In Vivo Mouse Model of Spinal Implant Infection

Podsumowanie

The protocol describes a novel in vivo mouse model of spinal implant infection where a stainless-steel k-wire implant is infected with bioluminescent Staphylococcus aureus Xen36. Bacterial burden is monitored longitudinally with bioluminescent imaging and confirmed with colony forming unit counts after euthanasia.

Streszczenie

Spine implant infections portend poor outcomes as diagnosis is challenging and surgical eradication is at odds with mechanical spinal stability. The purpose of this method is to describe a novel mouse model of spinal implant infection (SII) that was created to provide an inexpensive, rapid, and accurate in vivo tool to test potential therapeutics and treatment strategies for spinal implant infections.

In this method, we present a model of posterior-approach spinal surgery in which a stainless-steel k-wire is transfixed into the L4 spinous process of 12-week old C57BL/6J wild-type mice and inoculated with 1 x 10³ CFU of a bioluminescent strain of Staphylococcus aureus Xen36 bacteria. Mice are then longitudinally imaged for bioluminescence in vivo on post-operative days 0, 1, 3, 5, 7, 10, 14, 18, 21, 25, 28, and 35. Bioluminescence imaging (BLI) signals from a standardized field of view are quantified to measure in vivo bacterial burden.

To quantify bacteria adhering to implants and peri-implant tissue, mice are euthanized and the implant and surrounding soft tissue are harvested. Bacteria are detached from the implant by sonication, cultured overnight and then colony forming units (CFUs) are counted. The results acquired from this method include longitudinal bacterial counts as measured by in vivo S. aureus bioluminescence (mean maximum flux) and CFU counts following euthanasia.

While prior animal models of instrumented spine infection have involved invasive, ex vivo tissue analysis, the mouse model of SII presented in this paper leverages noninvasive, real time in vivo optical imaging of bioluminescent bacteria to replace static tissue study. Applications of the model are broad and may include utilizing alternative bioluminescent bacterial strains, incorporating other types of genetically engineered mice to contemporaneously study host immune response, and evaluating current or investigating new diagnostic and therapeutic modalities such as antibiotics or implant coatings.

Wprowadzenie

The purpose of this method is to describe a novel mouse model of spinal implant infection (SII). This model was designed to provide an inexpensive and accurate tool to flexibly assess the effect of host, pathogen, and/or implant variables in vivo. Testing potential therapeutics and treatment strategies for spinal implant infections in this model is aimed at guiding research development prior to application in larger animal models and clinical trials.

Implant related infection after spine surgery is a devastating complication and unfortunately occurs in approximately 3–8% of patients undergoing elective spine surgery^1,2,3,4,5 and up to 65% of patients undergoing multilevel or revision surgery⁶. Treatment of spinal implant infections often requires multiple hospitalizations, multiple surgeries, and prolonged antibiotic therapy. SIIs portend poor patient outcomes including neurological compromise, disability, and an increased risk of mortality. Management of SII is extremely expensive, costing upwards of $900,000 per patient⁷.

Staphylococcus aureus is the most common virulent pathogen of SII^8,9,10,11. Bacteria can seed the hardware directly during surgery, through the wound during the postoperative period, or later via hematogenous spread. In the presence of metal implants, S. aureus form biofilm that protects the bacteria from antibiotic therapy and immune cells. While removal of infected hardware may help effectively eradicate an infection, this is frequently not feasible in the spine without causing destabilization and risking neurologic compromise¹².

In the absence of explanting infected hardware, novel approaches are needed to prevent, detect, and treat SII. Historically, there have been limited animal models of SII to efficiently assess the safety and efficacy of novel therapies. Previous animal models of SII require large numbers of animals and collection of data points requiring euthanasia including colony counting, histology, and culture^13,14,15. Lacking longitudinal in vivo monitoring, these models only provide one data point per animal and are therefore expensive and inefficient.

Previous work studying a mouse model of knee arthroplasty infection established the value and accuracy of noninvasive in vivo optical imaging to longitudinally monitor infection burden¹⁶. The detection of bioluminescence allows bacterial burden to be quantified over a longitudinal time course in a single animal humanely, accurately, and efficiently. Moreover, prior studies have demonstrated a high correlation between in vivo bioluminescence and CFUs adherent to implants¹⁷. The capacity to track infection over time, has led to a more nuanced understanding of implant related infection. In addition, monitoring longitudinal infection in this way, has allowed the effectiveness of antibiotic therapy and novel antimicrobials to be accurately assessed^16,17,18.

Leveraging these tools, we developed and validated a model of postoperative spinal implant infection. In the method presented, we utilize an inoculum of bioluminescent S. aureus Xen36 to establish an in vivo mouse model of SII to longitudinally monitor bacterial burden^16,17,18. This novel model provides a valuable tool to efficiently test potential detection, prevention, and treatment strategies for SII prior to their application in larger animal models and clinical trials.

Protokół

All animals were handled in strict accordance with good animal practice as defined in the federal regulations as set forth in the Animal Welfare Act (AWA), the 1996 Guide for the Care and Use of Laboratory Animals, PHS Policy for the Humane Care and Use of Laboratory Animals, as well as the institution’s policies and procedures as set forth in the Animal Care and Use Training Manual, and all animal work was approved by the University of California Los Angeles Chancellor’s Animal Research Committee (ARC).

1. S. aureus bioluminescent strain choice

1. Use the bioluminescent S. aureus strain Xen36 as the inoculum of interest.
   NOTE: This strain was derived from the parental strain S. aureus ATCC-49525, which is a clinical isolate from a septic patient. S. aureus Xen36 uniquely utilizes a luxABCDE operon, which is optimized and integrated into the host’s native plasmid.¹⁹ As a result, the Xen36 strain is capable of producing a blue-green bioluminescent light with a peak wavelength emission of 490 nm. This emission signal is only produced by living metabolically active bacterial organisms.

2. Preparation of S. aureus for inoculation

1. Add 200 μg/mL kanamycin to Luria Broth plus 1.5% agar to isolate S. aureus Xen36 from potential contaminants, utilizing the kanamycin resistance gene linked to the lux operon¹⁹.
2. Streak S. aureus Xen36 bacteria onto tryptic soy agar plates (tryptic soy broth [TSB] plus 1.5% agar) and incubate at 37 °C for 12-16 h.
3. Isolate single colonies of S. aureus Xen36 and individually culture in TSB for 12-16 h at 37 °C in a shaking incubator (200 rpm).
4. Dilute resultant culture at a 1:50 ratio.
5. Culture for additional 2 h at 37 °C to isolate midlogarithmic phase bacteria.
6. Pellet, resuspend, and wash bacteria in phosphate buffered saline (PBS) three times.
7. Measure the absorbance at 600 nm. The ideal OD600 is between 0.700 and 0.750 which corresponds to 4x10⁵ CFU/mL. Perform serial dilutions to achieve desired bacterial inoculum (1 x 10³  CFU/2 µL).
   NOTE: The optimal concentration of Xen36 for the establishment of a chronic infection was found to be 1 x 10³ CFU. Lower dosing of bacteria was cleared by the host immune system and higher dosing caused wound breakdown. Wound breakdown does not differentiate between a deep implant infection and a superficial wound infection and is therefore avoided in this model (Figure 1)²⁰.

3. Mice

1. Use 12-week old male C57BL/6J wild-type mice.
2. House mice in cages with a maximum of 4 at a time.
3. Keep water available at all times. Maintain a 12-hour light/dark cycle and do not perform experimentation during the dark phase of the cycle.
4. Use alfalfa-free chow for feeding due to potential interference with fluorescent signaling.
5. Have research or veterinary staff assess mice daily to ensure the well-being of the animals throughout the entirety of the experiment.

4. Mouse surgical procedures

1. Induce anesthesia by placing mice in an isoflurane (2%) chamber for approximately 5 minutes. Confirm appropriate depth of anesthesia by monitoring respirations to remain rhythmic and slower than when awake and not changing in response to noxious stimuli (e.g., surgical manipulation, toe pinch).
2. Transfer anesthetized mice to a preparation station and remove hair from the sacrum to the upper thoracic spine with rodent clippers.
3. Clean and sterilize the skin with triple washes of alternating betadine solution and isopropyl alcohol.
4. Transfer anesthetized and sterilized mice in the prone position to a sterile surgical bed maintaining anesthesia with administration of inhaled isoflurane (2%) via nose cone.
5. Maximally flex the hips and identify the position of the knee at the level of the spine to approximate the lumbar 4 vertebral body.
6. Make a longitudinal 2 cm incision through skin with a 15-blade surgical scalpel.
7. Palpate the spinous processes to confirm midline and continue the incision down to bone.
8. Dissect subperiosteally on the right side of the L4 spinous process, extending laterally to the transverse process.
9. Pass an absorbable braided suture size 5-0 cephalad and caudad to the L4 body through the fascia and leave open, in preparation for future closure.
10. Using a 25 G spinal needle, ream the spinous process of L4 using a 25 G spinal needle and insert a 0.1 mm diameter, 1 cm long “L-shaped” surgical grade stainless-steel implant along the lamina with the long arm laying cephalad.
11. Inoculate the implant with 1 x 10³ CFUs/2 µL bioluminescent S. aureus Xen36, taking care to ensure all solution contacts the implant.
12. Wait approximately 10 seconds before tying the previously passed absorbable suture following inoculation to ensure containment of inoculum on the implant.
13. Close skin in running fashion with absorbable suture.
14. Administer pain medicine via subcutaneous injection of buprenorphine (0.1 mg/kg) immediately postop and then every 12 hours for 3 days thereafter.
15. Recover mice on a heating pad and monitor for return to normal activity.
16. Obtain postoperative radiographs to confirm appropriate placement of implant.

5. Longitudinal In vivo bioluminescence imaging to measure bacterial burden

1. Anesthetize mice with inhaled isoflurane (2%). Confirm appropriate depth of anesthesia by monitoring respirations to remain rhythmic and slower than when awake and not changing in response to noxious stimuli (e.g., surgical manipulation, toe pinch).
2. Remove hair from the sacrum to the upper thoracic spine with rodent clippers.
3. Load mice onto field of view of bioluminescent imaging platform to perform in vivo bioluminescence imaging (BLI)¹⁹.
4. Capture bioluminescent signal over a 5 min acquisition time. Utilize large binning settings with a 15 cm field of view (B).
5. Repeat steps 5.1-5.4 on postoperative days 0, 1, 3, 5, 7, 10, 14, 18, 21, 25, 28, and 35 (or other days based on specific experimental design) to monitor bacterial burden.
6. Present BLI data via color scale and overlay on a grayscale photograph. Isolate a standard ovoid region of interest (ROI) using BLI software to quantify BLI in total flux (photons per second) or mean maximum flux (photons/second/centimeter²/steradian).

6. Quantify bacteria adherent to implants and surrounding tissue

1. Euthanize mice on POD 35 or an alternative post-operative date of choice with exposure to carbon dioxide in accordance with AVMA Guidelines. Confirm euthanasia with secondary cervical dislocation.
2. Sterilize the dorsal skin according to Step 4.3 and position the mouse prone on a sterile surgical field.
3. Sharply incise the previous incision using a 15-blade surgical scalpel.
4. Use sterile scissors to bluntly dissect to the L4 spinous process and identify the surgical implant.
5. Use a needle driver to gently twist and remove the implant from its position in the L4 spinous process.
6. Using sterile forceps and scissors, harvest approximately 0.1 g of spinous process bone and soft tissue immediately surrounding the surgical implant and place in 1 mL of PBS in small conical rhino tube with 4 sharp homogenizing beads.
7. Record weight of soft tissue by weighing conical tube before and after harvest.
8. Place the implant in 0.5 mL of 0.3% Tween-80 in TSB and sonicate for 15 min.
9. Vortex the resulting implant suspension for 2 min and culture overnight for 12-16 h.
10. Homogenize the soft tissue and spinous processes previously placed in 1 ml PBS surrounding the implant using homogenizer.
11. Vortex the resulting soft tissue suspension for 5 min and culture overnight for 12-16 h.
12. After overnight culture, count CFU from the implant and surrounding tissues, respectively. Express value as total CFU/g harvested for soft tissue and CFU/mL for sonicated implant.

Wyniki

The procedure presented here was used to assess the efficacy of antibiotic regimens in an in vivo mouse model of SII. Specifically, the efficacy of combination vancomycin and rifampin antibiotic therapy was compared to vancomycin monotherapy and untreated infected controls.

Prior to surgery, mice were randomized to either combination therapy, monotherapy, or infected control. A statistical power analysis was performed to calculate sample size. Anticipated means of mean maximum flux 1 x 10^...

Dyskusje

Implant related infections in the spine portend poor outcomes for patients^1,2,3,4,5. Unlike many other areas in the body, infected hardware in the spine frequently cannot be removed due to the risk of instability and neurologic compromise. This unique challenge in the setting of biofilm bacteria resistant to systemic antibiotic therapy necessitate novel approa...

Materiały

Name	Company	Catalog Number	Comments
Analytical Balance ME104	Mettler Toledo	30029067	120 g capacity, 0.1 mg readability, backlit LCD, internal adjustment, metal base
BD Bacto Tryptic Soy Broth	Becton Dickinson (BD)	BD 211825	BD Bacto Tryptic Soy Broth (Soybean-Casein Digest Medium)
Biomate 3S UV-VIS Spectrophotometer	Thermo Scientific	840-208300	Spectrophotometer; Thermo Scientific; BioMate 3S; Six-position cell holder; Spectral bandwidth: 1.8nm; Long-life xenon lamp; Store up to 40 test methods; 16L x 13W x 9 in. H; 19 lb.; 100/240V US line cord
Bioshield 720+ swinging bucket rotor	Thermo Scientific	75003183	Rotor, Swinging bucket; Thermo Scientific; BIOShield 720 high speed; Capacity: 4 x 180mL (0.72L); Angle: 90 deg. ; Max. speed/RCF: 6300rpm/7188 x g; Max. radius: 16.2cm
Branson Ultrasonics 2510R-MTH (Sonicator)	Branson Ultrasonics	CPX952217R	*similar model, our model is discontinued* Branson Ultrasonics MH Series Heated Ultrasonic Cleaning Bath, 120V, 0.75 gal
Bullet Blender Storm Homogenizer	Next Advance	BBY24M	The Bullet Blender Storm is the most powerful member of the Bullet Blender family. Homogenize up to 24 of your toughest samples (mouse femur, skin, cartilage, tumor, etc.) in just minutes. Air cooling™ minimizes sample heat up. Uses 1.5ml screw-cap RINO® tubes or snap-cap Eppendorf® Safe-lock™ tubes.
Germinator 500	Electron Microscopy Sciences	66118-10	The Germinator 500 is designed to decontaminate metal micro-dissecting instruments only. It is to be used exclusively for research purposes. The Germinator 500 should not be used as a substitute for traditional methods of terminal sterilization. Effective sterilization cannot be assured due to lack of routine sterilization-efficacy monitoring methods for glass bead sterilization. The Germinator 500 has been designed and built to pass the Validation of Dry Sterilizer Spore Suspension Test: USP XXIII, Part 1211.
Heracell 150i CO2 Incubator	Thermo Scientific	51026282	Single 150L
IVIS Lumina X5 Imaging System	Perkin Elmer	CLS148590	The IVIS Lumina X5 high-throughput 2D optical imaging system combines high-sensitivity bioluminescence and fluorescence with high-resolution x-ray into a compact system that fits on your benchtop. With an expanded 5 mouse field of view for 2D optical imaging plus our unique line of accessories to accelerate setup and labeling, it has never been easier or faster to get robust data—and answers—on anatomical and molecular aspects of disease.
MAXQ 4450 Digtial Incubating Bench Shaker	Thermo Scientific	SHKE4450	Shaker, Incubated; Thermo Scientific; Digital; MaxQ 4450; Speed 15 to 500rpm +/-1rpm; 5 deg. C above ambient to 80 deg. C; 120V 50/60Hz
PBS, Phosphate Buffered Saline	Fisher Bioreagents	BP24384	PBS, Phosphate Buffered Saline, 1X Solution, pH 7.4
Sorvall Legend Micro 21 Centrifuge, Ventilated	Thermo Scientific	75002436	24 x 1.5/2.0mL rotor with ClickSeal biocontainment lid
SORVALL LEGEND X1R 120V Centrifuge	Thermo Scientific	75004261	Centrifuge, Benchtop; Thermo Scientific; Sorvall Legend X1R (Refrigerated), 1L capacity; Max. Speed/RCF 15,200rpm/25,830 x g; CFC-free cooling -10C to +40C; 120V 60Hz
Staphylococcus aureus - Xen36	Perkin Elmer	119243	Staphylococcus aureus - Xen36 bioluminescent pathogenic bacteria for in vivo and in vitro drug discovery. This product was derived from a parental strain from the American Type Culture Collection, used under license. Staph. aureus-Xen36 possesses a stable copy of the Photorhabdus luminescens lux operon on the native plasmid.
TUTTNAUER AUTOCLAVE 2540E 120V	Heidolph Tuttnauer	23210401	Sterilizer, Benchtop; Heidolph; Tuttnauer; Model 2540E; Self-contained design with refillable reservoir controls water purity for sterilization; 120V 50/60Hz; 1400w. With electronic controls
Tween 80	Fisher Bioreagents	BP338-500	Tween 80, Fisher BioReagents, Non-ionic detergent for selective protein extraction
Vortex mixer VX-200	Labnet Internation	S0200	120V touch or continuous mixer, 230V: 0 - 2,850 rpm,120V: 0 - 3,400 rpm
0.9% Sodium Chloride	Pfizer Injectables/Hospira	00409-4888-10	0.9% Sodium Chloride Injection, USP