A novel method for the detection and diagnosis of virus infections in honey bees

被引:11
作者
Huang, Shaokang [1 ,2 ]
Li, Jianghong [2 ]
Zhang, Yi [1 ,3 ]
Li, Zhiguo [2 ]
Evans, Jay D. [1 ]
Rose, Robyn [4 ]
Gilligan, Todd M. [5 ]
LeBrun, Anne [5 ]
He, Nan [2 ]
Zheng, Teng [6 ]
Zhang, Tiyin [6 ]
Hamilton, Michele [1 ]
Chen, Yan Ping [1 ]
机构
[1] USDA ARS, Bee Res Lab, Beltsville, MD 20705 USA
[2] Fujian Agr & Forestry Univ, Coll Anim Sci Bee Sci, Fuzhou 350002, Fujian, Peoples R China
[3] Guangdong Acad Sci, Inst Zool, Guangdong Key Lab Anim Conservat & Resource Utili, Guangdong Publ Lab Wild Anim Conservat & Utilizat, Guangzhou 510260, Peoples R China
[4] Farm Prod & Conservat, 1400 Independence Ave SW, Washington, DC 20250 USA
[5] US Anim & Plant Hlth Inspect Serv, USDA, Natl Program Manager Honey Bee Hlth, Riverdale, MD 20737 USA
[6] Tech Ctr Fuzhou Customs, Fuzhou 350000, Fujian, Peoples R China
关键词
Honey bee; Viruses; Immune peptides; Detection; Diagnosis; Hemolymph; Lifespan; DEFORMED WING VIRUS; COMPLETE GENOME SEQUENCE; PARALYSIS VIRUS; INNATE IMMUNITY; PREVALENCE;
D O I
10.1016/j.jviromet.2021.114163
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In terms of infectious diseases caused by a variety of microorganisms, the ability to promptly and accurately identify the causative agents is the first step on the path to all types of effective management of such infections. Among the various factors that are affecting global bee health, viruses have often been linked to honey bee colony losses and they pose a serious threat to the fraction of agriculture that depends on the service of polli-nators. Over the past few decades, PCR-based molecular methods have provided powerful tools for rapid, spe-cific, and sensitive detection and the quantification of difficult-to-grow pathogenic microorganisms such as viruses in honey bees. However, PCR-based methods require nucleic acid extraction and purification, which can be quite laborious and time-consuming and they involve the use of organic solvents and chaotropic agents like phenol and chloroform which are volatile and highly toxic. In response, we developed a novel and non-sacrificial method for detecting viral infections in honey bees. As little as 1 mu l of hemolymph was collected from adult workers, larvae, and queens of bee colonies by puncturing the soft inter-tergal integument between the second and third dorsal tergum with a fine glass capillary. The hemolymph was then diluted and subjected to RT-PCR analysis directly. The puncture wound caused by the glass capillary was found to heal automatically and rapidly without any trouble and the lifespan of the experimental workers remained unaffected. Using this method, we detected multiple viruses including Deformed wing virus (DWV), Black queen cell virus (BQCV), and Sacbrood virus (SBV) in infected bees. Furthermore, expressed tran-scripts that indicate the induction of innate immune response to the virus infections were also detected in the hemolymph of infected bees. The simplicity and cost-effectiveness of this innovative approach will allow it to be a valuable, time-saving, safer, and more environmentally friendly contribution to bee disease management programs.
引用
收藏
页数:7
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