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Differential susceptibility of C57BL/6NCr and B6.Cg-Ptprc(a )mice to commensal bacteria after whole body irradiation in translational bone marrow transplant studies
BACKGROUND: The mouse is an important and widely utilized animal model for bone marrow transplant (BMT) translational studies. Here, we document the course of an unexpected increase in mortality of congenic mice that underwent BMT. METHODS: Thirty five BMTs were analyzed for survival differences uti...
Autores principales: | , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2292684/ https://www.ncbi.nlm.nih.gov/pubmed/18307812 http://dx.doi.org/10.1186/1479-5876-6-10 |
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author | Duran-Struuck, Raimon Hartigan, Adam Clouthier, Shawn G Dyson, Melissa C Lowler, Kathi Gatza, Erin Tawara, Isao Toubai, Tomomi Weisiger, Elisabeth Hugunin, Kelly Reddy, Pavan Wilkinson, John E |
author_facet | Duran-Struuck, Raimon Hartigan, Adam Clouthier, Shawn G Dyson, Melissa C Lowler, Kathi Gatza, Erin Tawara, Isao Toubai, Tomomi Weisiger, Elisabeth Hugunin, Kelly Reddy, Pavan Wilkinson, John E |
author_sort | Duran-Struuck, Raimon |
collection | PubMed |
description | BACKGROUND: The mouse is an important and widely utilized animal model for bone marrow transplant (BMT) translational studies. Here, we document the course of an unexpected increase in mortality of congenic mice that underwent BMT. METHODS: Thirty five BMTs were analyzed for survival differences utilizing the Log Rank test. Affected animals were evaluated by physical examination, necropsy, histopathology, serology for antibodies to infectious disease, and bacterial cultures. RESULTS: Severe bacteremia was identified as the main cause of death. Gastrointestinal (GI) damage was observed in histopathology. The bacteremia was most likely caused by the translocation of bacteria from the GI tract and immunosuppression caused by the myeloablative irradiation. Variability in groups of animals affected was caused by increased levels of gamma and X-ray radiation and the differing sensitivity of the two nearly genetically identical mouse strains used in the studies. CONCLUSION: Our retrospective analysis of thirty five murine BMTs performed in three different laboratories, identified C57BL/6NCr (Ly5.1) as being more radiation sensitive than B6.Cg-Ptprc(a)/NCr (Ly5.2). This is the first report documenting a measurable difference in radiation sensitivity and its effects between an inbred strain of mice and its congenic counterpart eventually succumbing to sepsis after BMT. |
format | Text |
id | pubmed-2292684 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-22926842008-04-12 Differential susceptibility of C57BL/6NCr and B6.Cg-Ptprc(a )mice to commensal bacteria after whole body irradiation in translational bone marrow transplant studies Duran-Struuck, Raimon Hartigan, Adam Clouthier, Shawn G Dyson, Melissa C Lowler, Kathi Gatza, Erin Tawara, Isao Toubai, Tomomi Weisiger, Elisabeth Hugunin, Kelly Reddy, Pavan Wilkinson, John E J Transl Med Research BACKGROUND: The mouse is an important and widely utilized animal model for bone marrow transplant (BMT) translational studies. Here, we document the course of an unexpected increase in mortality of congenic mice that underwent BMT. METHODS: Thirty five BMTs were analyzed for survival differences utilizing the Log Rank test. Affected animals were evaluated by physical examination, necropsy, histopathology, serology for antibodies to infectious disease, and bacterial cultures. RESULTS: Severe bacteremia was identified as the main cause of death. Gastrointestinal (GI) damage was observed in histopathology. The bacteremia was most likely caused by the translocation of bacteria from the GI tract and immunosuppression caused by the myeloablative irradiation. Variability in groups of animals affected was caused by increased levels of gamma and X-ray radiation and the differing sensitivity of the two nearly genetically identical mouse strains used in the studies. CONCLUSION: Our retrospective analysis of thirty five murine BMTs performed in three different laboratories, identified C57BL/6NCr (Ly5.1) as being more radiation sensitive than B6.Cg-Ptprc(a)/NCr (Ly5.2). This is the first report documenting a measurable difference in radiation sensitivity and its effects between an inbred strain of mice and its congenic counterpart eventually succumbing to sepsis after BMT. BioMed Central 2008-02-28 /pmc/articles/PMC2292684/ /pubmed/18307812 http://dx.doi.org/10.1186/1479-5876-6-10 Text en Copyright © 2008 Duran-Struuck et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Duran-Struuck, Raimon Hartigan, Adam Clouthier, Shawn G Dyson, Melissa C Lowler, Kathi Gatza, Erin Tawara, Isao Toubai, Tomomi Weisiger, Elisabeth Hugunin, Kelly Reddy, Pavan Wilkinson, John E Differential susceptibility of C57BL/6NCr and B6.Cg-Ptprc(a )mice to commensal bacteria after whole body irradiation in translational bone marrow transplant studies |
title | Differential susceptibility of C57BL/6NCr and B6.Cg-Ptprc(a )mice to commensal bacteria after whole body irradiation in translational bone marrow transplant studies |
title_full | Differential susceptibility of C57BL/6NCr and B6.Cg-Ptprc(a )mice to commensal bacteria after whole body irradiation in translational bone marrow transplant studies |
title_fullStr | Differential susceptibility of C57BL/6NCr and B6.Cg-Ptprc(a )mice to commensal bacteria after whole body irradiation in translational bone marrow transplant studies |
title_full_unstemmed | Differential susceptibility of C57BL/6NCr and B6.Cg-Ptprc(a )mice to commensal bacteria after whole body irradiation in translational bone marrow transplant studies |
title_short | Differential susceptibility of C57BL/6NCr and B6.Cg-Ptprc(a )mice to commensal bacteria after whole body irradiation in translational bone marrow transplant studies |
title_sort | differential susceptibility of c57bl/6ncr and b6.cg-ptprc(a )mice to commensal bacteria after whole body irradiation in translational bone marrow transplant studies |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2292684/ https://www.ncbi.nlm.nih.gov/pubmed/18307812 http://dx.doi.org/10.1186/1479-5876-6-10 |
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