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10.1016/j.virol.2020.08.018

http://scihub22266oqcxt.onion/10.1016/j.virol.2020.08.018
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suck abstract from ncbi


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pmid33059319      Virology 2021 ; 552 (ä): 43-51
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  • Epithelial-mesenchymal transition of absorptive enterocytes and depletion of Peyer s patch M cells after PEDV infection #MMPMID33059319
  • Chen YM; Helm ET; Groeltz-Thrush JM; Gabler NK; Burrough ER
  • Virology 2021[Jan]; 552 (ä): 43-51 PMID33059319show ga
  • This study focused on intestinal restitution including phenotype switching of absorptive enterocytes and the abundance of different enterocyte subtypes in weaned pigs after porcine epidemic diarrhea virus (PEDV) infection. At 10 days post-PEDV-inoculation, the ratio of villus height to crypt depth in both jejunum and ileum had restored, and the PEDV antigen was not detectable. However, enterocytes at the villus tips revealed epithelial-mesenchymal transition (EMT) in the jejunum in which E-cadherin expression decreased while expression of N-cadherin, vimentin, and Snail increased. Additionally, there was reduced expression of actin in microvilli and Zonula occludens-1 (ZO-1) in tight junctions. Moreover, the protein concentration of transforming growth factor beta1 (TGFbeta1), which mediates EMT and cytoskeleton alteration, was increased. We also found a decreased number of Peyer's patch M cells in the ileum. These results reveal incomplete restitution of enterocytes in the jejunum and potentially impaired immune surveillance in the ileum after PEDV infection.
  • |*Epithelial-Mesenchymal Transition[MESH]
  • |Animals[MESH]
  • |Cadherins/metabolism[MESH]
  • |Coronavirus Infections/immunology/pathology/*veterinary/virology[MESH]
  • |Enterocytes/*pathology[MESH]
  • |Gastroenteritis, Transmissible, of Swine/immunology/*pathology/virology[MESH]
  • |Ileum/immunology/pathology[MESH]
  • |Intestinal Mucosa/pathology[MESH]
  • |Jejunum/immunology/pathology[MESH]
  • |Microvilli/pathology[MESH]
  • |Peyer's Patches/*pathology[MESH]
  • |Porcine epidemic diarrhea virus/*pathogenicity[MESH]
  • |Swine[MESH]
  • |Tight Junctions/pathology[MESH]
  • |Transforming Growth Factor beta1/metabolism[MESH]


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