Zika Virus Targets Multiple Tissues and Cell Types During the First Trimester of Pregnancy

Autor: Francisco Veas, Nabila Jabrane-Ferrat
Přispěvatelé: Toulouse Institute for Infectious and Inflammatory Diseases, University of Toulouse, CNRS, INSERM, UPS, Toulouse, France. (Infinity), Hydrosciences Montpellier (HSM), Institut national des sciences de l'Univers (INSU - CNRS)-Institut de Recherche pour le Développement (IRD)-Université Montpellier 2 - Sciences et Techniques (UM2)-Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS), Centre de Physiopathologie Toulouse Purpan (CPTP), Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Institut de Recherche pour le Développement (IRD), Kobinger G., Racine T.
Jazyk: angličtina
Rok vydání: 2020
Předmět:
0301 basic medicine
MESH: Zika Virus / metabolism
[SDV]Life Sciences [q-bio]
Umbilical cord
Zika virus
0302 clinical medicine
MESH: Macrophages / pathology
MESH: Pregnancy
MESH: Chlorocebus aethiops
MESH: Placenta / pathology
MESH: Zika Virus Infection / pathology
MESH: Animals
030212 general & internal medicine
Fetal placenta
Maternal-fetal transmission
MESH: Pregnancy Trimester
First

MESH: Organ Specificity
ComputingMilieux_MISCELLANEOUS
MESH: Primary Cell Culture / methods
biology
Umbilical cord mesenchymal stem cells
MESH: Pregnancy Complications
Infectious / virology

MESH: Trophoblasts / pathology
MESH: Umbilical Cord / virology
3. Good health
Trophoblasts
MESH: Infectious Disease Transmission
Vertical

medicine.anatomical_structure
MESH: Trophoblasts / virology
embryonic structures
[SDV.MP.VIR]Life Sciences [q-bio]/Microbiology and Parasitology/Virology
MESH: Fetus / virology
[SDV.IMM]Life Sciences [q-bio]/Immunology
MESH: Macrophages / virology
Cellular Tropism
MESH: Zika Virus / pathogenicity
MESH: Virus Cultivation / methods
MESH: Vero Cells
MESH: Viral Load / methods
03 medical and health sciences
Placenta
medicine
MESH: Pregnancy Complications
Infectious / pathology

MESH: Specimen Handling / methods
MESH: Tissue Distribution
MESH: Umbilical Cord / pathology
First trimester pregnancy
Fetus
Pregnancy
MESH: Humans
MESH: Zika Virus Infection / virology
Macrophages
Mesenchymal stem cell
Trophoblast
Maternal decidua basalis
Zika virus infection
MESH: Fetus / pathology
biology.organism_classification
medicine.disease
Virology
030104 developmental biology
Hofbauer cells
MESH: Placenta / virology
MESH: Pregnancy Complications
Infectious / metabolism

Decidual fibroblasts
MESH: Female
Zdroj: Zika Virus
Zika Virus, 2142, Springer US, pp.235-249, 2020, Methods in Molecular Biology, ⟨10.1007/978-1-0716-0581-3_18⟩
Zika Virus : Methods and protocols
Kobinger G.; Racine T. Zika Virus : Methods and protocols, 2142, Humana, pp.235-249, 2020, Methods in Molecular Biology, 978-1-0716-0580-6. ⟨10.1007/978-1-0716-0581-3_18⟩
Methods in Molecular Biology ISBN: 9781071605806
DOI: 10.1007/978-1-0716-0581-3_18⟩
Popis: International audience; The 2016 Zika virus (ZIKV) outbreak in the Americas has been characterized by an increased association frequency of fetal neuropathological abnormalities. To have a comprehensive and accurate knowledge of key elements of the clinically observed neurologic dysfunctions in Zika-infected babies, ZIKV transmission from mother to fetus needs to be deeply studied. Thus, it is important to determine the role of both virus-targeted cells and tissues within the mother-fetus interface. Cellular tropism and mechanisms of ZIKV transmission from mother to the fetus during early pregnancy still remain unknown on many aspects. To improve the characterization of the maternal-fetal ZIKV transmission, we have set up an ex vivo model using an organ culture approach with a light-invasive sampling from the first trimester of pregnancy samples. Thus, here we provide evidence that circulating epidemic ZIKV strains from Latin America widely target and destroy reproductive tissues, including the decidua basalis, fetal placenta, and umbilical cord. In addition, we show that ZIKV is able to differentially replicate in a large range of both maternal and fetal cells, including decidual fibroblasts and macrophages, fetal trophoblast and Hofbauer cells, as well as umbilical cord mesenchymal stem cells. This primary and broad ZIKV cellular tropism and the resulting abundant cytopathic-induced tissue effects during the first trimester of pregnancy show the upstream path of clinically observed congenital damages.
Databáze: OpenAIRE