Back to Search
Start Over
Blood group substances as potential therapeutic agents for the prevention and treatment of infection with noroviruses proving novel binding patterns in human tissues.
- Source :
-
PloS one [PLoS One] 2014 Feb 18; Vol. 9 (2), pp. e89071. Date of Electronic Publication: 2014 Feb 18 (Print Publication: 2014). - Publication Year :
- 2014
-
Abstract
- Blood group-related glycans determining ABO and Lewis blood groups are known to function as attachment factors for most of the norovirus (NoV) strains. To identify binding specificity of each NoV, recombinant norovirus-like particles (VLPs) and human saliva samples with different ABO, Lewis phenotypes and secretor status have been commonly applied. When binding specificities of VLPs prepared from 16 different genotypes of NoVs in GI and GII genogroups were characterized in samples of human gastric mucosa compared to human saliva based on blood group phenotypes, considerable differences were observed for several strains. Novel binding specificities determined by an ELISA using preparations from human gastric mucosa were also ascertained by immunohistochemical analyses using human jejunal mucosa, widely believed to be susceptible to NoV infection. Further, A, B and O(H) blood group substances prepared from porcine and squid tissues were found to be effective for preventing ABO blood group-specific binding of VLPs to both saliva and mucosa samples. Therefore, these blood group substances might have potential for the prevention and treatment of NoV infection.
- Subjects :
- Animals
Blood Group Antigens therapeutic use
Decapodiformes
Enzyme-Linked Immunosorbent Assay
Gastric Mucosa metabolism
Humans
Immunohistochemistry
Polysaccharides blood
Protein Binding physiology
Saliva metabolism
Swine
Virion metabolism
Blood Group Antigens metabolism
Caliciviridae Infections blood
Caliciviridae Infections prevention & control
Norovirus metabolism
Polysaccharides metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1932-6203
- Volume :
- 9
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- PloS one
- Publication Type :
- Academic Journal
- Accession number :
- 24558470
- Full Text :
- https://doi.org/10.1371/journal.pone.0089071