Plant viruses are the causal agents of many plant diseases and the subsequent economic losses, es�mated to be US$60 billion worldwide each year. The melon necro�c spot virus (MNSV) is a small, single-stranded, posi�ve-sense RNA virus that belongs to the genus Gammacarmovirus and encodes five proteins. The coat protein (CP) is composed of three dis�nct domains. The R domain is responsible for binding to different RNA molecules and can be divided into two subdomains: R1 and R2. This domain is connected to the S domain by the arm region, which is also part of the RNA binding domain. The main func�on of the S domain is genome protec�on and transmission when forming virions. It is followed by the P domain, which is the interac�on site for the vector fungus zoospores. The discovery of a dual transit pep�de in the amino-terminal part of the CP was the star�ng point of this thesis. Early in MNSV infec�on, the new synthesized CP is imported into chloroplasts and mitochondria, while the cytoplasmic pool increases as the infec�on progresses. Inhibi�ng this dual transport leads to an increase in the RNA silencing suppressor ac�vity of the CP. However, far from resul�ng in an enhanced infec�on development, systemic spread was impaired. Therefore, the accumula�on of cytoplasmic CP may cause an increase in viral replica�on and overexpression of p29, an auxiliary replicase that causes morphological altera�ons, ROS, and necrosis that may restrict viral movement. Thus, a new role for CP targe�ng would be to avoid excessive viral replica�on by modula�ng the suppressor ac�vity to manage the balance between plant defense and viral counter-defense, leading to a compa�ble interac�on.Unfortunately, Arabidopsis thaliana is not a host for MNSV. Thus, to beter understand the molecular mechanism behind the CP dual targe�ng, the receptors and pores of the Nicotiana benthamiana mitochondrial and chloroplast outer membrane translocons were genome iden�fied, and some func�onal characteriza�on was carried out. We assigned the following names NbToc75-III, NbToc34, NbToc90, NbToc120, NbToc159A, NbToc159B, NbTic22-III for chloroplast translocon components, and NbTom40, NbTom20-1, NbTom20-2, NbOm64 for mitochondrion translocon components. The func�onal characteriza�on was mainly carried out by virus-induced gene silencing (VIGS) and RT-qPCR, revealing a func�onal redundancy higher than that reported for Arabidopsis homologs. Addi�onally, VIGS was also used to evaluate the relevance of each translocon component in MNSV infec�on, and together with