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Glucose-mediated proliferation of a gut commensal bacterium promotes Plasmodium infection by increasing mosquito midgut pH

Plant-nectar-derived sugar is the major energy source for mosquitoes, but its influence on vector competence for malaria parasites remains unclear. Here, we show that Plasmodium berghei infection of Anopheles stephensi results in global metabolome changes, with the most significant impact on glucose...

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Autores principales: Wang, Mengfei, An, Yanpeng, Gao, Li, Dong, Shengzhang, Zhou, Xiaofeng, Feng, Yuebiao, Wang, Penghua, Dimopoulos, George, Tang, Huiru, Wang, Jingwen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8116483/
https://www.ncbi.nlm.nih.gov/pubmed/33882310
http://dx.doi.org/10.1016/j.celrep.2021.108992
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author Wang, Mengfei
An, Yanpeng
Gao, Li
Dong, Shengzhang
Zhou, Xiaofeng
Feng, Yuebiao
Wang, Penghua
Dimopoulos, George
Tang, Huiru
Wang, Jingwen
author_facet Wang, Mengfei
An, Yanpeng
Gao, Li
Dong, Shengzhang
Zhou, Xiaofeng
Feng, Yuebiao
Wang, Penghua
Dimopoulos, George
Tang, Huiru
Wang, Jingwen
author_sort Wang, Mengfei
collection PubMed
description Plant-nectar-derived sugar is the major energy source for mosquitoes, but its influence on vector competence for malaria parasites remains unclear. Here, we show that Plasmodium berghei infection of Anopheles stephensi results in global metabolome changes, with the most significant impact on glucose metabolism. Feeding on glucose or trehalose (the main hemolymph sugars) renders the mosquito more susceptible to Plasmodium infection by alkalizing the mosquito midgut. The glucose/trehalose diets promote proliferation of a commensal bacterium, Asaia bogorensis, that remodels glucose metabolism in a way that increases midgut pH, thereby promoting Plasmodium gametogenesis. We also demonstrate that the sugar composition from different natural plant nectars influences A. bogorensis growth, resulting in a greater permissiveness to Plasmodium. Altogether, our results demonstrate that dietary glucose is an important determinant of mosquito vector competency for Plasmodium, further highlighting a key role for mosquito-microbiota interactions in regulating the development of the malaria parasite.
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spelling pubmed-81164832021-05-13 Glucose-mediated proliferation of a gut commensal bacterium promotes Plasmodium infection by increasing mosquito midgut pH Wang, Mengfei An, Yanpeng Gao, Li Dong, Shengzhang Zhou, Xiaofeng Feng, Yuebiao Wang, Penghua Dimopoulos, George Tang, Huiru Wang, Jingwen Cell Rep Article Plant-nectar-derived sugar is the major energy source for mosquitoes, but its influence on vector competence for malaria parasites remains unclear. Here, we show that Plasmodium berghei infection of Anopheles stephensi results in global metabolome changes, with the most significant impact on glucose metabolism. Feeding on glucose or trehalose (the main hemolymph sugars) renders the mosquito more susceptible to Plasmodium infection by alkalizing the mosquito midgut. The glucose/trehalose diets promote proliferation of a commensal bacterium, Asaia bogorensis, that remodels glucose metabolism in a way that increases midgut pH, thereby promoting Plasmodium gametogenesis. We also demonstrate that the sugar composition from different natural plant nectars influences A. bogorensis growth, resulting in a greater permissiveness to Plasmodium. Altogether, our results demonstrate that dietary glucose is an important determinant of mosquito vector competency for Plasmodium, further highlighting a key role for mosquito-microbiota interactions in regulating the development of the malaria parasite. 2021-04-20 /pmc/articles/PMC8116483/ /pubmed/33882310 http://dx.doi.org/10.1016/j.celrep.2021.108992 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ).
spellingShingle Article
Wang, Mengfei
An, Yanpeng
Gao, Li
Dong, Shengzhang
Zhou, Xiaofeng
Feng, Yuebiao
Wang, Penghua
Dimopoulos, George
Tang, Huiru
Wang, Jingwen
Glucose-mediated proliferation of a gut commensal bacterium promotes Plasmodium infection by increasing mosquito midgut pH
title Glucose-mediated proliferation of a gut commensal bacterium promotes Plasmodium infection by increasing mosquito midgut pH
title_full Glucose-mediated proliferation of a gut commensal bacterium promotes Plasmodium infection by increasing mosquito midgut pH
title_fullStr Glucose-mediated proliferation of a gut commensal bacterium promotes Plasmodium infection by increasing mosquito midgut pH
title_full_unstemmed Glucose-mediated proliferation of a gut commensal bacterium promotes Plasmodium infection by increasing mosquito midgut pH
title_short Glucose-mediated proliferation of a gut commensal bacterium promotes Plasmodium infection by increasing mosquito midgut pH
title_sort glucose-mediated proliferation of a gut commensal bacterium promotes plasmodium infection by increasing mosquito midgut ph
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8116483/
https://www.ncbi.nlm.nih.gov/pubmed/33882310
http://dx.doi.org/10.1016/j.celrep.2021.108992
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