Lymphocytes serve as a reservoir for Listeria monocytogenes growth during infection of mice

Denise S. McElroy, Taylor J. Ashley, Sarah E.F. D'Orazio

Research output: Contribution to journalArticlepeer-review

16 Scopus citations

Abstract

It is widely reported that Listeria monocytogenes can infect virtually all cell types, however, the degree to which this facultative intracellular pathogen can infect lymphocytes has not been well characterized. Previous studies have shown that a subset of lymphocytes, including activated T cells, are susceptible to apoptosis following exposure to L. monocytogenes, but the ability of the bacteria to replicate in the cytosol of lymphocytes prior to cell death was not examined. In this report, we demonstrate that intracellular L. monocytogenes can survive and multiply in vitro in a variety of transformed cell lines of lymphocytic origin. Intracellular L. monocytogenes were also recovered from splenic B cells, T cells, and NK cells following intravenous infection of mice. In fact, lymphocyte-associated L. monocytogenes comprised a substantial portion of the total bacterial burden in the spleen throughout the course of murine infection and B cell-deficient mice had significantly lower titers of bacteria present in the spleen following intravenous infection. These results suggest that lymphocytes can be a reservoir for L. monocytogenes growth in vivo.

Original languageEnglish
Pages (from-to)214-221
Number of pages8
JournalMicrobial Pathogenesis
Volume46
Issue number4
DOIs
StatePublished - Apr 2009

Bibliographical note

Funding Information:
We thank Beth Garvy for providing the J H knockout mice, Jennifer Strange and Greg Baumann for technical assistance, and Ando van der Velden for critical review of the manuscript. This work was supported by a grant from the Center for Research Resources (P20 RR20171) to S.E.F.D.

Funding

We thank Beth Garvy for providing the J H knockout mice, Jennifer Strange and Greg Baumann for technical assistance, and Ando van der Velden for critical review of the manuscript. This work was supported by a grant from the Center for Research Resources (P20 RR20171) to S.E.F.D.

FundersFunder number
National Center for Research ResourcesP20 RR20171
National Center for Research ResourcesP20RR020171

    Keywords

    • B cells
    • Intracellular pathogen
    • T cells

    ASJC Scopus subject areas

    • Microbiology
    • Infectious Diseases

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