Junji Hosokawa-Muto

Dr. Junji Hosokawa-Muto

orcid

Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 August 2015 in Journal of Forensic and Legal Medicine
Verified
Journal Article
Closed access
JHJunji Hosokawa-Muto
Junji Hosokawa-Muto
YFYoshihito Fujinami
Yoshihito Fujinami
NMNatsuko Mizuno
Natsuko Mizuno

27 June 2019 in Forensic Science, Medicine and Pathology
Verified
Journal Article
Closed access
PDF file
JHJunji Hosokawa-Muto
Junji Hosokawa-Muto
HSHiroki Sakai
Hiroki Sakai
YSYukiko Sassa
Yukiko Sassa
YFYoshihito Fujinami
Yoshihito Fujinami
MKMai Kishimoto
Mai Kishimoto
HNHiroaki Nakahara
Hiroaki Nakahara

1 December 2015 in Forensic Science International
Verified
Journal Article
Closed access
YFYoshihito Fujinami
Yoshihito Fujinami
JHJunji Hosokawa-Muto
Junji Hosokawa-Muto
NMNatsuko Mizuno
Natsuko Mizuno

1 November 2013 in Journal of Forensic and Legal Medicine
Verified
Journal Article
Closed access
JHJunji Hosokawa-Muto
Junji Hosokawa-Muto
YFYoshihito Fujinami
Yoshihito Fujinami
NMNatsuko Mizuno
Natsuko Mizuno

14 January 2022 in Diagnostics
Verified
Journal Article
Open access
PDF file
JHJunji Hosokawa-Muto
Junji Hosokawa-Muto
YSYukiko Sassa-O’brien
Yukiko Sassa-O’brien
YFYoshihito Fujinami
Yoshihito Fujinami
HNHiroaki Nakahara
Hiroaki Nakahara
When examining infectious samples, rapid identification of the pathogenic agent is required for diagnosis and treatment or for investigating the cause of death. In our previous study, we applied exhaustive amplification using non-specific primers (the rapid determination system of viral genome sequences, the RDV method) to identify the causative virus via swab samples from a cat with a suspected viral infection. The purpose of the current study is to investigate suitable methods for the rapid identification of causative pathogens from infected tissue samples. First, the influenza virus was inoculated into mice to prepare infected tissue samples. RNA extracted from the mouse lung homogenates was transcribed into cDNA and then analyzed using the RDV method and next-generation sequencing, using MiSeq and MinION sequencers. The RDV method was unable to detect the influenza virus in the infected tissue samples. However, influenza virus reads were detected using next-generation sequencing. Comparing MiSeq and MinION, the time required for library and sequence preparation was shorter for MinION sequencing than for MiSeq sequencing. We conclude that when a causative virus needs to be rapidly identified from an infectious sample, MinION sequencing is currently the method of choice.

1 January 2008 in Seibutsu Butsuri
Verified
Journal Article
Open access
PDF file
KYKei-Ichi Yamaguchi
Kei-Ichi Yamaguchi
TMTomoharu Matsumoto
Tomoharu Matsumoto
JHJunji Hosokawa-Muto
Junji Hosokawa-Muto
KKKazuo Kuwata
Kazuo Kuwata
Japan's largest platform for academic e-journals: J-STAGE is a full text database for reviewed academic papers published by Japanese societies