Human anaplasmosis caused by Anaplasma phagocytophilum (Ap) is now the second most prevalent tick-borne illness in North America, with increasing incidence also in Europe and Asia. The acute, pro-inflammatory syndrome is characterized by high fever, pancytopenia and elevated serum transaminases, requiring hospitalization in >36% of patients, with an overall mortality rate of ~1%. A major impediment to understanding the mechanisms whereby these obligate intracellular bacteria cause disease has been the lack of reproducible systems for mutagenesis to study gene function. This has been partially overcome with the establishment of a library containing ~1,200 intra- and intergenic insertions using human cells to select mutants. The broad, long-term goals of this renewal application are to use the principles of functional genomics to understand how Ap bacteria use their genome and specific genes to thrive in two biologically vastly different hosts, mammals and ticks, and cause human disease. Our central hypothesis is that many mutations that are tolerated in an in vitro human cell culture system will nevertheless produce a deficient phenotype in human and tick cells in vitro, and in mice and ticks. Therefore, we 1) plan to catalogue and develop the currently uncharacterized library into a resource for the scientific community. We will test the hypothesis that mutants selected in a human promyelocyte cell line will allow detailed analyses of the molecular basis of gene function in cell cultures from humans and ticks. We propose a high throughput screen of candidate mutants for defective infectivity in mice and ticks, and analyses for changes in phenotype in vitro using human and tick cell culture systems. 2) We will use advanced imaging technology, proteomics and 2-hybrid bacterial screens to reveal intracellular trafficking of secreted effectors and their interactions with host targets, with emphasis on T4SS structures and effectors, other secreted proteins, outer membrane proteins and hypothetical proteins that were selected using bioinformatics-based predictions. 3) We hypothesize that mutants selected in vector tick cell culture will additionally identify genes that are essential for growth in human cells, and which are not represented in the current library. To do this, we will refine methods for selection of transposon mutants in tick cel culture using constructs designed for facile complementation of mutants with wild-type gene sequences to restore function, and develop site-directed mutagenesis using CRISPR/Cas9 mediated allelic exchange. Investigators from three collaborating laboratories will join in this effort to maximize advancement of research plans. The knowledge gained will broadly impact the field of rickettsiology and identify the molecular basis underlying pathogenic mechanisms and survival strategies of arthropod-borne intracellular bacteria. These efforts will enable a gian step forward in functional genomics and enable rational design of vaccines and drugs for the Rickettsiales, a group that includes severe pathogens, e.g., Ap, Ehrlichia chaffeensis, Rickettsia rickettsii and R. prowazekii for which such tools are either lacking or in great need of refinement

Public Health Relevance

Human anaplasmosis caused by Anaplasma phagocytophilum (Ap) is now the second most important tick- borne illness in North America, presenting as an acute, pro-inflammatory syndrome characterized by high fever and anemia that requires hospitalization in >36% of patients, and has an unacceptably high mortality rate of ~1%, despite available antibiotic treatment. A major impediment to understanding the mechanisms whereby these obligate intracellular bacteria cause disease has been our inability to genetically alter these disease agents to study gene function. This proposal addresses these knowledge gaps by providing a large collection of Ap with specific genetic defects that will be studied to reveal their role in disrupting host cell function, and identify efficient drugs and vaccines, knowledge which will be broadly applicable also to other severe disease agents in its class such as those causing typhus and Rocky Mountain spotted fever.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI042792-20
Application #
9830002
Study Section
Vector Biology Study Section (VB)
Program Officer
Perdue, Samuel S
Project Start
1998-05-01
Project End
2020-11-30
Budget Start
2019-12-01
Budget End
2020-11-30
Support Year
20
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Minnesota Twin Cities
Department
Zoology
Type
Earth Sciences/Resources
DUNS #
555917996
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
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