Sanches Tiago L M, Cunha Larissa D, Silva Grace K, Guedes Paulo M M, Silva João Santana, Zamboni Dario S
Department of Cell Biology, University of São Paulo, Medical School Ribeirão Preto, FMRP/USP, São Paulo, Brazil.
Department of Biochemistry and Immunology, University of São Paulo, Medical School Ribeirão Preto, FMRP/USP, São Paulo, Brazil.
PLoS One. 2014 Mar 20;9(3):e91640. doi: 10.1371/journal.pone.0091640. eCollection 2014.
Chagas disease develops upon infection with the protozoan parasite Trypanosoma cruzi and undergoes an acute phase characterized by massive parasite replication and the presence of parasites in the blood. This condition is known as acute phase parasitemia. This initial stage may result in a cure, in the development of the chronic stages of the disease or in the death of the infected host. Despite intensive investigation related to the characterization of the acute and chronic phases of the disease, the cause-effect relationship of acute phase parasitemia to the outcome of the disease is still poorly understood. In this study, we artificially generated a heterogeneously controlled mouse population by intercrossing F1 mice obtained from a parental breeding of highly susceptible A/J with highly resistant C57BL/6 mouse strains. This F2 population was infected and used to assess the correlation of acute phase parasitemia with the longevity of the animals. We used nonparametric statistical analyses and found a significant association between parasitemia and mortality. If males and females were evaluated separately, we found that the former were more susceptible to death, although parasitemia was similar in males and females. In females, we found a strong negative correlation between parasitemia and longevity. In males, however, additional factors independent of parasitemia may favor mouse mortality during the development of the disease. The correlations of acute phase parasitemia with mortality reported in this study may facilitate an appropriate prognostic approach to the disease in humans. Moreover, these results illustrate the complexity of the mammalian genetic traits that regulate host resistance during Chagas disease.
恰加斯病由原生动物寄生虫克氏锥虫感染引发,会经历一个急性期,其特征是寄生虫大量繁殖且血液中存在寄生虫。这种情况被称为急性期寄生虫血症。这个初始阶段可能导致治愈、疾病进入慢性阶段或受感染宿主死亡。尽管对该疾病急性期和慢性期的特征进行了深入研究,但急性期寄生虫血症与疾病转归之间的因果关系仍未得到充分理解。在本研究中,我们通过将从高度易感的A/J与高度抗性的C57BL/6小鼠品系的亲本杂交获得的F1小鼠进行杂交,人工构建了一个异质性受控的小鼠群体。这个F2群体被感染,并用于评估急性期寄生虫血症与动物寿命的相关性。我们使用非参数统计分析,发现寄生虫血症与死亡率之间存在显著关联。如果分别评估雄性和雌性,我们发现前者更容易死亡,尽管雄性和雌性的寄生虫血症相似。在雌性中,我们发现寄生虫血症与寿命之间存在强烈的负相关。然而,在雄性中,独立于寄生虫血症的其他因素可能在疾病发展过程中有利于小鼠死亡。本研究中报道的急性期寄生虫血症与死亡率的相关性可能有助于对人类该疾病采取适当的预后方法。此外,这些结果说明了在恰加斯病期间调节宿主抗性的哺乳动物遗传特征的复杂性。