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Intra-host dynamics of co-infecting parasite genotypes in asymptomatic malaria patients

机译:无症状疟疾患者中共感染寄生虫基因型的宿主内动态

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摘要

Malaria-infected individuals often harbor mixtures of genetically distinct parasite genotypes. We studied intra-host dynamics of parasite genotypes co-infecting asymptomatic adults in an area of intense malaria transmission in Chikhwawa, Malawi. Serial blood samples (5 ml) were collected over seven consecutive days from 25 adults with asymptomatic Plasmodium falciparum malaria and analyzed to determine whether a single peripheral blood sample accurately captures within-host parasite diversity. Blood samples from three of the participants were also analyzed by limiting dilution cloning and SNP genotyping of the parasite clones isolated to examine both the number and relatedness of co-infecting parasite haplotypes. We observed rapid turnover of co-infecting parasite genotypes in 88% of the individuals sampled (n = 22) such that the genetic composition of parasites infecting these individuals changed dramatically over the course of seven days of follow up. Nineteen of the 25 individuals sampled (76%) carried multiple parasite genotypes at baseline. Analysis of serial blood samples from three of the individuals revealed that they harbored 6, 12 and 17 distinct parasite haplotypes respectively. Approximately 70% of parasite haplotypes recovered from the three extensively sampled individuals were unrelated (proportion of shared alleles <83.3%) and were deemed to have primarily arisen from superinfection (inoculation of unrelated parasite haplotypes through multiple mosquito bites). The rest were related at the half-sib level or greater and were deemed to have been inoculated into individual human hosts via parasite co-transmission from single mosquito bites. These findings add further to the growing weight of evidence indicating that a single blood sample poorly captures within-host parasite diversity and underscore the importance of repeated blood sampling to accurately capture within-host parasite ecology. Our data also demonstrate a more pronounced role for parasite co-transmission in generating within-host parasite diversity in high transmission settings than previously assumed. Taken together, these findings have important implications for understanding the evolution of drug resistance, malaria transmission, parasite virulence, allocation of gametocyte sex ratios and acquisition of malaria immunity.
机译:疟疾感染者经常携带遗传上不同的寄生虫基因型的混合物。我们研究了在马拉维奇克瓦瓦严重疟疾传播地区共同感染无症状成年人的寄生虫基因型的寄主内动力学。从连续25天连续7天收集了25例无症状恶性疟原虫疟疾的连续血样,并进行分析以确定单个外周血样是否能准确捕获宿主体内的寄生虫多样性。还通过限制稀释度克隆和分离出的寄生虫克隆的SNP基因分型来分析来自三名参与者的血样,以检查共感染寄生虫单倍型的数量和相关性。我们观察到88%的个体中共感染寄生虫基因型的快速转换(n = 22),因此在随访的7天中,感染这些个体的寄生虫的遗传组成发生了巨大变化。在25位样本中,有19位(76%)在基线时携带多种寄生虫基因型。对来自三个个体的连续血样的分析显示,它们分别具有6、12和17个不同的寄生虫单倍型。从三个广泛采样的个体中回收的大约70%的寄生虫单倍型是无关的(共有等位基因的比例<83.3%),并被认为主要来自于超级感染(通过多次蚊子叮咬接种无关的寄生虫单倍型)。其余的与半同胞水平或更高相关,并被认为是通过单蚊叮咬的寄生虫共传播而被接种到单个人宿主中的。这些发现进一步增加了越来越多的证据,这些证据表明单个血液样本不能很好地捕获宿主内寄生虫的多样性,并强调了重复采血对准确捕获宿主内寄生虫生态的重要性。我们的数据还证明,在高传播环境下,寄生共生在产生寄主内寄生多样性方面比以前假设的更为明显。综上所述,这些发现对理解耐药性,疟疾传播,寄生虫毒力,配子细胞性别比的分配以及获得疟疾免疫力具有重要意义。

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