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Protein regulation strategies of the mouse spleen in response to Babesia microti infection

BACKGROUND: Babesia is a protozoan parasite that infects red blood cells in some vertebrates. Some species of Babesia can induce zoonoses and cause considerable harm. As the largest immune organ in mammals, the spleen plays an important role in defending against Babesia infection. When infected with...

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Autores principales: Xue, Xiaomin, Ren, Shuguang, Yang, Xiaohong, Masoudi, Abolfazl, Hu, Yuhong, Wang, Xiaoshuang, Li, Hongxia, Zhang, Xiaojing, Wang, Minjing, Wang, Hui, Liu, Jingze
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7814643/
https://www.ncbi.nlm.nih.gov/pubmed/33468223
http://dx.doi.org/10.1186/s13071-020-04574-5
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author Xue, Xiaomin
Ren, Shuguang
Yang, Xiaohong
Masoudi, Abolfazl
Hu, Yuhong
Wang, Xiaoshuang
Li, Hongxia
Zhang, Xiaojing
Wang, Minjing
Wang, Hui
Liu, Jingze
author_facet Xue, Xiaomin
Ren, Shuguang
Yang, Xiaohong
Masoudi, Abolfazl
Hu, Yuhong
Wang, Xiaoshuang
Li, Hongxia
Zhang, Xiaojing
Wang, Minjing
Wang, Hui
Liu, Jingze
author_sort Xue, Xiaomin
collection PubMed
description BACKGROUND: Babesia is a protozoan parasite that infects red blood cells in some vertebrates. Some species of Babesia can induce zoonoses and cause considerable harm. As the largest immune organ in mammals, the spleen plays an important role in defending against Babesia infection. When infected with Babesia, the spleen is seriously injured but still actively initiates immunomodulatory responses. METHODS: To explore the molecular mechanisms underlying the immune regulation and self-repair of the spleen in response to infection, this study used data-independent acquisition (DIA) quantitative proteomics to analyse changes in expression levels of global proteins and in phosphorylation modification in spleen tissue after Babesia microti infection in mice. RESULTS: After mice were infected with B. microti, their spleens were seriously damaged. Using bioinformatics methods to analyse dynamic changes in a large number of proteins, we found that the spleen still initiated immune responses to combat the infection, with immune-related proteins playing an important role, including cathepsin D (CTSD), interferon-induced protein 44 (IFI44), interleukin-2 enhancer-binding factor 2 (ILF2), interleukin enhancer-binding factor 3 (ILF3) and signal transducer and activator of transcription 5A (STAT5A). In addition, some proteins related to iron metabolism were also involved in the repair of the spleen after B. microti infection, including serotransferrin, lactoferrin, transferrin receptor protein 1 (TfR1) and glutamate-cysteine ligase (GCL). At the same time, the expression and phosphorylation of proteins related to the growth and development of the spleen also changed, including protein kinase C-δ (PKC-δ), mitogen-activated protein kinase (MAPK) 3/1, growth factor receptor-bound protein 2 (Grb2) and P21-activated kinase 2 (PAK2). CONCLUSIONS: Immune-related proteins, iron metabolism-related proteins and growth and development-related proteins play an important role in the regulation of spleen injury and maintenance of homeostasis. This study provides an important basis for the diagnosis and treatment of babesiosis. [Image: see text]
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spelling pubmed-78146432021-01-19 Protein regulation strategies of the mouse spleen in response to Babesia microti infection Xue, Xiaomin Ren, Shuguang Yang, Xiaohong Masoudi, Abolfazl Hu, Yuhong Wang, Xiaoshuang Li, Hongxia Zhang, Xiaojing Wang, Minjing Wang, Hui Liu, Jingze Parasit Vectors Research BACKGROUND: Babesia is a protozoan parasite that infects red blood cells in some vertebrates. Some species of Babesia can induce zoonoses and cause considerable harm. As the largest immune organ in mammals, the spleen plays an important role in defending against Babesia infection. When infected with Babesia, the spleen is seriously injured but still actively initiates immunomodulatory responses. METHODS: To explore the molecular mechanisms underlying the immune regulation and self-repair of the spleen in response to infection, this study used data-independent acquisition (DIA) quantitative proteomics to analyse changes in expression levels of global proteins and in phosphorylation modification in spleen tissue after Babesia microti infection in mice. RESULTS: After mice were infected with B. microti, their spleens were seriously damaged. Using bioinformatics methods to analyse dynamic changes in a large number of proteins, we found that the spleen still initiated immune responses to combat the infection, with immune-related proteins playing an important role, including cathepsin D (CTSD), interferon-induced protein 44 (IFI44), interleukin-2 enhancer-binding factor 2 (ILF2), interleukin enhancer-binding factor 3 (ILF3) and signal transducer and activator of transcription 5A (STAT5A). In addition, some proteins related to iron metabolism were also involved in the repair of the spleen after B. microti infection, including serotransferrin, lactoferrin, transferrin receptor protein 1 (TfR1) and glutamate-cysteine ligase (GCL). At the same time, the expression and phosphorylation of proteins related to the growth and development of the spleen also changed, including protein kinase C-δ (PKC-δ), mitogen-activated protein kinase (MAPK) 3/1, growth factor receptor-bound protein 2 (Grb2) and P21-activated kinase 2 (PAK2). CONCLUSIONS: Immune-related proteins, iron metabolism-related proteins and growth and development-related proteins play an important role in the regulation of spleen injury and maintenance of homeostasis. This study provides an important basis for the diagnosis and treatment of babesiosis. [Image: see text] BioMed Central 2021-01-19 /pmc/articles/PMC7814643/ /pubmed/33468223 http://dx.doi.org/10.1186/s13071-020-04574-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Xue, Xiaomin
Ren, Shuguang
Yang, Xiaohong
Masoudi, Abolfazl
Hu, Yuhong
Wang, Xiaoshuang
Li, Hongxia
Zhang, Xiaojing
Wang, Minjing
Wang, Hui
Liu, Jingze
Protein regulation strategies of the mouse spleen in response to Babesia microti infection
title Protein regulation strategies of the mouse spleen in response to Babesia microti infection
title_full Protein regulation strategies of the mouse spleen in response to Babesia microti infection
title_fullStr Protein regulation strategies of the mouse spleen in response to Babesia microti infection
title_full_unstemmed Protein regulation strategies of the mouse spleen in response to Babesia microti infection
title_short Protein regulation strategies of the mouse spleen in response to Babesia microti infection
title_sort protein regulation strategies of the mouse spleen in response to babesia microti infection
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7814643/
https://www.ncbi.nlm.nih.gov/pubmed/33468223
http://dx.doi.org/10.1186/s13071-020-04574-5
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