Keller Judith I, Ballif Bryan A, St Clair Riley M, Vincent James J, Monroy M Carlota, Stevens Lori
Department of Biology, University of Vermont, Burlington, Vermont, United States of America.
Laboratorio de Entomología Aplicada y Parasitología, Escuela de Biología, Facultad de Ciencias Químicas y Farmacia, Universidad de San Carlos de Guatemala, Ciudad de Guatemala, Guatemala.
PLoS One. 2017 Dec 12;12(12):e0189647. doi: 10.1371/journal.pone.0189647. eCollection 2017.
Chagas disease is a complex vector borne parasitic disease involving blood feeding Triatominae (Hemiptera: Reduviidae) insects, also known as kissing bugs, and the vertebrates they feed on. This disease has tremendous impacts on millions of people and is a global health problem. The etiological agent of Chagas disease, Trypanosoma cruzi (Kinetoplastea: Trypanosomatida: Trypanosomatidae), is deposited on the mammalian host in the insect's feces during a blood meal, and enters the host's blood stream through mucous membranes or a break in the skin. Identifying the blood meal sources of triatomine vectors is critical in understanding Chagas disease transmission dynamics, can lead to identification of other vertebrates important in the transmission cycle, and aids management decisions. The latter is particularly important as there is little in the way of effective therapeutics for Chagas disease. Several techniques, mostly DNA-based, are available for blood meal identification. However, further methods are needed, particularly when sample conditions lead to low-quality DNA or to assess the risk of human cross-contamination. We demonstrate a proteomics-based approach, using liquid chromatography tandem mass spectrometry (LC-MS/MS) to identify host-specific hemoglobin peptides for blood meal identification in mouse blood control samples and apply LC-MS/MS for the first time to Triatoma dimidiata insect vectors, tracing blood sources to species. In contrast to most proteins, hemoglobin, stabilized by iron, is incredibly stable even being preserved through geologic time. We compared blood stored with and without an anticoagulant and examined field-collected insect specimens stored in suboptimal conditions such as at room temperature for long periods of time. To our knowledge, this is the first study using LC-MS/MS on field-collected arthropod disease vectors to identify blood meal composition, and where blood meal identification was confirmed with more traditional DNA-based methods. We also demonstrate the potential of synthetic peptide standards to estimate relative amounts of hemoglobin acquired when insects feed on multiple blood sources. These LC-MS/MS methods can contribute to developing Ecohealth control strategies for Chagas disease transmission and can be applied to other arthropod disease vectors.
恰加斯病是一种复杂的媒介传播寄生虫病,涉及吸血的锥蝽(半翅目:猎蝽科)昆虫,也被称为接吻虫,以及它们所吸食血液的脊椎动物。这种疾病对数以百万计的人产生了巨大影响,是一个全球性的健康问题。恰加斯病的病原体克氏锥虫(动基体目:锥虫科)在昆虫吸血时随粪便沉积在哺乳动物宿主身上,并通过黏膜或皮肤破损处进入宿主的血流。确定锥蝽媒介的血餐来源对于理解恰加斯病的传播动态至关重要,有助于识别传播循环中其他重要的脊椎动物,并辅助管理决策。由于恰加斯病几乎没有有效的治疗方法,后者尤为重要。有几种技术,大多基于DNA,可用于血餐鉴定。然而,还需要进一步的方法,特别是当样本条件导致DNA质量较低或评估人类交叉污染风险时。我们展示了一种基于蛋白质组学的方法,使用液相色谱串联质谱(LC-MS/MS)来鉴定小鼠血液对照样本中用于血餐鉴定的宿主特异性血红蛋白肽,并首次将LC-MS/MS应用于二色锥蝽昆虫媒介,追踪血源到物种。与大多数蛋白质不同,由铁稳定的血红蛋白极其稳定,甚至能在地质时间中保存下来。我们比较了添加抗凝剂和未添加抗凝剂储存的血液,并检查了在室温等次优条件下长时间储存的野外采集昆虫标本。据我们所知,这是第一项使用LC-MS/MS对野外采集的节肢动物疾病媒介进行血餐成分鉴定的研究,并且血餐鉴定通过更传统的基于DNA的方法得到了证实。我们还展示了合成肽标准物在估计昆虫吸食多种血源时获得的血红蛋白相对量方面的潜力。这些LC-MS/MS方法有助于制定恰加斯病传播的生态健康控制策略,并可应用于其他节肢动物疾病媒介。