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  • 1
    In: Journal of Virology, American Society for Microbiology, Vol. 96, No. 13 ( 2022-07-13)
    Abstract: Porcine epidemic diarrhea virus (PEDV) is the globally distributed alphacoronavirus that can cause lethal watery diarrhea in piglets, causing substantial economic damage. However, the current commercial vaccines cannot effectively the existing diseases. Thus, it is of great necessity to identify the host antiviral factors and the mechanism by which the host immune system responds against PEDV infection required to be explored. The current work demonstrated that the host protein, the far upstream element-binding protein 3 (FUBP3), could be controlled by the transcription factor TCFL5, which could suppress PEDV replication through targeting and degrading the nucleocapsid (N) protein of the virus based on selective autophagy. For the ubiquitination of the N protein, FUBP3 was found to recruit the E3 ubiquitin ligase MARCH8/MARCHF8, which was then identified, transported to, and degraded in autolysosomes via NDP52/CALCOCO2 (cargo receptors), resulting in impaired viral proliferation. Additionally, FUBP3 was found to positively regulate type-I interferon (IFN-I) signaling and activate the IFN-I signaling pathway by interacting and increasing the expression of tumor necrosis factor (TNF) receptor-associated factor 3 (TRAF3). Collectively, this study showed a novel mechanism of FUBP3-mediated virus restriction, where FUBP3 was found to degrade the viral N protein and induce IFN-I production, aiming to hinder the replication of PEDV. IMPORTANCE PEDV refers to the alphacoronavirus that is found globally and has re-emerged recently, causing severe financial losses. In PEDV infection, the host activates various host restriction factors to maintain innate antiviral responses to suppress virus replication. Here, FUBP3 was detected as a new host restriction factor. FUBP3 was found to suppress PEDV replication via the degradation of the PEDV-encoded nucleocapsid (N) protein via E3 ubiquitin ligase MARCH8 as well as the cargo receptor NDP52/CALCOCO2. Additionally, FUBP3 upregulated the IFN-I signaling pathway by interacting with and increasing tumor necrosis factor (TNF) receptor-associated factor 3 (TRAF3) expression. This study further demonstrated that another layer of complexity could be added to the selective autophagy and innate immune response against PEDV infection are complicated.
    Type of Medium: Online Resource
    ISSN: 0022-538X , 1098-5514
    Language: English
    Publisher: American Society for Microbiology
    Publication Date: 2022
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  • 2
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 2022
    In:  Monthly Notices of the Royal Astronomical Society Vol. 518, No. 1 ( 2022-11-12), p. 87-92
    In: Monthly Notices of the Royal Astronomical Society, Oxford University Press (OUP), Vol. 518, No. 1 ( 2022-11-12), p. 87-92
    Abstract: We investigate archival Hubble Space Telescope ACS/SBC F140LP observations of NGC 1399 to search for evidence of multiple stellar populations in extragalactic globular clusters. Enhanced far-ultraviolet (FUV) populations are thought to be indicators of He-enhanced second generation populations in globular clusters, specifically extreme/blue horizontal branch stars. Out of 149 globular clusters in the field of view, 58 have FUV counterparts with magnitudes brighter than 28.5. Six of these FUV-detected globular clusters are also detected in X-rays, including one ultraluminous X-ray source (LX & gt; 1039 erg/s). While optically bright clusters corresponded to brighter FUV counterparts, we observe FUV emission from both metal-rich and metal-poor clusters, which implies that the FUV excess is not dependent on optical colour. We also find no evidence that the cluster size influences the FUV emission. The clusters with X-ray emission are not unusually FUV bright, which suggests that even the ultraluminous X-ray source does not provide significant FUV contributions. NGC 1399 is only the fourth galaxy to have its globular cluster system probed for evidence of FUV-enhanced populations, and we compare these clusters to previous studies of the Milky Way, M31, M87, and the brightest cluster in M81. These sources indicate that many globular clusters likely host extreme HB stars and/or second generation stars, and highlight the need for more complete FUV observations of extragalactic globular cluster systems.
    Type of Medium: Online Resource
    ISSN: 0035-8711 , 1365-2966
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2022
    detail.hit.zdb_id: 2016084-7
    SSG: 16,12
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  • 3
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 1997
    In:  Chromatographia Vol. 46, No. 7-8 ( 1997-10), p. 430-436
    In: Chromatographia, Springer Science and Business Media LLC, Vol. 46, No. 7-8 ( 1997-10), p. 430-436
    Type of Medium: Online Resource
    ISSN: 0009-5893 , 1612-1112
    RVK:
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 1997
    detail.hit.zdb_id: 2019091-8
    detail.hit.zdb_id: 80097-1
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  • 4
    In: Gene, Elsevier BV, Vol. 827 ( 2022-06), p. 146480-
    Type of Medium: Online Resource
    ISSN: 0378-1119
    RVK:
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2022
    detail.hit.zdb_id: 1491012-3
    SSG: 12
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  • 5
    In: Microbiological Research, Elsevier BV, Vol. 274 ( 2023-09), p. 127423-
    Type of Medium: Online Resource
    ISSN: 0944-5013
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2023
    detail.hit.zdb_id: 2051526-1
    detail.hit.zdb_id: 1189614-0
    SSG: 12
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  • 6
    Online Resource
    Online Resource
    Wiley ; 2001
    In:  Surface and Interface Analysis Vol. 32, No. 1 ( 2001-08), p. 32-37
    In: Surface and Interface Analysis, Wiley, Vol. 32, No. 1 ( 2001-08), p. 32-37
    Abstract: Telomeres are an essential nucleoprotein structure at the ends of all eukaryotic chromosomes. Studies on the structure and function of telomeres have received particular attention owing to their possible significance to ageing and cancer. In this work, human telomere from HeLa cells were isolated and purification by bio‐gel P‐2 column. Large duplex loops with a tail were first observed directly in the purified telomeric DNA species by atomic force microscopy (AFM). The lengths of the loop and tail are ∼2.5 ± 0.5 and 2.0 ± 1.5 kb, respectively. The AFM images also showed that the circular portion of loops is assumed to be a double‐stranded structure according to its apparent height, but to be a triplex or tetraplex structure for the loop–tail junction. These results indicate that telomeres in human cells may end in large loops, which is an advantage in further studies on the structure and function of telomeres in cells and provides a new procedure for the study of telomere structure. Copyright © 2001 John Wiley & Sons, Ltd.
    Type of Medium: Online Resource
    ISSN: 0142-2421 , 1096-9918
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2001
    detail.hit.zdb_id: 2023881-2
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  • 7
    In: Virology Journal, Springer Science and Business Media LLC, Vol. 17, No. 1 ( 2020-12)
    Abstract: Porcine epidemic diarrhea virus (PEDV) infection causes an acute enteric tract infectious disease characterized by vomiting, anorexia, dehydration, weight loss and high mortality in neonatal piglets. During PEDV infection, the spike protein (S) is a major virion structural protein interacting with receptors and inducing neutralizing antibodies. However, the neutralizing B-cell epitopes within PEDV S protein have not been well studied. Methods To accurately identify the important immunodominant region of S1, the purified truncated S1 proteins (SA, SB, SC, SD and SE) were used to immunize BALB/c mice to prepare polyclonal antibodies. The antisera titers were determined by indirect ELISA, western blot and IFA after four immunizations to find the important immunodominant region of S1, and then purified the immunodominant region of S1 protein and immunized mice to generate the special antibodies, and then used recombinant peptides to determine the B-cell epitopes of monoclonal antibodies. Results Five antisera of recombinant proteins of the spike protein region of PEDV were generated and we found that only the polyclonal antibody against part of the S1 region (signed as SE protein, residues 666–789) could recognize the native PEDV. Purified SE protein was used to immunize BALB/c mice and generate mAb 2E10. Pepscan of the SE protein demonstrated that SE16 ( 722 SSTFNSTREL 731 ) is the minimal linear epitope required for reactivity with the mAb 2E10. Further investigation indicated that the epitope SE16 was localized on the surface of PEDV S protein in the 3D structure. Conclusions A mAb 2E10 that is specifically bound to PEDV was generated and identified a specific linear B-cell epitope (SE16, 722 SSTFNSTREL 731 ) of the mAb. The epitope region of PEDV S1 localized in the different regions in comparison with the earlier identified epitopes. These findings enhance the understanding of the PEDV spike protein structure for vaccine design and provide a potential use for developing diagnostic methods to detect PEDV.
    Type of Medium: Online Resource
    ISSN: 1743-422X
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2020
    detail.hit.zdb_id: 2160640-7
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  • 8
    In: Alzheimer's & Dementia, Wiley
    Abstract: We aimed to describe baseline amyloid‐beta (Aβ) and tau‐positron emission tomograrphy (PET) from Longitudinal Early‐onset Alzheimer's Disease Study (LEADS), a prospective multi‐site observational study of sporadic early‐onset Alzheimer's disease (EOAD). METHODS We analyzed baseline [18F]Florbetaben (Aβ) and [18F] Flortaucipir (tau)‐PET from cognitively impaired participants with a clinical diagnosis of mild cognitive impairment (MCI) or AD dementia aged  〈  65 years. Florbetaben scans were used to distinguish cognitively impaired participants with EOAD (Aβ+) from EOnonAD (Aβ−) based on the combination of visual read by expert reader and image quantification. RESULTS 243/321 (75.7%) of participants were assigned to the EOAD group based on amyloid‐PET; 231 (95.1%) of them were tau‐PET positive (A+T+). Tau‐PET signal was elevated across cortical regions with a parietal‐predominant pattern, and higher burden was observed in younger and female EOAD participants. DISCUSSION LEADS data emphasizes the importance of biomarkers to enhance diagnostic accuracy in EOAD. The advanced tau‐PET binding at baseline might have implications for therapeutic strategies in patients with EOAD. HIGHLIGHTS 72% of patients with clinical EOAD were positive on both amyloid‐ and tau‐PET. Amyloid‐positive patients with EOAD had high tau‐PET signal across cortical regions. In EOAD, tau‐PET mediated the relationship between amyloid‐PET and MMSE. Among EOAD patients, younger onset and female sex were associated with higher tau‐PET.
    Type of Medium: Online Resource
    ISSN: 1552-5260 , 1552-5279
    Language: English
    Publisher: Wiley
    Publication Date: 2023
    detail.hit.zdb_id: 2201940-6
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  • 9
    In: Microbiology Spectrum, American Society for Microbiology, Vol. 9, No. 2 ( 2021-10-31)
    Abstract: Emerging coronaviruses (CoVs) can cause severe diseases in humans and animals, and, as of yet, none of the currently available broad-spectrum drugs or vaccines can effectively control these diseases. Host antiviral proteins play an important role in inhibiting viral proliferation. One of the isoforms of cytoplasmic poly(A)-binding protein (PABP), PABPC4, is an RNA-processing protein, which plays an important role in promoting gene expression by enhancing translation and mRNA stability. However, its function in viruses remains poorly understood. Here, we report that the host protein, PABPC4, could be regulated by transcription factor SP1 and broadly inhibits the replication of CoVs, covering four genera ( Alphacoronavirus , Betacoronavirus , Gammacoronavirus , and Deltacoronavirus ) of the Coronaviridae family by targeting the nucleocapsid (N) protein through the autophagosomes for degradation. PABPC4 recruited the E3 ubiquitin ligase MARCH8/MARCHF8 to the N protein for ubiquitination. Ubiquitinated N protein was recognized by the cargo receptor NDP52/CALCOCO2, which delivered it to the autolysosomes for degradation, resulting in impaired viral proliferation. In addition to regulating gene expression, these data demonstrate a novel antiviral function of PABPC4, which broadly suppresses CoVs by degrading the N protein via the selective autophagy pathway. This study will shed light on the development of broad anticoronaviral therapies. IMPORTANCE Emerging coronaviruses (CoVs) can cause severe diseases in humans and animals, but none of the currently available drugs or vaccines can effectively control these diseases. During viral infection, the host will activate the interferon (IFN) signaling pathways and host restriction factors in maintaining the innate antiviral responses and suppressing viral replication. This study demonstrated that the host protein, PABPC4, interacts with the nucleocapsid (N) proteins from eight CoVs covering four genera ( Alphacoronavirus , Betacoronavirus , Gammacoronavirus , and Deltacoronavirus ) of the Coronaviridae family. PABPC4 could be regulated by SP1 and broadly inhibits the replication of CoVs by targeting the nucleocapsid (N) protein through the autophagosomes for degradation. This study significantly increases our understanding of the novel host restriction factor PABPC4 against CoV replication and will help develop novel antiviral strategies.
    Type of Medium: Online Resource
    ISSN: 2165-0497
    Language: English
    Publisher: American Society for Microbiology
    Publication Date: 2021
    detail.hit.zdb_id: 2807133-5
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  • 10
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 2022
    In:  Monthly Notices of the Royal Astronomical Society Vol. 518, No. 3 ( 2022-11-30), p. 3386-3396
    In: Monthly Notices of the Royal Astronomical Society, Oxford University Press (OUP), Vol. 518, No. 3 ( 2022-11-30), p. 3386-3396
    Abstract: Ultraluminous X-ray sources (ULXs) in globular clusters (GCs) are low-mass X-ray binaries that achieve high X-ray luminosities through a currently uncertain accretion mechanism. Using archival Chandra and Hubble Space Telescope observations, we perform a volume-limited search (≲70 Mpc) of 21 of the most massive ($\gt 10^{11.5} \, \mathrm{M}_\odot$) early-type galaxies to identify ULXs hosted by GC candidates. We find a total of 34 ULX candidates above the expected background within five times the effective radius of each galaxy, with 10 of these ($\sim 29.4{{\ \rm per\ cent}}$) potentially hosted by a GC. A comparison of the spatial and luminosity distributions of these new candidate GC ULXs with previously identified GC ULXs shows that they are similar: both samples peak at LX ∼ a few × 1039 erg s−1 and are typically located within a few effective radii of their host galaxies.
    Type of Medium: Online Resource
    ISSN: 0035-8711 , 1365-2966
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2022
    detail.hit.zdb_id: 2016084-7
    SSG: 16,12
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