Deformed Wing Virus Implicated in Overwintering Honeybee Colony Losses
The worldwide decline in honeybee colonies during the past 50 years has often been linked to the spread of the parasitic mite Varroa destructor and its interaction with certain honeybee viruses. Recently in the United States, dramatic honeybee losses (colony collapse disorder) have been reported; ho...
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Veröffentlicht in: | Applied and Environmental Microbiology 2009-11, Vol.75 (22), p.7212-7220 |
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creator | Highfield, Andrea C El Nagar, Aliya Mackinder, Luke C.M Noël, Laure M.-L.J Hall, Matthew J Martin, Stephen J Schroeder, Declan C |
description | The worldwide decline in honeybee colonies during the past 50 years has often been linked to the spread of the parasitic mite Varroa destructor and its interaction with certain honeybee viruses. Recently in the United States, dramatic honeybee losses (colony collapse disorder) have been reported; however, there remains no clear explanation for these colony losses, with parasitic mites, viruses, bacteria, and fungal diseases all being proposed as possible candidates. Common characteristics that most failing colonies share is a lack of overt disease symptoms and the disappearance of workers from what appears to be normally functioning colonies. In this study, we used quantitative PCR to monitor the presence of three honeybee viruses, deformed wing virus (DWV), acute bee paralysis virus (ABPV), and black queen cell virus (BQCV), during a 1-year period in 15 asymptomatic, varroa mite-positive honeybee colonies in Southern England, and 3 asymptomatic colonies confirmed to be varroa mite free. All colonies with varroa mites underwent control treatments to ensure that mite populations remained low throughout the study. Despite this, multiple virus infections were detected, yet a significant correlation was observed only between DWV viral load and overwintering colony losses. The long-held view has been that DWV is relatively harmless to the overall health status of honeybee colonies unless it is in association with severe varroa mite infestations. Our findings suggest that DWV can potentially act independently of varroa mites to bring about colony losses. Therefore, DWV may be a major factor in overwintering colony losses. |
doi_str_mv | 10.1128/AEM.02227-09 |
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Recently in the United States, dramatic honeybee losses (colony collapse disorder) have been reported; however, there remains no clear explanation for these colony losses, with parasitic mites, viruses, bacteria, and fungal diseases all being proposed as possible candidates. Common characteristics that most failing colonies share is a lack of overt disease symptoms and the disappearance of workers from what appears to be normally functioning colonies. In this study, we used quantitative PCR to monitor the presence of three honeybee viruses, deformed wing virus (DWV), acute bee paralysis virus (ABPV), and black queen cell virus (BQCV), during a 1-year period in 15 asymptomatic, varroa mite-positive honeybee colonies in Southern England, and 3 asymptomatic colonies confirmed to be varroa mite free. All colonies with varroa mites underwent control treatments to ensure that mite populations remained low throughout the study. Despite this, multiple virus infections were detected, yet a significant correlation was observed only between DWV viral load and overwintering colony losses. The long-held view has been that DWV is relatively harmless to the overall health status of honeybee colonies unless it is in association with severe varroa mite infestations. Our findings suggest that DWV can potentially act independently of varroa mites to bring about colony losses. Therefore, DWV may be a major factor in overwintering colony losses.</description><identifier>ISSN: 0099-2240</identifier><identifier>EISSN: 1098-5336</identifier><identifier>EISSN: 1098-6596</identifier><identifier>DOI: 10.1128/AEM.02227-09</identifier><identifier>PMID: 19783750</identifier><identifier>CODEN: AEMIDF</identifier><language>eng</language><publisher>Washington, DC: American Society for Microbiology</publisher><subject>Animals ; Apis mellifera ; Bees ; Bees - parasitology ; Bees - virology ; Biological and medical sciences ; Colony Collapse - parasitology ; Colony Collapse - virology ; Correlation analysis ; DNA, Viral - genetics ; England ; Fundamental and applied biological sciences. Psychology ; Insect Viruses - genetics ; Insect Viruses - physiology ; Invertebrate Microbiology ; Microbiology ; Parasites ; Picornaviridae - genetics ; Picornaviridae - physiology ; Seasons ; Studies ; Time Factors ; Varroidae - virology ; Viral Load ; Viruses</subject><ispartof>Applied and Environmental Microbiology, 2009-11, Vol.75 (22), p.7212-7220</ispartof><rights>2015 INIST-CNRS</rights><rights>Copyright American Society for Microbiology Nov 2009</rights><rights>Copyright © 2009, American Society for Microbiology 2009</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c565t-bcdb22c46010c2b9f5e170e28dc83ea1c18c6aee003398d9847d703bf85e9d3</citedby><cites>FETCH-LOGICAL-c565t-bcdb22c46010c2b9f5e170e28dc83ea1c18c6aee003398d9847d703bf85e9d3</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/PMC2786540/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2786540/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,3175,3176,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22137106$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19783750$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Highfield, Andrea C</creatorcontrib><creatorcontrib>El Nagar, Aliya</creatorcontrib><creatorcontrib>Mackinder, Luke C.M</creatorcontrib><creatorcontrib>Noël, Laure M.-L.J</creatorcontrib><creatorcontrib>Hall, Matthew J</creatorcontrib><creatorcontrib>Martin, Stephen J</creatorcontrib><creatorcontrib>Schroeder, Declan C</creatorcontrib><title>Deformed Wing Virus Implicated in Overwintering Honeybee Colony Losses</title><title>Applied and Environmental Microbiology</title><addtitle>Appl Environ Microbiol</addtitle><description>The worldwide decline in honeybee colonies during the past 50 years has often been linked to the spread of the parasitic mite Varroa destructor and its interaction with certain honeybee viruses. Recently in the United States, dramatic honeybee losses (colony collapse disorder) have been reported; however, there remains no clear explanation for these colony losses, with parasitic mites, viruses, bacteria, and fungal diseases all being proposed as possible candidates. Common characteristics that most failing colonies share is a lack of overt disease symptoms and the disappearance of workers from what appears to be normally functioning colonies. In this study, we used quantitative PCR to monitor the presence of three honeybee viruses, deformed wing virus (DWV), acute bee paralysis virus (ABPV), and black queen cell virus (BQCV), during a 1-year period in 15 asymptomatic, varroa mite-positive honeybee colonies in Southern England, and 3 asymptomatic colonies confirmed to be varroa mite free. All colonies with varroa mites underwent control treatments to ensure that mite populations remained low throughout the study. Despite this, multiple virus infections were detected, yet a significant correlation was observed only between DWV viral load and overwintering colony losses. The long-held view has been that DWV is relatively harmless to the overall health status of honeybee colonies unless it is in association with severe varroa mite infestations. Our findings suggest that DWV can potentially act independently of varroa mites to bring about colony losses. Therefore, DWV may be a major factor in overwintering colony losses.</description><subject>Animals</subject><subject>Apis mellifera</subject><subject>Bees</subject><subject>Bees - parasitology</subject><subject>Bees - virology</subject><subject>Biological and medical sciences</subject><subject>Colony Collapse - parasitology</subject><subject>Colony Collapse - virology</subject><subject>Correlation analysis</subject><subject>DNA, Viral - genetics</subject><subject>England</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Insect Viruses - genetics</subject><subject>Insect Viruses - physiology</subject><subject>Invertebrate Microbiology</subject><subject>Microbiology</subject><subject>Parasites</subject><subject>Picornaviridae - genetics</subject><subject>Picornaviridae - physiology</subject><subject>Seasons</subject><subject>Studies</subject><subject>Time Factors</subject><subject>Varroidae - virology</subject><subject>Viral Load</subject><subject>Viruses</subject><issn>0099-2240</issn><issn>1098-5336</issn><issn>1098-6596</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpd0c9v0zAUB3ALgVgZ3DhDhAQnMp7tJrYvSFPZ2KSiHcaPo-U4L62nxO7sZFP_e1xabcDJkv3RV9_nR8hrCieUMvnp9OzbCTDGRAnqCZlRULKsOK-fkhmAUiVjczgiL1K6AYA51PI5OaJKSC4qmJHzL9iFOGBb_HJ-Vfx0cUrF5bDpnTVjvnW-uLrDeO_8iHEnLoLHbYNYLEIf_LZYhpQwvSTPOtMnfHU4j8n1-dn3xUW5vPp6uThdlraqq7FsbNswZuc1ULCsUV2FVAAy2VrJ0VBLpa0NIgDnSrZKzkUrgDedrFC1_Jh83qdupiZXtujHaHq9iW4wcauDcfrfF-_WehXuNBOyruaQAz4cAmK4nTCNenDJYt8bj2FKmtEKasF5hu_-gzdhij6PphlUqs6ldujjHtmYPyFi99CEgt7tRufd6D-70aAyf_N3-0d8WEYG7w_AJGv6LhpvXXpwjFEuKNSP5dZutb53EbVJgzY4aFFlpQWjLKO3e9SZoM0q5qAf1wwoB1orKfKUvwHh2KtQ</recordid><startdate>20091101</startdate><enddate>20091101</enddate><creator>Highfield, Andrea C</creator><creator>El Nagar, Aliya</creator><creator>Mackinder, Luke C.M</creator><creator>Noël, Laure M.-L.J</creator><creator>Hall, Matthew J</creator><creator>Martin, Stephen J</creator><creator>Schroeder, Declan C</creator><general>American Society for Microbiology</general><general>American Society for Microbiology (ASM)</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7T7</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>SOI</scope><scope>5PM</scope></search><sort><creationdate>20091101</creationdate><title>Deformed Wing Virus Implicated in Overwintering Honeybee Colony Losses</title><author>Highfield, Andrea C ; El Nagar, Aliya ; Mackinder, Luke C.M ; Noël, Laure M.-L.J ; Hall, Matthew J ; Martin, Stephen J ; Schroeder, Declan C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c565t-bcdb22c46010c2b9f5e170e28dc83ea1c18c6aee003398d9847d703bf85e9d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Animals</topic><topic>Apis mellifera</topic><topic>Bees</topic><topic>Bees - parasitology</topic><topic>Bees - virology</topic><topic>Biological and medical sciences</topic><topic>Colony Collapse - parasitology</topic><topic>Colony Collapse - virology</topic><topic>Correlation analysis</topic><topic>DNA, Viral - genetics</topic><topic>England</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Insect Viruses - genetics</topic><topic>Insect Viruses - physiology</topic><topic>Invertebrate Microbiology</topic><topic>Microbiology</topic><topic>Parasites</topic><topic>Picornaviridae - genetics</topic><topic>Picornaviridae - physiology</topic><topic>Seasons</topic><topic>Studies</topic><topic>Time Factors</topic><topic>Varroidae - virology</topic><topic>Viral Load</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Highfield, Andrea C</creatorcontrib><creatorcontrib>El Nagar, Aliya</creatorcontrib><creatorcontrib>Mackinder, Luke C.M</creatorcontrib><creatorcontrib>Noël, Laure M.-L.J</creatorcontrib><creatorcontrib>Hall, Matthew J</creatorcontrib><creatorcontrib>Martin, Stephen J</creatorcontrib><creatorcontrib>Schroeder, Declan C</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Applied and Environmental Microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Highfield, Andrea C</au><au>El Nagar, Aliya</au><au>Mackinder, Luke C.M</au><au>Noël, Laure M.-L.J</au><au>Hall, Matthew J</au><au>Martin, Stephen J</au><au>Schroeder, Declan C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Deformed Wing Virus Implicated in Overwintering Honeybee Colony Losses</atitle><jtitle>Applied and Environmental Microbiology</jtitle><addtitle>Appl Environ Microbiol</addtitle><date>2009-11-01</date><risdate>2009</risdate><volume>75</volume><issue>22</issue><spage>7212</spage><epage>7220</epage><pages>7212-7220</pages><issn>0099-2240</issn><eissn>1098-5336</eissn><eissn>1098-6596</eissn><coden>AEMIDF</coden><abstract>The worldwide decline in honeybee colonies during the past 50 years has often been linked to the spread of the parasitic mite Varroa destructor and its interaction with certain honeybee viruses. Recently in the United States, dramatic honeybee losses (colony collapse disorder) have been reported; however, there remains no clear explanation for these colony losses, with parasitic mites, viruses, bacteria, and fungal diseases all being proposed as possible candidates. Common characteristics that most failing colonies share is a lack of overt disease symptoms and the disappearance of workers from what appears to be normally functioning colonies. In this study, we used quantitative PCR to monitor the presence of three honeybee viruses, deformed wing virus (DWV), acute bee paralysis virus (ABPV), and black queen cell virus (BQCV), during a 1-year period in 15 asymptomatic, varroa mite-positive honeybee colonies in Southern England, and 3 asymptomatic colonies confirmed to be varroa mite free. All colonies with varroa mites underwent control treatments to ensure that mite populations remained low throughout the study. Despite this, multiple virus infections were detected, yet a significant correlation was observed only between DWV viral load and overwintering colony losses. The long-held view has been that DWV is relatively harmless to the overall health status of honeybee colonies unless it is in association with severe varroa mite infestations. Our findings suggest that DWV can potentially act independently of varroa mites to bring about colony losses. Therefore, DWV may be a major factor in overwintering colony losses.</abstract><cop>Washington, DC</cop><pub>American Society for Microbiology</pub><pmid>19783750</pmid><doi>10.1128/AEM.02227-09</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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source | American Society for Microbiology; MEDLINE; EZB-FREE-00999 freely available EZB journals; PubMed Central; Alma/SFX Local Collection |
subjects | Animals Apis mellifera Bees Bees - parasitology Bees - virology Biological and medical sciences Colony Collapse - parasitology Colony Collapse - virology Correlation analysis DNA, Viral - genetics England Fundamental and applied biological sciences. Psychology Insect Viruses - genetics Insect Viruses - physiology Invertebrate Microbiology Microbiology Parasites Picornaviridae - genetics Picornaviridae - physiology Seasons Studies Time Factors Varroidae - virology Viral Load Viruses |
title | Deformed Wing Virus Implicated in Overwintering Honeybee Colony Losses |
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