Przewodowski Włodzimierz, Przewodowska Agnieszka
Plant Breeding and Acclimatization Institute - National Research Institute, Department of Potato Protection and Seed Science at Bonin, Poland.
PLoS One. 2017 Jan 9;12(1):e0169785. doi: 10.1371/journal.pone.0169785. eCollection 2017.
The quarantine bacterium Clavibacter michiganensis subsp. sepedonicus (Cms) causes bacterial ring rot (BRR) in potato but is difficult to detect, hampering the diagnosis of this disease. ELISA immunoassays have not been widely used to detect Cms because commercially available anti-Cms antibodies detect mainly EPS-producing bacteria and can fail to detect strains that do not produce EPS. In the current study, we developed a new type of polyclonal antibody that specifically detects Clavibacter michiganensis subsp. sepedonicus bacteria irrespective of their EPS level. We first found that the presence of bacterial EPS precluded quantitative measurement of bacteria by currently available immunoenzymatic methods, but that washing Cms cells with acidic and basic buffers to remove EPS before analysis successfully standardized ELISA results. We used a mix of three strains of Cms with diverse EPS levels to generate antigen for production of antibodies recognizing Cms cells with and without an EPS layer (IgG-EPS and IgG-N-EPS, respectively). The resulting IgG-N-EPS recognized almost all Cms strains tested in this work regardless of their mucoidal level. The availability of this new antibody renders immunological diagnostics of Cms more sensitive and reliable, as our newly developed antibodies can be used in many type of immunoassays. This work represents an important step forward in efforts to diagnose and prevent the spread of BRR, and the methods and solutions developed in this work are covered by six Polish, one European and one US patents.
检疫性细菌密执安棒杆菌马铃薯环腐亚种(Cms)可引发马铃薯细菌性环腐病(BRR),但难以检测,这阻碍了该病害的诊断。酶联免疫吸附测定(ELISA)免疫分析尚未广泛用于检测Cms,因为市售的抗Cms抗体主要检测产生胞外多糖(EPS)的细菌,可能无法检测不产生EPS的菌株。在本研究中,我们开发了一种新型多克隆抗体,可特异性检测密执安棒杆菌马铃薯环腐亚种细菌,而不论其EPS水平如何。我们首先发现,细菌EPS的存在妨碍了通过现有免疫酶法对细菌进行定量测量,但在分析前用酸性和碱性缓冲液洗涤Cms细胞以去除EPS,成功使ELISA结果标准化。我们使用了三株EPS水平不同的Cms菌株混合物来制备抗原,以生产识别有和没有EPS层的Cms细胞的抗体(分别为IgG-EPS和IgG-N-EPS)。所得的IgG-N-EPS识别了本研究中测试的几乎所有Cms菌株,而不论其黏液水平如何。这种新抗体的可用性使Cms的免疫诊断更加灵敏和可靠,因为我们新开发的抗体可用于多种免疫分析。这项工作是在诊断和预防BRR传播方面向前迈出的重要一步,并且本工作中开发的方法和解决方案已获得六项波兰专利、一项欧洲专利和一项美国专利。