Trichophyton ment. var interdigitale
Summary
Trichophyton mentagrophytes var. goetzii and Trichophyton mentagrophytes var. interdigitale have recently been reclassified as the same species, T. interdigitale. T. interdigitale is, along with T. rubrum, the most common cause of dermatophytosis in humans, a highly prevalent infectious disease. T. interdigitalis causes tinea pedis and onychomycosis predominantly. Trichophyton allergens have been implicated in the pathogenicity of both atopic and allergic airway disease. The route of exposure has not been elucidated. Three T. interdigitalis allergens are currently recognized.
Epidemiology
Worldwide distribution
Trichophyton mentagrophytes and T. rubrum are the most common pathogens associated with onychomycosis. However, some geographical variation is reported; in Libya, the most common cause of onychomycosis in women is yeasts of the genus Candida, whereas in men, it is T. violaceum, T. rubrum, T. mentagrophytes and Microsporum canis.
The epidemiology of anthropophilic T. interdigitale strains are similar to that of T rubrum. T. interdigitale is the cause of 4–8% of infections in Europe. An analysis of Trichophyton spp. contaminating nail dust from salons in different regions of Australia found that T. interdigitale was the most prevalent dermatophyte. Thought to be associated with the widespread abuse of topical steroid-containing creams, the underlying cause is widely reported as T. interdigitale. ITS analysis, however, has shown it is T. mentagrophytes.
A link between allergic skin disease and dermatophyte infection has been proposed. One study found a 79% prevalence of sensitization to Trichophyton spp. amongst patients with concurrent allergic skin disease and dermatophyte infection termed atopic-chronic dermatophytosis syndrome. This observation supports the findings of a controlled prospective trial from China, which found that 84.9% of patients with chronic urticaria and dermatophytosis were sensitized (as determined by skin prick test) to T. mentagrophytes.
Route Of Exposure
Main
The primary route of exposure to Trichophyton spp. is not fully understood. Sensitization to Trichophyton-specific allergen is common in patients with clinical dermatophytosis, suggesting hypersensitivity is due to transdermal contact with the allergen. However, there is evidence that Trichophyton hypersensitivity may also play a role in late-onset asthma and allergic rhinitis and that route of exposure may be inhalation, particularly in those patients with no concurrent dermatophytosis. Alternatively, Trichophyton spp. allergens may elicit hypersensitivity through a yet-to-be described mechanism.
Clinical Relevance
Trichophyton spp. allergens have been implicated in the pathogenesis of atopic dermatitis, late-onset asthma and allergic rhinitis. Trichophyton-specific allergens have been shown to have the unusual capacity to induce either immediate- (ITH) or delayed- (DTH) type hypersensitivity. In some patients, both immune responses are induced. The type of immune response induced is strongly associated with the clinical profile of dermatophyte disease. Whereas DTH is associated with acute inflammatory dermatophytosis with resolution, ITH results in persistent low-grade infection. It is proposed this is a dysregulated immune response and the mechanism for the association between chronic dermatophytosis and clinical hypersensitivity. This is supported by evidence of monosensitivity to dermatophyte antigens in patients with ”intrinsic” asthma. Furthermore, sensitization to Trichophyton spp. allergens is a possible risk factor for more severe disease amongst patients with asthma. T. mentagrophytes has also been implicated as an allergen in a small subgroup of patients with cholinergic urticaria.
Cross-Reactivity
A study found that a significant number of patients with allergic bronchopulmonary aspergillosis and Aspergillus-sensitized asthma were sensitized to T. mentagrophytes var. goetzii, indicating the possibility that patients are erroneously diagnosed with sensitivity to Aspergillosis spp. allergens. Furthermore, a study from China has demonstrated sensitization to T. mentagrophytes (as well as E. flocculosum and T. rubrum) in T. rubrum culture-positive patients, indicating cross-reactivity between the three dermatophytes.
References
- Ziółkowska G, Nowakiewicz A, Gnat S, Trościańczyk A, Zięba P, Dziedzic B. Molecular identification and classification of Trichophyton mentagrophytes complex strains isolated from humans and selected animal species. Mycoses. 2015;58.
- Heidemann S, Monod M, Gräser Y. Signature polymorphisms in the internal transcribed spacer region relevant for the differentiation of zoophilic and anthropophilic strains of Trichophyton interdigitale and other species of T. mentagrophytes sensu lato. Br J Dermatol. 2010;162(2):282-95.
- Celestrino GA, Verrinder Veasey J, Benard G, Sousa MGT. Host immune responses in dermatophytes infection. Mycoses. 2021;64(5):477-83.
- Nenoff P, Herrmann J, Gräser Y. Trichophyton mentagrophytes sive interdigitale? A dermatophyte in the course of time. J Dtsch Dermatol Ges. 2007;5(3):198-202.
- de Hoog GS, Dukik K, Monod M, Packeu A, Stubbe D, Hendrickx M, et al. Toward a Novel Multilocus Phylogenetic Taxonomy for the Dermatophytes. Mycopathologia. 2017;182(1-2):5-31.
- Nenoff P, Verma SB, Uhrlaß S, Burmester A, Gräser Y. A clarion call for preventing taxonomical errors of dermatophytes using the example of the novel Trichophyton mentagrophytes genotype VIII uniformly isolated in the Indian epidemic of superficial dermatophytosis. Mycoses. 2019;62(1):6-10.
- Ilkit M, Durdu M. Tinea pedis: the etiology and global epidemiology of a common fungal infection. Crit Rev Microbiol. 2015;41(3):374-88.
- Shi Y, Niu Q, Yu X, Jia X, Wang J, Lin D, et al. Assessment of the function of SUB6 in the pathogenic dermatophyte Trichophyton mentagrophytes. Med Mycol. 2016;54(1):59-71.
- Singh A, Masih A, Khurana A, Singh PK, Gupta M, Hagen F, et al. High terbinafine resistance in Trichophyton interdigitale isolates in Delhi, India harbouring mutations in the squalene epoxidase gene. Mycoses. 2018;61(7):477-84.
- Čmoková A, Rezaei-Matehkolaei A, Kuklová I, Kolařík M, Shamsizadeh F, Ansari S, et al. Discovery of New Trichophyton Members, T. persicum and T. spiraliforme spp. nov., as a Cause of Highly Inflammatory Tinea Cases in Iran and Czechia. Microbiol Spectr. 2021;9(2):e0028421.
- Nenoff P, Verma SB, Vasani R, Burmester A, Hipler UC, Wittig F, et al. The current Indian epidemic of superficial dermatophytosis due to Trichophyton mentagrophytes-A molecular study. Mycoses. 2019;62(4):336-56.
- Woodfolk JA. Allergy and Dermatophytes. Clinical Microbiology Reviews. 2005;18(1):30-43.
- Hainsworth S, Hubka V, Lawrie AC, Carter D, Vanniasinkam T, Grando D. Predominance of Trichophyton interdigitale Revealed in Podiatric Nail Dust Collections in Eastern Australia. Mycopathologia. 2020;185(1):175-85.
- Zhang M, Liu F, Liu H, Shen Y, Kong Q, Sang H. Sensitization and cross-reactions of dermatophyte and Candida albicans allergens in patients with chronic urticaria. Int J Dermatol. 2016;55(10):1138-42.
- Fukutomi Y, Taniguchi M. Sensitization to fungal allergens: Resolved and unresolved issues. Allergol Int. 2015;64(4):321-31.
- Goldman DL, Huffnagle GB. Potential contribution of fungal infection and colonization to the development of allergy. Med Mycol. 2009;47(5):445-56.
- Altrichter S, Schumacher P, Alraboni O, Wang Y, Hiragun M, Hide M, et al. Sensitization against skin resident fungi is associated with atopy in cholinergic urticaria patients. Clinical and Translational Allergy. 2020;10(1):18.
- allergome.org. Trichophyton 2021 [cited 2022 25.01.22]. Available from: http://www.allergome.org/script/search_step2.php.
