4.4 Review

CRISPR/Cas advancements for genome editing, diagnosis, therapeutics, and vaccine development for Plasmodium parasites, and genetic engineering of Anopheles mosquito vector

Journal

INFECTION GENETICS AND EVOLUTION
Volume 109, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.meegid.2023.105419

Keywords

Malaria; Functional genomics; CRISPR; Cas9; Drug resistance; Plasmodium transgenic lines; Anopheles

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Malaria, a vector-borne disease, remains a significant global health concern with more than 200 million cases. It is crucial to develop novel antimalarial drugs and effective vaccines to eliminate and eradicate malaria. The CRISPR/Cas nuclease system has been confirmed as a proficient genome editing tool for species-specific diagnosis, drug resistance research, and gene drive to control the Anopheles population. The integration of traditional and novel molecular techniques can greatly enhance research quality. The development of a CRISPR/Cas-based diagnostic kit for specific detection of Plasmodium species or drug resistance markers is urgently needed, as well as the ability to modify parasite genomes to better understand pathogenesis.
Malaria as vector-borne disease remains important health concern with over 200 million cases globally. Novel antimalarial medicines and more effective vaccines must be developed to eliminate and eradicate malaria. Appraisal of preceding genome editing approaches confirmed the CRISPR/Cas nuclease system as a novel proficient genome editing system and a tool for species-specific diagnosis, and drug resistance researches for Plasmodium species, and gene drive to control Anopheles population. CRISPR/Cas technology, as a handy tool for genome editing can be justified for the production of transgenic malaria parasites like Plasmodium transgenic lines expressing Cas9, chimeric Plasmodium transgenic lines, knockdown and knockout transgenic parasites, and transgenic parasites expressing alternative alleles, and also mutant strains of Anopheles such as only male mosquito populations, generation of wingless mosquitoes, and creation of knock-out/ knock-in mutants. Though, the incorporation of traditional methods and novel molecular techniques could noticeably enhance the quality of results. The striking development of a CRISPR/Cas-based diagnostic kit that can specifically diagnose the Plasmodium species or drug resistance markers is highly required in malaria settings with affordable cost and highspeed detection. Furthermore, the advancement of genome modifications by CRISPR/Cas technologies resolves contemporary restrictions to culturing, maintaining, and analyzing these parasites, and the aptitude to investigate parasite genome functions opens up new vistas in the better understanding of pathogenesis.

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