Abstract

BackgroundThe immune system is a key biological system present in vertebrates. Exposure to pathogens elicits various defensive immune mechanisms that protect the host from potential threats and harmful substances derived from pathogens such as parasites, bacteria, and viruses. The complex immune system of humans and many other vertebrates can be divided into two major categories: the innate and the adaptive immune systems. At present, analysis of the complex interactions between the two subsystems that regulate host defense and inflammatory responses remains challenging.ResultsBased on time-course microarray data following primary and secondary infection of zebrafish by Candida albicans, we constructed two intracellular protein–protein interaction (PPI) networks for primary and secondary responses of the host. 57 proteins and 341 PPIs were identified for primary infection while 90 proteins and 385 PPIs were identified for secondary infection. There were 20 proteins in common while 37 and 70 proteins specific to primary and secondary infection. By inspecting the hub proteins of each network and comparing significant changes in the number of linkages between the two PPI networks, we identified TGF-β signaling and apoptosis as two of the main functional modules involved in primary and secondary infection.Smad7, a member of the inhibitor SMADs, was identified to be a key protein in TGF-β signaling involved in secondary infection only. Indeed, the Smad7-dependent feedback system is related to the TGF-β signaling pathway and the immune response, suggesting that Smad7 may be an important regulator of innate and adaptive immune responses in zebrafish. Furthermore, we found that apoptosis was differentially involved in the two infection phases; more specifically, whereas apoptosis was promoted in response to primary infection, it was inhibited during secondary infection.ConclusionsOur initial in silico analyses pave the way for further investigation into the interesting roles played by the TGF-β signaling pathway and apoptosis in innate and adaptive immunity in zebrafish. Such insights could lead to therapeutic advances and improved drug design in the continual battle against infectious diseases.Electronic supplementary materialThe online version of this article (doi:10.1186/s12918-014-0116-0) contains supplementary material, which is available to authorized users.

Highlights

  • The immune system is a key biological system present in vertebrates

  • Strategy The method used to construct the dynamic intracellular protein–protein interaction (PPI) networks was divided into three key steps: (i) data selection and preprocessing, (ii) selection of the target protein pool, and (iii) construction of the refined PPI networks for zebrafish

  • The same procedure was applied to construct the zebrafish intracellular PPI network for primary and secondary infection on the basis of time-course microarray data obtained from the corresponding experiments

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Summary

Introduction

The immune system is a key biological system present in vertebrates. Exposure to pathogens elicits various defensive immune mechanisms that protect the host from potential threats and harmful substances derived from pathogens such as parasites, bacteria, and viruses. The immune system can generally be divided into two main categories: the innate immune system and the adaptive immune system [1] The former is responsible for nonspecific immune responses and serves as the front line for rapid defense against foreign invading pathogens [2]. The use of zebrafish to study immunity against infectious disease, including those due to bacterial or viral infections, is rapidly increasing [4,5]. Zebrafish possesses both innate and adaptive immune systems, making it a suitable model organism for investigating immune mechanisms in vertebrates and mammals [4]

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