A single-cell RNA-seq atlas of Schistosoma mansoni identifies a key regulator of blood feeding

Author:

Wendt George1ORCID,Zhao Lu1ORCID,Chen Rui1ORCID,Liu Chenxi2ORCID,O’Donoghue Anthony J.2ORCID,Caffrey Conor R.2,Reese Michael L.13ORCID,Collins James J.1ORCID

Affiliation:

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

2. Center for Discovery and Innovation in Parasitic Diseases, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California, San Diego, 9500 Gilman Dr., La Jolla, CA 92093, USA.

3. Department of Biochemistry, UT Southwestern Medical Center, Dallas, TX 75390, USA.

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

Bill and Melinda Gates Foundation

Welch Foundation

Wellcome

NIAID

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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