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Protein & Peptide Letters

Editor-in-Chief

ISSN (Print): 0929-8665
ISSN (Online): 1875-5305

Research Article

Plasmodium falciparum Heat Shock Protein 70 Lacks Immune Modulatory Activity

Author(s): Ofentse Jacob Pooe, Gabriele Köllisch, Holger Heine and Addmore Shonhai*

Volume 24, Issue 6, 2017

Page: [503 - 510] Pages: 8

DOI: 10.2174/0929866524666170214141909

Price: $65

Abstract

Background: Heat shock protein 70 (Hsp70) family are conserved molecules that constitute a major part of the cell’s protein folding machinery. The role of Hsp70s of parasitic origin in host cell immune modulation has remained contentious. This is largely due to the fact that several studies implicating Hsp70 in immune modulation rely on the use of recombinant protein derived from bacteria which is often fraught with lipopolysaccharide (LPS) contamination. For this reason, there is need to clarify the role of parasite Hsp70 in modulating host immune cells. Objective: The current study sought to investigate the role of Plasmodium falciparum Hsp70 (PfHsp70) in immune modulation.

Method: We expressed recombinant PfHsp70 using three bacterial expression hosts: E. coli XL1 Blue, E. coli ClearColi BL21 and Brevibacillus choshinensis, respectively. We further investigated the immunostimulatory capability of PfHsp70 by monitoring cytokine production by murine immune cells cultured in the presence of the protein.

Results: Recombinant PfHsp70 produced using E. coli XL1 Blue expression host induced IL6 and IL8 cytokines. On the other hand, PfHsp70 produced in E. coli ClearColi and B. choshinensis expression systems was associated with no detectable traces of LPS and exhibited no immunomodulatory activity.

Conclusion: Our findings demonstrate that PfHsp70 does not possess immunomodulatory function. Furthermore, our study further confirm E. coli ClearColi and B. choshinensis as appropriate expression systems for the production of LPS-free recombinant protein.

Keywords: Plasmodium falciparum Hsp70, recombinant protein, immune modulation, lipopolysaccharide, TLR2, TLR4.

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