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利用脂多糖特异性单克隆抗体开发基于微珠的Luminex检测法,以检测布鲁氏菌属的生物威胁。

Development of a bead-based Luminex assay using lipopolysaccharide specific monoclonal antibodies to detect biological threats from Brucella species.

作者信息

Silbereisen Angelika, Tamborrini Marco, Wittwer Matthias, Schürch Nadia, Pluschke Gerd

机构信息

Department of Medical Parasitology and Infection Biology, Swiss Tropical and Public Health Institute, Basel, Switzerland.

University of Basel, Basel, Switzerland.

出版信息

BMC Microbiol. 2015 Oct 5;15:198. doi: 10.1186/s12866-015-0534-1.

Abstract

BACKGROUND

Brucella, a Gram-negative bacterium, is classified as a potential bioterrorism agent mainly due to the low dose needed to cause infection and the ability to transmit the bacteria via aerosols. Goats/sheep, cattle, pigs, dogs, sheep and rodents are infected by B. melitensis, B. abortus, B. suis, B. canis, B. ovis and B. neotomae, respectively, the six classical Brucella species. Most human cases are caused by B. melitensis and B. abortus. Our aim was to specifically detect Brucellae with 'smooth' lipopolysaccharide (LPS) using a highly sensitive monoclonal antibody (mAb) based immunological assay.

METHODS

To complement molecular detection systems for potential bioterror agents, as required by international biodefense regulations, sets of mAbs were generated by B cell hybridoma technology and used to develop immunological assays. The combination of mAbs most suitable for an antigen capture assay format was identified and an immunoassay using the Luminex xMAP technology was developed.

RESULTS

MAbs specific for the LPS O-antigen of Brucella spp. were generated by immunising mice with inactivated B. melitensis or B. abortus cells. Most mAbs recognised both B. melitensis and B. abortus and antigen binding was not impeded by inactivation of the bacterial cells by γ irradiation, formalin or heat treatment, a step required to analyse the samples immunologically under biosafety level two conditions. The Luminex assay recognised all tested Brucella species with 'smooth' LPS with detection limits of 2×10(2) to 8×10(4) cells per mL, depending on the species tested. Milk samples spiked with Brucella spp. cells were identified successfully using the Luminex assay. In addition, the bead-based immunoassay was integrated into a multiplex format, allowing for simultaneous, rapid and specific detection of Brucella spp., Bacillus anthracis, Francisella tularensis and Yersinia pestis within a single sample.

CONCLUSION

Overall, the robust Luminex assay should allow detection of Brucella spp. in both natural outbreak and bio-threat situations.

摘要

背景

布鲁氏菌是一种革兰氏阴性菌,主要因其导致感染所需剂量低以及能够通过气溶胶传播细菌,而被列为潜在的生物恐怖主义病原体。山羊/绵羊、牛、猪、狗、绵羊和啮齿动物分别被马尔他布鲁氏菌、流产布鲁氏菌、猪布鲁氏菌、犬布鲁氏菌、绵羊布鲁氏菌和新墨西哥布鲁氏菌感染,这六种是经典的布鲁氏菌物种。大多数人类病例由马尔他布鲁氏菌和流产布鲁氏菌引起。我们的目的是使用基于高灵敏度单克隆抗体(mAb)的免疫测定法特异性检测具有“光滑”脂多糖(LPS)的布鲁氏菌。

方法

为了按照国际生物防御法规的要求补充针对潜在生物恐怖病原体的分子检测系统,通过B细胞杂交瘤技术制备了多组单克隆抗体,并用于开发免疫测定法。确定了最适合抗原捕获测定形式的单克隆抗体组合,并开发了使用Luminex xMAP技术的免疫测定法。

结果

通过用灭活的马尔他布鲁氏菌或流产布鲁氏菌细胞免疫小鼠,产生了对布鲁氏菌属LPS O抗原具有特异性的单克隆抗体。大多数单克隆抗体能识别马尔他布鲁氏菌和流产布鲁氏菌,并且通过γ射线照射、福尔马林或热处理使细菌细胞失活不会妨碍抗原结合,这是在生物安全二级条件下对样品进行免疫分析所需的步骤。Luminex测定法能够识别所有具有“光滑”LPS的测试布鲁氏菌物种,检测限为每毫升2×10²至8×10⁴个细胞,具体取决于所测试的物种。使用Luminex测定法成功鉴定了添加了布鲁氏菌属细胞的牛奶样品。此外,基于微珠的免疫测定法被整合到多重检测形式中,能够在单个样品中同时、快速且特异性地检测布鲁氏菌属、炭疽芽孢杆菌、土拉弗朗西斯菌和鼠疫耶尔森菌。

结论

总体而言,强大的Luminex测定法应能够在自然爆发和生物威胁情况下检测布鲁氏菌属。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b536/4595103/db6d68b631de/12866_2015_534_Fig2_HTML.jpg

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