The latter finding may be explained by the use of a reference FM OMV as the common antigen in ELISA; however, it is more likely that the relatively few antigens with increased expression in MC.6M OMVs contributed only marginally to the total antibody levels. The SBA result was probably attributable to the increased expression of a small number of surface proteins, LPS or a combination of the two with the ability to induce bactericidal antibodies. Apoptosis inhibitor As bactericidal activity is an immunological surrogate for protection [37], this observation may prove to be important for future OMV vaccine development. About 3% (64/2005) of the proteins were

differentially expressed. The majority (41/64, 64%) of the differentially

expressed proteins were present in higher amounts in OMVs produced in MC.6M. They included the proteins OpcA, MafA, NspA, TdfH, OMP NMB0088, lipoprotein NMB1126/1164 and the uncharacterized OMP NMB2134. Of these, OpcA, MafA, NspA and NMB0088 have all previously been shown to induce bactericidal antibodies in mice [25], [38], [39] and [40]. The higher level of these cell-surface proteins probably contributed to the increase in bactericidal antibodies elicited by the MC.6M OMVs. The relative contribution of antibodies to OpcA may have been underestimated in this study, as the target strain used in the SBA only expressed low levels of the protein [17], [25] and [41]. In addition, combination of antibodies to less abundant upregulated Talazoparib mw OMPs may also have contributed synergistically to increase the bactericidal titres obtained with the vaccine prepared from cells

grown in MC.6M [36]. As MC.6M is less complex than FM, it was not surprising to find that in adapting to the synthetic medium the meningococcus increased the expression of specific cell-surface proteins. Expression of the FetA protein, which belongs to the family of TonB-dependent receptors, is normally repressed in iron-rich media [42]. Its inconsistent expression in both FM and MC.6M suggested that batches of both media varied in the amount of readily available iron for meningococcal growth. However, variations in iron availability alone were unlikely to account for all observed changes. With heptaminol the exception of LbpB, there was no evidence of increased expression of other iron-repressed surface proteins, such as transferrin-binding protein or haem receptors, in the OMV preparations from bacteria grown in MC.6M. Like iron-regulated proteins, TdfH also belongs to the family of TonB-dependent receptors. It also shares homology with haem receptors but does not appear to be involved in iron uptake [15]. Unlike FetA, it was found to be expressed consistently by different batches of meningococci grown in MC.6M, suggesting that the induction of TdfH was not dependent upon fluctuations in iron levels. In contrast with the iron-repressed fetA gene, the nspA gene is known to be iron-activated [43].