Cargando…

The male mosquito contribution towards malaria transmission: Mating influences the Anopheles female midgut transcriptome and increases female susceptibility to human malaria parasites

Mating causes dramatic changes in female physiology, behaviour, and immunity in many insects, inducing oogenesis, oviposition, and refractoriness to further mating. Females from the Anopheles gambiae species complex typically mate only once in their lifetime during which they receive sperm and semin...

Descripción completa

Detalles Bibliográficos
Autores principales: Dahalan, Farah Aida, Churcher, Thomas S., Windbichler, Nikolai, Lawniczak, Mara K. N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6837289/
https://www.ncbi.nlm.nih.gov/pubmed/31697788
http://dx.doi.org/10.1371/journal.ppat.1008063
_version_ 1783467062757163008
author Dahalan, Farah Aida
Churcher, Thomas S.
Windbichler, Nikolai
Lawniczak, Mara K. N.
author_facet Dahalan, Farah Aida
Churcher, Thomas S.
Windbichler, Nikolai
Lawniczak, Mara K. N.
author_sort Dahalan, Farah Aida
collection PubMed
description Mating causes dramatic changes in female physiology, behaviour, and immunity in many insects, inducing oogenesis, oviposition, and refractoriness to further mating. Females from the Anopheles gambiae species complex typically mate only once in their lifetime during which they receive sperm and seminal fluid proteins as well as a mating plug that contains the steroid hormone 20-hydroxyecdysone. This hormone, which is also induced by blood-feeding, plays a major role in activating vitellogenesis for egg production. Here we show that female Anopheles coluzzii susceptibility to Plasmodium falciparum infection is significantly higher in mated females compared to virgins. We also find that mating status has a major impact on the midgut transcriptome, detectable only under sugar-fed conditions: once females have blood-fed, the transcriptional changes that are induced by mating are likely masked by the widespread effects of blood-feeding on gene expression. To determine whether increased susceptibility to parasites could be driven by the additional 20E that mated females receive from males, we mimicked mating by injecting virgin females with 20E, finding that these females are significantly more susceptible to human malaria parasites than virgin females injected with the control 20E carrier. Further RNAseq was carried out to examine whether the genes that change upon 20E injection in the midgut are similar to those that change upon mating. We find that 79 midgut-expressed genes are regulated in common by both mating and 20E, and 96% (n = 76) of these are regulated in the same direction (up vs down in 20E/mated). Together, these findings show that male Anopheles mosquitoes induce changes in the female midgut that can affect female susceptibility to P. falciparum. This implies that in nature, males might contribute to malaria transmission in previously unappreciated ways, and that vector control strategies that target males may have additional benefits towards reducing transmission.
format Online
Article
Text
id pubmed-6837289
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-68372892019-11-14 The male mosquito contribution towards malaria transmission: Mating influences the Anopheles female midgut transcriptome and increases female susceptibility to human malaria parasites Dahalan, Farah Aida Churcher, Thomas S. Windbichler, Nikolai Lawniczak, Mara K. N. PLoS Pathog Research Article Mating causes dramatic changes in female physiology, behaviour, and immunity in many insects, inducing oogenesis, oviposition, and refractoriness to further mating. Females from the Anopheles gambiae species complex typically mate only once in their lifetime during which they receive sperm and seminal fluid proteins as well as a mating plug that contains the steroid hormone 20-hydroxyecdysone. This hormone, which is also induced by blood-feeding, plays a major role in activating vitellogenesis for egg production. Here we show that female Anopheles coluzzii susceptibility to Plasmodium falciparum infection is significantly higher in mated females compared to virgins. We also find that mating status has a major impact on the midgut transcriptome, detectable only under sugar-fed conditions: once females have blood-fed, the transcriptional changes that are induced by mating are likely masked by the widespread effects of blood-feeding on gene expression. To determine whether increased susceptibility to parasites could be driven by the additional 20E that mated females receive from males, we mimicked mating by injecting virgin females with 20E, finding that these females are significantly more susceptible to human malaria parasites than virgin females injected with the control 20E carrier. Further RNAseq was carried out to examine whether the genes that change upon 20E injection in the midgut are similar to those that change upon mating. We find that 79 midgut-expressed genes are regulated in common by both mating and 20E, and 96% (n = 76) of these are regulated in the same direction (up vs down in 20E/mated). Together, these findings show that male Anopheles mosquitoes induce changes in the female midgut that can affect female susceptibility to P. falciparum. This implies that in nature, males might contribute to malaria transmission in previously unappreciated ways, and that vector control strategies that target males may have additional benefits towards reducing transmission. Public Library of Science 2019-11-07 /pmc/articles/PMC6837289/ /pubmed/31697788 http://dx.doi.org/10.1371/journal.ppat.1008063 Text en © 2019 Dahalan et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Dahalan, Farah Aida
Churcher, Thomas S.
Windbichler, Nikolai
Lawniczak, Mara K. N.
The male mosquito contribution towards malaria transmission: Mating influences the Anopheles female midgut transcriptome and increases female susceptibility to human malaria parasites
title The male mosquito contribution towards malaria transmission: Mating influences the Anopheles female midgut transcriptome and increases female susceptibility to human malaria parasites
title_full The male mosquito contribution towards malaria transmission: Mating influences the Anopheles female midgut transcriptome and increases female susceptibility to human malaria parasites
title_fullStr The male mosquito contribution towards malaria transmission: Mating influences the Anopheles female midgut transcriptome and increases female susceptibility to human malaria parasites
title_full_unstemmed The male mosquito contribution towards malaria transmission: Mating influences the Anopheles female midgut transcriptome and increases female susceptibility to human malaria parasites
title_short The male mosquito contribution towards malaria transmission: Mating influences the Anopheles female midgut transcriptome and increases female susceptibility to human malaria parasites
title_sort male mosquito contribution towards malaria transmission: mating influences the anopheles female midgut transcriptome and increases female susceptibility to human malaria parasites
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6837289/
https://www.ncbi.nlm.nih.gov/pubmed/31697788
http://dx.doi.org/10.1371/journal.ppat.1008063
work_keys_str_mv AT dahalanfarahaida themalemosquitocontributiontowardsmalariatransmissionmatinginfluencestheanophelesfemalemidguttranscriptomeandincreasesfemalesusceptibilitytohumanmalariaparasites
AT churcherthomass themalemosquitocontributiontowardsmalariatransmissionmatinginfluencestheanophelesfemalemidguttranscriptomeandincreasesfemalesusceptibilitytohumanmalariaparasites
AT windbichlernikolai themalemosquitocontributiontowardsmalariatransmissionmatinginfluencestheanophelesfemalemidguttranscriptomeandincreasesfemalesusceptibilitytohumanmalariaparasites
AT lawniczakmarakn themalemosquitocontributiontowardsmalariatransmissionmatinginfluencestheanophelesfemalemidguttranscriptomeandincreasesfemalesusceptibilitytohumanmalariaparasites
AT dahalanfarahaida malemosquitocontributiontowardsmalariatransmissionmatinginfluencestheanophelesfemalemidguttranscriptomeandincreasesfemalesusceptibilitytohumanmalariaparasites
AT churcherthomass malemosquitocontributiontowardsmalariatransmissionmatinginfluencestheanophelesfemalemidguttranscriptomeandincreasesfemalesusceptibilitytohumanmalariaparasites
AT windbichlernikolai malemosquitocontributiontowardsmalariatransmissionmatinginfluencestheanophelesfemalemidguttranscriptomeandincreasesfemalesusceptibilitytohumanmalariaparasites
AT lawniczakmarakn malemosquitocontributiontowardsmalariatransmissionmatinginfluencestheanophelesfemalemidguttranscriptomeandincreasesfemalesusceptibilitytohumanmalariaparasites