PLRV-infected Plants Research Articles

Plant Viruses Transmitted in Two Different Modes Produce Differing Effects on Small RNA-Mediated Processes in Their Aphid Vector

Transmission of plant viruses by aphids involves multitrophic interactions among host plants, aphid vectors, and plant viruses. Here, we used small RNA (sRNA) sequencing to visualize the sRNA response of Myzus persicae to two plant viruses that M. persicae transmits in different modes: the nonpersistent Potato virus Y (PVY) versus the persistent Potato leafroll virus (PLRV). Aphids exposed to PLRV produced significantly less 22 mers aligned to the aphid genome, and an abundance of 26 to 27 mers, many of which were predicted to be piRNA. Additionally, expression of Buchnera aphidicola tRNA-derived sRNAs was influenced by PLRV and, to a lesser extent, PVY, suggesting that plant viruses alter the aphid-endosymbiont relationship. Finally, aphids exposed to PLRV-infected plants generated an abundance of unusually long sRNAs and a reduced number of 22 mers against an aphid virus, Myzus persicae densovirus (MpDNV) and had higher MpDNV titer. Expression of the PLRV silencing suppressor P0 in plants recapitulated the increase in MpDNV titer in the absence of PLRV infection. Our results show that plant viruses transmitted in two different modes cause distinct effects on their vector with regards to post-transcriptional gene regulation, symbiosis with Buchnera, and the antiviral immune response of aphids to an aphid-infecting densovirus.

Disruption of Chloroplast Function Through Downregulation of Phytoene Desaturase Enhances the Systemic Accumulation of an Aphid-Borne, Phloem-Restricted Virus.

Chloroplasts play a central role in pathogen defense in plants. However, most studies explaining the relationship between pathogens and chloroplasts have focused on pathogens that infect mesophyll cells. In contrast, the family Luteoviridae includes RNA viruses that replicate and traffic exclusively in the phloem. Recently, our lab has shown that Potato leafroll virus (PLRV), the type species in the genus Polerovirus, forms an extensive interaction network with chloroplast-localized proteins that is partially dependent on the PLRV capsid readthrough domain (RTD). In this study, we used virus-induced gene silencing to disrupt chloroplast function and assess the effects on PLRV accumulation in two host species. Silencing of phytoene desaturase (PDS), a key enzyme in carotenoid, chlorophyll, and gibberellic acid (GA) biosynthesis, resulted in a substantial increase in the systemic accumulation of PLRV. This increased accumulation was attenuated when plants were infected with a viral mutant that does not express the RTD. Application of GA partially suppressed the increase in virus accumulation in PDS-silenced plants, suggesting that GA signaling also plays a role in limiting PLRV infection. In addition, the fecundity of the aphid vector of PLRV was increased when fed on PDS-silenced plants relative to PLRV-infected plants.

Responses of Aphid Vectors of Potato leaf roll virus to Potato Varieties.

Potato leaf roll virus (PLRV) can reduce tuber yield and quality in potato. Green peach aphid (Myzus persicae [Sulzer]) and potato aphid (Macrosiphum euphorbiae [Thomas]) are the two most important potato-colonizing PLRV vectors in the Pacific Northwest. We compared My. persicae and Ma. euphorbiae densities and PLRV incidences among potato varieties in the field to clarify the relationships between aphid abundance and PLRV incidence in plants. Aphids were sampled weekly over three years in the potato varieties Russet Burbank, Ranger Russet, and Russet Norkotah in a replicated field trial. In all years, My. persicae was more abundant than Ma. euphorbiae, representing at least 97% of samples. My. persicae densities did not differ among potato varieties across years; very low numbers of Ma. euphorbiae precluded such statistical comparisons for this species. PLRV infection did not differ significantly among potato varieties, although the percent of PLRV-infected plants differed among years when all varieties were combined (46% in 2013, 29% in 2011, 13% in 2012). For Ranger Russet and Russet Norkotah, PLRV incidence was positively correlated with aphid abundance as well as proportion of PLRV-positive aphids. In Russet Burbank, only aphid abundance was positively correlated with PLRV infection. Our results suggest that the three most commonly grown potato varieties in our region do not differ in their susceptibility to PLRV infection, and that aphid density was a consistent indicator of the risk of infection by this virus across varieties. Both of these findings can be used to hone PLRV monitoring and modeling efforts.

Increased susceptibility of potato to Rhizoctonia diseases in Potato leafroll virus-infected plants

In Hokkaido potato fields, tubers produced from the plants with leaf curl symptoms caused by potato leaf roll virus (PLRV) were noted to be more densely covered with Rhizoctonia sclerotia. This observation led us to hypothesize that potato infected with PLRV would have an increased susceptibility to Rhizoctonia solani. To test this hypothesis, in a pot experiment, we inoculated PLRV-infected mother tubers with Rhizoctonia. As a result, PLRV-infected plants produced significantly fewer and smaller tubers than virus-free plants did, suggesting that PLRV-infected plants are more susceptible than virus-free plants to R. solani. Virus-free seed tubers should thus be used to reduce Rhizoctonia diseases.

Infection Pattern of PVY and PLRV in Potato Tubers Obtained from Potato Plants Infected with Both the Viruses

Experiments were conducted to study the plant growth and tuber yield of the seed potato collected from PVY and PLRV infected plants. The seed potatoes were graded as under size (<28 mm), A grade ( 28-40 mm), B grade (41-55 mm) and over size (>55 mm) which were planted following RCBD in the field. Third generation seed potatoes of Diamant variety were used. The incidence of viruses was confirmed by DAS-ELISA. The incidence of PVY and PLRV was 100% in the plants raised from under size tubers. The lowest plant height, stem number/hill, tuber weight /hill was recorded in plants raised from under size tuber. It was observed that some of the plants raised from tubers A grade, B grade and oversize tubers remained virus free even when the tubers were collected from virus infected plants.

Detection of potato leafroll virus isolated from potato fields in Tehran province in aphids by immunocapture reverse transcription polymerase chain reaction

The surveys conducted during 2006 and 2007 revealed the infection of the virus in potato fields in Tehran province. Due to the important roll of aphids in transmission of the virus, immunocapture reverse transcription polymerase chain reaction (IC-RT-PCR) and reverse transcription polymerase chain reaction (RT-PCR) was developed using potato leafroll virus (PLRV) specific antibodies and specific primer pair (20 mer) located in the virus capsid gene to detect the virus in aphids. A 336-bp PCR product was detected from aphids (Myzus persicae) which had been fed on PLRV-infected plants. The PCR band was specific to PLRV as determined in PLRV-infected plants. This inquiry shows that this method is applicable to assess viroliferous nature of aphids in yellow -pan traps during season.

Changes in Green Peach Aphid Responses to Potato Leafroll Virus–Induced Volatiles Emitted During Disease Progression

Previous research has shown that green peach aphids, Myzus persicae (Sulzer), preferentially settle on leaflets of potato plants (Solanum tuberosum L.) infected with potato leafroll virus (PLRV) compared with sham-inoculated controls, at least in part because of aphid responses to volatile cues from the plants. The prior work used plants 4 wk after inoculation. In this study, aphid emigration from the vicinity of leaflets of PLRV-infected plants at 2, 4, 6, 8, and 10 wk after inoculation was compared with emigration from leaflets of sham-inoculated control plants. For the bioassay, 30 aphids were placed directly above a test leaflet on screening to exclude gustatory and tactile cues and in darkness to exclude visual cues. The numbers emigrating were recorded every 10 min for 1 h. Volatile organic compounds (VOCs) were collected from the headspace of the test plants, quantified, and compared among treatments. In bioassays with leaflets of upper nodes of the plants, aphid immigration rates were significantly lower from leaflets of PLRV-infected plants than from sham-inoculated plants at 4 and 6 wk after inoculation, but not at 2, 8, and 10 wk after inoculation. In bioassays with leaflets from lower nodes, emigration did not differ between PLRV-infected plants and sham-inoculated plants at any stage in the infection. Volatile compounds detectable in the headspace of intact plants at 2, 4, and 8 wk after inoculation (or sham inoculation) changed with plant age and with disease progression, potentially explaining behavioral responses of the aphids.

Effect of an Alternate Weed Host, Hairy Nightshade, <I>Solanum sarrachoides</I>, on the Biology of the Two Most Important Potato Leafroll Virus (Luteoviridae: Polerovirus) Vectors, <I>Myzus persicae</I> and <I>Macrosiphum euphorbiae</I> (Aphididae: Homoptera)

Hairy nightshade, Solanum sarrachoides (Sendtner), is a ubiquitous weed in potato agro-ecosystems and nonagricultural lands of southeastern Idaho and the Pacific Northwest. This weed increases the complexity of the Potato leafroll virus (PLRV) (Luteoviridae: Polervirus)-potato pathosystem by serving as aphid and virus reservoir. Previous field studies showed higher densities of green peach aphid, Myzus persicae (Sulzer), and potato aphid, Macrosiphum euphorbiae (Thomas), the two most important vectors of PLRV, on S. sarrachoides compared with potato plants in the same fields. Some of the S. sarrachoides plants sampled in these surveys tested positive for PLRV. Viral infections can alter the physiology of plant hosts and aphid performance on such plants. To understand better the potential effects of S. sarrachoides on the PLRV-potato-aphid pathosystem, the life histories of M. persicae and M. euphorbiae were compared on virus-free and PLRV-infected S. sarrachoides and potato. Individual nymphs of each aphid species were held in clip cages on plants from each treatment to monitor their development, survival, and reproductive output. Nymphal survival for both aphids across plant species was higher on S. sarrachoides than on potato, and, within plant species, it was higher on PLRV-infected plants than on noninfected plants. With a few exceptions, similar patterns occurred for fecundity, reproductive periods, adult longevity, and intrinsic rate of increase. The enhanced performance of aphids on S. sarrachoides and on PLRV-infected plants could alter the vector population dynamics and thus the PLRV-disease epidemiology in fields infested with this weed.

Effect of an Alternate Weed Host, Hairy Nightshade,Solanum sarrachoides, on the Biology of the Two Most Important Potato Leafroll Virus (Luteoviridae: Polerovirus) Vectors,Myzus persicaeandMacrosiphum euphorbiae(Aphididae: Homoptera)

Hairy nightshade, Solanum sarrachoides (Sendtner), is a ubiquitous weed in potato agro-ecosystems and nonagricultural lands of southeastern Idaho and the Pacific Northwest. This weed increases the complexity of the Potato leafroll virus (PLRV) (Luteoviridae: Polervirus)-potato pathosystem by serving as aphid and virus reservoir. Previous field studies showed higher densities of green peach aphid, Myzus persicae (Sulzer), and potato aphid, Macrosiphum euphorbiae (Thomas), the two most important vectors of PLRV, on S. sarrachoides compared with potato plants in the same fields. Some of the S. sarrachoides plants sampled in these surveys tested positive for PLRV. Viral infections can alter the physiology of plant hosts and aphid performance on such plants. To understand better the potential effects of S. sarrachoides on the PLRV-potato-aphid pathosystem, the life histories of M. persicae and M. euphorbiae were compared on virus-free and PLRV-infected S. sarrachoides and potato. Individual nymphs of each aphid species were held in clip cages on plants from each treatment to monitor their development, survival, and reproductive output. Nymphal survival for both aphids across plant species was higher on S. sarrachoides than on potato, and, within plant species, it was higher on PLRV-infected plants than on noninfected plants. With a few exceptions, similar patterns occurred for fecundity, reproductive periods, adult longevity, and intrinsic rate of increase. The enhanced performance of aphids on S. sarrachoides and on PLRV-infected plants could alter the vector population dynamics and thus the PLRV-disease epidemiology in fields infested with this weed.

Myzus persicae is Arrested More by Blends Than by Individual Compounds Elevated in Headspace of PLRV-Infected Potato

Volatiles from potato plants (Solanum tuberosum L.) infected with Potato leaf roll virus (PLRV) attract and arrest the principal vector of PLRV, the green peach aphid, Myzus persicae (Sulzer), more strongly than volatiles from non-infected plants. The total concentration of volatiles detectable in the headspace of PLRV-infected plants is greater than that in the headspace of non-infected controls, and the relative composition is altered. To determine the basis of the aphid response to PLRV-infection-induced volatiles from potato, behavioral bioassays were conducted. We measured arrestment of aphids by individual components, by synthetic blends of these, and by a naturally occurring blend by using an emigration rate bioassay, and quantified observations of the behavior of individual aphids. The components tested were those elevated at least twofold in response to PLRV infection. Before conducting the behavioral bioassays, electroantennograms confirmed the electrophysiological responses of aphids to the components of the blend. For bioassays, individual compounds or blends were tested by applying them in solution to paper strips at concentrations designed to mimic those present in the headspace of the plants. All bioassays were conducted by placing aphids on fine-mesh screening positioned above treated paper strips. Arrestment was measured by placing groups of 30 aphids directly over the treated strips and counting the number moving away at 10-min intervals for 50 min. Among the individual compounds tested, only beta-pinene was a mild arrestant. The other compounds did not elicit significant changes in arrestment or behavior at a range of physiologically relevant concentrations. In contrast, synthetic blends that mimicked the concentration and composition present in headspace of PLRV-infected potato plants arrested aphids significantly more strongly than blends mimicking volatiles from the headspace of non-infected plants. The naturally occurring blend collected from headspace of PLRV-infected plants also arrested M. persicae more strongly than the blend collected from headspace of non-infected plants. Aphid behavior was quantified by directly observing individual aphids and recording their activities during a 5-min period on screening above strips treated with test materials. Few differences in time budgets were observed among aphids exposed to individual components, but synthetic blends and trapped headspace volatiles from PLRV-infected plants resulted in significantly less time spent walking by aphids than synthetic blends and trapped headspace from non-infected controls. Our results indicate that arrestment of M. persicae by PLRV-infected plants requires the blend of volatile organic compounds released by these plants and is not produced in response to a single compound.

Effect of Mixed Viral Infections (Potato Virus Y–Potato Leafroll Virus) on Biology and Preference of Vectors Myzus persicae and Macrosiphum euphorbiae (Hemiptera: Aphididae)

Mixed viral infections of heterologous viruses such as Potato virus Y (family Potyviridae, genus Potyvirus, PVY) and Potato leafroll virus (family Luteoviridae, genus Polerovirus, PLRV) are a regular occurrence in Idaho’s potato, Solanum tuberosum (L.), cropping systems. An increased number of plant samples from Idaho’s potato fields over the past 2 yr has serologically tested positive for both PVY and PLRV via double antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA) and exhibited more severe symptoms than singly-infected plants (PVY or PLRV). Several studies have extensively examined the mixed infection phenomenon but to the best of our knowledge, none have examined the effect of such infections on vector biology and preference. Laboratory studies were conducted to examine the effect of mixed viral (PVY–PLRV) infection on the fecundity and preference of two of the most efficient PVY and PLRV vectors, the green peach aphid, Myzus persicae (Sulzer), and the potato aphid, Macrosiphum euphorbiae (Thomas) (Hemiptera: Aphididae). M. persicae and M. euphorbiae adults were clip-caged (one adult per cage) to leaflets of PVY, PLRV, PVY–PLRV-infected, and noninfected potato plants. The number of nymphs produced in all four treatments was recorded after 96 h. M. persicae and M. euphorbiae fecundity was significantly higher on mixed infected plants than on singly infected plants or noninfected plants. Preference of alatae and apterae of M. persicae and M. euphorbiae was determined with the use of settling bioassays. Both alatae and apterae of M. persicae and M. euphorbiae preferentially settled on PVY–PLRV-infected plants than on singly infected plants (PVY or PLRV) or noninfected plants.

Volatiles from potato plants infected with potato leafroll virus attract and arrest the virus vector, Myzus persicae (Homoptera: Aphididae).

The influence of viral disease symptoms on the behaviour of virus vectors has implications for disease epidemiology. Here we show that previously reported preferential colonization of potatoes infected by potato leafroll virus (genus Polerovirus) (luteovirus) (PLRV) by alatae of Myzus persicae, the principal aphid vector of PLRV, is influenced by volatile emissions from PLRV-infected plants. First, in our bioassays both differential immigration and emigration were involved in preferential colonization by aphids of PLRV-infected plants. Second, M. persicae apterae aggregated preferentially, on screening above leaflets of PLRV-infected potatoes as compared with leaflets from uninfected plants, or from plants infected with potato virus X (PVX) or potato virus Y (PVY). Third, the aphids aggregated preferentially on screening over leaflet models treated with volatiles collected from PLRV-infected plants as compared with those collected from uninfected plants. The specific cues eliciting the aphid responses were not determined, but differences between headspace volatiles of infected and uninfected plants suggest possible ones.

Six viruses identified in potato plants grown in Alabama, U.S.A.

A survey was conducted for virus-infected potato plants in commercial production fields in Baldwin, Cullman, DeKalb, and Jackson counties in Alabama. Infected plants were assessed visually, i.e., on the basis of occurrence of virus-like symptoms, and by enzyme-linked immunosorbent assay (ELISA). In 1997, potato plants were tested for Cucumber mosaic virus (CMV), Potato virus Y (PVY) and Tobacco etch virus (TEV). PVY was detected from foliar samples collected from Baldwin, Cullman, and Jackson counties. Neither CMV nor TEV were detected in any of the samples. In 1998, potato plants were once again tested for the presence of CMV, PVY, and TEV, with additional analyses for Potato viruse A (PVA), Potato M (PVM), Potato S (PVS), Potato X (PVX), and Potato leafroll virus (PLRV). Four viruses were detected from potato leaf samples collected from Baldwin County: PVS, PVX, PVY, and PLRV. Samples collected from DeKalb and Jackson counties were shown to be infected with CMV, PVA, PVS, PVX, and PVY. Identification of virus infection based on visual assessment was relatively inconsistent with the exception of PLRV-infected potato plants, which had upward curled leaves. The expression of infection by PVA, PVS, PVX, and PVY varied; some infected potato plants were symptomless while others had reddening of leaves that sometimes included a mild mosaic. This is the first report to identify viruses in commercially-grown potato plants in Alabama.

Transformation of tobacco and potato with cDNA encoding the full-length genome of Potato leafroll virus: evidence for a novel virus distribution and host effects on virus multiplication

A full-length cDNA copy of the genome of Potato leafroll virus (PLRV) was introduced into the genome of tobacco and potato plants by Agrobacterium tumefaciens-mediated transformation. Transgenic lines were obtained in which the transgene was readily detected by PCR with DNA extracted from T(1) tobacco seedlings and clonally multiplied potato plants. PLRV-specific genomic and sub- genomic RNAs, coat protein antigen and virus particles were detected in transgenic plants. Aphids fed on the transgenic tobacco plants readily transmitted PLRV to test plants. Infected transgenic tobacco plants, like non-transgenic (WT) PLRV-infected plants, displayed no symptoms of the infection but transgenic plants of potato were severely stunted. In parallel tests, the mean PLRV titres in WT tobacco plants and transgenic tobacco plants were 600 and 630 ng virus/g leaf, respectively, although differences in PLRV titres among transgenic plants were much greater than those among infected WT plants. In similar tests with potato, the mean PLRV titre of WT plants was 50 ng virus/g leaf whereas higher concentrations (up to 3400 ng virus/g leaf) accumulated in transgenic potato plants. In tissue prints of stems, PLRV was detected in similar proportions of phloem cells in transgenic and infected WT plants. In transgenic tobacco and potato plants, but not in infected WT plants, a few stem epidermal cells also contained virus. From tissue prints of transgenic tobacco leaves, it was estimated that about one in 40000 mesophyll cells contained virus, but in transgenic potato, a greater proportion of mesophyll cells was infected.

Immunological analysis of potato leafroll luteovirus (PLRV) P1 expression identifies a 25 kDa RNA-binding protein derived via P1 processing.

Mono- and polyclonal antibodies directed against different domains of the potato leafroll luteovirus (PLRV) P1 (ORF1) protein were applied to the analysis of P1 expression during PLRV replication in planta. Western analyses detected P1 and a protein of approximately 25 kDa (P1-C25) that accumulated to readily detectable amounts in PLRV-infected plants, but was not detected by in vitro cell-free translation of P1. P1-C25 represents the C-terminus of P1 and is a proteolytic cleavage product produced during P1 processing. On the basis of its molecular weight, the N-terminus of P1-C25 is either identical to or located adjacent to the previously identified PLRV genome-linked protein, VPg. P1-C25 is not associated with virus particles, and subcellular localization experiments detected P1-C25, but not P1, in the membrane and cytoplasmic fractions of PLRV-infected cells. In addition, P1-C25 exhibits nucleic acid-binding properties. On the basis of its biosynthesis, localization and biochemical properties, P1-C25 may facilitate the formation of P1/PLRV RNA complexes in which the spatial proximity allows for covalent bond formation between PLRV RNA and VPg.

Assembly of virus-like particles in insect cells infected with a baculovirus containing a modified coat protein gene of potato leafroll luteovirus.

DNA encoding the coat protein (P3) of a Scottish isolate of potato leafroll virus (PLRV) was inserted into the genome of Autographa californica nucleopolyhedrovirus (AcNPV) such that the coat protein was expressed either in an unmodified form or with the addition of the amino acid sequence MHHHHHHGDDDDKDAMG at the N terminus (P3-6H). Insect cells infected with these recombinant baculoviruses accumulated substantial amounts of P3 and P3-6H. P3 could not be recovered from cell extracts unless it was denatured in SDS but a proportion of the P3-6H was recoverable in a soluble form in non-denaturing conditions. Immunogold labelling of sections of infected cells showed that P3 accumulated in nuclei in large amorphous bodies. In contrast, although much of the P3-6H also accumulated in nuclei, it formed virus-like particles (VLP) which were often grouped in close-packed, almost cystalline arrays. When electron microscope grids coated with antibodies to PLRV were floated on cell extracts containing P3-6H, VLP were trapped which were indistinguishable from PLRV particles trapped from extracts of PLRV-infected plants. The VLP co- sedimented in sucrose gradients with PLRV particles which suggests that the VLP contained RNA. VLP collected from sucrose density gradient fractions contained protein which reacted with nickel chelated to nitrilotriacetic acid, a histidine-specific reagent. Cells infected with either recombinant baculovirus also synthesized a protein, with an Mr of about 17000, which was shown to be the translation product of the P4 gene which is in the +1 reading frame within the coat protein gene. This protein was also found in the nuclear fraction of infected cells but was more readily soluble than was P3.

Detection of potato leafroll virus in single aphids by the reverse transcription polymerase chain reaction and its potential epidemiological application.

A reverse transcription and polymerase chain reaction (RT-PCR) system was developed using two 20-mer primers located in the potato leafroll virus (PLRV) capsid gene. A 336-bp PCR product was detected from aphids (Myzus persicae) which had been fed on PLRV-infected plants. The PCR band was specific to PLRV as determined by Southern blots and detection by a PLRV-specific probe. As little as 5 min exposure of aphids to PLRV-infected leaves resulted in the presence of PLRV-specific bands in 13% of aphids. However, the percentage of PLRV-positive aphids increased with longer exposure to infected sources and reached 90% after 3-4 days of feeding. PLRV can be detected from a single viruliferous aphid or a single viruliferous aphid combined with up to 29 non-viruliferous aphids. PLRV can be detected from freshly collected aphids, those stored at -70 degrees C, or those stored in 70% ethanol at room temperature for extended periods. This method is applicable to assess the viruliferous nature of aphids caught in yellow-pan traps during the growing season or stored for over a year.

Acquisition of potato leafroll virus byMyzus persicae from secondarily-infected potato plants of different genotypes

The acquisition of potato leafroll virus (PLRV) byMyzus persicae nymphs from the top leaves of potato plants was studied throughout a growing season in relation to the antigen titre in those leaves and the feeding behaviour of the aphid. Secondarily-infected plants of eight potato genotypes with different levels of field resistance served as virus sources. Early in the growing season, plants were efficient sources for virus acquisition. The amount of viral antigen detected inM. persicae nymphs fed on the top leaves was strongly correlated with the titres of viral antigen in these leaves. Virus acquisition from the top leaves of older potato plants was markedly impaired and could not be correlated with their virus titre. With increasing age of the potato plants and the development of virus symptoms, the virus titre in the leaves declined and the initial weak correlation between the virus titre and field resistance ratings disappeared. Thus, screening secondarily-infected potato plants for field resistance to PLRV based on the concentration of viral antigen in leaves or in aphids fed on them should be avoided later in the growing season. The feeding rate ofM. persicae, measured by the number of honeydew droplets excreted, did not account for the reduced uptake of virus from older plants since it was not influenced by the age of the plant. Throughout the growing season, the feeding rate ofM. persicae nymphs on PLRV-infected plants was higher on genotypes with low levels of field resistance to PLRV than on genotypes with high ones.

Potato Leaf Roll Virus 3' Genome Organization: Sequence of the Coat Protein Gene and Identification of a Viral Subgenomic RNA

(...) The coat protein gene contains 624 nucleotides and encodes a protein of 208 amino acids with a calculated molecular weight of 23.2 kDa. This gene is located internal to the 3'-end of the genome, contains the complete overlap of an open reading frame (ORF) encoding a 17.4 kDa protein, and is followed in-frame by an ORF encoding a 56.4 kDa protein. Northern blot hybridization experiments have identified a 3'-positioned viral subgenomic RNA produced in PLRV-infected plants. This subgenomic RNA is not encapsidated and, by analogy to other RNA plant viruses, is likely the mRNA for expression of the 3'-portion of the genome (...)

Potato Leafroll Virus: Evaluation of Resistance in Potato Cultivars

Potato Leafroll Virus: Evaluation of Resistance in Potato Cultivars