Proteomic Analysis of Exudates from Chronic Ulcer of Diabetic Foot Treated with Scorpion Antimicrobial Peptide

Author:

Tan Zhixiang1ORCID,Yu Zhiguo2,Xu Xiaobo3,Meng Lanxia4ORCID,Yu Mosheng1ORCID,Tao Rui1ORCID,Wu Yingliang3ORCID,Zhu Zhanyong1ORCID

Affiliation:

1. Department of Plastic Surgery, Renmin Hospital of Wuhan University, Wuhan, Hubei, China

2. Department of Emergency, Central People’s Liberation Army, Wuhan, Hubei 430060, China

3. State Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan, Hubei 430060, China

4. Department of Neurology, Renmin Hospital of Wuhan University, Wuhan, Hubei 430060, China

Abstract

Scorpion peptides have good therapeutic effect on chronic ulcer of diabetic foot, but the related pharmacological mechanism has remained unclear. The different proteins and bacteria present in ulcer exudates from chronic diabetic foot patients, treated with scorpion antimicrobial peptide at different stages, were analyzed using isobaric tags for quantification-labeled proteomics and bacteriological methods. According to the mass spectrometry data, a total of 1865 proteins were identified qualitatively, and the number of the different proteins was 130 (mid/early), 401 (late/early), and 310 (mid, late/early). In addition, functional annotation, cluster analysis of effects and the analysis of signal pathway, transcription regulation, and protein-protein interaction network were carried out. The results showed that the biochemical changes of wound microenvironment during the treatment involved activated biological functions such as protein synthesis, cell proliferation, differentiation, migration, movement, and survival. Inhibited biological functions such as cell death, inflammatory response, immune diseases, and bacterial growth were also involved. Bacteriological analysis showed that Burkholderia cepacia was the main bacteria in the early and middle stage of ulcer exudate and Staphylococcus epidermidis in the late stage. This study provides basic data for further elucidation of the molecular mechanism of diabetic foot.

Funder

Wuhan University

Publisher

Hindawi Limited

Subject

Cell Biology,Immunology

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