Evaluation of a polymerase chain reaction assay for the diagnosis of bovine trypanosomiasis and epidemiological surveillance in Bolivia.

Jose Luis Gonzales, Tudor W Jones, Kim Picozzi, Hugo Ribera Cuellar
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引用次数: 32

Abstract

BACKGROUND: Sporadic outbreaks of bovine trypanosomiasis have been reported in Bolivia since 1996 when T. vivax and T. evansi were identified for the first time by parasitological means. However, comprehensive epidemiological information concerning T. vivax and T. evansi in the country is lacking. Current parasitological and serological diagnostic methods for trypanosomiasis have important limitations either in their sensitivity or specificity, which can result in unreliable data when applied in epidemiological studies. PCR assays are a recently developed procedure that might help to overcome the constraints of parasitological and serological assays. Therefore, the objective of this study was to evaluate PCR assays as a diagnostic tool for epidemiological studies in Bolivia. RESULTS: PCR assays for diagnosis of trypanosome infection in cattle were evaluated for their ability to detect trypanosome DNA in blood spots samples collected from cattle in four different provinces from the Bolivian lowlands and the results compared with those obtained with standard parasitological Micro Haematocrit Centrifugation Technique (MHCT) and stained smears and serological methods (Card Agglutination Test for T. evansi (CATT), and Antibody ELISAs for T. vivax and T. congolense). Kappa agreement analysis showed a significant agreement between PCR assays and results from parasitological methods but there was no agreement when PCR was compared with serological assays. Some samples from T. vivax smear positive animals were negative by PCR, therefore modifications to the PCR assay conditions were undertaken to try to improve agreement between PCR and parasitological assays. Changes in the template DNA concentration or the use of an alternative primer set resulted in improvements in the PCR detection rate, but not all the parasitologically positive samples were detected by PCR. Results from PCR assays for T. vivax and T. evansi were combined with results from parasitological and serological assays to provide information on prevalence rates for the four provinces from where the samples were obtained. CONCLUSION: The present study established evidence of the usefulness of PCR as diagnostic tool for epidemiological studies and confirmed that cattle trypanosomiasis appears to be endemic in several regions of the Bolivian lowlands.

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玻利维亚牛锥虫病的聚合酶链反应诊断及流行病学监测评价。
背景:自1996年首次通过寄生虫学方法发现间日疟原虫和伊瓦西疟原虫以来,玻利维亚报告了牛锥虫病的零星暴发。然而,该国缺乏关于间日疟原虫和伊文氏疟原虫的全面流行病学信息。目前用于锥虫病的寄生虫学和血清学诊断方法在敏感性或特异性方面存在重大局限性,这可能导致在流行病学研究中应用时数据不可靠。PCR检测是最近发展起来的一种方法,可能有助于克服寄生虫学和血清学检测的局限性。因此,本研究的目的是评价PCR检测作为玻利维亚流行病学研究的诊断工具。结果:对用于诊断牛锥虫感染的PCR检测方法在玻利维亚低地4个不同省份采集的牛血斑样本中检测锥虫DNA的能力进行了评估,并将结果与标准寄生虫学微红细胞压积离心技术(MHCT)、染色涂片和血清学方法(伊万氏绦虫卡凝集试验(CATT)、间日疟原虫和刚果锥虫抗体elisa)获得的结果进行了比较。Kappa一致性分析显示,PCR检测结果与寄生虫学检测结果有显著的一致性,但与血清学检测结果不一致。一些间日疟原虫涂片阳性动物的样本经PCR检测呈阴性,因此对PCR检测条件进行了修改,试图提高PCR与寄生虫学检测结果之间的一致性。改变模板DNA浓度或使用其他引物组可提高PCR检出率,但并非所有寄生虫学阳性样品都能被PCR检测到。将间日疟原虫和伊文氏疟原虫的PCR检测结果与寄生虫学和血清学检测结果相结合,以提供获取样本的4个省份的流行率信息。结论:本研究确立了PCR作为流行病学研究诊断工具的有效性证据,并证实牛锥虫病似乎在玻利维亚低地的几个地区流行。
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Consultation meeting on the development of therapeutic vaccines for post kala azar dermal leishmaniasis. In silico, biologically-inspired modelling of genomic variation generation in surface proteins of Trypanosoma cruzi. Genetic diversity of Leishmania amazonensis strains isolated in northeastern Brazil as revealed by DNA sequencing, PCR-based analyses and molecular karyotyping. Dynamics of infection and competition between two strains of Trypanosoma brucei brucei in the tsetse fly observed using fluorescent markers. Consultative meeting to develop a strategy for treatment of cutaneous leishmaniasis. Institute Pasteur, Paris. 13-15 June, 2006.
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