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A Pathogen Secreted Protein as a Detection Marker for Citrus Huanglongbing

机译:病原体分泌蛋白作为柑橘黄龙病的检测标记

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摘要

The citrus industry is facing an unprecedented crisis due to Huanglongbing (HLB, aka citrus greening disease), a bacterial disease associated with the pathogen Candidatus Liberibacter asiaticus (CLas) that affects all commercial varieties. Transmitted by the Asian citrus psyllid (ACP), CLas colonizes citrus phloem, leading to reduced yield and fruit quality, and eventually tree decline and death. Since adequate curative measures are not available, a key step in HLB management is to restrict the spread of the disease by identifying infected trees and removing them in a timely manner. However, uneven distribution of CLas cells in infected trees and the long latency for disease symptom development makes sampling of trees for CLas detection challenging. Here, we report that a CLas secreted protein can be used as a biomarker for detecting HLB infected citrus. Proteins secreted from CLas cells can presumably move along the phloem, beyond the site of ACP inoculation and CLas colonized plant cells, thereby increasing the chance of detecting infected trees. We generated a polyclonal antibody that effectively binds to the secreted protein and developed serological assays that can successfully detect CLas infection. This work demonstrates that antibody-based diagnosis using a CLas secreted protein as the detection marker for infected trees offers a high-throughput and economic approach that complements the approved quantitative polymerase chain reaction-based methods to enhance HLB management programs.
机译:由于黄龙病(HLB,又称柑橘绿化病),一种与病原体假丝酵母念珠菌(CLas)有关的细菌性疾病,影响了所有商业品种,柑橘业正面临前所未有的危机。 CLas由亚洲柑橘木虱(ACP)传播,在柑橘韧皮部定居,导致产量和果实品质下降,并最终导致树木枯死和死亡。由于没有足够的治疗措施,HLB管理中的关键步骤是通过识别受感染的树木并及时清除它们来限制疾病的传播。但是,受感染树木中CLas细胞的分布不均匀以及疾病症状发展的潜伏期长,使得为CLas检测而对树木进行采样具有挑战性。在这里,我们报告说,CLas分泌蛋白可用作检测HLB感染柑橘的生物标记。从CLas细胞分泌的蛋白质大概可以沿着韧皮部移动,超出ACP接种部位和CLas定植的植物细胞的位置,从而增加了检测被感染树木的机会。我们产生了一种与分泌蛋白有效结合的多克隆抗体,并开发了可以成功检测CLas感染的血清学检测方法。这项工作表明,使用CLas分泌蛋白作为被感染树木的检测标志物的基于抗体的诊断提供了一种高通量和经济的方法,可补充已批准的基于定量聚合酶链反应的方法来增强HLB管理程序。

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