The Armadillo as a Model for Leprosy Nerve Function Impairment: Preventative and Therapeutic Interventions

Mycobacterium leprae infection of peripheral nerves and the subsequent nerve function impairment (NFI), especially in response to reactional episodes, are hallmarks of leprosy. Improved treatments for M. leprae-induced nerve injury are needed, as most if not all of the disability and stigma associated with leprosy arises from the direct or indirect effects of NFI. Nine-banded armadillos (Dasypus novemcinctus), like humans, exhibit the full clinical spectrum of leprosy and extensive involvement of the peripheral nerves. In this study, state-of-the-art technology was used to compare nerve function between uninfected and M. leprae-infected armadillos. Motor nerve conduction velocity (MNCV) and compound muscle action potential (cMAP), which measure changes in the rate of impulse conduction velocity and amplitude, revealed a progression of impairment that was directly correlated with the duration of M. leprae infection and enabled development of an objective nerve impairment scoring system. Ultrasonography accompanied by color Doppler imaging detected enlargement of the M. leprae-infected nerves and increased vascularity, possibly due to inflammation. Assessment of epidermal nerve fiber density (ENFD), which shows a length-dependent innervation in armadillos that is similar to humans, identified small fiber degeneration early after M. leprae infection. Staining for neuromuscular junction (NMJ) integrity, which is an indicator of signal transduction efficiency into skeletal muscle, discerned a markedly lower number and structural integrity of NMJ in M. leprae-infected armadillo footpads. These tools for assessing nerve injury were used to monitor the effects of intervention therapy. Two potential neuro-protective drugs, ethoxyquin (EQ) and 4-aminopyridine (4-AP), were tested for their ability to ameliorate peripheral nerve injury in M. leprae-infected armadillos. 4-AP treatment improved MNCV, cMAP, and EFND compared to untreated animals, while EQ had less effect. These results support the armadillo as a model for M. leprae-induced peripheral nerve injury that can provide insights toward the understanding of NFI progression and contribute to the preclinical investigation of the safety and efficacy of neuro-preventive and neuro-therapeutic interventions for leprosy.

Introduction

Mycobacterium leprae and the closely related Mycobacterium lepromatosis infect the Schwann cells of the peripheral nerves. This infection can result in neuropathy that affects at least a third (1, 2) of the individuals diagnosed with leprosy. Since treatment of the infection often does not lead to resolution of the neuropathy, the number of affected patients is cumulative. Consequently, ∼2 million people currently suffer from leprosy-related nerve function impairment (NFI) (3).

Leprosy neuritis has been well described clinically and histologically for more than 100 years (4–6). In humans, the ulnar, radial, median, and peroneal nerves are primarily involved (7). Robinson et al. (8) reported that the lateral plantar branch of the tibial nerve is also significantly affected. Unfortunately, the mechanisms of nerve injury following M. leprae infection are difficult to study in humans as these nerves cannot be biopsied. Therefore, most investigations have been in human, mouse, and rat Schwann cell tissue culture models (9–11) and to a limited extent in vivo in mice (12). The mouse, however, may not be a suitable model to study M. leprae-induced neuropathy as it is neither naturally susceptible to M. leprae infection, nor does it develop any appreciable nerve involvement (7).

Nine-banded armadillos (Dasypus novemcinctus), as well as red squirrels (13) and chimpanzees (14), can become naturally infected with M. leprae (15–18). Armadillos develop an extensive nerve involvement that closely resembles the neuropathy seen in humans (19, 20). In response to M. leprae infection, the majority (>70%) of armadillos show lepromatous-type disease, but borderline and tuberculoid responses are also found (21, 22).

Standardized tests that measure nerve damage are well established for humans (23) and there has been some use of these tests to evaluate neuropathy in persons affected by leprosy (2, 24–28). Validation of such tests in M. leprae-infected armadillos would support its use as an animal model to study leprosy NFI. Therefore, we present here several methods to assess peripheral neuropathy in armadillos at early, mid and late stages of leprosy disease. These include motor nerve conduction tests (MNCT), such as motor nerve conduction velocity (MNCV) and compound motor action potential (cMAP), peripheral nerve ultrasonography with Doppler imaging, quantification of epidermal nerve fiber density (ENFD), neuropathic changes in muscle physiological cross sectional area (PCSA), and evaluation of neuromuscular junction (NMJ) number and integrity. Following extensive validation of these tools in both uninfected and M. leprae-infected armadillos, two potential neuroprotective drugs were tested in a pilot study to determine the suitability of these methods to evaluate therapeutic interventions to arrest or prevent leprosy neuropathy.

Materials and Methods

Armadillos

Wild captured and captive born (genetically identical) nine-banded armadillos were used in this study. The female armadillo gives birth to four genetically identical siblings, which are hand raised and brought to the NHDP after they are weaned. The use of genetically identical siblings enables a higher statistical power for experimental interventions. All animals were conditioned to our facility for a period of 3–6 months (wild captured) or 12 months (captive born). During conditioning, the armadillos were housed in modified rabbit cages and received the following treatments: Penicillin (2 mL IM repeated at 5 days), Ivermectin (0.1 mL SC), Droncit (0.4 mL IM) and Meticorten (0.25 mL IM). At the end of the conditioning period, they were tested for the presence of anti-Phenolic glycolipid-1 (PGL-1) antibodies to determine the presence of pre-existing M. leprae infection. Armadillos with pre-existing infection were not used in this study. To determine their immune responsiveness to M. leprae, a Lepromin test (heat-killed nude mice footpad derived M. leprae strain Thai-53 at 1 × 10⁸ bacilli in 0.1 mL total volume) was administered by intradermal injection to the abdominal skin. After 21 days, the skin test sites were biopsied using a 4 mm biopsy punch and examined histopathologically to score the reactivity of each animal on the Ridley-Jopling scale (29, 30). Only those animals classified as lepromatous (LL) were included in this study.

Infection of Armadillos With Mycobacterium leprae

Armadillos were experimentally infected via intravenous (IV) inoculation of a suspension of 1 × 10⁹ viable M. leprae freshly harvested from nude mice footpads (31).

Anti-pGL-1 Antibody ELISA

PGL-1 antigen (BEI Resources) was used in immunoassays to detect anti-PGL-1 IgM circulating antibody levels in serum samples as previously described (32). Levels of OD > 0.700 (540 nm) were considered positive.

Light Microscopic and Electron Microscopic Studies

At the time of sacrifice the posterior tibial nerve was collected, fixed in 10% buffered formalin and processed for light microscopic studies, or fixed in 5% glutaraldehyde and processed for electron microscopic studies as previously described (33, 34).

Motor Nerve Conduction Test

Following anesthesia with 0.4 ml Detomidine and 0.6 ml Ketamine, the animals were placed in a wooden trough ventral side up inside a Faraday cage. Skin temperatures were taken on the medial aspect of each hind limb between the knee and hip to ensure that the MNCT tests were done at body temperatures of 31 ± 2.0°C, because high body temperatures (>35°C) can affect the speed of conduction velocity. An infrared thermometer was used to take the body temperature. We adapted a Cadwell Sierra Summit (Cadwell) portable electrophysiology unit for use with the armadillos. 6.5mm gold cup percutaneous electrodes were prepped with Ten20 conductive paste and used as active, reference, and ground electrodes. After the hind limbs were cleaned with alcohol, the reference electrode was placed at the sulcus of the third toe and the active electrode was placed on an intrinsic muscle between the third and fourth metatarsal bones midshaft. The ground electrode was placed on the anterior/lateral aspect of the hind limb. A cortical disposable stimulator (Natus Neurology) was used to produce a motor stimulus. This stimulator has two 2.2 mm gold plated tips with 5 mm spacing. The negative pole of the stimulator was placed posterior to the medial ankle maleolus for the distal stimulation site. Percutaneous stimulation of the posterior tibial nerve was done near the ankle (distal), and near the knee (proximal) on the medial/posterior shaft of the tibia. Measurements were taken from the proximal stimulation site to the active electrode and from the distal stimulation site to the active electrode to measure the distance between the stimulation sites. Recordings were always done at a supramaximal stimulus. Motor nerve conduction velocity (MNCV) was calculated using the formula: MNCV (in m/s) = (Distance between Proximal and Distal stimulation sites)/(Proximal Latency – Distal Latency). Compound Motor Action Potential (cMAP) amplitude was measured from baseline to negative peak and was recorded in millivolts (mV). Room temperature was maintained between 24 and 26°C throughout the procedure.

Ultrasonography of the Peripheral Nerves

Posterior tibial nerves were examined via ultrasonography using a SmartUS transducer probe with a linear broadband frequency of 7.5–15 MHz connected to a Sierra Summit basic system (Cadwell). Color Doppler imaging was used to detect blood flow in the posterior tibial nerves. The colors show the speed and direction of blood flow through the vessel. Flow that travels away from the transducer (negative Doppler shift) is depicted in blue. Flow traveling toward the transducer (positive Doppler shift) is depicted in red. Lighter shades of each color denote higher velocities.

Neuropathic Changes in Muscle Physiological Cross Sectional Area

Following euthanasia, each hind limb was disarticulated at the hip joint and frozen until dissection. The dissection technique used was adapted from Brand et al. (35). The skin, superficial fascia, and fat were removed from the limbs and upper leg muscles were removed for better visualization. Blunt dissection was used to isolate the foot muscles from surrounding tissue. The tendon of insertion was severed distal to the muscle, clamped with a hemostat, and pulled laterally from the tendon of origin. Both tendons were traced into the muscle belly, lightly teasing away the connective tissue holding the muscle in its fusiform shape (Figures 6A,B). This allowed the fibers to align parallel to each other as they course from the tendon of origin to the tendon of insertion. Muscle fibers were measured with a Fowler precision dial caliper. The muscles were severed at their tendon of origin and weighed on an Ohaus scale. The fiber length (in centimeters) and mass (in grams) for each muscle was entered into the following equation to obtain the muscle PCSA: PCSA = Mass/1.02/Fiber length. The PCSA values for each muscle were analyzed along with the MNCT values recorded for the respective hind limb to determine any association.

Evaluation of Neuromuscular Junctions in the Footpad Muscles

Three uninfected and five M. leprae-infected armadillos were used to evaluate integrity and numbers of NMJ in the intrinsic muscles of the hind footpads. Following euthanasia, intrinsic muscles from both hind footpads were carefully dissected and collected in 4% paraformaldehyde at 4°C. After fixing in paraformaldehyde for 4 h, the muscles were incubated overnight in 30% sucrose solution, embedded in OCT (Thermo Fisher Scientific), and stored at -80°C. Thirty μm longitudinal sections were prepared and stained with FITC-labeled Bungarotoxin (Sigma-Aldrich) and PE-labeled anti-myosin antibody (Sigma-Aldrich). A 30 mm² area through the entire thickness of the section was analyzed for the number and integrity of NMJ. Images were captured on an Olympus BX-70 microscope and analyzed using Image Pro software (Dimension, Cellsen).

Quantification of Epidermal Nerve Fiber Density in the Armadillo Hind Limb

Skin biopsies were obtained from the armadillo hind limb using a 3 mm biopsy punch. The biopsy was fixed in Zamboni solution (Newcomer Supply) for 24 h, washed with 0.08 M Sorenson’s phosphate buffer, fixed in cryoprotectant (0.2 M Sorenson’s phosphate buffer and Glycerol), and stored at -20°C. The biopsies were sectioned with a sliding microtome into 50 μm thick, frozen, vertical, free-floating sections. Four sections were randomly selected and immunostained with rabbit anti-PGP 9.5, a pan axonal marker (Chemicon, Temecula, CA, United States dilution 1:10,000). ENFD were determined following established counting rules (36–38).

Evaluation of Effectiveness of Neuroprotective Drugs in Preventing and Improving NFI in Mycobacterium leprae-Infected Armadillos

Five sets (3 pairs and 2 triplets) of M. leprae-infected siblings were randomly allocated into 3 treatment groups as follows: 4-Aminopyridine (4-AP) (N = 4), Ethoxyquin (EQ) (N = 3) and untreated control (N = 5). 4-AP (0.9 mg/day, Sigma-Aldrich) and EQ (2 mg/day, Sigma-Aldrich) were administered orally with the food on a daily basis. The treatment started when the set of animals showed a decrease in cMAP (about 3–7 months post-inoculation) and ended after 60 days. MNCT was performed before, during, and at the end of treatment. At the end of treatment, a 3 mm punch biopsy was collected from the hind leg and fixed in Zamboni fixative. The biopsies were washed, fixed in cryoprotectant, and stored at -80°C for quantification of ENFD.

Statistical Analysis

Mann–Whitney Rank Sum test and Spearman’s rank test was used to compare differences and correlation, respectively, between different groups using either GraphPad Instat software, version 3.10 (GraphPad Software, Inc.) or Sigma Plot version 12.0 (Systat Software, Inc.). p < 0.05 was considered significant.

Results

A total of 154 armadillos were used in this study, including 36 uninfected and 118 that were experimentally infected with M. leprae. All the animals were classified as LL.

Localization of Mycobacterium leprae in the Posterior Tibial Nerve of Infected Armadillos

Armadillos, like humans, exhibit peripheral nerve involvement upon M. leprae infection. Figure 1A depicts a posterior tibial nerve section from a M. leprae-infected armadillo showing the presence of intraneural acid-fast bacilli. Transmission electron microscopy shows M. leprae located inside the unmyelinated (Figure 1B) and myelinated (Figure 1C) Schwann cells. The effects of this nerve invasion, however, are poorly understood in this model. Therefore, in this study we adapted and applied several non-invasive and invasive tests to evaluate the resultant neuropathy.

FIGURE 1

Figure 1. Localization of M. leprae in the posterior tibial nerve of infected armadillos. (A) Posterior tibial nerve showing clumps of intraneural M. leprae (arrows); modified Fite/Faraco stain. Electron micrographs showing M. leprae (M. lep) within unmyelinated (B) and myelinated (C) Schwann cell (SC) located by the axon (AX) in the post-tibial nerve of an armadillo at 24 months post-experimental infection.

Determination of MNCV and cMAP Values in the Posterior Tibial Nerve of Uninfected Armadillos

Twenty-five uninfected armadillos were used to develop and standardize MNCT and obtain the normal values for MNCV and cMAP. Upon evaluation of the posterior tibial nerve of each hind limb, a mean MNCV of 62.09 ± 10.72 m/s (range = 88.24–43.75 m/s) was found, with no significant difference between the right and left hind limbs of an individual animal (Figure 2). The mean proximal amplitude was 1.53 ± 0.30 mV (range = 2.12–1.02 mV) and the mean distal amplitude was 1.55 ± 0.33 mV (range = 2.18–0.98 mV). Again, there were no large discrepancies between the right and left cMAP amplitudes of an individual animal. Based on this data we established that a MNCV of <40 m/s (mean - 2 SD) and a cMAP amplitude of <0.9mV (mean - 2 SD) should be considered abnormal for the posterior tibial nerves in armadillos.

FIGURE 2

Figure 2. Posterior tibial nerve conduction wave forms in uninfected armadillos. Motor Nerve Conduction Tests (MNCT) were performed on the posterior tibial nerve of uninfected armadillos (N = 25) using a Cadwell Sierra Summit portable electrophysiology unit. Representative wave forms are shown of a right posterior tibial (A) and left posterior tibial (B) nerve. Measurements were taken from the proximal stimulation site to the active electrode and distal stimulation site to the active electrode to measure the distance between stimulation sites. Compound muscle action potential (cMAP) was measured from onset (O) to the peak (P) in both ankle and knee in response to supra-maximal electrical stimulation.

Progression of Abnormal MNCV and cMAP in the Posterior Tibial Nerve of Mycobacterium leprae-Infected Armadillos and Development of a MNCT Scoring System

Mycobacterium leprae-infected armadillos began to exhibit a low cMAP (<0.9 mV) at an early stage of infection (∼4 months post-inoculation) (Figure 3A). As the animals progressed to later stages of leprosy disease they showed a further depressed cMAP (Figure 3B) and eventually complete block of conduction at the knee (Figure 3C). A reduction in cMAP (signifying axonal degeneration) was more common than slowing of MNCV (related to demyelination). Importantly, these results indicated that measurable motor nerve conduction deficit, especially reduced cMAP, could occur early in the course of infection in these animals.

FIGURE 3

Figure 3. Posterior tibial nerve conduction wave forms showing reduced compound muscle action potential (cMAP) in M. leprae-infected armadillos. MNCT were performed on the posterior tibial nerves of M. leprae-infected armadillos (N = 71). Representative motor nerve conduction wave forms depict early (A) (4 months infection) and mid (B) (9 months infection) stage leprosy disease and show abnormal wave forms with declining degrees of cMAPs (<0.9 mV). Armadillos progressing to late stage leprosy disease (12–24 months post-inoculation), exhibit conduction block at the knee (C).

Based on these results we developed the following simple qualitative MNCT scoring system to categorize the armadillos according to their MNCV and cMAP abnormal readings in the posterior tibial nerve. The animals with both normal MNCV and cMAP in both hind limbs were arbitrarily assigned a score of 5. Each abnormality, low MNCV or cMAP in each hind limb, was considered as 1-point, which was substracted from the normal score of 5 to obtain the MNCT for a particular animal as follows:

Score 5: animals having no abnormal MNCV or cMAP in either hind limbs.

Score 4: animals having only one abnormality, either slow MNCV (<40 m/s) or low cMAP (< 0.9mV) in only one hind limb.

Score 3: animals having any combination of two abnormal readings in the MNCV and/or cMAP.

Score 2: animals having any combination of three abnormal readings in the MNCV and/or cMAP.

Score 1: animals having abnormal MNCV and cMAP in both right and left hind limbs.

Therefore, an animal showing both abnormal MNCV and cMAP in both hind limbs will have a score of 5–4 = 1, the lowest possible in this system.

Correlation of MNCT With Disease Progression and Anti-PGL-1 Antibody Levels

A set of 20 M. leprae-infected armadillos were individually evaluated for NFI throughout their leprosy disease progression using the MNCT scoring system standardized above. Figure 4A shows the MNCT scores of individual animals at pre-inoculation and at 4, 9, 12, and 24 months post-inoculation. At time 0 (uninfected) all the animals show a score of 5 with no abnormalities in the MNCV or cMAP in either hind limb. The scores began to decrease as early as 4 months post-infection with the majority of animals showing low scores at the late stages of leprosy disease (12 and 24 months post-infection).

FIGURE 4

Figure 4. MNCT scores decrease with duration of infection and correlate with anti-PGL1 antibody titers. A longitudinal study (A) demonstrated negative correlation between the MNCT score and duration of M. leprae infection, indicating progressive nerve injury (N = 20). (B) Phenolic glycolipid I (PGL-1) antigen was used in an enzyme immunoassay to detect anti-PGL1 IgM circulating antibody levels in armadillo serum samples. Armadillos with high (>0.900 OD 540 nm) anti-PGL1 antibody titers have lower MNCT scores, while those with low (0.700–0.900 OD 540 nm) anti-PGL-1 antibody titers have higher MNCT scores (N = 71).

We have previously shown that antibody levels for the M. leprae-specific PGL-1 correlate with bacterial load in armadillos (39–41). In order to determine the correlation between anti-PGL-1 antibody levels and impaired nerve conduction, we stratified 71 M. leprae-infected armadillos at different stages of leprosy disease into two groups according to serum anti-PGL-1 IgM antibody levels. As shown in Figure 4B, sera with OD 540nm values between 0.700 and 0.900 were considered as a low (+) anti-PGL-1 titer group (30/71) while sera with OD values of >0.900 were considered as a high (++) anti-PGL-1 titer group (41/71). Overall, 80.3% (57/71) of infected armadillos developed measurable motor nerve conduction abnormality in at least one of their posterior tibial nerves (MNCT score < 5). Within the low anti-PGL-1 group, 73.3% (22/30) showed impaired nerve conduction in at least one hind limb while in the high anti-PGL-1 group, 85.4% (35/41) showed impaired nerve conduction (Figure 4B). Although no significant difference (p = 0.3297) was found in impaired nerve conduction between low and high PGL-1 groups, conduction abnormality among M. leprae-infected armadillos generally tends to increase with rising anti-PGL-1 antibody levels. In the low anti-PGL-1 group, 36.6% (11/30) of the animals had a score of 3 or below while in the high anti-PGL-1 group 61.0% (25/41) of the animals had a score of 3 or below. In addition, nearly all of the animals that developed conduction deficit also eventually exhibited signs of clinical neuropathy in their footpads. Decreased cMAP correlated well with the number of wounds and heavy calluses (r = -0.72, p = 0.02) on the plantar surface of the foot (data not shown). The occurrence of hypertrophic nails and nail avulsion also tend to increase along with decreasing cMAP and increased anti-PGL-1 antibodies.

Ultrasonography of the Posterior Tibial Nerves

Figure 5 shows ultrasonography of the posterior tibial nerve in transverse and longitudinal axes of uninfected (A and B) and M. leprae-infected (C and D) armadillos at an early stage (4 months post-inoculation) of leprosy disease. The posterior tibial nerve of the M. leprae-infected armadillo was larger when measured at the transverse axis (0.096 cm²; P: 13.1 mm) compared to the uninfected armadillo (0.037 cm²; P: 8.3 mm). Nerve enlargement can also been seen when examined at the longitudinal axis. Figure 5E shows the ultrasonography of the posterior tibial nerve of an M. leprae-infected armadillo at a late stage of leprosy disease. Increased blood flow, indicating possible inflammation, was seen using color Doppler imaging in an armadillo at 23 months post-M. leprae inoculation. Interestingly, this animal had a high level of anti-PGL-1 IgM antibody (2.104 at OD 540 nm). No increased blood flow (5F) was seen in an armadillo at a mid-stage disease (9 months post-inoculation) that was negative for anti-PGL-1 IgM antibody (0.225 at OD 540 nm).

FIGURE 5

Figure 5. M. leprae infection causes nerve enlargement in armadillo peripheral nerves. Ultrasonography of the posterior tibial nerve was performed using a SmartUS transducer probe with a linear broadband frequency of 1.5–15 MHz connected to a Sierra Summit basic system. The posterior tibial nerve is shown along its longitudinal (A) and transverse (B) axes in an uninfected armadillo and a M. leprae-infected armadillo [(C,D), respectively]. The nerve diameter of the M. leprae-infected armadillo is 0.096 cm² indicating nerve enlargement compared to the nerve diameter of the uninfected armadillo (0.037 cm²). Ultrasound with color Doppler imaging in M. leprae-infected armadillos showed increased blood flow in animals at late stage leprosy disease (23 months post-infection) that were positive for anti-PGL-1 antibodies (E) compared to armadillos that were negative for anti-PGL-1 antibodies at 9 months post-infection (F). The intense colors indicate lower velocity of the blood flow traveling away and toward the transducer (N = 4).

Neuropathic Changes in Muscle Physiological Cross Sectional Area

We examined the PCSA of footpad muscles of 18 armadillos, of which 10 were infected with M. leprae and 8 were uninfected (Figures 6A,B). The PCSA values of the small lateral flexor, lateral lumbrical (Figure 6C), and both insertions (medial and lateral) of the medial lumbrical muscles (Figure 6D) of the M. leprae-infected armadillos averaged 20% lower than that of the uninfected animals (p < 0.02). Furthermore, there were statistical differences (p = 0.008) between MNCT scores between the groups.

FIGURE 6

Figure 6. M. leprae infection causes atrophy of armadillo footpad muscles. Photographs of the dissection of a representative animal showing (A) the small lateral flexor muscle of the footpad and how the fibers run between the tendons and (B) the lumbrical muscles of the right hind limb that were released from their tendon of insertion. (C) Atrophy of small lateral flexor and lateral lumbrical muscles in M. leprae-infected armadillos compared to uninfected armadillos. (D) Atrophy of medial and lateral insertions of the medial lumbrical muscle in M. leprae-infected armadillos (N = 10) compared to uninfected armadillos (N = 8). *p < 0.05.

Integrity of the Neuromuscular Junction in the Footpad Muscles

Intrinsic muscle from the hind footpads of 3 uninfected and 5 M. leprae-infected late-stage armadillos were used to quantify the numbers and fragmentation of post-synaptic NMJ. A significant reduction (p = 0.0012) in the number of NMJs was observed in this muscle in M. leprae-infected armadillos (Figure 7A). Furthermore, ∼50% of the NMJs in the infected armadillos (Figure 7B) were fragmented when compared to those in uninfected animals.

FIGURE 7

Figure 7. M. leprae infection causes degeneration of neuromuscular junctions (NMJ’s) in the armadillo footpad muscles. The number of NMJs (A) is reduced (**p = 0.0012) in M. leprae-infected armadillos (terminal stage) as measured in 30μm-thick, 30² mm muscle sections. Fluorescent micrograph (B) of footpad intrinsic muscle in an M. leprae-infected armadillo showing NMJs (green, arrowheads) stained with FITC-α-bungarotoxin and muscle fibers (red) stained with PE-anti-myosin. (N = 8).

Evaluation of Effect of Neuroprotective Drugs in Preventing and Improving Nerve Function Impairment in Mycobacterium leprae-Infected Armadillos

Motor nerve conduction studies together with ENFD for sensory nerves were used to evaluate the ability of two neuroprotective drugs, 4-AP and EQ, to improve nerve function impairment in M. leprae-infected armadillos. Electrophysiological studies indicated that armadillos treated with 4-AP and EQ showed a significantly higher (p = 0.001 and p = 0.012, respectively) cMAP than the untreated controls at 1 month post-treatment (Figure 8a). No significant differences were seen in the cMAP between EQ and 4-AP treated animals (p = 0.105). At the end of the treatment all the untreated (N = 4) and EQ (N = 3) treated animals had a MNCT score of 3 while the 4-AP treated animals (N = 3) yielded MNCT scores of 3, 4 and 5. Similarly, armadillos treated with 4-AP showed higher ENFD than untreated controls and EQ treated armadillos; however, the differences in this limited number of animals did not reach significance (Figure 8b). Figure 8c depicts a skin section from an M. leprae-infected armadillo stained with PGP.9.5, showing fewer branching of the epithelial nerve fibers compared to a 4-AP-treated armadillo (Figure 8d). EQ-treated armadillo also shows fewer branching than 4-AP-treated armadillo (Figure 8e).

FIGURE 8

Figure 8. Evaluation of the effect of neuroprotective drugs on NFI in M. leprae infected armadillos. (a) Armadillos treated with 4-Aminopyridine- (4-AP) (N = 4) and Ethoxyquin (EQ) (N = 3) showed a significantly higher (***p = 0.001 and **p = 0.012, respectively) cMAP (mV) than the untreated controls (N = 5) at 1 month post-treatment. (b) Epithelial nerve fiber density (ENFD, #fibers/mm) in 4-AP- and EQ-treated and untreated armadillos. (c) Skin section from an untreated armadillo stained with PGP9.5 showing epidermal nerve fibers (arrows) terminating at the epidermis (epi). (d) Skin section from a 4-AP-treated armadillo showing more branching of the epidermal nerve fibers (arrows) and that the dermal nerve bundles are dense at the papillary dermis (derm) in comparison to the untreated armadillo. (e) Skin section from an EQ treated armadillo showing single epidermal nerve fibers (arrows) entering the epidermis. Scale bars = 50 μm.

Discussion

The lack of an effective animal model to study M. leprae-induced nerve injury has greatly hampered understanding of the mechanisms involved. Nine-banded armadillos are naturally susceptible to M. leprae infection (16, 17) and show the full histopathological spectrum of leprosy. More importantly, armadillos develop extensive peripheral nerve involvement due to M. leprae infection that closely resembles neuropathy in humans (19, 42). Previous histopathological studies performed in the armadillo posterior tibial nerve suggested that the localization of M. leprae in the peripheral nerve proceeds from outside in as opposed to an ascending-type of infection. Similar to human LL cases, infected armadillo nerves demonstrate a heavy infiltration of M. leprae-loaded nucleated cells in many fascicles of nerve trunks and invading demyelinating Schwann cells (5, 42, 43). However, due to the exotic nature of this animal model, no standardized methods are available to detect and accurately measure the degree of neuropathy or nerve damage in armadillos. Standardized tools to study the progression of neuropathy as well as to evaluate any therapeutic interventions are essential to advancing the armadillo as a model for NFI. The purpose of this study was to establish multiple non-invasive tests, like MNCT, ENFD and ultrasonography, which could be performed on the same animal to follow disease progression in the peripheral nerves. We also evaluated muscular atrophy and NMJ integrity in the footpad muscles as end-point assessments for the degree of neuro-muscular damage at the terminal stage of the disease. Together these tests form a robust set of tools to evaluate peripheral neuropathy in M. leprae-infected armadillos.

Neuropathies in humans are diagnosed using peripheral motor and sensory nerve conduction studies that evaluate the integrity of nerve-muscle and the somatosensory circuit (23). Motor nerve conduction studies are commonly performed by electrically stimulating (percutaneous) a peripheral motor or mixed nerve and recording the electrical response from a suitable muscle innervated by the same nerve. Analysis of the conduction velocity (MNCV), negative peak amplitude (cMAP), and the shape of the wave form following electrical stimulation reveal the degree of demyelination and axonal loss in the studied segment of the peripheral motor or mixed nerve. Demyelination results in slowing of conduction velocity measured in meters/second (m/s). In some cases, demyelination can also cause dispersed cMAP. In contrast, axonal loss leads to a decrease in the cMAP measured in millivolts (mV) (27). Since percutaneous nerve conduction studies are non-invasive, they are convenient ways to study onset and progress of peripheral neuropathy over time in the same subject.

Although the hard carapace and thick skin limit the number of nerves that may be examined in armadillos, we have developed and validated MNCT techniques and an MNCT scoring system that can be used to assess motor nerve conduction in both hind limbs by examining the posterior tibial nerve that lies beneath the skin surface between the ankle and knee and innervates the small lumbrical and flexor muscles of each foot. Similar to that seen in humans, leprosy is asymmetrical and manifests randomly in different nerves in these animals. Moreover, like in humans there is a high probability that the posterior tibial nerve will become involved, and that probability increases as the disease progresses (20, 42). We have shown in previous electron microscopy studies that posterior tibial nerves of armadillos progressing at 28 months post infection exhibited M. leprae within both myelinated and unmyelinated axons and Schwann cells. The axons showed edema with demyelination and axonal degenerative changes (20, 43).

Peripheral conduction deficit among M. leprae-infected armadillos began early in the course of their disease and progressed over time. Decreased cMAP amplitude (<0.9mV), which indicates axonal loss, was the most common impairment. M. leprae-infected armadillos rarely showed dispersed cMAP, which also indicates axon loss, but abnormal nerve conduction velocity (MNCV < 40 m/s) was observed. Some studies have reported demyelination as the main cause of nerve dysfunction in leprosy disease (44–46). Another study, however, found that axonal injuries occurred at a higher frequency than myelin injuries in the posterior tibial nerve (8). Hence, the sequence of events leading to nerve injury may vary among different nerves or an individual’s position in the clinical spectrum. 70% (14/20) of experimentally infected armadillos developed demonstrable conduction deficit in at least one of their posterior tibial nerves within 4 months of infection, and its onset generally coincided with detectable anti-PGL-1 IgM antibodies. Eventually, nearly all M. leprae-infected armadillos will exhibit neuropathy as their disease disseminates. As the disease progressed, both right and left posterior tibial nerves were compromised showing delayed MNCV, which is a consequence of demyelination of the nerve fibers, and in some cases total conduction block. Armadillos in very late stages of experimental leprosy may develop lesions in their footpads that can make MNCT difficult to perform or can produce inaccurate results. Extending our electrophysiological techniques to include sensory nerve and F-wave responses will likely increase the sensitivity of detecting peripheral neuropathy and will likely reveal even greater involvement of nerves at these early stages of infection. Nevertheless, our data clearly shows that in armadillos there is a significant association between the onset of the host immune response (anti-PGL-1 antibodies) and conduction abnormalities in the peripheral nerves of the lower extremities which progresses over time to manifest classical lesions in the foot.

Peripheral nerves are often enlarged in leprosy patients and ultrasonography is currently used to determine nerve enlargement (28, 47, 48). It provides an objective measure of the nerve dimensions in addition to revealing structural changes over a longer length of the nerve (49). Enlarged nerves of patients undergoing leprosy reactions show increased endoneurial and epineurial vascularity that can be measured by ultrasonography with color or power Doppler (24, 28). We also used ultrasonography of the posterior tibial nerve to show that armadillos, like humans, show enlargement of peripheral nerves due to M. leprae infection. Although leprosy reactions have not yet been determined in armadillos, increased vascularity, most likely due to inflammation, could be demonstrated using color Doppler (49). Unlike MNCT, ultrasonography can be done on multiple peripheral nerves of upper and lower extremities of the animal, thereby increasing the probability of detecting neuropathy in focal and asymmetric disease progression.

Monitoring warm/cold detection or grip dynometry are currently among the most effective early indicators of nerve injury in human leprosy, and these tests often show changes well before conduction abnormality is apparent (2, 35). Unfortunately, armadillos cannot grip objects and they are generally unresponsive to common temperature stimuli. However, Brand showed that the PCSA (cross sectional area/mass) of muscles in the leprotic hand could be used as a surrogate measure of grip strength and index muscle atrophy (35). We examined the PCSA of footpad muscles of M. leprae-infected and uninfected armadillos and found that the infected armadillos showed significant muscle atrophy indicated by lower fiber density compared to the uninfected armadillos. Additionally, we compared neuromuscular junction (NMJ) integrity and numbers in footpad intrinsic muscles, between end stage M. leprae-infected and uninfected armadillos and found significant loss of NMJs in infected armadillos. Further studies are required to understand the mechanisms of motor NMJ innervations and decay dynamics in M. leprae-infected armadillos and to evaluate reconnection of the NMJ’s, which can give important insights into possible therapeutic interventions to arrest or reverse loss of neuro-muscular function in leprosy.

Motor nerve conduction and sensory tests together with ultrasonography are suitable for evaluation of peripheral nerve function. Since these are non-invasive tests they can be used to follow disease progression in experimentally infected armadillos and consequently to evaluate efficacies of therapeutic and immune interventions in preventing or reversing peripheral nerve damage. Within sensory tests, quantification of ENFD is a test that is used to diagnose small fiber neuropathies including leprosy induced neuropathies (50). In small fiber sensory neuropathies associated with diabetes, HIV and idiopathic small fiber neuropathies, a decrease in epidermal density in the distal leg has been demonstrated (51–53). We have previously reported that armadillos show a length dependent innervation similar to humans (42, 50); therefore, this test can be used to diagnose small fiber neuropathies associated with M. leprae-infection in armadillos. Using MNCT, it was demonstrated that Lepvax, a vaccine against leprosy, showed some nerve protection in M. leprae-infected armadillos, indicated by higher cMAP recordings and restoration of axonal size of the tibial nerve fibers in vaccinated armadillos compared to the unvaccinated (43).

In the current study, we evaluated two neuroprotective drugs that have been used successfully in cancer models to ameliorate neuropathy following chemotherapy (54) and in acute peripheral nerve injury models promoting remyelination (55). EQ, a quinolone-based antioxidant, has been shown to prevent axonal loss in peripheral nerves of mice with chemotherapy-induced neurotoxicity. EQ provided a dose-dependent neuroprotection indicated by higher intraepidermal nerve fiber density and sensory nerve potential amplitude, and lower thermal hypoalgesia compared to the untreated controls (54). A second drug, 4-AP, has been used in Lambert-Eaton myasthenic syndrome and multiple sclerosis and acts by blocking potassium channels, prolonging action potentials, and increasing neurotransmitter release at the neuromuscular junction. It was also shown to be effective in promoting remyelination and axon regeneration in acute peripheral nerve injuries. In clinical trials, administration of 4-AP improved multiple neurological signs of multiple sclerosis such as vision, muscle strength and coordination (56, 57). 4-AP treatment in acute peripheral injury enhanced both the speed and extent of restoration of normal NCV and caused regenerative increases in axonal area, myelin thickness, and levels of the myelin-specific protein (55). Both EQ and 4-AP were effective in preventing demyelination and axon loss, and treatment resulted in higher epidermal nerve fiber density (ENFD) indicating higher sensory integrity in treated animals (54, 55). We used motor nerve conduction studies together with sensory tests (ENFD) to assess the effect of these two neuroprotective drugs (4-AP and EQ) in preventing and or improving nerve function impairment in M. leprae-infected armadillos in a limited pilot study. After one month of treatment, 4-AP improved motor nerve function in armadillos that were progressing at an early stage of leprosy disease, indicating that this drug merits further evaluation in this model. This pilot study shows that the armadillo model and the various nerve structure and function assessment methods validated in this study have the required sensitivity to evaluate efficacy of therapeutic interventions against peripheral neuropathy in leprosy.

In summary, multiple non-invasive and invasive methods to evaluate M. leprae-induced peripheral NFI in nine-banded armadillos were validated, and a quantitative nerve deficit scoring system was developed. The data clearly indicate that the armadillo lower extremity becomes heavily involved and exhibits many of the same abnormalities as seen in humans. This study further suggests that, like humans, armadillos suffer an insidious silent neuropathy that commences early in the infection, and serological screening can be useful to stage the disease status for nerve injury studies. These techniques detected pathological events at early stages of disease and will benefit future studies to elucidate mechanisms involved in early leprosy neuropathy. Moreover, the armadillo model and these tests to evaluate peripheral neuropathy will support the screening of new preventive interventions for leprosy control such as leprosy specific vaccines and chemotherapies to either prevent, arrest or reverse nerve damage.

Data Availability Statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Ethics Statement

The animal study was reviewed and approved by the NHDP Institutional Animal Care and Use Committee (Assurance #D16-000019 [A3031-01]) and was performed in accordance with the United States Department of Agriculture and Plant Health Inspection Service.

Author Contributions

MP and RL validated MNCT test and ultrasonography of peripheral nerves and analyzed the data. GE counted and analyzed the EFND data. JF was instrumental in validating the MNCT test. SW validated the ultrasonography in peripheral nerves in armadillos. LA and RT conceived the study and secured funding. MP, RL, and LA wrote the manuscript. All authors provided critical reviews and approved the submitted version.

Author Disclaimer

The views expressed in this article are solely the opinions of the authors and do not necessarily reflect the official policies of the U. S. Department of Health and Human Services or the Health Resources and Services Administration, nor does mention of the department or agency names imply endorsement by the U.S. Government.

Funding

This study was supported by the NIH/NIAID through an interagency agreement (No. AAI15006-005) with HRSA/HSB/NHDP.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Acknowledgments

We thank all the NHDP technicians especially Roena Stevenson, Rachel Walley, Vilma Marks and Judith Wiles for their excellent technical support. We also thank Kim Gusman and Dave Guarantano for their contributions to PCSA studies. We thank Denise Brasseaux and Alicia Hoard for their help in developing the MNCT test. We thank Gregory McCormick for his contribution with the TEM photographs.

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