Between a bug and a hard place: Trypanosoma cruzi genetic diversity and the clinical outcomes of Chagas disease

被引:142
|
作者
Messenger, Louisa A. [1 ]
Miles, Michael A. [1 ]
Bern, Caryn [2 ]
机构
[1] London Sch Hyg & Trop Med, Fac Infect Trop Dis, Dept Pathogen Mol Biol, London WC1, England
[2] Univ Calif San Francisco, Sch Med, Dept Epidemiol & Biostat, Global Hlth Sci, San Francisco, CA 94143 USA
基金
英国惠康基金; 英国生物技术与生命科学研究理事会; 美国国家卫生研究院;
关键词
cardiomyopathy; Chagas disease; congenital transmission; diagnostics; genetic diversity; oral outbreaks; reactivation; treatment; DISCRETE TYPING UNITS; POLYMERASE-CHAIN-REACTION; AMPLIFIED POLYMORPHIC DNA; SYLVATIC TRANSMISSION CYCLES; CHROMOSOMAL SIZE VARIATION; POSSIBLE ORAL-TRANSMISSION; CONGENITAL TRANSMISSION; TRIATOMA-INFESTANS; KINETOPLAST DNA; POPULATION-STRUCTURE;
D O I
10.1586/14787210.2015.1056158
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Over the last 30 years, concomitant with successful transnational disease control programs across Latin America, Chagas disease has expanded from a neglected, endemic parasitic infection of the rural poor to an urbanized chronic disease, and now a potentially emergent global health problem. Trypanosoma cruzi infection has a highly variable clinical course, ranging from complete absence of symptoms to severe and often fatal cardiovascular and/or gastrointestinal manifestations. To date, few correlates of clinical disease progression have been identified. Elucidating a putative role for T. cruzi strain diversity in Chagas disease pathogenesis is complicated by the scarcity of parasites in clinical specimens and the limitations of our contemporary genotyping techniques. This article systematically reviews the historical literature, given our current understanding of parasite genetic diversity, to evaluate the evidence for any association between T. cruzi genotype and chronic clinical outcome, risk of congenital transmission or reactivation and orally transmitted outbreaks.
引用
收藏
页码:995 / 1029
页数:35
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