Plant pathogen culture collections: it takes a village to preserve these resources vital to the advancement of agricultural security and plant pathology

ABSTRACT Plant pathogen culture collections are essential resources in our fight against plant disease and for connecting discoveries of the present with established knowledge of the past. However, available infrastructure in support of culture collections is in serious need of improvement, and we continually face the risk of losing many of these collections. As novel and reemerging plant pathogens threaten agriculture, their timely identification and monitoring depends on rapid access to cultures representing the known diversity of plant pathogens along with genotypic, phenotypic, and epidemiological data associated with them. Archiving such data in a format that can be easily accessed and searched is essential for rapid assessment of potential risk and can help track the change and movement of pathogens. The underexplored pathogen diversity in nature further underscores the importance of cataloguing pathogen cultures. Realizing the potential of pathogen genomics as a foundation for developing effective disease control also hinges on how effectively we use the sequenced isolate as a reference to understand the genetic and phenotypic diversity within a pathogen species. In this letter, we propose a number of measures for improving pathogen culture collections.     

Morphological, developmental and ecological evidence for a progenetic life cycle in Neochasmus (Digenea)

Seven species of fishes, Catostomus commersonii (Lacépède), Etheostoma nigrum Rafinesque, Micropterus dolomieu Lacépède, Notemigonus crysoleucas (Mitchill), Notropis hudsonius (Clinton), Perca flavescens (Mitchill), and Percina caprodes (Rafinesque) from the St. Lawrence River, Quebec, Canada, were found infected with progenetic specimens of Neochasmus spp. in the orbits and/or the body musculature. Worms displayed varying degrees of maturation. Eggs occupied the entirety of the worm in late stages of development and persisted as distinct clusters in situ after worm death. Populations of parasites were studied monthly in E. nigrum from one site between May and October in order to follow parasite recruitment, development and maturation. Recruitment of parasites was observed in young-of-the-year fish primarily in July and continued through October. Worms matured rapidly, displaying egg production within a month. Later developmental stages, in which eggs occupied most of the worm, and clusters of eggs became abundant by September. Infections in overwintered fish collected in May consisted mainly of worms in early stages of egg production and of clusters of eggs. When hatched artificially, eggs from the clusters released viable miracidia, indicating that they survive beyond the lifespan of the adult worm. It is suggested that progenesis is a fixed characteristic of the life cycle of these species, that egg dispersal requires the death of the host and that it is facilitated by predation. All prior records of Neochasmus spp. are examined, leading us to conclude that the role of the putative definitive host (primarily basses) has been reduced to that of a dispersal agent. Current hypotheses concerning the evolution and maintenance of progenesis are considered, but it is concluded that they do not apply to this host-parasite system.     

Genetic variability in the feeding behavior of crossbred growing cattle and associations with performance and feed efficiency

The objectives of the present study were to estimate genetic parameters for several feeding behavior traits in growing cattle, as well as the genetic associations among and between feeding behavior and both performance and feed efficiency traits. An additional objective was to investigate the use of feeding behavior traits as predictors of genetic merit for feed intake. Feed intake and live-weight data on 6,088 growing cattle were used of which 4,672 had ultrasound data and 1,548 had feeding behavior data. Feeding behavior traits were defined based on individual feed events or meal events (where individual feed events were grouped into meals). Univariate and bivariate animal linear mixed models were used to estimate (co)variance components. Heritability estimates (± SE) for the feeding behavior traits ranged from 0.19 ± 0.08 for meals per day to 0.61 ± 0.10 for feeding time per day. The coefficient of genetic variation per trait varied from 5% for meals per day to 22% for the duration of each feed event. Genetically heavier cattle, those with a higher daily energy intake (MEI), or those that grew faster had a faster feeding rate, as well as a greater energy intake per feed event and per meal. Better daily feed efficiency (i.e., lower residual energy intake) was genetically associated with both a shorter feeding time per day and shorter meal time per day. In a validation population of 321 steers and heifers, the ability of estimated breeding values (EBV) for MEI to predict (adjusted) phenotypic MEI was demonstrated; EBVs for MEI were estimated using multi-trait models with different sets of predictor traits such as liveweight and/or feeding behaviors. The correlation (± SE) between phenotypic MEI and EBV for MEI marginally improved (P < 0.001) from 0.64 ± 0.03 to 0.68 ± 0.03 when feeding behavior phenotypes from the validation population were included in a genetic evaluation that already included phenotypic mid-test metabolic live-weight from the validation population. This is one of the largest studies demonstrating that significant exploitable genetic variation exists in the feeding behavior of young crossbred growing cattle; such feeding behavior traits are also genetically correlated with several performance and feed efficiency metrics. Nonetheless, there was only a marginal benefit to the inclusion of time-related feeding behavior phenotypes in a genetic evaluation for MEI to improve the precision of the EBVs for this trait.     

Effect of application rate on the sensitivity of Erysiphe graminis f.sp. tritici to fenpropimorph

Two sprays of fenpropimorph per season were applied to a winter wheat field trial, at a range of rates, which included the full commercial rate, in order to test the effect of fenpropimorph sprays on the sensitivity of Erysiphe graminis f.sp. tritici. While a reduction in the sensitivity of the mildew isolates was detected after fungicide application, this was not dependent on the rate of fungicide applied. Reduced rates were not found to induce a larger shift towards insensitivity than the full commercial rate. Powdery mildew isolates were collected from 1993 to 1996 and their sensitivity to fenpropimorph determined in order to monitor sensitivity changes in the population. While a decline in sensitivity was noted from season to season, there was no correlation between a lower sensitivity and the rate of fenpropimorph previously used. Isolates collected in Scotland were found to be significantly less sensitive than those sampled in the south of England. ©1997 SCI     

Detection of pseudorabies virus antibody in swine serum and oral fluid specimens using a recombinant gE glycoprotein dual-matrix indirect ELISA

Pseudorabies (Aujeszky disease) virus (PRV) was eliminated from domestic swine in many countries using glycoprotein E (gE)-deleted vaccines and serum antibody gE ELISAs, but PRV continues to circulate in some regions and in most feral swine populations in the world. We created a dual-matrix (serum and oral fluid) indirect IgG gE ELISA (iELISA) and evaluated its performance using samples from 4 groups of 10 pigs each: negative control (NC), vaccination (MLV), PRV inoculation (PRV), and vaccination followed by challenge (MLV-PRV). All serum and oral fluid samples collected before PRV challenge and all NC samples throughout the study were negative for gE antibodies by commercial blocking ELISA (bELISA) and our iELISA. Nasal swab samples from 9 of 10 animals in the PRV group were gB quantitative PRC (qPCR) positive at 2 days post-inoculation (dpi). The oral fluid iELISA detected a significant S/P response in the PRV (p = 0.03) and MLV-PRV (p = 0.01) groups by 6 dpi. ROC analyses of serum bELISA (n = 428), serum iELISA (n = 426), and oral fluid iELISA (n = 247) showed no significant differences in performance (p > 0.05). Our data support the concept of PRV surveillance based on oral fluid samples tested by an indirect gE ELISA.     

Optimization of the lighting system for a Hydraulically Integrated Serial Turbidostat Algal Reactor (HISTAR): Economic implications

An estimated 28% of the production cost in HISTAR systems that are artificially illuminated is attributed to the lighting cost. This cost estimated is based on an operational configuration comprised of eight CFSTRs, a system dilution rate (D_s) of 0.640 d^?1, and 400 W metal halide lamps positioned at an elevation of 38.1 cm over the culture. Deterministic model simulations of the volumetric productivity (P_v), photosynthetic efficiency (E_o) and lighting cost (LC) under various management strategies, operational parameters and reactor design configurations were performed and compared to the simulation results obtained for the original configuration. The simulations showed that LC may be reduced by 35.5% by switching from a metal halide (MH) to high-pressure sodium (HPS) light source at an optimum system dilution rate D_s = 0.641 d^?1. LC may be reduced by an additional 17.8% through decreasing the lamp elevation to 25.4 cm. Increasing the wattage of the light source from 400 to 1000 W in the last six reactors would reduce the LC by 13% from the original cost. Overall, using HPS lamps at 25.4 cm height, with six 1000 W and two 400 W lamps at a D_s = 0.641 d^?1 will result in a 54% overall LC reduction compared to the original configuration of HISTAR. This represents a 13% reduction in the overall microalgal production cost for HISTAR.     

成功源于对"上帝"的优质服务——访德国蓝帜公司联合体总裁狄特·布如客拉赫博士德国机械设备制造业联合会(VDMA)主席

严谨、认真是德国人留给世界的印象,正是这一特点铸就了德国制造的商品质。对产品品质的追求延伸到了对每一个用户所使用产品的长久维护。真正做到“顾客就是上帝”是蓝帜以戌许多企业的成功源动力。[编按]