z-logo
open-access-imgOpen Access
Emodepside targets SLO-1 channels of Onchocerca ochengi and induces broad anthelmintic effects in a bovine model of onchocerciasis
Author(s) -
Germanus S. Bah,
Sebastian Schneckener,
Steffen Hahnel,
Nicolas H. Bayang,
Helena Fieseler,
Gabriele Schmuck,
Ralph Krebber,
Anouk Sarr,
Carsten Terjung,
Henrietta F. Ngangyung,
David Ekale,
Youssouf Mouliom Mfopit,
Lucien Rufener,
John GrahamBrown,
Vincent N. Tanya,
Martin Glenschek-Sieberth,
Daniel Kulke,
Benjamin L. Makepeace
Publication year - 2021
Publication title -
plos pathogens
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.719
H-Index - 206
eISSN - 1553-7374
pISSN - 1553-7366
DOI - 10.1371/journal.ppat.1009601
Subject(s) - onchocerciasis , anthelmintic , onchocerca , biology , wolbachia , onchocerca volvulus , microbiology and biotechnology , immunology , zoology , gene , genetics
Onchocerciasis (river blindness), caused by the filarial worm Onchocerca volvulus , is a neglected tropical disease mostly affecting sub-Saharan Africa and is responsible for >1.3 million years lived with disability. Current control relies almost entirely on ivermectin, which suppresses symptoms caused by the first-stage larvae (microfilariae) but does not kill the long-lived adults. Here, we evaluated emodepside, a semi-synthetic cyclooctadepsipeptide registered for deworming applications in companion animals, for activity against adult filariae ( i . e ., as a macrofilaricide). We demonstrate the equivalence of emodepside activity on SLO-1 potassium channels in Onchocerca volvulus and Onchocerca ochengi , its sister species from cattle. Evaluation of emodepside in cattle as single or 7-day treatments at two doses (0.15 and 0.75 mg/kg) revealed rapid activity against microfilariae, prolonged suppression of female worm fecundity, and macrofilaricidal effects by 18 months post treatment. The drug was well tolerated, causing only transiently increased blood glucose. Female adult worms were mostly paralyzed; however, some retained metabolic activity even in the multiple high-dose group. These data support ongoing clinical development of emodepside to treat river blindness.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom