通过新型视频显微镜测定法,针对鞭毛蛋白 A 或 B 的抗血清可抑制铜绿假单胞菌的运动。

IF 1.6 4区 医学 Q4 BIOCHEMICAL RESEARCH METHODS
Ethel Apolinario , James Sinclair , Myeongjin Choi , Kun Luo , Surekha Shridhar , Sharon M. Tennant , Raphael Simon , Erik Lillehoj , Alan Cross
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引用次数: 0

摘要

鞭毛介导的运动对铜绿假单胞菌(P. aeruginosa)的毒力至关重要。针对鞭毛蛋白的抗体可降低运动能力,抑制细菌从感染部位扩散。证明抗鞭毛虫运动抑制的标准软琼脂试验需要较长的培养时间,难以解释,而且需要大量抗体。我们开发了一种延时视频显微镜方法来分析抗鞭毛虫素对铜绿微囊藻运动的抑制作用,这种方法与软琼脂检测法相比具有多项优势。用A型或B型鞭毛蛋白免疫小鼠的抗血清与表达绿色荧光蛋白(GFP)的铜绿假单胞菌菌株PAO1(FlaB+)和表达GFP的铜绿假单胞菌菌株PAK(FlaA+)孵育。我们分析了以十秒时间间隔拍摄的视频中细菌的运动情况。在加入少量鞭毛蛋白抗血清后的几分钟内,我们在显微镜下观察到细菌运动明显减少。通过数据分析,我们能够量化试验血清中抗鞭毛虫素抗体对降低铜绿假单胞菌运动的功效。与标准的软琼脂运动抑制试验相比,这种评估抗鞭毛虫素抗体功能活性的新型视频显微镜方法需要的血清更少、时间更短、终点更稳定、可重复性更好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antisera against flagellin A or B inhibits Pseudomonas aeruginosa motility as measured by novel video microscopy assay

Flagellum-mediated motility is essential to Pseudomonas aeruginosa (P. aeruginosa) virulence. Antibody against flagellin reduces motility and inhibits the spread of the bacteria from the infection site. The standard soft-agar assay to demonstrate anti-flagella motility inhibition requires long incubation times, is difficult to interpret, and requires large amounts of antibody. We have developed a time-lapse video microscopy method to analyze anti-flagellin P. aeruginosa motility inhibition that has several advantages over the soft agar assay. Antisera from mice immunized with flagellin type A or B were incubated with Green Fluorescent Protein (GFP)-expressing P. aeruginosa strain PAO1 (FlaB+) and GFP-expressing P. aeruginosa strain PAK (FlaA+). We analyzed the motion of the bacteria in video taken in ten second time intervals. An easily measurable decrease in bacterial locomotion was observed microscopically within minutes after the addition of small volumes of flagellin antiserum. From data analysis, we were able to quantify the efficacy of anti-flagellin antibodies in the test serum that decreased P. aeruginosa motility. This new video microscopy method to assess functional activity of anti-flagellin antibodies required less serum, less time, and had more robust and reproducible endpoints than the standard soft agar motility inhibition assay.

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来源期刊
CiteScore
4.10
自引率
0.00%
发文量
120
审稿时长
3 months
期刊介绍: The Journal of Immunological Methods is devoted to covering techniques for: (1) Quantitating and detecting antibodies and/or antigens. (2) Purifying immunoglobulins, lymphokines and other molecules of the immune system. (3) Isolating antigens and other substances important in immunological processes. (4) Labelling antigens and antibodies. (5) Localizing antigens and/or antibodies in tissues and cells. (6) Detecting, and fractionating immunocompetent cells. (7) Assaying for cellular immunity. (8) Documenting cell-cell interactions. (9) Initiating immunity and unresponsiveness. (10) Transplanting tissues. (11) Studying items closely related to immunity such as complement, reticuloendothelial system and others. (12) Molecular techniques for studying immune cells and their receptors. (13) Imaging of the immune system. (14) Methods for production or their fragments in eukaryotic and prokaryotic cells. In addition the journal will publish articles on novel methods for analysing the organization, structure and expression of genes for immunologically important molecules such as immunoglobulins, T cell receptors and accessory molecules involved in antigen recognition, processing and presentation. Submitted full length manuscripts should describe new methods of broad applicability to immunology and not simply the application of an established method to a particular substance - although papers describing such applications may be considered for publication as a short Technical Note. Review articles will also be published by the Journal of Immunological Methods. In general these manuscripts are by solicitation however anyone interested in submitting a review can contact the Reviews Editor and provide an outline of the proposed review.
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