Araujo R N, Campos I T N, Tanaka A S, Santos A, Gontijo N F, Lehane M J, Pereira M H
Departamento de Parasitologia, Instituto de Ciências Biológicas, UFMG, Bloco 14, Sala 177, Av. Antônio Carlos 6627, Belo Horizonte, MG, Brazil.
Int J Parasitol. 2007 Oct;37(12):1351-8. doi: 10.1016/j.ijpara.2007.04.017. Epub 2007 May 10.
Every hematophagous invertebrate studied to date produces at least one inhibitor of coagulation. Among these, thrombin inhibitors have most frequently been isolated. In order to study the thrombin inhibitor from Triatoma brasiliensis and its biological significance for the bug, we sequenced the corresponding gene and evaluated its biological function. The T. brasiliensis intestinal thrombin inhibitor, termed brasiliensin, was sequenced and primers were designed to synthesize double strand RNA (dsRNA). Gene knockdown (RNAi) was induced by two injections of 15mug of dsRNA into fourth instar nymphs. Forty-eight hours after the second injection, bugs from each group were allowed to feed on hamsters. PCR results showed that injections of dsRNA reduced brasiliensin expression in the anterior midgut by approximately 71% in knockdown nymphs when compared with controls. The reduction in gene expression was confirmed by the thrombin inhibitory activity assay and the citrated plasma coagulation time assay which showed activity reductions of approximately 18- and approximately 3.5-fold, respectively. Knockdown nymphs ingested approximately 39% less blood than controls. In order to confirm the importance of brasiliensin in blood ingestion, fourth instar nymphs were allowed to ingest feeding solution alone or feeding solution containing 15U of thrombin prior to blood feeding. Fifty-five percent less blood was ingested by nymphs which were fed thrombin prior to blood feeding. The results suggest that anticoagulant activity in the midgut is an important determinant of the amount of blood taken from the host. The role of anticoagulants during blood ingestion is discussed in the light of this novel insight.
迄今为止,每一种接受研究的吸血无脊椎动物都会产生至少一种凝血抑制剂。其中,凝血酶抑制剂是最常被分离出来的。为了研究巴西锥蝽的凝血酶抑制剂及其对该昆虫的生物学意义,我们对相应基因进行了测序,并评估了其生物学功能。对巴西锥蝽肠道凝血酶抑制剂(命名为巴西抑酶肽)进行了测序,并设计引物来合成双链RNA(dsRNA)。通过向四龄若虫注射两次15微克的dsRNA来诱导基因敲除(RNA干扰)。第二次注射后48小时,每组的虫子被允许吸食仓鼠的血液。PCR结果显示,与对照组相比,注射dsRNA使敲除若虫中肠前部的巴西抑酶肽表达降低了约71%。凝血酶抑制活性测定和枸橼酸盐血浆凝血时间测定证实了基因表达的降低,结果分别显示活性降低了约18倍和约3.5倍。敲除若虫吸食的血液比对照组少约39%。为了证实巴西抑酶肽在血液摄取中的重要性,在吸血前让四龄若虫单独摄取喂食溶液或含有15单位凝血酶的喂食溶液。在吸血前喂食凝血酶的若虫摄取的血液减少了55%。结果表明,中肠中的抗凝活性是从宿主摄取血液量的一个重要决定因素。鉴于这一新的见解,讨论了抗凝剂在吸血过程中的作用。