4 results match your criteria: "Tokyo Medical and Dental Universitygrid.265073.5[Affiliation]"

Article Synopsis
  • - Neisseria meningitidis causes serious invasive meningococcal disease (IMD), and the rise of antibiotic-resistant strains is a significant global health issue.
  • - A study analyzed 87 N. meningitidis strains from Japan and found that most were still susceptible to key antibiotics except for penicillin, which had some resistant isolates.
  • - The research identified specific resistant lineages in Japan that could pose future risks, emphasizing the importance of monitoring antibiotic resistance to ensure effective treatment for IMD patients and their close contacts.
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-Encoding IncP-6 Plasmids in Citrobacter freundii and Klebsiella variicola Strains from Hospital Sewage in Japan.

Appl Environ Microbiol

April 2022

Department of Molecular Microbiology, Graduate School of Medicine and Dental Science, Tokyo Medical and Dental Universitygrid.265073.5, Bunkyo-ku, Tokyo, Japan.

Klebsiella pneumoniae carbapenemase (KPC) producers are an emerging threat to global health, and the hospital water environment is considered an important reservoir of these life-threatening bacteria. We characterized plasmids of KPC-2-producing Citrobacter freundii and Klebsiella variicola isolates recovered from hospital sewage in Japan. Antimicrobial susceptibility testing, whole-genome sequencing analysis, bacterial conjugation, and transformation experiments were performed for both KPC-2 producers.

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RASSF6, a member of the tumor suppressor Ras-association domain family (RASSF) proteins, regulates cell cycle arrest and apoptosis via p53 and plays a tumor suppressor role. We previously reported that RASSF6 blocks MDM2-mediated p53 degradation and enhances p53 expression. In this study, we demonstrated that RASSF6 has nuclear localization and nuclear export signals and that DNA damage triggers the nuclear accumulation of RASSF6.

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Viral protein U (Vpu) is an accessory protein encoded by human immunodeficiency virus type 1 (HIV-1) and certain simian immunodeficiency virus (SIV) strains. Some of these viruses were reported to use Vpu to overcome restriction by BST-2 of their natural hosts. Our own recent report revealed that Vpu of SIVgsn-99CM71 (SIVgsn71) antagonizes human BST-2 through two AxxxxxxxW motifs (AW and AW), whereas antagonizing BST-2 of its natural host, greater spot-nosed monkey (GSN), involved only the AW motif.

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