Cargando…
A natural Anopheles-associated Penicillium chrysogenum enhances mosquito susceptibility to Plasmodium infection
Whereas studies have extensively examined the ability of bacteria to influence Plasmodium infection in the mosquito, the tripartite interactions between non-entomopathogenic fungi, mosquitoes, and Plasmodium parasites remain largely uncharacterized. Here we report the isolation of a common mosquito-...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5039729/ https://www.ncbi.nlm.nih.gov/pubmed/27678168 http://dx.doi.org/10.1038/srep34084 |
_version_ | 1782456121370345472 |
---|---|
author | Angleró-Rodríguez, Yesseinia I. Blumberg, Benjamin J. Dong, Yuemei Sandiford, Simone L. Pike, Andrew Clayton, April M. Dimopoulos, George |
author_facet | Angleró-Rodríguez, Yesseinia I. Blumberg, Benjamin J. Dong, Yuemei Sandiford, Simone L. Pike, Andrew Clayton, April M. Dimopoulos, George |
author_sort | Angleró-Rodríguez, Yesseinia I. |
collection | PubMed |
description | Whereas studies have extensively examined the ability of bacteria to influence Plasmodium infection in the mosquito, the tripartite interactions between non-entomopathogenic fungi, mosquitoes, and Plasmodium parasites remain largely uncharacterized. Here we report the isolation of a common mosquito-associated ascomycete fungus, Penicillium chrysogenum, from the midgut of field-caught Anopheles mosquitoes. Although the presence of Pe. chrysogenum in the Anopheles gambiae midgut does not affect mosquito survival, it renders the mosquito significantly more susceptible to Plasmodium infection through a secreted heat-stable factor. We further provide evidence that the mechanism of the fungus-mediated modulation of mosquito susceptibility to Plasmodium involves an upregulation of the insect’s ornithine decarboxylase gene, which sequesters arginine for polyamine biosynthesis. Arginine plays an important role in the mosquito’s anti-Plasmodium defense as a substrate of nitric oxide production, and its availability therefore has a direct impact on the mosquito’s susceptibility to the parasite. While this type of immunomodulatory mechanism has already been demonstrated in other host-pathogen interaction systems, this is the first report of a mosquito-associated fungus that can suppress the mosquito’s innate immune system in a way that would favor Plasmodium infection and possibly malaria transmission. |
format | Online Article Text |
id | pubmed-5039729 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50397292016-09-30 A natural Anopheles-associated Penicillium chrysogenum enhances mosquito susceptibility to Plasmodium infection Angleró-Rodríguez, Yesseinia I. Blumberg, Benjamin J. Dong, Yuemei Sandiford, Simone L. Pike, Andrew Clayton, April M. Dimopoulos, George Sci Rep Article Whereas studies have extensively examined the ability of bacteria to influence Plasmodium infection in the mosquito, the tripartite interactions between non-entomopathogenic fungi, mosquitoes, and Plasmodium parasites remain largely uncharacterized. Here we report the isolation of a common mosquito-associated ascomycete fungus, Penicillium chrysogenum, from the midgut of field-caught Anopheles mosquitoes. Although the presence of Pe. chrysogenum in the Anopheles gambiae midgut does not affect mosquito survival, it renders the mosquito significantly more susceptible to Plasmodium infection through a secreted heat-stable factor. We further provide evidence that the mechanism of the fungus-mediated modulation of mosquito susceptibility to Plasmodium involves an upregulation of the insect’s ornithine decarboxylase gene, which sequesters arginine for polyamine biosynthesis. Arginine plays an important role in the mosquito’s anti-Plasmodium defense as a substrate of nitric oxide production, and its availability therefore has a direct impact on the mosquito’s susceptibility to the parasite. While this type of immunomodulatory mechanism has already been demonstrated in other host-pathogen interaction systems, this is the first report of a mosquito-associated fungus that can suppress the mosquito’s innate immune system in a way that would favor Plasmodium infection and possibly malaria transmission. Nature Publishing Group 2016-09-28 /pmc/articles/PMC5039729/ /pubmed/27678168 http://dx.doi.org/10.1038/srep34084 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Angleró-Rodríguez, Yesseinia I. Blumberg, Benjamin J. Dong, Yuemei Sandiford, Simone L. Pike, Andrew Clayton, April M. Dimopoulos, George A natural Anopheles-associated Penicillium chrysogenum enhances mosquito susceptibility to Plasmodium infection |
title | A natural Anopheles-associated Penicillium chrysogenum enhances mosquito susceptibility to Plasmodium infection |
title_full | A natural Anopheles-associated Penicillium chrysogenum enhances mosquito susceptibility to Plasmodium infection |
title_fullStr | A natural Anopheles-associated Penicillium chrysogenum enhances mosquito susceptibility to Plasmodium infection |
title_full_unstemmed | A natural Anopheles-associated Penicillium chrysogenum enhances mosquito susceptibility to Plasmodium infection |
title_short | A natural Anopheles-associated Penicillium chrysogenum enhances mosquito susceptibility to Plasmodium infection |
title_sort | natural anopheles-associated penicillium chrysogenum enhances mosquito susceptibility to plasmodium infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5039729/ https://www.ncbi.nlm.nih.gov/pubmed/27678168 http://dx.doi.org/10.1038/srep34084 |
work_keys_str_mv | AT anglerorodriguezyesseiniai anaturalanophelesassociatedpenicilliumchrysogenumenhancesmosquitosusceptibilitytoplasmodiuminfection AT blumbergbenjaminj anaturalanophelesassociatedpenicilliumchrysogenumenhancesmosquitosusceptibilitytoplasmodiuminfection AT dongyuemei anaturalanophelesassociatedpenicilliumchrysogenumenhancesmosquitosusceptibilitytoplasmodiuminfection AT sandifordsimonel anaturalanophelesassociatedpenicilliumchrysogenumenhancesmosquitosusceptibilitytoplasmodiuminfection AT pikeandrew anaturalanophelesassociatedpenicilliumchrysogenumenhancesmosquitosusceptibilitytoplasmodiuminfection AT claytonaprilm anaturalanophelesassociatedpenicilliumchrysogenumenhancesmosquitosusceptibilitytoplasmodiuminfection AT dimopoulosgeorge anaturalanophelesassociatedpenicilliumchrysogenumenhancesmosquitosusceptibilitytoplasmodiuminfection AT anglerorodriguezyesseiniai naturalanophelesassociatedpenicilliumchrysogenumenhancesmosquitosusceptibilitytoplasmodiuminfection AT blumbergbenjaminj naturalanophelesassociatedpenicilliumchrysogenumenhancesmosquitosusceptibilitytoplasmodiuminfection AT dongyuemei naturalanophelesassociatedpenicilliumchrysogenumenhancesmosquitosusceptibilitytoplasmodiuminfection AT sandifordsimonel naturalanophelesassociatedpenicilliumchrysogenumenhancesmosquitosusceptibilitytoplasmodiuminfection AT pikeandrew naturalanophelesassociatedpenicilliumchrysogenumenhancesmosquitosusceptibilitytoplasmodiuminfection AT claytonaprilm naturalanophelesassociatedpenicilliumchrysogenumenhancesmosquitosusceptibilitytoplasmodiuminfection AT dimopoulosgeorge naturalanophelesassociatedpenicilliumchrysogenumenhancesmosquitosusceptibilitytoplasmodiuminfection |