Affiliation:
1. School of Molecular Biosciences, College of Veterinary Medicine, Washington State University, Pullman, Washington, USA
Abstract
ABSTRACT
Coxiella burnetii
is the causative agent of Q fever, a zoonotic disease that threatens both human and animal health. Due to the paucity of experimental animal models, little is known about how host factors interface with bacterial components and affect pathogenesis. Here, we used
Drosophila melanogaster
, in conjunction with the biosafety level 2 (BSL2) Nine Mile phase II (NMII) clone 4 strain of
C. burnetii
, as a model to investigate host and bacterial components implicated in infection. We demonstrate that adult
Drosophila
flies are susceptible to
C. burnetii
NMII infection and that this bacterial strain, which activates the immune deficiency (IMD) pathway, is able to replicate and cause mortality in the animals. We show that in the absence of Eiger, the only known tumor necrosis factor (TNF) superfamily homolog in
Drosophila
,
Coxiella
-infected flies exhibit reduced mortality from infection. We also demonstrate that the
Coxiella
type 4 secretion system (T4SS) is critical for the formation of the
Coxiella
-containing vacuole and establishment of infection in
Drosophila
. Altogether, our data reveal that the
Drosophila
TNF homolog Eiger and the
Coxiella
T4SS are implicated in the pathogenesis of
C. burnetii
in flies. The
Drosophila
/NMII model mimics relevant aspects of the infection in mammals, such as a critical role of host TNF and the bacterial T4SS in pathogenesis. Our work also demonstrates the usefulness of this BSL2 model to investigate both host and
Coxiella
components implicated in infection.
Funder
HHS | NIH | National Institute of Allergy and Infectious Diseases
Washington State University
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
19 articles.
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