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使用实时聚合酶链反应(PCR)对诱蝇笼捕获的大量蝇类样本中的新大陆螺旋蝇(Chrysomya bezziana)进行特异性检测。

Specific detection of the Old World screwworm fly, Chrysomya bezziana, in bulk fly trap catches using real-time PCR.

作者信息

Jarrett S, Morgan J A T, Wlodek B M, Brown G W, Urech R, Green P E, Lew-Tabor A E

机构信息

Department of Employment, Economic Development and Innovation, Queensland Primary Industries and Fisheries, Animal Research Institute, Yeerongpilly, Queensland, Australia.

出版信息

Med Vet Entomol. 2010 Sep;24(3):227-35. doi: 10.1111/j.1365-2915.2010.00867.x. Epub 2010 May 17.

Abstract

The Old World screwworm fly (OWS), Chrysomya bezziana Villeneuve (Diptera: Calliphoridae), is a myiasis-causing blowfly of major concern for both animals and humans. Surveillance traps are used in several countries for early detection of incursions and to monitor control strategies. Examination of surveillance trap catches is time-consuming and is complicated by the presence of morphologically similar flies that are difficult to differentiate from Ch. bezziana, especially when the condition of specimens is poor. A molecular-based method to confirm or refute the presence of Ch. bezziana in trap catches would greatly simplify monitoring programmes. A species-specific real-time polymerase chain reaction (PCR) assay was designed to target the ribosomal DNA internal transcribed spacer 1 (rDNA ITS1) of Ch. bezziana. The assay uses both species-specific primers and an OWS-specific Taqman((R)) MGB probe. Specificity was confirmed against morphologically similar and related Chrysomya and Cochliomyia species. An optimal extraction protocol was developed to process trap catches of up to 1000 flies and the assay is sensitive enough to detect one Ch. bezziana in a sample of 1000 non-target species. Blind testing of 29 trap catches from Australia and Malaysia detected Ch. bezziana with 100% accuracy. The probability of detecting OWS in a trap catch of 50 000 flies when the OWS population prevalence is low (one in 1000 flies) is 63.6% for one extraction. For three extractions (3000 flies), the probability of detection increases to 95.5%. The real-time PCR assay, used in conjunction with morphology, will greatly increase screening capabilities in surveillance areas where OWS prevalence is low.

摘要

旧大陆螺旋蝇(OWS),即致倦库蚊(Chrysomya bezziana Villeneuve)(双翅目:丽蝇科),是一种对动物和人类都至关重要的引起蝇蛆病的丽蝇。多个国家使用监测诱捕器来早期发现入侵情况并监测控制策略。检查监测诱捕器捕获的苍蝇很耗时,而且由于存在形态相似、难以与致倦库蚊区分的苍蝇而变得复杂,尤其是当标本状况不佳时。一种基于分子的方法来确认或反驳诱捕器捕获物中是否存在致倦库蚊,将极大地简化监测计划。设计了一种物种特异性实时聚合酶链反应(PCR)检测方法,以靶向致倦库蚊的核糖体DNA内部转录间隔区1(rDNA ITS1)。该检测方法使用物种特异性引物和OWS特异性Taqman® MGB探针。针对形态相似和相关的库蚊属和绿蝇属物种确认了特异性。开发了一种最佳提取方案来处理多达1000只苍蝇的诱捕捕获物,该检测方法足够灵敏,能够在1000个非目标物种的样本中检测到一只致倦库蚊。对来自澳大利亚和马来西亚的29个诱捕捕获物进行的盲测以100%的准确率检测到了致倦库蚊。当OWS种群患病率较低(每1000只苍蝇中有1只)时,对50000只苍蝇的诱捕捕获物进行一次提取检测到OWS的概率为63.6%。进行三次提取(3000只苍蝇)时,检测概率增加到95.5%。与形态学结合使用的实时PCR检测方法,将大大提高OWS患病率较低的监测区域的筛查能力。

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