ABSTRACT
The selected Plasmodium falciparum isolates amplicons were sequenced to obtain the nucleotide
sequence alignment profile. The result from the sequence alignment was further blasted to determine
the phylogenic ancestry of the resistant genes. Nucleotide alignment of Plasmodium falciparum
multidrug resistant (PFMDR) genes and Plasmodium falciparum chloroquine resistant (PFCRT)
transporter from volunteered malaria patients isolates, obtained from general hospital Kachia and
general hospital Kafanchan Kaduna State were sequenced and blasted using BLAST N program. The
nucleotide sequences showed relatedness to imported isolates from Africa in Henan Province (Yang et
al., 2018). The phylogenetic studies showed relatedness to resistant Plasmodium falciparum gene from
Tripura. The FAST A profile of the nucleotide sequence of the different resistant genes and their
accession number from the gene bank were well documented. The observed Plasmodium falciparum
Chloroquine resistant transporter (PFCRT) (186 — 800bp) and Plasmodium falciparum Multidrug
resistant gene I (PFMDR1) (300 — 1200 bp) amplification for Artemether was identified as the genes
involved in resistance. The sequence arrangement of Plasmodium falciparum Chloroquine resistant
gene PFCRT 184 gene (500bp) from Kachia with Gene bank sequence ID MH266479.1 had 100%
percent relatedness when compared to PFCRT (500bp) from Kafanchan with sequence ID MH266479.
The Phylogenic tree with sequence ID 1274671 spans ten (10) generation. It was concluded that the
similarity in the percentage of sequence alignment between the genes isolated from Kachia isolates and
Kafanchan isolates indicated that human movement was responsible for the similar genes found in
both towns. The search for drug combinations should be intensified and the use of molecular method
to monitor antimalarial drug resistance in Kaduna State should be encouraged