Trinity College Dublin KARI-TRC Shirakawa Institute of Animal Genetics Genomic approaches to trypanosomiasis resistance - some surprises.

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Trinity College Dublin KARI-TRC Shirakawa Institute of Animal Genetics Genomic approaches to trypanosomiasis resistance - some surprises

Trinity College Dublin KARI-TRC Shirakawa Institute of Animal Genetics

Copyright Mike Enfield

Livestock in heterogeneous environments There is extraordinary diversity in livestock (and crops) across Africa. This is TOTALLY different from the situation in the West. And reflects the ‘environment’ working on the genome. Therefore there is information in the simple occurrence of a given genotype in a given environment.

Trypanosomiasis Is a fatal disease of livestock. The livestock equivalent of sleeping sickness in humans T. congolense, T. vivax T brucei rhodesiense T gambiense

Studying the tolerant/susceptible phenotype has problems: Separating cause from effect Separating relevant from irrelevant. Dominance of the ‘what is happening to this weeks trendy gene/protein/cytokine?’ approach.

Contribution of 10 genes from Boran and N’Dama cattle to reduction in degree of trypanosomosis Boran (relatively susceptible) The N’Dama and Boran each contribute trypanotolerance alleles at 5 of the 10 most significant QTL, indicating that a synthetic breed could have even higher tolerance than the N’Dama. N’Dama (tolerant)

MMU1 MMU17 MMU5 D17Mit16 D17Mit46 D17Mit7 D5Mit233 D5Mit24 D5Mit114 D1Mit102 D1Mit403 D1Nds2 D1Mit cM In mice, we mapped three genomic regions which determine survival time following T. congolense infection

PCA of Liver expression data

Studying the tolerant/susceptible phenotype STILL has the same problems! Separating cause from effect Separating relevant from irrelevant. Dominance of the ‘what is happening to this weeks trendy gene/protein/cytokine?’ approach.

Analysis (Fisher et al, NAR 35 (16)p ) What genes are differentially expressed genomewide? What pathways are they members of? What pathways involve genes in the QTL? What pathways are in both lists ? Prioritise the list by 'degree of change' Look at the biology of each network

Analysis It is important to stress that we do NOT require (or even expect) QTG themselves to be differentially expressed.

Cholesterol metabolism

C57 lite vs C57 regular - survival following Trypanosome challenge

Patients in ICU under tight glycaemic control

This is nothing to do with Trypanosomiasis - this is a general response.

Some conclusions

Overlaying QTL and expression data has been incredibly informative. (But don’t assume your QTG will be differentially expressed!) Expression analysis in cow and mouse has revealed some unexpected pathways and interactions. We have learned a lot about host response to trypanosomes, but also about: How to survive a tryps infection How to survive in an ICU in Northern England Fundamentals of genome regulation.

It may be that much of biological variation will turn-out to result from differential use of a small number of very general networks. (Why are we surprised that QTL often (usually?) fall apart when moved onto a new genetic background?) If you do high quality science there will be high quality - but unpredictable - outcomes.

Trinity College Dublin KARI-TRC Shirakawa Institute of Animal Genetics