Bacillus anthracis, the causative agent of anthrax disease, has remained as a top bioterrorism concern since the
2001 anthrax attack. B. anthracis causes anthrax through a combination of bacterial infection and toxemia. As a
major virulence factor, the anthrax lethal toxin (LT) plays an essential role during multiple steps of the disease.
Due to the rapid course of anthrax disease, in particular, the early non-specific, flu-like symptoms of inhalational
anthrax, patients usually seek medical assistance when the disease is already in the middle/late stages, making
the clinical management of anthrax patients an extremely challenging task. Current treatments include antibiotics
and anti-toxin antibodies that respectively eliminate the pathogen and neutralize the toxin. However, there is no
therapy available to deal with the cellular/tissue damage caused by LT already having reached its molecular
targets inside cells. Mortality usually follows when the host fails to repair this damage, the so called “point-of-no-
return” for current therapy. Thus, even with intensive medical care, the mortality rate of systemic anthrax is high,
reaching > 50%. Therefore, there is an urgent unmet clinical need to develop better targeted therapies to avert
anthrax-induced mortality. Our goal in this application is to discover the molecular mechanisms underlying LT-
induced lethality and to develop potential targeted therapeutics to treat patients beyond the “point-of-no-return”.
Here, we set out to determine the specific roles of disrupting each of the ERK, p38, and JNK pathways in anthrax-
induced lethality, discover the underlying molecular mechanisms, and develop the concept of reactivation
/mobilization of these pathways as a targeted therapy for anthrax-induced mortality. In Aim 1, we will determine
the role of specifically disrupting the ERK pathway in anthrax-induced lethality. Among the three core MAPK
pathways targeted by LT, the ERK pathway is fundamental to many biological processes, including cell
proliferation and survival. Thus, we hypothesize that disrupting the ERK pathway is the major cause of anthrax-
induced lethality. We will generate and use novel mouse models containing MEK alleles that are resistant to LT-
cleavage to understand the precise role of ERK pathway inactivation in anthrax pathogenesis. In Aim 2, we will
further determine the roles of disrupting the p38 and JNK pathways, the two major stress-activated pathways
that hosts activate in order to adapt to a myriad of unfavorable conditions, in anthrax pathogenesis. Based on
our strong preliminary data that the LT-disrupted MAPK pathways, in particular the ERK pathway, can be
reactivated by the addition of potent mitogens, in Aim 3, we will explore the ERK pathway reactivation as a
targeted therapy for anthrax-induced tissue damage.
Upon completion of these studies, it is our expectation that we will provide significant conceptual advances in
our understanding of the underlying molecular mechanisms of anthrax pathogenesis, and offer an evidence-
based framework for developing anthrax-targeted therapies, which will complement the current therapies with
antibiotics and anti-toxin antibodies, to prevent anthrax mortality, even at advanced stages of anthrax infection.
