The number of substrates oxidized by C. burnetii increases with decreasing oxygen availability. The ability of C. burnetii to oxidize substrates in different oxygen environments was assessed using PM. (A) C. burnetii genes encoding terminal oxidases associated with aerobic (cytochrome o) and microaerobic (cytochrome bd) metabolism suggested C. burnetii can respire under microaerophilic conditions. (B) Purified C. burnetii was added to PM-1 plates and incubated for 24 h in 20%, 5%, and 2.5% oxygen. The number of metabolites oxidized increased with decreasing oxygen tension, consistent with microaerophilic metabolism. Representative PM plate images are shown. (C) Seventeen substrates were efficiently oxidized by C. burnetii in 2.5% oxygen. Signal intensities were measured using an OmniLog detection system and expressed as relative OmniLog units (OLU). Quantitative analysis is representative of at least 3 independent experiments. Substrate key (rows A-H, columns 1–12): A1, no substrate control; A5, succinate; A8, L-proline; A11, D-mannose; B12, L-glutamate; C2, D-galactonic acid-γ-lactone; C9, α-D-glucose; D6, α-ketoglutarate; E1, L-glutamine; E12, adenosine; F5, fumarate; F6, bromo succinate; G4, L-threonine; G5, L-alanine; G9, mono methyl succinate; H8, pyruvate; H9, L-galactonic acid-γ-lactone; H11, phenylethylamine.