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Engineered Anopheles Immunity to Plasmodium Infection

A causative agent of human malaria, Plasmodium falciparum, is transmitted by Anopheles mosquitoes. The malaria parasite is under intensive attack from the mosquito's innate immune system during its sporogonic development. We have used genetic engineering to create immune-enhanced Anopheles step...

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Detalles Bibliográficos
Autores principales: Dong, Yuemei, Das, Suchismita, Cirimotich, Chris, Souza-Neto, Jayme A., McLean, Kyle J., Dimopoulos, George
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3245315/
https://www.ncbi.nlm.nih.gov/pubmed/22216006
http://dx.doi.org/10.1371/journal.ppat.1002458
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author Dong, Yuemei
Das, Suchismita
Cirimotich, Chris
Souza-Neto, Jayme A.
McLean, Kyle J.
Dimopoulos, George
author_facet Dong, Yuemei
Das, Suchismita
Cirimotich, Chris
Souza-Neto, Jayme A.
McLean, Kyle J.
Dimopoulos, George
author_sort Dong, Yuemei
collection PubMed
description A causative agent of human malaria, Plasmodium falciparum, is transmitted by Anopheles mosquitoes. The malaria parasite is under intensive attack from the mosquito's innate immune system during its sporogonic development. We have used genetic engineering to create immune-enhanced Anopheles stephensi mosquitoes through blood meal-inducible expression of a transgene encoding the IMD pathway-controlled NF-kB Rel2 transcription factor in the midgut and fat-body tissue. Transgenic mosquitoes showed greater resistance to Plasmodium and microbial infection as a result of timely concerted tissue-specific immune attacks involving multiple effectors. The relatively weak impact of this genetic modification on mosquito fitness under laboratory conditions encourages further investigation of this approach for malaria control.
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spelling pubmed-32453152012-01-03 Engineered Anopheles Immunity to Plasmodium Infection Dong, Yuemei Das, Suchismita Cirimotich, Chris Souza-Neto, Jayme A. McLean, Kyle J. Dimopoulos, George PLoS Pathog Research Article A causative agent of human malaria, Plasmodium falciparum, is transmitted by Anopheles mosquitoes. The malaria parasite is under intensive attack from the mosquito's innate immune system during its sporogonic development. We have used genetic engineering to create immune-enhanced Anopheles stephensi mosquitoes through blood meal-inducible expression of a transgene encoding the IMD pathway-controlled NF-kB Rel2 transcription factor in the midgut and fat-body tissue. Transgenic mosquitoes showed greater resistance to Plasmodium and microbial infection as a result of timely concerted tissue-specific immune attacks involving multiple effectors. The relatively weak impact of this genetic modification on mosquito fitness under laboratory conditions encourages further investigation of this approach for malaria control. Public Library of Science 2011-12-22 /pmc/articles/PMC3245315/ /pubmed/22216006 http://dx.doi.org/10.1371/journal.ppat.1002458 Text en Dong 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Dong, Yuemei
Das, Suchismita
Cirimotich, Chris
Souza-Neto, Jayme A.
McLean, Kyle J.
Dimopoulos, George
Engineered Anopheles Immunity to Plasmodium Infection
title Engineered Anopheles Immunity to Plasmodium Infection
title_full Engineered Anopheles Immunity to Plasmodium Infection
title_fullStr Engineered Anopheles Immunity to Plasmodium Infection
title_full_unstemmed Engineered Anopheles Immunity to Plasmodium Infection
title_short Engineered Anopheles Immunity to Plasmodium Infection
title_sort engineered anopheles immunity to plasmodium infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3245315/
https://www.ncbi.nlm.nih.gov/pubmed/22216006
http://dx.doi.org/10.1371/journal.ppat.1002458
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