Large-scale RNAi screening uncovers therapeutic targets in the parasite Schistosoma mansoni

Author:

Wang Jipeng1ORCID,Paz Carlos1ORCID,Padalino Gilda2ORCID,Coghlan Avril3ORCID,Lu Zhigang3ORCID,Gradinaru Irina1,Collins Julie N. R.1,Berriman Matthew3ORCID,Hoffmann Karl F.2,Collins James J.1ORCID

Affiliation:

1. Department of Pharmacology, UT Southwestern Medical Center, Dallas, TX 75390, USA.

2. Institute of Biological, Environmental and Rural Sciences (IBERS), Aberystwyth University, Aberystwyth, Wales, UK.

3. Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SA, UK.

Abstract

Schistosome biology illuminated Schistosomiasis is caused by a parasitic flatworm about which little is known. Therefore, options to combat human disease caused by schistosome infection are limited. To aid in our quest to develop treatments, two studies undertook molecular investigations of the parasite Schistosoma mansoni . By generating a single-cell atlas, Wendt et al. identified the developmental trajectory of the flatworm, including the blood-feeding gut required for its survival in the host. From these data, they found a gene required for gut development that, when knocked out through RNA interference, confers reduced pathology in infected mice. Wang et al. performed a large-scale RNA interference survey of S. mansoni and identified an essential pair of protein kinases that can be targeted by approved pharmacological intervention (see the Perspective by Anderson and Duraisingh). These molecular investigations add to our understanding of the schistosome parasite and provide biological information that may help to combat this neglected tropical disease. Science , this issue p. 1644 , p. 1649 ; see also p. 1562

Funder

Welch Foundation

Wellcome

NIAID

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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