TY - JOUR
T1 - Characterization of Plasmodium vivax pvmdr1 Polymorphisms in Isolates from Mangaluru, India
AU - Tacoli, Costanza
AU - Gai, Prabhanjan P.
AU - Siegert, Konrad
AU - Wedam, Jakob
AU - Kulkarni, Suyamindra S.
AU - Rasalkar, Rashmi
AU - Boloor, Archith
AU - Jain, Animesh
AU - Mahabala, Chakrapani
AU - Baliga, Shantaram
AU - Shenoy, Damodara
AU - Gai, Pramod
AU - Devi, Rajeshwari
AU - Mockenhaupt, Frank P.
PY - 2019/8/1
Y1 - 2019/8/1
N2 - India accounts for approximately half of the global Plasmodium vivax cases, but information as to the presence of chloroquine (CQ) resistance is scarce. In an observational study in Mangaluru, south-western India, of 116 vivax malaria patients analyzed, 89.5% (102/114) had cleared parasitemia on days two or three of CQ treatment. Two remaining patients presented on days four and five without parasitemia. One hundred eight isolates of these 116 patients were successfully sequenced for pvmdr1 polymorphisms. Eight non-synonymous polymorphisms but no wild-type isolate were detected. Ten pvmdr1 haplotypes were observed with mutations T958M and F1076L occurring in all isolates, whereas the candidate CQ resistance marker Y976F was present in one isolate only. Pvmdr1 polymorphisms were not associated with early parasite clearance. The high proportion of early parasite clearance and the virtual absence of pvmdr1 Y976F and of sextuple pvmdr1 mutants suggest that CQ in the study area is still sufficiently effective. However, the abundance of pvmdr1 mutations in the local parasite population warrants monitoring.
AB - India accounts for approximately half of the global Plasmodium vivax cases, but information as to the presence of chloroquine (CQ) resistance is scarce. In an observational study in Mangaluru, south-western India, of 116 vivax malaria patients analyzed, 89.5% (102/114) had cleared parasitemia on days two or three of CQ treatment. Two remaining patients presented on days four and five without parasitemia. One hundred eight isolates of these 116 patients were successfully sequenced for pvmdr1 polymorphisms. Eight non-synonymous polymorphisms but no wild-type isolate were detected. Ten pvmdr1 haplotypes were observed with mutations T958M and F1076L occurring in all isolates, whereas the candidate CQ resistance marker Y976F was present in one isolate only. Pvmdr1 polymorphisms were not associated with early parasite clearance. The high proportion of early parasite clearance and the virtual absence of pvmdr1 Y976F and of sextuple pvmdr1 mutants suggest that CQ in the study area is still sufficiently effective. However, the abundance of pvmdr1 mutations in the local parasite population warrants monitoring.
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U2 - 10.4269/ajtmh.19-0224
DO - 10.4269/ajtmh.19-0224
M3 - Article
C2 - 31218998
AN - SCOPUS:85071347379
SN - 0002-9637
VL - 101
SP - 416
EP - 417
JO - American Journal of Tropical Medicine and Hygiene
JF - American Journal of Tropical Medicine and Hygiene
IS - 2
ER -