Back to Search Start Over

Label-free LC-MS/MS proteomic analysis of the hemolymph of silkworm larvae infected with Beauveria bassiana

Authors :
Kun Gao
Chengxiang Hou
Ping Xu
Dingding Lü
Xijie Guo
Source :
Journal of Invertebrate Pathology. 166:107227
Publication Year :
2019
Publisher :
Elsevier BV, 2019.

Abstract

Beauveria bassiana, a pathogen of the economically important silkworm (Bombyx mori), causes serious losses in the sericulture industry; however, the mechanisms underlying B. bassiana infection and the silkworm response are not fully understood. To obtain new insights into the interaction between B. bassiana and its host, hemolymph samples from fifth instar silkworm larvae infected with B. bassiana were analyzed at 36-h post-inoculation using a label-free LC-MS/MS proteomic technique. In total, 671 proteins were identified in the hemolymph, including 87 differentially expressed proteins, 42 up-regulated and 45 down-regulated in infected larvae. Six were detected only in infected larvae, and five were detected only in uninfected larvae. Based on GO annotations, 48 of the differentially expressed proteins were involved in molecular functions, 42 were involved in biological processes, and 39 were involved in cell components. A KEGG pathway analysis indicated that these differentially expressed proteins participate in 85 signal transduction pathways, including the amoebiasis, MAPK signaling, Hippo signaling, Toll and Imd signaling, and lysosome pathways. The silkworm hemolymph is the main site for B. bassiana replication. We identified differentially expressed proteins involved in the regulation of the host response to B. bassiana infection, providing important experimental data for the identification of key factors contributing to the interaction between the pathogenic fungus and its host.

Details

ISSN :
00222011
Volume :
166
Database :
OpenAIRE
Journal :
Journal of Invertebrate Pathology
Accession number :
edsair.doi.dedup.....325b990c395622ee0ba159a72c3d9d3f
Full Text :
https://doi.org/10.1016/j.jip.2019.107227