Cargando…

Hematogenous dissemination of pathogenic and non-pathogenic Leptospira in a short-term murine model of infection

Leptospirosis is an emerging zoonosis caused by pathogenic Leptospira spp. Because rodents are natural hosts of Leptospira, rodent models of pathogenesis have been limited, but are valuable to understand infection in reservoir animals even in the absence of disease. Mouse models of infection provide...

Descripción completa

Detalles Bibliográficos
Autores principales: Surdel, Matthew C., Anderson, Phillip N., Hahn, Beth L., Coburn, Jenifer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9339599/
https://www.ncbi.nlm.nih.gov/pubmed/35923802
http://dx.doi.org/10.3389/fcimb.2022.917962
_version_ 1784760202341384192
author Surdel, Matthew C.
Anderson, Phillip N.
Hahn, Beth L.
Coburn, Jenifer
author_facet Surdel, Matthew C.
Anderson, Phillip N.
Hahn, Beth L.
Coburn, Jenifer
author_sort Surdel, Matthew C.
collection PubMed
description Leptospirosis is an emerging zoonosis caused by pathogenic Leptospira spp. Because rodents are natural hosts of Leptospira, rodent models of pathogenesis have been limited, but are valuable to understand infection in reservoir animals even in the absence of disease. Mouse models of infection provide advantages due to genetic tractability, so developing murine models of Leptospira infection is crucial for further understanding the biology of this organism. Previously our laboratory developed a short-term murine model of Borrelia burgdorferi hematogenous dissemination to investigate the role of adhesion proteins on bacterial survival and dissemination within a host. Here we adapt this model to Leptospira. C3H/HeJ mice are anesthetized, inoculated intravenously, and then bacteria are allowed to circulate for up to twenty-four hours. Mice are euthanized, perfused with saline, and tissues are harvested for culture and DNA purification. Bacterial burdens are determined by quantitative PCR. Reproducible burdens of bacteria were found in tissues upon inoculation with pathogens and non-pathogens, demonstrating the utility of this model to probe different Leptospira species and strains. Pathogenic L. interrogans has a significantly higher burden in blood, liver, kidney, and bladder at one-hour post-inoculation when compared to non-pathogenic L. biflexa. Colonization of the kidney is essential to the life cycle of pathogenic Leptospira in nature. Measurable burdens of non-pathogenic L. biflexa were found in numerous organs and live leptospires were recovered from blood samples for at least three hours post-inoculation, contrary to the previous belief that non-pathogenic leptospires are rapidly cleared. This short-term murine model of Leptospira hematogenous dissemination will allow for the interrogation of virulence factors potentially important for tissue colonization and evasion of host defenses, and represents a novel animal model for investigating determinants of Leptospira infection.
format Online
Article
Text
id pubmed-9339599
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-93395992022-08-02 Hematogenous dissemination of pathogenic and non-pathogenic Leptospira in a short-term murine model of infection Surdel, Matthew C. Anderson, Phillip N. Hahn, Beth L. Coburn, Jenifer Front Cell Infect Microbiol Cellular and Infection Microbiology Leptospirosis is an emerging zoonosis caused by pathogenic Leptospira spp. Because rodents are natural hosts of Leptospira, rodent models of pathogenesis have been limited, but are valuable to understand infection in reservoir animals even in the absence of disease. Mouse models of infection provide advantages due to genetic tractability, so developing murine models of Leptospira infection is crucial for further understanding the biology of this organism. Previously our laboratory developed a short-term murine model of Borrelia burgdorferi hematogenous dissemination to investigate the role of adhesion proteins on bacterial survival and dissemination within a host. Here we adapt this model to Leptospira. C3H/HeJ mice are anesthetized, inoculated intravenously, and then bacteria are allowed to circulate for up to twenty-four hours. Mice are euthanized, perfused with saline, and tissues are harvested for culture and DNA purification. Bacterial burdens are determined by quantitative PCR. Reproducible burdens of bacteria were found in tissues upon inoculation with pathogens and non-pathogens, demonstrating the utility of this model to probe different Leptospira species and strains. Pathogenic L. interrogans has a significantly higher burden in blood, liver, kidney, and bladder at one-hour post-inoculation when compared to non-pathogenic L. biflexa. Colonization of the kidney is essential to the life cycle of pathogenic Leptospira in nature. Measurable burdens of non-pathogenic L. biflexa were found in numerous organs and live leptospires were recovered from blood samples for at least three hours post-inoculation, contrary to the previous belief that non-pathogenic leptospires are rapidly cleared. This short-term murine model of Leptospira hematogenous dissemination will allow for the interrogation of virulence factors potentially important for tissue colonization and evasion of host defenses, and represents a novel animal model for investigating determinants of Leptospira infection. Frontiers Media S.A. 2022-07-18 /pmc/articles/PMC9339599/ /pubmed/35923802 http://dx.doi.org/10.3389/fcimb.2022.917962 Text en Copyright © 2022 Surdel, Anderson, Hahn and Coburn https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular and Infection Microbiology
Surdel, Matthew C.
Anderson, Phillip N.
Hahn, Beth L.
Coburn, Jenifer
Hematogenous dissemination of pathogenic and non-pathogenic Leptospira in a short-term murine model of infection
title Hematogenous dissemination of pathogenic and non-pathogenic Leptospira in a short-term murine model of infection
title_full Hematogenous dissemination of pathogenic and non-pathogenic Leptospira in a short-term murine model of infection
title_fullStr Hematogenous dissemination of pathogenic and non-pathogenic Leptospira in a short-term murine model of infection
title_full_unstemmed Hematogenous dissemination of pathogenic and non-pathogenic Leptospira in a short-term murine model of infection
title_short Hematogenous dissemination of pathogenic and non-pathogenic Leptospira in a short-term murine model of infection
title_sort hematogenous dissemination of pathogenic and non-pathogenic leptospira in a short-term murine model of infection
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9339599/
https://www.ncbi.nlm.nih.gov/pubmed/35923802
http://dx.doi.org/10.3389/fcimb.2022.917962
work_keys_str_mv AT surdelmatthewc hematogenousdisseminationofpathogenicandnonpathogenicleptospirainashorttermmurinemodelofinfection
AT andersonphillipn hematogenousdisseminationofpathogenicandnonpathogenicleptospirainashorttermmurinemodelofinfection
AT hahnbethl hematogenousdisseminationofpathogenicandnonpathogenicleptospirainashorttermmurinemodelofinfection
AT coburnjenifer hematogenousdisseminationofpathogenicandnonpathogenicleptospirainashorttermmurinemodelofinfection