The SCID Mouse Model for Identifying Virulence Determinants in Coxiella burnetii

• Published in: Frontiers in cellular and infection microbiology Vol. 7; p. 25
• Main Authors: van Schaik, Erin J, Case, Elizabeth D, Martinez, Eric, Bonazzi, Matteo, Samuel, James E
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers 03.02.2017; Frontiers Media S.A
• Subjects: Animals; Coxiella burnetii - pathogenicity; Disease Models, Animal; Host-Pathogen Interactions; Life Sciences; Mice; Mice, SCID; Microbiology; Microbiology and Parasitology; Q Fever - microbiology; Q Fever - pathology; Virulence; Virulence Factors - analysis; virulence; animal model; SCID mouse; C. burnetii; transposon mutagenesis; C burnetii
• ISSN: 2235-2988; 2235-2988
• DOI: 10.3389/fcimb.2017.00025

is an intracellular, zoonotic pathogen that is the causative agent of Q fever. Infection most frequently occurs after inhalation of contaminated aerosols, which can lead to acute, self-limiting febrile illness or more serve chronic infections such as hepatitis or endocarditis. Macrophages are the principal target cells during infection where resides and replicates within a unique phagolysosome-like compartment, the -containing vacuole (CCV). The first virulence determinant described as necessary for infection was full-length lipopolysaccarride (LPS); spontaneous rough mutants (phase II) arise after passage in immuno-incompetent hosts. Phase II are attenuated in immuno-competent animals, but are fully capable of infecting a variety of host cells . A clonal strain of the Nine Mile isolate (RSA439, clone 4), has a 26 KDa chromosomal deletion that includes LPS biosynthetic genes and is uniquely approved for use in BL2/ABL2 conditions. With the advances of axenic media and genetic tools for research, the characterization of novel virulence determinants is ongoing and almost exclusively performed using this attenuated clone. A major problem with predicting essential virulence loci with RSA439 is that, although some cell-autonomous phenotypes can be assessed in tissue culture, no animal model for assessing pathogenesis has been defined. Here we describe the use of SCID mice for predicting virulence factors of , in either independent or competitive infections. We propose that this model allows for the identification of mutations that are competent for intracellular replication , but attenuated for growth and predict essential innate immune responses modulated by the pathogen during infection as a central pathogenic strategy.