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Updated: May 26, 2026

Development of a Negative Selectable Marker for Entamoeba histolytica
Published on: December 12, 2010
An antibiotic selection marker for schistosome transgenesis
Gabriel Rinaldi1, Sutas Suttiprapa, José F Tort
1Department of Microbiology, Immunology and Tropical Medicine, School of Medicine & Health Sciences, The George Washington University, 2300 I Street NW, Washington, DC 20037, USA.
Researchers developed a new method for creating transgenic schistosomes using drug selection. This technique enriches for genetically modified worms, advancing research on parasitic helminths.
Area of Science:
- Parasitology
- Molecular Biology
- Genetics
Background:
- Drug selection is crucial for transgene studies in various organisms.
- Enriching transgenic schistosomes is vital for advancing helminth research.
- Current methods lack efficient drug selection for schistosomes.
Purpose of the Study:
- To establish a drug selection method for creating transgenic schistosomes.
- To adapt retroviral vectors for schistosome gene transfer.
- To demonstrate the enrichment of transgenic schistosomes using G418 selection.
Main Methods:
- Adapted murine leukemia retrovirus vectors for schistosome transduction.
- Determined G418 (geneticin) dose-response and lethal concentrations.
- Cultured transduced schistosomes in G418-containing media to assess neomycin resistance (neoR) transgene efficacy.
Main Results:
- Established lethal G418 concentrations for Schistosoma mansoni schistosomules.
- Demonstrated that the neoR transgene rescues transgenic schistosomes from G418 toxicity.
- Showed dose-dependent enrichment and increased neoR expression in transgenic schistosomes cultured with G418.
Conclusions:
- Successfully adapted retroviral vectors for schistosome transduction.
- Established G418 as an effective drug selection agent for transgenic schistosomes.
- This method will accelerate functional genomics research on neglected tropical disease-causing helminths.
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Antibiotic Selection
Transduction