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Temporal dynamics of the early immune response following Mycobacterium bovis infection of cattle. | LitMetric

AI Article Synopsis

  • Bovine tuberculosis, caused by Mycobacterium bovis, is a significant infectious disease affecting cattle globally, with varying responses to infection that are not fully understood.
  • A study using advanced assays revealed that cell-mediated immune responses (CMI) appeared as early as two weeks after infection, while antibody responses were also detectable in some cattle within four weeks.
  • The findings suggest a need for better biomarkers to predict infection outcomes, especially in low-and-middle income countries where traditional control methods, like test-and-slaughter, are impractical.

Article Abstract

Bovine tuberculosis is an infectious disease of global significance that remains endemic in many countries. Mycobacterium bovis infection in cattle is characterized by a cell-mediated immune response (CMI) that precedes humoral responses, however the timing and trajectories of CMI and antibody responses determined by newer generation assays remain undefined. Here we used defined-antigen interferon-gamma release assays (IGRA) and an eleven-antigen multiplex ELISA (Enferplex TB test) alongside traditional tuberculin-based IGRA and IDEXX M. bovis antibody tests to assess immune trajectories following experimental M. bovis infection of cattle. The results show CMI responses developed as early as two-weeks post-infection, with all infected cattle testing positive three weeks post-infection. Interestingly, 6 of 8 infected animals were serologically positive with the Enferplex TB assay as early as 4 weeks post-infection. As expected, application of the tuberculin skin test enhanced subsequent serological reactivity. Infrequent M. bovis faecal shedding was observed but was uncorrelated with observed immune trajectories. Together, the results show that early antibody responses to M. bovis infection are detectable in some individuals and highlight an urgent need to identify biomarkers that better predict infection outcomes, particularly for application in low-and-middle income countries where test-and-slaughter based control methods are largely unfeasible.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10831113PMC
http://dx.doi.org/10.1038/s41598-024-52314-xDOI Listing

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