Abstract:
:The rodent malaria parasite Plasmodium chabaudi chabaudi shares many features with human malaria species, including P. falciparum, and is the in vivo model of choice for many aspects of malaria research in the mammalian host, from sequestration of parasitized erythrocytes, to antigenic variation and host immunity and immunopathology. This protocol describes an optimized method for the transformation of mature blood-stage P.c. chabaudi and a description of a vector that targets efficient, single crossover integration into the P.c. chabaudi genome. Transformed lines are reproducibly generated and selected within 14-20 d, and show stable long-term protein expression even in the absence of drug selection. This protocol, therefore, provides the scientific community with a robust and reproducible method to generate transformed P.c. chabaudi parasites expressing fluorescent, bioluminescent and model antigens that can be used in vivo to dissect many of the fundamental principles of malaria infection.
journal_name
Nat Protocjournal_title
Nature protocolsauthors
Spence PJ,Cunningham D,Jarra W,Lawton J,Langhorne J,Thompson Jdoi
10.1038/nprot.2011.313subject
Has Abstractpub_date
2011-04-01 00:00:00pages
553-561issue
4eissn
1754-2189issn
1750-2799journal_volume
6pub_type
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