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Molecular Characterization and Functional Analysis of a Novel Calcium-Dependent Protein Kinase 4 from Eimeria tenella

Eimeria tenella is an obligate intracellular parasite that actively invades cecal epithelial cells of chickens. The basis of cell invasion is not completely understood, but some key molecules of host cell invasion have been discovered. This paper investigated the characteristics of calcium-dependent...

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Autores principales: Wang, Ziwen, Huang, Bing, Dong, Hui, Zhao, Qiping, Zhu, Shunhai, Xia, Weili, Xu, Shuaibin, Xie, Yuxiang, Cui, Xiaoxia, Tang, Min, Men, Qifei, Yang, Zhiyuang, Li, Cong, Zhu, Xuelong, Han, Hongyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5158193/
https://www.ncbi.nlm.nih.gov/pubmed/27977727
http://dx.doi.org/10.1371/journal.pone.0168132
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author Wang, Ziwen
Huang, Bing
Dong, Hui
Zhao, Qiping
Zhu, Shunhai
Xia, Weili
Xu, Shuaibin
Xie, Yuxiang
Cui, Xiaoxia
Tang, Min
Men, Qifei
Yang, Zhiyuang
Li, Cong
Zhu, Xuelong
Han, Hongyu
author_facet Wang, Ziwen
Huang, Bing
Dong, Hui
Zhao, Qiping
Zhu, Shunhai
Xia, Weili
Xu, Shuaibin
Xie, Yuxiang
Cui, Xiaoxia
Tang, Min
Men, Qifei
Yang, Zhiyuang
Li, Cong
Zhu, Xuelong
Han, Hongyu
author_sort Wang, Ziwen
collection PubMed
description Eimeria tenella is an obligate intracellular parasite that actively invades cecal epithelial cells of chickens. The basis of cell invasion is not completely understood, but some key molecules of host cell invasion have been discovered. This paper investigated the characteristics of calcium-dependent protein kinase 4 (EtCDPK4), a critical molecule in E. tenella invasion of host cells. A full-length EtCDPK4 cDNA was identified from E. tenella using rapid amplification of cDNA ends. EtCDPK4 had an open reading frame of 1803 bp encoding a protein of 600 amino acids. Quantitative real-time PCR and western blotting were used to explore differences in EtCDPK4 transcription and translation in four developmental stages of E. tenella. EtCDPK4 was expressed at higher levels in sporozoites, but translation was higher in second-generation merozoites. In vitro invasion inhibition assays explored whether EtCDPK4 was involved in invasion of DF-1 cells by E. tenella sporozoites. Polyclonal antibodies against recombinant EtCDPK4 (rEtCDPK4) inhibited parasite invasion, decreasing it by approximately 52%. Indirect immunofluorescence assays explored EtCDPK4 distribution during parasite development after E. tenella sporozoite invasion of DF-1 cells in vitro. The results showed that EtCDPK4 might be important in sporozoite invasion and development. To analyze EtCDPK4 functional domains according to the structural characteristics of EtCDPK4 and study the kinase activity of rEtCDPK4, an in vitro phosphorylation system was established. We verified that rEtCDPK4 was a protein kinase that was completely dependent on Ca(2+) for enzyme activity. Specific inhibitors of rEtCDPK4 activity were screened by kinase activity in vitro. Some specific inhibitors were applied to assays of DF-1 cell invasion by E. tenella sporozoites to confirm that the inhibitors functioned in vitro. W-7, H-7, H-89, and myristoylated peptide inhibited DF-1 invasion by E. tenella sporozoites. The experimental results showed that EtCDPK4 may be involved in E. tenella invasion of chicken cecal epithelial cells.
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spelling pubmed-51581932016-12-21 Molecular Characterization and Functional Analysis of a Novel Calcium-Dependent Protein Kinase 4 from Eimeria tenella Wang, Ziwen Huang, Bing Dong, Hui Zhao, Qiping Zhu, Shunhai Xia, Weili Xu, Shuaibin Xie, Yuxiang Cui, Xiaoxia Tang, Min Men, Qifei Yang, Zhiyuang Li, Cong Zhu, Xuelong Han, Hongyu PLoS One Research Article Eimeria tenella is an obligate intracellular parasite that actively invades cecal epithelial cells of chickens. The basis of cell invasion is not completely understood, but some key molecules of host cell invasion have been discovered. This paper investigated the characteristics of calcium-dependent protein kinase 4 (EtCDPK4), a critical molecule in E. tenella invasion of host cells. A full-length EtCDPK4 cDNA was identified from E. tenella using rapid amplification of cDNA ends. EtCDPK4 had an open reading frame of 1803 bp encoding a protein of 600 amino acids. Quantitative real-time PCR and western blotting were used to explore differences in EtCDPK4 transcription and translation in four developmental stages of E. tenella. EtCDPK4 was expressed at higher levels in sporozoites, but translation was higher in second-generation merozoites. In vitro invasion inhibition assays explored whether EtCDPK4 was involved in invasion of DF-1 cells by E. tenella sporozoites. Polyclonal antibodies against recombinant EtCDPK4 (rEtCDPK4) inhibited parasite invasion, decreasing it by approximately 52%. Indirect immunofluorescence assays explored EtCDPK4 distribution during parasite development after E. tenella sporozoite invasion of DF-1 cells in vitro. The results showed that EtCDPK4 might be important in sporozoite invasion and development. To analyze EtCDPK4 functional domains according to the structural characteristics of EtCDPK4 and study the kinase activity of rEtCDPK4, an in vitro phosphorylation system was established. We verified that rEtCDPK4 was a protein kinase that was completely dependent on Ca(2+) for enzyme activity. Specific inhibitors of rEtCDPK4 activity were screened by kinase activity in vitro. Some specific inhibitors were applied to assays of DF-1 cell invasion by E. tenella sporozoites to confirm that the inhibitors functioned in vitro. W-7, H-7, H-89, and myristoylated peptide inhibited DF-1 invasion by E. tenella sporozoites. The experimental results showed that EtCDPK4 may be involved in E. tenella invasion of chicken cecal epithelial cells. Public Library of Science 2016-12-15 /pmc/articles/PMC5158193/ /pubmed/27977727 http://dx.doi.org/10.1371/journal.pone.0168132 Text en © 2016 Wang et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Wang, Ziwen
Huang, Bing
Dong, Hui
Zhao, Qiping
Zhu, Shunhai
Xia, Weili
Xu, Shuaibin
Xie, Yuxiang
Cui, Xiaoxia
Tang, Min
Men, Qifei
Yang, Zhiyuang
Li, Cong
Zhu, Xuelong
Han, Hongyu
Molecular Characterization and Functional Analysis of a Novel Calcium-Dependent Protein Kinase 4 from Eimeria tenella
title Molecular Characterization and Functional Analysis of a Novel Calcium-Dependent Protein Kinase 4 from Eimeria tenella
title_full Molecular Characterization and Functional Analysis of a Novel Calcium-Dependent Protein Kinase 4 from Eimeria tenella
title_fullStr Molecular Characterization and Functional Analysis of a Novel Calcium-Dependent Protein Kinase 4 from Eimeria tenella
title_full_unstemmed Molecular Characterization and Functional Analysis of a Novel Calcium-Dependent Protein Kinase 4 from Eimeria tenella
title_short Molecular Characterization and Functional Analysis of a Novel Calcium-Dependent Protein Kinase 4 from Eimeria tenella
title_sort molecular characterization and functional analysis of a novel calcium-dependent protein kinase 4 from eimeria tenella
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5158193/
https://www.ncbi.nlm.nih.gov/pubmed/27977727
http://dx.doi.org/10.1371/journal.pone.0168132
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