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Chagas Disease at the Canine-Wildlife-Human-Vector Interface

机译:在犬野生动物 - 人类矢量界面的Chagas病

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The hemoflagellate protozoan Trypanosoma cruzi is the etiologic agent of Chagas disease, and infects humans, nonhuman primates, dogs, and other wild and domestic mammalian species. Active transmission of T. cruzi occurs throughout the Americas, including the southern USA, where infected hematophagous triatomine "kissing bug" vectors (Fig. 1) and wildlife reservoirs co-occur.1 Infection can occur through the introduction of infectious triatomine feces to skin lesions during or shortly after blood feeding. Oral transmission to animals may result from consumption of infected bugs or infected prey species.1 Congenital transmission has been documented in humans, canines, and other animals.1 T. cruzi genetic strain differences occur throughout the Americas,2 where parasite discrete typing units (DTUs) TcI-TcVI circulate and may be associated with different reservoir hosts, vector species, and variation in disease outcome. Infected individuals do not always develop clinical disease;1 and prognosis in initially asymptomatic individuals is largely unknown. In the USA, clinical T. cruzi infection in dogs is most commonly associated with cardiac disease.13 Dogs are important hosts throughout the Americas, and in some cases serve as sentinels of human diseaserisk across a landscape.4 Diagnosis of Chagas disease is most commonly based on clinical suspicion and antibody detection, but diagnostic tests are imperfect and confirmation of antibody status is best derived from the results of more than one independent assay, which is usually impracticable. Chagas disease is a notifiable infectious disease for humans in four states, including Texas, Tennessee, Massachusetts, and Arizona. Using a One Health approach, we have conducted epidemiological studies of T. cruzi in vectors, dogs, wildlife, and humans, with a focus on the high-risk state of Texas in order to characterize transmission cycles, identify risk factors, and identify points for management interventions to reduce disease risk; highlights are reviewed below.
机译:血红蛋白原生动物胰蛋白酶瘤Cruzi是Chagas疾病的病因,并且感染人类,非人类原始动物,狗和其他野生和家庭哺乳动物物种。在整个美洲,包括南方的克鲁齐的主动传播,其中受感染的血液血液“亲吻虫子”载体(图1)和野生动物储存器也可以通过引入皮肤传染性三角虫粪便来发生血液喂养后或不久的病变。对动物的口服传播可能是由于感染的虫子的消耗或受感染的猎物.1先天性传播已经记载了人类,犬和其他动物.1 T.Cruzi遗传应变差异在整个美洲发生,其中寄生虫离散输入单位( DTU)TCI-TCVI循环,可能与不同的储层宿主,载体物种和疾病结果的变异相关联。受感染的个体并不总是发展临床疾病; 1,最初无症状的个体的预后很大程度上是未知的。在美国,狗的临床T.Cruzi感染最常与心脏病有关.13狗是整个美洲的重要主持人,在某些情况下,横跨人类丧失的哨兵.4疾病的诊断最常见的疾病基于临床怀疑和抗体检测,但诊断测试是不完美的,并且抗体状态的确认是最优异的,从一个以上的独立测定结果中最好衍生,这通常是不切实际的。 Chagas疾病是四个州的人类的通知传染病,包括德克萨斯州,田纳西州,马萨诸塞州和亚利桑那。使用一个健康的做法,我们在为了表征传输周期进行了载体,狗,野生动物和人类锥虫的流行病学研究,重点是得克萨斯州的高风险状态,识别风险因素,并确定分用于减少疾病风险的管理干预措施;亮点是下面审查的。

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