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Effect of blood meal digestion and DNA extraction protocol on the success of blood meal source determination in the malaria vector Anopheles atroparvus

机译:血粉消化和DNA提取方案对疟疾载体Atroparvus血粉来源测定成功的影响

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摘要

Background: Host identification is an essential step in studies on the transmission dynamics of vector-borne\uddisease. Nowadays, molecular tools allow the identification of vertebrate hosts to the species level. However, the\udproportion of successful identifications is variable and may be affected by the quality of the samples and the\udlaboratory protocols. Here, the effect of two of these factors, namely the digestion status of mosquito blood meal\udand the DNA extraction procedure, on the success of host identification by amplification and sequencing of a\udfragment of the cytochrome oxidase 1 gene were tested.\udMethods: Mosquitoes collected both outdoors and indoors during 2012 in southern Spain were identified to\udspecies level and their blood meal digestion status recorded using the Sella score, a visual estimation of the\uddigestion status of mosquito blood meals. Each mosquito was assigned randomly to one of two DNA extraction\udprocedures: the quick and cheap HotSHOT procedure or the QIAGEN DNeasy Blood and TissueW kit and their hosts\udidentified by a molecular method.\udResults: Three hundred and forty-seven blood-fed mosquitoes belonging to Anopheles atroparvus (n=171), Culex\udperexiguus (n=84), Culex pipiens (n=43), Culex theileri (n=39), Culex modestus (n=5), Ochlerotatus caspius (n=4), Culiseta\udsp. (n=1) were included in this study. Overall, hosts were identified from 234 blood meals compromising at least 25\udspecies including mammals, birds and a single reptile. The success of host identification was lower in mosquitoes\udwith an advanced stage of blood meal digestion and for blood meals extracted using the HotSHOT procedure.\udConclusions: The success of host identification decreases with the advanced stage of mosquito blood meal\uddigestion, from 84.5% for recent blood meals to 25.0% for more digested ones. Using the QIAGEN kit, the\udidentification success improved by 17.6%, with larger increases at more advanced stages of blood meal digestion.\udAvailability of blood-fed females used to be very limited for studies of vector ecology, and these results may help\udto increase the efficiency of blood meal analyses. In addition, results obtained in this study clearly support that the\udpotential malaria vector An. atroparvus feeds on animals located outdoors but use human-made shelters for resting\udafter feeding
机译:背景:宿主识别是研究媒介传播\疾病的传播动力学的重要步骤。如今,分子工具可以识别物种的脊椎动物宿主。但是,成功识别的比例是可变的,并且可能会受到样品质量和实验室规程的影响。在这里,我们测试了这两个因素的影响,即蚊子血粉的消化状态和DNA提取程序,对通过细胞色素氧化酶1基因片段的扩增和测序成功鉴定宿主的影响。 :2012年在西班牙南部的室外和室内收集的蚊子被鉴定为\ udspecies水平,并使用Sella得分记录了他们的血粉消化状态,Sella得分是对蚊子血粉\ digdigested状态的视觉估计。每只蚊子被随机分配到两种DNA提取程序中:便宜的HotSHOT程序或QIAGEN DNeasy Blood and TissueW试剂盒,以及它们的宿主,通过分子方法鉴定。\ ud结果:347例属于阿波罗按蚊(n = 171),库克斯(Culex \ udperexiguus)(n = 84),淡水库蚊(Culex pipiens)(n = 43),库蚊(Thelexri)(n = 39),库克斯库蚊(n.5),库氏n鱼(n = 4)的蚊子),Culiseta \ udsp。 (n = 1)被纳入这项研究。总体上,从234份血粉中鉴定出宿主,这些血粉包括哺乳动物,鸟类和一只爬行动物,危害了至少25种物种。蚊子中的宿主识别成功率较低,\\随着高级血粉消化和使用HotSHOT程序提取的血粉中\\结论:宿主识别的成功率随着蚊子血粉\消化率的降低而降低,从84.5开始近期的血粉百分比为25.0%,较新的血粉百分比为25.0%。使用QIAGEN试剂盒,鉴定成功率提高了17.6%,在血粉消化的更高级阶段,鉴定成功率提高了。\ ud以母乳喂养的雌性动物在媒介生态学研究中的应用非常有限,这些结果可能会帮助\ udto提高血粉分析的效率。另外,这项研究中获得的结果清楚地证明了\潜在疟疾媒介An。黄萎龙以室外的动物为食,但使用人工庇护所休息/喂食后

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