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Clinical proteomic analysis of scrub typhus infection

Authors :
Hyun Seok Song
Sangyeop Lee
Ha Young Lee
Chi-Won Choi
Sangmi Jun
Chang-Seop Lee
Gun-Hwa Kim
Seung Il Kim
Sung Ho Yun
Edmond Changkyun Park
Source :
Clinical Proteomics, Clinical Proteomics, Vol 15, Iss 1, Pp 1-8 (2018)
Publication Year :
2017

Abstract

Background Scrub typhus is an acute and febrile infectious disease caused by the Gram-negative α-proteobacterium Orientia tsutsugamushi from the family Rickettsiaceae that is widely distributed in Northern, Southern and Eastern Asia. In the present study, we analysed the serum proteome of scrub typhus patients to investigate specific clinical protein patterns in an attempt to explain pathophysiology and discover potential biomarkers of infection. Methods Serum samples were collected from three patients (before and after treatment with antibiotics) and three healthy subjects. One-dimensional sodium dodecyl sulphate–polyacrylamide gel electrophoresis followed by liquid chromatography-tandem mass spectrometry was performed to identify differentially abundant proteins using quantitative proteomic approaches. Bioinformatic analysis was then performed using Ingenuity Pathway Analysis. Results Proteomic analysis identified 236 serum proteins, of which 32 were differentially expressed in normal subjects, naive scrub typhus patients and patients treated with antibiotics. Comparative bioinformatic analysis of the identified proteins revealed up-regulation of proteins involved in immune responses, especially complement system, following infection with O. tsutsugamushi, and normal expression was largely rescued by antibiotic treatment. Conclusions This is the first proteomic study of clinical serum samples from scrub typhus patients. Proteomic analysis identified changes in protein expression upon infection with O. tsutsugamushi and following antibiotic treatment. Our results provide valuable information for further investigation of scrub typhus therapy and diagnosis. Electronic supplementary material The online version of this article (10.1186/s12014-018-9181-5) contains supplementary material, which is available to authorized users.

Details

ISSN :
15426416
Volume :
15
Database :
OpenAIRE
Journal :
Clinical proteomics
Accession number :
edsair.doi.dedup.....97c8ab81b78f84a7f4b1b4143e30065f