Staff Publications

Staff Publications

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    'Staff publications' is the digital repository of Wageningen University & Research

    'Staff publications' contains references to publications authored by Wageningen University staff from 1976 onward.

    Publications authored by the staff of the Research Institutes are available from 1995 onwards.

    Full text documents are added when available. The database is updated daily and currently holds about 240,000 items, of which 72,000 in open access.

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Record number 454449
Title Dissecting the genetic architecture of resistance to orsay virus infection in C. elegans
Author(s) Sterken, M.G.; Wang, Y.; Snoek, L.B.; Volkers, R.J.M.; Riksen, J.A.G.; Bosman, K.J.; Pijlman, G.P.; Kammenga, J.E.
Source In: Proceedings of PhD Spring School Host-Microbe Interactomics. - - p. 12 - 12.
Event Host-Microbe Interactions, Wageningen, The Netherlands, 2014-06-02/2014-06-04
Department(s) Laboratory of Nematology
Business Economics
Laboratory of Virology
PE&RC
Publication type Abstract in scientific journal or proceedings
Publication year 2014
Abstract Host-pathogen interactions play a major role in evolutionary selection and in shaping natural genetic variation. Recent identification of viral infection in C. elegans has prompted research into understanding the underlying pathways of Orsay virus (OrV) infection in natural populations. Here we report the dissection of the genetic architecture of OrV infection. We found that wild type Hawaii CB4856 strain was more resistant to OrV than the canonical Bristol N2 strain. To gain insight into the genetic architecture of resistance, 52 fully sequenced recombinant inbred lines (CB4856 x N2 RILs) were exposed to OrV using our recently developed quantitative assay. This led to the identification of two distinct loci on chromosome IV associated with OrV resistance. These loci were both associated with a lower viral load in the CB4856 genotype. Strikingly, these loci do not harbour the recently found drh-1 locus, which encodes a RIG-I like helicase that plays an important role in antiviral RNAi. To verify our results and gain additional insight into the genetic architecture, a panel of 18 introgression lines (ILs) (together covering chromosome IV entirely) was exposed to OrV. Both loci could be verified by ILs, also showing more resistance against OrV infection with the CB4856 locus. Our results provide insight in the loci underlying the higher viral resistance in CB4856. They also form an important step toward identifying polymorphic genes underlying resistance to viral infection in C. elegans.
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