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Renal scar formation and kidney function following antibiotic-treated murine pyelonephritis
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 s...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5719254/ https://www.ncbi.nlm.nih.gov/pubmed/28882930 http://dx.doi.org/10.1242/dmm.030130 |
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author | Olson, Patrick D. McLellan, Lisa K. Liu, Alice Briden, Kelleigh L. Tiemann, Kristin M. Daugherty, Allyssa L. Hruska, Keith A. Hunstad, David A. |
author_facet | Olson, Patrick D. McLellan, Lisa K. Liu, Alice Briden, Kelleigh L. Tiemann, Kristin M. Daugherty, Allyssa L. Hruska, Keith A. Hunstad, David A. |
author_sort | Olson, Patrick D. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5719254 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-57192542017-12-11 Renal scar formation and kidney function following antibiotic-treated murine pyelonephritis Olson, Patrick D. McLellan, Lisa K. Liu, Alice Briden, Kelleigh L. Tiemann, Kristin M. Daugherty, Allyssa L. Hruska, Keith A. Hunstad, David A. Dis Model Mech Resource Article 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. The Company of Biologists Ltd 2017-11-01 /pmc/articles/PMC5719254/ /pubmed/28882930 http://dx.doi.org/10.1242/dmm.030130 Text en © 2017. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Resource Article Olson, Patrick D. McLellan, Lisa K. Liu, Alice Briden, Kelleigh L. Tiemann, Kristin M. Daugherty, Allyssa L. Hruska, Keith A. Hunstad, David A. Renal scar formation and kidney function following antibiotic-treated murine pyelonephritis |
title | Renal scar formation and kidney function following antibiotic-treated murine pyelonephritis |
title_full | Renal scar formation and kidney function following antibiotic-treated murine pyelonephritis |
title_fullStr | Renal scar formation and kidney function following antibiotic-treated murine pyelonephritis |
title_full_unstemmed | Renal scar formation and kidney function following antibiotic-treated murine pyelonephritis |
title_short | Renal scar formation and kidney function following antibiotic-treated murine pyelonephritis |
title_sort | renal scar formation and kidney function following antibiotic-treated murine pyelonephritis |
topic | Resource Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5719254/ https://www.ncbi.nlm.nih.gov/pubmed/28882930 http://dx.doi.org/10.1242/dmm.030130 |
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