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首页> 外文期刊>Diseases of Aquatic Organisms >Reverse transcriptase loop-mediated isothermal amplification assay for infectious hematopoietic necrosis virus in Oncorhynchus keta
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Reverse transcriptase loop-mediated isothermal amplification assay for infectious hematopoietic necrosis virus in Oncorhynchus keta

机译:逆转录酶环介导的等温扩增法测定柯克氏菌感染性造血坏死病毒

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摘要

ABSTRACT: A reverse transcriptase loop-mediated isothermal amplification (RT-LAMP) assay was developed for detecting infectious hematopoietic necrosis virus (IHNV) from chum salmon Oncorhynchus keta in South Korea with high specificity, sensitivity and rapidity. A set of 6 IHNV-specific primers was designed, based on the G-protein sequence of IHNV (PRT strain), recognizing 8 distinct sequences of the target RNA. The assay was optimized to detect IHNV at 63°C for 30 min. The limit of detection was 0.01 fg of RNA extracted from IHNV-infected CHSE-214 cells, compared with 1.0 fg for nested RT-PCR. The applicability of this RT-LAMP assay was further tested by comparison with nested RT-PCR using field samples. Of 473 samples tested, 191 samples (40.38%) were IHNV-positive by RT-LAMP, whereas 162 samples (34.25%) were IHNV-positive by nested RT-PCR. These results indicate that, because of its high sensitivity and rapidity, the RT-LAMP assay is useful for early diagnosis of IHN.
机译:摘要:开发了一种逆转录酶环介导的等温扩增(RT-LAMP)测定法,该方法可检测韩国Chum鲑 Oncorhynchus keta 的传染性造血坏死病毒(IHNV),具有很高的特异性,敏感性和快速性。基于IHNV(PRT株)的G蛋白序列,设计了6种IHNV特异性引物,识别出目标RNA的8个不同序列。该测定经过优化,可在63°C下检测30分钟的IHNV。检测极限是从感染IHNV的CHSE-214细胞中提取的RNA为0.01 fg,而嵌套式RT-PCR为1.0 fg。通过使用田间样品与巢式RT-PCR进行比较,进一步测试了此RT-LAMP分析的适用性。在473个样本中,有191个样本(40.38%)通过RT-LAMP检测为IHNV阳性,而162个样本(34.25%)通过嵌套式RT-PCR检测为IHNV阳性。这些结果表明,由于其高灵敏度和快速性,RT-LAMP分析可用于IHN的早期诊断。

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