Skip to main content
. 2009 Oct 30;5(10):e1000644. doi: 10.1371/journal.ppat.1000644

Table 1. P. falciparum Strains and Experimental Design Used in This Study.

Purpose Strain & sub-line Description Method of cDNA/gDNA preparation No. of cycles in culture No. of replicate hybridizations
Testing amplification method
a3D7 Laboratory Unamplified Many 2
Transcriptome analysis
3D7 Laboratory Amplified Many 2
bDd2 Laboratory Amplified Many 1
cT9/96 Laboratory Amplified Many 1
dP1 Field, severe Amplified 62 3
dP3 Field, severe Amplified 63 3
dP4 Field, mild Amplified 48 3
dP5 Field, mild Amplified 66 2
dP6 Field, mild Amplified 59 3
Gene copy number analysis
dP1.A As above Unamplified e+21 3
dP3.A Unamplified +24 3
dP4.A Unamplified +31 3
dP5.A Unamplified +21 3
dP6.A Unamplified +23 3
dP1.B Unamplified +8 1
dP4.B Unamplified +14 1
dP6.B Unamplified +8 1
a

Derived from a patient in the Netherlands living near the airport [131]. Believed to be of African origin.

b

Obtained by cloning of strain W2-mef, a clone of Indochina III/CDC that had been under long-term mefloquine pressure [132].

c

Obtained from Thailand [133],[134].

d

Obtained from Kilifi, Kenya, from patients admitted to the hospital with severe or mild malaria.

e

The “+” indicates the number of cycles of culture in addition to those in the top part of the table.