Intrahost selection of Plasmodium falciparum pfmdr1 alleles after antimalarial treatment on the northwestern border of Thailand.
BACKGROUND: Increased pfmdr1 copy number is associated with reduced susceptibility to structurally unrelated antimalarial drugs. We assessed how administration of different antimalarial drugs altered pfmdr1 polymorphism in parasites from patients who experienced treatment failure. METHODS: In studi...
| Main Authors: | , , , , , , , , |
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| Format: | Journal article |
| Language: | English |
| Published: |
2007
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| _version_ | 1797099645743136768 |
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| author | Uhlemann, A Mcgready, R Ashley, E Brockman, A Singhasivanon, P Krishna, S White, N Nosten, F Price, R |
| author_facet | Uhlemann, A Mcgready, R Ashley, E Brockman, A Singhasivanon, P Krishna, S White, N Nosten, F Price, R |
| author_sort | Uhlemann, A |
| collection | OXFORD |
| description | BACKGROUND: Increased pfmdr1 copy number is associated with reduced susceptibility to structurally unrelated antimalarial drugs. We assessed how administration of different antimalarial drugs altered pfmdr1 polymorphism in parasites from patients who experienced treatment failure. METHODS: In studies conducted on the northwestern border of Thailand, amplifications and single-nucleotide polymorphisms in pfmdr1 were compared before and after antimalarial drug treatment. RESULTS: Intrahost changes in pfmdr1 copy number were observed in 20% (26/132) of patients with recurrent infections. Among infections that recrudesced after mefloquine-containing regimens, increases in pfmdr1 copy number occurred in 68% (95% confidence interval [CI], 46%-85%), and decreases occurred in 2% (95% CI, 0.4%-11%) of isolates; corresponding proportions after artemether-lumefantrine were 25% (2/8) and 11% (2/19); after quinine, 50% (1/2) and 40% (4/10); and after artemisinins alone, 0% (0/10) and 19% (3/16) of isolates (overall P<.001). CONCLUSIONS: Intrahost selection based on pfmdr1 copy number occurs frequently in parasite populations within individual patients. Amplification confers multidrug resistance but probably imposes a significant fitness cost to the parasites. |
| first_indexed | 2024-03-07T05:26:39Z |
| format | Journal article |
| id | oxford-uuid:e0cb7131-7be8-4b3b-8e79-255b28ad15c3 |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-07T05:26:39Z |
| publishDate | 2007 |
| record_format | dspace |
| spelling | oxford-uuid:e0cb7131-7be8-4b3b-8e79-255b28ad15c32022-03-27T09:49:59ZIntrahost selection of Plasmodium falciparum pfmdr1 alleles after antimalarial treatment on the northwestern border of Thailand.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:e0cb7131-7be8-4b3b-8e79-255b28ad15c3EnglishSymplectic Elements at Oxford2007Uhlemann, AMcgready, RAshley, EBrockman, ASinghasivanon, PKrishna, SWhite, NNosten, FPrice, R BACKGROUND: Increased pfmdr1 copy number is associated with reduced susceptibility to structurally unrelated antimalarial drugs. We assessed how administration of different antimalarial drugs altered pfmdr1 polymorphism in parasites from patients who experienced treatment failure. METHODS: In studies conducted on the northwestern border of Thailand, amplifications and single-nucleotide polymorphisms in pfmdr1 were compared before and after antimalarial drug treatment. RESULTS: Intrahost changes in pfmdr1 copy number were observed in 20% (26/132) of patients with recurrent infections. Among infections that recrudesced after mefloquine-containing regimens, increases in pfmdr1 copy number occurred in 68% (95% confidence interval [CI], 46%-85%), and decreases occurred in 2% (95% CI, 0.4%-11%) of isolates; corresponding proportions after artemether-lumefantrine were 25% (2/8) and 11% (2/19); after quinine, 50% (1/2) and 40% (4/10); and after artemisinins alone, 0% (0/10) and 19% (3/16) of isolates (overall P<.001). CONCLUSIONS: Intrahost selection based on pfmdr1 copy number occurs frequently in parasite populations within individual patients. Amplification confers multidrug resistance but probably imposes a significant fitness cost to the parasites. |
| spellingShingle | Uhlemann, A Mcgready, R Ashley, E Brockman, A Singhasivanon, P Krishna, S White, N Nosten, F Price, R Intrahost selection of Plasmodium falciparum pfmdr1 alleles after antimalarial treatment on the northwestern border of Thailand. |
| title | Intrahost selection of Plasmodium falciparum pfmdr1 alleles after antimalarial treatment on the northwestern border of Thailand. |
| title_full | Intrahost selection of Plasmodium falciparum pfmdr1 alleles after antimalarial treatment on the northwestern border of Thailand. |
| title_fullStr | Intrahost selection of Plasmodium falciparum pfmdr1 alleles after antimalarial treatment on the northwestern border of Thailand. |
| title_full_unstemmed | Intrahost selection of Plasmodium falciparum pfmdr1 alleles after antimalarial treatment on the northwestern border of Thailand. |
| title_short | Intrahost selection of Plasmodium falciparum pfmdr1 alleles after antimalarial treatment on the northwestern border of Thailand. |
| title_sort | intrahost selection of plasmodium falciparum pfmdr1 alleles after antimalarial treatment on the northwestern border of thailand |
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