Sequence-based identification of Aspergillus, Fusarium and Mucorales in the clinical mycology laboratory: Where are we and where should we go from here? Balajee SA, Borman AM, Brandt ME, Cano J, Cuenca-Estrella M, Dannaoui E, Guarro J, Haase G, Kibbler CC, Meyer W, O'Donnell K, Petti CA, Rodriguez-Tudela JL, Sutton D, Velegraki A, Wickes BL J Clin Microbiol 2008 Dec 10 [abstract on PubMed] Must Read F1000 Factor 6.0 EndNote [citations on Google Scholar] [related articles] [full text] Selected by | Susanne Perkhofer and Cornelia Lass-Floerl Evaluated 16 Jan 2009 Browse relevant Sections View additional info Faculty Comments & Author Responses Faculty Member Comments Susanne Perkhofer and Cornelia LassFloerl In my opinion, this article is interesting as it highlights the advantages and limitations of species identification in Aspergillus, Fusarium and the Mucorales by molecular methods. The authors provide clear strategies to perform an ideal identification. University of Innsbruck, Austria Infectious Diseases New Finding The authors describe the need of comparative sequence identification of fungi due to the fact that there is a change of epidemiology of medically important fungi, a rise of novel organisms causing diseases, and species-species differences in antifungal susceptibilities of these fungi. The 'gold standard' to identify fungal species is the comparative sequence-based identification (ID). However, the authors state that the appropriate locus has to be determined very carefully as the gene target should be orthologous, with a high level of interspecies variation, low levels of intra-specific variation and should not undergo recombination. The use of nuclear ribosomal internal transcribed spacer region (ITS) sequencing is recommended for subgenus/section level identification but limitations arise for species identification within a given section (e.g. discrimination of A. fumigatus from A. lentulus, both section Fumigatus). The authors advise ITS locus sequencebased ID for identification of aspergilli, fusaria and mucorales. In case of species/strain ID comparative sequence analysis of protein coding regions should be used. This manuscript describes the problems and manifoldness of molecular identification of medically important fungi very clearly, and the authors point out that many factors affect percent identity scores including quality and length of query sequence and the number and accuracy of existing GenBank records for the same species and locus. In the end, it was a pleasure to have read such an interesting article as new molecular techniques will be an important step in making prompt diagnosis of fungal infections.