AI Article Synopsis

  • The study reveals that most bacteria in the gut are found outside of cells, but some need to replicate inside specific, yet unidentified, immune cells for effective spread.
  • Researchers identified that the majority of bacteria adhered to Ly6C monocytes, which did not efficiently take in the bacteria, suggesting that not all immune cells are good hosts for bacterial replication.
  • Interestingly, while certain monocytes showed increased CD64 expression and could support bacterial growth when becoming macrophages, inflammatory monocytes from bone marrow did not support such growth, indicating important distinctions in immune cell interactions with bacteria.

Article Abstract

After foodborne transmission of the facultative intracellular bacterial pathogen , most of the bacterial burden in the gut is extracellular. However, we previously demonstrated that intracellular replication in an as yet unidentified cell type was essential for dissemination and systemic spread of In this article, we show that the vast majority of cell-associated in the gut were adhered to Ly6C monocytes, a cell type that inefficiently internalized With bone marrow-derived in vitro cultures, high multiplicity of infection or the use of opsonized bacteria enhanced uptake of in CD64 monocytes, but very few bacteria reached the cell cytosol. Surprisingly, monocytes that had upregulated CD64 expression in transition toward becoming macrophages fully supported intracellular growth of In contrast, inflammatory monocytes that had increased CD64 expression in the bone marrow of BALB/c/By/J mice prior to exposure in the gut did not support growth. Thus, contrary to the perception that can infect virtually all cell types, neither naive nor inflammatory Ly6C monocytes served as a productive intracellular growth niche for These results have broad implications for innate immune recognition of in the gut and highlight the need for additional studies on the interaction of extracellular, adherent with the unique subsets of myeloid-derived inflammatory cells that infiltrate sites of infection.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360488PMC
http://dx.doi.org/10.4049/jimmunol.1602076DOI Listing

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