Resistance Profile, Terbinafine Resistance Screening and MALDI-TOF MS Identification of the Emerging Pathogen Trichophyton indotineae.

IF 3.6 3区 生物学 Q2 MYCOLOGY Mycopathologia Pub Date : 2024-03-14 DOI:10.1007/s11046-024-00835-4
Roelke De Paepe, Anne-Cécile Normand, Silke Uhrlaß, Pietro Nenoff, Renaud Piarroux, Ann Packeu
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Abstract

The emerging pathogen Trichophyton indotineae, often resistant to terbinafine (TRB), is known to cause severe dermatophytoses such as tinea corporis and tinea cruris. In order to achieve successful treatment for these infections, insight in the resistance profile of T. indotineae strains and rapid, reliable identification is necessary. In this research, a screening medium was tested on T. indotineae strains (n = 20) as an indication tool of TRB resistance. The obtained results were confirmed by antifungal susceptibility testing (AST) for TRB following the in vitro broth microdilution reference method. Additionally, AST was performed for eight other antifungal drugs: fluconazole, itraconazole, voriconazole, ketoconazole, griseofulvin, ciclopirox olamine, naftifine and amorolfine. Forty-five percent of the strains were confirmed to be resistant to terbinafine. The TRB resistant strains showed elevated minimal inhibitory concentration values for naftifine and amorolfine as well. DNA sequencing of the squalene epoxidase-encoding gene showed that TRB resistance was a consequence of missense point mutations in this gene, which led to amino acid substitutions F397L or L393F. MALDI-TOF MS was used as a quick, accurate identification tool for T. indotineae, as it can be challenging to distinguish it from closely related species such as Trichophyton mentagrophytes or Trichophyton interdigitale using morphological characteristics. While MALDI-TOF MS could reliably identify ≥ 95% of the T. indotineae strains (depending on the spectral library), it could not be used to successfully distinguish TRB susceptible from TRB resistant strains.

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新病原体毛癣菌的抗药性概况、特比萘芬抗药性筛选和 MALDI-TOF MS 鉴定。
新出现的病原体毛癣菌通常对特比萘芬(TRB)具有耐药性,可引起严重的皮肤癣菌病,如体癣和股癣。为了成功治疗这些感染,有必要深入了解靛癣菌株的抗药性特征,并进行快速、可靠的鉴定。在这项研究中,对一种筛选培养基(n = 20)进行了测试,作为 TRB 耐药性的指示工具。按照体外肉汤微稀释参考方法,对 TRB 进行了抗真菌药敏试验 (AST),确认了所获得的结果。此外,还对其他八种抗真菌药物进行了药敏试验:氟康唑、伊曲康唑、伏立康唑、酮康唑、格列齐特、环吡醇胺、萘替芬和阿莫罗芬。45%的菌株被证实对特比萘芬耐药。对 TRB 产生抗药性的菌株对萘替芬和阿莫罗芬的最小抑菌浓度值也有所升高。角鲨烯环氧化物酶编码基因的 DNA 测序表明,TRB 抗性是该基因发生错义点突变的结果,这种突变导致了 F397L 或 L393F 氨基酸置换。MALDI-TOF MS 被用作快速、准确地鉴定 T. indotineae 的工具,因为利用形态特征将其与紧密相关的物种(如脑毛癣菌或间位毛癣菌)区分开来具有挑战性。虽然 MALDI-TOF MS 能可靠地鉴定出≥ 95% 的 T. indotineae 菌株(取决于光谱库),但它不能用来成功区分 TRB 易感菌株和 TRB 耐药菌株。
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来源期刊
Mycopathologia
Mycopathologia 生物-真菌学
CiteScore
6.80
自引率
3.60%
发文量
76
审稿时长
3 months
期刊介绍: Mycopathologia is an official journal of the International Union of Microbiological Societies (IUMS). Mycopathologia was founded in 1938 with the mission to ‘diffuse the understanding of fungal diseases in man and animals among mycologists’. Many of the milestones discoveries in the field of medical mycology have been communicated through the pages of this journal. Mycopathologia covers a diverse, interdisciplinary range of topics that is unique in breadth and depth. The journal publishes peer-reviewed, original articles highlighting important developments concerning medically important fungi and fungal diseases. The journal highlights important developments in fungal systematics and taxonomy, laboratory diagnosis of fungal infections, antifungal drugs, clinical presentation and treatment, and epidemiology of fungal diseases globally. Timely opinion articles, mini-reviews, and other communications are usually invited at the discretion of the editorial board. Unique case reports highlighting unprecedented progress in the diagnosis and treatment of fungal infections, are published in every issue of the journal. MycopathologiaIMAGE is another regular feature for a brief clinical report of potential interest to a mixed audience of physicians and laboratory scientists. MycopathologiaGENOME is designed for the rapid publication of new genomes of human and animal pathogenic fungi using a checklist-based, standardized format.
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