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Published Date: 2012-05-14 09:28:53
Subject: PRO/EAFR> Malaria - East Africa: artemisinin resistance
Archive Number: 20120514.252480

MALARIA - EAST AFRICA: ARTEMISININ RESISTANCE
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Date: Sat 12 May 2012
Source: The East African [edited]
http://www.theeastafrican.co.ke/news/ACTS+resistant+malaria+comes+to+East+Africa/-/2558/1404370/-/vc71yb/-/index.html ACTs [artemisinin-based combination therapies]-resistant malaria comes to East Africa ---------------------------------------------------------------------- A strain of the malaria parasite _Plasmodium falciparum_ that is resistant to artemisinin, one of the most powerful anti-malarial drugs, has been found in East Africa. The strain tested positive in blood samples from foreigners who had travelled in Kenya and Tanzania and 9 other African countries. This particular strain had been found at the border of Thailand and Myanmar and had been predicted to be spreading to India and then Africa as resistance to other antimalarial drugs has done before. The results, according to the researchers from St George's, University of London, indicate that either the strain has spread to East Africa or the other African countries, or the local parasite has developed resistance. Although malaria control efforts have been scaled up in the region, the researchers say their findings are a further warning that the best weapons against malaria could be rendered obsolete. Sanjeev Krishna, the study lead researcher and professor at St George's, University of London, said resistance in parasite samples were taken from 11 of the 28 malaria-infected patients from East Africa and the other African countries. On average, artemether's effectiveness was reduced by half. Each parasite was found to have the same genetic mutations, said Dr Krishna. The artemisinin group of drugs is the most effective and widely used treatments for malaria. The drugs in this group are most powerful and less likely to be resisted by the malaria parasite when used with other drugs as artemisinin-based combination therapies (ACTs). The patients were infected by malaria parasite-carrying mosquitoes while travelling to East Africa and the other 9 sub-Saharan African countries, home to 90 percent of the one million people killed worldwide each year by malaria. The researchers then later tested samples from patients infected with the _Plasmodium falciparum_ parasite and the parasites were assessed for their sensitivity to 4 artemisinins: artemisinin itself, artemether, dihydroartemisinin, and artesunate. The results showed that 11 parasites showing artemether resistance had the same genetic mutations in an internal system called the calcium pump (this is used to transport calcium, crucial for the parasite to function). We already suspected that the calcium pump, which we first showed was a target for artemisinins to work on in 2003, had the potential to develop artemisinin resistance. But this had been difficult to confirm until now, said Dr Krishna. Artemether and ACTs are still very effective, but this study confirms our fears of how the parasite is mutating to develop resistance. Drug resistance could eventually become a devastating problem in Africa and not just in Southeast Asia where most of the world is watching for resistance. Dr Krishna noted that the effectiveness of the other artemisinins was not significantly affected by the mutations. This may be because they were able to work on other transport systems in the parasite, compensating for the effects of resistance mutations in the calcium pump. "At the moment, we do not know if the other artemisinins will follow suit, but given the shared chemistry they have with artemether it is tempting to think that they would, he added. The scientists argued that the resistance could be a result of the increasing use of ACTs, 300 million doses of which were dispensed worldwide in 2011. Greater use could offer the parasites more opportunities to develop genetic mutations that provide resistance. They say this could lead to a repeat of how the parasite developed resistance to pre-artemisinin drugs such as chloroquine. Incorrect use of anti-malarials, such as not completing the treatment course or taking substandard drugs, could aid this process. [Byline: Christabel Ligami] -- Communicated by: ProMED-mail from HealthMap alerts <promed@promedmail.org> [This report heralds the emergence of artemisinin resistance in East Africa and hence the need to enhance antimicrobial resistance surveillance for malaria in the region. Such efforts should be integrated into the existing malarial control efforts and programs on antimalarial use to contain the emergence of resistance in the region. HealthMap/ProMED-mail interactive maps for the East African countries can be seen at http://healthmap.org/r/1wa6 for Uganda; http://healthmap.org/r/1zkN for Kenya; http://healthmap.org/r/1KlV for Tanzania; http://healthmap.org/r/1f*m for Burundi; and http://healthmap.org/r/1jzc for Rwanda. - Mod.JFW]

See Also


Malaria - Nigeria 20120503.251439
Malaria - Angola 20120125.241242
Malaria - Ghana: (Central) 20120125.241240
2011
----
Malaria - Zimbabwe (02) 20110429.221583
Malaria - Tanzania (02): (Arusha) 20110428.221537
Malaria - Angola: (Huila) 20110427.221470
Malaria - Swaziland: (Hhohho) 20110408.220717
Malaria - Tanzania: (Mbeya) 20110305.219331
Malaria - South Africa: (Limpopo) 20110117.217254
2010
----
Malaria - France: ex Cameroon, imported infected mosquitoes 20101117.215287
Malaria - Zimbabwe (02) 20100722.209320
Malaria - Angola: (Kwanza Sul) 20100713.209154
Malaria - Ethiopia: epidemic alert 20100501.207072
Malaria - Zimbabwe: (Matabeleland North) 20100329.206436
Malaria - Kenya (02): highlands 20100307.205984
Malaria - Africa: counterfeit drugs 20100211.205424
Malaria - South Africa (04): (Mpumalanga) 20100120.205033
Malaria - Uganda: (Kabale) 20100113.204893
Malaria - South Africa (03): (Mpumalanga) 20100112.204861
Malaria - South Africa (02): (Limpopo) 20100111.204802
Malaria - Kenya: Mount Kenya, RFI 20100108.204735
Malaria - South Africa: (Limpopo) 20100101.204595]
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