4.6 Article

N-Glycolylneuraminic Acid in Animal Models for Human Influenza A Virus

期刊

VIRUSES-BASEL
卷 13, 期 5, 页码 -

出版社

MDPI
DOI: 10.3390/v13050815

关键词

influenza; animal model; N-glycolylneuraminic acid; N-acetylneuraminic acid; CMAH; sialic acid linkage; mouse; ferret

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资金

  1. ERC Starting Grant from the European Commission [802780]
  2. Beijerinck Premium of the Royal Dutch Academy of Sciences
  3. European Research Council (ERC) [802780] Funding Source: European Research Council (ERC)

向作者/读者索取更多资源

The initial step in influenza virus infection involves the binding of hemagglutinin to sialic acid-containing glycans on the cell surface. Different sialic acid modifications, such as Neu5Ac and Neu5Gc, play a role in infection. Common animal models used for studying human influenza include mice and ferrets, with the latter being preferred due to their similarity to humans in sialic acid content and susceptibility to infection.
The first step in influenza virus infection is the binding of hemagglutinin to sialic acid-containing glycans present on the cell surface. Over 50 different sialic acid modifications are known, of which N-acetylneuraminic acid (Neu5Ac) and N-glycolylneuraminic acid (Neu5Gc) are the two main species. Animal models with alpha 2,6 linked Neu5Ac in the upper respiratory tract, similar to humans, are preferred to enable and mimic infection with unadapted human influenza A viruses. Animal models that are currently most often used to study human influenza are mice and ferrets. Additionally, guinea pigs, cotton rats, Syrian hamsters, tree shrews, domestic swine, and non-human primates (macaques and marmosets) are discussed. The presence of NeuGc and the distribution of sialic acid linkages in the most commonly used models is summarized and experimentally determined. We also evaluated the role of Neu5Gc in infection using Neu5Gc binding viruses and cytidine monophosphate-N-acetylneuraminic acid hydroxylase (CMAH)(-/-) knockout mice, which lack Neu5Gc and concluded that Neu5Gc is unlikely to be a decoy receptor. This article provides a base for choosing an appropriate animal model. Although mice are one of the most favored models, they are hardly naturally susceptible to infection with human influenza viruses, possibly because they express mainly alpha 2,3 linked sialic acids with both Neu5Ac and Neu5Gc modifications. We suggest using ferrets, which resemble humans closely in the sialic acid content, both in the linkages and the lack of Neu5Gc, lung organization, susceptibility, and disease pathogenesis.

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