Cargando…

Profiles of Kelch mutations in Plasmodium falciparum across South Asia and their implications for tracking drug resistance

Artemisinin-based combination therapy (ACT) offers highly successful treatment of malaria. Emergence and spread of Plasmodium falciparum (Pf) parasites with decreased susceptibility to ACT in South-East Asia has caused concern worldwide. The current accepted criteria to assess artemisinin (ART) resi...

Descripción completa

Detalles Bibliográficos
Autores principales: Chhibber-Goel, Jyoti, Sharma, Amit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6796718/
https://www.ncbi.nlm.nih.gov/pubmed/31606696
http://dx.doi.org/10.1016/j.ijpddr.2019.10.001
_version_ 1783459671655317504
author Chhibber-Goel, Jyoti
Sharma, Amit
author_facet Chhibber-Goel, Jyoti
Sharma, Amit
author_sort Chhibber-Goel, Jyoti
collection PubMed
description Artemisinin-based combination therapy (ACT) offers highly successful treatment of malaria. Emergence and spread of Plasmodium falciparum (Pf) parasites with decreased susceptibility to ACT in South-East Asia has caused concern worldwide. The current accepted criteria to assess artemisinin (ART) resistance relies upon data on treatment failure, delayed parasite clearance at day 3 (DPC3), parasite clearance half-life (PCHL) and in-vitro/ex-vivo ring stage survival assays (RSAs). Interestingly, some studies suggest that DPC3 does not provide a distinct separation between ART sensitive/resistant strains, and RSA differences may also be inconclusive. More recently, recrudescence of ART treated Pf, independent of the presence of Kelch 13 (K13) mutation (C580Y), has been reported in the monkey malaria model suggesting that genes other than K13 like coronin, dhps, dhfr, crt, mdr1 and plasmepsin1 may contribute towards ACT failure. Here we have collated the distribution of K13 mutants from Pf strains in South Asia. A total of fifty Pf-K13 mutations have been studied for ART resistance in South Asia of which nine have been validated while eleven are potentials for ART resistance. The remaining thirty K13 mutations have been reported from various locations in South Asia but lack corroborative clinical data on ART resistance/ACT failure. Of the fifty, fourteen K13 mutations have been identified in India including four novel mutations (S549Y, G625R, N657H, D702N). Structural mapping of these K13 mutations does not offer any coherent explanation for their contribution towards ART resistance as they are scattered in the K13 structure. Thus, K13 mutations likely provide only a partial synopsis, and we propose that all suspect cases of ACT failure be assessed by: 1) DPC3, 2) PCHL, 3) in-vitro/ex-vivo RSAs and 4) GWAS data in an effort to annotate the resistance status of the parasites. These efforts may help in surveillance and containment of ART resistance/ACT failure in South Asia.
format Online
Article
Text
id pubmed-6796718
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-67967182019-10-22 Profiles of Kelch mutations in Plasmodium falciparum across South Asia and their implications for tracking drug resistance Chhibber-Goel, Jyoti Sharma, Amit Int J Parasitol Drugs Drug Resist Regular Article Artemisinin-based combination therapy (ACT) offers highly successful treatment of malaria. Emergence and spread of Plasmodium falciparum (Pf) parasites with decreased susceptibility to ACT in South-East Asia has caused concern worldwide. The current accepted criteria to assess artemisinin (ART) resistance relies upon data on treatment failure, delayed parasite clearance at day 3 (DPC3), parasite clearance half-life (PCHL) and in-vitro/ex-vivo ring stage survival assays (RSAs). Interestingly, some studies suggest that DPC3 does not provide a distinct separation between ART sensitive/resistant strains, and RSA differences may also be inconclusive. More recently, recrudescence of ART treated Pf, independent of the presence of Kelch 13 (K13) mutation (C580Y), has been reported in the monkey malaria model suggesting that genes other than K13 like coronin, dhps, dhfr, crt, mdr1 and plasmepsin1 may contribute towards ACT failure. Here we have collated the distribution of K13 mutants from Pf strains in South Asia. A total of fifty Pf-K13 mutations have been studied for ART resistance in South Asia of which nine have been validated while eleven are potentials for ART resistance. The remaining thirty K13 mutations have been reported from various locations in South Asia but lack corroborative clinical data on ART resistance/ACT failure. Of the fifty, fourteen K13 mutations have been identified in India including four novel mutations (S549Y, G625R, N657H, D702N). Structural mapping of these K13 mutations does not offer any coherent explanation for their contribution towards ART resistance as they are scattered in the K13 structure. Thus, K13 mutations likely provide only a partial synopsis, and we propose that all suspect cases of ACT failure be assessed by: 1) DPC3, 2) PCHL, 3) in-vitro/ex-vivo RSAs and 4) GWAS data in an effort to annotate the resistance status of the parasites. These efforts may help in surveillance and containment of ART resistance/ACT failure in South Asia. Elsevier 2019-10-04 /pmc/articles/PMC6796718/ /pubmed/31606696 http://dx.doi.org/10.1016/j.ijpddr.2019.10.001 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Regular Article
Chhibber-Goel, Jyoti
Sharma, Amit
Profiles of Kelch mutations in Plasmodium falciparum across South Asia and their implications for tracking drug resistance
title Profiles of Kelch mutations in Plasmodium falciparum across South Asia and their implications for tracking drug resistance
title_full Profiles of Kelch mutations in Plasmodium falciparum across South Asia and their implications for tracking drug resistance
title_fullStr Profiles of Kelch mutations in Plasmodium falciparum across South Asia and their implications for tracking drug resistance
title_full_unstemmed Profiles of Kelch mutations in Plasmodium falciparum across South Asia and their implications for tracking drug resistance
title_short Profiles of Kelch mutations in Plasmodium falciparum across South Asia and their implications for tracking drug resistance
title_sort profiles of kelch mutations in plasmodium falciparum across south asia and their implications for tracking drug resistance
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6796718/
https://www.ncbi.nlm.nih.gov/pubmed/31606696
http://dx.doi.org/10.1016/j.ijpddr.2019.10.001
work_keys_str_mv AT chhibbergoeljyoti profilesofkelchmutationsinplasmodiumfalciparumacrosssouthasiaandtheirimplicationsfortrackingdrugresistance
AT sharmaamit profilesofkelchmutationsinplasmodiumfalciparumacrosssouthasiaandtheirimplicationsfortrackingdrugresistance