Forward Genetics in Apicomplexa Biology: The Host Side of the Story

Forward genetic approaches have been widely used in parasitology and have proven their power to reveal the complexities of host-parasite interactions in an unbiased fashion. Many aspects of the parasite's biology, including the identification of virulence factors, replication determinants, anti...

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Published in:Frontiers in cellular and infection microbiology Vol. 12; p. 878475
Main Authors: Sánchez-Arcila, Juan C, Jensen, Kirk D C
Format: Journal Article
Language:English
Published: Switzerland Frontiers Media S.A 12-05-2022
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Summary:Forward genetic approaches have been widely used in parasitology and have proven their power to reveal the complexities of host-parasite interactions in an unbiased fashion. Many aspects of the parasite's biology, including the identification of virulence factors, replication determinants, antibiotic resistance genes, and other factors required for parasitic life, have been discovered using such strategies. Forward genetic approaches have also been employed to understand host resistance mechanisms to parasitic infection. Here, we will introduce and review all forward genetic approaches that have been used to identify host factors involved with Apicomplexa infections, which include classical genetic screens and QTL mapping, GWAS, ENU mutagenesis, overexpression, RNAi and CRISPR-Cas9 library screens. Collectively, these screens have improved our understanding of host resistance mechanisms, immune regulation, vaccine and drug designs for Apicomplexa parasites. We will also discuss how recent advances in molecular genetics give present opportunities to further explore host-parasite relationships.
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This article was submitted to Parasite and Host, a section of the journal Frontiers in Cellular and Infection Microbiology
Reviewed by: Jon P. Boyle, University of Pittsburgh, United States; George So Yap, Rutgers University, Newark, United States
Edited by: Jeroen P. J. Saeij, University of California, Davis, United States
ISSN:2235-2988
2235-2988
DOI:10.3389/fcimb.2022.878475