Malarone treatment failure not associated with previously described mutations in the cytochrome b gene

被引:44
作者
Wichmann, O [1 ]
Muehlen, M
Gruss, H
Mockenhaupt, FP
Suttorp, N
Jelinek, T
机构
[1] Humboldt Univ, Inst Trop Med, Charite, Berlin, Germany
[2] Humboldt Univ, Virchow Klinikum, Charite, Berlin, Germany
关键词
D O I
10.1186/1475-2875-3-14
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Malarone(R)(atovaquone-proguanil) is an effective drug for the treatment and prophylaxis of multidrug-resistant falciparum malaria. However, first cases of resistance have been reported, which are associated with mutations at codon 268 of the parasite's cytochrome b gene. We report the first case of Malarone(R) treatment failure from Central Africa. Drug concentration was well within curative range. Pre- and post-treatment Plasmodium falciparum isolates revealed codon 268 wild-type alleles, and no other mutations of the putative atovaquone-binding domain. These findings illustrate the spread of atovaquone-proguanil-resistance in Africa and question the usefulness of codon 268 as the only target for the surveillance of its emergence.
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共 10 条
  • [1] Evidence of Plasmodium falciparum malaria resistant to atovaquone and proguanil hydrochloride:: case reports
    Färnert, A
    Lindberg, J
    Gil, P
    Swedberg, G
    Berqvist, Y
    Thapar, MM
    Lindegårdh, N
    Berezcky, S
    Björkman, A
    [J]. BMJ-BRITISH MEDICAL JOURNAL, 2003, 326 (7390): : 628 - 629
  • [2] Fivelman Quinton L, 2002, Malar J, V1, P1
  • [3] Detection of atovaquone and Malarone™ resistance conferring mutations in Plasmodium falciparum cytochrome b gene (cytb)
    Gil, JP
    Nogueira, F
    Strömberg-Nörklit, J
    Lindberg, J
    Carrolo, M
    Casimiro, C
    Lopes, D
    Arez, AP
    Cravo, PV
    Rosário, VE
    [J]. MOLECULAR AND CELLULAR PROBES, 2003, 17 (2-3) : 85 - 89
  • [4] Mutations in Plasmodium falciparum cytochrome b that are associated with atovaquone resistance are located at a putative drug-binding site
    Korsinczky, M
    Chen, NH
    Kotecka, B
    Saul, A
    Rieckmann, K
    Cheng, Q
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (08) : 2100 - 2108
  • [5] Atovaquone-proguanil versus mefloquine for malaria prophylaxis in nonimmune travelers: Results from a randomized, double-blind study
    Overbosch, D
    Schilthuis, H
    Bienzle, U
    Behrens, RH
    Kain, KC
    Clarke, PD
    Toovey, S
    Knobloch, J
    Nothdurft, HD
    Shaw, D
    Roskell, NS
    Chulay, JD
    [J]. CLINICAL INFECTIOUS DISEASES, 2001, 33 (07) : 1015 - 1021
  • [6] Genetic confirmation of atovaquone-proguanil-resistant Plasmodium falciparum malaria acquired by a nonimmune traveler to East Africa
    Schwartz, E
    Bujanover, S
    Kain, KC
    [J]. CLINICAL INFECTIOUS DISEASES, 2003, 37 (03) : 450 - 451
  • [7] Different mutation patterns of atovaquone resistance to Plasmodium falciparum in vitro and in vivo:: rapid detection of codon 268 polymorphisms in the cytochrome b as potential in vivo resistance marker -: art. no. 5
    Schwöbel, B
    Alifrangis, M
    Salanti, A
    Jelinek, T
    [J]. MALARIA JOURNAL, 2003, 2 (1)
  • [8] Atovaquone, a broad spectrum antiparasitic drug, collapses mitochondrial membrane potential in a malarial parasite
    Srivastava, IK
    Rottenberg, H
    Vaidya, AB
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (07) : 3961 - 3966
  • [9] Treatment of uncomplicated multidrug-resistant falciparum malaria with artesunate-atovaquone-proguanil
    van Vugt, M
    Leonardi, E
    Phaipun, L
    Slight, T
    Thway, KL
    McGready, R
    Brockman, A
    Villegas, L
    Looareesuwan, S
    White, NJ
    Nosten, F
    [J]. CLINICAL INFECTIOUS DISEASES, 2002, 35 (12) : 1498 - 1504
  • [10] Preventing antimalarial drug resistance through combinations
    White, NJ
    [J]. DRUG RESISTANCE UPDATES, 1998, 1 (01) : 3 - 9