Panels

A and B in Figure  4 show that mice inoculated with doses as low as 10 CFU produced Abs against BpaC, which in turn demonstrates that this autotransporter is expressed by both B. mallei and B. pseudomallei during infection. Figure 4 ELISA with sera from mice that survived aerosol challenge with various doses of B. pseudomallei 1026b and B. mallei ATCC 23344. Serum samples were serially diluted and placed in duplicate wells of plates coated with purified His-tagged protein encompassing aa 392–1068 of B. pseudomallei 1026b BpaC. Goat α-mouse Abs conjugated to HRP check details were used as secondary Abs. The y-axis shows absorbance at a wavelength of 650 nm, which is indicative of antibody binding to antigens coating the plates. The x-axis represents two-fold dilutions of sera starting at 1:100 to 1:12,800. The results are expressed as the mean absorbance (±standard deviation). Closed circles show sera from mice inoculated with 104 B. pseudomallei bacteria (panel A). Open circles show sera from mice infected with 103 organisms (panels A and B). Open triangles show sera from mice

inoculated with Ganetespib cost 102 bacteria (panels A and B). Closed diamonds show sera from mice infected with 101 CFU of B. mallei ATCC 23344 (panel B). Blue squares represent sera from control mice that were inoculated with 50 μL of PBS using the Microsprayer (panels A and B). Of note, sera from mice that survived acute infection by B. pseudomallei and B. mallei are described elsewhere [67]. Discussion The genome of B. mallei ATCC Erastin 23344 has been reported to specify eight autotransporter gene products [49] and of these, only BoaA (adhesin, [55]) and BimA (intracellular motility protein, [11, 68]) have been functionally characterized. Both are classified as oligomeric autotransporters because they possess a short C-terminal transporter selleck chemical module predicted to form 4 β-strands, which anchor the molecules

on the bacterial surface. In the present study, we characterized a third B. mallei ATCC 2334 oligomeric autotransporter, BpaC (BMA1027). Comparative sequence analyses indicate that the gene product is conserved among B. mallei isolates (see Additional files 1 and 2) and resembles members of the Oca (oligomeric coiled-coil adhesin) sub-family of oligomeric autotransporter proteins [16, 19–21]. Consistent with this, inactivation of bpaC in the genome of B. mallei ATCC 23344 reduces adherence to monolayers of A549 (lung) and HEp-2 (larynx) cells grown in submerged cultures (Figure  3D and E, respectively). Though these cells are relevant to aerosol infection by B. mallei, they lack key features of the airway mucosa such as cilia and mucociliary activity. Ciliated cells contribute to preventing colonization of the respiratory tract by pathogenic agents by moving secretions (and trapped organisms) toward the laryngopharynx for expectoration or swallowing to the stomach (where the acidic pH neutralizes organisms). For these reasons, we measured the adherence of the B.