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dc.contributor.authorRitchie, Ryan
dc.contributor.authorBarrett, Michael
dc.contributor.authorMottram, Jeremy
dc.contributor.authorMyburgh, Elmarie
dc.date.accessioned2021-04-14T09:24:09Z
dc.date.available2021-04-14T09:24:09Z
dc.date.issued2020
dc.identifier.urihttps://library.oapen.org/handle/20.500.12657/47835
dc.description.abstractTraditional animal models for human African trypanosomiasis rely on detecting Trypanosoma brucei brucei parasitemia in the blood. Testing the efficacy of new compounds in these models is cumbersome because it may take several months after treatment before surviving parasites become detectable in the blood. To expedite compound screening, we have used a Trypanosoma brucei brucei GVR35 strain expressing red-shifted firefly luciferase to monitor parasite distribution in infected mice through noninvasive wholebody bioluminescence imaging. This protocol describes the infection and in vivo bioluminescence imaging of mice to assess compound efficacy against T. brucei during the two characteristic stages of disease, the hemolymphatic phase (stage 1) and the encephalitic or central nervous system phase (stage 2).en_US
dc.languageEnglishen_US
dc.subject.classificationthema EDItEUR::P Mathematics and Science::PS Biology, life sciencesen_US
dc.subject.otherFirefly luciferase, Trypanosoma brucei brucei, In vivo imaging, Bioluminescenceen_US
dc.titleChapter 48 In Vivo Bioluminescence Imaging to Assess Compound Efficacy Against Trypanosoma bruceien_US
dc.typechapter
oapen.identifier.doi10.1007/978-1-0716-0294-2_48en_US
oapen.relation.isPublishedBy6c6992af-b843-4f46-859c-f6e9998e40d5en_US
oapen.relation.isPartOfBook51e921c5-535d-483f-99fb-69b0c7d85e58en_US
oapen.relation.isFundedByd859fbd3-d884-4090-a0ec-baf821c9abfden_US
oapen.relation.isbn9781071602935en_US
oapen.relation.isbn9781071602966en_US
oapen.collectionWellcomeen_US
oapen.pages17en_US
oapen.grant.number104976,104111
oapen.grant.number104976,104111


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