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首页> 外文期刊>Infection, Genetics and Evolution: Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases >Regular treatments of praziquantel do not impact on the genetic make-up of Schistosoma mansoni in Northern Senegal
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Regular treatments of praziquantel do not impact on the genetic make-up of Schistosoma mansoni in Northern Senegal

机译:常规治疗吡喹酮对塞内加尔北部曼氏血吸虫的基因组成没有影响

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The Senegal River Basin (SRB) experienced a major epidemic of intestinal schistosomiasis in the early nineties, after the construction of a dam for irrigation purposes. Exceptionally low cure rates following praziquantel (PZQ) treatment at the onset of the epidemic raised concerns about PZQ resistant strains of Schistosoma mansoni, although they could also be attributed to the intense transmission at that time. A field study in the same region more than 15 years later found cure rates for S. mansoni still to be low, whereas Schistosomahaematobium responded well to treatment. We collected S. mansoni miracidia from children at base-line prior to treatment, six months after two PZQ treatments and two years after the start of the study when they had received a total of five PZQ treatments. In total, 434 miracidia from 12 children were successfully genotyped with at least six out of nine DNA microsatellite loci. We found no significant differences in the genetic diversity of, and genetic differentiation between parasite populations before and after repeated treatment, suggesting that PZQ treatment does not have an impact on the neutral evolution of the parasite. This is in stark contrast with a similar study in Tanzania where a significant decrease in genetic diversity was observed in S. mansoni miracidia after a single round of PZQ treatment We argue that PZQ resistance might play a role in our study area, although rapid re-infection cannot be excluded. It is important to monitor this situation carefully and conduct larger field studies with short-term follow-up after treatment. Since PZQ is the only general schistosomicide available, the possibility of PZQ resistance is of great concern both for disease control and for curative use in clinical practice
机译:塞内加尔河流域(SRB)在修建用于灌溉目的的水坝后,于90年代初经历了肠道血吸虫病的主要流行。吡喹酮(PZQ)流行后的极低治愈率引发了人们对曼氏血吸虫的PZQ耐药菌株的担忧,尽管它们也可以归因于当时的强烈传播。超过15年后在同一地区进行的现场研究发现,曼氏链球菌的治愈率仍然较低,而血吸虫血吸虫病对治疗的反应良好。我们在治疗前,两次PZQ治疗后六个月和研究开始后两年(共接受五次PZQ治疗)时,从基线儿童中收集了曼氏葡萄球菌性痴呆症。总共,成功地对来自12个儿童的434个酸血症与9个DNA微卫星基因座中的至少6个进行了基因分型。我们发现重复处理前后,寄生虫种群的遗传多样性和遗传分化之间无显着差异,这表明PZQ处理对寄生虫的中性进化没有影响。这与坦桑尼亚的一项类似研究形成鲜明对比,在坦桑尼亚进行的一轮PZQ治疗后,曼氏沙门氏菌的遗传多样性显着下降。我们认为,PZQ耐药性可能在我们的研究区域中起作用,尽管快速重新不能排除感染。重要的是要仔细监测这种情况,并在治疗后进行短期随访,以进行更大范围的田间研究。由于PZQ是唯一可用的常规血吸虫药,因此PZQ耐药性的可能性在疾病控制和临床实践中均备受关注

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