Jovel Irina Tatiana, Kofoed Poul-Erik, Rombo Lars, Rodrigues Amabelia, Ursing Johan
Malaria Research, Department of Microbiology, Tumour and Cell Biology, Karolinska Institutet, Stockholm, Sweden Departamento de Parasitología, Escuela de Microbiología, Facultad de Ciencias, Universidad Nacional Autónoma de Honduras (UNAH), Tegucigalpa, Honduras
Projecto de Saúde de Bandim, Indepth Network, Bissau, Guinea-Bissau Department of Paediatrics, Kolding Hospital, Kolding, Denmark.
Antimicrob Agents Chemother. 2015 Feb;59(2):872-9. doi: 10.1128/AAC.03554-14. Epub 2014 Nov 24.
In 2008, artemether-lumefantrine was introduced in Guinea-Bissau, West Africa, but quinine has also been commonly prescribed for the treatment of uncomplicated Plasmodium falciparum malaria. An efficacious high-dose chloroquine treatment regimen was used previously. Temporal and seasonal changes of genetic polymorphisms associated with altered drug susceptibility to chloroquine, lumefantrine, and quinine have been described. P. falciparum chloroquine resistance transporter (pfcrt) K76T, pfmdr1 gene copy numbers, pfmdr1 polymorphisms N86Y and Y184F, and pfmdr1 sequences 1034 to 1246 were determined using PCR-based methods. Blood samples came from virtually all (n=1,806) children<15 years of age who had uncomplicated P. falciparum monoinfection and presented at a health center in suburban Bissau (from 2003 to 2012). The pfcrt K76T and pfmdr1 N86Y frequencies were stable, and seasonal changes were not seen from 2003 to 2007. Since 2007, the mean annual frequencies increased (P<0.001) for pfcrt 76T (24% to 57%), pfmdr1 N86 (72% to 83%), and pfcrt 76+pfmdr1 86 TN (10% to 27%), and pfcrt 76T accumulated during the high transmission season (P=0.001). The pfmdr1 86+184 NF frequency increased from 39% to 66% (from 2003 to 2011; P=0.004). One sample had two pfmdr1 gene copies. pfcrt 76T was associated with a lower parasite density (P<0.001). Following the discontinuation of an effective chloroquine regimen, probably highly artemether-lumefantrine-susceptible P. falciparum (with pfcrt 76T) accumulated, possibly due to suboptimal use of quinine and despite a fitness cost linked to pfcrt 76T. (The studies reported here were registered at ClinicalTrials.gov under registration no. NCT00137514 [PSB-2001-chl-amo], NCT00137566 [PSB-2004-paracetamol], NCT00426439 [PSB-2006-coartem], NCT01157689 [AL-eff 2010], and NCT01704508 [Eurartesim 2012].).
2008年,蒿甲醚-本芴醇被引入西非的几内亚比绍,但奎宁也一直常用于治疗非复杂性恶性疟原虫疟疾。此前曾使用过一种有效的高剂量氯喹治疗方案。已描述了与氯喹、本芴醇和奎宁药物敏感性改变相关的基因多态性的时间和季节变化。使用基于聚合酶链反应(PCR)的方法测定了恶性疟原虫氯喹抗性转运蛋白(pfcrt)K76T、pfmdr1基因拷贝数、pfmdr1多态性N86Y和Y184F以及pfmdr1序列1034至1246。血样几乎来自所有(n = 1806)15岁以下患有非复杂性恶性疟原虫单一感染并到比绍郊区的一个健康中心就诊的儿童(2003年至2012年)。pfcrt K76T和pfmdr1 N86Y频率稳定,2003年至2007年未见季节变化。自2007年以来,pfcrt 76T(从24%增至57%)、pfmdr1 N86(从72%增至83%)和pfcrt 76 + pfmdr1 86 TN(从10%增至27%)的年均频率增加(P<0.001),且pfcrt 76T在高传播季节积累(P = 0.001)。pfmdr1 86 + 184 NF频率从39%增至66%(2003年至2011年;P = 0.004)。一个样本有两个pfmdr1基因拷贝。pfcrt 76T与较低的寄生虫密度相关(P<0.001)。在停用有效的氯喹治疗方案后,可能对蒿甲醚-本芴醇高度敏感的恶性疟原虫(具有pfcrt 76T)积累,这可能是由于奎宁使用不当,尽管pfcrt 76T存在适应性代价。(此处报告的研究已在ClinicalTrials.gov注册,注册号分别为NCT00137514 [PSB - 2001 - chl - amo]、NCT00137566 [PSB - 2004 - paracetamol]、NCT00426439 [PSB - 2006 - coartem]、NCT01157689 [AL - eff 2010]和NCT01704508 [Eurartesim 2012]。)