A sensitive and specific SYBR Green-based qPCR assay for detecting scale drop disease virus (SDDV) in Asian sea bass

生物 黑鲈 聚合酶链反应 病毒学 实时聚合酶链反应 DNA提取 荧光染料 病毒 分子生物学 亚临床感染 套式聚合酶链反应 基因 渔业 遗传学
作者
Sukhontip Sriisan,Chuenchit Boonchird,Siripong Thitamadee,Molruedee Sonthi,Ha Thanh Dong,Saengchan Senapin
出处
期刊:Diseases of Aquatic Organisms [Inter-Research]
卷期号:139: 131-137 被引量:16
标识
DOI:10.3354/dao03484
摘要

Scale drop disease virus (SDDV) is a megalocytivirus known to cause disease in Asian sea bass in Southeast Asia. To support SDDV diagnosis and surveillance, we report on a sensitive and specific SYBR Green qPCR assay. The qPCR primers were designed to target a 135 bp fragment of the SDDV ATPase gene. The optimized SDDV qPCR assay reliably detected 2 copies of a plasmid dsDNA control and did not cross-amplify DNA to any of 12 viral or bacterial pathogens commonly found in aquatic animals. When assessed with 86 field samples, the assay detected SDDV in DNA extracted from each of 34 scale drop disease-affected fish collected from 5 affected farms. The qPCR also detected SDDV in DNA from 30 of 52 overtly healthy fish collected from 9 farms where SDDV had not been detected previously, using a semi-nested conventional PCR. The higher sensitivity of our SDDV qPCR assay can thus be useful in detecting fish with subclinical/chronic infections. However, the qPCR showed that SDDV DNA loads varied from 8.0 × 10 2 to 6.8 × 10 4 viral DNA copies per 200 ng DNA template among the 8 organ tissue types sampled from 3 diseased fish. In circumstances requiring SDDV to be detected unequivocally in subclinical carriers with lower-level infection, qPCR testing of more than one type of tissue is advisable.
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