Trichophyton species: use of volatile fingerprints for rapid identification and discrimination.

dc.contributor.authorSahgal, Natasha
dc.contributor.authorMonk, Barry
dc.contributor.authorWasil, Mohammad
dc.contributor.authorMagan, Naresh
dc.date.accessioned2008-02-05T09:53:23Z
dc.date.available2008-02-05T09:53:23Z
dc.date.issued2006-12
dc.description.abstractBackground: Fungal infection of the skin is a common clinical problem, and laboratory confirmation of the diagnosis is important to ensure appropriate treatment. The identification of the species of fungus is also important, because different fungal species have different modes of transmission, and this may be of importance both in preventing re-infection or in avoidance of infection of others. Objective: This study examined the potential of using volatile production patterns for the detection and discrimination between four Trichophyton species (T. mentagrophytes, T. rubrum, T. verrucosum and T. violaceum) in vitro on solid media and in broth culture. Methods: Two different sensor array systems (conducting polymer and metal oxide sensors) were examined for comparing the qualitative volatile fingerprints produced by these species over periods of 24-120 hrs in the headspace. The relative sensitivity of detection of two of the species (T. mentagrophytes, T. rubrum) was determined for log1 to log7 inoculum levels over the same time period. Results: The conducting polymer based system was unable to differentiate between species based on volatile fingerprints over the experimental period. However, metal oxide-based sensor arrays were found to be able to differentiate between the four species within 96 hrs of growth using PCA analysis which accounted for approximately 93% of the data in PC1 and 2 based on the qualitative volatile production patterns. This differentiation was confirmed by the Cluster analysis of the data using Euclidean distance and Ward’s linkage. Studies of the sensitivity of detection showed that for T. mentagrophytes and T. rubrum it was possible to differentiate between log3, log5 and log7 inoculum levels within 96 hrs. Conclusions: This is the first detailed study of the use of qualitative volatile fingerprints for identification and discrimination of dermatophytes. This approach could have potential for rapid identification of patient samples reducing significantly the time to treatment.en_UK
dc.identifier.citationN. Sahgal, B. Monk, M. Wasil, N. Magan, Trichophyton species: use of volatile fingerprints for rapid identification and discrimination. British Journal of Dermatology, 2006, v155(6), 1209–1216.en_UK
dc.identifier.issn0007-0963
dc.identifier.urihttp://hdl.handle.net/1826/2288
dc.identifier.urihttp://dx.doi.org/10.1111/j.1365-2133.2006.07549.x
dc.language.isoenen_UK
dc.publisherBlackwell Publishingen_UK
dc.subjectTrichophyton speciesen_UK
dc.subjectearly detectionen_UK
dc.subjectelectronic noseen_UK
dc.subjectvolatile fingerprintsen_UK
dc.titleTrichophyton species: use of volatile fingerprints for rapid identification and discrimination.en_UK
dc.typePostprinten_UK

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