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Mentagrophytes - Çukurova Üniversitesi

Mentagrophytes - Çukurova Üniversitesi

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ABSTRACT<br />

COMPARISION OF IDENTIFICATION METHODS FOR THE<br />

DIFFERENTIATION OF TRICHOPHYTON RUBRUM FROM TRICHOPHYTON<br />

MENTAGROPHYTES<br />

Nowadays a rapid and striking change is observed in the taxonomy of<br />

dermatophytes. They are either re-grouped or re-named, in addition some<br />

varieties remain out of nomenclature giving origin to new species.<br />

The gold standard in laboratory diagnosis is sequencing analysis. But<br />

dermatophyte species are identified at the level of species according to colony<br />

characteristics, microscopic morphologies, growth requirements, physiological and<br />

biochemical characteristics due to infer-structural needs and high cost of<br />

molecular based researches. As changes are observed for a single dermatophyte<br />

species both for its morphology (colony pattern, pigments and growth rate) or<br />

physiology (in vitro hair perforation) and for its genotype (rRNA and mating<br />

patterns); the reliability of the method is questioned.<br />

Many micro-organisms belonging to Trichophyton rubrum complex are<br />

renamed i.e., T. fischeri, T. kanei, T. raubitschekii and similar are identified.<br />

Trichophyton interdigitale, and other micro-organisms pertaining to Trichophyton<br />

mentagrophytes sensu lato are re-classified by sequencing analysis. But one of the<br />

principal problems observed in mycology laboratory is the differentiation of T.<br />

rubrum from T. mentagrophytes using classical diagnostic methods. This study<br />

aimed to discuss the efficacy of morphological, physiological and biochemical<br />

diagnostic tests used in the laboratory identification of micro-organisms pertaining<br />

to both complexes before the current classification, in addition to interrogate their<br />

reliability in routine laboratory practice.<br />

In the study, T. fischeri CBS 100081, T. fluvimunionse CBS 592.68, T. kanei<br />

CBS 289.86, T. kuryangei CBS 422.67, T. kuryangei CBS 517.63, T. kuryangei CBS<br />

518.63, T. pervesii CBS 303.38, T. raubitschekii CBS 202.88, T. raubitschekii CBS<br />

287.86, T. raubitschekii CBS 100084, T. raubitschekii CBS 102856, T. rodhainii CBS<br />

376.49, T. rubrum CBS 302.60, T. rubrum CBS 363.53, T. rubrum CBS 363.62, T.<br />

rubrum CBS 392.58, T. rubrum var. nigricans CBS 100237, T. megninii CBS 389.58,<br />

T. asteroides CBS 424.63, T. langeronii CBS 764.84, T. mentagrophytes CBS 318.56,<br />

T. mentagrophytes var. mentagrophytes CBS 110.65, T. mentagrophytes var.<br />

mentagrophytes CBS 160.66, T. papillosum CBS 347.55, T. quinckeanum CBS<br />

572.75, Arthroderma benhamiae (MT-) CBS 807.72, A. benhamiae (MT+) CBS<br />

808.72, A. simii (MT-) CBS 417.65, A. simii (MT+) CBS 448.65, A. vanbreuseghemii<br />

CBS 428.63 and A. vanbreuseghemii CBS 558.66 obtained from Centraalbureau<br />

voor Schimmelcultures (CBS), Utrecht, the Netherlans were used.<br />

Urease reaction (in broth, in tube-agar and Petri agar), in vitro hair<br />

perforation test (blond child hair, sheep and goat hair), growth in corn-meal agar<br />

and bromcresol purple-milk solids-glucose agar (BCPMSG), Tween opacity test,<br />

xiii

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