SwePub
Sök i LIBRIS databas

  Extended search

onr:"swepub:oai:DiVA.org:uu-169794"
 

Search: onr:"swepub:oai:DiVA.org:uu-169794" > Detecting adenosine...

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Detecting adenosine triphosphatase 6 point mutations that may be associated with Plasmodium falciparum resistance to artemisinin : prevalence at baseline, before policy change in Uganda

Kamugisha, Erasmus (author)
Sendagire, Hakim (author)
KadduMukasa, Mark (author)
show more...
Enweji, Nizar (author)
Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi
Gheysari, Fatheme (author)
Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi
Swedberg, Göte (author)
Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi
Kironde, Fred (author)
show less...
 (creator_code:org_t)
2011
2011
English.
In: Tanzania Journal of Health Research. - 1821-6404. ; 13:1, s. 50-60
  • Journal article (peer-reviewed)
Abstract Subject headings
Close  
  • The artemisinin based combination therapy (ACT) of artemether and lumefantrine (Co-artem) has recently replaced chloroquine and fansidar as the first line treatment policy drug in Uganda. It is necessary to develop practical procedures to monitor the likely emergence and spread of artemisinin resistant P. falciparum strains. We have analyzed the genotypes of PfATP6 in parasites from 300 stored filter paper samples from malaria patients who were diagnosed and treated in the years 1999 to 2004 at three field sites in Uganda. This is a period just prior to introduction of Co-artem. In order to develop a simple molecular procedure for mutation detection, regions of PfATP6 encoding protein domains important in artemisinin binding was amplified by nested PCR. Three DNA products, which together contain most of the coding region of amino acids located within the putative active site of pfATP6 were readily amplified. The amplified DNA was digested by restriction enzymes and the fragments sized by agarose gel electrophoresis. For the important codons 260, 263 and 769, methods using engineered restriction sites were employed. We did not find mutations at codons for the key residues Lys 260, Leu263, Gln266, Ser769 and Asn1039. Nucleotide sequencing of pfATPase6 gene DNA from at least 15 clinical isolates confirmed the above findings and suggested that mutations at these amino acid residues have not emerged in our study sites.

Keyword

PfATP5
artemisinin
resistance
SERCA
Plasmodium falciparum
Uganda

Publication and Content Type

ref (subject category)
art (subject category)

Find in a library

To the university's database

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Search outside SwePub

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view