The quantitative estimation of the infection of bean seed with Pseudomonas phaseolicola (Burkh.) Dowson

A routine laboratory method for the detection of Pseudomonas phaseolicola in bean seed is described. The method will detect low levels of seed-borne infection and has been used in a statistical procedure (the most probable number method) to give an estimate of percentage infection. Infection in seeds harvested from heavily infected crops varied from 10 to 1%, compared with from 1% to less than 0.1% in commercial seed stocks. A high proportion of infected seeds failed to produce infected plants and this may account for the very low levels of primary infection reported in the field. Removal of seeds showing possible ‘symptoms’ of disease reduced, but did not eliminate, infection from seed stocks.     

Cytochemical localization and ultrastructure of Aspergillus flavus in cottonseed

Cottonseeds having fluorescent fibers were harvested from fields in Arizona and examined utilizing light microscopy and transmission electron microscopy. The occurrence of fluorescent fibers indicated that seeds had been infected by Aspergillus flavus during development. Presence of A. flavus was verified by plating portions of seeds with fluorescent fibers. Hyphae, conidial heads, and conidia were identified readily in differentially-stained cotyledon tissue processed for light microscopy. Utilization of transmission electron microscopy permitted observations on lignified seed coats and cotyledons of mature cottonseeds. Hyphae were located throughout the cotyledon and in the nonlignified layers of the seed coat. The identification of hyphae in cross sections of vessel elements within the seed coat provided ultrastructural evidence supporting the hypothesis that A. flavus may enter seeds via the vascular tissue. Controls for the microscopy studies included observations on cottonseeds with no visual signs of infection and on laboratory-grown cultures of A. flavus. These observations demonstrated that the hyphae localized within fluorescent seeds had features characteristic of A. flavus and that fungal-like structures do not occur within uninfected seeds.     

Celery leaf spot: sources of inoculum

The relative importance of infected celery seed, infected leaf debris in the soil, and infected wild celery, in the incidence of Septoria leaf spot in cultivated celery has been investigated. Infection can be caused when the sole source of inoculum is viable spores on the seed surface; such spores are considered to be the main cause of disease outbreaks. Of all the seed samples examined, 93% were infected by Septoria spp. In untreated seed samples, 40% carried viable spores which survived for up to 15 months on seed stored in the laboratory, and for longer periods on seed stored at -20d? C. However, ageing of seed is not recommended as a commercial control measure. The fungus was not found in seed embryos or endosperms but mycelium was present in pericarps and testas. Unconfirmed evidence suggests that in favourable circumstances new spores might be produced in old seed-borne pycnidia.     

Studies on the seed-borne phases of dark leaf spot Alternaria brassicicola and grey leaf spot Alternaria brassicaeof brassicas

Tests in Britain on samples of basic and commercial Brassica oleracea seed between 1976 and 1978 showed that many lots were infected with Alternaria brassicicola. A. brassicae was uncommon in basic seed in these years and in commercial seed harvested in 1976 and 1977 but was frequent in seed harvested in 1978. Most affected seeds were contaminated by surface-borne spores and mycelium of A. brassicicola but many were internally infected by the fungus situated within the seed-coat and in some seeds in the embryo tissues. Superficial contamination by the fungus declined rapidly after 2 yr in cabbage seeds stored at 10 °C, 50% r.h. but internal infection persisted for up to 12 yr. In some samples, internal infection was commonly associated with small shrivelled seeds. Surface contaminated and internally infected seeds transmitted the disease but seedling infection was more closely correlated with the latter.     

The biology of Peronospora viciae on pea: factors affecting the susceptibility of plants to local infection and systemic colonization

Peronospora viciae (Berk.) Casp. penetrated leaf disks of Pisum sativum L. through the cuticle. Resistance of pea plants and of individual leaves to infection by P. viciae increased with age, but decreased again at senescence. Resistance was shown by a restriction in fungal growth and sporulation and by a chlorotic reaction in the leaves. Systemic invasion followed infection of meristematic tissue, and was induced by inoculation into the apical bud of young plants, or on to the epicotyl or hypocotyl, but not roots of germinating seedlings. Most plants whose growth was retarded showed an increased resistance to systemic infection. Pods were infected externally by sporangia, rather than by mycelial growth through the peduncle and pedicel. Oospores and mycelium were found in the testas of some seeds, but seeds from infected pods did not give rise to infected seedlings.     

Occurrence of Alternaria japonica on Seeds of Wild and Cultivated Rocket

In vitro evaluation was carried out on seed samples of wild and cultivated rocket cultivars, most frequently grown in Italy, and obtained from farms affected by the leaf spot caused by Alternaria japonica in Piedmont and Lombardy during the fall of 2010. Twelve seed samples were collected and assayed for the presence of A. japonica. The pathogen was isolated only from not disinfected seeds. Among the two seed samples of cultivated rocket (Eruca vesicaria), only one was infected by A. japonica at a level of one infected seed out of 800. Four out of ten samples of wild (Diplotaxis tenuifolia) rocket seeds were contaminated by A. japonica with the highest level of infection detected in a single sample of 3 out of 800. All tested isolates of A. japonica obtained from seeds were pathogenic on both wild and cultivated rocket.     

In situ detection of mycoplasma contamination in cell cultures by fluorescent Hoechst 33258 stain

A simple, fast, and easily reproducible routine laboratory technique for detecting mycoplasma contamination in cell cultures is reported. Cells grown on a coverslip are fixed directly with Carnoy's, air-dried, stained with DNA-specific fluorescent Hoechst 33258, and examined microscopically. All cultures that were infected with mycoplasmas had readily discernible, small, morphologically uniform, bright fluorescent bodies in the extranuclear and intercellular space in contrast to the non-contaminated control cultures in which the extra-nuclear background appeared uniformly dark. To probe the degree of sensitivity to detect mycoplasmas, control cultures were infected with aliquots from serially diluted cells or media collected from Mycoplasma hyorhinus infected cultures. The lowest infection rate (0.40% by sampling 1 000 cells in average per culture 4–24 h after infection) scored presently, however, can easily be lowered by increasing sample size since a cell infected with even one mycoplasma can be discerned. These mycoplasmas resisted centrifugation at 2 500 rpm for 30 min and easily filtered through 0.22 μm pore-size filter membrane. Amazingly infection rate of 0.63% scored from 24 h post-infection incubation attained 100% contamination with several hundreds of mycoplasmas per host cell within 120 h.     

The influence of the testa, damage and seed dressing on the emergence of groundnut (Arachis hypogea)

The effects of damaging the testa and the application of seed dressings were examined in field trials on several short-and long-season cultivars of groundnut (Arachis hypogea) with differently-pigmented testas at Samaru, Nigeria, in 1967. There was a high correlation between the number of seedlings which emerged in these trials and the resistance or susceptibility of the seed to invasion by the fungus Aspergillus flavus, as assessed by laboratory tests. When the testa was undamaged the emergence of white (susceptible) seed was only 50% while that of coloured (resistant) seed was between 95 and 98%. Damage to the testa by scratching greatly decreased emergence. The application of seed dressing increased the emergence of susceptible seed and also restored the emergence of scratched seeds to the level of undamaged seeds. The effect of the complete removal of the testa was not counteracted by seed dressing; naked seeds, with and without dressing, gave c. 10% emergence. The importance of pigment in the testa, the condition of the seed and the effects of seed dressing are discussed.     

The field behaviour of seed-borne Ascochyta fabae and disease control in field beans

In field sowings at Cambridge 2–15% of field bean seeds carrying Ascochyta fabae produced seedlings with leaf lesions. The fungus spread for distances up to 10 m in an average season and usually infected the new crop of seed. The amount of such infection arising from a single lot varied widely when samples were grown at different centres, presumably because of differences in local weather conditions. Seed lots with approximately 1% infected seeds seem suitable for ware crop production but little or no A. fabae can be tolerated in seed intended for multiplication. Infection in British-grown commercial seed has been greatly reduced by the selection of clean seed. Health standards adopted in the Field Bean Seed Scheme may have eliminated A. fabae from one cultivar.     

The effect of iprodione on the seed-borne phase of Alternaria brassicicola

Alternaria brassicicola infection of Brassica oleracea seeds was effectively controlled by a dust application of iprodione (Rovral 50% w.P.). At 2.5 g a.i./kg the seed-borne fungus was usually eliminated from samples with up to 61.5% affected seeds (35.5% internally diseased) but higher levels of infection required increased doses for complete eradication of the fungus. The germination of healthy seeds, including samples from 7–yr-old stocks, on filter paper was unaffected by the treatment. However, the germination of diseased samples, particularly those internally infected with A. brassicicola, was improved. More seedlings emerged from iprodione treated than from untreated seeds in glasshouse soil but the differences were not significant. The application of gamma-hexachlorocyclohexane to iprodione treated seeds sown in soil did not adversely affect subsequent emergence or disease control. Disease control was maintained and germination was not affected by the treatment when treated infected seeds were stored for 2 yr at 10 °C, 50% r.h. In a field trial iprodione seed treatment reduced seedling infection in a cabbage crop grown from naturally diseased seeds (100% contaminated, 45.5% internally infected) from 5.6 to 0.04%.     

Verticillium dahliae (Kleb.) Infecting Pumpkin Seed

This study investigated the natural occurrence of Verticillium dahliae (Kleb.) infection in pumpkin (Cucurbita pepo L.) seed. The mean incidence of infection was found to be 21.0%. Isolates recovered from seeds were pathogenic to pumpkin (cultivar ‘Jamaican squash’). Surface sterilization by immersion in 0.6% sodium hypochlorite for 20 min eradicated V. dahliae from infected pumpkin seeds without affecting germinability. Plating of seed components revealed that the fungus was present in the seed coat but not in the embryo or cotyledons. In a growing‐on test, 25% of 6‐week‐old plants grown from untreated seeds were infected. Germination and production of normal seedlings were unaffected by V. dahliae infection of seeds. Verticillium dahliae in pumpkin seed was found to be external and transmissible to plants. The findings of this study are important in devising disease control strategies.     

Pyrenophora graminea on Winter Barley Seed: Effect on Disease Incidence and Yield Losses

Field experiments were carried out in 1982–83 and 1983–84 in Northern and Central Italy (3 locations) in order to investigate the effect of different levels of seed infection of Pyrenophora graminea on disease incidence and yield losses in ‘Perga’ winter barley. Six levels of natural seed infection, assessed by the deep-freezing blotter method have been compared in 8 row-plots, 7.5 m long, arranged in randomized blocks with 4 replications. The percentage of infected plants and tillers has been recorded in all locations and the yield in two of them. A highly significant correlation was found between seed infection, plant infection, tiller infection and yield reduction. Major ratios found were: infected seeds/infected seedlings 1: 0.4, infected tillers/yield loss 1: 0.9, infected seeds/yield loss 1: 0.3. The threshold of seed infection at which production was not significantly different from the healthy control was 14%. Therefore seed treatment is advisable, under the conditions of Northern and Central Italy, when the percentage of seed infection in commercial seed lots is above this level. A tolerance near zero is recommended in prebasic and basic seeds.     

Fungi that infect cottonseeds before harvest

As a part of an investigation of aflatoxins and other mycotoxins in cottonseeds at harvest, samples of seeds collected from the 1971 crop at locations across the U.S. Cotton Belt were examined to determine the kinds of microorganisms causing internal or seed-coat infection in the field. Aspergillus flavus infection was absent from all seeds examined from most areas but was present in some samples from Arizona, California, and Texas. Fusarium spp., Alternaria sp., and A. niger caused internal infection at many locations; Colletotrichum gossypii and Rhizopus stolonifer were present in seeds from some areas but were generally much less common. Many of the infections with A. niger were in the seed coat. Bacterial infections were fairly frequent. In a series of commerical samples from Arizona. A. flavus infection was found in 61% of seeds, with fiber showing the bright, greenish-yellow (BGY) fluorescence that is diagnostic for A. flavus boll rot. Aflatoxin contamination was also concentration in the same seeds. The above findings agree with previous data showing that aflatoxin contamination of cottonseeds before harvest occurs rarely, if at all, in most parts of the U.S. Cotton Belt and that when such contamination does occur, it tends to be concentrated in seeds with the BGY fluorescence in their fiber and seed fuzz.     

Leaching of Ions, Organic Molecules, and Enzymes from Seeds of Peanut (Arachis hypogea L.) Imbibing without Testas or with Intact Testas

Reducing sugars, phosphates, potassium ions, total electricallyconducting material, proteins, and phenolics leached from twovarieties of peanut (Arachis hypogea L. ) seeds during 24 himbibition in distilled water. The same substances leached fromthe seeds when testas were removed before imbibition. The quantitiesof substances leached from seeds without testas after 24 h,except protein and phenolics, were much greater than from seedswith intact testas. Time courses of leaching of sugars, phosphates,potassium ions, and of total electrically conducting materialshowed fastest leaching rates in the first hour of imbibition.In the first 4 h of imbibition more sugars leached from intactseeds than from seeds without testas. Peroxidase was presentin leachates from intact seeds but was undetectable in leachatesfrom seeds without testas. Hydrogen peroxide-reducing activitywas detected in 24 h leachates from intact seeds and from seedswithout testas. The activity was partly inhibited by 1 mM ascorbate.It was concluded that catalase was present in the leachates. The peanut testas were thin. Their presence around the embryodid not reduce the rate of imbibition as compared with thatof seeds without testas. Thus the greater leaching of some substancesin the absence of the testa could not be ascribed to the absenceof a physical barrier to water uptake.     

Dynamics of Neotyphodium endophyte infection in ageing seed pools: incidence of differential viability loss of endophyte,infected seed and non-infected seed

Symbiotic associations between grasses and vertically transmitted endophytic fungi are widespread in nature. Within grass populations, changes in the frequency of infected plants are driven by influence of the endophyte on the fitness of their hosts and by the efficiency of endophyte transmission from parent plants to their offspring. During the seed stage, the endophyte might influence the fitness of its host by affecting the rate of seed viability loss, whereas the efficiency of endophyte transmission is affected by losses of viability of the fungus within viable seeds. We assessed the viability losses of Lolium multiflorum seeds with high and low level of infection of the endophyte Neotyphodium occultans, as well as the loss of viability of the fungus itself, under accelerated seed ageing and under field conditions. Starting with high endophyte-infected accessions of L. multiflorum, we produced their low endophyte-infected counterparts by treating seeds with a fungicide, and subsequently multiplying seeds in adjacent plots allowing pollen exchange. In our accelerated ageing experiments, which included three accessions, high endophyte-infected seeds lost viability significantly faster than their low endophyte-infected counterpart, for only one accession. High endophyte-infected seeds of this particular accession absorbed more water than low endophyte-infected seeds. In contrast, the endophyte lost viability within live seeds of all three accessions, as the proportions of viable seeds producing infected seedlings decreased over time. In our field experiment, which included only one accession, high endophyte-infected seed lost viability significantly but only slightly faster than low endophyte-infected seed. In contrast, the loss of viability of the endophyte was substantial as the proportions of viable seeds producing infected seedlings decreased greatly over time. Moving the seeds from the air to the soil surface (simulating seed dispersion off the spikes) decreased substantially the rate of seed viability loss, but increased the rate of endophyte viability loss. Our experiments suggest that, in ageing seed pools, endophyte viability loss and differential seed mortality determine decreases in the proportions of endophyte-infected seeds in L. multiflorum. Endophyte viability loss within live seeds contributes substantially more to infection frequency changes than differential viability losses of infected and non-infected seeds.     

携带GFP发光基因人猴嵌合免疫缺陷病毒SHIV的构建及活性检测

目的获得正常感染宿主细胞并稳定表达绿色荧光的SHIV毒株,为后期建立发光SHIV/恒河猴感染模型奠定基础。方法通过分子克隆手段,将绿色荧光蛋白基因克隆到携带HIV-1包膜蛋白的SHIV病毒全基因组中,并在细胞水平检测各毒株的感染活性及荧光蛋白表达能力。结果得到一株可表达绿色荧光蛋白的病毒株SHIV-KB9nefGFP,并具有感染TZM-bl细胞系及猴PBMC的能力。结论该毒株在宿主细胞恒河猴PBMC中具有一定复制能力,希望通过后续的猴体内传代实验获得毒力更强的发光病毒。     

Far Red and White Light-promoted Utilization of Calcium by Seedlings of Phaseolus vulgaris L

The cotyledons and embryo axes of seeds of Phaseolus vulgaris L. cv. Pinto contained 16% of the total calcium in the seed. The remaining 84% was in the testas. There was no evidence that calcium in testas was used in seedling growth or that calcium was leached from seedlings during growth.     

Rapid detection of cowpea aphid-borne mosaic virus in cowpea seeds

Four cultivars of cowpea (Vigna unguiculata [L]. Walp.) were infected with cowpea aphid-borne mosaic virus (CABMV) by natural infection in field plots. Seeds taken from these plants were tested for the presence of the virus by ELISA and symptom observation on the plantlets grown from the seeds. A biotin/ streptavidin ELISA technique was used and found to be more sensitive than a standard ELISA protocol for detecting CABMV infection in seed. There was a good correlation between the ELISA detection of CABMV in tissue taken from single cowpea seeds and subsequent development of infected plants grown from the same seeds. The ELISA technique is reliable for selecting CABMV-free stocks of cowpea seeds.     

Immunofluorescent Cell Assay of Infectious Pancreatic Necrosis Virus

An immunofluorescent cell (IFC) assay technique was developed for the quantification of infectious pancreatic necrosis (IPN) virus of salmonid fishes. Cover slip cultures of rainbow trout gonad (RTG-2) cells were infected with diluted virus preparations. After incubation to permit antigen development, the cells were stained with antiviral fluorescent antibody, and the number of fluorescing (infected) cells was counted. Optimal conditions for the IFC assay procedure are: (i) the use of RTG-2 cells cultured for at least 3 days at 20 C; (ii) 1-h absorption of IPN virus to RTG-2 cells at 20 C or alternatively, 4 h at 4 C; (iii) staining the infected cell cultures at 10 to 12 h postinfection. A linear relationship between the relative concentration of virus in the inoculum and the number of fluorescent cells in the first cycle of infection was observed. The IFC assay method is more sensitive than the plaque method for the assay of IPN virus.     

Infection of the flowers and seed of parsnip by Itersonilia pastinacae

Seeding parsnip plants on four commercial holdings in Essex showed not only the root cankers and leaf spots associated with infection by Itersonilia pastinacae, but also extensive lesions on the petioles and necrosis of the inflorescences. These last-named symptoms were proved to be caused by I. pastinacae which could also be found on some of the seeds. Seed infection, though largely superficial, was sometimes more deep-seated. It could be eliminated by soaking the seed in an aqueous suspension of 0·2% thiram at 30 °C for 24 h. Heavily infected seed gave a low percentage of seedlings bearing cotyledon lesions: it is uncertain whether hypocotyl lesions, which also occurred, were caused directly by the fungus. An outdoor test failed to show that infected seed gave rise ultimately to roots bearing Itersonilia cankers: the significance of this and other possible sources of infection is discussed.