Multiple blood feeding in mosquitoes shortens the Plasmodium falciparum incubation period and increases malaria transmission potential

dc.contributor.authorShaw, W. Roberten
dc.contributor.authorHolmdahl, Inga E.en
dc.contributor.authorItoe, Maurice A.en
dc.contributor.authorWerling, Kristineen
dc.contributor.authorMarquette, Meghanen
dc.contributor.authorPaton, Douglas G.en
dc.contributor.authorSingh, Nareshen
dc.contributor.authorBuckee, Caroline O.en
dc.contributor.authorChilds, Lauren M.en
dc.contributor.authorCatteruccia, Flaminiaen
dc.date.accessioned2021-02-24T14:12:53Zen
dc.date.available2021-02-24T14:12:53Zen
dc.date.issued2020-12-31en
dc.description.abstractMany mosquito species, including the major malaria vector Anopheles gambiae, naturally undergo multiple reproductive cycles of blood feeding, egg development and egg laying in their lifespan. Such complex mosquito behavior is regularly overlooked when mosquitoes are experimentally infected with malaria parasites, limiting our ability to accurately describe potential effects on transmission. Here, we examine how Plasmodium falciparum development and transmission potential is impacted when infected mosquitoes feed an additional time. We measured P. falciparum oocyst size and performed sporozoite time course analyses to determine the parasite’s extrinsic incubation period (EIP), i.e. the time required by parasites to reach infectious sporozoite stages, in An. gambiae females blood fed either once or twice. An additional blood feed at 3 days post infection drastically accelerates oocyst growth rates, causing earlier sporozoite accumulation in the salivary glands, thereby shortening the EIP (reduction of 2.3 ± 0.4 days). Moreover, parasite growth is further accelerated in transgenic mosquitoes with reduced reproductive capacity, which mimic genetic modifications currently proposed in population suppression gene drives. We incorporate our shortened EIP values into a measure of transmission potential, the basic reproduction number R0, and find the average R0 is higher (range: 10.1%–12.1% increase) across sub-Saharan Africa than when using traditional EIP measurements. These data suggest that malaria elimination may be substantially more challenging and that younger mosquitoes or those with reduced reproductive ability may provide a larger contribution to infection than currently believed. Our findings have profound implications for current and future mosquito control interventions.en
dc.description.sponsorshipF.C. is funded by a Faculty Research Scholar Award by the Howard Hughes Medical Institute (HHMI) and the Bill & Melinda Gates Foundation (BMGF) (Grant ID: OPP1158190, www. hhmi.org), and by the National Institutes of Health (NIH) (R01 AI124165, R01 AI153404, www.nih. gov). L.M.C. is supported by the National Science Foundation (NSF) (Grant ID: 1853495, www.nsf. gov).en
dc.identifier.doihttps://doi.org/10.1371/journal.ppat.1009131en
dc.identifier.issue12en
dc.identifier.urihttp://hdl.handle.net/10919/102435en
dc.identifier.volume16en
dc.language.isoen_USen
dc.publisherPLOSen
dc.rightsAttribution 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en
dc.titleMultiple blood feeding in mosquitoes shortens the Plasmodium falciparum incubation period and increases malaria transmission potentialen
dc.title.serialPLOS Pathogensen
dc.typeArticle - Refereeden
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