Gonçalo Moniz Research Centre, Oswaldo Cruz Foundation, Rua Waldemar Falcão, 121 Brotas, Salvador, Bahia 40296-710, Brazil; Bahiana School of Medicine and Public Health, Av. Silveira Martins, n° 3386, Salvador, Bahia 41150-100, Brazil.
Bahiana School of Medicine and Public Health, Av. Silveira Martins, n° 3386, Salvador, Bahia 41150-100, Brazil.
Int J Parasitol. 2018 Dec;48(14):1149-1154. doi: 10.1016/j.ijpara.2018.10.001. Epub 2018 Oct 24.
Eradication or local extinction of the human parasite Schistosoma mansoni is a goal for many control programs. Population genetic analyses are helping to evaluate and guide these efforts, yet what to sample, how to sample and how densely to sample is not well established. We determined the S. mansoni allele frequency profile of nearly all infected inhabitants in two small Brazilian communities and created sub-samples representing 5-50% of all detected human infections (infrapopulations). Samples were selected at random with replacement, and each size class was replicated 100 times. Mean pairwise differentiation for all infrapopulations (Di) and the variance effective population size (Ne) were calculated for each sample. Prior to community-wide treatment, the true mean Di was moderate (0.095-0.123) and Ne large (>30,000). Most samples of <50% of those infected produced estimates outside of 5% of the true value. For estimates within 10%, sample sizes of >15% of all infrapopulations were required. At the 3 year follow-up after treatment, the Di increased and Ne was reduced by >15 fold. At this time sampling of >30-45% was needed to achieve the same accuracy. Following a second treatment and 4 years from baseline, the Di further increased and Ne decreased with little change in the sampling effort required. Extensive sampling is required for accurate estimates of these important population parameters. Characteristics such as population census size, infection prevalence, the community's treatment history and the degree of infrapopulation differentiation should be taken into account. The intensity of infection was weakly correlated with the ability of a single infrapopulation to represent the component population (Dic), indicating a tendency toward random acquisition of parasite genotypes. This also suggests that targeted sampling from those most heavily infected will better represent the genetic diversity of the whole community than a random sample of infrapopulations.
消除或局部灭绝人体寄生虫曼氏血吸虫是许多控制计划的目标。种群遗传分析有助于评估和指导这些努力,但采样什么、如何采样以及如何密集采样尚未得到很好的确定。我们确定了两个巴西小社区中几乎所有受感染居民的曼氏血吸虫等位基因频率谱,并创建了代表所有检测到的人类感染(亚种群)的 5-50%的亚样本。样本以有放回的方式随机选择,每个大小类别的样本重复 100 次。计算了所有亚种群的平均配对分化(Di)和有效种群大小(Ne)。在社区范围内进行治疗之前,真实的平均 Di 值适中(0.095-0.123),Ne 值较大(>30000)。大多数<50%的感染样本产生的估计值超出了真实值的 5%。对于估计值在 10%以内的情况,需要>15%的所有亚种群的样本量。在治疗后 3 年的随访中,Di 值增加,Ne 值减少了 15 倍以上。此时,需要>30-45%的采样才能达到相同的准确性。在第二次治疗和基线后 4 年,Di 值进一步增加,Ne 值进一步降低,而所需的采样工作量几乎没有变化。需要广泛采样才能准确估计这些重要的种群参数。人口普查规模、感染流行率、社区的治疗历史以及亚种群分化程度等特征都应考虑在内。感染强度与单个亚种群代表组成种群的能力(Dic)之间存在弱相关性,这表明寄生虫基因型的获得具有随机性。这也表明,与随机抽取亚种群样本相比,从感染最严重的人群中进行有针对性的抽样将更好地代表整个社区的遗传多样性。