Koh, Gavin C K W and Schreiber, M Fernanda and Bautista, Ruben and Maude, Rapeephan R and Dunachie, Susanna and Limmathurotsakul, Direk and Day, Nicholas P J and Dougan, Gordon and Peacock, Sharon J (2013) Host responses to melioidosis and tuberculosis are both dominated by interferon-mediated signaling. PloS one, 8 (1). e54961. ISSN 1932-6203.
Host Responses to Melioidosis and Tuberculosis Are Both Dominated by Interferon-Mediated Signaling.pdf
Download (521kB) | Preview
Melioidosis (Burkholderia pseudomallei infection) is a common cause of community-acquired sepsis in Northeast Thailand and northern Australia. B. pseudomallei is a soil saprophyte endemic to Southeast Asia and northern Australia. The clinical presentation of melioidosis may mimic tuberculosis (both cause chronic suppurative lesions unresponsive to conventional antibiotics and both commonly affect the lungs). The two diseases have overlapping risk profiles (e.g., diabetes, corticosteroid use), and both B. pseudomallei and Mycobacterium tuberculosis are intracellular pathogens. There are however important differences: the majority of melioidosis cases are acute, not chronic, and present with severe sepsis and a mortality rate that approaches 50% despite appropriate antimicrobial therapy. By contrast, tuberculosis is characteristically a chronic illness with mortality <2% with appropriate antimicrobial chemotherapy. We examined the gene expression profiles of total peripheral leukocytes in two cohorts of patients, one with acute melioidosis (30 patients and 30 controls) and another with tuberculosis (20 patients and 24 controls). Interferon-mediated responses dominate the host response to both infections, and both type 1 and type 2 interferon responses are important. An 86-gene signature previously thought to be specific for tuberculosis is also found in melioidosis. We conclude that the host responses to melioidosis and to tuberculosis are similar: both are dominated by interferon-signalling pathways and this similarity means gene expression signatures from whole blood do not distinguish between these two diseases.
|Subjects:||WC Communicabable diseases|
|Divisions:||Clinical Support > Infectious Diseases|
|Depositing User:||Preeti Puligari|
|Date Deposited:||25 Apr 2013 13:58|
|Last Modified:||25 Apr 2013 13:58|
Actions (login required)