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Article

Novel Compound MMV1804559 from the Global Health Priority Box Exhibits In Vitro and In Vivo Activity against Madurella mycetomatis

by
Jingyi Ma
1,
Kimberly Eadie
1,
Marij Schippers
1,
Ahmed Fahal
2,
Benoît Laleu
3,
Annelies Verbon
1 and
Wendy W. J. van de Sande
1,*
1
Department of Medical Microbiology and Infectious Diseases, Erasmus MC, University Medical Center Rotterdam, Dr. Molewaterplein 40, 3015GD Rotterdam, The Netherlands
2
Mycetoma Research Centre, Khartoum 1115, Sudan
3
MMV Medicines for Malaria Venture, 1215 Geneva, Switzerland
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2024, 25(11), 6227; https://doi.org/10.3390/ijms25116227
Submission received: 18 April 2024 / Revised: 24 May 2024 / Accepted: 2 June 2024 / Published: 5 June 2024
(This article belongs to the Special Issue Antifungal Drug Discovery: Progresses, Challenges, Opportunities)
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Versions Notes

Abstract

:
Objectives: Eumycetoma is a neglected tropical disease (NTD) characterized by subcutaneous lesions and the formation of grains. Attempts to treat eumycetoma involve a combination of antifungal treatment and surgery, although the outcome is frequently disappointing. Therefore, there is a need to identify novel antifungal drugs to treat eumycetoma. In this respect, Medicines for Malaria Venture (MMV) has assembled libraries of compounds for researchers to use in drug discovery research against NTD. Therefore, we screened two MMVOpen compound libraries to identify novel leads for eumycetoma. Methods: A total of 400 compounds from the COVID Box and the Global Health Priority Box were screened in vitro at 100 µM and 25 µM against the most common causative agents of eumycetoma, namely Madurella mycetomatis and Falciformispora senegalensis, and the resulting IC50 and MIC50 values were obtained. Compounds with an IC50 < 8 µM were identified for possible in vivo efficacy studies using an M. mycetomatis grain model in Galleria mellonella larvae. Results: Out of the 400 compounds, 22 were able to inhibit both M. mycetomatis and F. senegalensis growth at 100 µM and 25 µM, with compounds MMV1593278, MMV020335, and MMV1804559 being selected for in vivo testing. Of these three, only the pyrazolopyrimidine derivative MMV1804559 was able to prolong the survival of M. mycetomatis-infected G. mellonella larvae. Furthermore, the grains in MMV1804559-treated larvae were significantly smaller compared to the PBS-treated group. Conclusion: MMV1804559 shows promising in vitro and in vivo activity against M. mycetomatis.

1. Introduction

Mycetoma is a neglected tropical disease (NTD) that is associated with more than 90 different infectious agents, including both bacteria (actinomycetoma) and fungi (eumycetoma) [1]. It is characterized by subcutaneous swellings and the formation of grains [2,3] and is mainly endemic in countries with a dry climate, such as Sudan, Senegal, Mexico, and India. The most common causative agents of actinomycetoma are the bacteria Nocardia brasiliensis, Streptomyces somaliensis, and Actinomadura madurae, which either form white or yellow grains. The most common causative agents of eumycetoma are Madurella mycetomatis, Falciformispora senegalensis, and Trematosphaeria grisea, which all form black grains [2,3].
The treatment of mycetoma depends on its etiology. Actinomycetoma is treated by a combination of antimicrobial agents, resulting in a cure rate of >95% [4], while eumycetoma is treated with a combination of antifungal agents and surgery, resulting in a cure rate of <26% and an amputation rate of 6.1% [5]. Currently, itraconazole is the drug of choice for treating eumycetoma patients, being given in daily dosages ranging from 200 to 400 mg for at least 6 months. After this time, the lesion is surgically removed [6]. Itraconazole is very active in vitro against the most common causative agent of eumycetoma, with MIC values ranging from 0.003 to 1 µg/mL for M. mycetomatis, 0.016 to 0.125 µg/mL for F. senegalensis, and from 0.5 to 2 µg/mL for T. grisea. For M. mycetomatis, an epidemiological cut-off value of 1 µg/mL itraconazole has been reported [7]. However, itraconazole is unable to kill any fungal grains in patients; even after six months of treatment, the grains removed during surgery are still viable when they are cultured on agar [6]. After surgery, patients are treated for at least another 6 months with itraconazole at dosages of 400 mg/day, although the recurrence of fungal grains is still common [5]. Clinically, the main benefit of itraconazole with respect to fungal grains appears to be stimulating the creation of a fibrous capsule around the grains, which makes it easier to excise the complete lesion during surgery [6]. This sub-optimal clinical activity on eumycetoma patients was also previously demonstrated in both Galleria mellonella and murine models of infection, where itraconazole (like most other azoles) did not prolong the survival of infected larvae or prevent fungal grain formation in mice [8,9]. Obviously, novel drugs with novel modes of action need to be identified in order to improve current clinical treatment options for eumycetoma.
Therefore, in 2018, we established an Open Source drug discovery program for mycetoma, named MycetOS [10], and subsequently obtained several collections of compounds from the ‘open innovation program’ of Medicines for Malaria Venture (MMVOpen). The MMVOpen program aims to catalyze drug discovery in the field of neglected tropical diseases [11]. The compounds obtained were tested against M. mycetomatis, the main causative agent of eumycetoma [1,11], and later against other causative agents of eumycetoma. We also screened three MMV open access boxes: the pathogen box, stasis box, and pandemic response box [10,12]. From those boxes, we identified ravuconazole and olorofim as promising candidates, which were already in phase II trials for other fungal infections [12]. Additionally, the fenarimols and benzimidazoles showed high antifungal efficacy during our in vitro susceptibility testing and in our in vivo G. mellonella larvae model, possibly representing potential new classes of antifungal agents that could be chemically optimized to become more effective in penetrating the fungal grain in eumycetoma patients [10,12,13].
Since the start of the MycetOS project in 2018, MMV has launched two new open-access compound libraries, namely the COVID Box and the Global Health Priority Box [14,15,16]. The COVID Box contains 160 marketed compounds in development that possess known or predicted activity against SARS-CoV-2 [15], while the Global Health Priority Box contains 240 compounds that had previously been shown to have activity against (i) drug-resistant malaria (80 compounds), (ii) malaria carriage in various zoonotic vector species (80 compounds), or (iii) various neglected (non-mycetoma) and zoonotic diseases (80 compounds) [16]. Further, as our previous MycetOS research using MMV compound libraries had resulted in potential lead compounds, we hypothesized that screening these new compound libraries could identify additional novel lead compounds. Therefore, in this study, we set out to screen the COVID Box and the Global Health Priority Box from MMV against the two most common causative agents of eumycetoma in order to identify novel classes of compounds that could be further developed as treatments for eumycetoma. We screened these compound libraries in vitro against M. mycetomatis and Falciformispora senegalensis and then tested the most promising compounds in vivo using our M. mycetomatis-infected G. mellonella grain larvae model.

2. Results

2.1. Twenty-Two Compounds Were Able to Inhibit the Growth of Both M. mycetomatis and F. senegalensis in In Vitro Susceptibility Testing

In this study, we determined the in vitro activity of 160 compounds from the MMV COVID Box and 240 compounds from the MMV Global Health Priority Box (Figure 1). In total, this meant that 400 compounds were tested against both M. mycetomatis and F. senegalensis at 100 and 25 µM per compound. Of these, 115 compounds inhibited M. mycetomatis growth and 59 F. senegalensis growth at 100 µM (Figure 2A,B). Of these 115 compounds, 59 also inhibited the growth of M. mycetomatis at 25 µM, and 24 inhibited the growth of F. senegalensis at 25 µM, as seen in Figure 2C. In total, 22 compounds were active against both eumycetoma fungal species studied. Fifteen of these 22 compounds originated from the MMV COVID Box, and 7 originated from the MMV Global Health Priority Box (4 from the ZND plate and 3 from the MB2 plate) (Table 1).

2.2. MMV1593278, MMV020335, and MMV1804559 from the MMV Global Health Priority Box Had an IC50 below 8 µM for M. mycetomatis

In order to rank the in vitro activity of the 22 selected compounds showing ≥80% fungal growth inhibition, IC50 values were obtained against both M. mycetomatis and F. senegalensis. As can be seen in Figure 2D, three of these 22 compounds had an IC50 below 8 µM for M. mycetomatis but not for F. senegalensis. The IC50 of these compounds ranged between 16.95 µM and 20.01 µM for F. senegalensis (Figure 2D, Table 1). These three compounds (MMV1593278, MMV020335, and MMV1804559) originated from the MMV Global Health Priority Box. The chemical structures of these three compounds are shown in Figure 3. For these three compounds, the activities against eight additional M. mycetomatis isolates were determined and are shown in Table 2. For MMV1593278, the MICs ranged from 8 µM to 16 µM, and 8 µM was needed to inhibit the growth of 50% of the M. mycetomatis isolates tested. For MMV020335, the MICs ranged from 16 µM to 32 µM, and 32 µM was needed to inhibit the growth of 50% of the M. mycetomatis isolates tested. For MMV1804559, the MICs ranged from 8 µM to 32 µM, and 8 µM was needed to inhibit the growth of 50% of the M. mycetomatis isolates tested.

2.3. In Vivo Efficacy of MMV020335, MMV1593278 and MMV1804559 from the MMV Global Health Priority Box

Compounds MMV1593278 and MMV020335 were found to be non-toxic to G. mellonella larvae at 20 µM/larva. However, compound MMV1804559 significantly decreased the survival of healthy, uninfected G. mellonella larvae at 20 µM/larva and was therefore considered toxic. Lowering the concentration of MMV1804559 to 10 µM/larvae resolved the toxicity, as no healthy G. mellonella larvae died when treated with this concentration (Figure 4A). Compounds MMV1593278, MMV020335, and MMV1804559 were used in in vivo therapeutic efficacy experiments in M. mycetomatis-infected larvae, as they exhibited in vivo IC50 therapeutic efficacy values below 8 µM against this fungus. Results are shown in Figure 4A, where enhanced survival was noted in M. mycetomatis-infected larvae when treated with 10 µM/larva MMV1804559 (Log-Rank, p = 0.0313). To determine if combining MMV1804559 with 5.7 mg/kg itraconazole (ITZ) could further enhance therapeutic efficacy, a combination treatment was studied. As can be seen in Figure 4B, combining MMV1804559 with ITZ resulted in enhanced survival (Log-Rank p = 0.0465) when compared to the PBS-treated group. However, no enhanced survival was noted compared to the MMV1804559-only treated group (Log-Rank, p = 0.2814).

2.4. Smaller Grains Were Observed in Larvae Treated with MMV1804559

To determine the effect of MMV1804559 on grain formation, histology slides were prepared for M. mycetomatis-infected larvae treated with PBS, 10 µM MMV1804559, 5.7 mg/kg ITZ, or a combination therapy of 10 µM MMV1804559 and 5.7 mg/kg ITZ. As can be seen in Figure 5A, mature M. mycetomatis grains were formed on day 3. When larvae were treated with 10 µM/larva of MMV1804559, the grains inside the larvae were much smaller (Figure 5B, Table 3). This was also noted when larvae were treated with the combination ITZ and MMV1804559 (Figure 5D, Table 3), but not when larvae were treated with ITZ alone (Figure 5C, Table 3). Despite their smaller size, there was no other striking difference in the morphology of the grains (Figure 5A–D). Additionally, for all grains, cement material was noted between the fungal hyphae, as well as a capsule surrounding the grains. To quantify the difference in grain size, we calculated the number of grains at each grain size. As can be seen in Figure 5I, there were differences between the different treatment groups. The total number of grains (Figure 5J, Table 3) remained stable, but the number of large grains (Figure 5K, Table 3) (Mann–Whitney, p = 0.0159) and the average size of the grain (Figure 5L, Table 3) (Mann–Whitney, p = 0.0079) were lower in the MMV1804559-treated group compared to the PBS-treated group. Also, the combination of 10 µM/larva MMV1804559 and 5.7 mg/kg ITZ resulted in significantly smaller grains compared to PBS-treated larvae (Mann–Whitney, p = 0.0317). This was not the case when larvae were treated with ITZ alone.

3. Discussion

In this study, we screened two MMV open-access boxes as part of our Mycetoma Open Source drug discovery program (MycetOS) and identified MMV1804559 as a potential new lead compound [10,12].
MMV1804559 inhibited the growth of M. mycetomatis with an IC50 of 6.95 µM and an MIC50 of 8 µM. Furthermore, MMV1804559 treatment prolonged the survival of M. mycetomatis-infected larvae and resulted in smaller grains in the G. mellonella larva model of infection. Although very little has been published on MMV1804559, from its chemical structure, it can be seen that MMV1804559 is a pyrazolopyrimidine derivative. A subsequent sub-structure search in SciFinder® identified that close analogs of MMV1804559 have been developed as either Mer tyrosine kinase (MerTK) inhibitors [17,18,19,20,21] or dual-specificity tyrosine-regulated kinase 1 (DYRK1) inhibitors [22]. However, Mer is a receptor tyrosine kinase, and tyrosine kinases are not present in most fungal genomes [23]. Therefore, we hypothesized that the activity of MMV1804559 might occur through the fungal DYRK1. In Aspergillus spp., Candida albicans, Cryptococcus spp., and Schizosaccharomyces pombe, two DYRKs are encoded in their genomes, namely yak1 and pom1 [24]. In the M. mycetomatis genome, a homolog of pom1 (KXX76507) was found. Although there is no published research on the deletion of these specific genes in M. mycetomatis, it was noted that deleting both yak1 and pom1 in C. albicans completely blocked filamentation [24]. Additionally, in Aspergillus fumigatus, YakA was associated with septal plugging, which led to abrogated growth [25]. This effect on the filamentation in the fungi was also noted in in vivo animal models. For example, in an in vivo C. albicans dermatitis model, yak1 deletion mutants no longer produced polarized C. albicans growth but appeared to block morphogenesis in yeast cells [24]. In an A. fumigatus lung model, the A. fumigatus lesion size was much smaller when mice were infected with an A. fumigatus yakA deletion mutant compared to a wild-type isolate [25]. Both Yak1 and YakA in C. albicans and A. fumigatus could also be inhibited by beta-carboline compounds [24,25,26]. In A. fumigatus, these compounds blocked the recruitment of YakA to the septal pore [25], while in C. albicans, these compounds blocked biofilm formation in an ex vivo model of vaginal candidiasis and filamentation in the C. albicans dermatitis model [24,26]. Although pyrazolopyrimidines were not tested specifically as DYRK inhibitors in Candida species, it was established that pyrazolopyrimidines have antifungal activity against Candida [27]. In the set of compounds tested in this study, another pyrazolopyrimidine derivative, MMV022478, was active against Candida albicans, Candida auris, and Candida glabrata [28]. Furthermore, MMV022478 was also able to inhibit M. mycetomatis with an IC50 of 2.95 µM and prolong larval survival [10]. However, although MMV1804559 decreased the number and size of M. mycetomatis grains formed, MMV022478 did not [10]. Pom1 deletion mutants have not yet been studied in in vivo models. Taken together, these results indicate that pyrazolopyrimidines should be studied further as potential drug candidates for the treatment of eumycetoma.
Since the literature searches showed that close structural analogs of MMV1804559 were developed as human MerTK and DYRK1 inhibitors, it is likely that MMV1804559 not only inhibited fungal DYRKs but could have also inhibited the G. mellonella MerTK or DYRK1 kinases. Indeed, at 20 µM/larva, MMV1804559 showed toxicity in uninfected G. mellonella, which was also demonstrated in HepG2 cells. In these cells, a concentration of 3 µM MMV1804559 reduced cell viability by 50%. In humans, Mer is a receptor tyrosine kinase that functions as an innate immune system checkpoint in macrophages [23,29]. MerTK is a marker of anti-fibrotic macrophages, is important in the clearance of apoptotic cells, and induces specialized pro-resolving mediators, which results in the clearance of inflammation [30,31,32]. DYRKs play indispensable roles in signal transduction, cellular differentiation, and cell cycle control, as well as in inflammation. In THP-1 macrophages, the inhibition of DYRK1B resulted in a pro-inflammatory cytokine release [33].
Treatment with MMV1804559 resulted in significantly smaller grains in our in vivo M. mycetomatis grain model in G. mellonella. Unlike mammals, G. mellonella only has an innate immune system, and grain formation in G. mellonella is a four-step process in which both the fungus and host play a role [34,35]. Therefore, inhibiting MerTK, DYRK1, or both would most likely result in enhanced inflammation in the G. mellonella host. However, in our treated M. mycetomatis-infected larvae, no evidence of enhanced inflammation was observed. Therefore, as MMV1804559 had a clear effect on inhibiting the growth and grain formation in M. mycetomatis, the compound is most likely to exhibit a novel mode of action against this eumycetoma causative agent. Further, although the compound showed toxicity in our in vivo G. mellonella model, future investigations into improved compound-fungal structure-activity relationships (SAR) could promote the design of more analogs of this parent molecule that display increased fungal activity but with less toxic activity to the host. For example, such an approach has already proven successful for the compound MMV024478, where two structural modifications of this pyrazolopyrimidine not only increased its efficacy against the fungus Candida auris but also decreased its toxicity [28]. Thus, before being able to study the efficacy of this drug in a murine model, novel derivatives of the molecule need to be made that are more selective towards the fungus and less toxic for the mammalian host. The Mycetoma Open Source drug discovery project, MycetOS (https://github.com/OpenSourceMycetoma; accessed on 1 February 2024), is a suitable platform for future research in this area.

4. Materials and Methods

4.1. Strains

The MMV COVID Box and Global Health Priority Box compound libraries were initially screened against M. mycetomatis strain MM55 and F. senegalensis strain CBS197.79. MM55 was originally isolated at the Mycetoma Research Centre in Sudan in 1999 and maintained at ErasmusMC [36]. CBS197.79 was obtained from the Westerdijk Fungal Biodiversity Center in The Netherlands. To ensure that the activity was not confined to these two isolates, the most promising compounds were also screened against a further eight different M. mycetomatis isolates, namely, CBS132419, CBS132588, and CBS132589 (all originating from India), p1 (originating from Mali), PARIJS 15580 AL1 (originating from Algeria), SO1 (originating from Somalia), Peru72012 (originating from Peru), and CBS247.48 (country of origin unknown) to determine the concentrations that inhibited 50% of all isolates tested (MIC50). The CBS isolates were originally obtained from the Westerdijk Fungal Biodiversity Center in Utrecht. All isolates were identified to the species level by sequencing the internally transcribed spacer (ITS) region and maintained in the Erasmus MC laboratory on Sabouraud Dextrose agar plates (BD, Erembodegem, Belgium) [37].

4.2. Compound Boxes

The COVID Box and the Global Health Priority Box were kindly donated by MMV. The COVID Box consisted of two plates of 80 compounds, each with known or predicted activity against SARS-CoV-2 [15]. The Global Health Priority Box consisted of 240 compounds divided over three plates, each containing 80 compounds. The first plate consisted of 80 compounds with confirmed activity against drug-resistant malaria; the second plate consisted of 80 compounds with activity against neglected (non-mycetoma) and zoonotic diseases; and the third plate consisted of 80 compounds with activity against various zoonotic vector species, as demonstrated in the Innovative Vector Control Consortium (IVCC) [16]. Therefore, a total of 400 compounds were screened for activity against M. mycetomatis and F. senegalensis (Supplementary File S1).

4.3. In Vitro Susceptibility Assay

To determine the activity of the 400 compounds against the fungal isolates, an initial in vitro screening at concentrations of 100 µM and 25 µM was performed. For this, strains were transferred from Sabouraud culture plates to colorless RPMI 1640 working medium, which contained 0.35 g/L L-glutamine (Gibco, ThermoFisher, Bleiswijk, The Netherlands) and 1.98 mM 4-morpholinepropane sulfonic acid (MOPS; Sigma-Aldrich, Zwijndrecht, The Netherlands). The suspension was then sonicated for 10 s at 10 µm (Soniprep 150 Plus, Medical and Scientific Equipment, Cholet, France) to obtain hyphal fragments, and the resulting suspension was incubated for seven days at 37 °C, after which time the mycelia were harvested by centrifugation at 3400 rpm for 5 min. The harvested mycelium was again sonicated to obtain hyphal fragments, and a working hyphal suspension of 68–72% transmission at 660 nm (Novaspec II; Pharmacia Biotech, Uppsala, Sweden) was prepared in a colorless RPMI working medium. One µL of the diluted compound and 100 µL of hyphal suspension were added to the wells of a round-bottom 96-well plate (Costar 3799, Fisher Scientific, Breda, The Netherlands).
For M. mycetomatis, the plates were then incubated for seven days at 37 °C, after which time 10 µL of ready-to-use viability dye was added (i.e., 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium inner salt (MTS)) from the CellTiter 96® AQueous One Solution Cell Proliferation Assay (G3581, Promega, Leiden, The Netherlands). After 2 h incubation at 37 °C, 100 µL of supernatant was transferred to the well of a flat-bottomed plate, and the color intensity was measured at 490 nm using an Epoch 2 (BioTek, Santa Clara, CA, USA) microplate reader.
For F. senegalensis, 20 µL of 0.15 mg/mL resazurin was added, after which the plates were incubated for seven days at 37 °C. After seven days, 100 µL of supernatant was transferred to the wells of a flat-bottomed plate, and color intensity was measured at 600 nm using an Epoch 2 (BioTek, Santa Clara, CA, USA) microplate reader. A negative control (NC), consisting of only the culture medium and the viability dye, was used to correct the background signal.
Finally, the metabolic activity of the treated isolate was compared to the metabolic activity of the growth control (GC—no compounds added to the isolates) corrected by the NC using the following formulas [38]:
Complete growth inhibition (MIC) was assumed if a reduction in metabolic activity of >80% was measured. If compounds showed complete growth inhibition at both 100 µM and 25 µM for both species, the IC50 was determined by repeating the assay using a two-fold dilution of the compounds, ranging from 0.03 to 16 µM. The minimal inhibitory concentrations (MICs) against additional isolates of the fungal species used were determined using the identical dilution series.

4.4. Toxicity of Compounds in Galleria Mellonella Larvae

The toxicity of the compounds with promising in vitro activity was determined in five instar Galleria mellonella larvae (Bigbig SA.G.IP larvae, forelshop.be, Baal, Belgium). For this, compounds were diluted in 20 µM/20 µL PBS. Each compound was injected into a group of 15 uninfected, healthy larvae via the pro-leg using an insulin 29G U-100 needle (BD diagnostics, Erembodegem, Belgium). Larvae survival was monitored for 10 days. If a significantly decreased larval survival (compared to the PBS-treated larvae) or an overall larval survival <80% (compared to injection at time 0) was observed, the compound was considered toxic. If toxicity was observed, compound concentrations of 10 µM/20 µL PBS were used.

4.5. In Vivo Grain Model in Galleria Mellonella Larvae

A previously described in vivo eumycetoma grain model involving M. mycetomatis and the larvae of the invertebrate G. mellonella was used for in vivo compound library screening [8]. To determine the efficacy of the selected compounds, larvae were first infected with 4 mg of M. mycetomatis per larva. To obtain this inoculum, M. mycetomatis strain MM55 was cultured for two weeks at 37 °C in RPMI 1640 working medium containing 0.3 g/L L-glutamine, 20 mM MOPS, and 100 mg/L chloramphenicol. After two weeks, the mycelia were harvested by vacuum filtration through a 0.22 µm filter (Nalgene, Abcoude, The Netherlands). The resulting wet-weight mycelium was weighed and then sonicated for 2 min at 10 microns. The resulting homogeneous suspension was washed once in PBS and further diluted to generate an inoculum of 100 mg/mL M. mycetomatis. Forty microliters of fungal suspension were then injected into the last left pro-leg of a larva using an insulin 29G U-100 needle, resulting in the inoculation of 4 mg M. mycetomatis/larva. Next, five infected larvae were placed in a Petri dish containing Whatmann paper, which was incubated at 37 °C for 10 days. For compound testing, 15 larvae were treated with either PBS (negative control), itraconazole 5.7 mg/kg (positive control—Janssen Pharmaceuticals, Beerse, Belgium), MMV1593278 at 20 μM/larva, MMV02033520 at 20 μM/larva, MMV1804559 at 10 μM/larva, or a combination of 5.7 mg/kg itraconazole and 10 μM MMV1804559/larva. Each experiment was performed in triplicate. In each larva, each compound was injected three times with an insulin 29G U-100 needle, namely 4, 28, and 52 h after M. mycetomatis infection. Per injection, a different pro-leg was used. Larvae were monitored for ten days after compound administration, and their survival was recorded on a daily basis. Survival rates were compared on days four and ten using the Log-Rank test. An initial starting time for compound administration of 4 h post-infection was chosen as fungal grains were already visible in infected larvae at this time point.

4.6. Histology

Larvae were infected with M. mycetomatis and treated 4, 28, and 52 h after infection, as described above. At 96 h after infection, larvae were injected with 100 µL of 10% buffered formalin and transferred to containers containing 10% buffered formalin. After 24 h incubation in formalin, the larvae were dissected into two parts. Both parts of the larvae were embedded in paraffin, and sections of 5 µm were prepared. The sections were stained with hematoxylin and eosin (H&E) and Grocott methanamine silver and observed under a Canon EOS70D camera (Canon Inc., Amstelveen, The Netherlands) by two independent researchers to avoid individual bias. Every slide was visualized on EOS Utility software version 3.12.30 (Canon Inc., Amstelveen, The Netherlands) at 40× magnification. Grains were categorized into large, medium, or small sizes using an enlargement display frame of 250 µm and 160 µm (present in the Live View Shooting mode) and manually counted under a light microscope mounted using a Canon EOS70D camera. Counts were performed by two independent scientists, as previously described [39]. The sum of all large, medium, and small grains present in larvae was used to represent the total number of grains in the larvae [39]. To estimate the total size of grain present in the larvae, the sum of all grains in a larva was multiplied by the minimum size of their respective category (large: 0.02 mm2, medium: 0.01 mm2, and small: 0.005 mm2) [39]. The sum of the grain sizes of the three categories together was considered the total grain size. For each treatment group, five larvae were analyzed.

4.7. Data Analysis

A Log-Rank test was performed to compare the survival rate between the different compound treatment groups and the PBS-treated group. The Mann–Whitney test was used to calculate the difference in grain number and size. All calculations were performed in GraphPad Prism 10 (Dotmatics, Boston, MA, USA). A p-value of <0.05 was considered significant.

5. Conclusions

In conclusion, compound MMV1804559 from the MMV Global Health Priority box exhibits promising in vitro and in vivo activity against the eumycetoma-causing fungus M. mycetomatis. Further, its pronounced effect on fungal grains during M. mycetomatis infection of G. mellonella makes MMV1804559 an attractive compound for further study as part of our Open Source drug discovery program, MycetOS.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/ijms25116227/s1.

Author Contributions

W.W.J.v.d.S. designed the study. A.F. donated the strains, J.M., M.S. and K.E. performed experiments. J.M. calculated the data and wrote the draft of this manuscript. A.V., B.L. and W.W.J.v.d.S. supervised the research and revised the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by Stichting Erasmus Trusfonds grant 97030.2022.101.718, Aspasia grant 015.013.033 from the Dutch Research Council, and an EUR fellowship of the Erasmus University, all awarded to Wendy van de Sande. Jingyi Ma was supported by the CSC Scholarship 202008520048. The funders had no role in the design, data collection, interpretation, or decision to publish.

Data Availability Statement

Data are contained within the article or Supplementary Materials.

Acknowledgments

We would like to thank MMV for their support in designing and supplying the COVID Box. We would like to thank MMV, Bristol-Myers Squibb Company, and IVCC for their support in designing and supplying the Global Health Priority Box.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Van de Sande, W.W.J. Global burden of human mycetoma: A systematic review and meta-analysis. PLoS Neglected Trop. Dis. 2013, 7, e2550. [Google Scholar] [CrossRef] [PubMed]
  2. Oladele, R.O.; Ly, F.; Sow, D.; Akinkugbe, A.O.; Ocansey, B.K.; Fahal, A.H.; van de Sande, W.W.J. Mycetoma in West Africa. Trans. R. Soc. Trop. Med. Hyg. 2021, 115, 328–336. [Google Scholar] [CrossRef] [PubMed]
  3. Van de Sande, W.; Fahal, A.; Ahmed, S.A.; Serrano, J.A.; Bonifaz, A.; Zijlstra, E.; Eumycetoma Working Group. Closing the mycetoma knowledge gap. Med. Mycol. 2018, 56 (Suppl. 1), 153–164. [Google Scholar] [CrossRef] [PubMed]
  4. Welsh, O.; Al-Abdely, H.M.; Salinas-Carmona, M.C.; Fahal, A.H. Mycetoma Medical Therapy. PLoS Neglected Trop. Dis. 2014, 8, e3218. [Google Scholar] [CrossRef] [PubMed]
  5. Scolding, P.; Fahal, A.; Yotsu, R.R. Drug therapy for Mycetoma. Cochrane Database Syst. Rev. 2018, 2018, CD013082. [Google Scholar] [CrossRef]
  6. Fahal, A.; Rahman, I.; El-Hassan, A.; Rahman, M.A.E.; Zijlstra, E. The safety and efficacy of itraconazole for the treatment of patients with eumycetoma due to Madurella mycetomatis. Trans. R. Soc. Trop. Med. Hyg. 2011, 105, 127–132. [Google Scholar] [CrossRef] [PubMed]
  7. Nyuykonge, B.; Siddig, E.E.; Mhmoud, N.A.; Nyaoke, B.A.; Zijlstra, E.E.; Verbon, A.; Bakhiet, S.; Fahal, A.H.; van de Sande, W.W.J. Epidemiological cut-off values for itraconazole and ravuconazole for Madurella mycetomatis, the most common causative agent of mycetoma. Mycoses 2022, 65, 1170–1178. [Google Scholar] [CrossRef] [PubMed]
  8. Kloezen, W.; van Helvert-van Poppel, M.; Fahal, A.H.; Van De Sande, W.W.J. A Madurella mycetomatis Grain Model in Galleria mellonella Larvae. PLoS Neglected Trop. Dis. 2015, 9, e0003926. [Google Scholar] [CrossRef] [PubMed]
  9. Van de Sande, W.W.; van Vianen, W.; ten Kate, M.; Fahal, A.; Bakker-Woudenberg, I. Amphotericin B but not itraconazole is able to prevent grain formation in experimental Madurella mycetomatis mycetoma in mice. Br. J. Dermatol. 2015, 173, 1561–1562. [Google Scholar] [CrossRef] [PubMed]
  10. Lim, W.; Melse, Y.; Konings, M.; Duong, H.P.; Eadie, K.; Laleu, B.; Perry, B.; Todd, M.H.; Ioset, J.-R.; van de Sande, W.W.J. Addressing the most neglected diseases through an open research model: The discovery of fenarimols as novel drug candidates for eumycetoma. PLoS Neglected Trop. Dis. 2018, 12, e0006437. [Google Scholar] [CrossRef] [PubMed]
  11. Samby, K.; Willis, P.A.; Burrows, J.N.; Laleu, B.; Webborn, P.J.H. Actives from MMV Open Access Boxes? A suggested way forward. PLoS Pathog. 2021, 17, e1009384. [Google Scholar] [CrossRef] [PubMed]
  12. Lim, W.; Nyuykonge, B.; Eadie, K.; Konings, M.; Smeets, J.; Fahal, A.; Bonifaz, A.; Todd, M.; Perry, B.; Samby, K.; et al. Screening the pandemic response box identified benzimidazole carbamates, Olorofim and ravuconazole as promising drug candidates for the treatment of eumycetoma. PLoS Neglected Trop. Dis. 2022, 16, e0010159. [Google Scholar] [CrossRef] [PubMed]
  13. Lim, W.; Verbon, A.; van de Sande, W. Identifying novel drugs with new modes of action for neglected tropical fungal skin diseases (fungal skinNTDs) using an Open Source Drug discovery approach. Expert Opin. Drug Discov. 2022, 17, 641–659. [Google Scholar] [CrossRef] [PubMed]
  14. Kim, T.; Hanh, B.-T.; Heo, B.; Quang, N.; Park, Y.; Shin, J.; Jeon, S.; Park, J.-W.; Samby, K.; Jang, J. A Screening of the MMV Pandemic Response Box Reveals Epetraborole as A New Potent Inhibitor against Mycobacterium abscessus. Int. J. Mol. Sci. 2021, 22, 5936. [Google Scholar] [CrossRef] [PubMed]
  15. MMV about the COVID Box. Available online: https://www.mmv.org/mmv-open/covid-box/about-covid-box (accessed on 30 January 2024).
  16. MMV about the Global Health Priority Box. Available online: https://www.mmv.org/mmv-open/global-health-priority-box/about-global-health-priority-box (accessed on 30 January 2024).
  17. Wang, X.; Frye, S. Preparation of Pyrazolopyrimidine Compounds as Mer Tyrosine Kinase Inhibitors Useful for Treatment of Cancer, Infections, and Other Diseases. WO/2015/157125, 15 October 2015. [Google Scholar]
  18. Liu, J.; Yang, C.; Simpson, C.; Deryckere, D.; Van Deusen, A.; Miley, M.J.; Kireev, D.; Norris-Drouin, J.; Sather, S.; Hunter, D.; et al. Discovery of Novel Small Molecule Mer Kinase Inhibitors for the Treatment of Pediatric Acute Lymphoblastic Leukemia. ACS Med. Chem. Lett. 2012, 3, 129–134. [Google Scholar] [CrossRef] [PubMed]
  19. Liu, J.; Zhang, W.; Stashko, M.A.; DeRyckere, D.; Cummings, C.T.; Hunter, D.; Yang, C.; Jayakody, C.N.; Cheng, N.; Simpson, C.; et al. UNC1062, a new and potent Mer inhibitor. Eur. J. Med. Chem. 2013, 65, 83–93. [Google Scholar] [CrossRef] [PubMed]
  20. Wang, X.; Frye, S. MerTK-Specific Pyrazolopyrimidine Compounds. WO/2015/157122, 15 October 2015. [Google Scholar]
  21. Ji, N.; Mainolfi, N.; Weiss, M. MerTK Degraders and Uses Thereof. WO/2020/010210, 9 January 2020. [Google Scholar]
  22. Hoffman-La Roche, F.; Liu, W.; Luk, K.-C.T.; Zhang, X. Pyrazolo Pyrimidines as DYRK1A and DYRK1B Inhibitors. WO/2012/098068, 26 July 2012. [Google Scholar]
  23. Kosti, I.; Mandel-Gutfreund, Y.; Glaser, F.; Horwitz, B.A. Comparative analysis of fungal protein kinases and associated domains. BMC. Genom. 2010, 11, 133. [Google Scholar] [CrossRef] [PubMed]
  24. MacAlpine, J.; Liu, Z.; Hossain, S.; Whitesell, L.; Robbins, N.; Cowen, L.E. DYRK-family kinases regulate Candida albicans morphogenesis and virulence through the Ras1/PKA pathway. mBio 2023, 14, e0218323. [Google Scholar] [CrossRef] [PubMed]
  25. Van Rhijn, N.; Zhao, C.; Al-Furajij, N.; Storer, I.; Valero, C.; Gago, S.; Chown, H.; Baldin, C.; Fortune-Grant, R.; Bin Shuraym, H.; et al. Functional analysis of the Aspergillus fumigatus kinome reveals a DYRK kinase involved in septal plugging is a novel antifungal drug target. Res. Sq. 2023, rs-2960526. [Google Scholar]
  26. MacAlpine, J.; Daniel-Ivad, M.; Liu, Z.L.; Yano, J.; Revie, N.M.; Todd, R.T.; Stogios, P.J.; Sanchez, H.; O’Meara, T.R.; Tompkins, T.A.; et al. A small molecule produced by Lactobacillus species blocks Candida albicans filamentation by inhibiting a DYRK1-family kinase. Nat. Commun. 2021, 12, 6151. [Google Scholar] [CrossRef] [PubMed]
  27. Elgemeie, G.H.; Azzam, R.A.; Zaghary, W.A.; Khedr, M.A.; Elsherif, G.E. Medicinal Chemistry of Pyrazolopyrimidine Scaffolds Substituted with Different Heterocyclic Nuclei. Curr. Pharm. Des. 2022, 28, 3374–3403. [Google Scholar] [CrossRef] [PubMed]
  28. Pan, B.; Weerasinghe, H.; Sezmis, A.; McDonald, M.J.; Traven, A.; Thompson, P.; Simm, C. Leveraging the MMV Pathogen Box to Engineer an Antifungal Compound with Improved Efficacy and Selectivity against Candida auris. ACS Infect. Dis. 2023, 9, 1901–1917. [Google Scholar] [CrossRef] [PubMed]
  29. Ubil, E.; Zahid, K.R. Structure and functions of Mer, an innate immune checkpoint. Front. Immunol. 2023, 14, 1244170. [Google Scholar] [CrossRef] [PubMed]
  30. Zizzo, G.; Hilliard, B.A.; Monestier, M.; Cohen, P.L. Efficient Clearance of Early Apoptotic Cells by Human Macrophages Requires M2c Polarization and MerTK Induction. J. Immunol. 2012, 189, 3508–3520. [Google Scholar] [CrossRef] [PubMed]
  31. Scott, R.S.; McMahon, E.J.; Pop, S.M.; Reap, E.A.; Caricchio, R.; Cohen, P.L.; Earp, H.S.; Matsushima, G.K. Phagocytosis and clearance of apoptotic cells is mediated by MER. Nature 2001, 411, 207–211. [Google Scholar] [CrossRef] [PubMed]
  32. Cai, B.; Thorp, E.B.; Doran, A.C.; Subramanian, M.; Sansbury, B.E.; Lin, C.-S.; Spite, M.; Fredman, G.; Tabas, I. MerTK cleavage limits proresolving mediator biosynthesis and exacerbates tissue inflammation. Proc. Natl. Acad. Sci. USA 2016, 113, 6526–6531. [Google Scholar] [CrossRef] [PubMed]
  33. Blom, K.; Rubin, J.; Berglund, M.; Jarvius, M.; Lenhammar, L.; Parrow, V.; Andersson, C.; Loskog, A.; Fryknas, M.; Nygren, P.; et al. Mebendazole-induced M1 polarisation of THP-1 macrophages may involve DYRK1B inhibition. BMC Res. Notes 2019, 12, 234. [Google Scholar] [CrossRef] [PubMed]
  34. Ma, J.; Konings, M.; Verbon, A.; van de Sande, W.W.J. A Falciformispora senegalensis grain model in Galleria mellonella larvae. Med. Mycol. 2023, 61, myad070. [Google Scholar] [CrossRef] [PubMed]
  35. Sheehan, G.; Konings, M.; Lim, W.; Fahal, A.; Kavanagh, K.; van de Sande, W.W.J. Proteomic analysis of the processes leading to Madurella mycetomatis grain formation in Galleria mellonella larvae. PLoS Neglected Trop. Dis. 2020, 14, e0008190. [Google Scholar] [CrossRef] [PubMed]
  36. Smit, S.; Derks, M.F.; Bervoets, S.; Fahal, A.; van Leeuwen, W.; van Belkum, A.; van de Sande, W.W. Genome Sequence of Madurella mycetomatis mm55, Isolated from a Human Mycetoma Case in Sudan. Genome Announc. 2016, 4, e00418-16. [Google Scholar] [CrossRef] [PubMed]
  37. Nyuykonge, B.; Eadie, K.; Zandijk, W.H.A.; Ahmed, S.A.; Desnos-Ollivier, M.; Fahal, A.H.; de Hoog, S.; Verbon, A.; van de Sande, W.W.J.; Klaassen, C.H.W. A Short-Tandem-Repeat Assay (MmySTR) for Studying Genetic Variation in Madurella mycetomatis. J. Clin. Microbiol. 2021, 59, 10–1128. [Google Scholar] [CrossRef] [PubMed]
  38. Van de Sande, W.W.J. In vitro susceptibility testing for black grain eumycetoma causative agents. Trans. R. Soc. Trop. Med. Hyg. 2021, 115, 343–354. [Google Scholar] [CrossRef] [PubMed]
  39. Lim, W.; Konings, M.; Parel, F.; Eadie, K.; Strepis, N.; Fahal, A.; Verbon, A.; van de Sande, W.W.J. Inhibiting DHN- and DOPA-melanin biosynthesis pathway increased the therapeutic value of itraconazole in Madurella mycetomatis infected Galleria mellonella. Med. Mycol. 2022, 60, myac003. [Google Scholar] [CrossRef] [PubMed]
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Figure 1. Flow diagram for in vitro and in vivo evaluation of the MMV compounds tested. In total, 400 compounds were tested for growth inhibition of both M. mycetomatis and F. senegalensis at 100 µM and 25 µM. Fifteen of the 160 compounds present in the MMV COVID Box (green) inhibited the growth of both M. mycetomatis and F. senegalensis. A total of 7 of the 240 compounds from the MMV Global Health box (blue) were able to inhibit the growth of both fungi. The concentrations at which these 22 compounds were able to achieve a 50% (IC50) reduction in fungal growth for M. mycetomatis and F. senegalensis were determined, with three compounds from the MMV Global Health box achieving IC50 at a concentration below 8 µM for M. mycetomatis. Additionally, the MIC of these three compounds was determined against eight other M. mycetomatis isolates, and all three compounds were able to inhibit the growth of eight additional isolates, namely CBS132419, CBS132588, CBS132589, p1, PARIJS 15580 AL1, SO1, Peru72012, and CBS247.48. After subsequent toxicity and efficacy testing in G. mellonella larvae, it was found that one compound, compound MMV1804559, was able to prolong larval survival and, therefore, was considered a new lead compound.
Figure 1. Flow diagram for in vitro and in vivo evaluation of the MMV compounds tested. In total, 400 compounds were tested for growth inhibition of both M. mycetomatis and F. senegalensis at 100 µM and 25 µM. Fifteen of the 160 compounds present in the MMV COVID Box (green) inhibited the growth of both M. mycetomatis and F. senegalensis. A total of 7 of the 240 compounds from the MMV Global Health box (blue) were able to inhibit the growth of both fungi. The concentrations at which these 22 compounds were able to achieve a 50% (IC50) reduction in fungal growth for M. mycetomatis and F. senegalensis were determined, with three compounds from the MMV Global Health box achieving IC50 at a concentration below 8 µM for M. mycetomatis. Additionally, the MIC of these three compounds was determined against eight other M. mycetomatis isolates, and all three compounds were able to inhibit the growth of eight additional isolates, namely CBS132419, CBS132588, CBS132589, p1, PARIJS 15580 AL1, SO1, Peru72012, and CBS247.48. After subsequent toxicity and efficacy testing in G. mellonella larvae, it was found that one compound, compound MMV1804559, was able to prolong larval survival and, therefore, was considered a new lead compound.
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Figure 2. The activities of compounds from the MMV COVID Box and MMV Global Health Priority Box against the two main causative agents of eumycetoma, i.e., M. mycetomatis MM55 and F. senegalensis CBS197.79. In panel (A), the percentage growth of M. mycetomatis exposed to 100 µM of each compound is shown. In panel (B), the percentage growth of F. senegalensis exposed to 100 µM of each compound is shown. Each dot represents a single compound. A green dot indicates a compound that originated from the MMV COVID Box, and a blue dot indicates a compound that originated from the MMV Global Health Priority Box. Growth inhibition was indicated when the percentage growth of fungi was inhibited by ≥80%. (indicated by a dashed line). In panel (C), the percentage growth of M. mycetomatis (x-axis) and F. senegalensis (y-axis) exposed to a compound concentration of 25 µM is plotted. In total, 22 compounds had a percentage growth inhibition of ≥80% for both M. mycetomatis and F. senegalensis. In panel (D), the IC50 values in µM of these 22 selected compounds against M. mycetomatis (x-axis) and F. senegalensis (y-axis) are shown. The dashed line shows the 8 µM boundary, i.e., the IC50 concentration at which a compound would be selected for in vivo testing.
Figure 2. The activities of compounds from the MMV COVID Box and MMV Global Health Priority Box against the two main causative agents of eumycetoma, i.e., M. mycetomatis MM55 and F. senegalensis CBS197.79. In panel (A), the percentage growth of M. mycetomatis exposed to 100 µM of each compound is shown. In panel (B), the percentage growth of F. senegalensis exposed to 100 µM of each compound is shown. Each dot represents a single compound. A green dot indicates a compound that originated from the MMV COVID Box, and a blue dot indicates a compound that originated from the MMV Global Health Priority Box. Growth inhibition was indicated when the percentage growth of fungi was inhibited by ≥80%. (indicated by a dashed line). In panel (C), the percentage growth of M. mycetomatis (x-axis) and F. senegalensis (y-axis) exposed to a compound concentration of 25 µM is plotted. In total, 22 compounds had a percentage growth inhibition of ≥80% for both M. mycetomatis and F. senegalensis. In panel (D), the IC50 values in µM of these 22 selected compounds against M. mycetomatis (x-axis) and F. senegalensis (y-axis) are shown. The dashed line shows the 8 µM boundary, i.e., the IC50 concentration at which a compound would be selected for in vivo testing.
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Figure 3. Chemical structures of compounds MMV020335, MMV1804559, and MMV1593278 from the MMV Global Health box with an IC50 < 20% for M. mycetomatis.
Figure 3. Chemical structures of compounds MMV020335, MMV1804559, and MMV1593278 from the MMV Global Health box with an IC50 < 20% for M. mycetomatis.
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Figure 4. Survival curve of treatment therapy against M. mycetomatis-infected larvae using three selected compounds. In panel (A), the toxicity (dashed lines) and efficacy (solid lines) of MMV1593278 (red), MMV020335 (green), and MMV1804559 (blue) in G. mellonella larvae are shown. PBS was used as a growth control (black). Toxicity testing was performed in uninfected larvae at 20 µM/larva for all three compounds and 10 µM/larva for MMV1804559 (dark blue). Efficacy testing was performed using 20 µM/larva for MMV1593278 and MMV020335 and at 10 µM/larva for MMV1804559 in M. mycetomatis-infected larvae. All treated groups were compared with the PBS group via the Log-Rank test. Only MMV1804559 prolonged the survival of M. mycetomatis-infected larvae after 4 days (Log-Rank, p = 0.0223) and after 10 days (Log-Rank, p = 0.0313). Prolonged survival is indicated with an * at day 4 and day 10. No enhanced survival was noted for MMV1593278 and MMV020335. In panel (B), the efficacy of the combination of MMV1804559 with itraconazole (ITZ) is shown. The survival curves of larvae treated with PBS (black), MMV1804559 at 10 µM/larva (blue), 5.7 mg/kg ITZ (red), and the combination of MMV1804559 at 10 µM/larvae with 5.7 mg/kg ITZ (green) are shown. Significantly enhanced survival is indicated with an * and observed for larvae treated with MMV1804559 only (Log-Rank, p = 0.0313), the combination of MMV1804559 and ITZ after 4 days (Log-Rank, p = 0.0227), and the combination of MMV1804559 and ITZ after 10 days (Log-Rank, p = 0.0465). * indicates a p-value between 0.01 and 0.05.
Figure 4. Survival curve of treatment therapy against M. mycetomatis-infected larvae using three selected compounds. In panel (A), the toxicity (dashed lines) and efficacy (solid lines) of MMV1593278 (red), MMV020335 (green), and MMV1804559 (blue) in G. mellonella larvae are shown. PBS was used as a growth control (black). Toxicity testing was performed in uninfected larvae at 20 µM/larva for all three compounds and 10 µM/larva for MMV1804559 (dark blue). Efficacy testing was performed using 20 µM/larva for MMV1593278 and MMV020335 and at 10 µM/larva for MMV1804559 in M. mycetomatis-infected larvae. All treated groups were compared with the PBS group via the Log-Rank test. Only MMV1804559 prolonged the survival of M. mycetomatis-infected larvae after 4 days (Log-Rank, p = 0.0223) and after 10 days (Log-Rank, p = 0.0313). Prolonged survival is indicated with an * at day 4 and day 10. No enhanced survival was noted for MMV1593278 and MMV020335. In panel (B), the efficacy of the combination of MMV1804559 with itraconazole (ITZ) is shown. The survival curves of larvae treated with PBS (black), MMV1804559 at 10 µM/larva (blue), 5.7 mg/kg ITZ (red), and the combination of MMV1804559 at 10 µM/larvae with 5.7 mg/kg ITZ (green) are shown. Significantly enhanced survival is indicated with an * and observed for larvae treated with MMV1804559 only (Log-Rank, p = 0.0313), the combination of MMV1804559 and ITZ after 4 days (Log-Rank, p = 0.0227), and the combination of MMV1804559 and ITZ after 10 days (Log-Rank, p = 0.0465). * indicates a p-value between 0.01 and 0.05.
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Figure 5. Grains in histology slides of four treatment groups in M. mycetomatis-infected larvae. In this figure, H&E-stained (panels (A–D)) and Grocott-stained (panels (E–H)) M. mycetomatis grains formed in G. mellonella larvae are shown. Slides were prepared after 72 h of infection and treatment with PBS (panels (A) and (E)), 5.7 mg/kg ITZ treatment (panels (B) and (F)), 10 µM/larva MMV1804559 treatment (panels (C) and (G)), or the combination of both (panels (D) and (H)). The scale bars stand for 250 µm in each image. The grains were grouped into large (black arrow), medium (white arrow), and small (dashed arrow) grains. The number of grains that were classified as large (orange), medium (purple), and small (blue) in each slide is depicted in panel (I). The Mann–Whitney U-test was used to compare the difference in the total number of grains/larva (panel (J)), the total number of large grains (panel (K)), and the total size of the grains (panel (L)). No significant difference in total grain number (panel (J)) was noted. However, a significantly lower number of large grains was noted in larvae treated with MMV1804559 (Mann–Whitney, p = 0.0159) (Panel (K)). This also resulted in a significantly lower total grain size for larvae treated with MMV1804559 (red) (Mann–Whitney, p = 0.0079) or the combination MMV1804559 with ITZ (blue) (Mann–Whitney, p = 0.0317) (Panel (L)). Statistical significance is displayed as * (0.01 < p < 0.05) and ** (0.0001 < p < 0.01).
Figure 5. Grains in histology slides of four treatment groups in M. mycetomatis-infected larvae. In this figure, H&E-stained (panels (A–D)) and Grocott-stained (panels (E–H)) M. mycetomatis grains formed in G. mellonella larvae are shown. Slides were prepared after 72 h of infection and treatment with PBS (panels (A) and (E)), 5.7 mg/kg ITZ treatment (panels (B) and (F)), 10 µM/larva MMV1804559 treatment (panels (C) and (G)), or the combination of both (panels (D) and (H)). The scale bars stand for 250 µm in each image. The grains were grouped into large (black arrow), medium (white arrow), and small (dashed arrow) grains. The number of grains that were classified as large (orange), medium (purple), and small (blue) in each slide is depicted in panel (I). The Mann–Whitney U-test was used to compare the difference in the total number of grains/larva (panel (J)), the total number of large grains (panel (K)), and the total size of the grains (panel (L)). No significant difference in total grain number (panel (J)) was noted. However, a significantly lower number of large grains was noted in larvae treated with MMV1804559 (Mann–Whitney, p = 0.0159) (Panel (K)). This also resulted in a significantly lower total grain size for larvae treated with MMV1804559 (red) (Mann–Whitney, p = 0.0079) or the combination MMV1804559 with ITZ (blue) (Mann–Whitney, p = 0.0317) (Panel (L)). Statistical significance is displayed as * (0.01 < p < 0.05) and ** (0.0001 < p < 0.01).
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Table 1. IC50 values of the 22 most potent compounds against both M. mycetomatis and F. senegalensis.
Table 1. IC50 values of the 22 most potent compounds against both M. mycetomatis and F. senegalensis.
Compound IDLocationCompound Name or Chemical ClassIC50 of mm55 (µM)IC50 of CBS197.79 (µM)
Global Health Priority Box
MMV1804559Global Health Priority Box MB2 platePyrazolo [3,4-d]pyrimidine6.9516.95
MMV1593278Global Health Priority Box ZND plate2,4-Diaminopyrimidine7.3817.94
MMV020335Global Health Priority Box MB2 plateThieno[3,2-d]pyrimidine7.3915.00
MMV1542799Global Health Priority Box ZND platePurine-2,8-diamine8.8117.20
MMV1545674Global Health Priority Box ZND plate2,6-Diaminoimidazo[4,5-c]pyrimidine9.8317.26
MMV1542798Global Health Priority Box ZND plate2,8-Diaminopurine9.9516.15
MMV024638Global Health Priority Box MB2 platePyrrolo[2,3-c]pyridine11.4016.45
COVID Box
MMV637229COVID Box plate-BClemastine13.8015.97
MMV003461COVID Box plate-ANiclosamide14.7215.43
MMV003162COVID Box plate-AAstemizole15.2216.21
MMV1804244COVID Box plate-ATriparanol15.9715.51
MMV000016COVID Box plate-B(+)-Mefloquine16.3720.44
MMV001428COVID Box plate-BThiethylperazine16.6016.28
MMV638007COVID Box plate-BToremifene16.8816.26
MMV001871COVID Box plate-AChlorpromazine17.0016.83
MMV001829COVID Box plate-AFluphenazine17.0716.48
MMV1804190COVID Box plate-ABemcentinib17.2515.18
MMV001681COVID Box plate-BFluspirilene17.2815.26
MMV1580167COVID Box plate-BPonatinib17.5116.42
MMV1580492COVID Box plate-AOzanimod17.6415.84
MMV892669COVID Box plate-BDesmethyl ferroquine18.1916.24
MMV690733COVID Box plate-BOsimertinib18.2116.61
Note: Ranked by IC50 value against M. mycetomatis MM55.
Table 2. MIC50 values of three selected compounds from the Global Health Priority Box.
Table 2. MIC50 values of three selected compounds from the Global Health Priority Box.
StrainMMV1593278
MIC (µM)		MMV020335
MIC (µM)		MMV1804559
MIC (µM)
CBS1324198168
CBS1325888328
CBS1325898328
p1161632
PARIJS 15580 AL183216
SO181616
Peru7201283216
CBS247.488168
MM558328
MIC508328
Table 3. Data analysis of grain number and size in M. mycetomatis-infected larvae treated with single and combined therapy.
Table 3. Data analysis of grain number and size in M. mycetomatis-infected larvae treated with single and combined therapy.
NumberIn Vivo Significance (p-value)AVERAGE
Grain Number Per Size		Median of Total Grain NumberMann–Whitney
p-Value		Median of Large Grain NumberMann–Whitney
p-value		Median of Total Grain SizeMann–Whitney
p-Value
Day 4Day 10Large
(STDEV)		Medium
(STDEV)		Small
(STDEV)		Average
(STDEV)		 Average
(STDEV)		 Average
(STDEV)
Control
PBS5 4.10 (1.93)3.10 (0.63)5.50 (2.57)12.70 (2.91) 4.10 (1.93) 0.12 (0.03)
Global Health Priority Box
MMV15932785NSNS/////////
MMV0203355NSNS/////////
MMV18045595Increase survival (0.0223 *)Increase survival (0.0313 *)0.95 (0.67)2.10 (2.15)7.05 (1.24)10.10 (2.85)NS0.95 (0.67)0.0159 *0.04 (0.02)0.0079 **
ITZ5NSNS2.85 (1.75)3.85 (1.92)9.03 (3.59)16.00 (6.52)NS2.85 (1.75)NS0.10 0.05)NS
MMV1804559 + ITZ5Increase survival (0.0227 *)Increase survival (0.0465 *)1.80 (1.19)2.20 (1.30)5.20 (1.69)9.20 (0.82)NS1.80 (1.19)NS0.06 (0.03)0.0317 *
Note: significant differences are displayed as NS (Not significant, p > 0.05); * (0.01 < p < 0.05) and ** (0.001 < p < 0.01).
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Ma, J.; Eadie, K.; Schippers, M.; Fahal, A.; Laleu, B.; Verbon, A.; van de Sande, W.W.J. Novel Compound MMV1804559 from the Global Health Priority Box Exhibits In Vitro and In Vivo Activity against Madurella mycetomatis. Int. J. Mol. Sci. 2024, 25, 6227. https://doi.org/10.3390/ijms25116227

AMA Style

Ma J, Eadie K, Schippers M, Fahal A, Laleu B, Verbon A, van de Sande WWJ. Novel Compound MMV1804559 from the Global Health Priority Box Exhibits In Vitro and In Vivo Activity against Madurella mycetomatis. International Journal of Molecular Sciences. 2024; 25(11):6227. https://doi.org/10.3390/ijms25116227

Chicago/Turabian Style

Ma, Jingyi, Kimberly Eadie, Marij Schippers, Ahmed Fahal, Benoît Laleu, Annelies Verbon, and Wendy W. J. van de Sande. 2024. "Novel Compound MMV1804559 from the Global Health Priority Box Exhibits In Vitro and In Vivo Activity against Madurella mycetomatis" International Journal of Molecular Sciences 25, no. 11: 6227. https://doi.org/10.3390/ijms25116227

APA Style

Ma, J., Eadie, K., Schippers, M., Fahal, A., Laleu, B., Verbon, A., & van de Sande, W. W. J. (2024). Novel Compound MMV1804559 from the Global Health Priority Box Exhibits In Vitro and In Vivo Activity against Madurella mycetomatis. International Journal of Molecular Sciences, 25(11), 6227. https://doi.org/10.3390/ijms25116227

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