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  1. Article ; Online: Varicella Vaccine-Induced Infantile Zoster-Like Skin Rash.

    Sugai, Tatsuro / Fujita, Yasuyuki / Yamada, Souichi / Fukushi, Shuetsu / Inamura, Emi / Hatakeyama, Kinya / Shimizu, Satoko

    The Journal of pediatrics

    2022  Volume 251, Page(s) 218–219

    MeSH term(s) Humans ; Chickenpox/prevention & control ; Chickenpox Vaccine/adverse effects ; Exanthema/etiology ; Herpes Zoster ; Vaccines, Attenuated
    Chemical Substances Chickenpox Vaccine ; Vaccines, Attenuated
    Language English
    Publishing date 2022-08-23
    Publishing country United States
    Document type Case Reports
    ZDB-ID 3102-1
    ISSN 1097-6833 ; 0022-3476
    ISSN (online) 1097-6833
    ISSN 0022-3476
    DOI 10.1016/j.jpeds.2022.08.032
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Macacine alphaherpesvirus 1 (B Virus) Infection in Humans, Japan, 2019

    Souichi Yamada / Harutaka Katano / Yuko Sato / Tadaki Suzuki / Akihiko Uda / Keita Ishijima / Motoi Suzuki / Daigo Yamada / Shizuko Harada / Hitomi Kinoshita / Phu Hoang Anh Nguyen / Hideki Ebihara / Ken Maeda / Masayuki Saijo / Shuetsu Fukushi

    Emerging Infectious Diseases, Vol 30, Iss 1, Pp 177-

    2024  Volume 179

    Abstract: Two human patients with Macacine alphaherpesvirus 1 infection were identified in Japan in 2019. Both patients had worked at the same company, which had a macaque facility. The rhesus-genotype B virus genome was detected in cerebrospinal fluid samples ... ...

    Abstract Two human patients with Macacine alphaherpesvirus 1 infection were identified in Japan in 2019. Both patients had worked at the same company, which had a macaque facility. The rhesus-genotype B virus genome was detected in cerebrospinal fluid samples from both patients.
    Keywords Macacine alphaherpesvirus 1 ; B virus ; viruses ; zoonoses ; Japan ; Medicine ; R ; Infectious and parasitic diseases ; RC109-216
    Language English
    Publishing date 2024-01-01T00:00:00Z
    Publisher Centers for Disease Control and Prevention
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  3. Article ; Online: Macacine alphaherpesvirus 1 (B Virus) Infection in Humans, Japan, 2019.

    Yamada, Souichi / Katano, Harutaka / Sato, Yuko / Suzuki, Tadaki / Uda, Akihiko / Ishijima, Keita / Suzuki, Motoi / Yamada, Daigo / Harada, Shizuko / Kinoshita, Hitomi / Nguyen, Phu Hoang Anh / Ebihara, Hideki / Maeda, Ken / Saijo, Masayuki / Fukushi, Shuetsu

    Emerging infectious diseases

    2023  Volume 30, Issue 1, Page(s) 177–179

    Abstract: Two human patients with Macacine alphaherpesvirus 1 infection were identified in Japan in 2019. Both patients had worked at the same company, which had a macaque facility. The rhesus-genotype B virus genome was detected in cerebrospinal fluid samples ... ...

    Abstract Two human patients with Macacine alphaherpesvirus 1 infection were identified in Japan in 2019. Both patients had worked at the same company, which had a macaque facility. The rhesus-genotype B virus genome was detected in cerebrospinal fluid samples from both patients.
    MeSH term(s) Animals ; Humans ; Herpesvirus 1, Cercopithecine ; Japan/epidemiology ; Macaca mulatta ; Genotype ; Monkey Diseases
    Language English
    Publishing date 2023-12-12
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1380686-5
    ISSN 1080-6059 ; 1080-6040
    ISSN (online) 1080-6059
    ISSN 1080-6040
    DOI 10.3201/eid3001.230435
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: OLIG2 translocates to chromosomes during mitosis via a temperature downshift: A novel neural cold response of mitotic bookmarking.

    Hayashi, Shinichi / Seki-Omura, Ryohei / Yamada, Shintaro / Kamata, Taito / Sato, Yuki / Oe, Souichi / Koike, Taro / Nakano, Yousuke / Iwashita, Hikaru / Hirahara, Yukie / Tanaka, Susumu / Sekijima, Tsuneo / Ito, Takeshi / Yasukochi, Yoshiki / Higasa, Koichiro / Kitada, Masaaki

    Gene

    2023  Volume 891, Page(s) 147829

    MeSH term(s) Temperature ; Chromosomes ; Mitosis ; Chromatin
    Chemical Substances Chromatin
    Language English
    Publishing date 2023-09-23
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 391792-7
    ISSN 1879-0038 ; 0378-1119
    ISSN (online) 1879-0038
    ISSN 0378-1119
    DOI 10.1016/j.gene.2023.147829
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Regulatory non-coding RNAs in nervous system development and disease.

    Oe, Souichi / Kimura, Tominori / Yamada, Hisao

    Frontiers in bioscience (Landmark edition)

    2019  Volume 24, Issue 7, Page(s) 1203–1240

    Abstract: Recent evidence demonstrates that long non-coding RNAs (lncRNAs) regulate the expression of multiple genes in an epigenetic, transcriptional, or post-transcriptional manner. They are involved in various cellular phenomena, such as the recruitment of ... ...

    Abstract Recent evidence demonstrates that long non-coding RNAs (lncRNAs) regulate the expression of multiple genes in an epigenetic, transcriptional, or post-transcriptional manner. They are involved in various cellular phenomena, such as the recruitment of transcription factors, epigenetic chaperoning, control of alternative splicing, mRNA stability and translational activity, as well as acting as decoys against microRNAs. In this review, we summarize the pivotal roles of lncRNAs in regulation of the gene expression involved in neural cell differentiation, synaptogenesis and synaptic plasticity in the central nervous system (CNS). We also describe the aberrant expression of multiple lncRNAs involved in the pathogenesis of neurological diseases. The abnormal expression of lncRNAs leads to altered expression levels of target genes, which contributes to neurodegenerative diseases, such as in Alzheimer's disease and Parkinson's disease, and to the formation of tumors, such as glioma. Accordingly, we discuss recent findings for the modes of action of lncRNAs in normal CNS development and for aberrant lncRNA actions in the pathogenesis of neuronal diseases.
    MeSH term(s) Alzheimer Disease/genetics ; Cell Differentiation/genetics ; Central Nervous System/growth & development ; Central Nervous System/metabolism ; Gene Expression Regulation ; Humans ; Neurodegenerative Diseases/genetics ; Neuronal Plasticity/genetics ; Neurons/cytology ; Neurons/metabolism ; Parkinson Disease/genetics ; RNA, Long Noncoding/genetics
    Chemical Substances RNA, Long Noncoding
    Language English
    Publishing date 2019-06-01
    Publishing country Singapore
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 2704569-9
    ISSN 2768-6698 ; 1093-9946
    ISSN (online) 2768-6698
    ISSN 1093-9946
    DOI 10.2741/4776
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Cpeb1 expression is post‐transcriptionally regulated by AUF1, CPEB1, and microRNAs

    Souichi Oe / Shinichi Hayashi / Susumu Tanaka / Taro Koike / Yukie Hirahara / Rio Kakizaki / Sumika Sakamoto / Yasuko Noda / Hisao Yamada / Masaaki Kitada

    FEBS Open Bio, Vol 12, Iss 1, Pp 82-

    2022  Volume 94

    Abstract: Cytoplasmic polyadenylation element binding protein 1 (CPEB1) regulates the translation of numerous mRNAs. We previously showed that AU‐rich binding factor 1 (AUF1) regulates Cpeb1 expression through the 3’ untranslated region (3’UTR). To investigate the ...

    Abstract Cytoplasmic polyadenylation element binding protein 1 (CPEB1) regulates the translation of numerous mRNAs. We previously showed that AU‐rich binding factor 1 (AUF1) regulates Cpeb1 expression through the 3’ untranslated region (3’UTR). To investigate the molecular basis of the regulatory potential of the Cpeb1 3’UTR, here we performed reporter analyses that examined expression levels of Gfp reporter mRNA containing the Cpeb1 3’UTR. Our findings indicate that CPEB1 represses the translation of Cpeb1 mRNA and that miR‐145a‐5p and let‐7b‐5p are involved in the reduction in Cpeb1 expression in the absence of AUF1. These results suggest that Cpeb1 expression is post‐transcriptionally regulated by AUF1, CPEB1, and microRNAs.
    Keywords CPEB1 ; AUF1 ; miR‐145a‐5p ; let‐7b‐5p ; post‐transcriptional regulation ; Neuro2a cell ; Biology (General) ; QH301-705.5
    Language English
    Publishing date 2022-01-01T00:00:00Z
    Publisher Wiley
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  7. Article ; Online: Virulence of Herpes Simplex Virus 1 Harboring a UAG Stop Codon between the First and Second Initiation Codon in the Thymidine Kinase Gene.

    Nguyen, Phu Hoang Anh / Yamada, Souichi / Harada, Shizuko / Fukushi, Shuetsu / Mizuguchi, Masashi / Saijo, Masayuki

    Japanese journal of infectious diseases

    2021  Volume 75, Issue 4, Page(s) 368–373

    Abstract: Herpes simplex virus 1 (HSV-1)-TK (8UAG) expresses a truncated thymidine kinase (TK) translated from the second initiation codon due to a stop codon (UAG) at the 8th position (counted from the first initiation codon). Here, we showed that the sensitivity ...

    Abstract Herpes simplex virus 1 (HSV-1)-TK (8UAG) expresses a truncated thymidine kinase (TK) translated from the second initiation codon due to a stop codon (UAG) at the 8th position (counted from the first initiation codon). Here, we showed that the sensitivity of HSV-1-TK (8UAG) to acyclovir (ACV) is similar to that of the control HSV-1 wild-type (WT), which expresses an intact TK protein. However, HSV-1-TK (44UAG), which expresses a truncated TK due to a UAG codon at position 44, showed lower sensitivity to ACV. A mouse infection model was used to compare the virulence of HSV-1-TK (8UAG) and HSV-1-TK (44UAG) to that of HSV-1 WT. The 50% lethal dose (LD
    MeSH term(s) Acyclovir ; Animals ; Antiviral Agents/pharmacology ; Codon, Initiator/genetics ; Codon, Terminator/genetics ; Herpesvirus 1, Human/genetics ; Herpesvirus 1, Human/pathogenicity ; Mice ; Mutation ; Thymidine Kinase/genetics ; Virulence/genetics
    Chemical Substances Antiviral Agents ; Codon, Initiator ; Codon, Terminator ; Thymidine Kinase (EC 2.7.1.21) ; Acyclovir (X4HES1O11F)
    Language English
    Publishing date 2021-12-28
    Publishing country Japan
    Document type Journal Article
    ZDB-ID 1478383-6
    ISSN 1884-2836 ; 1344-6304
    ISSN (online) 1884-2836
    ISSN 1344-6304
    DOI 10.7883/yoken.JJID.2021.674
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Performance Evaluation of Real-Time RT-PCR Assays for the Detection of Severe Acute Respiratory Syndrome Coronavirus-2 Developed by the National Institute of Infectious Diseases, Japan.

    Shirato, Kazuya / Tomita, Yuriko / Katoh, Hiroshi / Yamada, Souichi / Fukushi, Shuetsu / Matsuyama, Shutoku / Takeda, Makoto

    Japanese journal of infectious diseases

    2021  Volume 74, Issue 5, Page(s) 465–472

    Abstract: Soon after the 2019 outbreak of coronavirus disease 2019 in Wuhan, China, a protocol for real-time RT-PCR assay detection of severe acute respiratory syndrome coronavirus (SARS-CoV-2) was established by the National Institute of Infectious Diseases (NIID) ...

    Abstract Soon after the 2019 outbreak of coronavirus disease 2019 in Wuhan, China, a protocol for real-time RT-PCR assay detection of severe acute respiratory syndrome coronavirus (SARS-CoV-2) was established by the National Institute of Infectious Diseases (NIID) in Japan. The protocol used Charité's nucleocapsid (Sarbeco-N) and NIID nucleocapsid (NIID-N2) assays. During the following months, SARS-CoV-2 spread and caused a global pandemic, and various SARS-CoV-2 sequences were registered in public databases, such as the Global Initiative on Sharing All Influenza Data (GISAID). In this study, we evaluated the S2 assay (NIID-S2) that was newly developed to replace the Sarbeco-N assay and the performance of the NIID-N2 and NIID-S2 assays, referring to mismatches in the primer/probe targeted region. We found that the analytical sensitivity and specificity of the NIID-S2 set were comparable to those of the NIID-N2 assay, and the detection rate for clinical specimens was identical to that of the NIID-N2 assay. Furthermore, among the available sequences (approximately 192,000), the NIID-N2 and NIID-S2 sets had 2.6% and 1.2% mismatched sequences, respectively, although most of these mismatches did not affect the amplification efficiency, except the 3' end of the NIID-N2 forward primer. These findings indicate that the previously developed NIID-N2 assay is suitable for the detection of SARS-CoV-2 with support from the newly developed NIID-S2 set.
    MeSH term(s) COVID-19/diagnosis ; COVID-19 Nucleic Acid Testing/methods ; Coronavirus Nucleocapsid Proteins/genetics ; DNA Primers/genetics ; Humans ; Japan ; Phosphoproteins/genetics ; RNA, Viral/analysis ; RNA, Viral/genetics ; SARS-CoV-2/genetics ; SARS-CoV-2/isolation & purification ; Sensitivity and Specificity ; Spike Glycoprotein, Coronavirus/genetics
    Chemical Substances Coronavirus Nucleocapsid Proteins ; DNA Primers ; Phosphoproteins ; RNA, Viral ; Spike Glycoprotein, Coronavirus ; nucleocapsid phosphoprotein, SARS-CoV-2 ; spike protein, SARS-CoV-2
    Language English
    Publishing date 2021-02-26
    Publishing country Japan
    Document type Evaluation Study ; Journal Article
    ZDB-ID 1478383-6
    ISSN 1884-2836 ; 1344-6304
    ISSN (online) 1884-2836
    ISSN 1344-6304
    DOI 10.7883/yoken.JJID.2020.1079
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Impact of Reinfection with SARS-CoV-2 Omicron Variants in Previously Infected Hamsters.

    Shiwa-Sudo, Nozomi / Sakai, Yusuke / Iwata-Yoshikawa, Naoko / Watanabe, Shinji / Yamada, Souichi / Kuroda, Yudai / Yamamoto, Tsukasa / Shirakura, Masayuki / Fujisaki, Seiichiro / Miyazaki, Kaya / Miura, Hideka / Nagata, Shiho / Fukushi, Shuetsu / Maeda, Ken / Hasegawa, Hideki / Suzuki, Tadaki / Nagata, Noriyo

    Journal of virology

    2023  Volume 97, Issue 1, Page(s) e0136622

    Abstract: The diversity of SARS-CoV-2 mutations raises the possibility of reinfection of individuals previously infected with earlier variants, and this risk is further increased by the emergence of the B.1.1.529 Omicron variant. In this study, we used ... ...

    Abstract The diversity of SARS-CoV-2 mutations raises the possibility of reinfection of individuals previously infected with earlier variants, and this risk is further increased by the emergence of the B.1.1.529 Omicron variant. In this study, we used an
    MeSH term(s) Animals ; Cricetinae ; COVID-19 ; Mesocricetus ; Reinfection ; RNA, Viral ; SARS-CoV-2/genetics
    Chemical Substances RNA, Viral
    Language English
    Publishing date 2023-01-12
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 80174-4
    ISSN 1098-5514 ; 0022-538X
    ISSN (online) 1098-5514
    ISSN 0022-538X
    DOI 10.1128/jvi.01366-22
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Pathological and virological findings of type I interferon receptor knockout mice upon experimental infection with Heartland virus.

    Fujii, Hikaru / Fukushi, Shuetsu / Yoshikawa, Tomoki / Nagata, Noriyo / Taniguchi, Satoshi / Shimojima, Masayuki / Yamada, Souichi / Tani, Hideki / Uda, Akihiko / Maeki, Takahiro / Harada, Shizuko / Kurosu, Takeshi / Lim, Chang Kweng / Nakayama, Eri / Takayama-Ito, Mutsuyo / Watanabe, Shumpei / Ebihara, Hideki / Morikawa, Shigeru / Saijo, Masayuki

    Virus research

    2023  Volume 340, Page(s) 199301

    Abstract: Heartland virus (HRTV) causes generalized symptoms, severe shock, and multiple organ failure. We previously reported that interferon-α/β receptor knockout ( ... ...

    Abstract Heartland virus (HRTV) causes generalized symptoms, severe shock, and multiple organ failure. We previously reported that interferon-α/β receptor knockout (IFNAR
    MeSH term(s) Animals ; Mice ; Receptor, Interferon alpha-beta/genetics ; Mice, Knockout ; Interferons ; Liver ; Interleukin-12 ; Interferon Type I ; Bunyaviridae
    Chemical Substances Receptor, Interferon alpha-beta (156986-95-7) ; Interferons (9008-11-1) ; Interleukin-12 (187348-17-0) ; Interferon Type I
    Language English
    Publishing date 2023-12-16
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 605780-9
    ISSN 1872-7492 ; 0168-1702
    ISSN (online) 1872-7492
    ISSN 0168-1702
    DOI 10.1016/j.virusres.2023.199301
    Database MEDical Literature Analysis and Retrieval System OnLINE

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