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An Aedes aegypti-associated fungus increases susceptibility to dengue virus by modulating gut trypsin activity

Transmission of dengue virus (DENV) requires successful completion of the infection cycle in the Aedes aegypti vector, which is initiated in the midgut tissue after ingestion of an infectious blood meal. While certain Ae. aegypti midgut-associated bacteria influence virus infection, little is known...

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Autores principales: Angleró-Rodríguez, Yesseinia I, Talyuli, Octavio AC, Blumberg, Benjamin J, Kang, Seokyoung, Demby, Celia, Shields, Alicia, Carlson, Jenny, Jupatanakul, Natapong, Dimopoulos, George
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5716662/
https://www.ncbi.nlm.nih.gov/pubmed/29205153
http://dx.doi.org/10.7554/eLife.28844
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author Angleró-Rodríguez, Yesseinia I
Talyuli, Octavio AC
Blumberg, Benjamin J
Kang, Seokyoung
Demby, Celia
Shields, Alicia
Carlson, Jenny
Jupatanakul, Natapong
Dimopoulos, George
author_facet Angleró-Rodríguez, Yesseinia I
Talyuli, Octavio AC
Blumberg, Benjamin J
Kang, Seokyoung
Demby, Celia
Shields, Alicia
Carlson, Jenny
Jupatanakul, Natapong
Dimopoulos, George
author_sort Angleró-Rodríguez, Yesseinia I
collection PubMed
description Transmission of dengue virus (DENV) requires successful completion of the infection cycle in the Aedes aegypti vector, which is initiated in the midgut tissue after ingestion of an infectious blood meal. While certain Ae. aegypti midgut-associated bacteria influence virus infection, little is known about the midgut-associated fungi (mycobiota), and how its members might influence susceptibility to DENV infection. We show that a Talaromyces (Tsp_PR) fungus, isolated from field-caught Ae. aegypti, render the mosquito more permissive to DENV infection. This modulation is attributed to a profound down-regulation of digestive enzyme genes and trypsin activity, upon exposure to Tsp_PR-secreted factors. In conclusion, we show for the first time that a natural mosquito gut-associated fungus can alter Ae. aegypti physiology in a way that facilitates pathogen infection.
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spelling pubmed-57166622017-12-06 An Aedes aegypti-associated fungus increases susceptibility to dengue virus by modulating gut trypsin activity Angleró-Rodríguez, Yesseinia I Talyuli, Octavio AC Blumberg, Benjamin J Kang, Seokyoung Demby, Celia Shields, Alicia Carlson, Jenny Jupatanakul, Natapong Dimopoulos, George eLife Microbiology and Infectious Disease Transmission of dengue virus (DENV) requires successful completion of the infection cycle in the Aedes aegypti vector, which is initiated in the midgut tissue after ingestion of an infectious blood meal. While certain Ae. aegypti midgut-associated bacteria influence virus infection, little is known about the midgut-associated fungi (mycobiota), and how its members might influence susceptibility to DENV infection. We show that a Talaromyces (Tsp_PR) fungus, isolated from field-caught Ae. aegypti, render the mosquito more permissive to DENV infection. This modulation is attributed to a profound down-regulation of digestive enzyme genes and trypsin activity, upon exposure to Tsp_PR-secreted factors. In conclusion, we show for the first time that a natural mosquito gut-associated fungus can alter Ae. aegypti physiology in a way that facilitates pathogen infection. eLife Sciences Publications, Ltd 2017-12-05 /pmc/articles/PMC5716662/ /pubmed/29205153 http://dx.doi.org/10.7554/eLife.28844 Text en © 2017, Angleró-Rodríguez et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Microbiology and Infectious Disease
Angleró-Rodríguez, Yesseinia I
Talyuli, Octavio AC
Blumberg, Benjamin J
Kang, Seokyoung
Demby, Celia
Shields, Alicia
Carlson, Jenny
Jupatanakul, Natapong
Dimopoulos, George
An Aedes aegypti-associated fungus increases susceptibility to dengue virus by modulating gut trypsin activity
title An Aedes aegypti-associated fungus increases susceptibility to dengue virus by modulating gut trypsin activity
title_full An Aedes aegypti-associated fungus increases susceptibility to dengue virus by modulating gut trypsin activity
title_fullStr An Aedes aegypti-associated fungus increases susceptibility to dengue virus by modulating gut trypsin activity
title_full_unstemmed An Aedes aegypti-associated fungus increases susceptibility to dengue virus by modulating gut trypsin activity
title_short An Aedes aegypti-associated fungus increases susceptibility to dengue virus by modulating gut trypsin activity
title_sort aedes aegypti-associated fungus increases susceptibility to dengue virus by modulating gut trypsin activity
topic Microbiology and Infectious Disease
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5716662/
https://www.ncbi.nlm.nih.gov/pubmed/29205153
http://dx.doi.org/10.7554/eLife.28844
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