Natural genetic variation in Drosophila melanogaster reveals genes associated with Coxiella burnetii infection. Issue 3 (23rd January 2021)

• Record Type: Journal Article
• Authors: Guzman, Rosa M; Howard, Zachary P; Liu, Ziying; Oliveira, Ryan D; Massa, Alisha T; Omsland, Anders; White, Stephen N; Goodman, Alan G
• Editors: Gleason, J
• Is Part Of: Genetics. Volume 217:Issue 3(2021)
• Publication Date: 2021-01-23
• Subjects: genome-wide association study -- bacteria -- pathogenesis -- immunity -- host response; Genetics -- Periodicals; 576.5
• DOI: 10.1093/genetics/iyab005
• Languages: English
• ISSNs: 0016-6731

Abstract

Abstract: The gram-negative bacterium Coxiella burnetii is the causative agent of Query (Q) fever in humans and coxiellosis in livestock. Host genetics are associated with C. burnetii pathogenesis both in humans and animals; however, it remains unknown if specific genes are associated with severity of infection. We employed the Drosophila Genetics Reference Panel to perform a genome-wide association study to identify host genetic variants that affect host survival to C. burnetii infection. The genome-wide association study identified 64 unique variants ( P < 10 −5 ) associated with 25 candidate genes. We examined the role each candidate gene contributes to host survival during C. burnetii infection using flies carrying a null mutation or RNAi knockdown of each candidate. We validated 15 of the 25 candidate genes using at least one method. This is the first report establishing involvement of many of these genes or their homologs with C. burnetii susceptibility in any system. Among the validated genes, FER and tara play roles in the JAK/STAT, JNK, and decapentaplegic/TGF-β signaling pathways which are components of known innate immune responses to C. burnetii infection. CG42673 and DIP-ε play roles in bacterial infection and synaptic signaling but have no previous association with C. burnetii pathogenesis. Furthermore, since the mammalian ortholog of CG13404 ( PLGRKT ) is an important regulator of macrophage function, CG13404 could play a role in host susceptibility to C. burnetii through hemocyte regulation. These insights provide a foundation for further investigation regarding the genetics of C. burnetii susceptibility across a wide variety of hosts.