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Upregulation of Atg5 and AIF gene expression in synchronization with programmed cellular death events in integumental epithelium of Bombyx mori induced by a dipteran parasitoid infection

Published online by Cambridge University Press:  23 September 2014

J. Anitha
Affiliation:
Proteomics Division, Seribiotech Research Laboratory, Central Silk Board, CSB-Kodathi Campus, Carmelram. P.O., Bangalore 560035, Karnataka, India
A.R. Pradeep*
Affiliation:
Proteomics Division, Seribiotech Research Laboratory, Central Silk Board, CSB-Kodathi Campus, Carmelram. P.O., Bangalore 560035, Karnataka, India
V. Sivaprasad
Affiliation:
Proteomics Division, Seribiotech Research Laboratory, Central Silk Board, CSB-Kodathi Campus, Carmelram. P.O., Bangalore 560035, Karnataka, India
*
*Author for correspondence Phone: 91+80+28440651 Fax: 91+80+28439597 E-mail: [email protected]

Abstract

Infection of the commercially important silkworm, Bombyx mori by a tachnid parasitoid, Exorista bombycis induced activation of genes and cellular responses associated with apoptosis in integumental epithelial cells. Composite cellular profile showed initial autophagy, intermediate endoplasmic reticulum degranulation and deformed nucleus as well as later DNA fragmentation indicating apoptosis. Two cell death-associated proteins, autophagy 5-like (Atg5L) and apoptosis-inducing factor (AIF), in addition to caspase, are identified from the infected integumental epithelium through mass spectrometric analysis. Genes encoding these proteins showed age-dependent activation after the infection as revealed by quantitative expression analysis. Atg5 showed early upregulation in association with signs of autophagy whereas AIF showed late upregulation in association with DNA condensation and fragmentation. Expression of AIF showed negative correlation with that of Atg5 after the infection. On the other hand, in control, caspase expression showed positive correlation with AIF expression indicative of regulated expression in normal larval epithelium, which was absent after infection. Activation of Atg5, AIF and caspase genes in close association with different cell death events revealed the synchronized differential expression of apoptosis-associated genes in response to the macroparasitism. Enhanced expression of Atg5, AIF and caspase genes coupled with the appearance of cell death symptoms indicate parasitism-induced activation of genetic machinery to modulate cell death events in the epithelium, which was hither to unknown in invertebrate systems.

Type
Research Papers
Copyright
Copyright © Cambridge University Press 2014 

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