Back to Search
Start Over
The effect of proteolytic enzymes and pH on GII.4 norovirus, during both interactions and non-interaction with Histo-Blood Group Antigens.
- Source :
-
Scientific reports [Sci Rep] 2020 Oct 21; Vol. 10 (1), pp. 17926. Date of Electronic Publication: 2020 Oct 21. - Publication Year :
- 2020
-
Abstract
- Human noroviruses (HuNoVs) are the leading cause of acute gastroenteritis worldwide. Histo-Blood Groups Antigens (HBGAs) have been described as attachment factors, promoting HuNoV infection. However, their role has not yet been elucidated. This study aims to evaluate the ability of HBGAs to protect HuNoVs against various factors naturally found in the human digestive system. The effects of acid pH and proteolytic enzymes (pepsin, trypsin, and chymotrypsin) on GII.4 virus-like particles (VLPs) and GII.4 HuNoVs were studied, both during interactions and non-interaction with HBGAs. The results showed that GII.4 VLPs and GII.4 HuNoVs behaved differently following the treatments. GII.4 VLPs were disrupted at a pH of less than 2.0 and in the presence of proteolytic enzymes (1,500 units/mL pepsin, 100 mg/mL trypsin, and 100 mg/mL chymotrypsin). VLPs were also partially damaged by lower concentrations of trypsin and chymotrypsin (0.1 mg/mL). Conversely, the capsids of GII.4 HuNoVs were not compromised by such treatments, since their genomes were not accessible to RNase. HBGAs were found to offer GII.4 VLPs no protection against an acid pH or proteolytic enzymes.
- Subjects :
- Capsid drug effects
Chymotrypsin pharmacology
Dose-Response Relationship, Drug
Humans
Hydrogen-Ion Concentration
Norovirus genetics
Norovirus metabolism
Pepsin A pharmacology
Trypsin pharmacology
Virus Attachment drug effects
Blood Group Antigens metabolism
Blood Group Antigens physiology
Caliciviridae Infections virology
Gastroenteritis virology
Norovirus drug effects
Norovirus pathogenicity
Peptide Hydrolases pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 2045-2322
- Volume :
- 10
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Scientific reports
- Publication Type :
- Academic Journal
- Accession number :
- 33087754
- Full Text :
- https://doi.org/10.1038/s41598-020-74728-z