Cargando…
Novel systems to study vector-pathogen interactions in malaria
Some parasitic diseases, such as malaria, require two hosts to complete their lifecycle: a human and an insect vector. Although most malaria research has focused on parasite development in the human host, the life cycle within the vector is critical for the propagation of the disease. The mosquito s...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10253182/ https://www.ncbi.nlm.nih.gov/pubmed/37305421 http://dx.doi.org/10.3389/fcimb.2023.1146030 |
_version_ | 1785056346338492416 |
---|---|
author | Parres-Mercader, Marina Pance, Alena Gómez-Díaz, Elena |
author_facet | Parres-Mercader, Marina Pance, Alena Gómez-Díaz, Elena |
author_sort | Parres-Mercader, Marina |
collection | PubMed |
description | Some parasitic diseases, such as malaria, require two hosts to complete their lifecycle: a human and an insect vector. Although most malaria research has focused on parasite development in the human host, the life cycle within the vector is critical for the propagation of the disease. The mosquito stage of the Plasmodium lifecycle represents a major demographic bottleneck, crucial for transmission blocking strategies. Furthermore, it is in the vector, where sexual recombination occurs generating “de novo” genetic diversity, which can favor the spread of drug resistance and hinder effective vaccine development. However, understanding of vector-parasite interactions is hampered by the lack of experimental systems that mimic the natural environment while allowing to control and standardize the complexity of the interactions. The breakthrough in stem cell technologies has provided new insights into human-pathogen interactions, but these advances have not been translated into insect models. Here, we review in vivo and in vitro systems that have been used so far to study malaria in the mosquito. We also highlight the relevance of single-cell technologies to progress understanding of these interactions with higher resolution and depth. Finally, we emphasize the necessity to develop robust and accessible ex vivo systems (tissues and organs) to enable investigation of the molecular mechanisms of parasite-vector interactions providing new targets for malaria control. |
format | Online Article Text |
id | pubmed-10253182 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102531822023-06-10 Novel systems to study vector-pathogen interactions in malaria Parres-Mercader, Marina Pance, Alena Gómez-Díaz, Elena Front Cell Infect Microbiol Cellular and Infection Microbiology Some parasitic diseases, such as malaria, require two hosts to complete their lifecycle: a human and an insect vector. Although most malaria research has focused on parasite development in the human host, the life cycle within the vector is critical for the propagation of the disease. The mosquito stage of the Plasmodium lifecycle represents a major demographic bottleneck, crucial for transmission blocking strategies. Furthermore, it is in the vector, where sexual recombination occurs generating “de novo” genetic diversity, which can favor the spread of drug resistance and hinder effective vaccine development. However, understanding of vector-parasite interactions is hampered by the lack of experimental systems that mimic the natural environment while allowing to control and standardize the complexity of the interactions. The breakthrough in stem cell technologies has provided new insights into human-pathogen interactions, but these advances have not been translated into insect models. Here, we review in vivo and in vitro systems that have been used so far to study malaria in the mosquito. We also highlight the relevance of single-cell technologies to progress understanding of these interactions with higher resolution and depth. Finally, we emphasize the necessity to develop robust and accessible ex vivo systems (tissues and organs) to enable investigation of the molecular mechanisms of parasite-vector interactions providing new targets for malaria control. Frontiers Media S.A. 2023-05-26 /pmc/articles/PMC10253182/ /pubmed/37305421 http://dx.doi.org/10.3389/fcimb.2023.1146030 Text en Copyright © 2023 Parres-Mercader, Pance and Gómez-Díaz https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cellular and Infection Microbiology Parres-Mercader, Marina Pance, Alena Gómez-Díaz, Elena Novel systems to study vector-pathogen interactions in malaria |
title | Novel systems to study vector-pathogen interactions in malaria |
title_full | Novel systems to study vector-pathogen interactions in malaria |
title_fullStr | Novel systems to study vector-pathogen interactions in malaria |
title_full_unstemmed | Novel systems to study vector-pathogen interactions in malaria |
title_short | Novel systems to study vector-pathogen interactions in malaria |
title_sort | novel systems to study vector-pathogen interactions in malaria |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10253182/ https://www.ncbi.nlm.nih.gov/pubmed/37305421 http://dx.doi.org/10.3389/fcimb.2023.1146030 |
work_keys_str_mv | AT parresmercadermarina novelsystemstostudyvectorpathogeninteractionsinmalaria AT pancealena novelsystemstostudyvectorpathogeninteractionsinmalaria AT gomezdiazelena novelsystemstostudyvectorpathogeninteractionsinmalaria |