AI Article Synopsis

  • The study investigates the formation of granulomas connected to the resolution of Q fever caused by Coxiella burnetii, revealing that the underlying molecular processes are still not well understood.
  • Researchers created human granulomas using peripheral blood mononuclear cells (PBMCs) and C. burnetii-coated beads, finding that over 50% of the altered gene expressions were similar between responses to C. burnetii and BCG extracts, indicating a shared inflammatory pathway.
  • The findings highlight that inhibiting specific chemokines like CCL2 and CCL5 hampers granuloma formation, and the unique transcriptional profile of C. burnetii granulomas is significantly tied to the activation of type I interferon

Article Abstract

The formation of granulomas is associated with the resolution of Q fever, a zoonosis due to Coxiella burnetii; however the molecular mechanisms of granuloma formation remain poorly understood. We generated human granulomas with peripheral blood mononuclear cells (PBMCs) and beads coated with C. burnetii, using BCG extracts as controls. A microarray analysis showed dramatic changes in gene expression in granuloma cells of which more than 50% were commonly modulated genes in response to C. burnetii and BCG. They included M1-related genes and genes related to chemotaxis. The inhibition of the chemokines, CCL2 and CCL5, directly interfered with granuloma formation. C. burnetii granulomas also expressed a specific transcriptional profile that was essentially enriched in genes associated with type I interferon response. Our results showed that granuloma formation is associated with a core of transcriptional response based on inflammatory genes. The specific granulomatous response to C. burnetii is characterized by the activation of type 1 interferon pathway.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4266094PMC
http://dx.doi.org/10.3389/fcimb.2014.00172DOI Listing

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