Cellier Gilles, Arribat Sandrine, Chiroleu Frédéric, Prior Philippe, Robène Isabelle
Tropical Pests and Diseases Unit, Plant Health Laboratory, ANSESSaint-Pierre, France.
UMR Peuplements Végétaux et Bioagresseurs en Milieu Tropical, CIRADSaint-Pierre, France.
Front Plant Sci. 2017 May 24;8:821. doi: 10.3389/fpls.2017.00821. eCollection 2017.
is a well-known agricultural and ecological threat worldwide. The complexity of the species complex (Rssc) represents a challenge for the accurate characterization of epidemiological strains by official services and research laboratories. The majority of protocols only focus on a narrow range of strains; however, this species complex includes strains that represent major constraints and are under strict regulation. The main drawback associated with the current methods of detecting and characterizing Rssc strains is their reliance on combining different protocols to properly characterize the strains at the ecotype level, which require time and money. Therefore, we used microarray technology (ArrayTube) to develop a standard protocol, which characterizes 17 major groups of interest in the Rssc, in a single multiplex reaction. These 17 majors groups are linked with a phylogenetic assignation (phylotypes, sequevars), but also with an ecotype assignation associated with a range of hosts (e.g., brown rot, Moko). Probes were designed with a 50-mer length constraint and thoroughly evaluated for any flaws or secondary structures. The strains are characterized based on a DNA extraction from pure culture. Validation data showed strong intra-repeatability, inter-repeatability, and reproducibility as well as good specificity. A hierarchical analysis of the probe groups is suitable for an accurate characterization. Compared with single marker detection tests, the method described in this paper addresses efficiently the issue of combining several tests by testing a large number of phylogenetic markers in a single reaction assay. This custom microarray (RsscAT) represents a significant improvement in the epidemiological monitoring of Rssc strains worldwide, and it has the potential to provide insights for phylogenetic incongruence of Rssc strains based on the host of isolation and may be used to indicate potentially emergent strains.
是全球范围内广为人知的农业和生态威胁。该物种复合体(Rssc)的复杂性给官方服务机构和研究实验室准确鉴定流行病学菌株带来了挑战。大多数检测方案仅关注范围狭窄的菌株;然而,这个物种复合体包含一些构成主要限制因素且受到严格监管的菌株。当前检测和鉴定Rssc菌株方法的主要缺点是,它们依赖于组合不同的方案来在生态型水平上正确鉴定菌株,这既耗时又费钱。因此,我们使用微阵列技术(ArrayTube)开发了一种标准方案,该方案能在单一多重反应中鉴定Rssc中17个主要的目标菌群。这17个主要菌群不仅与系统发育分类(系统型、序列变种)相关,还与一系列宿主(如褐腐病、莫科病)相关的生态型分类有关。设计的探针长度限制为50个碱基对,并对其任何缺陷或二级结构进行了全面评估。基于从纯培养物中提取的DNA对菌株进行鉴定。验证数据显示出很强的内部重复性、相互重复性和再现性以及良好的特异性。对探针组进行层次分析适用于准确鉴定。与单标记检测试验相比,本文所述方法通过在单一反应测定中检测大量系统发育标记,有效解决了组合多个试验的问题。这种定制微阵列(RsscAT)代表了全球Rssc菌株流行病学监测的重大改进,它有可能基于分离宿主为Rssc菌株的系统发育不一致性提供见解,并可用于指示潜在的新出现菌株。