All Rickettsia genomes available were compared to discover specific sequences to design new sets of primers and probes. The specificity was verified in silico and against a panel of 30 rickettsial species. Sensitivity was determined using 10-fold serial dilutions. Finally, primers and probes that were both specific and sensitive were routinely used for the diagnosis of rickettsial infections from

clinical specimens. We retained sets of primers and probes to detect spotted fever group Rickettsia, typhus group Rickettsia,Rickettsia conorii,Rickettsia slovaca,Rickettsia africae and Rickettsia australis; 643 clinical samples were screened for the presence of Rickettsia DNA. Overall, 45 positive samples were detected, including 15 Rickettsia africae, nine R. conorii, five Rickettsia sibirica mongolitimonae, see more four R. slovaca, two R. australis, four Rickettsia massiliae, Nutlin-3 research buy one Rickettsia honei, one Rickettsia typhi and eight Rickettsia sp. Positive samples were detected mainly from cutaneous biopsies and swabs (31/45). Widespread use of real-time PCR is inexpensive and reduces delay in the diagnosis of rickettsial infections. These real-time PCR assays could be implemented easily in laboratories that have molecular facilities and may be added to existing molecular tools as a point-of-care strategy. Members of the genus

Rickettsia may be classified into spotted fever group (SFG) Rickettsia, typhus group (TG) Rickettsia, Rickettsia bellii group and Rickettsia canadensis group (Merhej & Raoult, 2011). Rickettsiae can be transmitted to humans by blood-sucking arthropods and are associated with specific diseases termed rickettsioses. For example, Rickettsia conorii is associated with Mediterranean spotted fever (MSF) (Parola et al., 2005), Rickettsia

africae with African tick-bite fever (ATBF) (Jensenius et al., 2003), Rickettsia sibirica ssp. Sorafenib molecular weight mongolitimonae with lymphangitis-associated rickettsiosis (LAR) (Fournier et al., 2005), Rickettsia slovaca with ‘scalp eschar and neck lymphadenopathy after tick bite’ (SENLAT) (Angelakis et al., 2010), Rickettsia australis with Queensland tick typhus (QTT) (Parola et al., 2005), Rickettsia typhi with murine typhus (Civen & Ngo, 2008) and Rickettsia honei with Flinders Island spotted fever (FISF) (Parola et al., 2005). When a rickettsiosis is clinically suspected, biological diagnosis can be obtained using serology, cell culture and/or molecular tools (Parola et al., 2005); among the molecular tools, real-time quantitative PCR (qPCR) is rapid and sensitive (Stenos et al., 2005; Henry et al., 2007; Kidd et al., 2008). Genomic approaches have recently increased our knowledge of Rickettsia sp., and massive amounts of genomic data have become available (Ogata et al., 2001; Fournier et al., 2007; Merhej & Raoult, 2011).