Expression Quantitative Trait Loci for Extreme Host Response to Influenza A in Pre-Collaborative Cross Mice

Author:

Bottomly Daniel12,Ferris Martin T13,Aicher Lauri D14,Rosenzweig Elizabeth14,Whitmore Alan13,Aylor David L35,Haagmans Bart L6,Gralinski Lisa E17,Bradel-Tretheway Birgit G14,Bryan Janine T14,Threadgill David W8,de Villena Fernando Pardo-Manuel135,Baric Ralph S179,Katze Michael G14,Heise Mark1139,McWeeney Shannon K1121011

Affiliation:

1. Pacific Northwest Regional Center of Excellence for Biodefense and Emerging Infectious Diseases Research, Portland, Oregon 97006

2. Oregon Clinical and Translational Research Institute, Oregon Health & Science University, Portland, Oregon 97239

3. Department of Genetics, University of North Carolina, Chapel Hill, North Carolina 27599

4. Department of Microbiology, School of Medicine, University of Washington, Seattle, Washington, 98195

5. Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, North Carolina, 27514

6. Erasmus Medical Center, 3000 CA Rotterdam, the Netherlands

7. Department of Epidemiology, University of North Carolina, Chapel Hill, North Carolina, 27599

8. Department of Genetics, North Carolina State University, Raleigh, North Carolina, 27695

9. Department of Microbiology and Immunology, University of North Carolina, Chapel Hill, North Carolina 27599

10. Division of Bioinformatics and Computational Biology, Medical Informatics and Clinical Epidemiology, Oregon Health & Science University, Portland, Oregon 97239

11. Division of Biostatistics, Public Health & Preventative Medicine, Oregon Health & Science University, Portland, Oregon 97239

Abstract

Abstract Outbreaks of influenza occur on a yearly basis, causing a wide range of symptoms across the human population. Although evidence exists that the host response to influenza infection is influenced by genetic differences in the host, this has not been studied in a system with genetic diversity mirroring that of the human population. Here we used mice from 44 influenza-infected pre-Collaborative Cross lines determined to have extreme phenotypes with regard to the host response to influenza A virus infection. Global transcriptome profiling identified 2671 transcripts that were significantly differentially expressed between mice that showed a severe (“high”) and mild (“low”) response to infection. Expression quantitative trait loci mapping was performed on those transcripts that were differentially expressed because of differences in host response phenotype to identify putative regulatory regions potentially controlling their expression. Twenty-one significant expression quantitative trait loci were identified, which allowed direct examination of genes associated with regulation of host response to infection. To perform initial validation of our findings, quantitative polymerase chain reaction was performed in the infected founder strains, and we were able to confirm or partially confirm more than 70% of those tested. In addition, we explored putative causal and reactive (downstream) relationships between the significantly regulated genes and others in the high or low response groups using structural equation modeling. By using systems approaches and a genetically diverse population, we were able to develop a novel framework for identifying the underlying biological subnetworks under host genetic control during influenza virus infection.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology

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