Garcia Melissa N, Burroughs Hadley, Gorchakov Rodion, Gunter Sarah M, Dumonteil Eric, Murray Kristy O, Herrera Claudia P
Department of Pediatrics, National School of Tropical Medicine, Baylor College of Medicine and Texas Children's Hospital, Houston, TX, USA.
Department of Tropical Medicine, Vector-Borne Infectious Disease Research Center, Tulane University, School of Public Health and Tropical Medicine, New Orleans, LA, USA.
Infect Genet Evol. 2017 Apr;49:151-156. doi: 10.1016/j.meegid.2017.01.016. Epub 2017 Jan 15.
The parasitic protozoan Trypanosoma cruzi, the causative agent of Chagas disease, is widely distributed throughout the Americas, from the southern United States (US) to northern Argentina, and infects at least 6 million people in endemic areas. Much remains unknown about the dynamics of T. cruzi transmission among mammals and triatomine vectors in sylvatic and peridomestic eco-epidemiological cycles, as well as of the risk of transmission to humans in the US. Identification of T. cruzi DTUs among locally-acquired cases is necessary for enhancing our diagnostic and clinical prognostic capacities, as well as to understand parasite transmission cycles. Blood samples from a cohort of 15 confirmed locally-acquired Chagas disease patients from Texas were used for genotyping T. cruzi. Conventional PCR using primers specific for the minicircle variable region of the kinetoplastid DNA (kDNA) and the highly repetitive genomic satellite DNA (satDNA) confirmed the presence of T. cruzi in 12/15 patients. Genotyping was based on the amplification of the intergenic region of the miniexon gene of T. cruzi and sequencing. Sequences were analyzed by BLAST and phylogenetic analysis by Maximum Likelihood method allowed the identification of non-TcI DTUs infection in six patients, which corresponded to DTUs TcII, TcV or TcVI, but not to TcIII or TcIV. Two of these six patients were also infected with a TcI DTU, indicating mixed infections in those individuals. Electrocardiographic abnormalities were seen among patients with single non-TcI and mixed infections of non-TcI and TcI DTUs. Our results indicate a greater diversity of T. cruzi DTUs circulating among autochthonous human Chagas disease cases in the southern US, including for the first time DTUs from the TcII-TcV-TcVI group. Furthermore, the DTUs infecting human patients in the US are capable of causing Chagasic cardiac disease, highlighting the importance of parasite detection in the population.
寄生原生动物克氏锥虫是恰加斯病的病原体,广泛分布于整个美洲,从美国南部到阿根廷北部,在流行地区至少感染600万人。关于克氏锥虫在野生和家庭周边生态流行病学循环中的哺乳动物和锥蝽媒介之间的传播动态,以及在美国传播给人类的风险,仍有许多未知之处。识别本地获得病例中的克氏锥虫离散分型单元(DTUs)对于提高我们的诊断和临床预后能力以及了解寄生虫传播周期至关重要。来自德克萨斯州15名确诊的本地获得性恰加斯病患者队列的血样用于克氏锥虫基因分型。使用针对动基体DNA(kDNA)的小环可变区和高度重复的基因组卫星DNA(satDNA)的特异性引物进行常规PCR,证实15名患者中有12名存在克氏锥虫。基因分型基于克氏锥虫微小外显子基因的基因间区域的扩增和测序。通过BLAST分析序列,并通过最大似然法进行系统发育分析,从而识别出6名患者感染了非TcI DTUs,分别对应于DTUs TcII、TcV或TcVI,但不包括TcIII或TcIV。这6名患者中有2名还感染了TcI DTU,表明这些个体存在混合感染。在单一非TcI感染以及非TcI和TcI DTUs混合感染的患者中均观察到心电图异常。我们的结果表明,在美国南部本地获得性人类恰加斯病病例中循环的克氏锥虫DTUs具有更大的多样性,首次包括来自TcII - TcV - TcVI组的DTUs。此外,在美国感染人类患者的DTUs能够导致恰加斯性心脏病,突出了在人群中检测寄生虫的重要性。