Evaluation of tuber-bearingSolanum species for symptomology,as diagnostic hosts,and sources of immunityto potato virus Y necrotic strain (PVYN)

A total of 258 Plant Introductions (PI) belonging to 69Solarium species were evaluated in the greenhouse for their reaction to the tobacco veinal necrosis strain of potato virus Y (PVY N). One hundred and thirty-one (50.7%) of the PI accessions produced mosaic symptoms ranging from mild to severe. Local lesion and veinal necrosis symptoms were observed in 19 PI accessions (7.3%) and a variety of other symptoms were observed in another 11 PI accessions (4.2%). Only 97 PI accessions (37.5%) were symptomless carriers of PVY^N. PI accession 473505 ofS. sparsipilum and PI accession 498021 ofS. brachycarpum developed local lesions and veinal necrosis with PVY^N, but necrotic spots and mosaic with PVY^o. Common mechanically-transmitted potato viruses A, S, M, and X did not interfere with PVY symptom development inS. sparsipilum andS. brachycarpum. Thus, PI 473505 and PI 498021 can be used as indicator plants for specific identification of PVY^N. PI accession 472819 ofS. chacoense developed local lesions with systemic spread in PVY^o, but without systemic spread in PVY^N. Thus, this can be used as a differential host plant for PVY strains. Two PI accessions ofS. stoloniferum, PI 160372 and 161171 were immune to PVY^N.     

Potato virus A lesions onPhysalis species

PVA produces distinct local lesions on open leaves ofPhysalis floridana, as does PVY. But, whereas PVA induced such lesions on detached leaves, PVY did not. PVX induced similar lesions, thus the test for PVA will be most useful in work with isolated cultures of PVA or with virus tested seed lines or in screening for resistance, where PVX is absent.P. floridana plants and leaves were best held at 15 to 18 C with low light intensity (4–5 K lux). From 4–6 week old potato plants, PVA was best obtained from lower leaves, ground in 0.05 M glycine — 0.03 M phosphate buffer, pH 9.2. One leaf disc infected with PVA could be detected in a composite sample with 9 discs from healthy leaves.P. angulata andP. pubescens may also be used for diagnosis of PVA. PVY becomes systemic in these species without inducing local lesions.     

Modification of serological techniques and their evaluation for detection of potato viruses in seed certification related activities

Development of alternative serological techniques to ELISA for detection of potato viruses offers advantages for monitoring virus incidence and for seed potato certification systems. Several trials showed that multiplex tissue print immunoassay (TPIA) and dot blot immunoassay (DBIA) might represent fast, practical, and sensitive alternatives for the detection of: Potato leaf roll virus (PLRV), Potato virus S (PVS), Potato virus X (PVX) and Potato virus Y (PVY), from green and/or tuber tissues. In TPIA, the specific precipitation patterns in infected tissues of leaf petioles or stem cross sections, observed with each virus, allowed identification of the specific virus or mixed infections in a single multiplex assay. For detection of PVY in green tissues, DBIA was shown to be over 50 times more sensitive than ELISA. TPIA and ELISA from the tuber stem end or from eyes might be used for rapid detection of PVY and PVS in seed potato tubers without prior germination. PVS was evenly distributed in potato tuber tissue, while PVY was localized in the vascular tissue beneath the epidermis, with irregular distribution along the periphery of the potato tuber. For laboratories in developing countries lacking time and facilities for tests based on tuber germination, monitoring for PVS and PVY using TPIA in tuber tissue may be a suitable alternative to ELISA.     

Population Growth of Myzus persicae on Potato Plants Infected with Different Strains and Variants of Potato virus Y

Potato virus Y (PVY) is one of the most economically important viruses affecting the potato crop. Several strains of the virus, including PVY^O, PVY^N, recombinant isolates; PVY^N:O (PVY ^N-Wi) and PVY^NTN and several variants of PVY^O have been reported from North American potato-production areas. The green peach aphid, Myzus persicae Sulzer, is a colonizer of potatoes and is considered the most important vector of PVY. The objective of this study was to measure the population growth of M. persicae on potato plants infected with different strains and genetic variants of PVY. The initial population of ten winged adults of M. persicae was allowed to develop on a potted plant for 12 days. Results clearly indicated that infections by different strains and genetic variants of PVY did not influence the population growth of M. persicae on potato plants during this period.     

马铃薯病毒外壳蛋白融合基因转化马铃薯及其抗病性分析

将多种病毒的有效核酸片断拼接成融合基因转入马铃薯可获得多抗马铃薯材料。针对马铃薯生产中分布广泛、危害严重并经常混合感染的马铃薯X病毒(PVX)、马铃薯Y病毒(PVY)、马铃薯卷叶病毒(PLRV)和马铃薯S病毒(PVS),开展了利用基因工程方法获得兼抗4种马铃薯病毒转基因马铃薯材料的研究。试验在前期获得含4种马铃薯病毒外壳蛋白基因片段的质粒pART27-XSYV-rh的基础上,通过根癌农杆菌(Agrobacterium tumefaciens)介导转化马铃薯(Solanum tuberosum)品种‘陇薯3号’,PCR扩增和PCR-Southern杂交证明,4价融合基因已整合到马铃薯基因组中。qRT-PCR分析表明,该融合基因在转基因植株中能正常表达。3株转基因植株的抗病性鉴定结果表明,2株对4种病毒同时具有抗性;1株对PLRV侵染表现阳性,对另外3种病毒同时具有抗性。     

The effect of metribuzin interaction with potato viruses X and Y on potato foliage,yield and grade

Foliar treatment of potato (Solanum tuberosum L.) with metribuzin at 0.57–1.0 lb/A caused a necrotic reaction in leaflets of plants infected with potato virus Y (PVY), but not in plants infected with potato virus X (PVX) or potato leafroll virus. Necrosis symptoms resulting from metribuzin-PVY interaction were distinct from symptoms of either PVY infection or of metribuzin injury. This reaction was similar in the Russet Burbank, Lemhi Russet, and Pioneer cultivars. Russet Burbank infected with PVY and PVX, alone or in combination, was treated with metribuzin to study herbicidevirus interaction effects on yield. Secondary PVY infection alone caused a 57% yield reduction, and when combined with PVX caused a 71% yield reduction. Although leaflet necrosis was induced by the metribuzin-PVY combination, there was no significant yield interaction. Results suggest that post-emergence application of metribuzin can be used as an aid for detecting and removing potato virus Y infected plants from potato seed fields     

Potato leafroll virus and potato virus Y in seed potatoes used to plant the North Carolina crop

Incidence of potato leafroll virus (PLRV) and potato virus Y (PVY) was determined in seed potatoes (Solatium tuberosum) from Canada, Maine, Minnesota, New York, North Dakota, Nebraska, Pennsylvania, and Wisconsin used to plant the North Carolina crop in 1977, 1978 and 1979. Incidence of PLRV ranged from 0–5.2% (X = 0.57%) and for PVY from 0-5.6% (X = 0.62%) from all sources (112 seed lots). All PVY isolates (177) tested from potato caused a very mild veinbanding and mottling onNicotiana tabacum cultivars NC 95 and NC 2326. No serological difference was detected between these isolates and the common strain of PVY from tobacco in North Carolina. Essentially no spread of PVY occurred in three potato fields observed each year of the study.     

Occurrence and Distribution of Potato Pests and Diseases in Kenya

Potato plays an important role in food security in Kenya but yields are low (<10 t/ha), and this is partly attributed to the lack of healthy planting material. This study is the first wide-scale survey to determine the occurrence and distribution of common potato pests and diseases in Kenyan seed (certified and quality declared) and ware crops. Potato crops growing on 101 farms in 21 districts were examined. Approximately 36% of plants in farmers’ fields sampled both during the long rains (main potato-growing season) and short rains seasons displayed virus-like disease symptoms. Six viruses (potato leafroll virus (PLRV), Potato virus A (PVA), potato virus M (PVM), potato virus S (PVS), potato virus X (PVX), and potato virus Y (PVY)) were detected using double antibody sandwich enzyme-linked immunosorbent assay in potato samples. Sequencing of polymerase chain reaction products from PVY-infected plants revealed the presence of recombinant strains of PVY (NTN and Wilga). Four aphid species, Macrosiphum euphorbiae, Aphis gossypii, Myzus persicae, and Aphis fabae, colonized potato in all districts, occurring in greater numbers west of the Great Rift Valley than to the east. There was a positive correlation between virus incidence and aphid numbers in the long rains (main) potato-growing season. PLRV, PVM, PVS, PVX, and PVY were detected in solanaceous weeds. Ralstonia solanacearum was detected in soils from 13 farms in 8 of the 18 districts surveyed. Approximately 38% of soil samples were infested with Meloidogyne spp. Phytophthora infestans isolates belonging to the US 1 and 2_A1 genotypes were identified. Although many economically important diseases are present in Kenya, the lower aphid incidence in districts east of the Great Rift Valley may indicate that these districts are more suitable for seed potato production.     

Genetic Resistances to Potato Leafroll Virus, Potato Virus Y, and Green Peach Aphid in Progeny ofSolanum etuberosum

Increasing prevalence of potato leafroll virus (PLRV) and potato virus Y (PVY) has been reported in seed and commercial potato production, resulting in the rejection of potatoes for certification and processing. Host plant resistance to PLRV and PVY and their primary vector, green peach aphid,Myzus persicae, could limit the spread of these viruses. Host plant resistance to PLRV, PVY, and green peach aphid has been identified in non-tuber-bearingSolanum etuberosum (PI 245939) and in its backcross 2 (BC₂) progeny. Resistance to green peach aphid involved a reduction in fecundity and adult aphid size. In addition, one BC₂ individual was identified as possessing a genetic factor that was detrimental to nymph survival. PVY resistance was identified in all five BC₂ progenies evaluated in a field screening under intense virus pressure. PLRV resistance was identified in two of the five BC₂ progeny. This resistance was stable in field and cage evaluations with large populations of viruliferous aphids. Based on the segregation of virus resistances in the BC₂ , PVY and PLRV resistances appear to result from the action of independent genetic mechanisms that reduce the levels of primary and secondary virus infection. Two BC₂ individuals, Etb 6-21-3 and Etb 6-21-5 were identified as having multiple resistances to PLRV, PVY, and green peach aphid derived fromS. etuberosum. This germplasm could prove useful to potato breeders in the development of virus-resistant cultivars.     

Resistance to potato viruses M,S, X and the spindle tuber virus in tuber-bearingSolanum species

On two separate occasions, some available accessions of tuber-bearingSolanum species were tested for resistance to potato viruses. Challenge inoculations were made mechanically with infective sap; and assessment was by sub-inoculation to differential host plants, supplemented by serological tests. In 1956–57, four accessions remained free from potato virus S (PVS), and nine remained free from PVM. In 1968–70, one or more clones of 11 accessions showed resistance to PVS—one of them,S. megistacrolobum, a diploid, apparently being hypersensitive. Resistance to PVX was found in seven accessions, and to PVM in two. There appeared to be resistance to the potato spindley tuber virus in five accessions.     

Evaluation of the enzyme-amplified ELISA for the detection of potato viruses A,M, S,X, Y,and leafroll

Various parameters,e.g. types of microtiter plate for DAS-ELISA (double antibody sandwich-enzyme-linked immunosorbent assay), use of fresh or frozen amplifier solutions for enzyme-amplified-ELISA, and use of sodium diethyldithiocarbamate (NaDIECA) in sample buffer in cocktail-ELISA were evaluated for the detection of potato viruses A, M, S, X, Y and leafroll from potato foliage. Dynatech Immulon immunoplates provided higher readings for all viruses. Fresh amplifier solution in amplifed-ELISA was superior to frozen solutions. Amplified ELISA gave only marginal improvement in the sensitivity over the standard DAS-ELISA. Addition of NaDIECA in sample buffer did not improve the detection of viruses in DAS-, amplified-, or cocktail-ELISA. Cocktail-ELISA can reduce antigen incubation time to as short as 15 min for PVA, PVM and PVX; 1 hr for PVY and PLRV; and 2–4 hr for PVS using pre-coated plates. Although amplified-ELISA is slightly more sensitive than DAS-ELISA for certain potato viruses, it is not suitable for large-scale indexing of potato viruses in Seed Certification Laboratories, in view of the additional steps needed in carrying out this procedure.     

Potato Virus Y transmission efficiency for some common aphids in Idaho

Green tile pan trap counts during the potato-growing season showed thatCapitophorus elaeagni (32%),Diuraphis noxia (27.7%), andMetopolophium dirhodum (15%) were the most abundant aphid species in potato fields at Aberdeen, Idaho.Acyrthosiphon pisum (22%),C. elaeagni (19%), andMetopolophium dirhodum (19%) were the most abundant species in potato fields at Tetonia, Idaho potato seed production areas. Eight species of aphids found to visit potato fields (C. elaeagni, D. noxia, M. dirhodum, Myzus persicae, Rhopalosiphum maidis, Rhopalosiphum padi, Schizaphis graminum, andSitobion avenue) were tested for Potato virus Y (PVY) transmission efficiency by timed probe experiments. Four of these species (D. noxia, M. dirhodum, M. persicae, andS. aoenae) and an additional three (Diuraphis frequens, Diuraphis mexicana, andDiuraphis tritici) were tested using mass inoculations.Capitophorus elaeagni, M. persicae, R. maidis, R. padi, andS. graminum all transmitted PVY in the timed probe experiments.Myzus persicae andD. noxia transmitted PVY in the mass inoculation experiments.     

The incidence of potato viruses X,Y and S in the Chilota potato collection

The 530 potato clones of the Chilota collection of the germplasm bank from the Universidad Austral de Chile were tested for potato viruses X (PVX), Y (PVY) and S (PVS) by means of NCM-ELISA (nitrocellulose membrane enzyme-linked immunosorbent assay). Four clones (0.8%) healthy for all 3 viruses simultaneously were detected. These clones could be resistant to the above mentioned viruses.     

Comparative levels of potato viruses S and Y infection of microplants and tuber-propagated plants in the field

The practice of transplanting microplants from tissue-culture to the field was compared to normal tuber propagation with respect to the transmission and translocation of potato virus S (PVS) and potato virus Y (PVY) to the daughter tubers of Red Pontiac, Shepody, Kennebec, and Russet Burbank cultivars in Prince Edward Island in 1984 and 1985. In general, the use of microplants to produce seed stocks appeared to increase the risk of infection with both viruses, although the results for tuber infection with PVY were only significant in one of the years.     

The infection pressure of potato leafroll virus and potato virus Y in relation to aphid populations in Cyprus

Summary The infection pressure of two viruses, potato leafroll (PLRV) and potato virus Y (PVY), both common in seed potatoes grown in Cyprus, was determined in three experiments in 1982–83. Virus-free bait plants, of potato and four other species, were exposed weekly to field infection during the growing season (March–June), and then returned to an aphid-free glasshouse for symptom expression. Only tobacco plants produced clear symptoms enabling reliable assessment of PVY infection pressure. When assessed with ELISA or by tuber indexing, the potato plants were efficient baits for both viruses whose infection period commenced at emergence (mid March to early April) and ended within 6–7 weeks. The seasonal trend of aphid populations, determined with Moericke traps or 100-leaf counts, correspond to that of virus spread. Correlation and regression analysis of aphid and virus data implicated the alate form ofMyzus persicae as the principal vector of both viruses.     

Environmental factors influencing aphid transmission of potato virus Y and potato leafroll virus

Summary The effect of temperature, relative humidity (RH) and light on aphid transmission of potato virus Y (PVY) and potato leafroll virus (PLRV) was studied using as vectorsMyzus persicae Sulz. andAphis gossypii Glov. Host susceptibility was enhanced by 48 h pre-inoculation exposure at 25°C and by 48 h post-inoculation exposure to 30°C. High RH (80%) in both pre- or postinoculation phases enhanced host susceptibility. Continuous fluorescent light (4000 lux) did not alter the rate of transmission of either virus. High RH (80–90%) and high temperature (25–30°C), when combined, increased virus transmission by 30–35%. Transmission rates were reduced by nearly 50% if RH was maintained at 50% in either of the two phases even if the temperature was 25 or 30°C. Both viruses were acquired by aphids earlier (13–20 days after inoculation) when the source plants were incubated at 25 or 30°C. Most virus was transmitted from plants inoculated with PVY 13 to 16 days and with PLRV 15 to 20 days previously. Transmission rates of PVY were enumerated from symptom expression on test plants and by Enzyme Linked Immunosorbent Assay (ELISA) whereas those of PLRV were enumerated from symptom expression alone.     

Soybean aphid,Aphis glycines Matsumura, a new vector ofPotato virus Y in potato

Soybean aphid (Aphis glycines Matsumura), an exotic species first discovered in the North Central region of the United States in 2000, is a competent vector of severalPotyviridae. Soybean aphid has high fecundity and produces alatae (winged morphs) readily, characteristics typical of proficient virus vectors. When soybean aphids were exposed toPotato virus Y (PVY)-infected potato plants and then clip-caged on healthy potato plants in groups of five or as single aphids, PVY transmission ranged from 14% to 75% across all experiments. PVY^o, PVYⁿ, and PVP^ntn strains were transmitted by soybean aphid.     

Reevaluation of the potato aphid,Macrosiphum euphorbiae (Thomas), as vector of potato virus Y

The effectiveness of the potato aphid,Macrosiphum euphorbiae (Thomas), to transmit potato virus Y (PVY) to potato has generally been overestimated because tobacco has been used as the indicator host. Our results demonstrate that, although apterousM. euphorbiae can acquire PVY from potato and tobacco plants and transmit it to tobacco plants, it does not readily transmit it to potato plants. Alatae only transmitted the virus to 4.5% of potato plants. This relative inability to transmit the virus to potato seems independent of potato cultivar. Results suggest that the role of the potato aphid in the spread of PVY in potatoes may be negligible.