Spread of antimicrobial resistance and shortage of novel antibiotics have led to an urgent need for new antibacterials. Although aminoglycoside antibiotics (AGs) are very potent anti-infectives, their use is largely restricted due to serious side-effects, mainly nephrotoxicity and ototoxicity. We evaluated the ototoxicity of various AGs selected from a larger set of AGs on the basis of their strong antibacterial activities against multidrug-resistant clinical isolates of the ESKAPE panel: gentamicin, gentamicin C1a, apramycin, paromomycin and neomycin. Following local round window application, dose-dependent effects of AGs on outer hair cell survival and compound action potentials showed gentamicin C1a and apramycin as the least toxic. Strikingly, although no changes were observed in compound action potential thresholds and outer hair cell survival following treatment with low concentrations of neomycin, gentamicin and paromomycin, the number of inner hair cell synaptic ribbons and the compound action potential amplitudes were reduced. This indication of hidden hearing loss was not observed with gentamicin C1a or apramycin at such concentrations. These findings identify the inner hair cells as the most vulnerable element to AG treatment, indicating that gentamicin C1a and apramycin are promising bases for the development of clinically useful antibiotics.
Currently, there is a critical shortage of effective antibiotics, and in particular, those needed to treat serious infections caused by Gram-negative pathogens belonging to the Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa and Enterobacter species (ESKAPE) group. These include carbapenemase-producing enterobacteria, multidrug-resistant (MDR) Pseudomonas aeruginosa and MDR Acinetobacter baumannii1,2, which are the pathogens that pose the highest risk in clinical practice. Although aminoglycoside antibiotics (AGs) show potent antimicrobial activity, important side-effects have severely curtailed their use, such as nephrotoxicity, loss of vestibular function (i.e., vestibulotoxicity) and permanent hearing impairment (i.e., cochleotoxicity)3,4. In the 1970’s, AGs were mostly replaced by other antibiotics that are safer and highly efficacious against Gram-negative infections, such as the fluoroquinolones. However, in recent years the rapid spread of fluoroquinolone-resistance has seriously reduced the efficacy of these compounds in the fight against severe bacterial infections, such as tuberculosis, pneumonia, peritonitis, bacteremia, and intra-abdominal and genitourinary tract infections5. The current rise in MDR pathogens has highlighted the important role AGs have as the ultimate weapons against life-threatening infections6,7,8. It is therefore of great importance to identify AGs that have strong antibacterial activity while lacking their most harmful side-effects.
We carried out an extensive study on the ototoxic activities of five selected natural AGs9 following their confirmation as potent antibiotics against a selection of MDR clinical isolates of the ESKAPE panel: Neomycin (Neo), gentamicin (GM), paromomycin (Paro), apramycin (Apra) and gentamicin C1a (GM C1a). Neo, GM and Paromomycin are AGs that are medically used (e.g., https://www.drugs.com/monograph/gentamicin-sulfate.html)10,11,12 despite their known ototoxicity. Their antibacterial activities were compared to those of apramycin and GM C1a (congener present in the commercial GM mixture). Although apramycin is an antibiotic that is currently used in veterinary medicine13, neither apramycin nor GM C1a have been used in the clinic. However, a few studies have indicated that apramycin and GM C1a are antibacterials with lower ototoxic activity14,15,16.
Our in-vitro and in-vivo assays indicated dose-dependent toxicity of each of the AGs tested. When their ototoxicity was examined in-vivo, there was no hair cell (HC) loss or compound action potential (CAP) threshold shifts 3 weeks after a single application of AGs to the round window membrane at the lowest concentration under study. However, for neomycin, GM and paromomycin, but not apramycin or GM C1a, this concentration induced a reduction in inner hair cell (IHC) ribbon numbers (i.e., IHC synaptopathy), and a worsening of the CAP amplitudes. At higher concentrations, the AGs additionally induced a reduction in summating potential (SP) amplitudes, which mainly represented mechanoelectrical transduction (MET) current-mediated IHC receptor potential responses from basal cochlear turns. Importantly, these data thereby demonstrated hidden hearing loss caused by neomycin, GM and paromomycin but not apramycin or GM C1a, at concentrations where outer hair cell (OHC) loss was not yet detectable. Thus the IHC was identified as the most vulnerable element of the inner ear to AG treatment, and the data indicated IHC synaptopathy as the earliest marker of AG-induced ototoxicity. These data suggest that current GM administration regimes adopted in the clinic (i.e., application of GM at reduced doses or at once-a-day intervals) to reduce the risk of nephrotoxicity and ototoxicity might still cause hidden hearing loss. Thus, this might translate into hearing impairment later in life, as has already been observed following noise exposure17. On the other hand, these results underline the potential of apramycin and GM C1a as promising drug leads for the development of safer AGs for the clinic.
Antibacterial efficacies of the selected aminoglycoside antibiotics
Isolation of the GM C1a congener was achieved following derivatization of the GM C complex in the GM mixture using benzyl chloroformate, which provided a mixture of carboxybenzyl (Cbz)-protected GM congeners that were detected and separated using preparative HPLC with UV detection (Supplementary Fig. S1; for details, see Supplementary Information). A Cbz-protection / deprotection strategy was subsequently applied (Supplementary Fig. S2; for details, see Supplementary Information) that yielded gram quantities of pure GM C1a in the form of a disulfate salt (Supplementary Fig. S3; for details, see Supplementary Information).
The antibiotic activities of the selected AGs were established against an ESKAPE panel of 61 MDR isolates (Table 1, Supplementary Table S1). High MIC90 values (>64 mg/L) were obtained for almost all of these compounds, with the exception of apramycin (MIC90, 32 mg/L). However, in terms of MIC50, the most active compounds were neomycin and paromomycin. Interestingly, although the MIC50 and MIC90 values of GM and GM C1a were similar, these two compounds showed different in-vitro activities against a large proportion of the isolates (Supplementary Table S2). The MICs determined for GM were within the defined quality control ranges for the three reference strains, as defined by the Clinical and Laboratory Standards Institute (CLSI, 2018). As the breakpoints for defining clinical categories are only established for GM, by the CLSI and the European Committee on Antimicrobial Susceptibility Testing, it is difficult at present to evaluate the clinical value of the information obtained for the other tested compounds, such as GM C1a and apramycin. However, if the in-vitro activity of GM C1a is evaluated considering the same breakpoints defined for GM, then 42.6% (26/61) and 6.6% (4/61) of the isolates tested would be susceptible (<8 mg/L) and intermediate resistant (8 mg/L), respectively, to GM C1a. Categorical breakpoints have been suggested for apramycin18 based on information from a National Antibiotic Resistance Monitoring Study report, and its susceptible, intermediate resistant, and resistant categories are defined at ≤8 mg/L, 16–32 mg/L, and ≥64 mg/L, respectively. Considering these breakpoints, 59.0% (36/61) and 31.1% (19/61) of the tested organisms would be susceptible and intermediate susceptible to apramycin, respectively (Table 1). Additionally, the MICs for apramycin were within the narrow range of 4 mg/mL to 16 mg/L for 82.0% (50/61) isolates, whereas only three isolates (K. pneumoniae [×2], A. baumannii) had MICs > 64 mg/L (Table 1, Supplementary Table S1).
Toxicity to otic cell lines varies among aminoglycoside antibiotics
In-vitro evaluation of the ototoxicities of neomycin, GM, paromomycin, apramycin and GM C1a was conducted on two immortalized otic cell lines (House Ear Institute-Organ of Corti 1 [HEI-OC1], OC-k3 cells), both derived from the organ of Corti of postnatal day 14 (P14) H-2Kb-tsA58 transgenic mice19,20,21. MTT tests (using 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide) were used to detect metabolically active cells in the cultures. Initial experiments were carried out with the ototoxic AGs GM and neomycin, to establish the optimal conditions for conducting these tests. Three AG concentrations (1, 2, 5 mM) were analyzed for three different incubation times (24, 48, 72 h). At 5 mM, both GM and neomycin were toxic to both cell lines following the 24-h treatment (Supplementary Fig. S4a). Application of 2 mM GM or neomycin for 48 hours resulted in a statistically significant loss of viability in the cultures, albeit this was significantly lower than for 5 mM GM or neomycin (Supplementary Fig. S4b). Overall, no increased toxicity was seen for the 72-h treatment with 5 mM GM or neomycin, compared to 48 h. On the other hand, 1 mM and 2 mM GM or neomycin for 24 h showed no significant toxicities for either cell line (Supplementary Fig. S4a). Therefore, in-vitro ototoxicity was thereafter evaluated by conducting MTT tests on cultures treated for 48 h with 2 and 5 mM AGs.
At 2 mM AG concentrations, only GM and neomycin were confirmed as toxic to both cell lines (Fig. 1a). A trend toward greater survival that did not reach statistical significance was seen for OC-k3 cells treated with 2 mM GM C1a (93.3% ± 5.9%; no significant loss of viability compared to controls; p > 0.1) compared to 2 mM GM (80.7% ± 0.8%; significant loss of viability compared to controls; p < 0.0001) (Fig. 1a). This difference was not seen for HEI-OC1 cells, where 2 mM GM C1a showed significant toxicity which was similar to that of 2 mM GM or neomycin (Fig. 1a). Paromomycin and apramycin at 2 mM did not show any toxicity toward either of these cell lines, with significantly higher survival for OC-k3 cells treated with 2 mM apramycin, compared to 2 mM GM.
Treatment of both of the cell lines with all of the AGs at 5 mM led to significant loss of viability (Fig. 1b), with neomycin as the most toxic. Interestingly, the cells showed differences in their responses to some of the AGs. The HEI-OC1 cells were significantly more resistant to GM and GM C1a than the OC-k3 cells, while they were more susceptible to apramycin. On OC-k3 cells apramycin was significantly less toxic than neomycin, GM, and GM C1a.
Thus, these in-vitro ototoxicity tests indicated that neomycin was the most toxic of these AGs, with apramycin and paromomycin showing lower ototoxicities. In addition, for the OC-k3 line, 2 mM GM C1a appeared to be less toxic than 2 mM GM. Overall, the responses of both of these cell lines to the AGs were comparable, although the HEI-OC1 cells were significantly more resistant to 5 mM GM and GM C1a, and more sensitive to 5 mM apramycin, compared to the OC-k3 cells.
Cochleotoxicity on organotypic cultures of cochlear epithelia varies among aminoglycoside antibiotics
These AGs were tested on organotypic cultures of cochlear epithelia obtained from new born (P3) mice. Cochlear explants were treated with 0.1 mM AGs for 23 h (Fig. 2), conditions under which OHC survival was ~50% following GM treatment (see Supplementary Information). As reported previously22,23, a gradient was observed in the vulnerability of HCs to AG toxicity, with the HCs in the basal area of the cochlear epithelium more susceptible to damage than those in the apical zone (Fig. 2a). Treatment with apramycin showed no HC toxicity (104.5% ± 6.3% OHC survival), as for paromomycin (95.9% ± 1.6% OHC survival). In contrast, significant HC toxicity was seen for GM C1a (76.7% ± 7.7% OHC survival; p < 0.05), GM (43.9% ± 4.6% OHC survival; p < 0.001), and neomycin (80.0% ± 8.4% OHC survival; p < 0.05) (Fig. 2b). GM was significantly more toxic than the other AGs, including the GM C1a congener (p < 0.01). Interestingly, an apical-to-basal gradient of IHC loss was consistently observed for both GM and GM C1a (Fig. 2a), which indicated greater vulnerability of IHCs compared to OHCs. The same effects on the explants were seen for lower concentrations of GM and GM C1a (0.05 mM), and the testing of a different commercial GM mixture yielded the same results.
In summary, this study on organotypic cultures of cochlear epithelia indicated the toxicities of GM C1a, GM and neomycin. Although GM C1a was toxic to the explants, it was significantly less toxic than the commercial GM mixture. Indeed, GM was the most toxic of the AGs, with no toxicities seen for organotypic cultures treated with either apramycin or paromomycin.
Dose-dependent elevation of compound action potential threshold shifts in the high frequency region varies among aminoglycoside antibiotics
Following the in-vitro studies, and to analyse the primary long-term ototoxic effects, we investigated the cochleotoxicity of these five AGs in an in-vivo guinea pig model, 3 weeks after application of each AG to the round window membrane. A hydrogel-based delivery system to the cochlea was used, which excluded indirect retrocochlear effects that might be caused by nephrotoxicity, for example, as described by Muller et al.24. These hydrogels have been successfully used in animal research and in the clinic, and they promote long-lasting effects25. Three defined AG concentrations were chosen (60 mg/mL, 210 mg/mL, 420 mg/mL) based on dose-response curves for neomycin and GM on CAP hearing thresholds. For this selected concentration range, none of the typical correlates of impaired vestibulo-ocular reflex, such as head tremble, head deviation, spontaneous nystagmus, eye deviation, body tilt or looping (not shown) were observed26 for any of the initial tests, not even at the highest AG concentrations tested. Impaired vestibulo-ocular reflex can result in loss of appetite and weight, which can lead to the death of the experimental animal. With the administration method used here, all 45 AG-treated animals survived. These observations confirm the advantage of local round window application in terms of a safe treatment, as it provides an animal model of AG-induced hearing loss with low mortality rates27,28.
The CAP measurements represent the summed response of the synchronous firing of all of the auditory nerve fibres (with lower or higher thresholds, and spontaneous firing rates)29,30. This allowed the extraction of direct response changes to sound within the cochlea following the AG application. To evaluate AG-induced cochleotoxicity on hearing function over time, the CAP threshold shifts were calculated by subtracting the CAP threshold before AG application from that after AG application. The CAP threshold shifts were analysed for round window application of the selected AG concentrations (60, 210 [data not shown], 420 mg/mL) after 60−90 min and for days 7, 14, and 21 (Supplementary Fig. S5a). All of the AGs showed dose-dependent CAP threshold increases, with the maximum values seen at day 7. The threshold shift differences were mainly at >4 kHz (i.e., corresponding to alterations in the ‘basal region’) in comparison to the measurements recorded at <4 kHz (‘mid region’). The CAP threshold shift between 60 min and 7 days also showed rapid onset and long-lasting elution times of the AGs from the hydrogel. The threshold shifts showed no changes from day 7 onwards at any of the frequencies (Supplementary Fig. S5a). The input-output function curves at day 21 showed that the AG-induced effects were mainly restricted to the ‘basal region’ (Supplementary Fig. S5a). The fine structure analysis of the CAP thresholds and amplitudes was completed with the data collected at the ‘basal region’ at both times (before application, day 21 following treatment), which indicated that 60 mg/mL, 210 mg/mL, and 420 mg/mL AGs induced dose-dependent increases in the CAP thresholds (Supplementary Fig. S5b; n = 3 animals/6 ears per AG). The CAP threshold differences for each AG 3 weeks after the round window application are illustrated in Fig. 3. In comparison to the vehicle-treated groups, application of 420 mg/mL of any of the AGs tested resulted in significant CAP threshold shifts (Fig. 3a; n = 3 animals/6 ears; p = 0.0024; GM C1a, p = 0.049; Apra, p = 0.001; GM, p = 0.0001; Paro, p = 0.016; Neo, p = 0.0005). When the AGs were applied at 210 mg/mL, GM, paromomycin, and neomycin also led to significant CAP increases (Fig. 3a; n = 3 animals/6 ears, p = 0.004), while those for GM C1a and apramycin did not reach statistical significance (p > 0.05, with CAP threshold shifts <10 dB). No significant CAP threshold increases were seen with any of the AGs when they were tested at a 60 mg/mL (Fig. 3a; n = 3 animals/6 ears; p = 0.21).
As the thresholds for sound-evoked neural potentials are not affected by diffuse neuronal loss as long as the OHCs are functioning normally31, a normal CAP threshold is expected to reflect intact OHCs. Surface preparations of cochleae from guinea pigs treated with 420 mg/mL of all of the tested AGs, or with 210 mg/mL GM, paromomycin or neomycin, showed extensive OHC loss in the basal turns (see Fig. 3b). To quantify this effect, the surviving OHCs were counted in whole mounts of the basal cochlear turn along the basilar membrane. This decrease in OHC density was significant with 420 mg/mL AGs (Fig. 3c; n = 3 ears per AG; p = 0.0086), although the OHC loss for animals treated with 210 mg/mL GM, paromomycin or neomycin did not reach statistical significance (Fig. 3c; n = 3 ears per AG; p = 0.11). In agreement with the reduced CAP threshold shifts recorded at cochlear midbasal turns (Supplementary Fig. S5a), no significant OHC loss was observed in the ‘mid region’ (data not shown). When the animals were treated with 60 mg/mL AGs, there was also no OHC loss in the ‘basal region’ (Fig. 3c; n = 3 ears per AG; p = 0.28). In support of the robustness of these findings, there was a significant negative correlation between the CAP threshold shifts and the density of the surviving OHCs, as shown for the ‘basal’ and ‘mid regions’ (Fig. 3d; r = −0.92; p < 0.001; n = 72).
Taken together, dose-dependent increases in the CAP thresholds were seen that correlated with the loss of OHCs in the basal regions of the cochlea. Apramycin and GM C1a showed the weakest effects on cochlear function, while GM, paromomycin and neomycin showed the highest toxicities.
Loss of compound action potential amplitude and synaptic ribbons varies among aminoglycoside antibiotics in the absence of compound action potential threshold shifts
To get a more detailed view of the distinct cochleotoxic action of each individual AG, the CAP amplitudes at 21 days post-treatment were compared to those before application. These CAP input-output functions reveal the functional status of the auditory nerve fibres/synapses in more detail. When 210 mg/mL (not shown; p = 0.022) and 420 mg/mL AGs were applied, significant decreases in the CAP amplitude were seen (Fig. 4a; lower panel; n = 6 ears per AG; p = 0.0009). Interestingly, there was also a significant decrease of the CAP amplitude at the ‘basal region’ in animals treated with 60 mg/mL GM, paromomycin or neomycin (Fig. 4a; upper panel; n = 6 ears per AG; p < 0.0001), although at this AG concentration the CAP thresholds were unchanged compared to the controls. No decrease in the CAP amplitude was seen for 60 mg/mL GM C1a or apramycin.
Considering that neither CAP threshold shifts nor OHC loss were observed following the administration of 60 mg/mL of any of the AGs, the decline in CAP amplitude after treatment with either GM, paromomycin or neomycin was surprising, and this indicated decreased sound responsiveness at the level of the IHCs. Interestingly, no significant changes in IHC density were observed for any of the AG treatments, neither for the ‘mid regions’ (not shown) nor for the ‘basal regions’ (Fig. 4b; n = 3 ears per AG; p > 0.05), which indicated that the decreased CAP amplitude after the lowest AG treatments is not linked to IHC loss.
Various studies have indicated that the number of presynaptic ribbon-like transmitter release sites at the base of IHCs can be used as an approximate readout of IHC afferent innervation32. These sites can be stained with antibodies directed against CtBP2/ RIBEYE (see Fig. 4e for a whole-mount preparation)32. When the synaptic ribbon numbers were counted in whole-mount cochlear explants of AG-treated animals, significant IHC ribbon decrease was observed in the basal turn (Fig. 4c,e; n = 3 ears per AG/12–16 IHCs per ear) of the animals treated with AGs at 420 mg/mL (p = 0.0011) (Fig. 4c), and 210 mg/mL (p = 0.0279; data not shown). This was also the case for 60 mg/mL GM, paromomycin or neomycin, as shown by the post-hoc tests (Fig. 4c,e; n = 3 ears per AG; p = 0.0051). Importantly, these findings indicated that GM, paromomycin and neomycin, but not GM C1a or apramycin, can induce a loss of CAP amplitude and IHC synaptic ribbons at concentrations that do not result in any OHC loss or elevation of CAP thresholds. Indeed, when the CAP amplitude was compared with the synaptic ribbon number in basal cochlear turns, a strong correlation was found (Fig. 4d; left panel; r = 0.86; p < 0.001; n = 34), while CAP threshold and IHC ribbon numbers did not correlate (Fig. 4d, right panel). Therefore, the CAP amplitude appears to be an adequate metric for synaptopathy.
Loss of summating potential amplitude, but not summating potential/compound action potential amplitude ratio, varies among aminoglycoside antibiotics in the absence of compound action potential threshold shifts
The detection of the SP reflects the direct current of receptor potentials. This applies mainly to that of IHCs33,34 in the basal cochlear turns35,36, as IHCs move in conjunction with the basilar membrane29. In contrast, OHCs in the base of the cochlea produce little direct-current receptor potential except at very high sound pressure levels37,38,39. SP responses thus provide a first indication of whether MET channel currents in the IHCs are intact or not30,40. On the other hand, enhanced SP/ action potential (AP) amplitude ratios (used as a measurement for CAP, and henceforth called the SP/CAP amplitude ratio) have been associated with IHC synaptopathy in cases such as auditory neuropathy due to mutations in the otoferlin gene41, and noise-induced hidden hearing loss42. On these bases, we analysed the SP amplitude and the SP/CAP amplitude ratios prior to AG application and at 21 days post-treatment (Fig. 5a, see Supplementary Fig. S5). At 21 days post-treatment with 60 mg/mL GM, paromomycin or neomycin, the SP amplitudes were significantly reduced compared to controls, GM C1a and apramycin (Fig. 5b; n = 6 ears per AG; post-hoc test p = 0.0001). Comparison of the SP/CAP amplitude ratios showed no significant differences among the two control groups and the five AG treatment groups (Fig. 5c; n = 6 ears per AG; p > 0.05). This indicated that GM, paromomycin and neomycin affect the SP amplitudes and CAP amplitudes in similar ways. In line with these data, the SP/CAP amplitude ratios were not influenced by the loss of synaptic ribbons (Fig. 5d; r = −0.24; p = 0.16; n = 32).
In summary, all of the AGs except GM C1a and apramycin induced deterioration of SPs and reduction in synaptic ribbon numbers at concentrations that were well below the levels that affect the hearing (CAP) thresholds. The observation that the SP/CAP amplitude ratio did not change following treatment with GM, paromomycin or neomycin suggests that the AGs induce changes to the SP and CAP amplitudes to comparable extents.
The AGs remain a vital clinical asset, as they are very potent bactericidal compounds. Although their use is restricted due to severe side-effects (mainly nephrotoxicity and ototoxicity), the current rise in MDR bacterial infections makes it necessary to develop novel derivatives that have high antibacterial activities but have significantly lower toxicities. We evaluated the ototoxicities of five AGs after demonstrating their efficacies against a set of MDR pathogens from the ESKAPE panel.
We were particularly interested here to compare apramycin and GM C1a, as two AGs that have not yet been brought into the clinical setting, with neomycin and GM, two AGs with some medical indications that show good antibacterial activities, but with strong ototoxicities. This interest was motivated by our demonstration that GM C1a showed activity against a panel of ESKAPE MDR pathogens that was comparable to that of the commercial GM complex used in the clinic. In addition, we had also recorded very promising activity for apramycin (currently used as a veterinary antibiotic) against the panel of MDR pathogens. The fifth AG, paromomycin, was also included in these analyses in light of its high efficacy against the tested ESKAPE isolates.
Ototoxicity was evaluated using in-vitro and in-vivo models. The otic OC-k3 and HEI-OC1 cell lines43,44,45,46,47,48,49,50 were used as the in-vitro models, in addition to cultures of cochlear epithelia. Although derived from the same tissue and at the same developmental stage, it is possible that these cell lines differ regarding the cell types from which they were derived, as has already been described for similar cell lines20. As this might affect the way the cultures respond to treatments, parallel tests were carried out on both. Here, similar data were obtained, although the HEI-OC1 cells were significantly more resistant than the OC-k3 cells to treatments with 5 mM GM and GM C1a. Additionally, 2 mM AG treatment of OC-k3 cells, but not HEI-OC1 cells, indicated lower ototoxicity of GM C1a compared to GM, which was in agreement with the observations on the cochlear explants and in the in-vivo model. Surprisingly, the application of GM or GM C1a to cochlear organotypic cultures resulted in the loss of large proportions of IHCs. This loss was specific to GM and GM C1a throughout the various experimental settings, but was not seen in the in-vivo model. Differences have been observed among AGs in the mechanisms by which they induce HC loss51. Some studies have also shown that IHCs in cochlear explants are more vulnerable than OHCs to, e.g., salicylate treatment or oxygen-glucose deprivation51,52. However, this has not been described for AGs. As this specific sensitivity of IHCs to GMs was not seen in the in-vivo model here, at developmental stages that more closely resembled the clinical setting, no further work was conducted to investigate this in more detail. With regards to apramycin, the results obtained in all of these models indicated a lower toxicity of apramycin compared to the reference AGs neomycin and GM. Different data were obtained for the evaluation of the ototoxic potential of paromomycin. The cell lines and the cochlear explants indicated low toxicity for paromomycin, similar to that of apramycin, while the in-vivo studies demonstrated that it was clearly ototoxic, and comparable to neomycin and GM. Divergent data from in-vitro and in-vivo ototoxicity models have been recorded previously53,54. These might be related to the presence of vulnerable cell types in-vivo that have a role in the overall response to treatment and that are not present in in-vitro models, or to differential differentiation stages and signalling pathways being activated in the in-vitro versus in-vivo models25,55,56,57. Altogether, the in-vivo work here demonstrated lower cochleotoxicity of apramycin and GM C1a, compared to neomycin, GM, and paromomycin.
Application of the AGs is believed to initially cause stereociliary damage, which will be followed by HC loss, mainly of OHCs in the basal (high frequency) region3, which have been considered to date as the most vulnerable element of the inner ear to AG treatment. In addition, some studies have shown damage to the spiral ganglion neurons, which was thought to occur secondary to HC loss58,59. On the other hand, recent animal studies have shown that noise exposure can lead to spiral ganglion neuron degeneration, even when HCs recover and thresholds return to normal32. In noise-exposed ears showing no acute or chronic HC loss, a reduction of up to 50% of the synapses between IHCs and cochlear neurons can occur. The same primary loss of cochlear synapses occurs in the aging ear17,60. This cochlear synaptopathy has been termed “hidden” because cochlear neural degeneration does not cause behavioural changes or elevated electrophysiological thresholds until it becomes extreme61,62. Thus, the concept of “hidden hearing loss” refers to a disorder where a pure tone audiogram fails to detect any existing cochlear pathology and auditory processing deficits32,63,64. In these instances, although there is poor auditory speech recognition due to loss of cochlear synapses to IHCs and auditory nerve degeneration, normal hearing thresholds are maintained64.
Regarding this aspect, it is interesting that the IHC synaptic ribbons that form between IHCs and spiral ganglion neurons can be damaged following AG treatment, and independently from OHC loss. This feature adds support to previous speculation about IHCs being the primary vulnerable element to AG applications in the inner ear65. In our present in-vivo studies, the animals receiving 60 mg/mL neomycin, GM or paromomycin (and not those receiving 60 mg/mL apramycin or GM 1Ca) showed decreased numbers of IHC synaptic ribbons and reduced CAP amplitude in the absence of HC loss. These observations are interesting for several reasons:
They confirm previously reported data that established a relationship between the amplitude of cochlear neural responses, such as auditory brainstem responses, and IHC synaptic ribbon loss, with both affected by aging60 and noise exposure32, and independent of hearing threshold loss66. We here used CAPs, which detect population responses of all of the auditory nerve fibers synchronously, which respond to an auditory stimulation of increasing sound pressure levels. The nature of this extracellular potential determines the response characteristic; i.e., more auditory fibers are activated with increasing sound pressure level. This leads to increase in the CAP amplitudes. Where fibers are not activated because their synaptic contact to the IHC is lost (e.g., in animal models of reduced ribbon counts or ribbon size in the presynapse67, using e.g. ouabain intoxication), a dose-dependent reduction in the size of the CAP amplitude is observed67. We can thus assume a direct association between the observed altered CAP amplitudes following AG treatment and the auditory nerve fiber contribution to the CAP response.
Our present in-vivo data demonstrate that animals that received 60 mg/mL neomycin, GM or paromomycin, but not those receiving 60 mg/mL apramycin or GM 1Ca, showed decreased SP amplitudes as a result of MET alterations, in parallel to decreased numbers of IHC ribbons and decreased CAP amplitude. As the SP/CAP amplitude ratio is not changed, both events may be related. When the AGs were applied at higher concentrations, they affected OHC survival with a strong decreasing gradient from the basal to the apical cochlear turns, which mainly means that OHCs in the basal cochlear turn are affected. In the basal cochlear turns (which represent higher frequencies) the SP is mainly generated by IHCs, at least at moderate intensities37,39. At higher frequencies, OHCs only contribute to the SP at high intensities (e.g., 110 dB sound pressure level). In the present study, the SP recordings were analyzed at 22.6 kHz and 80 dB sound pressure level, settings under which an OHC contribution should be minimal, or even absent.
Moreover, our data strongly support the concept that whether systemically or locally applied, AGs probably result in similar damage to the integrity of the IHC synapse, which will endanger IHC ribbon stability. Indeed, previous studies have shown IHC ribbon loss 2 weeks after an intraperitoneal injection of gentamicin65, which supports the concept that AGs can similarly affect IHC synapse integrity following systemic (intraperitoneal) or local application. In the absence of sufficient published data, we cannot however exclude that systemic administration of the lower concentrations of AGs might have yielded different results from the synaptopathy observed following the round window application; it is also hard to predict outcomes in human patients, which emphasizes the urgent need to attract industrial partners who can invest their efforts in the scaling up of isolation procedures, which is a step of great importance for patients in need of safer antibacterials.
For the mode of entry of AGs into HCs, two mechanisms have been proposed to date68,69,70: entry through the MET channels, which is regarded as the main route; and endocytosis. HC loss following AG entry appears to be mediated by mitochondrial dysfunction16,71, generation of reactive oxygen species3, and caspase activation72,73. It would thus be of interest to investigate whether the lower ototoxicity of apramycin and GM C1a might result from reduced affinity for MET channels, as has been demonstrated for some new sisomicin derivatives6,16,69,74,75,76. Indeed, although previous studies indicated ribbon loss following systemic treatment with 100 mg/kg GM, - loss that was not accompanied by any effects on stereocilia77-, we cannot exclude that structural damage to stereocilia rather than MET channel dysfunction affected SPs and CAP amplitudes following our AG administration protocol. This question can be addressed in future studies (e.g., using FM1-43X dye uptake assays).
In summary, this study has demonstrated the lower ototoxicity of the AGs apramycin and GM C1a, compared to those of the clinically used neomycin and GM. This translates into higher OHC survival and smaller changes in CAP thresholds following their application. Moreover, our studies have unveiled the potential of low concentrations of the AGs neomycin, GM and paromomycin to damage the IHC synapse and reduce CAP amplitudes preceding any damage to the OHCs. Gentamicin-induced loss of ribbon structures at the IHC has been observed before77,78. However, to date, no AGs have been differentially compared in terms of their potential to induce IHC synaptopathy, nor have auditory nerve functions been analysed to possibly link functional changes to damage to the IHC synapse. We observed reduced CAP amplitudes (but not CAP thresholds) linked to IHC ribbon loss upon AG treatment. The CAP amplitude changes might be reflected in supra-threshold ABR wave fine structures, which are currently not examined in routine clinical audiometry investigations. A decrease in SP amplitude following application of high AG concentrations was also indicative of the ongoing IHC dysfunction and altered mechanoelectrical transduction caused by AGs. While further studies are essential to analyse the effects of AGs on IHCs in more detail, our data point to the IHC as the primary target of AG treatment in the inner ear. The findings also emphasize the urgent need to consider the evaluation of supra-threshold ABR wave fine structure analysis as an approach for preclinical ototoxicity tests of AGs, as well as studying possible long-term ototoxic side effects of AGs in the clinic.
However, no IHC alterations were observed with apramycin or GM C1a, which further underlines the lower ototoxic potential of these compounds. Importantly, these AGs showed similar efficacies to neomycin and GM against a panel of ESKAPE pathogens. Based on these data, apramycin and GM C1a have potent antibacterial activities and low ototoxic potential, and thus they represent excellent starting points for chemical derivatization. Apramycin is already produced on an industrial scale as a veterinary product, and it is thus available in sufficient quantities. On the other hand, it is also highly relevant that the industrial production of individual AG congeners, such as GM C1a, can now be achieved following manual chemical derivatization79. Improvements in the biosynthetic processes for the production of individual components like GM C1a might therefore allow the industrial production of economically affordable antibiotics80. Although there are other pharmacological properties that apramycin and GM C1a will need to be evaluated for, such as their nephrotoxicity, the present data warrant further studies into these two AGs as promising candidates for translation into the clinical setting.
Aminoglycoside antibiotics and isolation of the congener GM C1a
Apramycin, GM and Neomycin were purchased from Glentham Life Sciences Ltd (UK); Paromomycin was purchased from AK Scientific Inc. (USA). Isolation of the GM C1a congener was carried out based on the procedure described by Grote and Johnson (2012)79. Benzyl chloroformate (Cbz)-protected derivatives of the GM complex were prepared so that they predominantly contained GM congeners of the C-series (see Supplementary Fig. S1), and these were separated by preparative HPLC (Supplementary Fig. S1). This strategy, followed by Cbz-deprotection (hydrogenation) and subsequent treatment with sulfuric acid, permitted the isolation of GM C1a in a pure form, as the sulfate salts (Supplementary Figs S2, S3). We established an efficient protocol for the isolation of gram quantities of the GM 1Ca congener, as described in the Supplementary Information.
For the evaluation of antibacterial activities and in-vitro ototoxicity testing, AGs were dissolved in distilled water at 50 mg/mL and sterilized by filtration. For in-vivo testing the AGs were prepared at three different concentrations (100, 350, 700 mg/mL) in demineralized water containing 1% polyethylene glycol (Sigma-Aldrich, St. Louis, MO, USA). Before surgery, each AG stock solution was diluted 3:2 in a 20% solution of Poloxamer 407 (Sigma-Aldrich, St. Louis, MO, USA), which provided 60, 210 and 420 mg/mL AG preparations in 1% polyethylene glycol and 20% Poloxamer 40725
Antibacterial activities of the selected aminoglycoside antibiotics against multidrug-resistant clinical isolates
Clinical isolates used in this study
A collection of 61 MDR isolates (as previously defined Magiorakos et al.)81 were cultured from clinical samples (one isolate per patient) from the bacterial collection of the clinical microbiology laboratory of the University Hospital Marqués de Valdecilla (Santander, Spain). The organisms were identified with the Vitek-2 system (BioMérieux, France), following the manufacturer indications, and were conserved at −80 °C in tryptic soy broth with 10% glycerol. ESKAPE refers to a series of bacterial pathogens that are associated with antimicrobial resistance: Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, and Enterobacter species. The following ESKAPE species with the indicated relevant resistance phenotypes were studied: 15 Escherichia coli, 10 of which produced extended-spectrum β-lactamases (ESBL), while 5 were not ESBL producers; 15 K. pneumoniae, 10 as ESBL producers, and 5 not ESBL producers; 11 P. aeruginosa, 7 as carbapenem resistant and 4 as carbapenem susceptible; 10 A. baumannii, as 5 carbapenem resistant and 5 as carbapenem susceptible; and 10 S. aureus, five as resistant to methicillin and five as susceptible to methicillin. Enterococcus spp. were not tested in this study, as these organisms are considered to be intrinsically resistant to AGs.
Antimicrobial susceptibility testing
Minimum inhibitory concentrations (MICs) of the five tested AGs were determined using in-house standardized broth microdilution, following CLSI guidelines (CLSI, 2012). Antimicrobial agents were tested in the range of 64 mg/L to 0.5 mg/L. After bacterial inoculation, the plates were incubated in air at 35 °C for 20 h. The MICs were read visually as the lowest concentration of AG inhibiting bacterial growth. E. coli ATCC 25922, P. aeruginosa ATCC 27853, and S. aureus ATCC 29213 were used as control strains. The MIC values calculated corresponded to concentrations that inhibited 50% (MIC50) and 90% (MIC90) of the 61 isolates.
In-vitro ototoxicity testing
Cell cultures and viability tests
The auditory OC-k3 and HEI-OC1 cell lines were cultured according to Kalinec et al.82, in high-glucose Dulbecco’s modified Eagle’s medium (Gibco, Grand Island, NY, USA) supplemented with 2 mM glutamine and 10% fetal bovine serum (Gibco, Grand Island, NY, USA), and in the absence of antibiotics. The cells were passaged at a density of 2 × 105 cells/mL and maintained under permissive conditions (i.e., 33 °C and 10% CO2, with addition of 50 U/mL interferon-γ (Sigma-Aldrich, St. Louis, MO, USA) to OC-k3 cultures).
When conducting MTT (Sigma Aldrich (St. Louis, MO, USA)) and ATP-based (Promega Corp, Madison, WI, USA) viability assays, the cells were plated onto 96-well flat-bottom plates (100 μL cell suspension/well) 24 h prior to AG treatment. Viability measurements were carried out following the manufacturer instruction.
The animal care, use and experimental protocols followed the national and institutional guidelines, and were reviewed and approved by the Animal Welfare Commissioner and the Regional Board of Animal Experimentation at the University of Tübingen and the University of Valladolid. All of the experiments were performed according to European Union Directive 2010/63/EU for the protection of animals used for experimental and other scientific purposes.
Organotypic cochlear cultures
Cochlear explants were prepared from postnatal day 3 (P3) C57/BL6 mice, according to the protocol described in Chen et al.83. Forty-eight hours after plating, they were treated with 0.1 mM AG for an additional 23 h, and subsequently fixed to stain the actin filaments in the stereocilia of the surviving HCs, with FITC-conjugated phalloidin (Molecular Probes Inc., Life Technologies, Eugene, OR, USA). Detailed information is provided in the Supplementary Information.
In-vivo ototoxicity testing
Animals and experimental groups
Forty-eight adult guinea pigs that weighed between 350 and 600 g were used (pigmented, BFA bunt) and bred in an in-house animal facility, according to the German ‘Law on Protecting Animals’ (Tierschutzgesetz) and in line with European Directive 2010/63/EU for the protection of animals used for experimental purposes. Three animals were treated with each AG concentration (60, 210, 420 mg/mL). The AG solutions were applied bilaterally (i.e., six ears analysed per group).
All animals were anesthetized with an intramuscular injection of a mixture of fentanyl citrate (0.025 mg/kg; Fentadon, Eurovet Animal Health), midazolam (0.2 mg/kg; Midazolam-Ratiopharm, Ratiopharm) and medetomidine hydrochloride (Sedator, 1 mg/kg; EurovetAnimalHealth). Additional doses (20% of the initial dose) were applied as necessary after 2 h. During surgery and routine functional measurements, the animals were placed on a heating pad to maintain their temperature at 37 °C. An incision was made bilaterally in the post-auricular region to expose the otic bulla, and then a small hole was made in the bulla to identify the round window and the basal turn of the cochlea.
For functional measurements, an insulated 0.125-mm-diameter gold wire (Goodfellow, Cambridgeshire, UK) with a small hook at one end was placed at the ridge above the round window. Bilaterally implanted electrodes were connected to a percutaneous socket, and then fixed with dental cement to the vertex.
Once normal hearing was confirmed in each animal through functional measurements, the AG solution (10 μL) was delivered bilaterally to the round window membrane of the cochlea. A micromanipulator was used to place a 20 μL microloader pipette tip (Eppendorf, catalogue no. 5242-956.003) on the round window, which was connected to a 50 μL Hamilton syringe. The pipette tip was removed 15 min after the application, and then the bulla was sealed with dental acrylic, followed by suturing of the skin. Once the surgery and the functional measurements were completed, the anesthesia was antagonized using a subcutaneous (s.c.) injection of a mixture of Naloxan (0.03 mg/kg), Flumazenil (0.1 mg/kg), and Atipamezol (1 mg/kg). For three consecutive days following surgery, the animals were given Meloxicam (analgesic, 0.5 mg/kg, s.c) and Enrofloxacin (antibiotic, 10 mg/kg, oral).
Functional measurement and data collection procedures
Functional measurements were performed at five time points (before application, 60−90 min, days 7, 14, 21). Measurements of CAPs were carried out under anesthesia in a soundproof chamber, and performed as described previously24 (Supplementary Information).
Tissue preparation, immunohistochemistry, and hair cell and ribbon counts
The animals were euthanized 21 days after AG application, while under deep anesthesia using an overdose of Narcoren (4 mL/kg). Then, the cochlear samples were collected, preserved, permeabilized, and blocked, as described previously84. The cochlear tissues were stained to detect the CtBP2 (C-terminal-binding protein 2), as described in Supplementary Information.
The in-vitro tests were each carried out in triplicate, for a minimum of three experiments (n = 3–8) carried out with each compound. All of the data are presented as means ± SD. Students’ t-tests were used to compare two groups, and two-way ANOVA with Holm-Sidak post-hoc analysis was used to compare three or more groups. The statistical software used was SigmaPlot v.11.0 (Systat). Values of p < 0.05 were considered to be statistically significant.
When evaluating the functional and histological data obtained from the in-vivo study, one-way ANOVA with Tukey’s multiple comparisons was used. To evaluate the correlation between the outcome variables and the histological findings, Pearsons correlations were used. All of the statistical analyses were performed using a commercially available software package (GraphPad Prism, GraphPad Software Inc., La Jolla, CA, USA). Values of p < 0.05 were considered to be statistically significant. All data are presented as means ± SD.
The datasets generated and/or analyzed during the current study are available from the corresponding authors upon request.
Maura, D., Ballok, A. E. & Rahme, L. G. Considerations and caveats in anti-virulence drug development. Current opinion in microbiology 33, 41–46, https://doi.org/10.1016/j.mib.2016.06.001 (2016).
Tacconelli, E. et al. Discovery, research, and development of new antibiotics: the WHO priority list of antibiotic-resistant bacteria and tuberculosis. The Lancet. Infectious diseases 18, 318–327, https://doi.org/10.1016/S1473-3099(17)30753-3 (2018).
Forge, A. & Schacht, J. Aminoglycoside antibiotics. Audiol Neurootol 5, 3–22, 13861 (2000).
Huth, M. E., Ricci, A. J. & Cheng, A. G. Mechanisms of aminoglycoside ototoxicity and targets of hair cell protection. Int J Otolaryngol 2011, 937861, https://doi.org/10.1155/2011/937861 (2011).
Cooper, M. A. & Shlaes, D. Fix the antibiotics pipeline. Nature 472, 32, https://doi.org/10.1038/472032a (2011).
Huth, M. E. et al. Designer aminoglycosides prevent cochlear hair cell loss and hearing loss. J Clin Invest 125, 583–592, https://doi.org/10.1172/JCI77424 (2015).
Vidal, L. et al. Efficacy and safety of aminoglycoside monotherapy: systematic review and meta-analysis of randomized controlled trials. J Antimicrob Chemother 60, 247–257, https://doi.org/10.1093/jac/dkm193 (2007).
Becker, B. & Cooper, M. A. Aminoglycoside antibiotics in the 21st century. ACS Chem Biol 8, 105–115, https://doi.org/10.1021/cb3005116 (2013).
Burnham, C. D., Leeds, J., Nordmann, P., O’Grady, J. & Patel, J. Diagnosing antimicrobial resistance. Nature reviews. Microbiology 15, 697–703, https://doi.org/10.1038/nrmicro.2017.103 (2017).
Sundar, S., Jha, T. K., Thakur, C. P., Sinha, P. K. & Bhattacharya, S. K. Injectable paromomycin for Visceral leishmaniasis in India. N Engl J Med 356, 2571–2581, https://doi.org/10.1056/NEJMoa066536 (2007).
van Hellemond, J. J., Molhoek, N., Koelewijn, R., Wismans, P. J. & van Genderen, P. J. Is paromomycin the drug of choice for eradication of Blastocystis in adults? J Infect Chemother 19, 545–548, https://doi.org/10.1007/s10156-012-0496-2 (2013).
Phongsamran, P. V., Kim, J. W., Cupo Abbott, J. & Rosenblatt, A. Pharmacotherapy for hepatic encephalopathy. Drugs 70, 1131–1148, https://doi.org/10.2165/10898630-000000000-00000 (2010).
Ramirez, M. S. & Tolmasky, M. E. Aminoglycoside modifying enzymes. Drug resistance updates: reviews and commentaries in antimicrobial and anticancer chemotherapy 13, 151–171, https://doi.org/10.1016/j.drup.2010.08.003 (2010).
Kobayashi, M., Umemura, M., Sone, M. & Nakashima, T. Differing effects on the inner ear of three gentamicin compounds: GM-C1, -C2 and -C1a. Acta oto-laryngologica 123, 916–922 (2003).
Kobayashi, M. et al. Comparisons of cochleotoxicity among three gentamicin compounds following intratympanic application. Acta oto-laryngologica 128, 245–249, https://doi.org/10.1080/00016480701558948 (2008).
Matt, T. et al. Dissociation of antibacterial activity and aminoglycoside ototoxicity in the 4-monosubstituted 2-deoxystreptamine apramycin. Proceedings of the National Academy of Sciences of the United States of America 109, 10984–10989, https://doi.org/10.1073/pnas.1204073109 (2012).
Viana, L. M. et al. Cochlear neuropathy in human presbycusis: Confocal analysis of hidden hearing loss in post-mortem tissue. Hearing research 327, 78–88, https://doi.org/10.1016/j.heares.2015.04.014 (2015).
Smith, K. P. & Kirby, J. E. Verification of an Automated, Digital Dispensing Platform for At-Will Broth Microdilution-Based Antimicrobial Susceptibility Testing. Journal of clinical microbiology 54, 2288–2293, https://doi.org/10.1128/JCM.00932-16 (2016).
Jat, P. S. et al. Direct derivation of conditionally immortal cell lines from an H-2Kb-tsA58 transgenic mouse. Proceedings of the National Academy of Sciences of the United States of America 88, 5096–5100 (1991).
Kalinec, F., Kalinec, G., Boukhvalova, M. & Kachar, B. Establishment and characterization of conditionally immortalized organ of corti cell lines. Cell Biol Int 23, 175–184, https://doi.org/10.1006/cbir.1998.0339 (1999).
Rivolta, M. N. & Holley, M. C. Cell lines in inner ear research. J Neurobiol 53, 306–318, https://doi.org/10.1002/neu.10111 (2002).
Richardson, G. P. & Russell, I. J. Cochlear cultures as a model system for studying aminoglycoside induced ototoxicity. Hearing research 53, 293–311 (1991).
Lowenheim, H., Kil, J., Gultig, K. & Zenner, H. P. Determination of hair cell degeneration and hair cell death in neomycin treated cultures of the neonatal rat cochlea. Hearing research 128, 16–26 (1999).
Muller, M., Tisch, M., Maier, H. & Lowenheim, H. Reduction of permanent hearing loss by local glucocorticoid application: Guinea pigs with acute acoustic trauma. Hno 65, 59–67, https://doi.org/10.1007/s00106-016-0266-z (2017).
El Kechai, N. et al. Recent advances in local drug delivery to the inner ear. Int J Pharm 494, 83–101, https://doi.org/10.1016/j.ijpharm.2015.08.015 (2015).
Stevens, D. M., Dutka, A. J. & Snyder, J. E. Vestibulo-ocular reflex gain as a measure of vestibular function in guinea pigs while in a recompression chamber: apparatus design and effects of nitrogen narcosis. The American journal of otology 16, 360–364 (1995).
Yorgason, J. G., Fayad, J. N. & Kalinec, F. Understanding drug ototoxicity: molecular insights for prevention and clinical management. Expert opinion on drug safety 5, 383–399, https://doi.org/10.1517/147403220.127.116.113 (2006).
Murillo-Cuesta, S. et al. Direct drug application to the round window: a comparative study of ototoxicity in rats. Otolaryngology–head and neck surgery: official journal of American Academy of Otolaryngology-Head and Neck Surgery 141, 584–590, https://doi.org/10.1016/j.otohns.2009.07.014 (2009).
Tasaki, I. Nerve impulses in individual auditory nerve fibers of guinea pig. Journal of neurophysiology 17, 97–122 (1954).
Ruttiger, L., Zimmermann, U. & Knipper, M. Biomarkers for Hearing Dysfunction: Facts and Outlook. ORL; journal for oto-rhino-laryngology and its related specialties 79, 93–111, https://doi.org/10.1159/000455705 (2017).
El-Badry, M. M. & McFadden, S. L. Electrophysiological correlates of progressive sensorineural pathology in carboplatin-treated chinchillas. Brain Res 1134, 122–130, https://doi.org/10.1016/j.brainres.2006.11.078 (2007).
Kujawa, S. G. & Liberman, M. C. Adding insult to injury: cochlear nerve degeneration after “temporary” noise-induced hearing loss. J Neurosci 29, 14077–14085, https://doi.org/10.1523/JNEUROSCI.2845-09.2009 (2009).
Durrant, J. D., Wang, J., Ding, D. L. & Salvi, R. J. Are inner or outer hair cells the source of summating potentials recorded from the round window? J Acoust Soc Am 104, 370–377 (1998).
Zheng, X. Y., Ding, D. L., McFadden, S. L. & Henderson, D. Evidence that inner hair cells are the major source of cochlear summating potentials. Hearing research 113, 76–88 (1997).
Liberman, M. C. Auditory-nerve response from cats raised in a low-noise chamber. J Acoust Soc Am 63, 442–455 (1978).
Oates, P. & Stapells, D. R. Frequency specificity of the human auditory brainstem and middle latency responses to brief tones. I. High-pass noise masking. J Acoust Soc Am 102, 3597–3608 (1997).
Russell, I. J. & Sellick, P. M. Low-frequency characteristics of intracellularly recorded receptor potentials in guinea-pig cochlear hair cells. J Physiol 338, 179–206 (1983).
Cody, A. R. & Russell, I. J. The response of hair cells in the basal turn of the guinea-pig cochlea to tones. J Physiol 383, 551–569 (1987).
Russell, I. J. & Kossl, M. Sensory transduction and frequency selectivity in the basal turn of the guinea-pig cochlea. Philos Trans R Soc Lond B Biol Sci 336, 317–324, https://doi.org/10.1098/rstb.1992.0064 (1992).
Patuzzi, R. B., Yates, G. K. & Johnstone, B. M. Outer hair cell receptor current and sensorineural hearing loss. Hearing research 42, 47–72 (1989).
Santarelli, R. et al. Abnormal cochlear potentials from deaf patients with mutations in the otoferlin gene. Journal of the Association for Research in Otolaryngology: JARO 10, 545–556, https://doi.org/10.1007/s10162-009-0181-z (2009).
Liberman, M. C., Epstein, M. J., Cleveland, S. S., Wang, H. & Maison, S. F. Toward a Differential Diagnosis of Hidden Hearing Loss in Humans. PLoS One 11, e0162726, https://doi.org/10.1371/journal.pone.0162726 (2016).
Previati, M. et al. Cisplatin cytotoxicity in organ of Corti-derived immortalized cells. J Cell Biochem 101, 1185–1197, https://doi.org/10.1002/jcb.21239 (2007).
Low, W. K., Sun, L., Tan, M. G., Chua, A. W. & Wang, D. Y. L-N-Acetylcysteine protects against radiation-induced apoptosis in a cochlear cell line. Acta oto-laryngologica 128, 440–445, https://doi.org/10.1080/00016480701762490 (2008).
Low, W. K., Kong, S. W. & Tan, M. G. Ototoxicity from combined Cisplatin and radiation treatment: an in vitro study. Int J Otolaryngol 2010, 523976, https://doi.org/10.1155/2010/523976 (2010).
Shin, Y. S. et al. A novel synthetic compound, 3-amino-3-(4-fluoro-phenyl)-1H-quinoline-2,4-dione, inhibits cisplatin-induced hearing loss by the suppression of reactive oxygen species: in vitro and in vivo study. Neuroscience 232, 1–12, https://doi.org/10.1016/j.neuroscience.2012.12.008 (2013).
Kim, Y. J. et al. Prevention of cisplatin-induced ototoxicity by the inhibition of gap junctional intercellular communication in auditory cells. Cell Mol Life Sci 71, 3859–3871, https://doi.org/10.1007/s00018-014-1594-3 (2014).
Kalinec, G., Thein, P., Park, C. & Kalinec, F. HEI-OC1 cells as a model for investigating drug cytotoxicity. Hearing research 335, 105–117, https://doi.org/10.1016/j.heares.2016.02.019 (2016).
Kalinec, G. M., Park, C., Thein, P. & Kalinec, F. Working with Auditory HEI-OC1 Cells. J Vis Exp, https://doi.org/10.3791/54425 (2016).
Teitz, T., Goktug, A. N., Chen, T. & Zuo, J. Development of Cell-Based High-Throughput Chemical Screens for Protection Against Cisplatin-Induced Ototoxicity. Methods Mol Biol 1427, 419–430, https://doi.org/10.1007/978-1-4939-3615-1_22 (2016).
Mazurek, B., Lou, X., Olze, H., Haupt, H. & Szczepek, A. J. In vitro protection of auditory hair cells by salicylate from the gentamicin-induced but not neomycin-induced cell loss. Neuroscience letters 506, 107–110, https://doi.org/10.1016/j.neulet.2011.10.060 (2012).
Amarjargal, N. et al. Differential vulnerability of outer and inner hair cells during and after oxygen-glucose deprivation in organotypic cultures of newborn rats. Physiological research 58, 895–902 (2009).
Oishi, N., Kendall, A. & Schacht, J. Metformin protects against gentamicin-induced hair cell death in vitro but not ototoxicity in vivo. Neuroscience letters 583, 65–69, https://doi.org/10.1016/j.neulet.2014.09.028 (2014).
Roldan-Fidalgo, A. et al. In vitro and in vivo effects of lutein against cisplatin-induced ototoxicity. Exp Toxicol Pathol 68, 197–204, https://doi.org/10.1016/j.etp.2016.01.003 (2016).
Francis, S. P. & Cunningham, L. L. Non-autonomous Cellular Responses to Ototoxic Drug-Induced Stress and Death. Frontiers in cellular neuroscience 11, 252, https://doi.org/10.3389/fncel.2017.00252 (2017).
Wood, M. B. & Zuo, J. The Contribution of Immune Infiltrates to Ototoxicity and Cochlear Hair Cell Loss. Frontiers in cellular neuroscience 11, 106, https://doi.org/10.3389/fncel.2017.00106 (2017).
Sun, S. et al. Inhibition of the activation and recruitment of microglia-like cells protects against neomycin-induced ototoxicity. Molecular neurobiology 51, 252–267, https://doi.org/10.1007/s12035-014-8712-y (2015).
Duan, M., Agerman, K., Ernfors, P. & Canlon, B. Complementary roles of neurotrophin 3 and a N-methyl-D-aspartate antagonist in the protection of noise and aminoglycoside-induced ototoxicity. Proceedings of the National Academy of Sciences of the United States of America 97, 7597–7602 (2000).
Bae, W. Y., Kim, L. S., Hur, D. Y., Jeong, S. W. & Kim, J. R. Secondary apoptosis of spiral ganglion cells induced by aminoglycoside: Fas-Fas ligand signaling pathway. Laryngoscope 118, 1659–1668, https://doi.org/10.1097/MLG.0b013e31817c1303 (2008).
Sergeyenko, Y., Lall, K., Liberman, M. C. & Kujawa, S. G. Age-related cochlear synaptopathy: an early-onset contributor to auditory functional decline. J Neurosci 33, 13686–13694, https://doi.org/10.1523/JNEUROSCI.1783-13.2013 (2013).
Woellner, R. C. & Schuknecht, H. F. Hearing loss from lesions of the cochlear nerve: an experimental and clinical study. Trans Am Acad Ophthalmol Otolaryngol 59, 147–149 (1955).
Lobarinas, E., Salvi, R. & Ding, D. Insensitivity of the audiogram to carboplatin induced inner hair cell loss in chinchillas. Hearing research 302, 113–120, https://doi.org/10.1016/j.heares.2013.03.012 (2013).
Schaette, R. & McAlpine, D. Tinnitus with a normal audiogram: physiological evidence for hidden hearing loss and computational model. J Neurosci 31, 13452–13457, https://doi.org/10.1523/JNEUROSCI.2156-11.2011 (2011).
Plack, C. J., Barker, D. & Prendergast, G. Perceptual consequences of “hidden” hearing loss. Trends Hear 18, https://doi.org/10.1177/2331216514550621 (2014).
Liu, K. et al. Cochlear inner hair cell ribbon synapse is the primary target of ototoxic aminoglycoside stimuli. Molecular neurobiology 48, 647–654, https://doi.org/10.1007/s12035-013-8454-2 (2013).
Moser, T. & Starr, A. Auditory neuropathy–neural and synaptic mechanisms. Nat Rev Neurol 12, 135–149, https://doi.org/10.1038/nrneurol.2016.10 (2016).
Bourien, J. et al. Contribution of auditory nerve fibers to compound action potential of the auditory nerve. Journal of neurophysiology 112, 1025–1039, https://doi.org/10.1152/jn.00738.2013 (2014).
Alharazneh, A. et al. Functional hair cell mechanotransducer channels are required for aminoglycoside ototoxicity. PLoS One 6, e22347, https://doi.org/10.1371/journal.pone.0022347 (2011).
Marcotti, W., van Netten, S. M. & Kros, C. J. The aminoglycoside antibiotic dihydrostreptomycin rapidly enters mouse outer hair cells through the mechano-electrical transducer channels. J Physiol 567, 505–521, https://doi.org/10.1113/jphysiol.2005.085951 (2005).
Hashino, E. & Shero, M. Endocytosis of aminoglycoside antibiotics in sensory hair cells. Brain Res 704, 135–140 (1995).
Shulman, E. et al. Designer aminoglycosides that selectively inhibit cytoplasmic rather than mitochondrial ribosomes show decreased ototoxicity: a strategy for the treatment of genetic diseases. J Biol Chem 289, 2318–2330, https://doi.org/10.1074/jbc.M113.533588 (2014).
Cheng, A. G., Cunningham, L. L. & Rubel, E. W. Hair cell death in the avian basilar papilla: characterization of the in vitro model and caspase activation. Journal of the Association for Research in Otolaryngology: JARO 4, 91–105, https://doi.org/10.1007/s10162-002-3016-8 (2003).
Cunningham, L. L., Cheng, A. G. & Rubel, E. W. Caspase activation in hair cells of the mouse utricle exposed to neomycin. J Neurosci 22, 8532–8540 (2002).
Kros, C. J., Rusch, A. & Richardson, G. P. Mechano-electrical transducer currents in hair cells of the cultured neonatal mouse cochlea. Proc Biol Sci 249, 185–193, https://doi.org/10.1098/rspb.1992.0102 (1992).
Ricci, A. Differences in mechano-transducer channel kinetics underlie tonotopic distribution of fast adaptation in auditory hair cells. Journal of neurophysiology 87, 1738–1748, https://doi.org/10.1152/jn.00574.2001 (2002).
Duscha, S. et al. Identification and evaluation of improved 4′-O-(alkyl) 4,5-disubstituted 2-deoxystreptamines as next-generation aminoglycoside antibiotics. MBio 5, e01827–01814, https://doi.org/10.1128/mBio.01827-14 (2014).
Liu, K. et al. Dynamic distribution of ototoxic gentamicin entry into inner hair cells of mice. Acta oto-laryngologica 134, 345–351, https://doi.org/10.3109/00016489.2013.875219 (2014).
Chen, L., Xiong, S., Liu, Y. & Shang, X. Effect of different gentamicin dose on the plasticity of the ribbon synapses in cochlear inner hair cells of C57BL/6J mice. Molecular neurobiology 46, 487–494, https://doi.org/10.1007/s12035-012-8312-7 (2012).
Grote, J. & Johnson, H. R. D. Methodology for the rapid separation of gentamicin components and regiospecific synthesis of gentamicin conjugates. Tetrahedron Letters 53, 6751–6754, https://doi.org/10.1016/j.tetlet.2012.09.113 (2012).
Li, S. et al. Methyltransferases of gentamicin biosynthesis. Proceedings of the National Academy of Sciences of the United States of America 115, 1340–1345, https://doi.org/10.1073/pnas.1711603115 (2018).
Magiorakos, A. P. et al. Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance. Clin Microbiol Infect 18, 268–281, https://doi.org/10.1111/j.1469-0691.2011.03570.x (2012).
Kalinec, G. M., Webster, P., Lim, D. J. & Kalinec, F. A cochlear cell line as an in vitro system for drug ototoxicity screening. Audiol Neurootol 8, 177–189, 71059 (2003).
Chen, F. Q., Schacht, J. & Sha, S. H. Aminoglycoside-induced histone deacetylation and hair cell death in the mouse cochlea. J Neurochem 108, 1226–1236, https://doi.org/10.1111/j.1471-4159.2009.05871.x (2009).
Bako, P. et al. Methyl methacrylate embedding to study the morphology and immunohistochemistry of adult guinea pig and mouse cochleae. J Neurosci Methods 254, 86–93, https://doi.org/10.1016/j.jneumeth.2015.07.017 (2015).
This study was supported by TRIH grants/Action on Hearing Loss (Grant No. Project No. T3_Petkovic), the Deutsche Forschungsgemeinschaft SPP 1608 RU 316/12-1; SPP1608 KN 316/12-1. The authors thank Prof. Federico Kalinec for kindly providing the otic cell lines, and Prof. Jochen Schacht for advice on the organotypic explant work. We also thank Sergio Díez-Hermano for help with the statistical analyses, as well as Cristina Sánchez and Yolanda Noriega for their assistance in confocal microscopy. Dr Marta Fernández-Martínez and Dr Luis Martínez-Martínez are supported by Plan Nacional de I + D + i 2013‐2016 and Instituto de Salud Carlos III, Subdirección General de Redes y Centros de Investigación Cooperativa, Ministerio de Economía, Industria y Competitividad, Spanish Network for Research in Infectious Diseases (REIPI RD16/0016/0007 and RD16/0016/0008, respectively), and co-financed by the European Development Regional Fund “A way to achieve Europe”, Operative Program Intelligent Growth 2014–2020.
Dr. Stefan Fujs and Dr. Gregor Kosec are shareholders of Acies Bio d.o.o. Their work has been funded by Acies Bio d.o.o. Masaaki Ishikawa, Nadia García-Mateo, Alen Čusak, Iris López-Hernández, Marta Fernández-Martínez, Marcus Müller, Lukas Rüttiger, Wibke Singer, Hubert Löwenheim, Luis Martínez-Martínez, Thomas Schimmang, Hrvoje Petković, Marlies Knipper and M. Beatriz Durán-Alonso declare that they have no conflicts of interest or competing financial interests.
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Ishikawa, M., García-Mateo, N., Čusak, A. et al. Lower ototoxicity and absence of hidden hearing loss point to gentamicin C1a and apramycin as promising antibiotics for clinical use. Sci Rep 9, 2410 (2019). https://doi.org/10.1038/s41598-019-38634-3
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