These dissimilar domains may be the epitopes recognized by the po

These dissimilar domains may be the epitopes recognized by the polyclonal antibodies binding to Wag31Mtb. RT-PCR was performed on cDNA prepared from M. smegmatis mc2155/pwag31Mtb and M. smegmatis mc2155Δrel/pwag31Mtb, and this showed that Rel has a positive effect on the expression of wag31Mtb (Fig. 2b, upper panel). The presence of wag31Mtb on a multicopy plasmid in M. smegmatis alters

both the cell shape and the colony morphologies in a rel-dependent Docetaxel price fashion (Fig. 3). In the presence of the shuttle vector pOLYG, the wild-type and ΔrelMsm colonies have raised ridges with average cell lengths of 2.1 ± 0.3 μm for mc2155/pOLYG and 3.4 ± 0.9 μm for ΔrelMsm/pOLYG (Fig. 3a and b). However, the presence of pwag31Mtb in both strains leads to a flattened, smoother colony formation. There are almost no colony ridges for mc2155/pwag31 (Fig. 3c), while the ΔrelMsm/pwag31 strain has a modest amount of ridges near the circumference of 17-AAG clinical trial colonies (Fig. 3d). For both strains, the presence of pwag31Mtb leads to shorter cells, with mc2155/pwag31 cells averaging 0.9 ± 0.4 μm in length and ΔrelMsm/pwag31 cells averaging 1.6 ± 0.3 μm in length (Fig. 3c and d insets, respectively). Smoother colony appearance suggests a change in the cell surface properties like a decrease in hydrophobicity. To

test this theory, cell dispersion was compared for cells grown in the presence or in the absence of the detergent Tween 80 (0.05% v/v) (Fig. 4). The absence of Tween 80 from standing cultures led to a 60% decrease in the levels of cell suspension, except for mc2155/pwag31Mtb cells, which remained dispersed even without the detergent. This is the first reported instance of Wag31 playing a role in altering mycobacterial cell surfaces. Wag31 was first identified as a mycobacterial antigen using serum antibodies of leprosy and tuberculosis patients (Hermans et al., 1995), which helps explain the observed humoral response Urease of rabbits to this protein (Fig. 1a). Wag31 was eventually discovered to be a homolog

of DivIVA, a protein known to regulate cell shape and cell division in gram-positive bacteria (Cha & Stewart, 1997; Cole et al., 1998; Flardh, 2003), and wag31 has been shown to be an essential gene in M. tuberculosis (Sassetti et al., 2003) and in M. smegmatis (Kang et al., 2005; Nguyen et al., 2007). Wag31 is receptive to extracellular signaling by two serine/threonine protein kinases, PknA and PknB, and the action of Wag31 as a determinant of cell shape is dependent on a protein phosphorylation domain in the protein (Kang et al., 2005). The bacterial role of Wag31 appears to be regulating cell division and cell shape as evident by the appearance of the protein at the poles of dividing cells (Nguyen et al., 2007; Kang et al., 2008), by its appearance on the cell surface of mycobacteria (He & De Buck, 2010), by wag31-dependent alterations in cell envelope proteins and lipids (Hamasha et al.

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