Urinary Tract Infection in a Small Animal Model: Transurethral Catheterization of Male and Female Mice

Summary

The established model of transurethral catheterization of mice allows the study of bladder pathologies, including urinary tract infection, but can only be performed in females. A new model of male transurethral instillation, presented here, will enable research in an area marked by strong clinical and epidemiological differences between the sexes.

Abstract

Urinary tract infections (UTI) are extremely common worldwide, incurring significant morbidity and healthcare-associated expenses. Small animal models, which accurately reflect disease establishment and progression, permit dissection of host-pathogen interactions and generation of immunity to infection. In mice, intravesical instillation of uropathogenic E. coli, the causative agent in more than 85% of community acquired UTI, recapitulates many of the stages of infection observed in humans. Until recently, however, UTI could only be modeled in female animals. This limitation has hindered the study of sex-related differences in UTI, as well as other bladder pathologies, such as cancer. Here, we describe a method to instill male mice that allows direct comparison between female and male animals and provide a detailed protocol to assess bladder tissue by flow cytometry as a means to better understand host responses to infection. Together, these approaches will aid in the identification of host factors that contribute to sex biases observed in UTI and other bladder-associated diseases.

Introduction

Urinary tract infections (UTI) are one of the most common infections in developed countries¹. Infection rates are similar between females and males among neonates and the elderly². Premenopausal adult women, however, have a greatly increased incidence of community-acquired UTI compared to men^2,3. Given that this disease primarily impacts women, fundamental and clinical research has overwhelmingly focused on UTI in females. However, UTI in men is a significant and understudied health care challenge⁴. Indeed, because UTI in men are associated with higher morbidity, these infections are routinely defined as complicated^4,5.

As our understanding of the central role of sex biases in physiology and pathology evolves, new methods are required to explore this previously neglected aspect of disease. Sex differences play an essential role in immunity and infection; females have higher incidence of autoimmune disease, while males are more susceptible to certain infections, such as tuberculosis, malaria, and HIV^6,7. Bladder cancer, another urologic pathology, is significantly more prevalent in men than in women, and several studies have shown a role for androgens in the development of malignancy^8,9,10,11,12. Notably, however, investigation of intravesical therapies for bladder cancer is performed exclusively in female animals, due to the inability to repeatedly catheterize male mice¹³.

The study of UTI pathogenesis relies heavily on rodent models of infection (e.g., mice and rats). Murine models of UTI may employ uropathogens originally isolated from human infections, such as uropathogenic E. coli (UPEC), Klebsiella, Enterococcus, Staphylococcus, or Proteus¹⁴. Typically, bacteria are introduced into the bladder via catheterization of the urethra. Following infection, bladders and kidneys can be removed to assess specific parameters of infection, such as bacterial colonization, tissue damage, or host immune response^15,16. Universally, however, only female animals are used for UTI research. Indeed, many studies have noted that, due to anatomical reasons, catheterization of male mice is not possible^13,17,18,19. More recently, a surgical approach to male instillation has been described, in which the abdomen is opened, the bladder is externally displaced by applying gentle pressure to the opening in the abdomen, and bacteria are injected into the bladder²⁰. This approach enables male infection, at the cost of surgical intervention. Thus, a major caveat of this approach includes the influence of inflammation, on the outcome of infection such as the potential to induce an anti-inflammatory wound-healing response to the incision²¹. As our interests include understanding sex bias in response to disease, we developed a method of bacterial intravesical instillation in male mice that more closely matches the long-established non-surgical transurethral approach used in female rodents²².

Our model builds upon an established methodology and provides the ability to directly compare the host immune response to UTI in female and male animals. This method will permit dissection of sex-based differences in infection, and potentially offer molecular and cellular clues to the pronounced differences in susceptibility and response to infection between the sexes. Additionally, this model has value beyond UTI studies, allowing the establishment of models to investigate other bladder-associated diseases, such as bladder cancer, prostatitis, under- or over-active bladder syndrome, and interstitial cystitis.

Protocol

Mouse experiments were conducted in accordance with approval of protocol number 2012-0024 by the Comité d'éthique en expérimentation animale Paris Centre et Sud (the ethics committee for animal experimentation), in application of the European Directive 2010/63 EU.

1. Preparation of Catheters

1. Prepare one pediatric intravenous-access cannula for each group of mice to be infected. Using the inbuilt spring mechanism, divest each cannula of its needle, as instructed by the manufacturer. Discard the needles, preserving only the plastic intravenous cannula.
2. Sterilize catheters in a laminar flow hood for one ultraviolet (U.V.) cycle, typically 25 - 30 min.
   Note: Catheters can be used for more than one mouse, however a new catheter should be used between experimental groups, sexes, or bacterial strains.

2. Preparation of Uropathogenic E. coli for Infection

1. At least two days prior to infection, using a sterile inoculation loop, streak UPEC from a frozen bacterial stock onto a Luria Broth (LB) agar plate, containing antibiotics if appropriate. Incubate at 37 °C overnight. Plates can be stored at 4 °C for up to one week.
2. In a 100 ml sterile Erlenmeyer flask, inoculate 10 ml LB, containing antibiotics if appropriate, with a single colony from the LB plate and incubate standing at 37 °C overnight (approximately 16 - 18 hr).
   Note: Standing cultures permit the expression of type 1 pili, which are necessary for infection²³. Cultures grown shaking will have less efficient pili expression, and therefore, inconsistent rates of infection.
3. Measure the optical density (OD)₆₀₀ of the overnight culture and calculate the number of bacteria per ml using a pre-determined growth curve. As an example, for UPEC strain UTI89, OD₆₀₀ = 0.35 is equivalent to 2 x 10⁸ CFU per ml, thus, an overnight culture with an OD₆₀₀ = 2.4 would be equivalent to 13.7 x 10⁸ CFU per ml. Empirically determine the relationship between the OD₆₀₀ and viable bacteria with every new strain employed for infection.
4. Determine the amount of bacteria needed by considering the number of animals to be infected and that each mouse should receive approximately 10⁷ colony-forming units (CFU) in 50 μl PBS. Include in the calculation the ~130 µl dead volume of the catheter and syringe nub and 100 µl needed to determine the inoculum.
   1. Spin the bacterial suspension in a tabletop microcentrifuge at 17,000 x g for 1 min and resuspend the resulting bacterial pellet at 2 x 10⁸ CFU per ml in PBS. Serially dilute an aliquot of this suspension and plate on LB agar, with antibiotics if appropriate, to determine the exact inoculum for each infection.
5. Draw the bacterial inoculum into a 1 ml syringe and attach the catheter to the end of the syringe. Tap the syringe to remove any air and depress the plunger to fill the dead air space in the catheter before beginning the instillation.

3. Preparation of Mice

1. Anesthetize mice via intraperitoneal injection of 100 mg/kg ketamine and 5 mg/kg xylazine. Supplemental heat can be provided. 
2. Ensure that each mouse is fully sedated by squeezing the footpad with medium pressure. Mice are fully sedated when they do not react and require 3 - 5 min to reach this state.
3. Place mice supine and apply medium pressure to the lower abdomen to empty the bladder of urine. Full bladders feel like a pea under the skin between the ileac crests.
   Note: Inhaled isoflurane has been used to catheterize female mice^15,22, however, it has not been tested whether male mice are sufficiently anesthetized by inhaled isoflurane for this procedure.

4. Transurethral Instillation of Female Mice

1. Using the non-dominant hand, place the thumb on the tail and a finger of the same hand on the abdomen of the mouse and apply gentle pressure in opposing directions to hold the mouse firmly in place.
2. Place the tip of the catheter perpendicular to the mouse at the urethral orifice. With gentle pressure, slide the catheter into the urethra, until the hub meets the urethral orifice, while simultaneously lowering the syringe so that it is parallel to the working surface. The catheter requires no lubrication. Do not push or force the catheter into the urethra. The catheter should slide smoothly and easily into the urethra, with little to no resistance.
   1. Before instilling the inoculum (step 4.3), once the catheter is in place, very gently pull the abdominal skin towards the head of the mouse with the finger from the non-dominant hand that is already on the abdomen of the mouse (step 4.1). If the catheter is in the urethra, the tissue composing the urethra orifice will not move, whereas if the catheter is incorrectly placed in the vagina, the tissue will move up and away from the catheter. This rapid test should be performed on each mouse.
3. When the hub of the catheter meets the urethral orifice, slowly dispense 50 µl of the bacterial inoculum. A slow instillation rate minimizes vesicoureteral reflux into the kidney. Slowly remove the catheter to prevent leakage, over a count of 5. Place mice in their cages in a supine position.

5. Transurethral Instillation of Male Mice

1. Place two thumb forceps cranially and caudally to the mouse's external genitalia. Retract the prepuce to fully expose the glans penis. Once the penis is externally positioned, release the thumb forceps.
2. Reposition the forceps to stabilize the protruding penis perpendicular to the animal, holding the organ gently but tautly. Visualize the urethral meatus and carefully introduce the catheter into the small opening at the tip of the organ. Gently guide the catheter into the penis, toward the body of the mouse, maintaining gentle tension with the forceps. The catheter requires no lubrication. Do not force the catheter into the penis; the catheter should slide smoothly into the urethra, indicating correct placement.
3. Once the hub of the catheter meets the tip of the penis, very slowly dispense 50 µl of the inoculum, while maintaining the position of the penis. The quality of the instillation can be noted at this time according to a predetermined instillation quality score, such as that shown in Figure 2.
4. Retract the catheter slowly, over a count of 5, to prevent leakage of the inoculum. Place mice in their cages in a supine position. Animals should begin to recover 30 - 45 min following administration of the anesthetic.

6. Determination of CFU in Infected Organs

1. At predetermined time-points, sacrifice mice using approved standard operating procedures (e.g., cervical dislocation or carbon dioxide overdose). Moisten the abdomen thoroughly with 70% ethanol to minimize contamination by fur.
2. Make an incision across the lower third of the mouse's abdomen of at least 2 cm using scissors and aseptically remove the bladder and any other desired organs, including but not limited to, kidneys, testis, seminal vesicles, or preputial glands, into 5 ml polypropylene snap cap tubes containing 1 ml sterile PBS. Keep all samples on ice.
3. Homogenize the organs with a handheld homogenizer until almost no solid tissue remains, approximately 15 - 60 sec depending on the organ. Fat does not homogenize well, and is easily recognizable as shiny beige-white tissue. Discard fat prior to or following homogenization. Wash the homogenizer in ethanol followed by PBS between each experimental or organ group.
   Note: Typically, use handheld homogenizers or bead mill homogenizers. While all of these systems have yielded similar results, as determined by direct comparison of bacterial CFU at 24 hr post-infection, the optimal conditions to homogenize host tissue while preserving bacterial viability should be determined empirically before performing this protocol routinely.
4. Perform serial dilutions of homogenized organ suspensions. Plate dilutions on LB agar plates, containing antibiotics when appropriate, and incubate overnight (~15 hr) at 37 °C. UPEC strains have very rapid doubling times and as such, care should be taken to not incubate the agar plates too long because this will hinder the ability to count individual colonies.

7. Flow Cytometric Analysis of Bladder Tissue

1. Prepare digestion buffer containing collagenase at 34 units/mL and DNase at 100 µg/mL, in PBS. Keep on ice. Prepare one 15 ml conical tube per animal to be analyzed and aliquot 1 ml digestion buffer per tube.
2. At predetermined timepoints, sacrifice mice using approved standard operating procedures (e.g., cervical dislocation or carbon dioxide overdose). Moisten the abdomen thoroughly with 70% ethanol to minimize contamination by fur.
3. Make an incision across the lower third of the mouse's abdomen of at least 2 cm using scissors and remove the entire bladder. Mince well with scissors, cutting the bladder into 2 - 3 mm² sized pieces, typically about 8 pieces.
   1. Add one minced bladder per tube containing digestion buffer. Shake to wash minced bladder tissue into the digestion buffer. Keep on ice until all bladders are dissected and minced.
4. Incubate minced bladders for 60 - 75 min at 37 °C, with vigorous shaking by hand for 5 s every 15 min. When the tissue has a glassy transparent appearance, resembling wet tissue paper, digestion is complete. Prolonged digestion will remove surface proteins from the cells needed for identification and should be avoided.
5. Inactivate the digestion enzymes by adding 2 - 3 mL of ice-cold flow cytometry buffer (PBS containing 2% fetal bovine serum (FBS) and 0.2 mM EDTA) and mix gently. Place tubes on ice.
6. To ensure a single cell suspension and to remove any connective tissue, pass the contents of the tube through a 100 µm filter placed in a 15 mL conical tube. Gently press any remaining tissue through the filter with the end of a syringe plunger. Wash the filter with an additional 2 mL flow cytometry buffer. Keep samples on ice.
7. Wash samples by centrifugation for 7 min at 200 x g, 4 °C. Resuspend pellets in 100 µL flow cytometry buffer containing Fc block, diluted to 5 µg/mL and transfer to a 96-well round bottom plate. After 10 - 15 min, add 100 µL desired antibody cocktail to each sample. Incubate samples for 30 - 45 min, on ice, protected from light.
   Note: Fc block is a reagent used to prevent the binding of the Fc portion of antibodies to cells expressing Fc receptors. Its purpose is to minimize nonspecific antibody binding. Determination of antibodies to use will be dependent upon the hypothesis being tested in the experiment and should be selected with input from the literature. In Figure 3, to measure the overall immune cell infiltration, an anti-CD45 antibody was employed, which is a pan-immune cell protein.
8. Wash samples by centrifugation for 7 min at 200 x g, 4 °C. Resuspend cell pellets in 200 µL flow cytometry buffer and pass samples through a 40 µm cell strainer on a 5 ml polystyrene tube just prior to acquisition on a flow cytometer.
9. Collect the entire sample on the flow cytometer. A good digestion will yield 200,000 - 400,000 cells, with 8,000 - 10,000 CD45⁺ immune cells from naïve mouse bladders, while infected organs will contain more cells¹⁶ (Figure 3).
   Note: Samples prepared for flow cytometric analysis cannot be used to evaluate CFU. It is not recommended to split the bladder into two parts as no evidence exists to demonstrate that UPEC colonization or immune cell infiltration is uniform throughout the tissue.

Results

In the development of this protocol, cohorts of female and male C57Bl/6 mice aged 6 to 8 weeks were instilled, and bacterial burden evaluated in bladders at time points ranging from 1 hr to 30 days. The results from these studies are detailed elsewhere (Zychlinsky Scharff et al., pending). Here, we present representative data from 24 hr infections. Notably, bacterial burden was equivalent between male and female mice at 24 hr post-infection (Figure 1). Little var...

Discussion

Transurethral instillation of male mice offers many new research opportunities into the influence of sex on bladder mucosal disease, but also presents several challenges. Foremost, one limitation is that the instillation may initially prove to be technically difficult, resulting in excessive inflammation during catheter insertion. Improvement in technique can be achieved by the instillation of dead mice with a colored solution, such as Evans blue dye. To confirm that the instillation is successful, bladders should be vis...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
BD Insyte Autoguard Shielded IV Catheters 24 G, 0.7 mm external diameter, 14 mM long	BD Medical	381811 or 381411*	* catalog number is country-dependent
inoculating loop	Greiner Bio-One	731171
LB Miller broth	Difco	244620
LB Miller agar	Difco	244520
Cuvettes	Bio-rad	223-9955
syringes	B Braun	9166017V
Thumb (Adson) forceps	Fine Science Tools	11006-12
5 ml tubes, polypropylene	Falcon	352063
Tissue Ruptor disposable probes	Qiagen	990890
15 ml flip cap tubes	Thermo Scientific	362694
DNAse	Invitrogen	18047019
Liberase TM	Sigma-Aldrich	5401119001	should be aliquotted and stored at -20 °C to avoid repeated freeze-thaw
100 µM MACS SmartStrainers	Miltenyi	130-098-463	compatible with 15 ml tubes, preferred
100 µm cell strainers	Falcon	352360	compatible with 50 ml tubes, if MACS Smart Strainers are not available
96 well plate	Falcon	353077
Fc block	BD Pharmingen	553142	anti-CD16/CD32
anti-mouse CD45 antibody	BD Biosciences	561487	many different fluorescent conjugation options are available
5 ml tubes polystyrene with filter cap	Falcon	352235
insulin syringe	Terumo	BS05M2913
hand held homogenizer	Qiagen	9001272	TissueRuptor
flow cytometer	BD Biosciences	N/A	Fortessa SORP
Flow cytometry software	BD Biosciences	N/A	Diva