posted on 2023-01-22, 22:27authored byVL Hunt, IJ Tsai, A Coghlan, AJ Reid, N Holroyd, BJ Foth, A Tracey', JA Cotton', EJ Stanley, H Beasley, HM Bennett, K Brooks, B Harsha, R Kajitani, A Kulkarni, D Harbecke, E Nagayasu, S Nichol, Y Ogura, MA Quail, N Randle, D Xia, NW Brattig, H Soblik, DM Ribeiro, A Sanchez-Flores, T Hayashi, T Itoh, DR Denver, Warwick GrantWarwick Grant, JD Stoltzfus, JB Lok, H Murayama, J Wastling, A Streit, T Kikuchi, M Viney, M Berriman
Soil-transmitted nematodes, including the Strongyloides genus, cause one of the most prevalent neglected tropical diseases. Here we compare the genomes of four Strongyloides species, including the human pathogen Strongyloides stercoralis, and their close relatives that are facultatively parasitic (Parastrongyloides trichosuri) and free-living (Rhabditophanes sp. KR3021). A significant paralogous expansion of key gene families - families encoding astacin-like and SCP/TAPS proteins - is associated with the evolution of parasitism in this clade. Exploiting the unique Strongyloides life cycle, we compare the transcriptomes of the parasitic and free-living stages and find that these same gene families are upregulated in the parasitic stages, underscoring their role in nematode parasitism.
Funding
The S. ratti transcriptome and proteome work was funded by Wellcome Trust grant 094462/Z/10/Z awarded to M.V., J.W. and M.B. The S. ratti, S. stercoralis, S. papillosus, P. trichosuri and Rhabditophanes sp. KR3021 genome sequencing and the S. venezuelensis optical mapping were funded by Wellcome Trust grant 098051. The S. venezuelensis work was supported by Japan Society for the Promotion of Science (JSPS) KAKENHI (24310142, 21590466 and 24780044), KAKENHI for Innovative Areas 'Genome Science' (221S0002) and the Integrated Research Project for Human and Veterinary Medicine of the University of Miyazaki. I.J.T. was supported by Academia Sinica. Work was funded by grants AI050668 and AI105856 from the US National Institutes of Health (NIH) to J.B.L. and by Resource-Related Research Grant RR02512 from the US NIH to M. Haskins, which provided research materials for the study. J.D.S. received support from US NIH training grant AI060516. A.K. was supported by a predoctoral stipend from the Max Planck Society. Work by AK., D.H. and A.S. was funded by the Max Planck Society.
History
Publication Date
2016-02-01
Journal
Nature Genetics
Volume
48
Issue
3
Pagination
9p. (p. 299-307)
Publisher
Nature Publishing Group
ISSN
1061-4036
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