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Updated: Feb 23, 2026

Bilateral Renal Ischemia-Reperfusion Model for Acute Kidney Injury in Mice
Published on: February 2, 2024
Renal scar formation and kidney function following antibiotic-treated murine pyelonephritis
Patrick D Olson1,2, Lisa K McLellan2, Alice Liu2
1Medical Scientist Training Program, Washington University School of Medicine, St Louis, MO 63110, USA.
Insights
A new male mouse model for pyelonephritis allows studying antibiotic treatment and long-term kidney damage. This model helps understand urinary tract infection (UTI) complications and potential new therapies.
Area of Science:
- Microbiology
- Nephrology
- Pediatrics
Background:
- Urinary tract infections (UTIs), often caused by uropathogenic Escherichia coli (UPEC), are common in children.
- Severe pyelonephritis can lead to renal scarring, hypertension, and chronic kidney disease.
- Existing preclinical UTI models using female mice have limitations in studying severe infection and recovery.
Purpose of the Study:
- To develop and optimize a preclinical model for studying the treatment, resolution, and sequelae of severe ascending pyelonephritis.
- To assess the efficacy of antibiotic treatment in a male mouse model of pyelonephritis.
- To investigate the long-term consequences of pyelonephritis following antibiotic therapy.
Main Methods:
- Utilized a novel mini-surgical bladder inoculation technique in male C3H/HeN mice to induce ascending pyelonephritis.
- Administered a 5-day ceftriaxone regimen starting at abscess development.
- Monitored infection resolution, histological changes, renal function, and late sequelae (scarring, hydronephrosis, chronic kidney disease) at various time points.
Main Results:
- Ceftriaxone treatment resolved bladder and kidney infections in most male mice.
- A minority of treated mice showed persistent histological abscesses or developed renal scars with fibrosis and inflammation.
- Antibiotic treatment preserved renal function, but hydronephrosis and occasional chronic kidney disease were observed as late effects.
Conclusions:
- The developed male mouse model effectively mimics human pyelonephritis, enabling study of treatment response and sequelae.
- This model provides a platform to investigate antibiotic efficacy and the emergence of long-term complications like renal scarring.
- Future research using this model can inform adjunctive therapies to reduce chronic complications of UTIs.
Abstract:
We present a new preclinical model to study treatment, resolution and sequelae of severe ascending pyelonephritis. Urinary tract infection (UTI), primarily caused by uropathogenic Escherichia coli (UPEC), is a common disease in children. Severe pyelonephritis is the primary cause of acquired renal scarring in childhood, which may eventually lead to hypertension and chronic kidney disease in a small but important fraction of patients. Preclinical modeling of UTI utilizes almost exclusively females, which (in most mouse strains) exhibit inherent resistance to severe ascending kidney infection; consequently, no existing preclinical model has assessed the consequences of recovery from pyelonephritis following antibiotic treatment. We recently published a novel mini-surgical bladder inoculation technique, with which male C3H/HeN mice develop robust ascending pyelonephritis, highly prevalent renal abscesses and evidence of fibrosis. Here, we devised and optimized an antibiotic treatment strategy within this male model to more closely reflect the clinical course of pyelonephritis. A 5-day ceftriaxone regimen initiated at the onset of abscess development achieved resolution of bladder and kidney infection. A minority of treated mice displayed persistent histological abscess at the end of treatment, despite microbiological cure of pyelonephritis; a matching fraction of mice 1 month later exhibited renal scars featuring fibrosis and ongoing inflammatory infiltrates. Successful antibiotic treatment preserved renal function in almost all infected mice, as assessed by biochemical markers 1 and 5 months post-treatment; hydronephrosis was observed as a late effect of treated pyelonephritis. An occasional mouse developed chronic kidney disease, generally reflecting the incidence of this late sequela in humans. In total, this model offers a platform to study the molecular pathogenesis of pyelonephritis, response to antibiotic therapy and emergence of sequelae, including fibrosis and renal scarring. Future studies in this system may inform adjunctive therapies that may reduce the long-term complications of this very common bacterial infection.
Related Concept Videos
Acute Kidney Injury IV: Diagnostic Studies and Prevention
Acute Pyelonephritis II: Diagnostic Studies and Management
Acute Pyelonephritis I: Introduction
Acute Kidney Injury II: Pathophysiology
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Acute Kidney Injury III: Clinical Manifestations

