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用于分析抗疟疾候选真菌生物农药的实时定量PCR:技术验证及首次应用

Real-time quantitative PCR for analysis of candidate fungal biopesticides against malaria: technique validation and first applications.

作者信息

Bell Andrew S, Blanford Simon, Jenkins Nina, Thomas Matthew B, Read Andrew F

机构信息

School of Biological Sciences, University of Edinburgh, West Mains Road, Edinburgh EH93JT, UK.

出版信息

J Invertebr Pathol. 2009 Mar;100(3):160-8. doi: 10.1016/j.jip.2009.01.006.

Abstract

Recent research has indicated that fungal biopesticides could augment existing malaria vector control tools. Here we present a set of methodologies to monitor the in vivo kinetics of entomopathogenic fungi in Anopheles in the presence or absence of malaria parasites using quantitative real-time PCR. Three qPCR assays were successfully developed for counting fungal genomes: "specific" assays capable of distinguishing two well characterized fungal entomopathogens Beauveria bassiana isolate IMI391510 and Metarhizium anisopliae var. acridum isolate IMI330189, both of which have previously been shown to be virulent to Anopheles mosquitoes, and a "generic" fungal assay for determining any fungal burden. A fourth assay to Plasmodium chabaudi enabled quantification of co-infecting malarial parasites. All qPCR assays provide sensitive, target-specific, and robust quantification over a linear range of greater than five orders of magnitude (seven orders of magnitude for the fungal assays). B. bassiana growth within mosquitoes exposed to three different conidial challenge doses was monitored using the B. bassiana-specific assay and represents the first description of entomopathogenic fungal replication within an insect host. This revealed that, irrespective of challenge dose, after several days of relatively little replication, a sudden on-set of substantial nuclear division occurs, accompanied by physical fungal growth (hyphae) within the mosquito haemocoel shortly before death. Exposure to higher densities of conidia resulted in significantly greater pick-up by mosquitoes and to elevated fungal burdens at each time point sampled. High fungal burdens, comparable to those identified in cadavers, were attained more rapidly and mortalities occurred earlier post-exposure with increasing challenge dose. The lines of research made possible by the qPCR assays described here will contribute to optimization of fungal biopesticides against malaria and other vector-borne diseases.

摘要

近期研究表明,真菌生物农药可增强现有的疟疾媒介控制工具。在此,我们介绍了一套方法,用于在存在或不存在疟原虫的情况下,使用定量实时PCR监测按蚊体内昆虫病原真菌的体内动力学。成功开发了三种用于计数真菌基因组的qPCR检测方法:“特异性”检测方法,能够区分两种特征明确的昆虫病原真菌球孢白僵菌分离株IMI391510和绿僵菌变种金龟子绿僵菌分离株IMI330189,这两种真菌此前均已证明对按蚊具有毒性;以及一种用于确定任何真菌负荷的“通用”真菌检测方法。针对查巴迪疟原虫的第四种检测方法能够对共感染的疟原虫进行定量。所有qPCR检测方法在大于五个数量级的线性范围内(真菌检测方法为七个数量级)都能提供灵敏、靶向特异性且稳健的定量结果。使用球孢白僵菌特异性检测方法监测了暴露于三种不同分生孢子攻击剂量的蚊子体内球孢白僵菌的生长情况,这是首次对昆虫病原真菌在昆虫宿主体内的复制进行描述。结果显示,无论攻击剂量如何,在经过几天相对较少的复制后,会突然出现大量核分裂,紧接着在蚊子死亡前不久,真菌在血腔中出现物理性生长(菌丝)。暴露于更高密度的分生孢子会导致蚊子摄取量显著增加,且在每个采样时间点真菌负荷都会升高。随着攻击剂量的增加,与在尸体中发现的真菌负荷相当的高真菌负荷出现得更快,暴露后死亡发生得更早。本文所述的qPCR检测方法所推动的一系列研究将有助于优化针对疟疾和其他媒介传播疾病的真菌生物农药。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a95/2666797/09934b7f92a1/gr1.jpg

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