Polarization of avian macrophages upon avian flavivirus infection.
Animals
Antiviral Agents
Cell Line
Cell Movement
Cell Polarity
Chickens
/ physiology
Ducks
/ physiology
Flavivirus
/ immunology
Flavivirus Infections
/ veterinary
Host Specificity
Macrophages
/ physiology
Monocytes
/ physiology
Nitric Oxide
/ metabolism
Phagocytosis
Poultry Diseases
/ virology
Specific Pathogen-Free Organisms
Virus Replication
Avian Tembusu virus
Macrophage polarization
Migration
Nitric oxide
Phagocytosis
Journal
Veterinary microbiology
ISSN: 1873-2542
Titre abrégé: Vet Microbiol
Pays: Netherlands
ID NLM: 7705469
Informations de publication
Date de publication:
May 2021
May 2021
Historique:
received:
23
10
2020
accepted:
18
03
2021
pubmed:
10
4
2021
medline:
28
9
2021
entrez:
9
4
2021
Statut:
ppublish
Résumé
Avian Tembusu virus (TMUV) is a newly emerging avian pathogenic flavivirus that spreads rapidly, has an expanding host range and undergoes cross-species transmission. Our previous study identified avian monocytes/macrophages as the key targets of TMUV infection, since the infection of host monocytes/macrophages was crucial for the replication, transmission, and pathogenesis of TMUV. The polarization of host macrophages determines the functional phenotypes of macrophages; however, the effect of TMUV infection on macrophage polarization remains unclear. Here, we analysed the expression spectra of the marker genes of macrophage polarization upon TMUV infection in the HD11 chicken macrophage cell line and primary monocytes/macrophages isolated from the peripheral blood of specific pathogen-free (SPF) chickens and ducks. We found that viral replication mainly induced M1 marker genes and triggered nitric oxide (NO) release at different levels, suggesting that TMUV infection led mainly to host macrophages polarizing into the classically activated (M1) type. The NO that was increased upon infection did not function as an antiviral agent against TMUV, since the replication of TMUV in HD11 cells was not affected by the addition of an organic NO donor. Furthermore, upon TMUV infection, polarized HD11 cells exhibited increased migration but reduced phagocytosis, as evidenced by scratch assay and neutral red uptake assay, respectively. Our present study characterized the polarization of host monocytes/macrophages upon TMUV infection, which may lay a foundation for further research on the immune escape mechanism and pathogenic mechanism of TMUV.
Identifiants
pubmed: 33836389
pii: S0378-1135(21)00067-5
doi: 10.1016/j.vetmic.2021.109044
pii:
doi:
Substances chimiques
Antiviral Agents
0
Nitric Oxide
31C4KY9ESH
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
109044Informations de copyright
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