Publications by authors named "Yukari Itakura"

Antibody-dependent enhancement (ADE) is one of the mechanisms associated with severe clinical outcomes in infections caused by certain viruses, including dengue virus (DENV). Several ADE assay systems have been established, including flow cytometric assays using live viruses, enzyme-linked immuno-sorbent assay (ELISA) for the detection of viral NS1, and luciferase reporter gene assays. Among these, the flow cytometric assay is the most commonly used to evaluate ADE activity; however, it has limitations such as high operational costs due to fixation and immunostaining procedures, as well as a long analysis time.

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Rabies vaccines require repeated immunization to robustly elicit neutralizing antibodies that prevent fatal diseases. Here, we analyzed rabies glycoprotein antibody repertoires at both polyclonal and monoclonal levels following repeated vaccination. Booster vaccination dramatically elevated the neutralizing activity of recalled antibodies, primarily targeting an immunodominant site III epitope with hydrophilic and rugged structures.

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  • Fruit bats can carry dangerous viruses like Nipah and Hendra, which can affect humans and animals.
  • Scientists found a new type of virus called MRV from fruit bats in Indonesia, showing it's the first time this virus has been detected in Southeast Asia.
  • The research revealed that this virus could make laboratory mice very sick, indicating it might be a serious health risk for both animals and people.
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  • Neutralization tests are more accurate than enzyme-linked immunosorbent assays for detecting orthoflavivirus infections, but they need live virus and biosafe labs.
  • Single-round infectious particles (SRIPs) offer a safer alternative as they can't replicate and still help detect neutralizing antibodies.
  • Producing SRIPs at a cooler temperature (28°C) rather than the standard 37°C increases their yield and retains the ability to trigger an immune response, making them useful for diagnostic tests.
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  • - Rabies virus (RABV) is a deadly virus that causes rabies, categorized into fixed laboratory strains and street strains found in the wild, each with different traits.
  • - The Toyohashi strain is a street strain from Japan that was derived from a rabid dog bite and has been used to create a reverse genetics system for research.
  • - Researchers developed a recombinant Toyohashi strain that allows tracking of viral proteins in living cells, making it a valuable resource for studying how rabies street strains replicate at the molecular level.
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  • A recent study found that Beiji nairovirus (BJNV), a tick-borne virus, is widely present in ticks across Japan, particularly in high-altitude areas and on the northern island where Ixodes ticks are prevalent.
  • Researchers identified three distinct types of nairoviruses in Japan—BJNV, Yichun nairovirus (YCNV), and a new Mikuni nairovirus (MKNV)—and noted that BJNV shows high genetic similarity to variants found in China and Russia.
  • The study underscores the importance of monitoring BJNV and related viruses due to their potential risks to public health, especially given evidence of cross-border transmission and unique genetic features in these
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  • Researchers are studying a new type of tick-borne virus called Yezo virus (YEZV), which causes fever after tick bites in parts of East Asia, particularly Japan and China.
  • They created a mouse model using special mice that lack certain immune receptors to better understand how this virus affects the body and to test potential antiviral treatments.
  • Mice infected with YEZV developed severe liver damage and died within six days, but those treated with the antiviral drug favipiravir survived, indicating it could be an effective treatment against this virus.
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  • - The study investigates the effectiveness of monotherapy with oral antiviral ensitrelvir and the anti-inflammatory corticosteroid methylprednisolone, as well as their combination, in treating hamsters infected with SARS-CoV-2, focusing on timing and therapeutic outcomes.
  • - Results showed that combining ensitrelvir and methylprednisolone significantly improved respiratory health and decreased pneumonia risk, even when treatment started two days post-infection, by reducing lung damage and inflammation.
  • - The findings underscore the potential benefits of using a combination therapy of antiviral and corticosteroid drugs for better lung pathology and inflammatory response management in COVID-19 cases, including those caused by the delta and omicron variants.
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The most conserved fusion loop (FL) domain present in the flavivirus envelope protein has been reported as a dominant epitope for cross-reactive antibodies to mosquito-borne flaviviruses (MBFVs). As a result, establishing accurate serodiagnosis for MBFV infections has been difficult as anti-FL antibodies are induced by both natural infection and following vaccination. In this study, we modified the most conserved FL domain to overcome this cross-reactivity.

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The emergence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron variants has led to concerns that ancestral SARS-CoV-2-based vaccines may not be effective against newly emerging Omicron subvariants. The concept of "imprinted immunity" suggests that individuals vaccinated with ancestral virus-based vaccines may not develop effective immunity against newly emerging Omicron subvariants, such as BQ.1.

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  • In late 2022, the SARS-CoV-2 Omicron subvariant XBB emerged from the recombination of two existing BA.2 lineages, BJ.1 and BM.1.1.1, during the summer of 2022.
  • XBB.1 shows strong resistance to vaccines designed for BA.2/5 and has increased fusogenicity, meaning it can fuse with human cells more efficiently due to changes in its spike protein.
  • Research indicates that while XBB.1 is pathogenic, its disease-causing potential in male hamsters is similar to or lower than that of the BA.2.75 variant, marking a notable adaptation in virus evolution through recombination.
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  • In late 2022, several Omicron subvariants emerged globally, characterized by specific amino acid changes in their spike proteins, indicating convergent evolution.
  • The study highlights a problematic lineage, BQ.1.1, which shows higher viral fitness due to five critical amino acid substitutions and better evasion of immune responses compared to the BA.5 subvariant.
  • In tests on hamsters, BQ.1.1 demonstrated lower pathogenicity than BA.5, revealing insights into the evolutionary patterns of Omicron subvariants up to 2022.
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Viral protein assembly and virion budding are tightly regulated to enable the proper formation of progeny virions. At this late stage in the virus life cycle, some enveloped viruses take advantage of the host endosomal sorting complex required for transport (ESCRT) machinery, which contributes to the physiological functions of membrane modulation and abscission. Bullet-shaped viral particles are unique morphological characteristics of rhabdoviruses; however, the involvement of host factors in rhabdovirus infection and, specifically, the molecular mechanisms underlying virion formation are not fully understood.

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  • Rotavirus A (RVA) is a virus that causes diarrhea in humans and animals, with recent discoveries showing it can be transmitted between bats, rodents, and potentially humans, highlighting its zoonotic potential.
  • Researchers isolated RVAs from an Egyptian fruit bat and a Natal multimammate mouse in Zambia, uncovering that one bat RVA strain had genetic similarities to an uncharacterized strain from Kenya, while the rodent RVA had novel genetic profiles.
  • The study found that both RVAs can infect mouse models and human intestinal tissue, showing that they have distinctive entry mechanisms and the ability to cause diarrhea, emphasizing the need for more detailed research on their virological properties.
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  • Oral antiviral agents, such as S-217622 (ensitrelvir), are being researched as effective treatments for COVID-19, alongside vaccination efforts.
  • S-217622 specifically targets the main protease of SARS-CoV-2, demonstrating significant antiviral activity and reducing viral load in infected hamsters.
  • This antiviral agent shows promise against various strains of the virus and is currently undergoing evaluation in a phase 3 clinical trial, highlighting its potential as an oral therapeutic option for COVID-19.
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Nelson Bay orthoreovirus (NBV) is an emerging bat-borne virus and causes respiratory tract infections in humans sporadically. Over the last two decades, several strains genetically related to NBV were isolated from humans and various bat species, predominantly in Southeast Asia (SEA), suggesting a high prevalence of the NBV species in this region. In this study, an orthoreovirus (ORV) belonging to the NBV species was isolated from Indonesian fruit bats' feces, tentatively named Paguyaman orthoreovirus (PgORV).

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  • The genus Flavivirus includes both harmful viruses spread by ticks and mosquitoes and harmless insect-specific flaviviruses (ISFVs).
  • Researchers analyzed the immune response to two ISFVs, Psorophora flavivirus (PSFV) and Barkeji virus (BJV), to compare their antigenic relationships with pathogenic mosquito-borne flaviviruses (MBFVs).
  • Findings revealed that the immune serum for PSFV recognized a broad range of MBFV antigens, while the serum for BJV had limited recognition, indicating that PSFV is more similar to MBFVs than BJV is.
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The amino acid residue at position 333 of the rabies virus (RABV) glycoprotein (G333) is a major determinant of RABV pathogenicity. Virulent RABV strains possess Arg, whereas the attenuated strain HEP-Flury (HEP) possesses Glu. To investigate the potential attenuation mechanism dependent on a single amino acid at G333, comparative analysis was performed between HEP and HEPR mutant with Arg.

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The increasing burden of tick-borne orthonairovirus infections, such as Crimean-Congo hemorrhagic fever, is becoming a global concern for public health. In the present study, we identify a novel orthonairovirus, designated Yezo virus (YEZV), from two patients showing acute febrile illness with thrombocytopenia and leukopenia after tick bite in Hokkaido, Japan, in 2019 and 2020, respectively. YEZV is phylogenetically grouped with Sulina virus detected in Ixodes ricinus ticks in Romania.

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  • A549 lung cells are normally resistant to SARS-CoV-2 due to low levels of the entry receptor ACE2 when grown in standard submerged cultures.
  • Adapting A549 cells to an air-liquid interface (ALI) culture causes them to develop a mucus layer and reduces a proliferation marker, making them more susceptible to SARS-CoV-2 infection.
  • This increased susceptibility is linked to higher expression of ACE2 and TMPRSS2 in ALI culture, and treatment with Camostat, a TMPRSS2 inhibitor, effectively reduced the infection rate in these modified cells.
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Severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) possesses a discriminative polybasic cleavage motif in its spike protein that is recognized by the host furin protease. Proteolytic cleavage activates the spike protein, thereby affecting both the cellular entry pathway and cell tropism of SARS-CoV-2. Here, we investigated the impact of the furin cleavage site on viral growth and pathogenesis using a hamster animal model infected with SARS-CoV-2 variants bearing mutations at the furin cleavage site (S gene mutants).

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Group A rotaviruses (RVAs) are representative enteric virus species and major causes of diarrhea in humans and animals. The RVA virion is a triple-layered particle, and the outermost layer consists of the glycoprotein VP7 and spike protein VP4. To increase the infectivity of RVA, VP4 is proteolytically cleaved into VP5* and VP8* subunits by trypsin; and these subunits form a rigid spike structure on the virion surface.

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Classical swine fever viruses (CSFVs) do typically not show cytopathic effect (CPE) in cell culture, while some strains such as vaccine strain the GPE induce CPE in the swine kidney-derived CPK-NS cell line cultured in serum-free medium. These latter strains commonly lack N-mediated inhibition of type-I interferon (IFN) induction. In order to explore the molecular mechanisms of GPE-induced CPE, we analyzed the cellular pathways involved.

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The evaluation of subvisible particles, including protein aggregates, in therapeutic protein products has been of great interest for both pharmaceutical manufacturers and regulatory agencies. To date, the flow imaging (FI) method has emerged as a powerful tool instead of light obscuration (LO) due to the fact that (1) protein aggregates contain highly transparent particles and thereby escape detection by LO and (2) FI provides detailed morphological characteristics of subvisible particles. However, the FI method has not yet been standardized nor listed in any compendium.

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It is often necessary to modify the dose or schedule of eribulin mesilate (Eri) because of adverse events. Therefore, we retrospectively investigated the optimal approach for Eri dose adjustment and/or dosage interval adjustment. Patients who received Eri at the institutions affiliated with the Division of Oncology of the Aichi Prefectural Society of Hospital Pharmacists between July 2011 and November 2013 were enrolled in this study.

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