López-Soriano Pablo, Noguera Patricia, Gorris María Teresa, Puchades Rosa, Maquieira Ángel, Marco-Noales Ester, López María M
Centro de Protección Vegetal, Instituto Valenciano de Investigaciones Agrarias, Moncada, Valencia, Spain.
Instituto Universitario de Reconocimiento Molecular y Desarrollo Tecnológico, Departamento de Química, Universitat Politècnica de València, València, Spain.
PLoS One. 2017 Apr 27;12(4):e0176201. doi: 10.1371/journal.pone.0176201. eCollection 2017.
Xanthomonas arboricola pv. pruni is a quarantine pathogen and the causal agent of the bacterial spot disease of stone fruits and almond, a major threat to Prunus species. Rapid and specific detection methods are essential to improve disease management, and therefore a prototype of a lateral flow immunoassay (LFIA) was designed for the detection of X. arboricola pv. pruni in symptomatic field samples. It was developed by producing polyclonal antibodies which were then combined with carbon nanoparticles and assembled on nitrocellulose strips. The specificity of the LFIA was tested against 87 X. arboricola pv. pruni strains from different countries worldwide, 47 strains of other Xanthomonas species and 14 strains representing other bacterial genera. All X. arboricola pv. pruni strains were detected and cross-reactions were observed only with four strains of X. arboricola pv. corylina, a hazelnut pathogen that does not share habitat with X. arboricola pv. pruni. The sensitivity of the LFIA was assessed with suspensions from pure cultures of three X. arboricola pv. pruni strains and with spiked leaf extracts prepared from four hosts inoculated with this pathogen (almond, apricot, Japanese plum and peach). The limit of detection observed with both pure cultures and spiked samples was 104 CFU ml-1. To demonstrate the accuracy of the test, 205 samples naturally infected with X. arboricola pv. pruni and 113 samples collected from healthy plants of several different Prunus species were analyzed with the LFIA. Results were compared with those obtained by plate isolation and real time PCR and a high correlation was found among techniques. Therefore, we propose this LFIA as a screening tool that allows a rapid and reliable diagnosis of X. arboricola pv. pruni in symptomatic plants.
李生黄单胞菌李致病型是一种检疫性病原菌,是核果类和杏仁细菌性穿孔病的病原,对李属物种构成重大威胁。快速且特异的检测方法对于改善病害管理至关重要,因此设计了一种用于检测有症状田间样本中李生黄单胞菌李致病型的侧向流动免疫分析(LFIA)原型。它是通过制备多克隆抗体,然后将其与碳纳米颗粒结合并组装在硝酸纤维素条上而开发的。针对来自全球不同国家的87株李生黄单胞菌李致病型菌株、47株其他黄单胞菌属菌株以及代表其他细菌属的14株菌株,对该LFIA的特异性进行了测试。所有李生黄单胞菌李致病型菌株均被检测到,仅与4株榛树病原菌李生黄单胞菌榛致病型菌株发生了交叉反应,该病原菌与李生黄单胞菌李致病型不共享栖息地。使用三株李生黄单胞菌李致病型菌株纯培养物的悬浮液以及用该病原菌接种的四种寄主(杏仁、杏、日本李和桃)制备的加标叶片提取物,评估了LFIA的灵敏度。在纯培养物和加标样本中观察到的检测限均为104 CFU ml-1。为了证明该检测的准确性,使用LFIA分析了205份自然感染李生黄单胞菌李致病型的样本以及从几种不同李属物种的健康植株上采集的113份样本。将结果与平板分离法和实时PCR法获得的结果进行比较,发现各技术之间具有高度相关性。因此,我们建议将这种LFIA作为一种筛查工具,用于对有症状植物中的李生黄单胞菌李致病型进行快速可靠的诊断。