Résumé
Palm lethal yellowing phytoplasmas (PLYPs) are a group of phytoplasmas that cause death in infected hosts across the tropics. Historically, detection and identification has relied on standard PCR, nested PCR, and restriction fragment length polymorphism. While these approaches are generally good, they are prone to error and contamination that is significantly lower or absent in modern approaches using quantitative PCR (qPCR) and digital PCR (dPCR). Additionally, these modern approaches are more time-efficient and consume fewer resources, making them more cost-effective in the long term. Recent studies have adapted dPCR and qPCR coupled with high-resolution melt curve analysis (HRMA) for PLYPs in the Caribbean/New World; however, these tools have not been developed for phytoplasmas in Africa and Madagascar. In this study, a duplex dPCR assay was developed with two specific assays, one for 'Candidatus Phytoplasma palmicola' and one for 'Ca. P. cocostanzaniae' and isolates from Madagascar. Additionally, primers targeting the secA gene were optimized and allowed for the separation of 'Ca. P. cocostanzaniae' and Malagasy isolates by approximately one degree Celsius. New primers were developed based on secA for 'Ca. P. palmicola' that allowed for the separation of the two subgroups (A and B) by HRMA by a difference of approximately one degree Celsius. These assays provide a valuable resource to explore aspects such as vector discovery and host range.