Ding Fang, Duan Yongping, Paul Cristina, Brlansky Ronald H, Hartung John S
USDA ARS Molecular Plant Pathology Laboratory, Beltsville, Maryland, United States of America; College of Plant Science and Technology, Huazhong Agricultural University, Wuhan, P. R. China.
USDA ARS Horticultural Research Laboratory, Fort Pierce, Florida, United States of America.
PLoS One. 2015 May 6;10(5):e0123939. doi: 10.1371/journal.pone.0123939. eCollection 2015.
'Candidatus Liberibacter asiaticus' (CaLas), a non-cultured member of the α-proteobacteria, is the causal agent of citrus Huanglongbing (HLB). Due to the difficulties of in vitro culture, antibodies against CaLas have not been widely used in studies of this pathogen. We have used an anti-OmpA polyclonal antibody based direct tissue blot immunoassay to localize CaLas in different citrus tissues and in periwinkle leaves. In citrus petioles, CaLas was unevenly distributed in the phloem sieve tubes, and tended to colonize in phloem sieve tubes on the underside of petioles in preference to the upper side of petioles. Both the leaf abscission zone and the junction of the petiole and leaf midrib had fewer CaLas bacteria compared to the main portions of the petiole and the midribs. Colonies of CaLas in phloem sieve tubes were more frequently found in stems with symptomatic leaves than in stems with asymptomatic leaves with an uneven distribution pattern. In serial sections taken from the receptacle to the peduncle, more CaLas were observed in the peduncle sections adjacent to the stem. In seed, CaLas was located in the seed coat. Many fewer CaLas were found in the roots, as compared to the seeds and petioles when samples were collected from trees with obvious foliar symptoms. The direct tissue blot immuno assay was adapted to whole periwinkle leaves infected by CaLas. The pathogen was distributed throughout the lateral veins and the results were correlated with results of qPCR. Our data provide direct spatial and anatomical information for CaLas in planta. This simple and scalable method may facilitate the future research on the interaction of CaLas and host plant.
“亚洲韧皮杆菌(暂定种)”(CaLas)是α-变形菌门中一种不可培养的成员,是柑橘黄龙病(HLB)的病原体。由于体外培养存在困难,针对CaLas的抗体尚未广泛应用于该病原体的研究中。我们使用了基于抗OmpA多克隆抗体的直接组织印迹免疫分析法,来定位CaLas在不同柑橘组织和长春花叶片中的位置。在柑橘叶柄中,CaLas在韧皮部筛管中分布不均,并且倾向于在叶柄下侧的韧皮部筛管中定殖,而非上侧。与叶柄和叶脉的主要部分相比,叶片脱落区以及叶柄与叶片中脉的连接处的CaLas细菌较少。与无症状叶片的茎相比,有症状叶片的茎中韧皮部筛管中的CaLas菌落更常见,且分布不均。在从花托到果梗的连续切片中,在靠近茎的果梗切片中观察到更多的CaLas。在种子中,CaLas位于种皮中。当从具有明显叶片症状的树上采集样本时,与种子和叶柄相比,根中发现的CaLas要少得多。直接组织印迹免疫分析法适用于被CaLas感染的整个长春花叶片。病原体分布在整个侧脉中,结果与qPCR结果相关。我们的数据为植物体内的CaLas提供了直接的空间和解剖学信息。这种简单且可扩展的方法可能会促进未来对CaLas与寄主植物相互作用的研究。