LAUSR

Simple Summary Phytoplasmas are a group of phloem-restricted phytopathogens that attack a huge number of wild and cultivated plants, causing heavy economic losses. They are transmitted by phloem-feeding insects of the order Hemiptera; the transmission process requires the vector to orally acquire the phytoplasma by feeding on an infected plant, becoming infective once it reaches the salivary glands after quite a long latency period. Since infection is retained for all of the insect’s life, acquisition at the nymphal stage is considered to be most effective because of the long time needed before pathogen inoculation. This work provides evidence for the reduced latency period needed by adults of the phytoplasma vector Euscelidius variegatus from flavescence dorée phytoplasma acquisition to transmission. Indeed, we demonstrate that adults can become infective as soon as 9 days from the beginning of phytoplasma acquisition. Our results support a reconsideration of the role of adults in phytoplasma epidemiology, by indicating their extended potential ability to complete the full transmission process. Abstract Phytoplasma transmission takes place by insect vectors through an Acquisition Access Period (AAP), Latency Period (LP) and Inoculation Access Period (IAP). Generally, phytoplasmas are believed to be transmitted more efficiently by nymphs because they need a long LP to reach the salivary glands before becoming infective. The transmission can start from adults as well, but in this case a long LP may exceed the insect’s lifespan. However, previous evidence has indicated that adults can undergo a shorter LP, even though little knowledge is available regarding the phytoplasma temporal dynamics during this period. Here, we investigate the minimum time required by the phytoplasma to colonize the vector midgut and salivary glands, and finally to be inoculated into a plant. We used the leafhopper Euscelidius variegatus to investigate the life cycle of flavescence dorée phytoplasma (FDP). Phytoplasma-free E. variegatus adults were left on broad beans (BBs) infected with FDP for an AAP of 7 days. Subsequently, they were individually transferred onto a healthy BB for seven different IAPs, each one lasting 24 h from day 8 to 14. Molecular analyses and fluorescence in situ hybridization were performed for FDP detection. FDP was found in the leafhopper midgut from IAP 1 with an infection rate reaching 50%, whereas in the salivary glands it was found from IAP 2 with an infection rate reaching 30%. FDP was also detected in BBs from IAP 4, with infection rates reaching 10%. Our results represent an important step to further deepen the knowledge of phytoplasma transmission and its epidemiology.