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. 2018 Sep 10;99(5):1128–1133. doi: 10.4269/ajtmh.18-0277

Table 1.

Summary of the Plasmodium vivax potential and confirmed cases identified in the Democratic Republic of the Congo during the 2013 DHS

Sample name Cluster Pfldh Microscopy RDT P. vivax–nested 18s rRNA PCR P. vivax by RT-PCR P. vivax by Sanger sequencing Duffy −33 T:C mutation
B5A7N 69 N N N P P P P
J6V8T 69 P P N P P P P
M2B5U* 69 P N P P P P P
T6B8J 69 P P P P P P P
Z6W9M 69 P N P P P P P
X3M5S* 144 P N N P N P P
Q8J6O 144 N N N P P P P
D9U3K 144 N N N P P P P
G0R3B 238 P P P P N N P
U1P9U* 238 P P P P P N P
O6Y4X 238 N N N P P P P
P8A6E* 298 P N P P N P P
I4G3V 298 P N P P P P P
N4M7L 298 N N P P P P P

DHS = Demographic Health Survey; pfldh = P. falciparum lactate dehydrogenase; RDT = rapid diagnostic test; * = index cases; P = positive; N = negative. The columns above provide information on the DHS cluster the case was identified in, whether the case was coinfected with Plasmodium falciparum as identified with real-time PCR for the pfldh gene, and whether the patient was considered positive for malaria by microscopy and RDT. In addition, each isolate has results for nested 18s rRNA P. vivax PCR, P. vivax real-time PCR, and P. vivax Sanger sequencing. Finally, the host genotype was sequenced for the −33 T:C mutation that predicts the Duffy-negative phenotype.3