Iridovirus and microsporidian linked to honey bee colony decline
In 2010 Colony Collapse Disorder (CCD), again devastated honey bee colonies in the USA, indicating that the problem is neither diminishing nor has it been resolved. Many CCD investigations, using sensitive genome-based methods, have found small RNA bee viruses and the microsporidia, Nosema apis and...
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creator | Bromenshenk, Jerry J Henderson, Colin B Wick, Charles H Stanford, Michael F Zulich, Alan W Jabbour, Rabih E Deshpande, Samir V McCubbin, Patrick E Seccomb, Robert A Welch, Phillip M Williams, Trevor Firth, David R Skowronski, Evan Lehmann, Margaret M Bilimoria, Shan L Gress, Joanna Wanner, Kevin W Cramer, Jr, Robert A |
description | In 2010 Colony Collapse Disorder (CCD), again devastated honey bee colonies in the USA, indicating that the problem is neither diminishing nor has it been resolved. Many CCD investigations, using sensitive genome-based methods, have found small RNA bee viruses and the microsporidia, Nosema apis and N. ceranae in healthy and collapsing colonies alike with no single pathogen firmly linked to honey bee losses.
We used Mass spectrometry-based proteomics (MSP) to identify and quantify thousands of proteins from healthy and collapsing bee colonies. MSP revealed two unreported RNA viruses in North American honey bees, Varroa destructor-1 virus and Kakugo virus, and identified an invertebrate iridescent virus (IIV) (Iridoviridae) associated with CCD colonies. Prevalence of IIV significantly discriminated among strong, failing, and collapsed colonies. In addition, bees in failing colonies contained not only IIV, but also Nosema. Co-occurrence of these microbes consistently marked CCD in (1) bees from commercial apiaries sampled across the U.S. in 2006-2007, (2) bees sequentially sampled as the disorder progressed in an observation hive colony in 2008, and (3) bees from a recurrence of CCD in Florida in 2009. The pathogen pairing was not observed in samples from colonies with no history of CCD, namely bees from Australia and a large, non-migratory beekeeping business in Montana. Laboratory cage trials with a strain of IIV type 6 and Nosema ceranae confirmed that co-infection with these two pathogens was more lethal to bees than either pathogen alone.
These findings implicate co-infection by IIV and Nosema with honey bee colony decline, giving credence to older research pointing to IIV, interacting with Nosema and mites, as probable cause of bee losses in the USA, Europe, and Asia. We next need to characterize the IIV and Nosema that we detected and develop management practices to reduce honey bee losses. |
doi_str_mv | 10.1371/journal.pone.0013181 |
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We used Mass spectrometry-based proteomics (MSP) to identify and quantify thousands of proteins from healthy and collapsing bee colonies. MSP revealed two unreported RNA viruses in North American honey bees, Varroa destructor-1 virus and Kakugo virus, and identified an invertebrate iridescent virus (IIV) (Iridoviridae) associated with CCD colonies. Prevalence of IIV significantly discriminated among strong, failing, and collapsed colonies. In addition, bees in failing colonies contained not only IIV, but also Nosema. Co-occurrence of these microbes consistently marked CCD in (1) bees from commercial apiaries sampled across the U.S. in 2006-2007, (2) bees sequentially sampled as the disorder progressed in an observation hive colony in 2008, and (3) bees from a recurrence of CCD in Florida in 2009. The pathogen pairing was not observed in samples from colonies with no history of CCD, namely bees from Australia and a large, non-migratory beekeeping business in Montana. Laboratory cage trials with a strain of IIV type 6 and Nosema ceranae confirmed that co-infection with these two pathogens was more lethal to bees than either pathogen alone.
These findings implicate co-infection by IIV and Nosema with honey bee colony decline, giving credence to older research pointing to IIV, interacting with Nosema and mites, as probable cause of bee losses in the USA, Europe, and Asia. We next need to characterize the IIV and Nosema that we detected and develop management practices to reduce honey bee losses.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0013181</identifier><identifier>PMID: 20949138</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Animals ; Anthonomus grandis ; Apiculture ; Apidae ; Apis cerana ; Apis mellifera ; Apoptosis ; Beekeeping ; Bees ; Bees - virology ; Biochemistry/Bioinformatics ; Biotechnology/Protein Chemistry and Proteomics ; Collapse ; Colonies ; Colony Collapse ; Concurrent infection ; Ecology/Environmental Microbiology ; Environmental quality ; European honeybee ; Gene expression ; Genomes ; Genomics ; Health aspects ; Honey ; Hymenoptera ; Infections ; Infectious Diseases/Fungal Infections ; Insect viruses ; Iridovirus - pathogenicity ; Mass Spectrometry ; Mass spectroscopy ; Microspora ; Microsporidia ; Microsporidia - pathogenicity ; Molecular biology ; Morphology ; Nosema ceranae ; Nosematidae ; Pathogens ; Peptides ; Plant pathology ; Plant sciences ; Proteins ; Proteomics ; Ribonucleic acid ; Risk assessment ; RNA ; RNA viruses ; Scientific imaging ; Studies ; Tipula ; United States ; Virology/Diagnosis ; Viruses</subject><ispartof>PloS one, 2010-10, Vol.5 (10), p.e13181</ispartof><rights>COPYRIGHT 2010 Public Library of Science</rights><rights>2010. This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. 2010</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c789t-fca792eab88f7fba30705f809a838063b37bda1410231adebf050b43c82f784a3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2950847/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2950847/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,729,782,786,866,887,2106,2932,23875,27933,27934,53800,53802</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20949138$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Leal, Walter S.</contributor><creatorcontrib>Bromenshenk, Jerry J</creatorcontrib><creatorcontrib>Henderson, Colin B</creatorcontrib><creatorcontrib>Wick, Charles H</creatorcontrib><creatorcontrib>Stanford, Michael F</creatorcontrib><creatorcontrib>Zulich, Alan W</creatorcontrib><creatorcontrib>Jabbour, Rabih E</creatorcontrib><creatorcontrib>Deshpande, Samir V</creatorcontrib><creatorcontrib>McCubbin, Patrick E</creatorcontrib><creatorcontrib>Seccomb, Robert A</creatorcontrib><creatorcontrib>Welch, Phillip M</creatorcontrib><creatorcontrib>Williams, Trevor</creatorcontrib><creatorcontrib>Firth, David R</creatorcontrib><creatorcontrib>Skowronski, Evan</creatorcontrib><creatorcontrib>Lehmann, Margaret M</creatorcontrib><creatorcontrib>Bilimoria, Shan L</creatorcontrib><creatorcontrib>Gress, Joanna</creatorcontrib><creatorcontrib>Wanner, Kevin W</creatorcontrib><creatorcontrib>Cramer, Jr, Robert A</creatorcontrib><title>Iridovirus and microsporidian linked to honey bee colony decline</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>In 2010 Colony Collapse Disorder (CCD), again devastated honey bee colonies in the USA, indicating that the problem is neither diminishing nor has it been resolved. Many CCD investigations, using sensitive genome-based methods, have found small RNA bee viruses and the microsporidia, Nosema apis and N. ceranae in healthy and collapsing colonies alike with no single pathogen firmly linked to honey bee losses.
We used Mass spectrometry-based proteomics (MSP) to identify and quantify thousands of proteins from healthy and collapsing bee colonies. MSP revealed two unreported RNA viruses in North American honey bees, Varroa destructor-1 virus and Kakugo virus, and identified an invertebrate iridescent virus (IIV) (Iridoviridae) associated with CCD colonies. Prevalence of IIV significantly discriminated among strong, failing, and collapsed colonies. In addition, bees in failing colonies contained not only IIV, but also Nosema. Co-occurrence of these microbes consistently marked CCD in (1) bees from commercial apiaries sampled across the U.S. in 2006-2007, (2) bees sequentially sampled as the disorder progressed in an observation hive colony in 2008, and (3) bees from a recurrence of CCD in Florida in 2009. The pathogen pairing was not observed in samples from colonies with no history of CCD, namely bees from Australia and a large, non-migratory beekeeping business in Montana. Laboratory cage trials with a strain of IIV type 6 and Nosema ceranae confirmed that co-infection with these two pathogens was more lethal to bees than either pathogen alone.
These findings implicate co-infection by IIV and Nosema with honey bee colony decline, giving credence to older research pointing to IIV, interacting with Nosema and mites, as probable cause of bee losses in the USA, Europe, and Asia. We next need to characterize the IIV and Nosema that we detected and develop management practices to reduce honey bee losses.</description><subject>Animals</subject><subject>Anthonomus grandis</subject><subject>Apiculture</subject><subject>Apidae</subject><subject>Apis cerana</subject><subject>Apis mellifera</subject><subject>Apoptosis</subject><subject>Beekeeping</subject><subject>Bees</subject><subject>Bees - virology</subject><subject>Biochemistry/Bioinformatics</subject><subject>Biotechnology/Protein Chemistry and Proteomics</subject><subject>Collapse</subject><subject>Colonies</subject><subject>Colony Collapse</subject><subject>Concurrent infection</subject><subject>Ecology/Environmental Microbiology</subject><subject>Environmental quality</subject><subject>European honeybee</subject><subject>Gene expression</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Health aspects</subject><subject>Honey</subject><subject>Hymenoptera</subject><subject>Infections</subject><subject>Infectious Diseases/Fungal Infections</subject><subject>Insect viruses</subject><subject>Iridovirus - pathogenicity</subject><subject>Mass Spectrometry</subject><subject>Mass spectroscopy</subject><subject>Microspora</subject><subject>Microsporidia</subject><subject>Microsporidia - pathogenicity</subject><subject>Molecular biology</subject><subject>Morphology</subject><subject>Nosema ceranae</subject><subject>Nosematidae</subject><subject>Pathogens</subject><subject>Peptides</subject><subject>Plant pathology</subject><subject>Plant sciences</subject><subject>Proteins</subject><subject>Proteomics</subject><subject>Ribonucleic acid</subject><subject>Risk assessment</subject><subject>RNA</subject><subject>RNA viruses</subject><subject>Scientific imaging</subject><subject>Studies</subject><subject>Tipula</subject><subject>United 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Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bromenshenk, Jerry J</au><au>Henderson, Colin B</au><au>Wick, Charles H</au><au>Stanford, Michael F</au><au>Zulich, Alan W</au><au>Jabbour, Rabih E</au><au>Deshpande, Samir V</au><au>McCubbin, Patrick E</au><au>Seccomb, Robert A</au><au>Welch, Phillip M</au><au>Williams, Trevor</au><au>Firth, David R</au><au>Skowronski, Evan</au><au>Lehmann, Margaret M</au><au>Bilimoria, Shan L</au><au>Gress, Joanna</au><au>Wanner, Kevin W</au><au>Cramer, Jr, Robert A</au><au>Leal, Walter S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Iridovirus and microsporidian linked to honey bee colony decline</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2010-10-06</date><risdate>2010</risdate><volume>5</volume><issue>10</issue><spage>e13181</spage><pages>e13181-</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>In 2010 Colony Collapse Disorder (CCD), again devastated honey bee colonies in the USA, indicating that the problem is neither diminishing nor has it been resolved. Many CCD investigations, using sensitive genome-based methods, have found small RNA bee viruses and the microsporidia, Nosema apis and N. ceranae in healthy and collapsing colonies alike with no single pathogen firmly linked to honey bee losses.
We used Mass spectrometry-based proteomics (MSP) to identify and quantify thousands of proteins from healthy and collapsing bee colonies. MSP revealed two unreported RNA viruses in North American honey bees, Varroa destructor-1 virus and Kakugo virus, and identified an invertebrate iridescent virus (IIV) (Iridoviridae) associated with CCD colonies. Prevalence of IIV significantly discriminated among strong, failing, and collapsed colonies. In addition, bees in failing colonies contained not only IIV, but also Nosema. Co-occurrence of these microbes consistently marked CCD in (1) bees from commercial apiaries sampled across the U.S. in 2006-2007, (2) bees sequentially sampled as the disorder progressed in an observation hive colony in 2008, and (3) bees from a recurrence of CCD in Florida in 2009. The pathogen pairing was not observed in samples from colonies with no history of CCD, namely bees from Australia and a large, non-migratory beekeeping business in Montana. Laboratory cage trials with a strain of IIV type 6 and Nosema ceranae confirmed that co-infection with these two pathogens was more lethal to bees than either pathogen alone.
These findings implicate co-infection by IIV and Nosema with honey bee colony decline, giving credence to older research pointing to IIV, interacting with Nosema and mites, as probable cause of bee losses in the USA, Europe, and Asia. We next need to characterize the IIV and Nosema that we detected and develop management practices to reduce honey bee losses.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>20949138</pmid><doi>10.1371/journal.pone.0013181</doi><tpages>e13181</tpages><oa>free_for_read</oa></addata></record> |
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identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2010-10, Vol.5 (10), p.e13181 |
issn | 1932-6203 1932-6203 |
language | eng |
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source | MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Public Library of Science (PLoS) Journals Open Access; PubMed Central; Free Full-Text Journals in Chemistry |
subjects | Animals Anthonomus grandis Apiculture Apidae Apis cerana Apis mellifera Apoptosis Beekeeping Bees Bees - virology Biochemistry/Bioinformatics Biotechnology/Protein Chemistry and Proteomics Collapse Colonies Colony Collapse Concurrent infection Ecology/Environmental Microbiology Environmental quality European honeybee Gene expression Genomes Genomics Health aspects Honey Hymenoptera Infections Infectious Diseases/Fungal Infections Insect viruses Iridovirus - pathogenicity Mass Spectrometry Mass spectroscopy Microspora Microsporidia Microsporidia - pathogenicity Molecular biology Morphology Nosema ceranae Nosematidae Pathogens Peptides Plant pathology Plant sciences Proteins Proteomics Ribonucleic acid Risk assessment RNA RNA viruses Scientific imaging Studies Tipula United States Virology/Diagnosis Viruses |
title | Iridovirus and microsporidian linked to honey bee colony decline |
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