PCR diagnostic methods for Ascosphaera infections in bees

被引:56
作者
James, RR [1 ]
Skinner, JS
机构
[1] USDA ARS, Bee Biol & Systemat Lab, Logan, UT 84321 USA
[2] Oregon State Univ, Dept Hort, Corvallis, OR 97331 USA
关键词
Apis mellifera; Ascosphaera; bees; chalkbrood; disease diagnosis; Megachile rotundata; PCR;
D O I
10.1016/j.jip.2005.08.004
中图分类号
Q95 [动物学];
学科分类号
071002 ;
摘要
Fungi in the genus Ascosphaera are the causative agents of chalkbrood, a major disease affecting bee larval viability. Identification of individual Ascosphaera species based on morphological features has been difficult due to a lack of distinguishing characteristics. Most identifications are based on the size and shape of the ascomata, spore balls and conidia. Unfortunately, much overlap occurs in the size of these structures, and some Ascosphaera species will not produce sexual structures in vitro. We report a quick and reliable diagnostic method for identifying Ascosphaera infections in Megachile bees (leafcutting bees) using PCR markers that employ genus-specific primers for Ascosphaera, and species-specific primers for species known to be associated with Megachile spp. Using these methods, species identifications can be performed directly on bees, including asymptornatic individuals. Furthermore, the PCR markers can detect co-infections of multiple Ascosphaera species in a single host. We also identified a marker for Ascosphaera apis, the predominant cause of chalkbrood in Apis inellifera, the honey bee. Our diagnostic methods eliminate the need for culturing samples, and could be used to process a large number of field collected bee larvae. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:98 / 103
页数:6
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