Literature DB >> 27573632

Artemisinin Resistance-Associated K13 Polymorphisms of Plasmodium falciparum in Southern Rwanda, 2010-2015.

Costanza Tacoli1, Prabhanjan P Gai1, Claude Bayingana2,3, Kevin Sifft1, Dominik Geus1, Jules Ndoli2,3, Augustin Sendegeya2,3, Jean Bosco Gahutu2,3, Frank P Mockenhaupt4.   

Abstract

Emerging artemisinin resistance is a threat to global malaria control. Mutations in the Plasmodium falciparum Kelch 13 (K13) propeller domain confer artemisinin resistance and constitute molecular markers for its detection and monitoring. We sequenced 222 P. falciparum isolates obtained from community children in the Huye District of southern Rwanda in 2010, 2014, and 2015 to investigate the presence of K13 polymorphisms. No polymorphisms were observed in 2010 but they were present in 2.5% and 4.5% in 2014 and 2015, respectively. In 2015, two isolates showed candidate K13 resistance mutations (P574L and A675V), which are common in southeast Asia and associated with delayed parasite clearance. K13 polymorphisms in southern Rwanda are infrequent but include variants associated with artemisinin resistance. Establishing correlations with local treatment response and in vitro resistance assays are needed in addition to further monitoring K13 polymorphisms in the study area. © The American Society of Tropical Medicine and Hygiene.

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Year:  2016        PMID: 27573632      PMCID: PMC5094222          DOI: 10.4269/ajtmh.16-0483

Source DB:  PubMed          Journal:  Am J Trop Med Hyg        ISSN: 0002-9637            Impact factor:   2.345


  17 in total

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Journal:  N Engl J Med       Date:  2016-06-23       Impact factor: 91.245

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Journal:  N Engl J Med       Date:  2014-07-31       Impact factor: 91.245

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Authors:  Jean-Bosco Gahutu; Christian Steininger; Cyprien Shyirambere; Irene Zeile; Neniling Cwinya-Ay; Ina Danquah; Christoph H Larsen; Teunis A Eggelte; Aline Uwimana; Corine Karema; Andre Musemakweri; Gundel Harms; Frank P Mockenhaupt
Journal:  Malar J       Date:  2011-05-18       Impact factor: 2.979

10.  Slow Clearance of Plasmodium falciparum in Severe Pediatric Malaria, Uganda, 2011-2013.

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Journal:  Emerg Infect Dis       Date:  2015-07       Impact factor: 6.883

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  31 in total

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2.  Polymorphisms in Plasmodium falciparum Kelch 13 and P. vivax Kelch 12 Genes in Parasites Collected from Three South Pacific Countries Prior to Extensive Exposure to Artemisinin Combination Therapies.

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3.  The Diversity of the Plasmodium falciparum K13 Propeller Domain Did Not Increase after Implementation of Artemisinin-Based Combination Therapy in Uganda.

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5.  Using an antimalarial in mosquitoes overcomes Anopheles and Plasmodium resistance to malaria control strategies.

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6.  Emergence and Spread of kelch13 Mutations Associated with Artemisinin Resistance in Plasmodium falciparum Parasites in 12 Thai Provinces from 2007 to 2016.

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7.  Artemisinin combination therapy fails even in the absence of Plasmodium falciparum kelch13 gene polymorphism in Central India.

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Review 8.  Artemisinin resistance: an important emerging clinical problem in tropical medicine.

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Authors:  Kevin C Sifft; Dominik Geus; Caritas Mukampunga; Jean Claude Mugisha; Felix Habarugira; Kira Fraundorfer; Claude Bayingana; Jules Ndoli; Irenee Umulisa; Corine Karema; George von Samson-Himmelstjerna; Toni Aebischer; Peter Martus; Augustin Sendegeya; Jean Bosco Gahutu; Frank P Mockenhaupt
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10.  Changing Prevalence of Potential Mediators of Aminoquinoline, Antifolate, and Artemisinin Resistance Across Uganda.

Authors:  Victor Asua; Melissa D Conrad; Ozkan Aydemir; Marvin Duvalsaint; Jennifer Legac; Elias Duarte; Patrick Tumwebaze; Deborah M Chin; Roland A Cooper; Adoke Yeka; Moses R Kamya; Grant Dorsey; Sam L Nsobya; Jeffrey Bailey; Philip J Rosenthal
Journal:  J Infect Dis       Date:  2021-03-29       Impact factor: 7.759

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