TY - JOUR
T1 - Cytomegalovirus infection of the rat developing brain in utero prominently targets immune cells and promotes early microglial activation
AU - Cloarec, Robin
AU - Bauer, Sylvian
AU - Luche, Hervé
AU - Buhler, Emmanuelle
AU - Pallesi-Pocachard, Emilie
AU - Salmi, Manal
AU - Courtens, Sandra
AU - Massacrier, Annick
AU - Grenot, Pierre
AU - Teissier, Natacha
AU - Watrin, Françoise
AU - Schaller, Fabienne
AU - Adle-Biassette, Homa
AU - Gressens, Pierre
AU - Malissen, Marie
AU - Stamminger, Thomas
AU - Streblow, Daniel N.
AU - Bruneau, Nadine
AU - Szepetowski, Pierre
N1 - Funding Information:
This work was supported by INSERM (Institut National de la Santé et de la Recherche Médicale), by ANR (Agence Nationale de la Recherche) grant EPILAND (ANR-2010-BLAN-1405 01), by FRM (Fondation pour la Recherche Médicale) grant ("Physiology and pathology of brain development", call 2012), and by the PACA (Provence-Alpes-Côte d'Azur) Regional Council. RC was a recipient of an INSERM/PACA (Institut National de la Santé et de la Recherche Médicale/ Provence-Alpes-Côte d'Azur)PhD fellowship and a recipient of a FRM (Fondation pour la Recherche Médicale) PhD fellowship (FDT20140930813). TS was supported by the Deutsche Forschungsgemeinschaft (SFB796). We thank F. Michel at inMAGIC (INMED Imaging Centre), F. Bader and S. Corby (INMED animal core facilities), L Castelein for technical support, H Child (Oxford University, UK) for his help as a trainee via the BIOTRAIL international student exchange program, and all the administrative staff at INMED. We also thank R. Charrel (EPV UMR_D190, Aix-Marseille University, France) for his advices at the onset of the project, G. Grauls (Department of Medical Microbiology, Maastricht University, The Netherlands) for the gift of anti-R44 producing hybridoma, A. Fontbonne (UMR 7260, Aix-Marseille University, France) for his help in inner ear analysis, and C. Sapet and O. Zelphati at OZ Biosciences (Marseille, France) for their kind help and support.
Funding Information:
Funding: This work was supported by INSERM (Institut National de la Santé et de la Recherche Médicale), by ANR (Agence Nationale de la Recherche) grant EPILAND (ANR-2010-BLAN-1405 01), by FRM (Fondation pour la Recherche Médicale) grant ("Physiology and pathology of brain development", call 2012), and by the PACA (Provence-Alpes-Côte d'Azur) Regional Council. RC was a recipient of an INSERM/PACA (Institut National de la Santé et de la Recherche Médicale/ Provence-
Funding Information:
Alpes-Côte d'Azur)PhD fellowship and a recipient of a FRM (Fondation pour la Recherche Médicale) PhD fellowship (FDT20140930813). TS was supported by the Deutsche Forschungsgemeinschaft (SFB796).
Publisher Copyright:
© 2016 Cloarec et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2016/7
Y1 - 2016/7
N2 - Background Congenital cytomegalovirus infections are a leading cause of neurodevelopmental disorders in human and represent a major health care and socio-economical burden. In contrast with this medical importance, the pathophysiological events remain poorly known. Murine models of brain cytomegalovirus infection, mostly neonatal, have brought recent insights into the possible pathogenesis, with convergent evidence for the alteration and possible involvement of brain immune cells. Objectives and Methods In order to confirm and expand those findings, particularly concerning the early developmental stages following infection of the fetal brain, we have created a model of in utero cytomegalovirus infection in the developing rat brain. Rat cytomegalovirus was injected intraventricularly at embryonic day 15 (E15) and the brains analyzed at various stages until the first postnatal day, using a combination of gene expression analysis, immunohistochemistry and multicolor flow cytometry experiments. Results Rat cytomegalovirus infection was increasingly seen in various brain areas including the choroid plexi and the ventricular and subventricular areas and was prominently detected in CD45low/int, CD11b+ microglial cells, in CD45high, CD11b+ cells of the myeloid lineage including macrophages, and in CD45+, CD11b– lymphocytes and non-B non-T cells. In parallel, rat cytomegalovirus infection of the developing rat brain rapidly triggered a cascade of pathophysiological events comprising: chemokines upregulation, including CCL2-4, 7 and 12; infiltration by peripheral cells including B-cells and monocytes at E17 and P1, and T-cells at P1; and microglia activation at E17 and P1. Conclusion In line with previous findings in neonatal murine models and in human specimen, our study further suggests that neuroimmune alterations might play critical roles in the early stages following cytomegalovirus infection of the brain in utero. Further studies are now needed to determine which role, whether favorable or detrimental, those putative double-edge swords events actually play.
AB - Background Congenital cytomegalovirus infections are a leading cause of neurodevelopmental disorders in human and represent a major health care and socio-economical burden. In contrast with this medical importance, the pathophysiological events remain poorly known. Murine models of brain cytomegalovirus infection, mostly neonatal, have brought recent insights into the possible pathogenesis, with convergent evidence for the alteration and possible involvement of brain immune cells. Objectives and Methods In order to confirm and expand those findings, particularly concerning the early developmental stages following infection of the fetal brain, we have created a model of in utero cytomegalovirus infection in the developing rat brain. Rat cytomegalovirus was injected intraventricularly at embryonic day 15 (E15) and the brains analyzed at various stages until the first postnatal day, using a combination of gene expression analysis, immunohistochemistry and multicolor flow cytometry experiments. Results Rat cytomegalovirus infection was increasingly seen in various brain areas including the choroid plexi and the ventricular and subventricular areas and was prominently detected in CD45low/int, CD11b+ microglial cells, in CD45high, CD11b+ cells of the myeloid lineage including macrophages, and in CD45+, CD11b– lymphocytes and non-B non-T cells. In parallel, rat cytomegalovirus infection of the developing rat brain rapidly triggered a cascade of pathophysiological events comprising: chemokines upregulation, including CCL2-4, 7 and 12; infiltration by peripheral cells including B-cells and monocytes at E17 and P1, and T-cells at P1; and microglia activation at E17 and P1. Conclusion In line with previous findings in neonatal murine models and in human specimen, our study further suggests that neuroimmune alterations might play critical roles in the early stages following cytomegalovirus infection of the brain in utero. Further studies are now needed to determine which role, whether favorable or detrimental, those putative double-edge swords events actually play.
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U2 - 10.1371/journal.pone.0160176
DO - 10.1371/journal.pone.0160176
M3 - Article
C2 - 27472761
AN - SCOPUS:85027258967
SN - 1932-6203
VL - 11
JO - PLoS One
JF - PLoS One
IS - 7
M1 - e0160176
ER -