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Jundishapur J Microbiol.

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https://doi.org/10.5812/jjm.115902

In Vitro Antifungal Activity of Luliconazole, Efinaconazole, and Nine Comparators Against Aspergillus and Candida Strains Isolated from Otomycosis

Author(s):
Gholamreza ShokoohiGholamreza ShokoohiGholamreza Shokoohi ORCID1, 2, Reza Rouhi SefidmazgiReza Rouhi Sefidmazgi2, 3, Mohammad EtehadnezhadMohammad Etehadnezhad1, 2, Bahram AhmadiBahram AhmadiBahram Ahmadi ORCID4, Javad JavidniaJavad JavidniaJavad Javidnia ORCID5, 6, Sadegh Nouripour-SisakhtSadegh Nouripour-SisakhtSadegh Nouripour-Sisakht ORCID7, Farhang HooshmandFarhang HooshmandFarhang Hooshmand ORCID2, 8, Ali Rezaei-MatehkolaeiAli Rezaei-MatehkolaeiAli Rezaei-Matehkolaei ORCID9, Seyede Nadia TabatabaeifarSeyede Nadia Tabatabaeifar10, Saham AnsariSaham AnsariSaham Ansari ORCID11,*
1Department of Medical Parasitology and Mycology, School of Medicine, Jahrom University of Medical Sciences, Jahrom, Iran
2Zoonosis Research Center, Jahrom University of Medical Sciences, Jahrom, Iran
3Department of Medical Otorhinolaryngology, Jahrom University of Medical Sciences, Jahrom, Iran
4Department of Medical Laboratory Sciences, Faculty of Paramedical, Bushehr University of Medical Sciences, Bushehr, Iran
5Department of Medical Mycology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran
6Student Research Committee, Mazandaran University of Medical Sciences, Sari, Iran
7Medicinal Plants Research Center, Yasuj University of Medical Sciences, Yasuj, Iran
8Department of Pathology, School of Medicine, Jahrom University of Medical Sciences, Jahrom, Iran
9Infectious and Tropical Diseases Research Center, Health Research Institute, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran
10Department of Internal Medicine, Sina Hospital, Tehran University of Medical Sciences, Tehran, Iran
11Department of Parasitology and Mycology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Jundishapur Journal of Microbiology:Vol. 14, issue 4; e115902
Published online:Jul 18, 2021
Article type:Research Article
Received:May 05, 2021
Accepted:Jul 05, 2021
How to Cite:Shokoohi G, Rouhi Sefidmazgi R, Etehadnezhad M, Ahmadi B, Javidnia J, et al. In Vitro Antifungal Activity of Luliconazole, Efinaconazole, and Nine Comparators Against Aspergillus and Candida Strains Isolated from Otomycosis.Jundishapur J Microbiol.2021;14(4):e115902.https://doi.org/10.5812/jjm.115902.

Abstract

Background:

Aspergillus and Candida species are the most commonly identified fungal pathogens in otomycosis. However, we usually encounter some difficulties in its treatment because many patients show resistance to antifungal agents and present a high recurrence rate.

Objectives:

The current research was conducted to compare the in vitro activities of luliconazole (LUL), and efinaconazole (EFN) and the nine comparators on Aspergillus and Candida strains isolated from otomycosis.

Methods:

The in vitro activities of nine common antifungal drugs (amphotericin B (AMB), voriconazole (VRC), fluconazole (FLU), itraconazole (ITC), ketoconazole (KTO), clotrimazole (CLO), nystatin (NYS), terbinafine (TRB), and caspofungin (CAS)) and two novel new azoles (LUL and EFN) against 108 clinical isolates of Aspergillus and Candida species obtained from otomycosis were assessed according to the CLSI broth microdilution document.

Results:

The LUL and EFN had the geometric mean minimum inhibitory concentrations (GM MICs) of 0.098 and 0.109 μg/mL against all Aspergillus strains, respectively. Furthermore, the GM MICs of all Candida isolates for LUL, EFN, CAS, CLO, VRC, AMB, ITC, KTO, FLU, NYS, and TRB were calculated to be 0.133, 0.144, 0.194, 0.219, 0.475, 0.537, 0.655, 1.277, 4.905, 9.372, and 13.592 μg/mL, respectively. Additionally, 6 (35.29%), 2 (11.7%), and 1 (5.88%) Candida isolates were resistant to FLU, CAS, and VRC, respectively.

Conclusions:

As the findings indicated, LUL and EFN showed the lowest GM MIC values against the examined species. Accordingly, these novel imidazole and triazole antifungal agents can be regarded as proper candidates for the treatment of otomycosis caused by Aspergillus and Candida strains.

Keywords
Otomycosis
Antifungal Susceptibility
Efinaconazole
Luliconazole

1. Background

Otomycosis, a superficial infection of the external ear induced by fungal pathogens, is a common condition in tropical and subtropical regions (1). The similarity of the clinical symptoms of otomycosis with those of other ear infections that cause the improper administration of antifungal drugs leads to resistance to antifungal drugs (2). Some Aspergillus and Candida species, which are the main causes of otomycosis, have an inherent resistance to several antifungal drugs (3). There is evidence regarding the isolation of the multidrug-resistant Candida species, namely Candida auris, one of the most threatening fungal species, from an external ear discharge (4).

Topical forms of clotrimazole, miconazole, bifonazole, ciclopirox olamine, tolnaftate, and amphotericin B, as well as triazoles, such as voriconazole, posaconazole, and itraconazole for oral administration are instances of accessible therapies for otomycosis (5, 6). Although the causative agents of otomycosis are commonly susceptible to most antifungal drugs in vivo and in vitro, treatment is a big challenge because frequent relapses and failures are observed, particularly in cases with complete removal of these organisms, which can act as a potential risk factor leading to the gradual increase of resistant species (7, 8). Thus, alternative antifungal agents with better activity and lower side effects can help to improve the controlling of these infections. Lately, the new imidazole agents, luliconazole and efinaconazole, were approved for the treatment of onychomycosis and dermatophytosis (9). Previous studies have also shown the potent activities of these antifungal agents against different strains of fungi (10-12).

2. Objectives

As far as we know, only limited data are available on the in vitro activities of these novel imidazoles, and triazoles against Aspergillus and Candida strains isolated from otomycosis (13). Therefore, the current research was performed to compare the in vitro activities of two novel antifungal agents, namely luliconazole (LUL) and efinaconazole (EFN), with those of amphotericin B (AMB), voriconazole (VRC), fluconazole (FLU), itraconazole (ITC), ketoconazole (KTO), clotrimazole (CLO), nystatin (NYS), terbinafine (TRB), and caspofungin (CAS) against Aspergillus and Candida strains isolated from otomycosis.

3. Methods

3.1. Fungal Isolates

A total of 91 clinical Aspergillus strains (Aspergillus tubingensis [n = 57], A. niger [n = 28], A. flavus [n = 5], and A. awamori [n = 1]) and 17 Candida strains (C. parapsilosis [n = 7], C. glabrata [n = 6], C. albicans [n = 3], and C. orthopsilosis [n = 1]) obtained from patients with otomycosis, in Jahrom, Iran. The genomic DNA of these fungal strains, previously extracted by the glass-bead phenol-chloroform (6). Candida isolates were identified at the species level based on molecular methods to obtain restriction digestion of the internal transcribed spacer rDNA region using the PCR‐restriction fragment length polymorphism (PCR-RFLP) method with the MspI restriction enzyme (14). The identification of the Aspergillus isolates was also accomplished by the amplification and sequencing of a fragment of the β-tubulin gene using beta-2A and beta-2B primers, respectively (15). Randomly selected isolates were reconfirmed by DNA sequencing of the ITS rDNA and β-tubulin regions. The obtained nucleotide sequences were deposited in GenBank under the accession numbers: MT348163- MT348208 and MT303056-MT303061.

3.2. In Vitro Antifungal Susceptibility Test

In vitro antifungal susceptibility of the yeast strains and mold isolates were tested based on the Clinical and Laboratory Standards Institute (CLSI) M27-A3/M60 and M38-A3, respectively (16-19). After the dilution of the antifungal drugs in the standard RPMI-1640 medium (Sigma, St. Louis, MO, USA.) with L-glutamine and without bicarbonate, they were buffered by 0.165 M-morpholinepropanesulfonic acid (MOPS) buffer (Sigma, St. Louis, MO, USA) and using NaOH, the acidity was adjusted to pH 7.0. Drug serial dilutions were then dispensed into 96-well microdilution trays at a concentration range of 0.016 - 16 µg/mL for ITC (Janssen Research Foundation, Beerse, Belgium), VRC (Pfizer, Central Research, Sandwich, United Kingdom), CLO (Sigma, St. Louis, MO, USA), KTO (Sigma, St. Louis, MO, USA), TRB (Sigma, St. Louis, MO, USA), CAS (Sigma, St. Louis, MO, USA), and AMB (Bristol-Myers-Squib, Woerden, The Netherlands). This concentration range was determined as 0.063 - 64 µg/mL for FLU (Pfizer) and NYS (Sigma, St. Louis, MO, USA) and 0.001 - 1 μg/mL for LUL (Sigma, St. Louis, MO, USA, and EFN (Sigma, St. Louis, MO, USA).

The spectrophotometric adjustment of homogeneous freshly yeast or conidial suspensions that cultured on Sabouraud dextrose agar containing chloramphenicol (50 mg/L) (SDA, Difco Laboratories, Detroit, MI, USA) was accomplished at a wavelength of 530 nm to the optical densities (ODs) of 75 - 77% and 80 - 82% for yeasts and molds, respectively. The final inocula suspension was adjusted to 0.5 - 2.5 × 103 and 0.4 - 5 × 104 conidia/mL for yeasts and molds, respectively, in RPMI-1640 with L-glutamine and without sodium bicarbonate (Sigma-Aldrich, St. Louis, MO, USA) and buffered at a pH 7.0 with 0.165 MOPS (Sigma-Aldrich, St. Louis, MO, USA).

Based on CLSI guidelines (CLSI M27-A3 and M27-S4 documents), Candida species were grown at 35°C, and microdilution plates were incubated at 35°C for 24h (if no growth was observed or growth was inadequate, incubation was extended to 48 h) and read visually (16). For Aspergillus species, plates were incubated at 35°C for 24 - 72h (18). After the incubation of the microdilution plates, they were visually examined to determine the minimum inhibitory concentration (MIC) values. Candida krusei (ATCC 6258), C. parapsilosis (ATCC 22019), and Paecilomyces variotii (ATCC 22319) were utilized as quality controls for each new series of MIC plates.

The determination of the MIC values of the yeasts and molds was performed based on the guidelines of the CLSI M27-A3/M60 and M38-A3, respectively (16-18). The geometric mean (GM) MICs, MIC50, MIC90, and MIC ranges were estimated for all antifungals. Susceptibility and resistance to antifungal drugs for Candida species isolates was evaluated based on CLSI-S4 and MIC value of various Aspergillus species and compared with epidemiological cutoff values (ECV) for in vitro susceptibility testing using the CLSI-M59 method (19). All tests were carried out in duplicate.

3.3. Statistical Analysis

The student’s t-test was utilized to determine the differences in the mean values using SPSS software (version 16.0) at a significance level of ≤ 0.05.

4. Results

Tables 1 and 2 present the GM MIC, MIC range, MIC50, and when appropriate MIC90 of the studied antifungals. The LUL and EFN had the GM MICs of 0.098 and 0.109 μg/mL against all Aspergillus strains, respectively. These values were obtained to be 0.377, 0.777, 3.568, 3.695, 4.922, 8.311, 8.503, 0.146, and 13.739 μg/mL for VRC, CLO, ITC, FLU, AMB, KTO, CAS, TRB, and NYS, respectively. The comparison of the susceptibilities of the strains revealed a high MIC value for A. niger in all drugs, except for LUL, EFN, and TRB, which had low MICs. With regard to the Candida isolates, the GM MICs LUL, EFN, CAS, CLO, VRC, AMB, ITC, KTO, FLU, NYS, and TRB were calculated to be 0.133, 0.144, 194, 0.219, 0.475, 0.537, 0.655, 1.277, 4.905, 9.372, and 13.592 μg/mL, respectively (Table 2). A total of 7 (41.1%) and 4 (23.5%) Candida isolates were found to be susceptible-dose-dependent to FLU and VRC, respectively. Additionally, 6 (35.29%), 2 (11.7%), and 1 (5.88%) Candida isolates were resistant to FLU, CAS, and VRC, respectively (Table 2).

Table 1.In Vitro Antifungal Susceptibilities of 91 Aspergillus Strains Isolated from Otomycosis Against the Eleven Antifungal Agents
Species (No.)RangeMIC Parameters (µg/mL)Ra
G-meanMIC50MIC90
All Aspergillus Strains (n = 91)-
AMB0.06 - > 164.9221632
NYS0.25 - 3213.7391632
FLU0.12 - 323.695416
ITC0.25 - > 163.5684> 16
VRC0.06 - > 160.3770.252
KTO0.25 - > 168.3118> 16
CLO0.06 - 80.77712
EFN0.031 - 0.50.1090.060.25
LUL0.031 - 0.50.0980.060.25
CAS0.25 - > 168.503> 16> 16
TRB0.031 - 160.1460.121
A. tubingensis (n = 57)-
AMB0.06 - > 163.7358> 16
NYS0.25 - 329.718832
FLU0.12 - 82.47748
ITC0.25 - > 163.3742> 16
VRC0.06 - 20.2760.251
KTO0.25 - > 167.171816
CLO0.06 - 20.60112
EFN0.06 - 0.50.1270.120.25
LUL0.031 - 0.50.1200.120.5
CAS0.25 - > 164.85916> 16
TRB0.06 - 80.1790.122
A. niger (n = 28)
AMB0.12 - > 1611.85316> 1627
NYS8 - 3223.7763232-
FLU4 - 3210.247816-
ITC1 - > 165.3848> 1618
VRC0.25 - > 160.8200.524
KTO0.5 - > 1611.88816> 16-
CLO0.12 - 81.80624-
EFN0.06 - 0.50.0990.060.25-
LUL0.06 - 0.250.0790.060.25-
CAS8 - > 1626.25116> 1628
TRB0.031 - 160.1280.060.25-
A. flavus (n = 5)
AMB0.25 - 160.758NDND0
NYS16 - 3227.858NDND-
FLU0.25 - 81.149NDND-
ITC0.25 - > 160.871NDND1
VRC0.06 - 0.50.186NDND0
KTO2 - > 166.063NDND-
CLO0.06 - 20.214NDND-
EFN0.06 - 0.0310.035NDND-
LUL0.0310.031NDND-
CAS0.25 - > 166.964NDND4
TRB0.031 - 0.060.040NDND-
A. awamori (n = 1)-
AMB8NDNDND
NYS32NDNDND
FLU4NDNDND
ITC1NDNDND
VRC0.25NDNDND
KTO8NDNDND
CLO0.06NDNDND
EFN0.06NDNDND
LUL0.06NDNDND
CAS> 16NDNDND
TRB0.031NDNDND

In Vitro Antifungal Susceptibilities of 91 Aspergillus Strains Isolated from Otomycosis Against the Eleven Antifungal Agents

Table 2.In Vitro Antifungal Susceptibilities of 17 Candida Strains Isolated from Otomycosis Against the Eleven Antifungal Agents
Species (No.)RangeMIC Parameters (µg/mL)
G-meanMIC50MIC90SSDDR
All Candida strains (n = 17)
AMB0.06 - 80.5370.54---
NYS0.06 - 329.3721632---
FLU0.25 - 644.905432476
ITC0.12 - 160.65512---
VRC0.031 - > 160.4750.254641
KTO0.5 - 81.27714---
CLO0.031 - 40.2190.250.5---
EFN0.06 - 10.1440.060.5---
LUL0.06 - 0.50.1330.060.5---
CAS0.031 - 40.1940.12215-2
TRB0.25 - > 1613.592>16>16---
C. parapsilosis (n = 7)
AMB0.06 - 80.403NDND---
NYS0.06 - 324.819NDND---
FLU0.25 - 642.972NDND4-3
ITC0.12 - 160.244NDND---
VRC0.031 - 320.075NDND52-
KTO0.5 - 82.208NDND---
CLO0.031 - 40.136NDND---
EFN0.06 - 10.247NDND---
LUL0.06 - 0.50.203NDND---
CAS0.031 - 40.606NDND7--
TRB0.25 - > 166.563NDND---
C. glabrata (n = 6)
AMB0.5 - 80.794NDND---
NYS0.06 - 168.979NDND---
FLU4 - 644.489NDND-6-
ITC0.122NDND---
VRC0.06 - 43.564NDND---
KTO0.5 - 10.561NDND---
CLO0.031 - 40.397NDND---
EFN0.06 - 0.50.085NDND---
LUL0.06 - 0.250.076NDND---
CAS0.031 - 20.069NDND5-1
TRB> 1632NDND---
C. albicans (n = 3)
AMB0.06 - 81NDND---
NYS0.06 - 3232NDND---
FLU0.25 - 6410.079NDND-12
ITC0.12 - 161.243NDND---
VRC0.031 - 320.783NDND111
KTO0.5 - 81.259NDND---
CLO0.031 - 40.249NDND---
EFN0.06 - 10.097NDND---
LUL0.06 - 0.50.122NDND---
CAS0.031 - 40.124NDND2-1
TRB0.25 - > 1612.699NDND---
C. orthopsilosis (n = 1)
AMB0.060.06NDND---
NYS3232NDND---
FLU3232NDND--1
ITC0.120.12NDND---
VRC0.250.25NDND-1-
KTO44NDND---
CLO0.120.12NDND---
EFN0.250.25NDND---
LUL0.250.25NDND---
CAS0.120.12NDND1--
TRB1616NDND---

In Vitro Antifungal Susceptibilities of 17 Candida Strains Isolated from Otomycosis Against the Eleven Antifungal Agents

5. Discussion

The present research assessed the in vitro susceptibility testing of 108 molecularly well-characterized Aspergillus, and Candida isolates recovered from otomycosis patients to LUL, a novel imidazole, and EFN, a novel triazole, and comparing them with other antifungal drugs. The LUL and EFN are new imidazole and triazole agents, which their efficacy in the management of dermatophytosis and onychomycosis has been recently confirmed. The literature is indicative of the potent activities of these antifungals against dermatophytes, C. albicans, dematiaceous fungi, Malassezia, and azole-resistant and azole-susceptible A. fumigatus strains (7, 12, 20-22). However, to the best of our knowledge, there is no report regarding the resistance of these species to these drugs. As the results of the current research indicated, LUL (0.098 μg/mL) and EFN (0.109 μg/mL) had the lowest GM MICs against Aspergillus strains. The MIC ranges of LUL against A. niger and A. tubingensis isolates were 0.06 - 0.25 and 0.031 - 0.5 μg/mL, respectively. These values for EFN were 0.06 - 0.5 and 0.06 - 0.5 μg/mL, respectively (Table 1).

In a study performed by Hivary et al., the MICs of LUL against A. niger and A. tubingensis, as the predominant agents of otomycosis, were in the ranges of 0.00024 - 0.125 μg/mL and 0.00024 - 0.125 μg/mL, respectively (20). In addition, the MIC value presented by Tupaki-Sreepurna et al. demonstrated that EFN was more potent than other azoles against different non-dermatophytic fungi (21). The EFN MIC values was estimated at < 0.25 μg/mL for Aspergillus (12, 21, 23). Our results revealed low MIC values for EFN and LUL against Aspergillus, which is in line with other reports (12, 21, 23). In the current research, TRB had the GM MICs of 0.040, 0.128, and 0.179 μg/mL against A. flavus, A. niger, and A. tubingensis, respectively. The TRB (Lamisil) is a safe allylamine antifungal used both topically and orally for the management of infections, such as pityriasis versicolor, cutaneous candidiasis, and dermatophytosis (24). Based on a study by Mosquera et al., this drug had potent activities against Aspergillus species (25). In the present study, TRB had a lower GM MIC against A. flavus and A. niger compared to the values reported by Moore et al. (26). The VRC and CLO are other antifungal agents utilized for the treatment of Aspergillus-induced infections.

The susceptibility of Aspergillus species to these antifungals was also investigated in the present study. The comparison of VRC and CLO with ITC, FLU, KTO, and AMB revealed a lower GM MIC for VRC and CLO against Aspergillus species. The results of previous studies are indicative of the resistance of this species to VRC (27). Sutton et al. suggested VRC as an agent that can be used clinically for the treatment of refractory invasive aspergillosis and should be prioritized over the conventional AMB treatment (28). There are reports regarding the growing resistance of ITC to A. fumigatus (29). On the contrary, black aspergilli (MIC > 16 µg/mL) showed resistance to ITC in more than 50% of cases, without any clear mechanisms explaining this resistance (30). Our results showed that the common black aspergilli species (e.g., A. niger and A. tubingensis) showed higher ITC resistance.

Ototopical FLU is used for the management of otomycosis, especially against Aspergillus (31). The GM MICs of FLU against A. niger, A. tubingensis, and A. flavus were obtained to be 10.2, 2.47, and 1.14 μg/mL, respectively (Table 1). Our results revealed FLU resistance in 6 isolates (35.29%), which is in line with other reports indicating in vitro FLU resistance (32). Evidence is suggestive of the higher susceptibility of A. niger and A. tubingensis accounting for mild to systemic aspergillosis to AMB under in vitro conditions. However, these cases undergo frequent relapses and failures in spite of using antifungal therapy; accordingly, their therapeutic values are challenging (33).

In the present study, AMB MICs ranged between 0.06 and > 16 μg/mL for Aspergillus species, which is similar to the results reported by Oakley et al., but in contrast to those obtained by Kaya et al. (34, 35). Among the tested antifungal agents, KTO, CAS, and NYS had higher GM MICs against Aspergillus species compared to other drugs. Our data showed that A. flavus was more susceptible to LUL and EFN than A. niger and A. tubingensis. Nevertheless, aspergilli recovered from the external auditory canal demonstrated higher susceptibility to LUL, EFN, and TRB. Therefore, these topical agents can be considered as effective treatments for aspergillosis. In this study, the susceptibility of Candida isolates recovered from otomycosis was tested for the eleven drugs. The LUL (GM = 0.133μg/mL) and EFN (GM = 0.144 μg/mL) had the lowest MICs for Candida isolates. The LUL and EFN have an unclear sensitivity, dose dependence, or resistance range because of the lack of an acceptable breakpoint for Candida species.

The GM MICs of LUL and EFN for C. glabrata were obtained to be 0.076 and 0.085 μg/mL, respectively. These values were 0.122 and 0.097 μg/mL for C. albicans and 0.203 and 0.247 μg/mL for C. parapsilosis, respectively. Our results revealed that C. glabrata had lower MICs for LUL and EFN than C. parapsilosis and C. albicans strains. Niwano et al. (36) and Koga et al. (37) were the first researchers reporting a very low MIC for LUL and EFN (MIC range: 0.031 - 0.13 and 0.031 - 0.25 µg/mL, respectively) against C. albicans. Niwano et al., comparing oral LUL and FLU in a murine model of systemic candidiasis, reported the lower efficacy of LUL compared to that of FLU (36, 38). In the current study, CAS had a GM MIC of 0.194 μg/mL against Candida species. The previous studies have also confirmed the potent in vitro activity of this drug against Candida strains (39). Based on our results, NYS and TRB had the highest MIC values against Candida isolates, which is consistent with the results reported in the literature (40). However, Candida isolates also showed resistance to FLU, VRC, and CAS.

5.1. Conclusions

Our findings revealed that LUL and EFN had the highest in vitro activities against Aspergillus (GM MICs of 0.098 and 0.109 μg/mL, respectively) and Candida (GM MICs of 0.133 and 0.144 μg/mL, respectively) strains. In most of the cases, the novel topical triazoles and imidazoles (EFN and LUL) appeared to show good antifungal activities. The findings of the present research could be useful in promoting the significance of antifungal susceptibility testing for appropriate treatment.

Acknowledgments

Footnotes

References

  • 1.
    Agarwal P, Devi LS. Otomycosis in a rural community attending a Tertiary Care Hospital: Assessment of risk factors and identification of fungal and bacterial agents. J Clin Diagn Res. 2017;11(6):DC14-8. [PubMed ID: 28764159]. [PubMed Central ID: PMC5535352]. https://doi.org/10.7860/JCDR/2017/25865.10068.
  • 2.
    Jia X, Liang Q, Chi F, Cao W. Otomycosis in Shanghai: Aetiology, clinical features and therapy. Mycoses. 2012;55(5):404-9. [PubMed ID: 21999222]. https://doi.org/10.1111/j.1439-0507.2011.02132.x.
  • 3.
    Van Der Linden JW, Warris A, Verweij PE. Aspergillus species intrinsically resistant to antifungal agents. Med Mycol. 2011;49 Suppl 1:S82-9. [PubMed ID: 20662634]. https://doi.org/10.3109/13693786.2010.499916.
  • 4.
    Chakrabarti A, Singh S. Multidrug-resistant Candida auris: An epidemiological review. Expert Rev Anti Infect Ther. 2020;18(6):551-62. [PubMed ID: 32237924]. https://doi.org/10.1080/14787210.2020.1750368.
  • 5.
    Jimenez-Garcia L, Celis-Aguilar E, Diaz-Pavon G, Munoz Estrada V, Castro-Urquizo A, Hernandez-Castillo N, et al. Efficacy of topical clotrimazole vs. topical tolnaftate in the treatment of otomycosis. A randomized controlled clinical trial. Braz J Otorhinolaryngol. 2020;86(3):300-7. [PubMed ID: 30826311]. https://doi.org/10.1016/j.bjorl.2018.12.007.
  • 6.
    Kiakojuri K, Mahdavi Omran S, Roodgari S, Taghizadeh Armaki M, Hedayati MT, Shokohi T, et al. Molecular identification and antifungal susceptibility of yeasts and molds isolated from patients with otomycosis. Mycopathologia. 2021;186(2):245-57. [PubMed ID: 33718990]. https://doi.org/10.1007/s11046-021-00537-1.
  • 7.
    Taheri Rizi Z, Abastabar M, Fakhim H, Ilkit M, Ahangarkani F, Javidnia J, et al. Antifungal activity of a novel triazole, efinaconazole and nine comparators against 354 molecularly identified Aspergillus isolates. Mycopathologia. 2020;185(2):357-65. [PubMed ID: 32112265]. https://doi.org/10.1007/s11046-020-00434-z.
  • 8.
    Anwar K, Gohar MS. Otomycosis; clinical features, predisposing factors and treatment implications. Pak J Med Sci. 2014;30(3):564-7. [PubMed ID: 24948980]. [PubMed Central ID: PMC4048507]. https://doi.org/10.12669/pjms.303.4106.
  • 9.
    Rezaei-Matehkolaei A, Khodavaisy S, Alshahni MM, Tamura T, Satoh K, Abastabar M, et al. In vitro antifungal activity of novel triazole efinaconazole and five comparators against dermatophyte isolates. Antimicrob Agents Chemother. 2018;62(5). [PubMed ID: 29530856]. [PubMed Central ID: PMC5923135]. https://doi.org/10.1128/AAC.02423-17.
  • 10.
    Shokoohi GR, Badali H, Mirhendi H, Ansari S, Rezaei-Matehkolaei A, Ahmadi B, et al. In vitro activities of luliconazole, Lanoconazole, and efinaconazole compared with those of five antifungal drugs against melanized fungi and relatives. Antimicrob Agents Chemother. 2017;61(11). [PubMed ID: 28848012]. [PubMed Central ID: PMC5655049]. https://doi.org/10.1128/AAC.00635-17.
  • 11.
    Moslem M, Mahmoudabadi AZ. The high efficacy of luliconazole against environmental and otomycosis Aspergillus flavus strains. Iran J Microbiol. 2020;12(2):170-6. [PubMed ID: 32494352]. [PubMed Central ID: PMC7244823].
  • 12.
    Jo Siu WJ, Tatsumi Y, Senda H, Pillai R, Nakamura T, Sone D, et al. 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(4):1610-6. [PubMed ID: 23318803]. [PubMed Central ID: PMC3623347]. https://doi.org/10.1128/AAC.02056-12.
  • 13.
    Gharaghani M, Halvaeezadeh M, Ali Jalaee G, Taghipour S, Kiasat N, Zarei Mahmoudabadi A. Antifungal susceptibility profiles of otomycosis etiological agents in Ahvaz, Iran. Curr Med Mycol. 2020;6(2):18-22. [PubMed ID: 33628977]. [PubMed Central ID: PMC7888522]. https://doi.org/10.18502/CMM.6.2.2696.
  • 14.
    Shokoohi G, Rasekh-Jahromi A, Solhjoo K, Hasannezhad A, Nouripour-Sisakht S, Ahmadi B, et al. Molecular characterization and antifungal susceptibility of Candida species isolated from vulvovaginitis in Jahrom city, South of Iran. Jundishapur J Microbiol. 2020;13(10). https://doi.org/10.5812/jjm.106825.
  • 15.
    Shokohi G, Mirhendi H, Kordbacheh P, Nikaeen M, Rezaei-Matehkolaei A, Abastabar M. Morphological and genotypic identification of some environmental isolates of Aspergillus in Iran based on beta-tubulin gene sequencing. J Isfahan Med Sch. 2012;29(166).
  • 16.
    Clinical and Laboratory Standards Institute. Reference method for broth dilution antifungal susceptibility testing of yeasts; approved standard, CLSI document M27-A3 and Supplement S. 3. Wayne, PA, USA: Clinical and Laboratory Standards Institute; 2008.
  • 17.
    Clinical and Laboratory Standards Institute. Performance standards for antifungal susceptibility testing of yeasts, CLSI document M60. 1st ed. Wayne, PA, USA: Clinical and Laboratory Standards Institute; 2017.
  • 18.
    Clinical and Laboratory Standards Institute. Reference method for broth dilution antifungal susceptibility testing of filamentous fungi; approved standard. CLSI document M38- A3. Wayne, PA, USA: Clinical and Laboratory Standards Institute; 2017.
  • 19.
    Clinical and Laboratory Standards Institute. Epidemiological cutoff values for antifungal susceptibility testing, M59. 3rd ed. Wayne, PA, USA: Clinical and Laboratory Standards Institute; 2018.
  • 20.
    Hivary S, Fatahinia M, Halvaeezadeh M, Mahmoudabadi AZ. The potency of luliconazole against clinical and environmental Aspergillus nigri complex. Iran J Microbiol. 2019;11(6):510-9. [PubMed ID: 32148683]. [PubMed Central ID: PMC7048962].
  • 21.
    Tupaki-Sreepurna A, Jishnu BT, Thanneru V, Sharma S, Gopi A, Sundaram M, et al. An assessment of in vitro antifungal activities of efinaconazole and itraconazole against common non-dermatophyte fungi causing onychomycosis. J Fungi (Basel). 2017;3(2). [PubMed ID: 29371538]. [PubMed Central ID: PMC5715924]. https://doi.org/10.3390/jof3020020.
  • 22.
    Shokoohi G, Ansari S, Abolghazi A, Gramishoar M, Nouripour-Sisakht S, Mirhendi H, et al. The first case of fingernail onychomycosis due to Neoscytalidium novaehollandiae, molecular identification and antifungal susceptibility. J Mycol Med. 2020;30(1). 100920. [PubMed ID: 31892498]. https://doi.org/10.1016/j.mycmed.2019.100920.
  • 23.
    Shokoohi G, Javidnia J, Mirhendi H, Rasekh-Jahromi A, Rezaei-Matehkolaei A, Ansari S, et al. Molecular identification and antifungal susceptibility profiles of Candida dubliniensis and Candida africana isolated from vulvovaginal candidiasis: A single-centre experience in Iran. Mycoses. 2021;64(7):771-9. [PubMed ID: 33811780]. [PubMed Central ID: PMC8251901]. https://doi.org/10.1111/myc.13280.
  • 24.
    Zarei Mahmoudabadi A, Seifi Z, Gharaghani M. Lamisil, a potent alternative antifungal drug for otomycosis. Curr Med Mycol. 2015;1(1):18-21. [PubMed ID: 28680976]. [PubMed Central ID: PMC5490317]. https://doi.org/10.18869/acadpub.cmm.1.1.18.
  • 25.
    Mosquera J, Sharp A, Moore CB, Warn PA, Denning DW. In vitro interaction of terbinafine with itraconazole, fluconazole, amphotericin B and 5-flucytosine against Aspergillus spp. J Antimicrob Chemother. 2002;50(2):189-94. [PubMed ID: 12161398]. https://doi.org/10.1093/jac/dkf111.
  • 26.
    Moore CB, Walls CM, Denning DW. In vitro activities of terbinafine against Aspergillus species in comparison with those of itraconazole and amphotericin B. Antimicrob Agents Chemother. 2001;45(6):1882-5. [PubMed ID: 11353643]. [PubMed Central ID: PMC90563]. https://doi.org/10.1128/AAC.45.6.1882-1885.2001.
  • 27.
    Manavathu EK, Cutright JL, Loebenberg D, Chandrasekar PH. A comparative study of the in vitro susceptibilities of clinical and laboratory-selected resistant isolates of Aspergillus spp. to amphotericin B, itraconazole, voriconazole and posaconazole (SCH 56592). J Antimicrob Chemother. 2000;46(2):229-34. [PubMed ID: 10933645]. https://doi.org/10.1093/jac/46.2.229.
  • 28.
    Sutton DA, Sanche SE, Revankar SG, Fothergill AW, Rinaldi MG. In vitro amphotericin B resistance in clinical isolates of Aspergillus terreus, with a head-to-head comparison to voriconazole. J Clin Microbiol. 1999;37(7):2343-5. [PubMed ID: 10364610]. [PubMed Central ID: PMC85155]. https://doi.org/10.1128/JCM.37.7.2343-2345.1999.
  • 29.
    Chowdhary A, Kathuria S, Xu J, Meis JF. Emergence of azole-resistant aspergillus fumigatus strains due to agricultural azole use creates an increasing threat to human health. PLoS Pathog. 2013;9(10). e1003633. [PubMed ID: 24204249]. [PubMed Central ID: PMC3812019]. https://doi.org/10.1371/journal.ppat.1003633.
  • 30.
    Howard SJ, Harrison E, Bowyer P, Varga J, Denning DW. Cryptic species and azole resistance in the Aspergillus niger complex. Antimicrob Agents Chemother. 2011;55(10):4802-9. [PubMed ID: 21768508]. [PubMed Central ID: PMC3186969]. https://doi.org/10.1128/AAC.00304-11.
  • 31.
    Yadav SPS, Gulia JS, Jagat S, Goel AK, Aggarwal N. Role of ototopical fluconozole and clotrimazole in management of otomycosis. Indian J Otol. 2007;13:12-5.
  • 32.
    Yenisehirli G, Bulut Y, Guven M, Gunday E. In vitro activities of fluconazole, itraconazole and voriconazole against otomycotic fungal pathogens. J Laryngol Otol. 2009;123(9):978-81. [PubMed ID: 19454132]. https://doi.org/10.1017/S0022215109005489.
  • 33.
    Galiger C, Brock M, Jouvion G, Savers A, Parlato M, Ibrahim-Granet O. Assessment of efficacy of antifungals against Aspergillus fumigatus: value of real-time bioluminescence imaging. Antimicrob Agents Chemother. 2013;57(7):3046-59. [PubMed ID: 23587947]. [PubMed Central ID: PMC3697358]. https://doi.org/10.1128/AAC.01660-12.
  • 34.
    Oakley KL, Moore CB, Denning DW. In vitro activity of the echinocandin antifungal agent LY303,366 in comparison with itraconazole and amphotericin B against Aspergillus spp. Antimicrob Agents Chemother. 1998;42(10):2726-30. [PubMed ID: 9756785]. [PubMed Central ID: PMC105927]. https://doi.org/10.1128/AAC.42.10.2726.
  • 35.
    Kaya AD, Kiraz N. In vitro susceptibilities of Aspergillus spp. causing otomycosis to amphotericin B, voriconazole and itraconazole. Mycoses. 2007;50(6):447-50. [PubMed ID: 17944704]. https://doi.org/10.1111/j.1439-0507.2007.01409.x.
  • 36.
    Niwano Y, Seo A, Kanai K, Hamaguchi H, Uchida K, Yamaguchi H. Therapeutic efficacy of lanoconazole, a new imidazole antimycotic agent, for experimental cutaneous candidiasis in guinea pigs. Antimicrob Agents Chemother. 1994;38(9):2204-6. [PubMed ID: 7811048]. [PubMed Central ID: PMC284713]. https://doi.org/10.1128/AAC.38.9.2204.
  • 37.
    Koga H, Nanjoh Y, Makimura K, Tsuboi R. In vitro antifungal activities of luliconazole, a new topical imidazole. Med Mycol. 2009;47(6):640-7. [PubMed ID: 19115136]. https://doi.org/10.1080/13693780802541518.
  • 38.
    Taghipour S, Kiasat N, Shafiei S, Halvaeezadeh M, Rezaei-Matehkolaei A, Zarei Mahmoudabadi A. Luliconazole, a new antifungal against Candida species isolated from different sources. J Mycol Med. 2018;28(2):374-8. [PubMed ID: 29198426]. https://doi.org/10.1016/j.mycmed.2017.11.004.
  • 39.
    Katiraee F, Khosravi AR, Khalaj V, Hajiabdolbaghi M, Khaksar AA, Rasoulinejad M. In vitro antifungal susceptibility of oral candida species from Iranian HIV infected patients. Tehran Univ Med J. 2012;70(2):96-103.
  • 40.
    Martin MV, Dinsdale RC. Nystatin-resistance of candida albicans isolates from two cases of oral candidiasis. Br J Oral Surg. 1982;20(4):294-8. [PubMed ID: 6760890]. https://doi.org/10.1016/s0007-117x(82)80026-7.
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