Please use this identifier to cite or link to this item: http://www.repositorio.ufop.br/handle/123456789/11192
Title: Using label-free shotgun proteomics and systems biology to explore the complex immune dynamic of splenomegaly during acute schistosomiasis mansoni.
Authors: Cosenza Contreras, Miguel de Jesus
metadata.dc.contributor.advisor: Borges, William de Castro
Keywords: Schistosoma mansoni
Baço
Proteômica
Helmintíase
Inflamação
Issue Date: 2019
metadata.dc.contributor.referee: Magalhães, Lizandra Guidi
Vieira, Paula Melo de Abreu
Borges, William de Castro
Citation: COSENZA CONTRERAS, Miguel de Jesus. Using label-free shotgun proteomics and systems biology to explore the complex immune dynamic of splenomegaly during acute schistosomiasis mansoni. 2019. 92 f. Dissertação (Mestrado em Ciências Biológicas) - Núcleo de Pesquisas em Ciências Biológicas, Universidade Federal de Ouro Preto, Ouro Preto, 2018.
Abstract: Schistosomiasis is a neglected tropical disease that affect millions of people worldwide and it is caused by the infection with parasites of the genus Schistosoma. When caused by S. mansoni, schistosomiasis is characterized by the formation of liver granuloma, due to the presence of eggs trapped in the tissue, and the concurrent development of liver fibrosis that could lead to life lasting chronic complications. In this context, the spleen has been demonstrated to be a very responsible organ, with splenomegaly being one of the major hallmarks of schistosomiasis. Nevertheless, it has received little attention in terms of which immune and molecular mechanisms could be governing this host-parasite interplay and the development of this condition. In this study, we used mass spectrometry-based shotgun proteomics combined with systems biology tools to explore the complex molecular dynamic in the spleen at the acute phase of inflammation in a mice model of infection by S. mansoni. More than fifty hundred proteins were identified in the spleen proteome, and 325 of them were differentially expressed between infected and control individuals. Functional enrichment analyses showed that most differentially expressed proteins were categorized within pathways of innate and adaptive immunity, DNA replication, vesicle transport and catabolic metabolism. There was a significant enrichment of pathways associated with antigen processing and presentation, with an increased expression of MHC class II proteins and the negative regulation of cysteine and serine proteases. Indications of metabolic reprogramming were also found, with the downregulation of a set of proteins related to mitochondrial metabolism. It was also possible to establish a link between the variation in protein expression in the spleens with variations in subpopulations of spleen cells as revealed by flow cytometry analyses. These suggested the increased proportion of MHC-II-presenting macrophages with the higher abundance of MHC-II proteins measured by mass spectrometry. With this, we presented the first proteomic shotgun analysis of the spleen during schistosomiasis, offering new insights on the understanding of immune mechanisms associated with the establishment of the disease and other processes of immune modulation related to the host-parasite interplay.
Description: Programa de Pós-Graduação em Ciências Biológicas. Núcleo de Pesquisas em Ciências Biológicas, Pró-Reitoria de Pesquisa de Pós Graduação, Universidade Federal de Ouro Preto.
URI: http://www.repositorio.ufop.br/handle/123456789/11192
metadata.dc.rights.license: Autorização concedida ao Repositório Institucional da UFOP pelo(a) autor(a) em 03/05/2019 com as seguintes condições: disponível sob Licença Creative Commons 4.0 que permite copiar, distribuir e transmitir o trabalho desde que sejam citados o autor e o licenciante. Não permite o uso para fins.
Appears in Collections:PPCBIOL - Mestrado (Dissertações)

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