Assessment of the Applicability of Capsid-Integrity Assays for Detecting Infectious Norovirus Inactivated by Heat or UV Irradiation
Autor: | David N. Lees, David I. Walker, Connaire L. Jenkins, Lisa J. Cross, James A. Lowther, Tina A. Stapleton |
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Rok vydání: | 2019 |
Předmět: |
0301 basic medicine
Hot Temperature Swine Ultraviolet Rays Epidemiology RNase P viruses Health Toxicology and Mutagenesis 030106 microbiology 010501 environmental sciences Real-Time Polymerase Chain Reaction medicine.disease_cause 01 natural sciences Virus Bacteriophage 03 medical and health sciences Capsid Ribonucleases Virology Enterovirus Infections medicine Animals Humans Coliphage Caliciviridae Infections 0105 earth and related environmental sciences Infectivity biology Gastric Mucins Norovirus RNA biology.organism_classification Biocatalysis Virus Inactivation Food Science |
Zdroj: | Food and Environmental Virology. 11:229-237 |
ISSN: | 1867-0342 1867-0334 |
DOI: | 10.1007/s12560-019-09390-4 |
Popis: | Human noroviruses are the leading cause of viral gastroenteritis. In the absence of a practical culture technique for routine analysis of infectious noroviruses, several methods have been developed to discriminate between infectious and non-infectious viruses by removing non-viable viruses prior to analysis by RT-qPCR. In this study, two such methods (RNase and porcine gastric mucin) which were designed to remove viruses with compromised capsids (and therefore assumed to be non-viable), were assessed for their ability to quantify viable F-specific RNA bacteriophage (FRNAP) and human norovirus following inactivation by UV-C or heat. It was found that while both methods could remove a proportion of non-viable viruses, a large proportion of non-viable virus remained to be detected by RT-qPCR, leading to overestimations of the viable population. A model was then developed to determine the proportion of RT-qPCR detectable RNA from non-viable viruses that must be removed by such methods to reduce overestimation to acceptable levels. In most cases, nearly all non-viable virus must be removed to reduce the log overestimation of viability to within levels that might be considered acceptable (e.g. below 0.5 log10). This model could be applied when developing alternative pre-treatment methods to determine how well they should perform to be comparable to established infectivity assays. |
Databáze: | OpenAIRE |
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