The Growing Problem of Antifungal Resistance in Onychomycosis and Other Superficial Mycoses.


Journal

American journal of clinical dermatology
ISSN: 1179-1888
Titre abrégé: Am J Clin Dermatol
Pays: New Zealand
ID NLM: 100895290

Informations de publication

Date de publication:
Mar 2021
Historique:
accepted: 28 11 2020
pubmed: 24 12 2020
medline: 13 7 2021
entrez: 23 12 2020
Statut: ppublish

Résumé

Superficial mycoses are becoming increasingly resistant to current antifungal medications. As alternative therapeutic options are limited, the increasing frequency of reports of antifungal resistance is alarming. This epidemic parallels the rise of antibiotic resistance; however, the significance of this problem has yet to gain global attention. Here, we discuss the reports of antifungal resistance from around the world, present our own experience with treatment-resistant infections, and examine alternative treatment strategies. The majority of reports of recalcitrant infections indicate terbinafine resistance as the causative factor. Single-point mutations in the squalene oxidase gene is the most reported mechanism of resistance to terbinafine. Mixed infections of dermatophytes with non-dermatophyte molds and/or yeasts are becoming more prevalent and contributing to the resistant nature of these infections. The key to selecting an effective antifungal therapy for a recalcitrant infection is identification of the infectious organisms(s) and testing susceptibility of the organism(s) to antifungal drugs. Combination and sequential therapy regimens are options, but both require active monitoring for hepatic and renal function, drug interactions, and other adverse effects. Selected topical antifungals with a wide spectrum of activity may also be considerations in some clinical presentations. Innovative treatment regimens and novel therapeutics are needed to overcome the rising epidemic of antifungal resistance.

Identifiants

pubmed: 33354740
doi: 10.1007/s40257-020-00580-6
pii: 10.1007/s40257-020-00580-6
doi:

Substances chimiques

Antifungal Agents 0
Terbinafine G7RIW8S0XP

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

149-157

Références

Panda S, Verma S. The menace of dermatophytosis in India: the evidence that we need. Indian J Dermatol Venereol Leprol. 2017;83:281–4. https://doi.org/10.4103/ijdvl.IJDVL_224_17 .
doi: 10.4103/ijdvl.IJDVL_224_17 pubmed: 28366915
Verma S, Madhu R. The Great Indian epidemic of superficial dermatophytosis: an appraisal. Indian J Dermatol. 2017;62:227–36. https://doi.org/10.4103/ijd.IJD_206_17 .
doi: 10.4103/ijd.IJD_206_17 pubmed: 28584364 pmcid: 5448256
Havlickova B, Czaika VA, Friedrich M. Epidemiological trends in skin mycoses worldwide. Mycoses. 2008;51:2–15. https://doi.org/10.1111/j.1439-0507.2008.01606.x .
doi: 10.1111/j.1439-0507.2008.01606.x pubmed: 18783559
Davies J, Davies D. Origins and evolution of antibiotic resistance. Microbiol Mol Biol Rev MMBR. 2010;74:417–33. https://doi.org/10.1128/MMBR.00016-10 .
doi: 10.1128/MMBR.00016-10 pubmed: 20805405
Seebacher C, Bouchara J-P, Mignon B. Updates on the epidemiology of dermatophyte infections. Mycopathologia. 2008;166:335–52. https://doi.org/10.1007/s11046-008-9100-9 .
doi: 10.1007/s11046-008-9100-9 pubmed: 18478365
Singh S, Beena PM. Profile of dermatophyte infections in Baroda. Indian J Dermatol Venereol Leprol. 2003;69:281–3.
pubmed: 17642912
Nenoff P, Verma SB, Vasani R, Burmester A, Hipler U-C, Wittig F, Krüger C, Nenoff K, Wiegand C, Saraswat A, Madhu R, Panda S, Das A, Kura M, Jain A, Koch D, Gräser Y, Uhrlaß S. The current Indian epidemic of superficial dermatophytosis due to Trichophyton mentagrophytes-a molecular study. Mycoses. 2019;62:336–56. https://doi.org/10.1111/myc.12878 .
doi: 10.1111/myc.12878 pubmed: 30561859
Gupta AK, Ryder JE, Chow M, Cooper EA. Dermatophytosis: the management of fungal infections. Skinmed. 2005;4:305–10.
doi: 10.1111/j.1540-9740.2005.03435.x
Mukherjee PK, Leidich SD, Isham N, Leitner I, Ryder NS, Ghannoum MA. Clinical Trichophyton rubrum strain exhibiting primary resistance to terbinafine. Antimicrob Agents Chemother. 2003;47:82–6.
doi: 10.1128/AAC.47.1.82-86.2003
Osborne CS, Leitner I, Hofbauer B, Fielding CA, Favre B, Ryder NS. Biological, biochemical, and molecular characterization of a new clinical Trichophyton rubrum isolate resistant to terbinafine. Antimicrob Agents Chemother. 2006;50:2234–6. https://doi.org/10.1128/AAC.01600-05 .
doi: 10.1128/AAC.01600-05 pubmed: 16723593 pmcid: 1479141
Singh A, Masih A, Khurana A, Singh PK, Gupta M, Hagen F, Meis JF, Chowdhary A. High terbinafine resistance in Trichophyton interdigitale isolates in Delhi, India harbouring mutations in the squalene epoxidase gene. Mycoses. 2018;61:477–84. https://doi.org/10.1111/myc.12772 .
doi: 10.1111/myc.12772 pubmed: 29577447
Yamada T, Maeda M, Alshahni MM, Tanaka R, Yaguchi T, Bontems O, Salamin K, Fratti M, Monod M. Terbinafine resistance of trichophyton clinical isolates caused by specific point mutations in the squalene epoxidase gene. Antimicrob Agents Chemother. 2017. https://doi.org/10.1128/AAC.00115-17 .
doi: 10.1128/AAC.00115-17 pubmed: 29269432 pmcid: 5740349
Rudramurthy SM, Shankarnarayan SA, Dogra S, Shaw D, Mushtaq K, Paul RA, Narang T, Chakrabarti A. Mutation in the squalene epoxidase gene of Trichophyton interdigitale and Trichophyton rubrum associated with allylamine resistance. Antimicrob Agents Chemother. 2018. https://doi.org/10.1128/AAC.02522-17 .
doi: 10.1128/AAC.02522-17 pubmed: 30126956 pmcid: 6201112
Hiruma J, Kitagawa H, Noguchi H, Kano R, Hiruma M, Kamata H, Harada K. Terbinafine-resistant strain of Trichophyton interdigitale strain isolated from a tinea pedis patient. J Dermatol. 2019;46:351–3. https://doi.org/10.1111/1346-8138.14809 .
doi: 10.1111/1346-8138.14809 pubmed: 30768808
Burmester A, Hipler U-C, Hensche R, Elsner P, Wiegand C. Point mutations in the squalene epoxidase gene of Indian ITS genotype VIII T. mentagrophytes identified after DNA isolation from infected scales. Med Mycol Case Rep. 2019;26:23–4. https://doi.org/10.1016/j.mmcr.2019.09.001 .
doi: 10.1016/j.mmcr.2019.09.001 pubmed: 31667055 pmcid: 6812012
Hsieh A, Quenan S, Riat A, Toutous-Trellu L, Fontao L. A new mutation in the SQLE gene of Trichophyton mentagrophytes associated to terbinafine resistance in a couple with disseminated tinea corporis. J Mycol Med. 2019;29:352–5. https://doi.org/10.1016/j.mycmed.2019.100903 .
doi: 10.1016/j.mycmed.2019.100903 pubmed: 31611164
Saunte DML, Hare RK, Jørgensen KM, Jørgensen R, Deleuran M, Zachariae CO, Thomsen SF, Bjørnskov-Halkier L, Kofoed K, Arendrup MC. Emerging terbinafine resistance in trichophyton: clinical characteristics, squalene epoxidase gene mutations, and a reliable EUCAST method for detection. Antimicrob Agents Chemother. 2019. https://doi.org/10.1128/AAC.01126-19 .
doi: 10.1128/AAC.01126-19 pubmed: 31383665 pmcid: 6761549
Süß A, Uhrlaß S, Ludes A, Verma SB, Monod M, Krüger C, Nenoff P. Extensive tinea corporis due to a terbinafine-resistant Trichophyton mentagrophytes isolate of the Indian genotype in a young infant from Bahrain in Germany. Hautarzt Z Dermatol Venerol Verwandte Geb. 2019;70:888–96. https://doi.org/10.1007/s00105-019-4431-7 .
doi: 10.1007/s00105-019-4431-7
Singh S, Chandra U, Anchan VN, Verma P, Tilak R. Limited effectiveness of four oral antifungal drugs (fluconazole, griseofulvin, itraconazole and terbinafine) in the current epidemic of altered dermatophytosis in India: results of a randomized pragmatic trial. Br J Dermatol. 2020. https://doi.org/10.1111/bjd.19146 .
doi: 10.1111/bjd.19146 pubmed: 33332578
Ebert A, Monod M, Salamin K, Burmester A, Uhrlaß S, Wiegand C, Hipler U-C, Krüger C, Koch D, Wittig F, Verma SB, Singal A, Gupta S, Vasani R, Saraswat A, Madhu R, Panda S, Das A, Kura MM, Kumar A, Poojary S, Schirm S, Gräser Y, Paasch U, Nenoff P. Alarming India-wide phenomenon of antifungal resistance in dermatophytes: a multicentre study. Mycoses. 2020;63:717–28. https://doi.org/10.1111/myc.13091 .
doi: 10.1111/myc.13091 pubmed: 32301159
Salehi Z, Shams-Ghahfarokhi M, Razzaghi-Abyaneh M. Antifungal drug susceptibility profile of clinically important dermatophytes and determination of point mutations in terbinafine-resistant isolates. Eur J Clin Microbiol Infect Dis. 2018;37:1841–6. https://doi.org/10.1007/s10096-018-3317-4 .
doi: 10.1007/s10096-018-3317-4 pubmed: 29980898
Järv H, Uhrlass S, Simkin T, Nenoff E, Alvarado Ramirez E, Chryssanthou E, Monod M. Terbinafine resistant Trichophyton mentagrophytes genotype VIII, Indian type, isolated in Finland. In: 9th Trends Med. Mycol. Held 11-14 Oct. 2019 Nice Fr. Organ. Auspices EORTC-IDG ECMM, Journal of Fungi, Nice, France, 2019: p. P039.
Gallo JG, Woods M, Graham RM, Jennison AV. A severe transmissible Majocchi’s granuloma in an immunocompetent returned traveler. Med Mycol Case Rep. 2017;18:5–7. https://doi.org/10.1016/j.mmcr.2017.07.003 .
doi: 10.1016/j.mmcr.2017.07.003 pubmed: 28725545 pmcid: 5502794
Rengasamy M, Shenoy MM, Dogra S, Asokan N, Khurana A, Poojary S, Jayaraman J, Valia AR, Sardana K, Kolalapudi S, Marfatia Y, Rao PN, Bhat RM, Kura M, Pandhi D, Barua S, Kaushal V. Indian Association of Dermatologists, Venereologists and Leprologists (IADVL) Task Force against Recalcitrant Tinea (ITART) Consensus on the Management of Glabrous Tinea (INTACT). 2020;11:502–19. Indian Dermatol Online J. https://doi.org/10.4103/idoj.IDOJ_233_20 .
Majid I, Sheikh G, Kanth F, Hakak R. Relapse after oral terbinafine therapy in dermatophytosis: a clinical and mycological study. Indian J Dermatol. 2016;61:529–33. https://doi.org/10.4103/0019-5154.190120 .
doi: 10.4103/0019-5154.190120 pubmed: 27688443 pmcid: 5029239
Singh S, Shukla P. End of the road for terbinafine? Results of a pragmatic prospective cohort study of 500 patients. Indian J Dermatol Venereol Leprol. 2018;84:554–7. https://doi.org/10.4103/ijdvl.IJDVL_526_17 .
doi: 10.4103/ijdvl.IJDVL_526_17 pubmed: 29893296
Khurana A, Masih A, Chowdhary A, Sardana K, Borker S, Gupta A, Gautam RK, Sharma PK, Jain D. Correlation of in vitro susceptibility based on MICs and squalene epoxidase mutations with clinical response to terbinafine in patients with tinea corporis/cruris. Antimicrob Agents Chemother. 2018. https://doi.org/10.1128/AAC.01038-18 .
doi: 10.1128/AAC.01038-18 pubmed: 30275090 pmcid: 6256768
Taghipour S, Shamsizadeh F, Pchelin IM, Rezaei-Matehhkolaei A, Zarei Mahmoudabadi A, Valadan R, Ansari S, Katiraee F, Pakshir K, Zomorodian K, Abastabar M. Emergence of terbinafine resistant trichophyton mentagrophytes in Iran, harboring mutations in the squalene epoxidase (SQLE) gene. Infect Drug Resist. 2020;13:845–50. https://doi.org/10.2147/IDR.S246025 .
doi: 10.2147/IDR.S246025 pubmed: 32214830 pmcid: 7078656
Nofal A, Fawzy MM, El-Hawary EE. Successful treatment of resistant onychomycosis with voriconazole in a liver transplant patient. Dermatol Ther. 2020. https://doi.org/10.1111/dth.14014 .
doi: 10.1111/dth.14014 pubmed: 33006221
Schøsler L, Andersen LK, Arendrup MC, Sommerlund M. Recurrent terbinafine resistant Trichophyton rubrum infection in a child with congenital ichthyosis. Pediatr Dermatol. 2018;35:259–60. https://doi.org/10.1111/pde.13411 .
doi: 10.1111/pde.13411 pubmed: 29341312
Digby SS, Hald M, Arendrup MC, Hjort SV, Kofoed K. Darier disease complicated by terbinafine-resistant Trichophyton rubrum: a case report. Acta Dermatol Venereol. 2017;97:139–40. https://doi.org/10.2340/00015555-2455 .
doi: 10.2340/00015555-2455
Santos HL, Lang EAS, Segato F, Rossi A, Martinez-Rossi NM. Terbinafine resistance conferred by multiple copies of the salicylate 1-monooxygenase gene in Trichophyton rubrum. Med Mycol. 2018;56:378–81. https://doi.org/10.1093/mmy/myx044 .
doi: 10.1093/mmy/myx044 pubmed: 28582544
Chen E, Ghannoum M, Elewski BE. Treatment-resistant tinea corporis, a potential public health issue. Br J Dermatol. 2020. https://doi.org/10.1111/bjd.19420 .
doi: 10.1111/bjd.19420 pubmed: 33428216 pmcid: 7262186
Gawaz A, Weisel G. Mixed infections are a critical factor in the treatment of superficial mycoses. Mycoses. 2018;61:731–5. https://doi.org/10.1111/myc.12794 .
doi: 10.1111/myc.12794 pubmed: 29774605
Gupta AK, Stec N, Summerbell RC, Shear NH, Piguet V, Tosti A, Piraccini BM. Onychomycosis: a review. J Eur Acad Dermatol Venereol JEADV. 2020. https://doi.org/10.1111/jdv.16394 .
doi: 10.1111/jdv.16394 pubmed: 33351973
Newland JG, Abdel-Rahman SM. Update on terbinafine with a focus on dermatophytoses. Clin Cosmet Investig Dermatol CCID. 2009;2:49–63.
pubmed: 21436968
Novartis Pharmaceuticals Corporation. Product monograph Lamisil (terbinafine hydrochloride). 2011. http://webprod3.hc-sc.gc.ca/dpd-bdpp/info.do?lang=eng&code=13990 . Accessed 21 Aug 2012.
Gupta AK, Taborda VBA, Taborda PRO, Shemer A, Nakrieko K-A. High prevalence of mixed infections in global onychomycosis. 2020.
Sharma P, Bhalla M, Thami GP, Chander J. Evaluation of efficacy and safety of oral terbinafine and itraconazole combination therapy in the management of dermatophytosis. J Dermatol Treat. 2020;31:749–53. https://doi.org/10.1080/09546634.2019.1612835 .
doi: 10.1080/09546634.2019.1612835
Arendrup MC, Jørgensen KM, Guinea J, Lagrou K, Chryssanthou E, Hayette M-P, Barchiesi F, Lass-Flörl C, Hamal P, Dannaoui E, Chowdhary A, Meletiadis J. Multicentre validation of a EUCAST method for the antifungal susceptibility testing of microconidia-forming dermatophytes. J Antimicrob Chemother. 2020;75:1807–19. https://doi.org/10.1093/jac/dkaa111 .
doi: 10.1093/jac/dkaa111 pubmed: 32303059
Hof H. A new, broad-spectrum azole antifungal: posaconazole–mechanisms of action and resistance, spectrum of activity. Mycoses. 2006;49(Suppl 1):2–6. https://doi.org/10.1111/j.1439-0507.2006.01295.x .
doi: 10.1111/j.1439-0507.2006.01295.x pubmed: 16961575
Gupta AK, Foley KA, Versteeg SG. New antifungal agents and new formulations against dermatophytes. Mycopathologia. 2017;182:127–41. https://doi.org/10.1007/s11046-016-0045-0 .
doi: 10.1007/s11046-016-0045-0 pubmed: 27502503
Hachem R, Assaf A, Numan Y, Shah P, Jiang Y, Chaftari A-M, Raad II. Comparing the safety and efficacy of voriconazole versus posaconazole in the prevention of invasive fungal infections in high-risk patients with hematological malignancies. Int J Antimicrob Agents. 2017;50:384–8. https://doi.org/10.1016/j.ijantimicag.2017.03.021 .
doi: 10.1016/j.ijantimicag.2017.03.021 pubmed: 28694233
Gupta AK, Daigle D. A critical appraisal of once-daily topical luliconazole for the treatment of superficial fungal infections. Infect Drug Resist. 2016;9:1–6. https://doi.org/10.2147/IDR.S61998 .
doi: 10.2147/IDR.S61998 pubmed: 26848272 pmcid: 4723097
Jo Siu WJ, Tatsumi Y, Senda H, Pillai R, Nakamura T, Sone D, Fothergill A. Comparison of in vitro antifungal activities of efinaconazole and currently available antifungal agents against a variety of pathogenic fungi associated with onychomycosis. Antimicrob Agents Chemother. 2013;57:1610–6. https://doi.org/10.1128/AAC.02056-12 .
doi: 10.1128/AAC.02056-12 pubmed: 23318803 pmcid: 3623347
Valeant Canada LP. PrJublia
Coronado D, Merchant T, Chanda S, Zane LT. In vitro nail penetration and antifungal activity of tavaborole, a boron-based pharmaceutical. J Drugs Dermatol JDD. 2015;14:609–14.
pubmed: 26091387
Anacor Pharmaceuticals. Kerydin
Gupta AK, Stec N. Recent advances in therapies for onychomycosis and its management. F1000Research. 2019. https://doi.org/10.12688/f1000research.18646.1 .
doi: 10.12688/f1000research.18646.1 pubmed: 32047596 pmcid: 6979471
Gupta AK, Versteeg SG, Shear NH. Onychomycosis in the 21st century: an update on diagnosis, epidemiology, and treatment. J Cutan Med Surg. 2017;21:525–39. https://doi.org/10.1177/1203475417716362 .
doi: 10.1177/1203475417716362 pubmed: 28639462
Shen JJ, Jemec GBE, Arendrup MC, Saunte DML. Photodynamic therapy treatment of superficial fungal infections: a systematic review. Photodiagn Photodyn Ther. 2020. https://doi.org/10.1016/j.pdpdt.2020.101774 .
doi: 10.1016/j.pdpdt.2020.101774
Saoji V, Madke B. Efficacy of salicylic acid peel in dermatophytosis. Indian J Dermatol Venereol Leprol. 2019. https://doi.org/10.4103/ijdvl.IJDVL_853_18 .
doi: 10.4103/ijdvl.IJDVL_853_18 pubmed: 31650983
Huang T-H, Lan C-CE. Cutaneous chromoblastomycosis effectively treated with local heat monotherapy. Clin Exp Dermatol. 2019;44:461–2. https://doi.org/10.1111/ced.13780 .
doi: 10.1111/ced.13780 pubmed: 30280420

Auteurs

Aditya K Gupta (AK)

Mediprobe Research Inc., 645 Windermere Road, London, ON, N5X 2P1, Canada. agupta@mediproberesearch.com.
Division of Dermatology, Department of Medicine, University of Toronto School of Medicine, Toronto, Canada. agupta@mediproberesearch.com.

Helen J Renaud (HJ)

Mediprobe Research Inc., 645 Windermere Road, London, ON, N5X 2P1, Canada.

Emma M Quinlan (EM)

Mediprobe Research Inc., 645 Windermere Road, London, ON, N5X 2P1, Canada.

Neil H Shear (NH)

Division of Dermatology, Department of Medicine, University of Toronto School of Medicine, Toronto, Canada.
Division of Dermatology, Sunnybrook Health Sciences Centre, Toronto, Canada.

Vincent Piguet (V)

Division of Dermatology, Department of Medicine, University of Toronto School of Medicine, Toronto, Canada.
Division of Dermatology, Women's College Hospital, Toronto, Canada.

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