aphrophilus, C. hominis, E. corrodens, P. multocida and Capnocytophaga sp. other than C. canimorsus, which are characterised by typical biochemical key reactions that readily differentiate them from other fastidious GNR. In contrast, genera of Moraxella and Neisseria represent a challenge for the biochemical identification. Both genera often show similar biochemical reaction patterns, e.g., positive oxidase reaction or missing acid production from glucose, sucrose, Selleck Bucladesine maltose, mannitol, and xylose in semisolid Caspase Inhibitor VI clinical trial cystine-trypticase agar medium; furthermore, the morphology in the Gram-stain does often not differentiate Moraxella and Neisseria species [13]. As alternative to conventional

phenotypic methods, we analysed a subgroup of 80 isolates of fastidious GNR by the commercially available colorimetric VITEK 2 NH card (bioMérieux). Despite the limited database, this system supports the identification of fastidious GNR similar to that of conventional biochemical reactions by identifying 31% and 9% of the isolates to correct species and genus level, respectively. Accurate identification of clinically relevant selleck chemicals isolates of fastidious GNR is important for adequate interpretation and reporting as infectious agents and susceptibility testing [1]. However, in a routine diagnostic microbiology laboratory it is not feasible to subject all clinical isolates to molecular analyses for

identification. Mahlen et al. proposed an efficient strategy by applying selective criteria such as discordant morphologic

or biochemical results and knowledge of validity of phenotypic testing of isolates of Gram-negative bacilli [23]. Based on our data, we propose a cost-efficient algorithm, which is based on the knowledge of easy-to-identify organisms by conventional phenotypic methods and molecular analyses by the 16S rRNA gene for other difficult-to-differentiate species of this group. For identification of fastidious GNR conventional biochemical reactions and 16S Fludarabine rRNA gene sequence analysis can be implemented in a diagnostic laboratory as follows: (i) conventional biochemical identification of A. aphrophilus, C. hominis, E. corrodens, and P. multocida based on the typical reaction pattern is reliable; and (ii) any other result including Capnocytophaga sp. should be subjected to molecular methods by 16S rRNA gene analysis when accurate identification is of concern. By applying this approach to the 158 fastidious GNR analysed in our study, at least a third (32%) of the isolates would be readily identified by conventional phenotypic methods without laborious molecular analyses. Conclusions In time of cost-effectiveness and rapid development of newer identification methods such as MALDI-TOF MS, an efficient strategy for difficult-to-identify bacteria is mandatory as alternative method.