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Steroid Hormone Function Controls Non-competitive Plasmodium Development in Anopheles
Author(s) -
Kristine Werling,
W. Robert Shaw,
Maurice A. Itoe,
Kathleen A. Westervelt,
Perrine Marcenac,
Douglas G. Paton,
Duo Peng,
Naresh Singh,
Andrea L. Smidler,
Adam South,
Amy Deik,
Liliana Mâncio-Silva,
Allison Demas,
Sandra March,
Eric Calvo,
Sangeeta N. Bhatia,
Clary B. Clish,
Flaminia Catteruccia
Publication year - 2019
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2019.02.036
Subject(s) - biology , anopheles gambiae , plasmodium falciparum , malaria , anopheles , plasmodium (life cycle) , host (biology) , vector (molecular biology) , transmission (telecommunications) , zoology , parasite hosting , immunology , ecology , genetics , engineering , world wide web , computer science , gene , electrical engineering , recombinant dna
Transmission of malaria parasites occurs when a female Anopheles mosquito feeds on an infected host to acquire nutrients for egg development. How parasites are affected by oogenetic processes, principally orchestrated by the steroid hormone 20-hydroxyecdysone (20E), remains largely unknown. Here we show that Plasmodium falciparum development is intimately but not competitively linked to processes shaping Anopheles gambiae reproduction. We unveil a 20E-mediated positive correlation between egg and oocyst numbers; impairing oogenesis by multiple 20E manipulations decreases parasite intensities. These manipulations, however, accelerate Plasmodium growth rates, allowing sporozoites to become infectious sooner. Parasites exploit mosquito lipids for faster growth, but they do so without further affecting egg development. These results suggest that P. falciparum has adopted a non-competitive evolutionary strategy of resource exploitation to optimize transmission while minimizing fitness costs to its mosquito vector. Our findings have profound implications for currently proposed control strategies aimed at suppressing mosquito populations.

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