کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
3406683 1223585 2013 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Development and application of antibody microarray for lymphocystis disease virus detection in fish
موضوعات مرتبط
علوم زیستی و بیوفناوری ایمنی شناسی و میکروب شناسی ویروس شناسی
پیش نمایش صفحه اول مقاله
Development and application of antibody microarray for lymphocystis disease virus detection in fish
چکیده انگلیسی


• Antibody microarray with high specificity was developed for LCDV detection in fish.
• Influences of supports, markers and storage time on sensitivity were tested.
• The lowest detection limit of microarray was 68.6 ng/ml of LCDV.
• The microarray has a shelf-life of more than 8 months at −20 °C.
• It has a concordance rate of 100% with ELISA and 98% with IFAT in LCDV detection.

Lymphocystis disease virus (LCDV) is the causative agent of lymphocystis disease affecting marine and freshwater fish worldwide. Here an antibody microarray was developed and employed to detect LCDV in fish. Rabbit anti-LCDV serum was arrayed on agarose gel-modified slides as capture antibody, and Cy3-conjugated anti-LCDV monoclonal antibody (MAbs) was added as detection antibody. The signals were imaged with a laser chip scanner and analyzed by corresponding software. To improve the sensitivity, different substrate binders (poly-l-lysine, MPTS, aldehyde, APES and agarose gel modified slides, and commercially available amino-modified slides), markers (fluorescein isothiocyanate, Cy3, horseradish peroxidase, biotin or colloidal gold) conjugated to anti-LCDV Mabs, and storage time of the antibody were assessed. The results showed that the antibody microarrays based on agarose gel-modified slides gave a lower detection limit of 0.55 μg/ml of LCDV when Cy3 and HRP conjugated anti-LCDV MAbs were used as detection antibody; and the lowest detectable LCDV protein concentration was 0.0686 μg/ml when streptavidin–biotin conjugated to anti-LCDV MAbs served as detection antibody. The developed antibody microarray proved to have a high specificity for LCDV detection and a shelf-life of more than 8 months at −20 °C. Furthermore, the LCDV detection results of the microarray in fish gills or fins (n = 50) presented a concordance rate of 100% with enzyme-linked immunosorbent assay (ELISA) and 98% with immunofluorescence assay technique (IFAT). These results revealed that the developed antibody microarray could serve as an effective tool for diagnostic and epidemiological studies of LCDV in fish.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Virological Methods - Volume 189, Issue 2, May 2013, Pages 243–249
نویسندگان
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