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Anaplasma phagocytophilum Ats-1 enhances exosome secretion through Syntenin-1

Anaplasma phagocytophilum is an intracellular obligate parasite that causes granulocytic anaplasmosis. Effector Ats-1 is an important virulence factor of A. phagocytophilum. Multiomics screening and validation has been used to determine that Ats-1 regulates host cell apoptosis and energy metabolism...

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Autores principales: Li, Ruirui, Ma, Zhongchen, Zheng, Wei, Xiao, Yangyang, Wang, Zhen, Yi, Jihai, Wang, Yong, Chen, Chuangfu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10523776/
https://www.ncbi.nlm.nih.gov/pubmed/37759206
http://dx.doi.org/10.1186/s12866-023-03023-4
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author Li, Ruirui
Ma, Zhongchen
Zheng, Wei
Xiao, Yangyang
Wang, Zhen
Yi, Jihai
Wang, Yong
Chen, Chuangfu
author_facet Li, Ruirui
Ma, Zhongchen
Zheng, Wei
Xiao, Yangyang
Wang, Zhen
Yi, Jihai
Wang, Yong
Chen, Chuangfu
author_sort Li, Ruirui
collection PubMed
description Anaplasma phagocytophilum is an intracellular obligate parasite that causes granulocytic anaplasmosis. Effector Ats-1 is an important virulence factor of A. phagocytophilum. Multiomics screening and validation has been used to determine that Ats-1 regulates host cell apoptosis and energy metabolism through the respiratory chain mPTP axis. In this study, a total of 19 potential binding proteins of Ats-1 in host cells were preliminarily screened using a yeast two-hybrid assay, and the interaction between syntenin-1 (SDCBP) and Ats-1 was identified through immunoprecipitation. Bioinformatics analysis showed that SDCBP interacted with SDC1, SDC2, and SDC4 and participated in the host exosome secretion pathway. Further studies confirmed that Ats-1 induced the expression of SDC1, SDC2, and SDC4 in HEK293T cells through SDCBP and increased the exosome secretion of these cells. This indicated that SDCBP played an important role in Ats-1 regulating the exosome secretion of the host cells. These findings expand our understanding of the intracellular regulatory mechanism of A. phagocytophilum, which may enhance its own infection and proliferation by regulating host exosome pathways. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-023-03023-4.
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spelling pubmed-105237762023-09-28 Anaplasma phagocytophilum Ats-1 enhances exosome secretion through Syntenin-1 Li, Ruirui Ma, Zhongchen Zheng, Wei Xiao, Yangyang Wang, Zhen Yi, Jihai Wang, Yong Chen, Chuangfu BMC Microbiol Research Anaplasma phagocytophilum is an intracellular obligate parasite that causes granulocytic anaplasmosis. Effector Ats-1 is an important virulence factor of A. phagocytophilum. Multiomics screening and validation has been used to determine that Ats-1 regulates host cell apoptosis and energy metabolism through the respiratory chain mPTP axis. In this study, a total of 19 potential binding proteins of Ats-1 in host cells were preliminarily screened using a yeast two-hybrid assay, and the interaction between syntenin-1 (SDCBP) and Ats-1 was identified through immunoprecipitation. Bioinformatics analysis showed that SDCBP interacted with SDC1, SDC2, and SDC4 and participated in the host exosome secretion pathway. Further studies confirmed that Ats-1 induced the expression of SDC1, SDC2, and SDC4 in HEK293T cells through SDCBP and increased the exosome secretion of these cells. This indicated that SDCBP played an important role in Ats-1 regulating the exosome secretion of the host cells. These findings expand our understanding of the intracellular regulatory mechanism of A. phagocytophilum, which may enhance its own infection and proliferation by regulating host exosome pathways. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-023-03023-4. BioMed Central 2023-09-27 /pmc/articles/PMC10523776/ /pubmed/37759206 http://dx.doi.org/10.1186/s12866-023-03023-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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
Li, Ruirui
Ma, Zhongchen
Zheng, Wei
Xiao, Yangyang
Wang, Zhen
Yi, Jihai
Wang, Yong
Chen, Chuangfu
Anaplasma phagocytophilum Ats-1 enhances exosome secretion through Syntenin-1
title Anaplasma phagocytophilum Ats-1 enhances exosome secretion through Syntenin-1
title_full Anaplasma phagocytophilum Ats-1 enhances exosome secretion through Syntenin-1
title_fullStr Anaplasma phagocytophilum Ats-1 enhances exosome secretion through Syntenin-1
title_full_unstemmed Anaplasma phagocytophilum Ats-1 enhances exosome secretion through Syntenin-1
title_short Anaplasma phagocytophilum Ats-1 enhances exosome secretion through Syntenin-1
title_sort anaplasma phagocytophilum ats-1 enhances exosome secretion through syntenin-1
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10523776/
https://www.ncbi.nlm.nih.gov/pubmed/37759206
http://dx.doi.org/10.1186/s12866-023-03023-4
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