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Prevalence of T. rubrum and T. interdigitale Exhibiting High MICs to Terbinafine in Clinical Samples Analyzed in the Portuguese Mycology Reference Laboratory

dc.contributor.authorSchirmer, Helena
dc.contributor.authorHenriques, Camila
dc.contributor.authorSimões, Helena
dc.contributor.authorVeríssimo, Cristina
dc.contributor.authorSabino, Raquel
dc.date.accessioned2026-02-19T15:39:29Z
dc.date.available2026-02-19T15:39:29Z
dc.date.issued2025-01-25
dc.description.abstractCutaneous fungal infections represent a significant burden worldwide with a high impact on public health. Accurate identification of dermatophyte species causing these infections is vital for an appropriate treatment. Terbinafine is the primary agent against Trichophyton species due to its clinical efficacy; however, cases of elevated minimum inhibitory concentration (MIC) have been reported, raising clinical and epidemiological concerns. Herein, we aimed to detect Trichophyton rubrum and Trichophyton interdigitale isolates collected from clinical samples with terbinafine-high MICs (TRB-hMIC). A total of 168 isolates, recovered from 2017 to 2023, were identified as T. rubrum complex (140/83.4%) or T. interdigitale (28/16.7%) and further screened regarding their terbinafine susceptibility. Four isolates with capacity to grow in terbinafine media were detected by screening, and these and a further sixteen random isolates were submitted to the broth microdilution method. This methodology confirmed the four (2.4%) isolates as TRB-hMIC. One T. rubrum and three T. interdigitale showed a minimum inhibitory concentration (MIC) higher than 1 mg/L. Partial sequencing of the SQLE gene identified point mutations in T. rubrum (Phe397Iso) and in one T. interdigitale (Phe397Leu) isolate. Notably, in the other two T. interdigitale isolates with TRB-hMIC, no point mutations in the SQLE gene were identified. In conclusion, TRB-hMIC isolates (T. rubrum and T. interdigitale) were identified in clinical samples analyzed in Portugal, as antifungal susceptibility testing is a crucial routine for identifying treatment failures and also for epidemiological purposes aiming to monitor the dynamics of terbinafine resistance.eng
dc.description.sponsorshipThis work was supported by the Young ISHAM Training Fellowship.
dc.identifier.citationPathogens. 2025 Jan 25;14(2):115. doi: 10.3390/pathogens14020115
dc.identifier.doi10.3390/pathogens14020115
dc.identifier.eissn2076-0817
dc.identifier.pmid40005492
dc.identifier.urihttp://hdl.handle.net/10400.18/10952
dc.language.isoeng
dc.peerreviewedyes
dc.publisherMDPI
dc.relation.hasversionhttps://www.mdpi.com/2076-0817/14/2/115
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectTrichophyton
dc.subjectAntifungal Resistance
dc.subjectDermatophytes
dc.subjectSqualene Epoxidase Mutations
dc.subjectTerbinafine
dc.subjectResistência aos Antimicrobianos
dc.titlePrevalence of T. rubrum and T. interdigitale Exhibiting High MICs to Terbinafine in Clinical Samples Analyzed in the Portuguese Mycology Reference Laboratoryeng
dc.typejournal article
dcterms.referenceshttps://www.mdpi.com/2076-0817/14/2/115
dspace.entity.typePublication
oaire.citation.issue2
oaire.citation.startPage115
oaire.citation.titlePathogens
oaire.citation.volume14
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85

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