McQueen Philip G, McKenzie F Ellis
Center for Information Technology and Fogarty International Center, National Institutes of Health, Bethesda, Maryland 20892-5620, USA.
Am J Trop Med Hyg. 2006 Jul;75(1):112-25.
We assess the consequences of competition for red blood cells (RBCs) in co-infections with the two major agents of human malaria, Plasmodium vivax and Plasmodium falciparum, using differential equations to model the population dynamics of RBCs and parasites. P. vivax parasitizes only the youngest RBCs, but this can reduce the broader RBC population susceptible to P. falciparum. We found that competition for RBCs typically causes one species to suppress the other, depending on their relative reproduction rates and timing of inoculation. However, if the species' reproduction rates are nearly equal, transient increases in RBC production stimulated by the presence of P. falciparum may boost P. vivax parasitemia above its single-species infection level. Conversely, P. falciparum parasitemia is rarely enhanced above its single-species level. Furthermore, transients in RBC production can induce coupled oscillations in the parasitemia of both species. These results are remarkably robust to changes in model parameters.
我们使用微分方程来模拟红细胞和疟原虫的种群动态,评估在人类疟疾的两种主要病原体——间日疟原虫和恶性疟原虫共同感染中对红细胞(RBCs)的竞争后果。间日疟原虫仅寄生于最年轻的红细胞,但这会减少对恶性疟原虫易感的更广泛的红细胞群体。我们发现,对红细胞的竞争通常会导致一个物种抑制另一个物种,这取决于它们的相对繁殖率和接种时间。然而,如果物种的繁殖率几乎相等,由恶性疟原虫的存在刺激的红细胞生成的短暂增加可能会使间日疟原虫血症高于其单物种感染水平。相反,恶性疟原虫血症很少会增强到高于其单物种水平。此外,红细胞生成的瞬变可诱导两个物种的虫血症发生耦合振荡。这些结果对模型参数的变化具有显著的稳健性。