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

Many 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 mala...

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Main Authors: W Robert Shaw, Inga E Holmdahl, Maurice A Itoe, Kristine Werling, Meghan Marquette, Douglas G Paton, Naresh Singh, Caroline O Buckee, Lauren M Childs, Flaminia Catteruccia
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2020-12-01
Series:PLoS Pathogens
Online Access:https://doi.org/10.1371/journal.ppat.1009131
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spelling doaj-918b87ae3b8c4bc3b752fc8e20e7d3c92021-04-21T17:55:50ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742020-12-011612e100913110.1371/journal.ppat.1009131Multiple blood feeding in mosquitoes shortens the Plasmodium falciparum incubation period and increases malaria transmission potential.W Robert ShawInga E HolmdahlMaurice A ItoeKristine WerlingMeghan MarquetteDouglas G PatonNaresh SinghCaroline O BuckeeLauren M ChildsFlaminia CatterucciaMany 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.https://doi.org/10.1371/journal.ppat.1009131
collection DOAJ
language English
format Article
sources DOAJ
author W Robert Shaw
Inga E Holmdahl
Maurice A Itoe
Kristine Werling
Meghan Marquette
Douglas G Paton
Naresh Singh
Caroline O Buckee
Lauren M Childs
Flaminia Catteruccia
spellingShingle W Robert Shaw
Inga E Holmdahl
Maurice A Itoe
Kristine Werling
Meghan Marquette
Douglas G Paton
Naresh Singh
Caroline O Buckee
Lauren M Childs
Flaminia Catteruccia
Multiple blood feeding in mosquitoes shortens the Plasmodium falciparum incubation period and increases malaria transmission potential.
PLoS Pathogens
author_facet W Robert Shaw
Inga E Holmdahl
Maurice A Itoe
Kristine Werling
Meghan Marquette
Douglas G Paton
Naresh Singh
Caroline O Buckee
Lauren M Childs
Flaminia Catteruccia
author_sort W Robert Shaw
title Multiple blood feeding in mosquitoes shortens the Plasmodium falciparum incubation period and increases malaria transmission potential.
title_short Multiple blood feeding in mosquitoes shortens the Plasmodium falciparum incubation period and increases malaria transmission potential.
title_full Multiple blood feeding in mosquitoes shortens the Plasmodium falciparum incubation period and increases malaria transmission potential.
title_fullStr Multiple blood feeding in mosquitoes shortens the Plasmodium falciparum incubation period and increases malaria transmission potential.
title_full_unstemmed Multiple blood feeding in mosquitoes shortens the Plasmodium falciparum incubation period and increases malaria transmission potential.
title_sort multiple blood feeding in mosquitoes shortens the plasmodium falciparum incubation period and increases malaria transmission potential.
publisher Public Library of Science (PLoS)
series PLoS Pathogens
issn 1553-7366
1553-7374
publishDate 2020-12-01
description Many 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.
url https://doi.org/10.1371/journal.ppat.1009131
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