Publications by authors named "Emma Heckenberg"

Epstein-Barr virus has evolved with its human host leading to an intimate relationship where infection of antibody-producing B cells mimics the process by which these cells normally recognize foreign antigens and become activated. Virtually everyone in the world is infected by adulthood and controls this virus pushing it into life-long latency. However, immune-suppressed individuals are at high risk for EBV+ cancers.

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Mycobacterium tuberculosis () is a bacterium that exclusively resides in human hosts and remains a dominant cause of morbidity and mortality among infectious diseases worldwide. Host protection against infection is dependent on the function of immunity-related GTPase clade M (IRGM) proteins. Polymorphisms in human associate with altered susceptibility to mycobacterial disease, and human IRGM promotes the delivery of into degradative autolysosomes.

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Enteroviruses are among the most common viral infectious agents of humans and cause a broad spectrum of illness, which can range from mild and self-limiting to severe. Severe outcomes of enteroviral infections can include aseptic meningitis, bronchitis, acute liver failure, hand-foot-mouth disease (HFMD), hemorrhagic conjunctivitis, or acute flaccid myelitis and other paralytic syndromes. Enteroviruses initiate their replicative life cycles by attaching to a broad range of cell surface receptors, which play direct roles in the clinical outcomes of enteroviral infections.

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Article Synopsis
  • Lymphoblastoid cell lines (LCLs) are created from B cells infected with Epstein-Barr virus (EBV) and are important for research in areas like viral oncology and immunology.
  • This study used single-cell RNA sequencing to analyze five LCLs, revealing significant differences in gene expression related to immune responses and viral activity.
  • The research also developed a simulation model to show how the initial variation in B cells and random factors during culture can lead to diverse outcomes in seemingly identical cell populations.
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