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Chronic Q fever is caused by persistent infection with the Gram-negative bacterium Coxiella burnetii . The mechanisms underlying this persistence remain elusive, but the presence of the bacteria in the bone marrow of C. burnetii -infected patients has been demonstrated. Therefore, we investigated the potential role of osteoclasts, the bone-resorbing cells, in harboring C. burnetii during infection. The histological analysis of bones from a murine model of Q fever revealed the presence of C. burnetii inside osteoclasts. In vitro infection assays confirmed that osteoclasts can be infected with C. burnetii and supported bacterial replication in a type IVB secretion system (T4BSS)-dependent manner. Wild-type C. burnetii infection inhibited osteoclast differentiation and bone-resorbing activity, while the T4BSS mutant enhanced the differentiation and bone-degrading function of osteoclasts. Taken together, our findings identify osteoclasts as a potential host cell for C. burnetii . This opens new perspectives on the mechanisms that may underlie chronic Q fever as well as questioning the putative consequences on bone biology in chronically affected patients.
Lai et al. (Fri,) studied this question.