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基于细胞色素b基因的PCR-RFLP方法鉴定野外捕获白蛉体内的血餐

Identification of blood meals in field captured sand flies by a PCR-RFLP approach based on cytochrome b gene.

作者信息

González Estela, Gállego Montserrat, Molina Ricardo, Abras Alba, Alcover M Magdalena, Ballart Cristina, Fernández Anna, Jiménez Maribel

机构信息

Unidad de Entomología Médica, Servicio de Parasitología, Centro Nacional de Microbiología, Instituto de Salud Carlos III, Ctra. Majadahonda-Pozuelo s/n, 28220 Majadahonda, Madrid, Spain.

Laboratori de Parasitologia, Facultat de Farmàcia, Universitat de Barcelona (UB), Spain; ISGlobal, Barcelona Ctr. Int. Health Res. (CRESIB), Hospital Clínic-Universitat de Barcelona, Barcelona, Spain.

出版信息

Acta Trop. 2015 Dec;152:96-102. doi: 10.1016/j.actatropica.2015.08.020. Epub 2015 Sep 3.

Abstract

Leishmaniasis is a vector-borne disease transmitted by phlebotomine sand flies. Information about blood meal preferences in sand flies is essential to understand the epidemiology of the disease to adopt control measures. In previous studies, a polymerase chain reaction (PCR) of 359bp fragment of the conserved gene cytochrome b (cyt b) and further sequencing were applied in the study of blood meal sources in sand flies collected in the area of a leishmaniasis outbreak in southwest Madrid, Spain, providing significant information about blood meal preferences in the focus. In this work, a PCR-restriction fragment length polymorphism (RFLP) targeting a fragment of 359bp of vertebrate cyt b gene was developed. Restriction endonucleases HaeIII and HinfI generated specific patterns consistent with the blood meal sources found in sand flies. The protocol has been validated with twenty six engorged females collected in the field with CDC traps. Blood meals from nine vertebrates were identified based on PCR-cyt b and sequencing-human, dog, cat, horse, hare, rabbit, sheep, goat and chicken - and mixed blood meals (sheep/human; sheep/goat) - and successfully distinguished by PCR-RFLP. Therefore, this approach is an efficient and reliable alternative method to be applied in entomological surveys.

摘要

利什曼病是一种由白蛉传播的媒介传播疾病。了解白蛉的血餐偏好信息对于理解该疾病的流行病学以及采取控制措施至关重要。在先前的研究中,对西班牙马德里西南部利什曼病暴发地区采集的白蛉血餐来源研究采用了对保守基因细胞色素b(cyt b)的359bp片段进行聚合酶链反应(PCR)并进一步测序的方法,提供了有关该疫源地白蛉血餐偏好的重要信息。在这项工作中,开发了一种针对脊椎动物cyt b基因359bp片段的PCR-限制性片段长度多态性(RFLP)方法。限制性内切酶HaeIII和HinfI产生了与白蛉中发现的血餐来源一致的特定模式。该方案已通过用疾控中心诱捕器在野外采集的26只饱血雌虫进行了验证。基于PCR-cyt b和测序确定了来自9种脊椎动物的血餐——人类、狗、猫、马、野兔、兔子、绵羊、山羊和鸡——以及混合血餐(绵羊/人类;绵羊/山羊)——并通过PCR-RFLP成功区分。因此,这种方法是一种可应用于昆虫学调查的高效且可靠的替代方法。

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