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用于快速检测白斑综合征病毒(WSSV)的现场可用侧向流动免疫测定法。

Field-Usable Lateral Flow Immunoassay for the Rapid Detection of White Spot Syndrome Virus (WSSV).

作者信息

Kulabhusan Prabir Kumar, Rajwade Jyutika M, Sugumar Vimal, Taju Gani, Sahul Hameed A S, Paknikar Kishore M

机构信息

Nanobioscience Group, Agharkar Research Institute, Pune, India.

OIE Reference Laboratory for WTD, C. Abdul Hakeem College, Melvisharam, Tamilnadu, India.

出版信息

PLoS One. 2017 Jan 3;12(1):e0169012. doi: 10.1371/journal.pone.0169012. eCollection 2017.

Abstract

BACKGROUND

White spot disease (WSD), a major threat to sustainable aquaculture worldwide, is caused by White spot syndrome virus (WSSV). The diagnosis of WSD relies heavily on molecular detection of the virus by one-step PCR. These procedures are neither field-usable nor rapid enough considering the speed at which the virus spreads. Thus, development of a rapid, reliable and field-usable diagnostic method for the detection of WSSV infection is imperative to prevent huge economic losses.

METHODS/PRINCIPAL FINDINGS: Here, we report on the development of a lateral flow immunoassay (LFIA) employing gold nanoparticles conjugated to a polyclonal antibody against VP28 (envelope protein of WSSV). The LFIA detected WSSV in 20 min and showed no cross-reactivity with other shrimp viruses, viz. Monodon Baculovirus (MBV), Hepatopancreatic parvovirus (HPV) and Infectious Hypodermal and Hematopoietic Necrosis virus (IHHNV). The limit of detection (LOD) of the assay, as determined by real-time PCR, was 103 copies of WSSV. In a time course infectivity experiment, ~104 WSSV particles were injected in Litopenaeus vannamei. The LFIA could rapidly ( 20 min) detect the virus in different tissues after 3 h (hemolymph), 6 h (gill tissue) and 12 h (head soft tissue, eye stalk, and pleopod) of infection. Based on these findings, a validation study was performed using 75 field samples collected from different geographical locations in India. The LFIA results obtained were compared with the conventional "gold standard test", viz. one-step PCR. The analysis of results in 2x2 matrix indicated very high sensitivity (100%) and specificity (96.77%) of LFIA. Similarly, Cohen's kappa coefficient of 0.983 suggested "very good agreement" between the developed LFIA and the conventional one-step PCR.

CONCLUSION

The LFIA developed for the rapid detection of WSSV has an excellent potential for use in the field and could prove to be a boon to the aquaculture industry.

摘要

背景

白斑病(WSD)是全球可持续水产养殖的主要威胁,由白斑综合征病毒(WSSV)引起。WSD的诊断严重依赖于通过一步法PCR对病毒进行分子检测。考虑到病毒传播的速度,这些方法既不便于现场使用,也不够快速。因此,开发一种快速、可靠且便于现场使用的诊断方法来检测WSSV感染对于防止巨大的经济损失至关重要。

方法/主要发现:在此,我们报告了一种侧向流动免疫分析(LFIA)的开发,该分析采用了与抗VP28(WSSV包膜蛋白)多克隆抗体偶联的金纳米颗粒。LFIA在约20分钟内检测到WSSV,并且与其他虾类病毒没有交叉反应,即对虾杆状病毒(MBV)、肝胰腺细小病毒(HPV)和传染性皮下及造血组织坏死病毒(IHHNV)均无交叉反应。通过实时PCR确定的该分析的检测限(LOD)为103个WSSV拷贝。在一个时间进程感染性实验中,向凡纳滨对虾注射了约104个WSSV颗粒。LFIA能够在感染3小时(血淋巴)、6小时(鳃组织)和12小时(头部软组织、眼柄和腹足)后快速(约20分钟)检测到不同组织中的病毒。基于这些发现,使用从印度不同地理位置收集的75份现场样本进行了验证研究。将获得的LFIA结果与传统的“金标准测试”即一步法PCR进行比较。2x2矩阵中的结果分析表明LFIA具有非常高的灵敏度(100%)和特异性(96.77%)。同样,科恩kappa系数为0.9 (100%) and specificity (96.77%) of LFIA. Similarly, Cohen's kappa coefficient of 0.983 suggested "very good agreement" between the developed LFIA and the conventional one-step PCR.

结论

开发的用于快速检测WSSV的LFIA在现场使用方面具有巨大潜力,可能会成为水产养殖业的福音。 83表明开发的LFIA与传统的一步法PCR之间“非常吻合”。

结论

开发的用于快速检测WSSV的LFIA在现场使用方面具有巨大潜力,可能会成为水产养殖业的福音。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d1d/5207695/2b68dbd64570/pone.0169012.g001.jpg

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