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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Published inPloS one Vol. 5; no. 10; p. e13181
Main Authors 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
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 06.10.2010
Public Library of Science (PLoS)
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Summary: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.
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Conceived and designed the experiments: JJB CBH CHW RAC. Performed the experiments: JJB REJ SVD PEM MML JCG RAC. Analyzed the data: JJB CBH PEM PMW RAC. Contributed reagents/materials/analysis tools: SLB KWW RAC. Wrote the paper: JJB CBH CHW MFS AWZ REJ SVD PEM RAS TW DRF SLB RAC. Coordinated overall research team: JJB. Conducted statistical analyses: CBH. Coordinated Army (ECBC) research: CHW. Directed proteomics research: MFS. Organized Army research contribution: AWZ. Conducted proteomics analysis: REJ SVD. Analyzed results using bioinformatics: REJ SVD. Contributed Information Technology guidance: RAS. Set up and annotated proteomics data base: PMW. Consulted on all aspects of Iridoviruses: TW. Coordinated efforts with US Army: DRF. Guided epidemiology approach: EWS. Directed graduate student research: KWW.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0013181