Cargando…

Brucella suis Vaccine Strain 2 Induces Endoplasmic Reticulum Stress that Affects Intracellular Replication in Goat Trophoblast Cells In vitro

Brucella has been reported to impair placental trophoblasts, a cellular target where Brucella efficiently replicates in association with the endoplasmic reticulum (ER), and ultimately trigger abortion in pregnant animals. However, the precise effects of Brucella on trophoblast cells remain unclear....

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Xiangguo, Lin, Pengfei, Li, Yang, Xiang, Caixia, Yin, Yanlong, Chen, Zhi, Du, Yue, Zhou, Dong, Jin, Yaping, Wang, Aihua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4746994/
https://www.ncbi.nlm.nih.gov/pubmed/26904517
http://dx.doi.org/10.3389/fcimb.2016.00019
_version_ 1782414910658969600
author Wang, Xiangguo
Lin, Pengfei
Li, Yang
Xiang, Caixia
Yin, Yanlong
Chen, Zhi
Du, Yue
Zhou, Dong
Jin, Yaping
Wang, Aihua
author_facet Wang, Xiangguo
Lin, Pengfei
Li, Yang
Xiang, Caixia
Yin, Yanlong
Chen, Zhi
Du, Yue
Zhou, Dong
Jin, Yaping
Wang, Aihua
author_sort Wang, Xiangguo
collection PubMed
description Brucella has been reported to impair placental trophoblasts, a cellular target where Brucella efficiently replicates in association with the endoplasmic reticulum (ER), and ultimately trigger abortion in pregnant animals. However, the precise effects of Brucella on trophoblast cells remain unclear. Here, we describe the infection and replication of Brucella suis vaccine strain 2 (B.suis.S2) in goat trophoblast cells (GTCs) and the cellular and molecular responses induced in vitro. Our studies demonstrated that B.suis.S2 was able to infect and proliferate to high titers, hamper the proliferation of GTCs and induce apoptosis due to ER stress. Tunicamycin (Tm), a pharmacological chaperone that strongly mounts ER stress-induced apoptosis, inhibited B.suis.S2 replication in GTCs. In addition, 4 phenyl butyric acid (4-PBA), a pharmacological chaperone that alleviates ER stress-induced apoptosis, significantly enhanced B.suis.S2 replication in GTCs. The Unfolded Protein Response (UPR) chaperone molecule GRP78 also promoted B.suis.S2 proliferation in GTCs by inhibiting ER stress-induced apoptosis. We also discovered that the IRE1 pathway, but not the PERK or ATF6 pathway, was activated in the process. However, decreasing the expression of phosphoIRE1α and IRE1α proteins with Irestatin 9389 (IRE1 antagonist) in GTCs did not affect the proliferation of B.suis.S2. Although GTC implantation was not affected upon B.suis.S2 infection, progesterone secretion was suppressed, and prolactin and estrogen secretion increased; these effects were accompanied by changes in the expression of genes encoding key steroidogenic enzymes. This study systematically explored the mechanisms of abortion in Brucella infection from the viewpoint of pathogen invasion, ER stress and reproductive endocrinology. Our findings may provide new insight for understanding the mechanisms involved in goat abortions caused by Brucella infection.
format Online
Article
Text
id pubmed-4746994
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-47469942016-02-22 Brucella suis Vaccine Strain 2 Induces Endoplasmic Reticulum Stress that Affects Intracellular Replication in Goat Trophoblast Cells In vitro Wang, Xiangguo Lin, Pengfei Li, Yang Xiang, Caixia Yin, Yanlong Chen, Zhi Du, Yue Zhou, Dong Jin, Yaping Wang, Aihua Front Cell Infect Microbiol Microbiology Brucella has been reported to impair placental trophoblasts, a cellular target where Brucella efficiently replicates in association with the endoplasmic reticulum (ER), and ultimately trigger abortion in pregnant animals. However, the precise effects of Brucella on trophoblast cells remain unclear. Here, we describe the infection and replication of Brucella suis vaccine strain 2 (B.suis.S2) in goat trophoblast cells (GTCs) and the cellular and molecular responses induced in vitro. Our studies demonstrated that B.suis.S2 was able to infect and proliferate to high titers, hamper the proliferation of GTCs and induce apoptosis due to ER stress. Tunicamycin (Tm), a pharmacological chaperone that strongly mounts ER stress-induced apoptosis, inhibited B.suis.S2 replication in GTCs. In addition, 4 phenyl butyric acid (4-PBA), a pharmacological chaperone that alleviates ER stress-induced apoptosis, significantly enhanced B.suis.S2 replication in GTCs. The Unfolded Protein Response (UPR) chaperone molecule GRP78 also promoted B.suis.S2 proliferation in GTCs by inhibiting ER stress-induced apoptosis. We also discovered that the IRE1 pathway, but not the PERK or ATF6 pathway, was activated in the process. However, decreasing the expression of phosphoIRE1α and IRE1α proteins with Irestatin 9389 (IRE1 antagonist) in GTCs did not affect the proliferation of B.suis.S2. Although GTC implantation was not affected upon B.suis.S2 infection, progesterone secretion was suppressed, and prolactin and estrogen secretion increased; these effects were accompanied by changes in the expression of genes encoding key steroidogenic enzymes. This study systematically explored the mechanisms of abortion in Brucella infection from the viewpoint of pathogen invasion, ER stress and reproductive endocrinology. Our findings may provide new insight for understanding the mechanisms involved in goat abortions caused by Brucella infection. Frontiers Media S.A. 2016-02-09 /pmc/articles/PMC4746994/ /pubmed/26904517 http://dx.doi.org/10.3389/fcimb.2016.00019 Text en Copyright © 2016 Wang, Lin, Li, Xiang, Yin, Chen, Du, Zhou, Jin and Wang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Wang, Xiangguo
Lin, Pengfei
Li, Yang
Xiang, Caixia
Yin, Yanlong
Chen, Zhi
Du, Yue
Zhou, Dong
Jin, Yaping
Wang, Aihua
Brucella suis Vaccine Strain 2 Induces Endoplasmic Reticulum Stress that Affects Intracellular Replication in Goat Trophoblast Cells In vitro
title Brucella suis Vaccine Strain 2 Induces Endoplasmic Reticulum Stress that Affects Intracellular Replication in Goat Trophoblast Cells In vitro
title_full Brucella suis Vaccine Strain 2 Induces Endoplasmic Reticulum Stress that Affects Intracellular Replication in Goat Trophoblast Cells In vitro
title_fullStr Brucella suis Vaccine Strain 2 Induces Endoplasmic Reticulum Stress that Affects Intracellular Replication in Goat Trophoblast Cells In vitro
title_full_unstemmed Brucella suis Vaccine Strain 2 Induces Endoplasmic Reticulum Stress that Affects Intracellular Replication in Goat Trophoblast Cells In vitro
title_short Brucella suis Vaccine Strain 2 Induces Endoplasmic Reticulum Stress that Affects Intracellular Replication in Goat Trophoblast Cells In vitro
title_sort brucella suis vaccine strain 2 induces endoplasmic reticulum stress that affects intracellular replication in goat trophoblast cells in vitro
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4746994/
https://www.ncbi.nlm.nih.gov/pubmed/26904517
http://dx.doi.org/10.3389/fcimb.2016.00019
work_keys_str_mv AT wangxiangguo brucellasuisvaccinestrain2inducesendoplasmicreticulumstressthataffectsintracellularreplicationingoattrophoblastcellsinvitro
AT linpengfei brucellasuisvaccinestrain2inducesendoplasmicreticulumstressthataffectsintracellularreplicationingoattrophoblastcellsinvitro
AT liyang brucellasuisvaccinestrain2inducesendoplasmicreticulumstressthataffectsintracellularreplicationingoattrophoblastcellsinvitro
AT xiangcaixia brucellasuisvaccinestrain2inducesendoplasmicreticulumstressthataffectsintracellularreplicationingoattrophoblastcellsinvitro
AT yinyanlong brucellasuisvaccinestrain2inducesendoplasmicreticulumstressthataffectsintracellularreplicationingoattrophoblastcellsinvitro
AT chenzhi brucellasuisvaccinestrain2inducesendoplasmicreticulumstressthataffectsintracellularreplicationingoattrophoblastcellsinvitro
AT duyue brucellasuisvaccinestrain2inducesendoplasmicreticulumstressthataffectsintracellularreplicationingoattrophoblastcellsinvitro
AT zhoudong brucellasuisvaccinestrain2inducesendoplasmicreticulumstressthataffectsintracellularreplicationingoattrophoblastcellsinvitro
AT jinyaping brucellasuisvaccinestrain2inducesendoplasmicreticulumstressthataffectsintracellularreplicationingoattrophoblastcellsinvitro
AT wangaihua brucellasuisvaccinestrain2inducesendoplasmicreticulumstressthataffectsintracellularreplicationingoattrophoblastcellsinvitro