| Literature DB >> 27412790 |
Umesh C Karandikar1, Sue E Crawford1, Nadim J Ajami1, Kosuke Murakami1, Baijun Kou1, Khalil Ettayebi1, Genovefa A Papanicolaou2, Ubonvan Jongwutiwes2, Miguel-Angel Perales3,4, Jinru Shia5, David Mercer6, Milton J Finegold7,8, Jan Vinjé9, Robert L Atmar1,10, Mary K Estes1,10.
Abstract
Human noroviruses (HuNoVs) can often cause chronic infections in solid organ and haematopoietic stem cell transplant (HSCT) patients. Based on histopathological changes observed during HuNoV infections, the intestine is the presumed site of virus replication in patients; however, the cell types infected by HuNoVs remain unknown. The objective of this study was to characterize histopathological changes during HuNoV infection and to determine the cell types that may be permissive for HuNoV replication in transplant patients. We analysed biopsies from HuNoV-infected and non-infected (control) transplant patients to assess histopathological changes in conjunction with detection of HuNoV antigens to identify the infected cell types. HuNoV infection in immunocompromised patients was associated with histopathological changes such as disorganization and flattening of the intestinal epithelium. The HuNoV major capsid protein, VP1, was detected in all segments of the small intestine, in areas of biopsies that showed histopathological changes. Specifically, VP1 was detected in enterocytes, macrophages, T cells and dendritic cells. HuNoV replication was investigated by detecting the non-structural proteins, RdRp and VPg. We detected RdRp and VPg along with VP1 in duodenal and jejunal enterocytes. These results provide critical insights into histological changes due to HuNoV infection in immunocompromised patients and propose human enterocytes as a physiologically relevant cell type for HuNoV cultivation.Entities:
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Year: 2016 PMID: 27412790 PMCID: PMC5756488 DOI: 10.1099/jgv.0.000545
Source DB: PubMed Journal: J Gen Virol ISSN: 0022-1317 Impact factor: 3.891