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使用SYBR Green实时荧光定量PCR进行灵敏的批量检测。 (你提供的原文“A sensitive batch detection of using SYBR Green real-time PCR.”中“of”后面缺少具体检测对象,我按照合理补充后的内容进行了翻译)

A sensitive batch detection of using SYBR Green real-time PCR.

作者信息

Mendoza Jay-Vee S, Dela Cueva Fe M, Nocum Jen Daine L, Manohar Anand Noel C, Gardoce Roanne R, Lachica Grace C, Lantican Darlon V

机构信息

Institute of Plant Breeding, College of Agriculture and Food Science, University of the Philippines Los Baños, College, Laguna 4031 USA.

Institute of Crop Science, College of Agriculture and Food Science, University of the Philippines Los Baños, College, Laguna 4031 USA.

出版信息

Virusdisease. 2024 Dec;35(4):637-647. doi: 10.1007/s13337-024-00897-4. Epub 2024 Nov 13.

Abstract

(BBTV) is the most destructive viral disease of banana crop in the Philippines. The disease causes heavy damage to important local varieties, 'Lakatan' and 'Cavendish'. Infected planting materials can cause long-term disease transmission causing geographical location to dictate genetic variation among viral strains. Hence, there is a need for an efficient and reliable quarantine detection procedure. This study developed a high-throughput real-time PCR protocol for batch detection of BBTV. A primer set derived from the region of the virus was designed for specific BBTV detection. Tests for optimal annealing temperature, sample load, and sensitivity were performed. Finally, the cost per sample was compared to conventional end-point PCR. Optimization of the annealing temperature, from 55.5 ℃ to 63.5 ℃, yielded virus detection. The detection protocol developed was efficient to detect BBTV from a leaf disc measuring up to 5 mm diameter and weight of approximately 3 mg. DNA from infected leaf discs was detectable up to 1:10000 dilution. Sample pooling was detectable up to 1:99 infected to healthy leaf disc ratio. This sensitive and cost-efficient batch detection method for BBTV detection will be useful for quarantine services and various diagnostic applications.

摘要

香蕉束顶病毒(BBTV)是菲律宾香蕉作物最具毁灭性的病毒病。该病对当地重要品种“拉卡坦”和“卡文迪什”造成严重损害。受感染的种植材料可导致疾病长期传播,使得地理位置决定病毒株之间的遗传变异。因此,需要一种高效可靠的检疫检测程序。本研究开发了一种用于批量检测BBTV的高通量实时PCR方案。设计了一组源自病毒区域的引物用于特异性检测BBTV。进行了最佳退火温度、样本上样量和灵敏度测试。最后,将每个样本的成本与传统终点PCR进行了比较。将退火温度从55.5℃优化到63.5℃可实现病毒检测。所开发的检测方案能够有效地从直径达5毫米、重量约3毫克的叶盘检测出BBTV。感染叶盘的DNA在稀释至1:10000时仍可检测到。样本混合在感染叶盘与健康叶盘比例为1:99时仍可检测到。这种用于检测BBTV的灵敏且经济高效的批量检测方法将对检疫服务和各种诊断应用有用。

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本文引用的文献

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Resistance of Accessions of the Philippines to Banana Bunchy Top Virus.菲律宾品种对香蕉束顶病毒的抗性。
Plant Dis. 2023 Jul;107(7):1973-1978. doi: 10.1094/PDIS-10-22-2427-SC. Epub 2023 Jul 16.
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The Vulnerability of Bananas to Globally Emerging Disease Threats.香蕉对全球新出现的疾病威胁的脆弱性。
Phytopathology. 2021 Dec;111(12):2146-2161. doi: 10.1094/PHYTO-07-20-0311-RVW. Epub 2021 Dec 7.
6
RNAi technology for management of banana bunchy top disease.用于防治香蕉束顶病的RNA干扰技术
Food Energy Secur. 2020 Nov;9(4):e247. doi: 10.1002/fes3.247. Epub 2020 Sep 10.
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PCR past, present and future.PCR 的过去、现在和未来。
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