Evidence map›Paper›PMID 31238932›Full record

ArticleMalaria journal2019

Improvement of an in vitro drug selection method for generating transgenic Plasmodium berghei parasites.

Akira Soga, Takahiro Shirozu, Mami Ko-Ketsu, Shinya Fukumoto

Abstract read
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Article in Malaria journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Akira SogaNational Research Center for Protozoan Diseases, Obihiro University of Agriculture and Veterinary Medicine, Inada-cho, Obihiro, Hokkaido, 080-8555, Japan.
Takahiro ShirozuNational Research Center for Protozoan Diseases, Obihiro University of Agriculture and Veterinary Medicine, Inada-cho, Obihiro, Hokkaido, 080-8555, Japan.
Mami Ko-KetsuNational Research Center for Protozoan Diseases, Obihiro University of Agriculture and Veterinary Medicine, Inada-cho, Obihiro, Hokkaido, 080-8555, Japan.
Shinya FukumotoNational Research Center for Protozoan Diseases, Obihiro University of Agriculture and Veterinary Medicine, Inada-cho, Obihiro, Hokkaido, 080-8555, Japan. fukumoto@obihiro.ac.jp.

Funding

Japan Society for the Promotion of Science (JP) 18J10448Japan Society for the Promotion of Science (JP) JP16H05026Japan Society for the Promotion of Science (JP) JP16K15035Japan Society for the Promotion of Science (JP) JP26304038
6 · The paper itself

Abstract

backgroundReverse genetics approaches have become powerful tools to dissect the biology of malaria parasites. In a previous study, development of an in vitro drug selection method for generating transgenic parasite of Plasmodium berghei was reported. Using this method, two novel and independent selection markers using the P. berghei heat shock protein 70 promoter was previously established. While the approach permits the easy and flexible genetic manipulation of P. berghei, shortcomings include a low variety in promoter options to drive marker gene expression and increased complexity of the selection procedure. In this study, addressing these issues was attempted.

methodsTo secure a variety of promoters, the use of a P. berghei elongation factor-1α promoter for marker gene expression was attempted. To simplify the procedure of in vitro selection, the establishment of a two cell-cycle culture method and its application for drug selection were attempted.

resultsThe P. berghei elongation factor-1α (pbef-1α) promoter, which is commonly used to drive marker gene expression, was successfully applied as an alternative promoter model for marker gene expression, using the parasite's codon-optimized marker sequence. To simplify the in vitro selection method, a two cell-cycle culture method in which the merozoite was released by filtration of the culture containing matured schizont-infected erythrocytes was also developed and successfully applied for drug selection.

conclusionThe pbef-1α promoter was successfully applied in an in vitro selection system. The in vitro selection procedure also could be simplified for practical use using a two cell-cycle culture method. These improvements provide a more versatile platform for the genetic manipulation of P. berghei.

Indexed as

AnimalsAntimalarialsCell Culture TechniquesFemaleMalariaMiceMice, Inbred BALB CMice, Inbred ICRMicroorganisms, Genetically-ModifiedPlasmodium bergheiAntimalarialsDrug selectionPlasmodium bergheiTransgenic parasite

Identifiers

PMID31238932
PMCPMC6593524

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