This proposal examines infection with the facultative intracellular pathogen Listeria monocytogenes (LM), focusing on the early stage when LM is multiplying in tissues at a high exponential rate. During this period, precisely by the 48th hour, there is extensive lymphocyte death by apoptosis in lymphoid organs. The death is caused by the LM virulent pore forming protein Listeriolysin O (LLO). This proposal is based on three observations, the finding of extensive lymphocyte apoptosis in infective foci, our finding ex vivo and in vivo, that LLO is apoptogenic to lymphocytes; and observations indicating that the lymphocyte death stage may be linked to a period of lower resistance. The lower resistance became evident when SCID mice were found to handle the exponential growth phase better than normal mice. Pointedly, SCID mice injected with lymphocytes at the same time of infection, reverted to the pattern seen in normal mice, with higher LM burden. The plans include examining the molecular basis of LLO action on cells, to in vivo analysis of how LLO may be acting, plus an evaluation of the changes that take place in lymphoid organs at the time of the apoptotic phase. Accordingly, how LLO induces apoptotic death of lymphocytes is examined in detail. Preliminary evidence indicates that LLO initiates an intracellular proteolytic pathway that results in the death program. Experiments are planned to determine the nature of this pathway. Having a better understanding and pinpointing critical molecules in the death pathway may allow the infection to be modulated by targeting such molecules in a number of ways. Another important issue to examine is whether lymphocytes vary in their susceptibility to LLO apoptosis depending on their set and/or activation states: this issue is tackled by both in vivo and ex vivo experiments with purified cells. A LM that expresses LLO as a membrane protein is being engineered, in order to explore whether it is extracellular LLO that causes the lymphocyte death. The proposal includes a number of different approaches in order to determine whether lymphocyte apoptosis modulates in a negative way the infectious process. In summary, listeriosis is a powerful system to examine the relevance of lymphocyte death to the outcome of an infectious disease.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI062832-03
Application #
7151483
Study Section
Bacteriology and Mycology Subcommittee 2 (BM)
Program Officer
Mills, Melody
Project Start
2004-12-01
Project End
2009-11-30
Budget Start
2006-12-01
Budget End
2007-11-30
Support Year
3
Fiscal Year
2007
Total Cost
$362,679
Indirect Cost
Name
Washington University
Department
Pathology
Type
Schools of Medicine
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Valderrama, Carolina; Clark, Amy; Urano, Fumihiko et al. (2017) Listeria monocytogenes induces an interferon-enhanced activation of the integrated stress response that is detrimental for resolution of infection in mice. Eur J Immunol 47:830-840
MacDuff, Donna A; Reese, Tiffany A; Kimmey, Jacqueline M et al. (2015) Phenotypic complementation of genetic immunodeficiency by chronic herpesvirus infection. Elife 4:
Lee, Sang Hun; Carrero, Javier A; Uppaluri, Ravindra et al. (2013) Identifying the initiating events of anti-Listeria responses using mice with conditional loss of IFN-? receptor subunit 1 (IFNGR1). J Immunol 191:4223-34
Carrero, Javier Antonio (2013) Confounding roles for type I interferons during bacterial and viral pathogenesis. Int Immunol 25:663-9
Carrero, Javier A; Vivanco-Cid, Hector; Unanue, Emil R (2012) Listeriolysin o is strongly immunogenic independently of its cytotoxic activity. PLoS One 7:e32310
Carrero, Javier A; Unanue, Emil R (2012) Mechanisms and immunological effects of apoptosis caused by Listeria monocytogenes. Adv Immunol 113:157-74
Unanue, Emil R; Carrero, Javier A (2012) Studies with Listeria monocytogenes lead the way. Adv Immunol 113:1-5
Edelson, Brian T; Bradstreet, Tara R; Hildner, Kai et al. (2011) CD8?(+) dendritic cells are an obligate cellular entry point for productive infection by Listeria monocytogenes. Immunity 35:236-48
Edelson, Brian T; Bradstreet, Tara R; KC, Wumesh et al. (2011) Batf3-dependent CD11b(low/-) peripheral dendritic cells are GM-CSF-independent and are not required for Th cell priming after subcutaneous immunization. PLoS One 6:e25660
Aoshi, Taiki; Carrero, Javier A; Konjufca, Vjollca et al. (2009) The cellular niche of Listeria monocytogenes infection changes rapidly in the spleen. Eur J Immunol 39:417-25

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