4.6 Article

Tissue distribution of angiotensin-converting enzyme 2 (ACE2) receptor in wild animals with a focus on artiodactyls, mustelids and phocids

Journal

ONE HEALTH
Volume 16, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.onehlt.2023.100492

Keywords

ACE2; Wildlife; Ungulate; Mustelid; Phocid; Respiratory tract; Intestinal tract

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Natural cases of SARS-CoV-2 transmission to animals have been observed in free-ranging white-tailed deer and farmed American mink. The distribution of ACE2 receptors in the respiratory and intestinal tissues of various wild and semi-domesticated mammals was characterized to understand its potential effect on viral tropism. ACE2 receptor expression was detected in the bronchial or bronchiolar epithelium of several deer species, camel, badger, stoat, hippopotamus, harbor seal, and hooded seal. ACE2 receptor expression in the nasal mucosal epithelium was high in European badger and stoat. Expression of ACE2 receptor in intestinal cells was found across multiple mammalian taxa. These findings demonstrate the potential for ACE2-mediated viral infection in a variety of wild mammals and highlight the variability of ACE2 receptor expression within species.
Natural cases of zooanthroponotic transmission of SARS-CoV-2 to animals have been reported during the COVID-19 pandemic, including to free-ranging white-tailed deer (Odocoileus virginianus) in North America and farmed American mink (Neovison vison) on multiple continents. To understand the potential for angiotensin-converting enzyme 2 (ACE2)-mediated viral tropism we characterised the distribution of ACE2 receptors in the respiratory and intestinal tissues of a selection of wild and semi-domesticated mammals including artiodactyls (cervids, bovids, camelids, suids and hippopotamus), mustelid and phocid species using immunohistochemistry. Expres-sion of the ACE2 receptor was detected in the bronchial or bronchiolar epithelium of several European and Asiatic deer species, Bactrian camel (Camelus bactrianus), European badger (Meles meles), stoat (Mustela erminea), hippopotamus (Hippopotamus amphibious), harbor seal (Phoca vitulina), and hooded seal (Cystophora cristata). Further receptor mapping in the nasal turbinates and trachea revealed sparse ACE2 receptor expression in the mucosal epithelial cells and occasional occurrence in the submucosal glandular epithelium of Western roe deer (Capreolus capreolus), moose (Alces alces alces), and alpaca (Vicunga pacos). Only the European badger and stoat expressed high levels of ACE2 receptor in the nasal mucosal epithelium, which could suggest high susceptibility to ACE2-mediated respiratory infection. Expression of ACE2 receptor in the intestinal cells was ubiquitous across multiple taxa examined. Our results demonstrate the potential for ACE2-mediated viral infection in a selection of wild mammals and highlight the intra-taxon variability of ACE2 receptor expression, which might influence host susceptibility and infection.

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