Low-Cost Gait Analysis for Behavioral Phenotyping of Mouse Models of Neuromuscular Disease

Summary

Footprint analysis is a low-cost alternative to digitized gait analysis programs for researchers quantifying movement abnormalities in mice. Because of its speed, simplicity, and longitudinal potential, it is ideal for behavioral phenotyping of mouse models.

Abstract

Measurement of animal locomotion is a common behavioral tool used to describe the phenotype of a given disease, injury, or drug model. The low-cost method of gait analysis demonstrated here is a simple but effective measure of gait abnormalities in murine models. Footprints are analyzed by painting a mouse’s feet with non-toxic washable paint and allowing the subject to walk through a tunnel on a sheet of paper. The design of the testing tunnel takes advantage of natural mouse behavior and their affinity for small dark places. The stride length, stride width, and toe spread of each mouse is easily measured using a ruler and a pencil. This is a well-established and reliable method, and it generates several metrics that are analogous to digital systems. This approach is sensitive enough to detect changes in stride early in phenotype presentation, and due to its non-invasive approach, it allows for testing of groups across life-span or phenotypic presentation.

Introduction

Locomotion requires complex neurological and musculoskeletal coordination, and deficits in a single aspect of motor pathways can produce observable gait abnormalities^1,2. Gait analysis is a critical tool for researchers testing mouse models because it provides quantifiable behavioral data on how a given disease, injury, or drug impacts an animal’s movement³. However, digitized gait analysis requires the purchase of a treadmill, a camera, and associated software, which can be prohibitively expensive for researchers. Gait analysis is often used intermittently to track longitudinal changes in motor function, hence it may be difficult to justify the expenditure if sporadically used⁴. Although digitized analyses may provide more detailed gait metrics than simple footprint analysis, these more complex measures are not always necessary or relevant for the characterization of a behavioral phenotype⁵.

Here we present a low-cost manual footprint analysis method as a quick and sensitive alternative to digitized gait analysis programs^6,7. Manual footprint analysis has been demonstrated to detect significant gait differences in a multitude of murine disease models^{4,7,8,9,10,11,12,13,14,15,16,17}, and in at least one case, this low-cost method identified changes in gait that were not detected by a common digitized gait analysis program¹². The total cost of materials is nominal, and it can be easily adapted to other rodent research models.

While there are many different gait metrics from which data can be drawn, the method we describe focuses on three specific metrics: stride length, stride width (a.k.a. “track width”), and toe spread. It is important to note that the parameters to be assessed should be determined on a model-by-model basis. This method of gait analysis is not designed to measure cognitive function, and it is not recommended for studies that require complex biomechanical measurements of gait¹⁶.

We present behavioral data from a cohort of pre- and post-symptomatic mice modeling X-linked Spinal and Bulbar Muscular Atrophy (SBMA), a neuromuscular disease characterized by motor neuron degeneration and muscle atrophy. These mice develop progressive deficits in gait that coincide with the onset of other disease-specific phenotypes. This demonstrates the validity and specificity of this method, and confirms that it can reliably discriminate between affected and non-affected animals.

The experimental mice in this study were 2.5 (pre-symptomatic) and 9-month-old (post-symptomatic) BAC fxAR121 transgenic mice on a C57BL/6 background (n_expt=12). This model was generated in our lab and has been fully characterized as a powerful mouse model of SBMA⁹. Non-transgenic littermates were used as controls (n_ctrl=8). SBMA is a sex-limited disease which fully manifests in males only, so male mice were used exclusively for this study. During planning stages, researchers must take into account the National Institutes of Health’s considerations of sex as a biological variable to determine group sizes and composition¹⁸.

Protocol

All testing conducted with mice was reviewed and approved by the Institutional Animal Care and Use Committee (IACUC) of Duke University. Personnel responsible for testing and scoring must be blinded to animal genotype or experimental condition until gait analysis and scoring of papers has been completed for the entire cohort.

1. Testing material preparation

1. Conduct testing with a tunnel built from 3 pre-cut clear acrylic panels that are 0.375 inches thick. Assemble tunnel by gluing panels together with a sealant that specifically bonds acrylic and will not emit odors when dried.
   1. For standard C57BL/6 mice, use the following tunnel measurements: 2.5 in. wide, 3 in. high, and 13 in. long. Mice must be able to comfortably walk through the tunnel and take enough steps (>4) so that gait can be measured.
2. Construct the goal chamber with pre-cut gray acrylic panels 0.375 inches thick, glued together with the same sealant as used on the tunnel. The interior measurements of the chamber are 4 in. wide, 4 in. long, and 3 in. tall. Match the opening of this chamber to the opening of the tunnel (2.5 in. wide x 3.0 in. tall). Because the mice naturally prefer darkened spaces to well-lit spaces, use material that is opaque and dark in color.
3. Use paper for tracking steps that is thick and smooth (watercolor paper works well). Cut individual papers strips to be slightly wider and longer than the width and length of the tunnel. If using the tunnel dimensions described here, cut papers to 15 in. long by 3.5 in. wide.
4. Use two contrasting colors (e.g., green and purple) of non-toxic washable water-based paint. Assign one color for hind-limbs, the second one for forelimbs. Mice will lick the remaining paint from their feet after testing, so the selected paint must be completely non-toxic.
5. Use two round barrel paintbrushes, one for each paint color (~0.5 cm in diameter, tapered/pointed brush tip).
6. Select a ruler with markings down to millimeters, and a caliper with measurements down to 0.1 mm. Pencil is recommended to write on the scoring papers.
7. Optional: For animals with high anxiety or low motivation, provide a behavioral incentive in the goal chamber. This can include small amounts of sterilized sunflower seeds (placed in the home cage 2 days prior to testing to allow habituation). On the day of testing, place sunflower seeds inside the goal chamber to encourage mice to walk through without stopping.

2. Data collection

1. If testing is performed in a separate room, acclimate the mice to the new room for 30 minutes and then start the behavioral assays. Additionally, because mice are naturally nocturnal, ensure all mice are fully awake and alert for at least 5 minutes before testing.
2. Prepare the testing setup by positioning the tunnel over the paper and marking the paper with mouse ID and testing date. Position the goal chamber at the end of the tunnel, connecting both open ends. Add sunflower seeds at the end of the tunnel (inside the goal chamber) for motivation if needed.
3. Remove the mouse to be tested from its cage and grip it firmly by its scruff, making sure to grip the tail to stabilize movement of its hind limbs.
4. Paint forepaws so the entire underside of all toes and the center of the foot are fully covered in paint. Repeat this with a contrasting color of paint on its hind paws. Wipe off any paint that the mouse gets on other parts of its body with a clean damp cloth to prevent smudges that may interfere with data collection.
   NOTE: Mouse handling must be performed by experienced researchers to minimize animal stress.
5. Place the mouse at the start of the tunnel and allow it to walk all the way into the goal chamber, and then retrieve the mouse, gently wipe off its feet with a water-dampened cloth, and return it to its home cage.
6. Allow paper with footprints to dry fully before scoring. Wipe down the testing area and tunnel with ethanol or an equivalent cleaning solution in between each animal.

3. Scoring criteria

1. Use steps that are consistently spaced with clear, non-smudged footprints for scoring. Figure 1B is a good example of a footprint sequence that can be scored. In order to generate sufficient scoring data, there must be at least 2 consecutive steps from each foot, but 4-6 steps per foot is recommended. Do not include the first and last footprints on the paper, as they are unlikely to represent normal gait because the mouse is changing its walking speed.
2. Use stride length, stride width, and toe spread as three different measures of gait that can be analyzed using this method.
   NOTE: Stride length and width require clear sequential prints where the forefoot region is well defined in paint. Toe spread does not require sequential prints for scoring, only clear prints of the first and last toes on a single foot. However, if a given footprint is not included in measurements of stride length or width, it cannot not be scored for toe spread. All three measures are assessed in centimeters.
   1. Define stride length as the distance between two sequential footprints created by the same foot (i.e., one stride) (Figure 1A, 1B).
      1. With a pencil, draw a 2-4 mm circle around the fore-foot region of both forelimb footprints (identified by assigned color above) in a single stride and draw a line between them using a ruler.
      2. Record the distance between two prints from the middle of each circle (i.e. center of each foot pad) as Right-Fore 1 (RF1) or Left-Fore 1 (LF1).
      3. Repeat for all steps that can be scored (RF2, LF2, RF3, LF3 and so on).
      4. Repeat for right and left hind-limb footprints.
      5. Average all individual recorded stride distances for each limb. For statistical analysis, individual cohort members can be averaged together.
   2. Define stride width as the measure of distance between left and right forelimbs or hind-limbs (Figure 1A, 1B).
      1. To assess this distance, draw and measure a line from the circled forefoot region of one hind-limb that intersects perpendicularly with the line for stride length on the contralateral hind-limb.
      2. Repeat this for all hind-limb prints that can be scored, and then average the measurements. The method of calculation for stride width is the same for fore- and hind-limbs.
   3. Define toe spread as the distance between the first and last toes on a single fore- or hind-limb footprint (Figure 1A, 1B).
      1. Use calipers to measure the distance between the tip of the first toe print and the tip of the last toe print.
      2. Repeat for all hind-limb prints that can be scored and average the measurements. The method of calculation for toe spread is the same for fore- and hind-limbs.
3. If the paper cannot be scored, allow the animal to rest for 10 minutes before trying again.

Results

With sufficient numbers of animals, this procedure is capable of detecting gait differences between mouse genotypes, within the same strain over time. Figure 1B shows representative traces of footprint images collected in our lab, using a mouse model of X-linked Spinal and Bulbar Muscular Atrophy (SBMA), a neurodegenerative disorder affecting lower motor neurons and skeletal muscle. We have previously reported that male BAC fxAR121 transgenic mice develop significant weight loss, impairments...

Discussion

Using the low-cost gait analysis method described above, we show successful identification of several parameters of gait dysfunction at post-symptomatic ages in the BAC fxAR121 mouse model of SBMA. Decreases in stride length are consistent with prior SBMA studies of mouse models and human patients⁹. We also show for the first time that there are significant differences in hind-limb toe spread in symptomatic SBMA mice compared to non-transgenic littermate controls. Interestingly, decreases in hind ...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
Caliper	n/a	n/a	must have markings down to 0.1 mm
Craft Glue	E6000	n/a
Footprint Paint (Tempera Paint)	Artmind	n/a	must be non-toxic
Round Barrel Paintbrushes	Symply Simmons	n/a	0.5 cm diameter
Ruler	n/a	n/a	must have markings down to millimeters
Scoring Paper (Watercolor Pads)	Canson	n/a	cut to size
Tunnel and Goal Chamber	Interstate Plastics	n/a	cut to size