iTRAQ-based comparative proteomic analysis of cells infected with Eimeria tenella sporozoites

Eimeria tenella is an obligate intracellular parasite that actively invades cecal epithelial cells of chickens. When E. tenella infects a host cell, the host produces a corresponding change to deal with damage caused by this infection. To date, our knowledge on the mechanism of how the host cell res...

Full description

Bibliographic Details
Main Authors: Zhao Zongping, Zhao Qiping, Zhu Shunhai, Huang Bing, Lv Ling, Chen Ting, Yan Ming, Han Hongyu, Dong Hui
Format: Article
Language:English
Published: EDP Sciences 2019-01-01
Series:Parasite
Subjects:
Online Access:https://www.parasite-journal.org/articles/parasite/full_html/2019/01/parasite180108/parasite180108.html
_version_ 1797641333814329344
author Zhao Zongping
Zhao Qiping
Zhu Shunhai
Huang Bing
Lv Ling
Chen Ting
Yan Ming
Han Hongyu
Dong Hui
author_facet Zhao Zongping
Zhao Qiping
Zhu Shunhai
Huang Bing
Lv Ling
Chen Ting
Yan Ming
Han Hongyu
Dong Hui
author_sort Zhao Zongping
collection DOAJ
description Eimeria tenella is an obligate intracellular parasite that actively invades cecal epithelial cells of chickens. When E. tenella infects a host cell, the host produces a corresponding change to deal with damage caused by this infection. To date, our knowledge on the mechanism of how the host cell responds to E. tenella infection is highly limited at both the molecular and cellular levels. In this study, isobaric tags for relative and absolute quantitation (iTRAQ) coupled with LC-MS/MS was used to screen the differentially expressed proteins (DEPs) in BHK-21 cells infected with E. tenella sporozoites for 24 h post infection. In total, 6139 non-redundant distinct proteins were identified and 195 of these were found to have a fold change ratio ≥1.3 or ≤0.7 and p < 0.05, including 151 up-regulated proteins and 44 down-regulated proteins. The reliability of the proteomic data was further validated with qPCR and western blot. Gene Ontology enrichment indicated that the up-regulated DEPs were mainly involved in binding and catalytic activity, whereas the down-regulated DEPs were catalytic activity and molecular function regulators. Furthermore, KEGG pathway analysis showed that the DEPs participated in the PI3K-Akt, chemokine, Ras, Wnt, and p53 signaling pathways and so on, and the up-regulated and down-regulated DEPs mainly related to the ribosome and mRNA surveillance pathway, respectively. The data in this study provide an important basis to further analyze E. tenella host cell interactions.
first_indexed 2024-03-11T13:44:07Z
format Article
id doaj.art-47b733d2c1ab428eaff94e31f4eec4c6
institution Directory Open Access Journal
issn 1776-1042
language English
last_indexed 2024-03-11T13:44:07Z
publishDate 2019-01-01
publisher EDP Sciences
record_format Article
series Parasite
spelling doaj.art-47b733d2c1ab428eaff94e31f4eec4c62023-11-02T11:02:43ZengEDP SciencesParasite1776-10422019-01-0126710.1051/parasite/2019009parasite180108iTRAQ-based comparative proteomic analysis of cells infected with Eimeria tenella sporozoitesZhao ZongpingZhao QipingZhu ShunhaiHuang BingLv LingChen TingYan MingHan HongyuDong HuiEimeria tenella is an obligate intracellular parasite that actively invades cecal epithelial cells of chickens. When E. tenella infects a host cell, the host produces a corresponding change to deal with damage caused by this infection. To date, our knowledge on the mechanism of how the host cell responds to E. tenella infection is highly limited at both the molecular and cellular levels. In this study, isobaric tags for relative and absolute quantitation (iTRAQ) coupled with LC-MS/MS was used to screen the differentially expressed proteins (DEPs) in BHK-21 cells infected with E. tenella sporozoites for 24 h post infection. In total, 6139 non-redundant distinct proteins were identified and 195 of these were found to have a fold change ratio ≥1.3 or ≤0.7 and p < 0.05, including 151 up-regulated proteins and 44 down-regulated proteins. The reliability of the proteomic data was further validated with qPCR and western blot. Gene Ontology enrichment indicated that the up-regulated DEPs were mainly involved in binding and catalytic activity, whereas the down-regulated DEPs were catalytic activity and molecular function regulators. Furthermore, KEGG pathway analysis showed that the DEPs participated in the PI3K-Akt, chemokine, Ras, Wnt, and p53 signaling pathways and so on, and the up-regulated and down-regulated DEPs mainly related to the ribosome and mRNA surveillance pathway, respectively. The data in this study provide an important basis to further analyze E. tenella host cell interactions.https://www.parasite-journal.org/articles/parasite/full_html/2019/01/parasite180108/parasite180108.htmliTRAQEimeria tenellaSporozoitesBHK-21 cellsDifferentially expressed proteins
spellingShingle Zhao Zongping
Zhao Qiping
Zhu Shunhai
Huang Bing
Lv Ling
Chen Ting
Yan Ming
Han Hongyu
Dong Hui
iTRAQ-based comparative proteomic analysis of cells infected with Eimeria tenella sporozoites
Parasite
iTRAQ
Eimeria tenella
Sporozoites
BHK-21 cells
Differentially expressed proteins
title iTRAQ-based comparative proteomic analysis of cells infected with Eimeria tenella sporozoites
title_full iTRAQ-based comparative proteomic analysis of cells infected with Eimeria tenella sporozoites
title_fullStr iTRAQ-based comparative proteomic analysis of cells infected with Eimeria tenella sporozoites
title_full_unstemmed iTRAQ-based comparative proteomic analysis of cells infected with Eimeria tenella sporozoites
title_short iTRAQ-based comparative proteomic analysis of cells infected with Eimeria tenella sporozoites
title_sort itraq based comparative proteomic analysis of cells infected with eimeria tenella sporozoites
topic iTRAQ
Eimeria tenella
Sporozoites
BHK-21 cells
Differentially expressed proteins
url https://www.parasite-journal.org/articles/parasite/full_html/2019/01/parasite180108/parasite180108.html
work_keys_str_mv AT zhaozongping itraqbasedcomparativeproteomicanalysisofcellsinfectedwitheimeriatenellasporozoites
AT zhaoqiping itraqbasedcomparativeproteomicanalysisofcellsinfectedwitheimeriatenellasporozoites
AT zhushunhai itraqbasedcomparativeproteomicanalysisofcellsinfectedwitheimeriatenellasporozoites
AT huangbing itraqbasedcomparativeproteomicanalysisofcellsinfectedwitheimeriatenellasporozoites
AT lvling itraqbasedcomparativeproteomicanalysisofcellsinfectedwitheimeriatenellasporozoites
AT chenting itraqbasedcomparativeproteomicanalysisofcellsinfectedwitheimeriatenellasporozoites
AT yanming itraqbasedcomparativeproteomicanalysisofcellsinfectedwitheimeriatenellasporozoites
AT hanhongyu itraqbasedcomparativeproteomicanalysisofcellsinfectedwitheimeriatenellasporozoites
AT donghui itraqbasedcomparativeproteomicanalysisofcellsinfectedwitheimeriatenellasporozoites