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10.1016/j.virol.2019.12.007

http://scihub22266oqcxt.onion/10.1016/j.virol.2019.12.007
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suck abstract from ncbi


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pmid32056711      Virology 2020 ; 541 (ä): 136-140
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  • The use of cells from ANPEP knockout pigs to evaluate the role of aminopeptidase N (APN) as a receptor for porcine deltacoronavirus (PDCoV) #MMPMID32056711
  • Stoian A; Rowland RRR; Petrovan V; Sheahan M; Samuel MS; Whitworth KM; Wells KD; Zhang J; Beaton B; Cigan M; Prather RS
  • Virology 2020[Feb]; 541 (ä): 136-140 PMID32056711show ga
  • The coronaviruses, porcine epidemic diarrhea virus (PEDV), transmissible gastroenteritis virus (TGEV), and porcine deltacoronavirus (PDCoV) represent important sources of neonatal diarrhea on pig farms. The requirement for aminopeptidase N (APN) as a receptor for TGEV, but not for PEDV, is well established. In this study, the biological relevance of APN as a receptor for PDCoV was tested by using CRISPR/Cas9 to knockout the APN gene, ANPEP, in pigs. Porcine alveolar macrophages (PAMs) from ANPEP knockout (KO) pigs showed resistance to PDCoV infection. However, lung fibroblast-like cells, derived from the ANPEP KO PAM cultures, supported PDCoV infection to high levels. The results suggest that APN is a receptor for PDCoV in PAMs but is not necessary for infection of lung-derived fibroblast cells. The infection of the ANPEP KO pigs with PDCoV further confirmed that APN is dispensable as a receptor for PDCoV.
  • |Animals[MESH]
  • |CD13 Antigens/genetics/*physiology[MESH]
  • |Coronavirus Infections/*etiology[MESH]
  • |Gastroenteritis, Transmissible, of Swine/etiology[MESH]
  • |Gene Knockout Techniques[MESH]
  • |Porcine epidemic diarrhea virus/physiology[MESH]
  • |Receptors, Virus/*physiology[MESH]
  • |Swine[MESH]


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