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A single-cell RNA-seq atlas of Schistosoma mansoni identifies a key regulator of blood feeding
Author(s) -
George Wendt,
Lu Zhao,
Rui Chen,
Chenxi Liu,
Anthony J. O’Donoghue,
Conor R. Caffrey,
Michael L. Reese,
James J. Collins
Publication year - 2020
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.abb7709
Subject(s) - flatworm , schistosoma mansoni , biology , schistosoma , parasite hosting , rna interference , tropical disease , rna , disease , schistosomiasis , computational biology , gene , immunology , virology , genetics , helminths , zoology , pathology , medicine , world wide web , computer science
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 parasiteSchistosoma mansoni . By generating a single-cell atlas, Wendtet 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. Wanget al. performed a large-scale RNA interference survey ofS. 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

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