Progression of Plasmodium berghei through Anopheles stephensi is density-dependent.

It is well documented that the density of Plasmodium in its vertebrate host modulates the physiological response induced; this in turn regulates parasite survival and transmission. It is less clear that parasite density in the mosquito regulates survival and transmission of this important pathogen....

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Main Authors: Robert E Sinden, Emma J Dawes, Yasmene Alavi, Joanna Waldock, Olivia Finney, Jacqui Mendoza, Geoff A Butcher, Laura Andrews, Adrian V Hill, Sarah C Gilbert, María-Gloria Basáñez
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2007-12-01
Series:PLoS Pathogens
Online Access:https://journals.plos.org/plospathogens/article/file?id=10.1371/journal.ppat.0030195&type=printable
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author Robert E Sinden
Emma J Dawes
Yasmene Alavi
Joanna Waldock
Olivia Finney
Jacqui Mendoza
Geoff A Butcher
Laura Andrews
Adrian V Hill
Sarah C Gilbert
María-Gloria Basáñez
author_facet Robert E Sinden
Emma J Dawes
Yasmene Alavi
Joanna Waldock
Olivia Finney
Jacqui Mendoza
Geoff A Butcher
Laura Andrews
Adrian V Hill
Sarah C Gilbert
María-Gloria Basáñez
author_sort Robert E Sinden
collection DOAJ
description It is well documented that the density of Plasmodium in its vertebrate host modulates the physiological response induced; this in turn regulates parasite survival and transmission. It is less clear that parasite density in the mosquito regulates survival and transmission of this important pathogen. Numerous studies have described conversion rates of Plasmodium from one life stage to the next within the mosquito, yet few have considered that these rates might vary with parasite density. Here we establish infections with defined numbers of the rodent malaria parasite Plasmodium berghei to examine how parasite density at each stage of development (gametocytes; ookinetes; oocysts and sporozoites) influences development to the ensuing stage in Anopheles stephensi, and thus the delivery of infectious sporozoites to the vertebrate host. We show that every developmental transition exhibits strong density dependence, with numbers of the ensuing stages saturating at high density. We further show that when fed ookinetes at very low densities, oocyst development is facilitated by increasing ookinete number (i.e., the efficiency of ookinete-oocyst transformation follows a sigmoid relationship). We discuss how observations on this model system generate important hypotheses for the understanding of malaria biology, and how these might guide the rational analysis of interventions against the transmission of the malaria parasites of humans by their diverse vector species.
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institution OA Journals
issn 1553-7366
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publishDate 2007-12-01
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record_format Article
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spelling doaj-art-8953d27e55dd4aaca3e26bbbfe106a7a2025-08-20T02:38:27ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742007-12-01312e19510.1371/journal.ppat.0030195Progression of Plasmodium berghei through Anopheles stephensi is density-dependent.Robert E SindenEmma J DawesYasmene AlaviJoanna WaldockOlivia FinneyJacqui MendozaGeoff A ButcherLaura AndrewsAdrian V HillSarah C GilbertMaría-Gloria BasáñezIt is well documented that the density of Plasmodium in its vertebrate host modulates the physiological response induced; this in turn regulates parasite survival and transmission. It is less clear that parasite density in the mosquito regulates survival and transmission of this important pathogen. Numerous studies have described conversion rates of Plasmodium from one life stage to the next within the mosquito, yet few have considered that these rates might vary with parasite density. Here we establish infections with defined numbers of the rodent malaria parasite Plasmodium berghei to examine how parasite density at each stage of development (gametocytes; ookinetes; oocysts and sporozoites) influences development to the ensuing stage in Anopheles stephensi, and thus the delivery of infectious sporozoites to the vertebrate host. We show that every developmental transition exhibits strong density dependence, with numbers of the ensuing stages saturating at high density. We further show that when fed ookinetes at very low densities, oocyst development is facilitated by increasing ookinete number (i.e., the efficiency of ookinete-oocyst transformation follows a sigmoid relationship). We discuss how observations on this model system generate important hypotheses for the understanding of malaria biology, and how these might guide the rational analysis of interventions against the transmission of the malaria parasites of humans by their diverse vector species.https://journals.plos.org/plospathogens/article/file?id=10.1371/journal.ppat.0030195&type=printable
spellingShingle Robert E Sinden
Emma J Dawes
Yasmene Alavi
Joanna Waldock
Olivia Finney
Jacqui Mendoza
Geoff A Butcher
Laura Andrews
Adrian V Hill
Sarah C Gilbert
María-Gloria Basáñez
Progression of Plasmodium berghei through Anopheles stephensi is density-dependent.
PLoS Pathogens
title Progression of Plasmodium berghei through Anopheles stephensi is density-dependent.
title_full Progression of Plasmodium berghei through Anopheles stephensi is density-dependent.
title_fullStr Progression of Plasmodium berghei through Anopheles stephensi is density-dependent.
title_full_unstemmed Progression of Plasmodium berghei through Anopheles stephensi is density-dependent.
title_short Progression of Plasmodium berghei through Anopheles stephensi is density-dependent.
title_sort progression of plasmodium berghei through anopheles stephensi is density dependent
url https://journals.plos.org/plospathogens/article/file?id=10.1371/journal.ppat.0030195&type=printable
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