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dc.contributor.authorParres-Mercader, Marina
dc.contributor.authorPance, Alena
dc.contributor.authorGómez-Díaz, Elena
dc.date.accessioned2023-06-19T10:45:01Z
dc.date.available2023-06-19T10:45:01Z
dc.date.issued2023-05-26
dc.identifier.citationParres-Mercader , M , Pance , A & Gómez-Díaz , E 2023 , ' Novel systems to study vector-pathogen interactions in malaria ' , Frontiers Cellular and Infection Microbiology , vol. 13 , 1146030 , pp. 1-13 . https://doi.org/10.3389/fcimb.2023.1146030
dc.identifier.issn2235-2988
dc.identifier.otherJisc: 1135612
dc.identifier.urihttp://hdl.handle.net/2299/26438
dc.description© 2023 Parres-Mercader, Pance and Gómez-Díaz. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). https://creativecommons.org/licenses/by/4.0/
dc.description.abstractSome 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.en
dc.format.extent13
dc.format.extent2827914
dc.language.isoeng
dc.relation.ispartofFrontiers Cellular and Infection Microbiology
dc.subjecttissue explant
dc.subjectmembrane feeding assay (MFA)
dc.subjectorganoids
dc.subjectPlasmodium
dc.subjectAnopheles
dc.subjectmosquito
dc.subjectMalaria
dc.subjectHumans
dc.subjectAnimals
dc.subjectMosquito Vectors
dc.subjectTechnology
dc.subjectCulicidae
dc.subjectEnvironment
dc.subjectMicrobiology (medical)
dc.subjectInfectious Diseases
dc.subjectMicrobiology
dc.subjectImmunology
dc.titleNovel systems to study vector-pathogen interactions in malariaen
dc.contributor.institutionSchool of Life and Medical Sciences
dc.contributor.institutionCentre for Research in Mechanisms of Disease and Drug Discovery
dc.description.statusPeer reviewed
dc.identifier.urlhttp://www.scopus.com/inward/record.url?scp=85161721582&partnerID=8YFLogxK
rioxxterms.versionofrecord10.3389/fcimb.2023.1146030
rioxxterms.typeOther
herts.preservation.rarelyaccessedtrue


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