Triazole Resistance in Aspergillus spp.: A Worldwide Problem?

Since the first description of an azole-resistant A. fumigatus strain in 1997, there has been an increasing number of papers describing the emergence of azole resistance. Firstly reported in the USA and soon after in Europe, it has now been described worldwide, challenging the management of human aspergillosis. The main mechanism of resistance is the modification of the azole target enzyme: 14-α sterol demethylase, encoded by the cyp51A gene; although recently, other resistance mechanisms have also been implicated. In addition, a shift in the epidemiology has been noted with other Aspergillus species (mostly azole resistant) increasingly being reported as causative agents of human disease. This paper reviews the current situation of Aspergillus azole resistance and its implications in the clinical setting.


Introduction
Invasive aspergillosis (IA) is a life-threatening infection caused by ubiquitous saprophytic Aspergillus species, which are the most common cause of invasive mold infections worldwide, especially in immunocompromised patients [1]. Aspergillus fumigatus is the leading agent of IA [2] but also of all other forms of aspergillosis, including allergic bronchopulmonary aspergillosis (ABPA), chronic pulmonary aspergillosis (CPA) and aspergilloma [3]. This fungus produces billions of airborne conidia due to an abundant asexual reproduction cycle and has the ability of surviving in very different environments, such as those with temperatures up to 60˝C [4].
Despite the mortality and morbidity of IA remaining high due mainly to difficulties in early diagnosis, the survival rates of these patients have improved due to advances in diagnostics and treatment. The triazoles, itraconazole (ITC), voriconazole (VRC) and posaconazole (POS), are the mainstay of treatment for aspergillosis. Isavuconazole is a new extended-spectrum triazole, and its activity against Aspergillus has been proven [5]. Triazoles are the only anti-Aspergillus agents that are orally available, making them essential for long-term therapy [6]. Although VRC is recommended as first-line therapy for IA [7,8], ITC is still commonly used for chronic and allergic non-invasive forms of aspergillosis [8,9], and POS was shown to reduce the number of invasive fungal infections in neutropenic patients [10]. Additionally, there are some alternative therapies to triazoles that can function as rescue treatments, such as echinocandins or amphotericin B [8].
target (Cyp51A, a 14α sterol demethylase), although other mechanisms within A. fumigatus have been investigated.

Cyp51A Mutations
Up to now, most of the A. fumigatus azole resistant strains have been associated with point mutations or overexpression of cyp51A. The cyp51A encodes a 14α-sterol-demethylase, a key enzyme in the ergosterol biosynthesis pathway [22]. Ergosterol is the main component of fungal cell membranes. Triazoles bind with one of the nitrogen atoms of the triazole ring to the iron atom in the heme group located at the active site of Cyp51A [22]. This way, demethylation of C-14 of lanosterol is blocked, and ergosterol is not synthesized. Lack of ergosterol alters membrane fluidity and leads to fungal cell death [1]. Several single-nucleotide polymorphisms (SNPs), responsible for cyp51A amino acid substitutions, with or without tandem repeats in the promoter region of the gene, have been described. Both mechanisms affect the binding of azoles to the enzyme and lead to the development of resistance.
There are a few point mutations located at hot spot codons, whose link to azole resistance has been corroborated: (i) those associated with glycine 54 (G54), linked to cross-resistance to ITC and POS [23,24]; and (ii) amino acid substitutions at methionine 220 (M220), associated with different patterns of reduced susceptibility for triazoles [25]. Mutations in glycine 138 (G138), causing simultaneous resistance to itraconazole and voriconazole [26], and glycine 448 (G448S), resulting in VRC resistance, with some reduction in ITC and POS susceptibility, have also being reported in several studies [27][28][29]. Other point mutations, such as P216L, F219C, F219I, A284T, Y431C, G432S and G434C, have been occasionally described related to azole resistance, but further research is needed in order to confirm its role in the development of resistance [17,18,[30][31][32][33][34][35][36]. In addition, a group of polymorphisms resulting in amino acid changes (F46Y, M172V, N248T, D255E and E427K) is frequently reported, alone or in combination, related to different patterns of susceptibility (they have been detected in azole susceptible and resistant strains), with consistently higher MICs than the wild type strains, although not always exceeding the breakpoint for resistance. More research is needed in order to determine the implication of each amino acid substitution (if any) in the azole profile shown by these strains ( Table 1). All of these point mutations are generally described in strains isolated from patients that have been undergoing azole treatment.
A second group of cyp51A alterations with different resistance mechanisms has been reported, being normally described as panazole resistant. In A. fumigatus, this type of azole cross-resistance depends on specific mutations in cyp51A in combination with alterations in the promoter region, leading to multiazole-resistant strains [12,37,38]. These mechanisms are generated by combinations of cyp51A modifications: (i) the integration of a 34-bp tandem repeat (TR 34 ) in the promoter region of the gene, leading to an overexpression of cyp51A along with a substitution of leucine 98 to histidine (TR 34 /L98H) [37]; this alteration is the most frequently identified resistance mechanism found in environmental A. fumigatus strains [39]; (ii) a 46-bp tandem repeat insertion in the promoter region and substitutions of tyrosine 121 to phenylalanine and threonine 289 to alanine (TR 46 /Y121F/T289A) [40], which is related to VRC resistance; and (iii) a 53-bp tandem repeat in the promoter region without any cyp51A amino acid substitution [41,42].
One of the first studies on azole cross-resistance in A. fumigatus was performed in 17 clinical A. fumigatus isolates that were ITC resistant. These strains showed cross-resistance between ITC and POS, which have a similar molecule structure, but not with VRC [43,44]. Cross-resistance between azoles was studied by Howard et al. showing that 74% of the ITC resistant isolates studied were cross-resistant to POS and 65% to VRC [17]. The newest triazole isavuconazole has shown higher MICs in strains with reduced susceptibilities to other triazoles and presented a high degree of correlation with VRC susceptibility results [45]. In addition, other azole fungicides are widely used for crop protection (DMIs), which exhibit a related molecule structure to medical triazoles, leading to development of cross-resistance with azole in clinical use [46].

Azole Resistance Mechanisms are cyp51A Independent
Although triazole resistance in A. fumigatus is mainly attributed to cyp51A target mutations, a recent survey of resistant isolates in Manchester showed that >50% of resistant isolates had no mutation in cyp51A or its promoter [98]. There is also a reported case of a Dutch patient with chronic granulomatous disease treated with azole-echinocandin combination therapy, whose resistant isolate revealed a four-to-five-fold increased expression of cyp51A without having any cyp51A alterations [2]. Therefore, other mechanisms of resistance in clinical azole-resistant isolates without cyp51A mutations need to be explored.
Overexpression of cyp51B. In A. fumigatus, Cyp51 proteins are encoded by two different, but related genes sharing 63% sequence identity, cyp51A and cyp51B [21]. As described before, most of the azole-resistant strains have alterations in cyp51A; however, the role of cyp51B in A. fumigatus azole resistance remains unclear. Several cyp51B polymorphisms/mutations have been observed, but have never been linked to resistance. Only one study with a clinical azole-resistant isolate without cyp51A mutation or over-expression showed an over-expression of cyp51B [99]. Further studies are required to clearly define the relationship between this mechanism and azole resistance.
Overexpression of efflux pumps. Fungi have to beat intracellular toxin accumulation in order to successfully colonize human hosts [1]. This is achieved by efflux pumps, of which there are two main categories: ATP-binding cassette (ABC) proteins, primary transporters that take advantage of ATP hydrolysis, and major facilitator superfamily (MFS) pumps, secondary transporters that use the proton-motive force across the plasma membrane [100]. In A. fumigatus, at least 49 ABC family transporters and 278 MFS genes have been described, which is more than four-times the number identified in yeasts like Saccharomyces cerevisiae [101]. However, in A. fumigatus, despite the great number of existing genes encoding transporters, little is known about the connection between ABC or MFS efflux pumps and triazole resistance. To date, only five transporter genes are known to be related to azole resistance: AfuMDR1, AfuMDR2, AfuMDR3, AfuMDR4 and AtrF.
AfuMDR1 and AfuMDR2 ATP-binding cassette transporters were the first described, raising the possibility that these two genes could be directly involved in drug efflux in A. fumigatus [102]. Another ABC transporter, atrF, was cloned from a clinical isolate of A. fumigatus resistant to ITC, and five-fold higher levels of atrF mRNA compared to those in susceptible strains were revealed [103]. AfuMDR3 and AfuMDR4 were identified to be connected with triazole resistance in a study where resistant A. fumigatus mutants showed either constitutive high-level expression of both transporters or induction of expression when exposed to ITC. Two out of 23 mutants seemed to be ITC resistant due to overexpression of these genes, although evidence of a direct relationship between them and an ITC resistant phenotype is lacking. AfuMDR3 has great similarity to MFS, and AfuMDR4 is a member of the ABC proteins family [24]. Additionally, AfuMDR4 has been shown to be induced with VRC in complex A. fumigatus biofilm populations and that this contributes to azole resistance [104]. Furthermore, exposure of a clinical azole-susceptible A. fumigatus isolate to VRC showed upregulation of five transporters of the ABC superfamily (abcA-E) and three of the MFS (mfsA-C) [105]. Lastly, a demonstrated link between transporters and azole resistance was the azole-induced expression of cdr1B. A cdr1B deleted mutant resulted in a four-fold susceptibility reduction in ITC MICs in an A. fumigatus clinical resistant isolate [106]. However, further studies are warranted in order to properly understand the relationship between the overexpression of pump efflux and azole resistance mechanisms in A. fumigatus.
Cholesterol import. The import of exogenous cholesterol under aerobic conditions, as a substitute for ergosterol after azole treatment, has also been described as a mechanism of resistance. The activity of ITC against A. fumigatus is compromised when cholesterol serum in RPMI medium is present [107]. In A. fumigatus, a sterol-regulatory element binding protein (SrbA) that plays a role in the azole resistance by erg11 (cyp51A) regulation has been characterized [108]. The srbA null mutant (∆srbA) was highly susceptible to FLC and VRC, which was explained by a reduction in erg11A transcript in response to both azoles. However, further studies on the genetic regulatory network mediated by SrbA in A. fumigatus and its role in triazole drug interactions need to be carried out [109,110].
Role of Hsp90. Heat shock protein 90 (Hsp90) is a eukaryotic molecular chaperone that helps crucial regulatory proteins in their folding, transport and maturation steps under environmental stress. Its involvement in the resistance of Candida albicans to azole and echinocandin antifungals is well established, but the function of Hsp90 in A. fumigatus remains unclear [111]. Using S. cerevisiae mutants expressing different levels of this chaperone, it was revealed that Hsp90 potentiates the acquisition of azole resistance and plays a key role in its continuance once it has been acquired. In C. albicans and Aspergillus terreus, Hsp90 inhibitors can beat azole and echinocandin resistance in vivo [112]. However, the mechanisms by which Hsp90 controls these functions remain to be fully investigated.
HapE mutation. Another described mechanism is caused by a mutation in HapE, a CCAAT-binding transcription factor complex subunit. Two isogenic isolates with the wild-type cyp51A genotype, one azole susceptible isolated before treatment and the second with a resistant phenotype isolated post-treatment, were whole-genome sequenced in order to detect the resistance conferring mutation. Six out of a sixty-nine of identified point mutations in protein-coding regions were confirmed, and sexual crossing experiments revealed that a P88L substitution in HapE was the only one leading to resistance in progeny. This mutation in HapE can lead to a resistant phenotype by itself, as it was proven by cloning the mutated hapE gene into an azole-susceptible reference strain. This increase in resistance has been suggested to be due to a gain of function mutation if the mutated Hap-complex binds to a CCAAT-box in the promoter region of cyp51A and induces its expression [113].

Prevalence of Azole Resistance in Aspergillus fumigatus throughout the World
To date, Europe is the continent with the highest reported azole resistance in A. fumigatus ( Table 2). Two reports in the late 2000s in the Netherlands and UK raised the alarm about an increase of azole resistance cases. The first one, in 2007, involved a series of Dutch patients suffering IA caused by panazole resistant strains, even those who had not been under azole treatment. One new resistance mechanism was found in these strains, TR 34 /L98H [37,38]. The second study, in 2009, described a wide range of cyp51A mutations found in patients in the U.K., becoming clear that a dramatic increase in azole resistance in A. fumigatus was occurring [17]. Since then, azole resistant cases in clinical samples have been reported in almost every European country, including Austria [70], Belgium [68,76,92,94], Denmark [35,61,66,70], France [19,27,30,48,50,73,91,114], Germany [32,47,51,60,72], Greece [115], Italy [36], The Netherlands [18,20,37,38,40,41,53,65,67,[74][75][76], Poland [69,116], Portugal [117], Romania [118], Spain [12,23,25,29,34,37,49,63,70,93,119], Sweden [120], Turkey [71] and the UK [17,26,31,33,65]. Even though G54 and M220 point mutations have been occasionally reported in Europe since they were described [12,17,18,20,23,25,32,35,48,50,51,60,71], the TR 34 /L98H is by far the most common mutation found, both in environmental and clinical samples. Since its first report in 2007 in Spanish and Dutch isolates [37], TR 34 /L98H has been detected across Europe (Figure 1) [12,32,35,38,41,48,50,51,53,60,67,69,71,75]. In 2009 a new resistance mechanism, TR 46 /Y121F/T289A, was identified in The Netherlands [40]. Since then, it has also been reported in several countries [39,51,60,66,67,75,76,[91][92][93]. Azole resistance in environmental strains in Europe has been commonly detected, with TR 34 /L98H and TR 46 /Y121F/T289A being the most often described mechanisms (Figure 1), and therefore, their emergence has been related with the extensive use of agricultural fungicides. Van der Linden et al. found that out of 140 environmental resistant strains, 14 had the TR 46 /Y121F/T289A mechanism, while 126 had TR 34 /L98H [40]. In Germany, an analysis of 455 environmental isolates revealed 45 that harbored the TR 34 /L98H mutation and six TR 46 /Y121F/T289A [47]. Another analysis reported 16% resistance (to ITC and POS) in environmental A. fumigatus isolates in Italy [36]. Other, less frequent point mutations have been described as related to the azole-resistant phenotype, but further research is needed in order to confirm it.   Reports from Asiatic countries suggest that triazole resistance rates in Asia are lower than in Europe ( Table 2). The first two reports describing azole resistance in A. fumigatus in this area were published in 2005. One was from clinical strains from Taiwan, where two out of 40 isolates showed Reports from Asiatic countries suggest that triazole resistance rates in Asia are lower than in Europe ( Table 2). The first two reports describing azole resistance in A. fumigatus in this area were published in 2005. One was from clinical strains from Taiwan, where two out of 40 isolates showed azole resistance, but mutations in cyp51A were not investigated [125]; and the second one was based on six isogenic isolates obtained from a Chinese patient treated with azoles and suffering from lung aspergilloma. ITC resistance was found in four post-treatment isolates, one of them with a M220I mutation and the rest with G54R [54]. Several other cases have been reported since then. The ARTEMIS global antifungal susceptibility program included more than 100 medical centers worldwide and detected several clinical isolates from China that had a TR 34 /L98H resistance mechanism [123]. This alteration has also been reported in 7.9% of the multi-azole resistant strains isolated from azole-naïve patients in Taiwan [87] and in three out of fourteen resistant clinical isolates in Pakistan [85]. In contrast, TR 34 /L98H has not been described in Japan, with reports showing a low azole resistant strains rate. Kikuchi et al. found three resistant isolates out of 171 A. fumigatus clinical strains isolated between 1987 and 2008 [121]. Some novel mutations have been reported in this country, such as the P216L [97] or F332K [126], and the G448S and TR 46 /Y121F/T289A mechanisms were recently identified in Japan for the first time [64,95]. Azole resistance prevalence in A. fumigatus is also low in India, where three studies revealed the presence of TR 34 /L98H as the resistance mechanism in clinical isolates: 44 out of 630 (6.9%), two out of 103 (1.9%) and 10 out of 685 (1.5%) [3,80,81]. Similar findings have been observed in Middle East countries, like Iran (3.5% of clinical samples) [84] or Kuwait (two out of 16 clinical isolates and one out of 50 environmental isolates) [77]. Azole resistance in environmental strains in Asia is also lower than in Europe (Table 2). In fact, a recent report on the use of azole fungicides on a pumpkin farm revealed no azole resistance in 50 A. fumigatus isolates [127]. Several environmental studies have been performed in India, describing the TR 46 /Y121F/T289A mechanism for the first time in Asia in isolates from agricultural fields [82] and showing that 44 out of 630 A. fumigatus sampled from the soil of paddy fields, tea gardens, cotton trees, flower pots and indoor air of hospitals were resistant and harbored the TR 34 /L98H resistance mechanism [81]. A report from Iran described 12.2% of environmental resistant strains [79], and in Kuwait, 7% of environmental samples were also resistant [78], all of them carrying TR 34 /L98H. This difference in environmental azole resistance rates between Asia and Europe could be due to the lower use of azole fungicides in Asian countries [128].
The first study involving a large number of isolates in the U.S. included 181 A. fumigatus isolates from transplant patients with proven IA from 2001-2006 (multicenter prospective study). Only one of these isolates was triazole resistant [122] and indicates a low azole resistance prevalence in this country. Similarly, 1096 A. fumigatus clinical strains from all over the U.S. collected between 2011 and 2013 were studied; 51 of them were sequenced for cyp51A mutations. One isolate possessed the M220I mutation in cyp51A, and 13 isolates had another mutation, I242V; TR 34 /L98H was not identified [62]. A recent comprehensive study in the U.S. included 220 clinical A. fumigatus isolates obtained from 2001-2014, with the description of two isolates harboring TR 34 /L89H mutations and the other two with TR 46 /Y121F/T289A. This was the first report of both resistance mechanisms in A. fumigatus isolates in the United States. Other point mutations detected in the 26 azole resistant strains were G54R/W/E, M220I/K/V, G138S/C, G448S and F219S [58]. To our knowledge, no environmental sample studies have been reported in this country yet, but there is also lower use of fungicides in the U.S. as compared to Europe [128].
Some investigations have been carried out in South American countries, such as Brazil, where six out of 170 clinical A. fumigatus collected between 2000 and 2012 showed azole resistance, but neither the TR 34 /L98H nor the TR 46 /Y121F/T289A mechanisms were found [129]. An environmental study has been carried out in Colombia, known to be the fourth country in the world for pesticide use, 30% of which are fungicides. Sixty soil samples from flower beds and flower fields were analyzed, describing one TR 34 /L98H, 17 TR 46 /Y121F/T289A and one TR53 isolates [88]. Colombia is the second biggest flower exporter after The Netherlands, which could explain the high environmental azole resistance rate in A. fumigatus [129].
Azole resistance has also been reported in Africa; 15 out of 108 environmental samples taken in Tanzania were azole resistant, 11 of them with the TR 34 /L98H mutation and four with TR 46 /Y121F/T289A [90]. Another study in the same country describes G54E as responsible for 46.4% of resistant environmental A. fumigatus isolates from this country [118]. To our knowledge, no reports from clinical samples have been published in Africa yet.
In Australia, 418 A. fumigatus clinical strains were collected from 2000-2013, revealing nine isolates with reduced susceptibility to ITC, VRC and POS. All of them had between two and five amino acid substitutions, including G54R, F46Y, Y431S, G448S, M172V, N248T, D255E, E427K and TR 34 /L98H, the latter being identified in two isolates. The first TR 34 /L98H A. fumigatus was recovered in 2004, and it is believed to be Australian-acquired in a patient on long-term ITC therapy, while the second isolate was suspected to have been acquired in Europe while the patient was travelling in 2012 [59].

Azole Resistance in Other Aspergillus Species
A shift in epidemiology of fungal infections towards a greater number of species able to cause disease in humans has occurred [130]. The leading cause of IA is A. fumigatus (85%), followed by A. flavus (5%-10%), A. terreus (2%-10%) and A. niger (2%-3%) [100]. However, the use of molecular tools has led to the description of new species within the genus Aspergillus. Some of these species are considered cryptic or sibling because they are difficult to differentiate by classical methods, and they have been frequently misidentified. Their prevalence in the clinical setting has been reported to be between 10% and 15% in two studies. The TRANSNET (Transplant-Associated Infection Surveillance Network) study included 218 Aspergillus isolates from transplant recipients with proven or probable IA from 2001-2006 from the U.S. and documented an 11% cryptic species [131]. The FILPOP study (population-based survey of filamentous fungi) from Spain described 15% cryptic species among 323 isolates analyzed [119]. The importance of these cryptic species in the clinical setting is based on their different susceptibility profile, as they are frequently more resistant to the antifungals available [132]. As these cryptic species are difficult to differentiate, it has been recommended that when using classical identification methods in the clinical setting, an Aspergillus isolate should be classified to the "species complex" level, thereby accounting for gathering all closely-related cryptic species.
The A. niger includes A. tubingensis, the second most frequent species of the complex in clinical isolates, and has been found with similar prevalence as A. niger in some studies [76,119]. Aspergillus awamori and A. foetidus have also been described in clinical samples, although there is debate about their classification as new species or subspecies of A. niger [138]. The susceptibility profile of these species is isolate dependent, and three patterns have been described regarding ITC: low MICs, high MICs and isolates that show a paradoxical effect (which are able to grow in the presence of high antifungal concentrations, but remain fully susceptible at intermediate-to-low concentrations [139]) for this antifungal [140]. Aspergillus niger and A. awamori have been reported to have higher MICs to azoles than A. tubingensis [141].
Aspergillus flavus is the second most common Aspergillus causing IA, and it is reported as the most prevalent in countries with arid climates, such as those in the Middle East, Africa and Southeast Asia, as it is capable of surviving in extreme conditions [142]. Aspergillus alliaceus is part of the A. flavus complex. This species has elevated MICs to AmB and echinocandins, but is variable regarding azoles. The first report describing A. alliaceus stated that ITC was the most active antifungal in vitro against this mold [143], but the first study reporting IA caused by A. alliaceus (together with A. flavus) defined VRC as the best option for treatment, as the isolate tested was resistant to ITC and POS [144]. VRC resistance has also been reported in clinical strains of A. flavus, and T788G and Y319H mutations in the cyp51C gene have been found to be associated with these high MICs to VRC [145,146].
Aspergillus terreus shows high MICs to AmB both in vitro [147,148] and in vivo [149], and reduced susceptibility to azoles has also been described. A study from 2012 reports a cyp51A mutation, M217I, in some clinical A. terreus isogenic isolates causing ITC resistance [150]. The A. terreus complex includes Aspergillus alabamensis, A. floccosus, A. neoafricanus, A. aureoterreus A. hortai, A. pseudoterreus [151] and Aspergillus citrinoterreus. They all have high MICs to AmB, but A. hortai and A. citrinoterreus are more susceptible to azoles than A. terreus [152,153].
The Aspergillus ustus complex is known for its elevated MICs to most drugs. Aspergillus calidoustus was described in 2008 as being able to grow at 37˝C, in contrast to A. ustus, and has been isolated from human infections [154]. Triazoles have been reported to be inactive in vitro against A. calidoustus [122], and the same has been reported of other antifungal classes, so it is considered a multiresistant species. Other cryptic species with high MICs to all antifungals in this complex are A. keveii and A. insuetus, also isolated from clinical samples [155].

Treatment Options
Mortality rates in patients infected with azole-resistant strains (ITC > 2 µg/mL, VRC > 2 µg/mL, POS > 0.5 µg/mL, determined by the CLSI reference method) are higher than those affected with azole-susceptible ones (88% vs. 30%-50%) [53]. As mentioned above, VRC is the primary treatment for IA, but liposomal amphotericin B (L-AMB) is recommended as an alternative therapy [156]. L-AMB was demonstrated to develop no cross-resistance in a murine model of disseminated azole-resistant aspergillosis, being either active against azole-susceptible or azole-resistant strains [157]. However, this drug is not recommended to treat infections caused by A. terreus or other AMB-resistant species. Another approach to consider is an antifungal combination therapy that leads to a synergistic response. A great number of in vitro, in vivo and clinical studies have tested various antifungal combinations and found some of them effective against A. fumigatus [158]. Recent studies have focused on the combination of an azole, normally VRC, with an echinocandin, both for azole-susceptible and azole-resistant A. fumigatus strains. The efficacy of this combined therapy mainly relies on anidulafungin (AND) [159], which is currently not licensed for the treatment of IA. In one clinical study, mortality rates were 27.5% for monotherapy and 19.3% for combined therapy of VRC and AND [160]. In a murine model, AND was successful against 45% of VRC-resistant strains when used as monotherapy [161]. Further studies for combined therapy are warranted in order to find alternative treatment options, given the limitations of current monotherapy. Although azole-resistant strains have been present in clinical samples for more than two decades, it has been suggested that first-line therapy should remain as azoles whilst local azole resistance prevalence remains below 10% [162]. Still, therapeutic options for IA should be revised taking this issue into account.

Conclusions and Recommendations for Clinical Practice
Clinical and environmental triazole resistance in Aspergillus species is a growing public health concern that has become a worldwide problem. Even though the highest rates of triazole resistance have been described in Europe, several cases have been reported in every continent, and new resistance mechanisms are being described. Despite A. fumigatus being the most common Aspergillus species, triazole resistance has also been identified in many cryptic species of Aspergillus. Therefore, the morphological identification of an isolate cannot always drive the treatment strategy. We recommend performing antifungal susceptibility testing on every Aspergillus isolate associated with IA in order to select the best antifungal treatment. In addition, the prevalence of resistant strains should be investigated in every country to understand the prevalence of resistance and to adjust therapeutic options where high rates of resistant isolates are present. Moreover, the development of molecular methods to detect azole resistance in culture-negative infections could be very useful in laboratory practice.
It is important to investigate more extensively the origin of environmental samples that are resistant to triazoles, since measures to reduce the use of agricultural azoles could be an important step in reducing resistance rates in the clinical setting, as stated in the technical report published by the European Centre for Disease prevention and Control (ECDC) [163].