Investigating Alterations in Caecum Microbiota After Traumatic Brain Injury in Mice

Podsumowanie

Presented here is a protocol to induce diffuse traumatic brain injury using a lateral fluid percussion device followed by the collection of the caecum content for gut microbiome analysis.

Streszczenie

Increasing evidence shows that the microbiota-gut-brain axis plays an important role in the pathogenesis of brain diseases. Several studies also demonstrate that traumatic brain injuries cause changes to the gut microbiota. However, mechanisms underlying the bidirectional regulation of the brain-gut axis remain unknown. Currently, few models exist for studying the changes in gut microbiota after traumatic brain injury. Therefore, the presented study combines protocols for inducing traumatic brain injury using a lateral fluid percussion device and analysis of caecum samples following injury for investigating alterations in the gut microbiome. Alterations of the gut microbiota composition after traumatic brain injury are determined using 16S-rDNA sequencing. This protocol provides an effective method for studying the relationships between enteric microorganisms and traumatic brain injury.

Wprowadzenie

Traumatic brain injury (TBI) is a global public health problem and the leading cause of death and disability in young adults^1,2. TBI causes many deaths every year, and survivors experience a variety of physical, psychiatric, emotional, and cognitive disabilities. Therefore, TBI is a heavy burden to a patient's family and societal resources. TBI involves both the primary brain injury that occurs at the time of trauma and any secondary brain injuries that develop hours to months following initial injury. Secondary brain injury is mediated by several biochemical cascades, which are not only detrimental to the brain but also have significant negative effects on various organ systems, including the gastrointestinal system³.

Currently, there are three models to induce TBI in animal experiments: fluid percussion injury, control cortical impact (CCI), and weight drop acceleration. Lateral fluid percussion injury (LFPI) is the most commonly used model to establish diffuse brain injury (DAI)⁴. The device produces brain injury through a craniectomy by applying a brief fluid pressure pulse to the intact dura. This pulse is created by the strike of the pendulum. LFPI is a reproducible and controllable modeling method for TBI research.

The microbiome is defined as the collective genomes of all microorganisms that reside in the human body. Intestinal microbes in particular not only play an important role in intestinal homeostasis and function but also regulate many aspects of host physiology and the functioning of other organs⁵. In recent years, there is increasing evidence that indicates that gut microbiota regulate brain development and function via brain-gut axes⁶. Disruption of the gut microbiota has been linked to several brain function disorders including Parkinson's disease, mood disorders, and autism⁷. Recently, preclinical studies have also reported that acute brain injury can induce changes in gut microbiota^8,9.

A study by Treangen et al.¹⁰ found significant decreases in three microbial species and increases in two microbial species after CCI-induced TBI. This evidence indicates that modulation of gut microbiota may be a therapeutic method in TBI management. However, the mechanisms underlying brain injury-induced gut microbiota changes remain unknown. For this reason, a relatively simple and efficient model of studying the changes in gut microbiota after TBI is required. Therefore, the present study presents a protocol to examine alterations in gut microbiota after TBI in mice.

Protokół

All procedures performed were approved by the Experimental Animal Ethics Committee of Zhejiang University. All instruments and materials used in surgery are sterile. The TBI proceudre takes about 20 minutes.

1. Animal care

1. Use 5- to 6-week-old male C57BL/6J mice (20-25 g of weight) in this experiment.
2. Maintain mice on a 12 h/12 h light/dark cycle, and make sure they receive food and water ad libitum. Provide the same amounts of food and water to both the sham and TBI groups throughout the study.
3. Make all efforts to minimize the animal pain and discomfort.

2. Induction of traumatic brain injury

1. Inject Ketamine (80-100 mg/kg)/Xylazine (10 mg/kg) IP for anesthesia. Test the depth of anesthesia using an eye reflex or pain reflex. Use artificial tears or lubricant eye ointment to keep the eyes from drying.
2. After anesthesia, put the mouse in prone position. Use a temperature-controlled heating pad to maintain the temperature at 37 °C during the surgery and for 30 min after TBI.
3. Shave the hair of the incision area.
4. Disinfect the scalp with 70% ethanol using three alternating scrubs, then incise the scalp in a sagittal plane.
5. Use forceps to retract the incision on both sides and separate the periosteum slightly.
6. Use a marker to draw a circle (3 mm diameter) on the right parietal area of the skull, 2 mm away from the midline.
7. Drill the skull with an electric drill. Ensure that this step is operated carefully to protect the dura from being damaged.
8. Remove the bone flap and expose a small bone window (3 mm in diameter).
9. Place a plastic injury cannula (internal diameter = 2.5 mm, length = 8 mm) over the craniotomy and cement the cannula to the skull using a dental acrylic.
10. Fill the cannula with sterile 0.9% NaCl (normal saline) using a syringe (5 mL) to ensure that there are no bubbles in the cannula.
11. Turn on the oscilloscope and amplifier and ensure that the high-pressure tube of the lateral fluid percussion injury (LFPI) device is free of air bubbles. Test the device by delivering about 10 pulses until it gives a steady signal. Adjust the angle of the pendulum starting position to reach a pulse intensity of about 2.0 atm.
12. Connect the injury cannula to the LFPI device. Induce brain injury by pulling the trigger and releasing the pendulum. Then, obtain a pulse and transmit it to the dura through the entire closed fluid-filled tubing system.
13. Operate the mice in the sham group with the same surgical procedure. Do not perform the LFPI.

3. Post-surgery treatment

1. After inducing the brain injury, remove the plastic cannula and suture the incision. During surgery administer buprenorphine (2mg/kg) SQ or IP and thereafter every 6-12 h for three days.
2. Lay the mouse on a heating pad until it is ambulatory. Set the temperature of the heating pad to 37 °C to accelerate anesthetic resuscitation.
3. Put the mouse back in the cage and administer food and water ad libitum.

4. Laparotomy and sample collection from the caecum

1. Euthanize the mice by CO₂ followed by cervical dislocation at the corresponding time points.
   NOTE: In this experiment, the chosen time points were 1 h, 6 h, 1 d, 3 d, and 7 d post-traumatic brain injury to analyze the dynamic evolution of gut microbiota.
2. Remove the hair from the surface of the abdomen. Disinfect the abdomen with 70% ethanol.
3. Place a sterile drape over the mouse. Make an incision from the lower abdomen midline, just above the prepuce in the male mice.
4. After the intestines are exposed, locate the cecum and gently separated it from other intestinal tracts. Avoid grasping the cecum with toothed or sharp forceps. Use atraumatic forceps, such as Adson forceps with serrations.
5. Cut the caecum with sharp scissors.
6. Extract the caecum contents manually onto sterile dressing and store the contents in 1.5 mL microcentrifuge tubes.
7. Store the caecum contents at -80 °C until microbiome analysis.

5. DNA extraction and 16S-rDNA sequencing and data analysis

1. Isolation of DNA from feces
   NOTE: A commercially available DNA isolation kit (Table of Materials) was used for this experiment.
   1. Use a scalpel to scrape 300 mg of feces in a 2 mL microcentrifuge tube and place the tube on ice.
   2. Add 1 mL of inhibit buffer to each sample. Vortex continuously for 1 min or until the feces sample is thoroughly homogenized.
   3. Centrifuge the sample at the maximum speed for 1 min to pellet the feces particles.
   4. Pipette 2 µL of proteinase K into a new 2 mL microcentrifuge tube. Pipet 600 µL of the supernatant from step 5.1.3 into the 2 mL microcentrifuge tube containing proteinase K. Then, add 600 µL of Buffer 1 and vortex for 15 s.
   5. Incubate the sample at 70 °C for 10 min.
   6. Add 600 µL of 100% ethanol to the lysate (1:1 ratio) and mix by vortexing. Centrifuge at the maximum speed briefly to remove drops from the inside of the tube lid.
   7. Apply 600 µL of the lysate to the spin column. Centrifuge at the maximum speed for 1 min. Discard the flow-through. Repeat this step one more time. Then, transfer the column into a new 2 mL collection tube.
   8. Open the spin column and add 500 µL of Buffer 2. Centrifuge at the maximum speed for 1 min. Remove the column and place it in a new 2 mL collection tube.
   9. Add 500 µL of Buffer 3 into the column. Centrifuge at the maximum speed for 3 min. Discard the flow-through. Repeat the centrifugation process once to ensure the Buffer 3 is completely eluted.
   10. Place the spin column into a new tube 2 mL collection tube and pipette 200 µL of Buffer 4 directly onto the membrane. Incubate for 1 min at room temperature (RT), then centrifuge at the maximum speed for 1 min to elute DNA.
2. 16S-rDNA sequencing and data analysis
   1. Use 20-30 ng of DNA to generate amplicons.
   2. Use commercially available primers designed for the relatively conserved regions bordering the V3 and V4 hypervariable regions of bacteria 16S rDNA. The forward primers containing the sequence "CCTACGGRRBGCASCAGKVRVGAAT" and reverse primers containing the sequence "GGACTACNVGGGTWTCTAATCC" were used in the present study.
   3. Make the PCR reactions mixture by adding 2.5 µL of Buffer 1, 2 µL of dNTPs, 1 µL of each primer, 0.5 µL of DNA polymerase, and 20 ng of template DNA in a tube. Use ddH₂O to adjust the reaction system to 25 µL.
   4. Set the PCR reaction parameters as follows: perform the pre-denaturation at 94 °C for 3 min once. Perform denaturation at 94 °C for 5 s, anneal at 57 °C for 90 s, extend at 72°C for 10 s, and repeat this 24x.
   5. Perform PE250/300 paired-end sequencing according to the manufacturer's instruction and use QIIME data analysis package for 16S rRNA data analysis.
      NOTE: In this experiment, the DNA sequencing and data analysis were primarily done by a professional sequencing company.

Wyniki

Establishment of TBI is shown in Figure 1. After anesthesia and disinfection, the scalp was incised sagittally (Figure 1A). A craniotomy (3 mm in diameter) was trephined into the skull over the right parietal cortex with an electric drill, the dura was kept intact (Figure 1B,C). A plastic injury cannula was placed over the bone window and cemented to the skull using dental acrylic (<...

Dyskusje

Presented here is a simple and efficient protocol to determine changes in cecal microbiota after TBI in mice. Induction of brain injury and collection of caecum content samples are critical parts of the protocol.

Despite researchers having studied the changes of gut microbiota following TBI, the brain injury used in these studies were CCI-⁸ and weight drop/impact-induced models⁹. However, the CCI model mostly replicates brain contusion, and the w...

Materiały

Name	Company	Catalog Number	Comments
DNA isolation kit	QIAGEN	51604	For fast purification of genomic DNA from stool samples
Gene analysis service	GENEWIZ		Gene analyse service
Heating pad	Shanghai SAFE Biotech Co.	TR-200	heating pad
Injector	The First Affiliated Hospital, School of Medicine, Zhejiang University		injector
LFPI device	Virginia Commonwealth University	FP302	LFPI device
Micro cranial drill	RWD Life Science	78061	Micro cranial drill
Povidone Iodine	The First Affiliated Hospital, School of Medicine, Zhejiang University		Povidone Iodine