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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2021
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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. |
format | Online Article Text |
id | pubmed-8116483 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
record_format | MEDLINE/PubMed |
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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