The exclusively blood-feeding blacklegged tick Ixodes scapularis is the most medically relevant vector of infectious diseases in the United States. Despite the public health importance of I. scapularis, which transmits over six pathogens, including the Lyme disease spirochete Borrelia burgdorferi, this non-insect arthropod vector is understudied. The molecular details of vector-pathogen interactions and non-insect arthropod immune responses remain relatively poorly characterized. The recent description of the tick immune deficiency (IMD) pathway elucidated one facet of the tick response to B. burgdorferi. The IMD pathway is centrally regulated by the E3 ubiquitin ligase X-linked inhibitor of apoptosis (XIAP), which serves to polyubiquitylate target proteins, forming ubiquitin scaffolds. Substrates of XIAP in the context of tick-B. burgdorferi interactions remain unknown. In this F31 application, we report an interacting partner, p47, which is shown to participate in the tick immune response to B. burgdorferi by restricting pathogen acquisition in I. scapularis. The central hypothesis of the proposed research is that XIAP binds and polyubiquitylates p47 in a lysine (K)63-dependent manner. We will investigate this hypothesis in two aims.
In Aim 1, the molecular and biophysical details of the XIAP-p47 interaction will be systematically examined by using p47 deletion mutants in binding assays with XIAP, as well as surface plasmon resonance and isothermal titration calorimetry.
In Aim 2, biochemical interactions between XIAP and p47 will be investigated by performing in vitro polyubiquitylation assays and mass spectrometry to identify which residues of p47 are polyubiquitylated. By completing the aims of the proposed research, we will characterize a substrate of XIAP, which will improve our understanding of the tick IMD pathway. These findings will also contribute to unraveling novel scientific paradigms in tick-pathogen interactions.

Public Health Relevance

The blacklegged tick Ixodes scapularis is the principal arthropod vector of disease in the United States and transmits over six diverse pathogens, including the Lyme disease spirochete Borrelia burgdorferi. We will use biochemical and biophysical methods to characterize the interaction between an immune deficiency regulator and a substrate. Our findings will contribute toward characterizing the tick immune deficiency pathway, which may lead to the development of new tick-focused strategies to prevent Lyme disease transmission.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
5F31AI138440-02
Application #
9663197
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Costero-Saint Denis, Adriana
Project Start
2018-02-05
Project End
2020-02-04
Budget Start
2019-02-05
Budget End
2020-02-04
Support Year
2
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Maryland Baltimore
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
188435911
City
Baltimore
State
MD
Country
United States
Zip Code
21201
McClure Carroll, Erin E; Wang, Xiaowei; Shaw, Dana K et al. (2018) p47 licenses activation of the immune deficiency pathway in the tick Ixodes scapularis. Proc Natl Acad Sci U S A :