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

Abstract Background Reverse 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 indepe...

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Main Authors: Akira Soga, Takahiro Shirozu, Mami Ko-ketsu, Shinya Fukumoto
Format: Article
Language:English
Published: BMC 2019-06-01
Series:Malaria Journal
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12936-019-2851-6
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author Akira Soga
Takahiro Shirozu
Mami Ko-ketsu
Shinya Fukumoto
author_facet Akira Soga
Takahiro Shirozu
Mami Ko-ketsu
Shinya Fukumoto
author_sort Akira Soga
collection DOAJ
description Abstract Background Reverse 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. Methods To 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. Results The 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. Conclusion The 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.
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spelling doaj.art-b23b7b8dde04403093dd186adc7b98c92022-12-22T01:30:38ZengBMCMalaria Journal1475-28752019-06-011811910.1186/s12936-019-2851-6Improvement of an in vitro drug selection method for generating transgenic Plasmodium berghei parasitesAkira Soga0Takahiro Shirozu1Mami Ko-ketsu2Shinya Fukumoto3National Research Center for Protozoan Diseases, Obihiro University of Agriculture and Veterinary MedicineNational Research Center for Protozoan Diseases, Obihiro University of Agriculture and Veterinary MedicineNational Research Center for Protozoan Diseases, Obihiro University of Agriculture and Veterinary MedicineNational Research Center for Protozoan Diseases, Obihiro University of Agriculture and Veterinary MedicineAbstract Background Reverse 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. Methods To 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. Results The 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. Conclusion The 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.http://link.springer.com/article/10.1186/s12936-019-2851-6Plasmodium bergheiTransgenic parasiteDrug selection
spellingShingle Akira Soga
Takahiro Shirozu
Mami Ko-ketsu
Shinya Fukumoto
Improvement of an in vitro drug selection method for generating transgenic Plasmodium berghei parasites
Malaria Journal
Plasmodium berghei
Transgenic parasite
Drug selection
title Improvement of an in vitro drug selection method for generating transgenic Plasmodium berghei parasites
title_full Improvement of an in vitro drug selection method for generating transgenic Plasmodium berghei parasites
title_fullStr Improvement of an in vitro drug selection method for generating transgenic Plasmodium berghei parasites
title_full_unstemmed Improvement of an in vitro drug selection method for generating transgenic Plasmodium berghei parasites
title_short Improvement of an in vitro drug selection method for generating transgenic Plasmodium berghei parasites
title_sort improvement of an in vitro drug selection method for generating transgenic plasmodium berghei parasites
topic Plasmodium berghei
Transgenic parasite
Drug selection
url http://link.springer.com/article/10.1186/s12936-019-2851-6
work_keys_str_mv AT akirasoga improvementofaninvitrodrugselectionmethodforgeneratingtransgenicplasmodiumbergheiparasites
AT takahiroshirozu improvementofaninvitrodrugselectionmethodforgeneratingtransgenicplasmodiumbergheiparasites
AT mamikoketsu improvementofaninvitrodrugselectionmethodforgeneratingtransgenicplasmodiumbergheiparasites
AT shinyafukumoto improvementofaninvitrodrugselectionmethodforgeneratingtransgenicplasmodiumbergheiparasites