid><doi>10.1371/journal.ppat.1002735</doi><oa>free_for_read</oa></addata></record> |
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subjects | Agriculture Animals Bees Bees - immunology Bees - parasitology Biology Coinfection - immunology Coinfection - veterinary Health aspects Host-Parasite Interactions - immunology Host-parasite relationships Immunology Infections Insect Viruses - immunology Mite Infestations - complications Mite Infestations - immunology Mite Infestations - veterinary NF-kappa B - immunology Parasites Pathogenic microorganisms Physiological aspects Plant reproduction Real-Time Polymerase Chain Reaction RNA Virus Infections - complications RNA Virus Infections - immunology RNA Virus Infections - veterinary RNA Viruses - immunology Statistical methods Varroidae - immunology Veterinary Science Viral infections Virulence (Microbiology) |
title | Synergistic parasite-pathogen interactions mediated by host immunity can drive the collapse of honeybee colonies |
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