Co‐localization of Middle East respiratory syndrome coronavirus (MERS‐CoV) and dipeptidyl peptidase‐4 in the respiratory tract and lymphoid tissues of pigs and llamas

This study investigated the co‐localization of the Middle East respiratory syndrome coronavirus (MERS‐CoV) and its receptor dipeptidyl peptidase‐4 (DPP4) by immunohistochemistry (IHC) across respiratory and lymphoid organs of experimentally MERS‐CoV infected pigs and llamas. Also, scanning electron...

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Veröffentlicht in:Transboundary and emerging diseases 2019-03, Vol.66 (2), p.831-841
Hauptverfasser: Te, Nigeer, Vergara‐Alert, Júlia, Lehmbecker, Annika, Pérez, Mónica, Haagmans, Bart L., Baumgärtner, Wolfgang, Bensaid, Albert, Segalés, Joaquim
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container_title Transboundary and emerging diseases
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creator Te, Nigeer
Vergara‐Alert, Júlia
Lehmbecker, Annika
Pérez, Mónica
Haagmans, Bart L.
Baumgärtner, Wolfgang
Bensaid, Albert
Segalés, Joaquim
description This study investigated the co‐localization of the Middle East respiratory syndrome coronavirus (MERS‐CoV) and its receptor dipeptidyl peptidase‐4 (DPP4) by immunohistochemistry (IHC) across respiratory and lymphoid organs of experimentally MERS‐CoV infected pigs and llamas. Also, scanning electron microscopy was performed to assess the ciliary integrity of respiratory epithelial cells in both species. In pigs, on day 2 post‐inoculation (p.i.), DPP4‐MERS‐CoV co‐localization was detected in medial turbinate epithelium. On day 4 p.i., the virus/receptor co‐localized in frontal and medial turbinate epithelial cells in pigs, and epithelial cells distributed unevenly through the whole nasal cavity and in the cervical lymph node in llamas. MERS‐CoV viral nucleocapsid was mainly detected in upper respiratory tract sites on days 2 and 4 p.i. in pigs and day 4 p.i. in llamas. No MERS‐CoV was detected on day 24 p.i. in any tissue by IHC. While pigs showed severe ciliary loss in the nasal mucosa both on days 2 and 4 p.i. and moderate loss in the trachea on days 4 and 24 p.i., ciliation of respiratory organs in llamas was not significantly affected. Obtained data confirm the role of DPP4 for MERS‐CoV entry in respiratory epithelial cells of llamas. Notably, several nasal epithelial cells in pigs were found to express viral antigen but not DPP4, suggesting the possible existence of other molecule/s facilitating virus entry or down regulation of DPP4 upon infection.
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subjects Animals
Bone
Camelids, New World - virology
Coronaviridae
Coronavirus Infections - veterinary
Coronavirus Infections - virology
Coronaviruses
Dipeptidyl Peptidase 4 - metabolism
dipeptidyl peptidase‐4 (DPP4)
Dipeptidyl-peptidase IV
Epithelial cells
Epithelium
Immunohistochemistry
Immunohistochemistry - veterinary
Inoculation
llama
Localization
Lymph nodes
Lymphoid tissue
Lymphoid Tissue - enzymology
Microscopy, Electron, Scanning - veterinary
Middle East respiratory syndrome coronavirus (MERS‐CoV)
Middle East Respiratory Syndrome Coronavirus - pathogenicity
Mucosa
Nose
Nucleocapsids
Organs
Original
Peptidase
pig
Real-Time Polymerase Chain Reaction - veterinary
Receptors, Virus - metabolism
Respiratory diseases
Respiratory organs
Respiratory System - enzymology
Respiratory tract
RNA, Viral - genetics
Scanning electron microscopy
Swine
Swine Diseases - virology
Tissues
Trachea
Viruses
title Co‐localization of Middle East respiratory syndrome coronavirus (MERS‐CoV) and dipeptidyl peptidase‐4 in the respiratory tract and lymphoid tissues of pigs and llamas
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