53 research outputs found

    A Regulatory Role for NBS1 in Strand-Specific Mutagenesis during Somatic Hypermutation

    Get PDF
    Activation-induced cytidine deaminase (AID) is believed to initiate somatic hypermutation (SHM) by deamination of deoxycytidines to deoxyuridines within the immunoglobulin variable regions genes. The deaminated bases can subsequently be replicated over, processed by base excision repair or mismatch repair, leading to introduction of different types of point mutations (G/C transitions, G/C transversions and A/T mutations). It is evident that the base excision repair pathway is largely dependent on uracil-DNA glycosylase (UNG) through its uracil excision activity. It is not known, however, which endonuclease acts in the step immediately downstream of UNG, i.e. that cleaves at the abasic sites generated by the latter. Two candidates have been proposed, an apurinic/apyrimidinic endonuclease (APE) and the Mre11-Rad50-NBS1 complex. The latter is intriguing as this might explain how the mutagenic pathway is primed during SHM. We have investigated the latter possibility by studying the in vivo SHM pattern in B cells from ataxia-telangiectasia-like disorder (Mre11 deficient) and Nijmegen breakage syndrome (NBS1 deficient) patients. Our results show that, although the pattern of mutations in the variable heavy chain (VH) genes was altered in NBS1 deficient patients, with a significantly increased number of G (but not C) transversions occurring in the SHM and/or AID targeting hotspots, the general pattern of mutations in the VH genes in Mre11 deficient patients was only slightly altered, with an increased frequency of A to C transversions. The Mre11-Rad50-NBS1 complex is thus unlikely to be the major nuclease involved in cleavage of the abasic sites during SHM, whereas NBS1 might have a specific role in regulating the strand-biased repair during phase Ib mutagenesis

    Investigation of hospital discharge cases and SARS-CoV-2 introduction into Lothian care homes

    Get PDF
    Background The first epidemic wave of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) in Scotland resulted in high case numbers and mortality in care homes. In Lothian, over one-third of care homes reported an outbreak, while there was limited testing of hospital patients discharged to care homes. Aim To investigate patients discharged from hospitals as a source of SARS-CoV-2 introduction into care homes during the first epidemic wave. Methods A clinical review was performed for all patients discharges from hospitals to care homes from 1st March 2020 to 31st May 2020. Episodes were ruled out based on coronavirus disease 2019 (COVID-19) test history, clinical assessment at discharge, whole-genome sequencing (WGS) data and an infectious period of 14 days. Clinical samples were processed for WGS, and consensus genomes generated were used for analysis using Cluster Investigation and Virus Epidemiological Tool software. Patient timelines were obtained using electronic hospital records. Findings In total, 787 patients discharged from hospitals to care homes were identified. Of these, 776 (99%) were ruled out for subsequent introduction of SARS-CoV-2 into care homes. However, for 10 episodes, the results were inconclusive as there was low genomic diversity in consensus genomes or no sequencing data were available. Only one discharge episode had a genomic, time and location link to positive cases during hospital admission, leading to 10 positive cases in their care home. Conclusion The majority of patients discharged from hospitals were ruled out for introduction of SARS-CoV-2 into care homes, highlighting the importance of screening all new admissions when faced with a novel emerging virus and no available vaccine

    SARS-CoV-2 Omicron is an immune escape variant with an altered cell entry pathway

    Get PDF
    Vaccines based on the spike protein of SARS-CoV-2 are a cornerstone of the public health response to COVID-19. The emergence of hypermutated, increasingly transmissible variants of concern (VOCs) threaten this strategy. Omicron (B.1.1.529), the fifth VOC to be described, harbours multiple amino acid mutations in spike, half of which lie within the receptor-binding domain. Here we demonstrate substantial evasion of neutralization by Omicron BA.1 and BA.2 variants in vitro using sera from individuals vaccinated with ChAdOx1, BNT162b2 and mRNA-1273. These data were mirrored by a substantial reduction in real-world vaccine effectiveness that was partially restored by booster vaccination. The Omicron variants BA.1 and BA.2 did not induce cell syncytia in vitro and favoured a TMPRSS2-independent endosomal entry pathway, these phenotypes mapping to distinct regions of the spike protein. Impaired cell fusion was determined by the receptor-binding domain, while endosomal entry mapped to the S2 domain. Such marked changes in antigenicity and replicative biology may underlie the rapid global spread and altered pathogenicity of the Omicron variant

    A critical examination of the virtual organization and the mutual dependencies of trust, communication, and collaborative learning

    No full text
    Includes bibliographical references (pages [137]-151)Within the past decade, the way we do business has changed dramatically. The electronic superhighway has allowed us to expand our thinking in terms of customers, employees and information. A greater concern with work-family balance has resulted in more people preferring flexible schedules and choices about the location of the workplace. Company rightsizing resulted in more independent contractors and small specialty firms as people took a chance on stretching their entrepreneurial abilities. These events have all contributed to the formation of a new type of organizational structure: the virtual organization. This ethnographic study explores the concept of the virtual organization in general, and investigates what makes a virtual organization effective from the point of view of the individuals who work in such structures. The study also shows how adult-education principles are integral to the workings of a virtual organization. Virtual organization workers in all levels of the organization, and representing several different industries, contributed to this study. Over a period of 10 years, informal discussions, formal interviews, and personal experience yielded information about working in a virtual organization. The pivotal themes that emerged from the study are trust, communication, and collaborative learning. In order to succeed in a virtual organization, workers need to trust one another. The higher the degree of trust, the more communication will occur between virtual workers. When an organization is working optimally, the virtual workers are participating with each other and trusting one another to lead the team in their particular area of subject-matter expertise. In this way, active communication and a high level of trust can lead to collaborative learning. Trust, communication, and collaborative learning is the symbiotic relationship that forms the foundation upon which a virtual organization can build and thrive. The ultimate ability of management to create an environment where a virtual worker is encouraged to trust, communicate, and learn from other workers will be a key determinant in the virtual organization's success. Policies encouraging this environment and reflecting human-resources development principles are recommended to managers at the conclusion of this study.Ed.D. (Doctor of Education
    corecore