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10.1111/1348-0421.12498

http://scihub22266oqcxt.onion/10.1111/1348-0421.12498
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28675506!7168434!28675506
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suck abstract from ncbi


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pmid28675506      Microbiol+Immunol 2017 ; 61 (8): 318-327
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  • Determination of the cell tropism of serotype 1 feline infectious peritonitis virus using the spike affinity histochemistry in paraffin-embedded tissues #MMPMID28675506
  • Cham TC; Chang YC; Tsai PS; Wu CH; Chen HW; Jeng CR; Pang VF; Chang HW
  • Microbiol Immunol 2017[Aug]; 61 (8): 318-327 PMID28675506show ga
  • Unlike for serotype II feline coronaviruses (FCoV II), the cellular receptor for serotype I FCoV (FCoV I), the most prevalent FCoV serotype, is unknown. To provide a platform for assessing the pattern by which FCoV I attaches to its host receptor(s), HEK293 cell lines that stably express the ectodomains of the spike (S) proteins derived from a FCoV I feline enteric coronavirus strain UU7 (FECV UU7) and a feline infectious peritonitis virus strain UU4 (FIPV UU4) were established. Using the recombinant S proteins as probes to perform S protein affinity histochemistry in paraffin-embedded tissues, although no tissue or enteric binding of FECV UU7 S protein was detected, it was found that by immunohistochemistry that the tissue distribution of FIPV UU4 S protein-bound cells correlated with that of FIPV antigen-positive cells and lesions associated with FIP and that the affinity binding of FIPV UU4 S protein on macrophages was not affected by enzymatic removal of host cell-surface sialic acid with neuraminidase. These findings suggest that a factor(s) other than sialic acid contribute(s) to the macrophage tropism of FIPV strain UU4. This approach allowed obtaining more information about both virus-host cell interactions and the biological characteristics of the unidentified cellular receptor for FCoV I.
  • |*Virus Attachment[MESH]
  • |Animals[MESH]
  • |Cats[MESH]
  • |Cell Line[MESH]
  • |Coronavirus, Feline/*metabolism[MESH]
  • |HEK293 Cells[MESH]
  • |Host-Pathogen Interactions/physiology[MESH]
  • |Humans[MESH]
  • |Macrophages/virology[MESH]
  • |N-Acetylneuraminic Acid/chemistry[MESH]
  • |Protein Binding/genetics/physiology[MESH]
  • |Receptors, Virus/*metabolism[MESH]
  • |Serogroup[MESH]
  • |Spike Glycoprotein, Coronavirus/genetics/*metabolism[MESH]


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