“…A prerequisite to control the spread of viruses in forest trees or woody crops is to have a sensitive and specific diagnostic procedure at hand. Viruses in these plants are often difficult to detect because of their low and uneven concentration within the tissues (G arrett et al, 1985; W erner et al, 1997). Furthermore, the presence of secondary metabolites such as tannins and polysaccharides complicate the analysis of virus‐infected plant material (C lark et al, 1976; N ewbury and P ossingham , 1977; S ingh et al, 2002).…”
Section: Discussionmentioning
confidence: 99%
“…Thus, although EMARAV could not be identified as the causative agent of the ringspot disease yet, and although the transmission of the virus is still unclear, a rapid spreading through commercial distribution of infected seedlings from nurseries of the virus should be avoided by establishing a reliable detection method for EMARAV. High sensitivity of this analysis is essential because of the low concentration and heterogeneous distribution of virus particles in woody plants (G arrett et al, 1985; W erner et al, 1997).…”
Chlorotic ringspots and mottling on leaves of European mountain ash (Sorbus aucuparia L.) are typical symptoms of the widely distributed ringspot disease. We found a novel plant RNA virus with a multipartite genome associated with these symptoms, called European mountain ash ringspot-associated virus (EMARAV). This virus is not classified yet but shows certain similarities to members of the virus family Bunyaviridae. Characterization of the complete viral genome of EMARAV allowed us to develop two sensitive procedures, which enable the specific detection in its host plant. By raising an antiserum against the N-terminal part of the putative nucleocapsid protein p3, the detection of EMARAV, respectively its proteins, in leaf extracts is now feasible. A second diagnostic tool, the reverse transcription-PCR (RT-PCR), allows the detection of EMARAV with even higher sensitivity. One specific primer pair was deduced from each of the four viral genomic RNAs to amplify minute amounts of the virus in various plant tissues.
“…A prerequisite to control the spread of viruses in forest trees or woody crops is to have a sensitive and specific diagnostic procedure at hand. Viruses in these plants are often difficult to detect because of their low and uneven concentration within the tissues (G arrett et al, 1985; W erner et al, 1997). Furthermore, the presence of secondary metabolites such as tannins and polysaccharides complicate the analysis of virus‐infected plant material (C lark et al, 1976; N ewbury and P ossingham , 1977; S ingh et al, 2002).…”
Section: Discussionmentioning
confidence: 99%
“…Thus, although EMARAV could not be identified as the causative agent of the ringspot disease yet, and although the transmission of the virus is still unclear, a rapid spreading through commercial distribution of infected seedlings from nurseries of the virus should be avoided by establishing a reliable detection method for EMARAV. High sensitivity of this analysis is essential because of the low concentration and heterogeneous distribution of virus particles in woody plants (G arrett et al, 1985; W erner et al, 1997).…”
Chlorotic ringspots and mottling on leaves of European mountain ash (Sorbus aucuparia L.) are typical symptoms of the widely distributed ringspot disease. We found a novel plant RNA virus with a multipartite genome associated with these symptoms, called European mountain ash ringspot-associated virus (EMARAV). This virus is not classified yet but shows certain similarities to members of the virus family Bunyaviridae. Characterization of the complete viral genome of EMARAV allowed us to develop two sensitive procedures, which enable the specific detection in its host plant. By raising an antiserum against the N-terminal part of the putative nucleocapsid protein p3, the detection of EMARAV, respectively its proteins, in leaf extracts is now feasible. A second diagnostic tool, the reverse transcription-PCR (RT-PCR), allows the detection of EMARAV with even higher sensitivity. One specific primer pair was deduced from each of the four viral genomic RNAs to amplify minute amounts of the virus in various plant tissues.
“…Thus, seeds and pollen can play a role in the epidemiology of some almond-infecting ilarviruses. For instance, the presence of PDV and PNRSV in pollen grains may lead, in principle, to both a direct transmission (to the seeds at least) through fertilization mediated by pollinating insects and an indirect transmission by thrips (Garret et al, 1985). The epidemiological role of seeds seems important only for PNRSV, which is the least economically relevant of the three ilarviruses.…”
The major and most widespread virus‐induced disorder of almond is a complex disease called mosaic. The disease is characterized by a variety of symptoms ranging from bright chrome‐yellow (calico) to chlorotic discolorations, localized necrosis of the leaf blade, leaf curling, bud failure, fasciations, rosetting, stunting and bushy growth. Three ilarviruses, apple mosaic (ApMV), prune dwarf (PDV) and prunus necrotic ringspot (PNRSV), are associated with almond mosaic throughout the Mediterranean, and are involved to different extents in its aetiology. Apple chlorotic leaf spot trichovirus (ACLSV) may also be present in mosaic‐affected plants, and is sometimes associated with a chlorotic leafroll condition. Two epoviruses, tomato ringspot (ToRSV) and tomato black ring (TBRV), have been reported from the USA and Europe as the agents of diseases called yellow bud mosaic and enations, respectively. Plum pox potyvirus (PPV) and another filamentous virus, prunus latent virus (PLV), can also infect almond. Brown line and decline, a putative phytoplasma disease, occurs in California, together with the leaf scorch induced by the xylem‐limited bacterium Xylella fastidiosa. A stem pitting lot associated with nepovirus infection and a graft‐union necrosis apparently not caused by phytoplasmas have been reported from Italy. Infections by hop stunt viroid (HSVd) were recently reported from Spain.
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