Volume 4
Journal of Infectious Diseases and Treatment
ISSN: 2472-1093
Page 57
Euro Infectious Diseases 2018 &
Histopathology 2018
September 27-29, 2018
&
JOINT EVENT
September 27-29, 2018 Rome, Italy
5
th
International Conference on
Histopathology & Cytopathology
10
th
Euro-Global Conference on
Infectious Diseases
A study on genomic diversity of norovirus using deep sequencing approach
InSun Joo, JeongSu Lee, EunSook An, SiYeon Ju
and
MinHee Jeong
National Institute of Food and Drug Safety Evaluation, Korea
A
study on genomic diversity of norovirus using deep sequencing approach: Norovirus (NoVs) are the leading cause of
epidemic and sporadic gastroenteritis outbreaks worldwide affecting across all age groups, responsible for approximately
90% of all outbreak of viral gastroenteritis. Each year, mortality due to NoV is estimated at 570-800 in the United States, with
approximately $777 million in health-care costs. NoV, a genus within the
Caliciviridae
family, is small non-enveloped virus
with a positive single-stranded RNA genome of 7.5-7.7 kb organized into three open reading frames (ORFs). ORF1 encodes
six non-structural proteins, including RNA dependent RNA polymerase (RdRP). ORF2, ORF3 encode VP1 and VP2 capsid
proteins. Generally, the genome of RNA virus has been known to change constantly from mutational event and revealed novel
variant. In the previous reports, the NoV GII.4 strains had been known to evolve at a rate of 4.3-9.0X10-4 mutations per site
per year and to share a most recent common ancestor in the early 1980s. The goal of this study was to analyze NoV complete
sequence and detect variants using next generation sequencing (NGS) method. Sequence reads of NoV were constructed
to GII.4 whole genome sequence and were assembled with reference genome. In phylogenetic analysis, the sequence was
clustered with 2006b variants. Moreover, VP1 (i.e. capsid protein) were revealed that the amino acid sequence altered three
sites in hyper variable domains, and it led to changes in protein structure. Continued molecular studies of NoV by NGS,
including approaching of complete genome, is important for monitoring emerging strains in our strategy to prevent of NoV
outbreaks in Korea.
jis901@korea.krJ Infec Dis Treat 2018, Volume 4
DOI: 10.21767/2472-1093-C1-003




