sakazakii, lower panel). In general, the 36 kDa protein was the most common among all Cronobacter OMP profiles. It was detected by immnunoblotting in 5 out of the 12 tested Cronobacter strains (Figure 2, lower panel; lanes, 5, 6, 9, 10, 11; C. sakazakii, C. turicensis, C. sakazakii, C. sakazakii, NU7441 concentration C. muytjensii, respectively), and a 42 kDa protein was detected in two C. sakazakii isolates (Figure 2, lower panel; lanes, 1 and 12), while a 41 kDa protein was detected in two isolates

(C. sakazakii, and C. muytjensii, lower lanes 4 and 8 respectively). In addition, proteins of 37 and 39 kDa were detected each in one C. sakazakii isolate (Figure 2, lower panel; lanes 2 and 3, respectively). OMPs from a number of non-Cronobacter species were also tested for reactivity against the purified MAbs by immunoblotting. Unlike the single band pattern observed in Cronobacter OMP LY294002 research buy Immunoblot profiles, the non-Cronobacter immunoblot profiles exhibited a double-band pattern corresponding to MW of 38 and 41 kDa (Figure 3 lower panel; lanes 3, 4, 6 and 7 representing strains; E. coli, P. aeroginusa, Salmonella,

and S. sonnii respectively). In addition, C. freundii (Figure 3 lower panel; lane 2) exhibited only one protein corresponding to 40 kDa, while the only Gram-positive control strain (L. ivanovii, lane 5) exhibited the same two bands with a higher MW (39 and 42 kDa) Selleck CUDC-907 than those which appeared in samples from the Gram-negative isolates. In order to determine which surface antigen the MAbs

were bound to, OMPs and LPS extracted from Cronobacter muytjensii ATCC 51329 (strain used for immunization) were analyzed by SDS-PAGE, DOC-PAGE and immunoblotting. All MAbs (A1, B5, 2C2, C5 and A4) displayed strong and specific reaction against a 44 kDa OMP (Figure 4). Although these MAbs were produced from two different fusion experiments, they all reacted new strongly and specifically against the same 44 kDa OMP. Furthermore, to compare the epitope specificity of all MAbs, additive index ELISA was conducted for each pair of the MAbs. All scores obtained were very low and fall in the range of 0 to 10 indicating that all MAbs were raised against the same epitope within the 44 kDa OMP. Figure 2 SDS-PAGE (Upper) and Immunoblot (Lower) of OMPs extracted from different Cronobacter strains probed with MAb 2C2. M: Molecular weight marker; 1: C. muytjensii ATCC 51329; 2: C4; 3: C6; 4: C13; 5: Jor93; 6: Jor170; 7: Jor44; 8: Jor112; 9: Jor146A; 10: Jor146B; 11: Jor149; 12: Jor160A. Figure 3 SDS-PAGE (Upper) and Immunoblot (Lower) of OMPs extracted from different Non- Cronobacter strains probed with MAb 2C2. M: Molecular weight marker; 1: C. muytjensii ATCC 51329; 2: Citrobacter freundii; 3: E. coli; 4: Pseudomonas aeruginosa; 5: Listeria ivanovii; 6: Salmonella; 7: Shigella sonnii Figure 4 Immunoblot for SDS-PAGE gel of OMP extracted from C. muytjensii ATCC 51329 and probed with all MAbs.