Response of the honey bee (Apis mellifera) proteome to Israeli acute paralysis virus (IAPV) infection

被引:10
|
作者
Michaud, Sarah [1 ]
Boncristiani, Humberto F., Jr. [2 ]
Gouw, Joost W. [1 ]
Strand, Micheline K. [3 ]
Pettis, Jeffrey [4 ]
Rueppell, Olav [2 ]
Foster, Leonard J. [1 ]
机构
[1] Univ British Columbia, Ctr High Throughput Biol, Dept Biochem & Mol Biol, Vancouver, BC V6T 1Z4, Canada
[2] Univ N Carolina, Dept Biol, Greensboro, NC 27403 USA
[3] US Army, Res Off, Div Life Sci, Res Triangle Pk, NC 27709 USA
[4] USDA ARS, Bee Res Lab, Beltsville, MD 20705 USA
基金
加拿大健康研究院; 加拿大创新基金会; 美国食品与农业研究所; 加拿大自然科学与工程研究理事会;
关键词
Apis mellifera; Israeli acute paralysis virus; Dicistroviridae; mass spectrometry; proteomics; QUANTITATIVE PROTEOMICS; VARROA-DESTRUCTOR; IMMUNE; PATHOGEN; REVEALS; HOST;
D O I
10.1139/cjz-2014-0181
中图分类号
Q95 [动物学];
学科分类号
071002 ;
摘要
Recent declines in honey bee (Apis mellifera L., 1758) populations worldwide have spurred significant research into the impact of pathogens on colony health. The role of the Israeli acute paralysis virus (IAPV) on hive mortality has become of particular concern since being correlated with colony losses. However, the molecular interactions between IAPV and its host remain largely unknown. To investigate changes in host protein expression during IAPV infection, mass-spectrometry-based quantitative proteomics was used to compare IAPV-infected and healthy pupae. Proteins whose expression levels changed significantly during infection were identified and functional analysis was performed to determine host systems and pathways perturbed by IAPV infection. Among the A. mellifera proteins most affected by IAPV, those involving translation and the ubiquitin-proteasome pathway were most highly enriched and future investigation of these pathways will be useful in identifying host proteins required for infection. This analysis represents an important first step towards understanding the honey bee host response to IAPV infection through the systems-level analysis of protein expression.
引用
收藏
页码:711 / 720
页数:10
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