Identifying genetic susceptibility to Aspergillus fumigatus infection using collaborative cross mice and RNA‐Seq approach

Author:

Yosief Roa'a H. S.1ORCID,Lone Iqbal M.1,Nachshon Aharon2ORCID,Himmelbauer Heinz3,Gat‐Viks Irit2,Iraqi Fuad A.1ORCID

Affiliation:

1. Department of Clinical Microbiology and Immunology, Sackler Faculty of Medicine Tel‐Aviv University Tel‐Aviv Israel

2. School of Molecular Cell Biology and Biotechnology, George S. Wise Faculty of Life Sciences Tel Aviv University Tel Aviv Israel

3. Institute of Computational Biology, Department of Biotechnology, University of Natural Resources and Life Sciences, Muthgasse 18 1190 Vienna Austria

Abstract

AbstractBackgroundAspergillus fumigatus (Af) is one of the most ubiquitous fungi and its infection potency is suggested to be strongly controlled by the host genetic background. The aim of this study was to search for candidate genes associated with host susceptibility to Aspergillus fumigatus (Af) using an RNAseq approach in CC lines and hepatic gene expression.MethodsWe studied 31 male mice from 25 CC lines at 8 weeks old; the mice were infected with Af. Liver tissues were extracted from these mice 5 days post‐infection, and next‐generation RNA‐sequencing (RNAseq) was performed. The GENE‐E analysis platform was used to generate a clustered heat map matrix.ResultsSignificant variation in body weight changes between CC lines was observed. Hepatic gene expression revealed 12 top prioritized candidate genes differentially expressed in resistant versus susceptible mice based on body weight changes. Interestingly, three candidate genes are located within genomic intervals of the previously mapped quantitative trait loci (QTL), including Gm16270 and Stox1 on chromosome 10 and Gm11033 on chromosome 8.ConclusionsOur findings emphasize the CC mouse model's power in fine mapping the genetic components underlying susceptibility towards Af. As a next step, eQTL analysis will be performed for our RNA‐Seq data. Suggested candidate genes from our study will be further assessed with a human cohort with aspergillosis.

Funder

Tel Aviv University

Publisher

Wiley

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