Differentiating Peromyscus leucopus bone marrow-derived macrophages for characterization of responses to Borrelia burgdorferi and lipopolysaccharide

ABSTRACT Currently, most tools utilized in host-pathogen interaction studies depend on the use of human or mouse (Mus musculus) cells and tissues. While these species have led to countless breakthroughs in our understanding of infectious disease, there are undoubtedly important biological processes...

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發表在:Infection and Immunity
Main Authors: Christopher C. Wells, Tanja Petnicki-Ocwieja, Shumin Tan, Stephen C. Bunnell, Sam R. Telford, Linden T. Hu, Jeffrey S. Bourgeois
格式: Article
語言:英语
出版: American Society for Microbiology 2025-07-01
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在線閱讀:https://journals.asm.org/doi/10.1128/iai.00581-24
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author Christopher C. Wells
Tanja Petnicki-Ocwieja
Shumin Tan
Stephen C. Bunnell
Sam R. Telford
Linden T. Hu
Jeffrey S. Bourgeois
author_facet Christopher C. Wells
Tanja Petnicki-Ocwieja
Shumin Tan
Stephen C. Bunnell
Sam R. Telford
Linden T. Hu
Jeffrey S. Bourgeois
author_sort Christopher C. Wells
collection DOAJ
container_title Infection and Immunity
description ABSTRACT Currently, most tools utilized in host-pathogen interaction studies depend on the use of human or mouse (Mus musculus) cells and tissues. While these species have led to countless breakthroughs in our understanding of infectious disease, there are undoubtedly important biological processes that are missed by limiting studies to these two vertebrate species. For instance, it is well-established that a common deermouse in North America, Peromyscus leucopus, has unique interactions with microbes, which likely shape its ability to serve as a critical reservoir for numerous zoonotic pathogens, including a Lyme disease spirochete, Borrelia burgdorferi. In this work, we expand the immunological toolkit to study P. leucopus biology by performing the first differentiation of deermouse bone marrow to macrophages using P. leucopus M-CSF producing HEK293T cells. We find that P. leucopus BMDMs generated through this method behave broadly very similarly to C57BL/6J macrophages generated with the L-929 supernatant, although RNA sequencing revealed modest differences in transcriptomic responses to B. burgdorferi and lipopolysaccharide. In particular, differences in Il-10 induction and caspase expression were observed between the species.
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spelling doaj-art-fdc107aa28f74232a6e1e35c4e7bfe862025-10-17T16:23:44ZengAmerican Society for MicrobiologyInfection and Immunity0019-95671098-55222025-07-0193710.1128/iai.00581-24Differentiating Peromyscus leucopus bone marrow-derived macrophages for characterization of responses to Borrelia burgdorferi and lipopolysaccharideChristopher C. Wells0Tanja Petnicki-Ocwieja1Shumin Tan2Stephen C. Bunnell3Sam R. Telford4Linden T. Hu5Jeffrey S. Bourgeois6Department of Immunology, Tufts University, Boston, Massachusetts, USATufts Lyme Disease Initiative, Tufts University, Boston, Massachusetts, USADepartment of Molecular Biology and Microbiology, Tufts University, Boston, Massachusetts, USADepartment of Immunology, Tufts University, Boston, Massachusetts, USATufts Lyme Disease Initiative, Tufts University, Boston, Massachusetts, USATufts Lyme Disease Initiative, Tufts University, Boston, Massachusetts, USATufts Lyme Disease Initiative, Tufts University, Boston, Massachusetts, USAABSTRACT Currently, most tools utilized in host-pathogen interaction studies depend on the use of human or mouse (Mus musculus) cells and tissues. While these species have led to countless breakthroughs in our understanding of infectious disease, there are undoubtedly important biological processes that are missed by limiting studies to these two vertebrate species. For instance, it is well-established that a common deermouse in North America, Peromyscus leucopus, has unique interactions with microbes, which likely shape its ability to serve as a critical reservoir for numerous zoonotic pathogens, including a Lyme disease spirochete, Borrelia burgdorferi. In this work, we expand the immunological toolkit to study P. leucopus biology by performing the first differentiation of deermouse bone marrow to macrophages using P. leucopus M-CSF producing HEK293T cells. We find that P. leucopus BMDMs generated through this method behave broadly very similarly to C57BL/6J macrophages generated with the L-929 supernatant, although RNA sequencing revealed modest differences in transcriptomic responses to B. burgdorferi and lipopolysaccharide. In particular, differences in Il-10 induction and caspase expression were observed between the species.https://journals.asm.org/doi/10.1128/iai.00581-24Peromyscus leucopusBorrelia burgdorferiBorreliella burgdorferiLyme diseaselipopolysaccharideLPS
spellingShingle Christopher C. Wells
Tanja Petnicki-Ocwieja
Shumin Tan
Stephen C. Bunnell
Sam R. Telford
Linden T. Hu
Jeffrey S. Bourgeois
Differentiating Peromyscus leucopus bone marrow-derived macrophages for characterization of responses to Borrelia burgdorferi and lipopolysaccharide
Peromyscus leucopus
Borrelia burgdorferi
Borreliella burgdorferi
Lyme disease
lipopolysaccharide
LPS
title Differentiating Peromyscus leucopus bone marrow-derived macrophages for characterization of responses to Borrelia burgdorferi and lipopolysaccharide
title_full Differentiating Peromyscus leucopus bone marrow-derived macrophages for characterization of responses to Borrelia burgdorferi and lipopolysaccharide
title_fullStr Differentiating Peromyscus leucopus bone marrow-derived macrophages for characterization of responses to Borrelia burgdorferi and lipopolysaccharide
title_full_unstemmed Differentiating Peromyscus leucopus bone marrow-derived macrophages for characterization of responses to Borrelia burgdorferi and lipopolysaccharide
title_short Differentiating Peromyscus leucopus bone marrow-derived macrophages for characterization of responses to Borrelia burgdorferi and lipopolysaccharide
title_sort differentiating peromyscus leucopus bone marrow derived macrophages for characterization of responses to borrelia burgdorferi and lipopolysaccharide
topic Peromyscus leucopus
Borrelia burgdorferi
Borreliella burgdorferi
Lyme disease
lipopolysaccharide
LPS
url https://journals.asm.org/doi/10.1128/iai.00581-24
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