A Native Hymenopteran Predator of \u3ci\u3eAgonopterix Alstroemeriana\u3c/i\u3e (Lepidoptera: Oecophoridae) in East-Central Illinois

Agonopterix alstroemeriana is a European oecophorid moth that defoliates poison hemlock (Conium maculatum), a noxious Eurasian weed extensively naturalized throughout temperate Australia, New Zealand, North America, and South America. Throughout western North America, and increasingly in the Midwest and Northeast, A. alstroemeriana has been utilized in poison hemlock eradication programs. We report, for the first time, predation on A. alstroemeriana by Euodynerus foraminatus (Hymenoptera: Eumenidae), a native solitary wasp that paralyzes these and other lepidopteran larvae and uses them to provision its nests. The presence of an effective predator may reduce the impact of A. alstroemeriana in biological control programs

A Native Hymenopteran Predator of \u3ci\u3eAgonopterix Alstroemeriana\u3c/i\u3e (Lepidoptera: Oecophoridae) in East-Central Illinois

Agonopterix alstroemeriana is a European oecophorid moth that defoliates poison hemlock (Conium maculatum), a noxious Eurasian weed extensively naturalized throughout temperate Australia, New Zealand, North America, and South America. Throughout western North America, and increasingly in the Midwest and Northeast, A. alstroemeriana has been utilized in poison hemlock eradication programs. We report, for the first time, predation on A. alstroemeriana by Euodynerus foraminatus (Hymenoptera: Eumenidae), a native solitary wasp that paralyzes these and other lepidopteran larvae and uses them to provision its nests. The presence of an effective predator may reduce the impact of A. alstroemeriana in biological control programs

Evaluation of a hospital-based integrated model of eye care for diabetic retinopathy assessment: A multimethod study

Objectives Diabetic eye disease is a leading cause of blindness but can be mitigated by regular eye assessment. A framework of issues, developed from the literature of barriers to eye assessment, was used to structure an examination of perceptions of a new model of care for diabetic retinopathy from the perspective of staff using the model, and health professionals referring patients to the new service. Design Multimethod: interviews and focus groups, and a separate survey. Setting A new clinic based on an integrated model of care was established at a hospital in outer metropolitan Sydney, Australia in 2017. Funded jointly by Centre for Eye Health (CFEH) and the hospital, the clinic was equipped and staffed by optometrists who work alongside the ophthalmologists in the existing hospital eye clinic. Participants Five (of seven) hospital staff working in the clinic (ophthalmologists and administrative officers) or referring to it from other departments (endocrinologists); nine optometrists from CFEH who developed or worked in the clinic; 10 community-based optometrists as potential referrers. Results The new clinic was considered to have addressed known barriers to eye assessment, including access, assistance for patients unable/unwilling to organise eye checks and efficient management of human resources. The clinic optimised known drivers of this model of care: providing clear scope of practice and protocols for shared care between optometrists and ophthalmologists, good communication between referrers and eye professionals and a collegial approach promoting interprofessional trust. Remaining areas of concern were few referrals from general practitioners, fewer referrals from hospital endocrinologists than expected and issues with stretched administrative capacity. There were also perceived mismatches between the priorities of hospital management and aims of the clinic. Conclusions The new model was considered to have addressed many of the barriers to assessment. While there remain issues with the model, there were also unexpected benefits

Underdeveloped RPE Apical Domain Underlies Lesion Formation in Canine Bestrophinopathies

Canine bestrophinopathy (cBest) is an important translational model for BEST1-associated maculopathies in man that recapitulates the broad spectrum of clinical and molecular disease aspects observed in patients. Both human and canine bestrophinopathies are characterized by focal to multifocal separations of the retina from the RPE. The lesions can be macular or extramacular, and the specific pathomechanism leading to formation of these lesions remains unclear. We used the naturally occurring canine BEST1 model to examine factors that underlie formation of vitelliform lesions and addressed the susceptibility of the macula to its primary detachment in BEST1-linked maculopathies

Metabolic analysis of the interaction between plants and herbivores

Insect herbivores by necessity have to deal with a large arsenal of plant defence metabolites. The levels of defence compounds may be increased by insect damage. These induced plant responses may also affect the metabolism and performance of successive insect herbivores. As the chemical nature of induced responses is largely unknown, global metabolomic analyses are a valuable tool to gain more insight into the metabolites possibly involved in such interactions. This study analyzed the interaction between feral cabbage (Brassica oleracea) and small cabbage white caterpillars (Pieris rapae) and how previous attacks to the plant affect the caterpillar metabolism. Because plants may be induced by shoot and root herbivory, we compared shoot and root induction by treating the plants on either plant part with jasmonic acid. Extracts of the plants and the caterpillars were chemically analysed using Ultra Performance Liquid Chromatography/Time of Flight Mass Spectrometry (UPLCT/MS). The study revealed that the levels of three structurally related coumaroylquinic acids were elevated in plants treated on the shoot. The levels of these compounds in plants and caterpillars were highly correlated: these compounds were defined as the ‘metabolic interface’. The role of these metabolites could only be discovered using simultaneous analysis of the plant and caterpillar metabolomes. We conclude that a metabolomics approach is useful in discovering unexpected bioactive compounds involved in ecological interactions between plants and their herbivores and higher trophic levels.

Catchment-scale patterns of geomorphic activity and vegetation distribution in an alpine glacier foreland (Kaunertal Valley, Austria)

The interaction between geomorphological and ecological processes plays a significant role in determining landscape patterns in glacier forelands. However, the spatial organization of this biogeomorphic mosaic remains unclear due to limited catchment-scale data. To address this gap, we used a multi-proxy analysis to map potential geomorphic activity related to surface changes induced by sediment transport on drift-mantled slopes and a glaciofluvial plain. High-resolution vegetation data were used to generate a catchment-scale map delineating vegetation cover and stability thresholds. The two maps were integrated, and an exploratory regression analysis was conducted to investigate the influence of geomorphic activity on vegetation colonization. The multi-proxy analysis resulted in an accurate mapping of catchment-wide geomorphic activity, with a validation accuracy ranging from 75.3% through field mapping to 85.9% through plot sampling. Through vegetation cover mapping, we identified biogeomorphic stability thresholds, revealing a mosaic of vegetation distribution. Distinct colonization patterns emerged across different geomorphic process groups, influenced by process magnitude and the time since the last disturbance event. The exploratory regression analysis showed that vegetation distribution is significantly affected by geomorphic processes. Based on the overlay of results regarding geomorphic activity and vegetation distribution, we suggest an age-independent framework that indicates four potential situations of biogeomorphic succession

Identical Mutation in a Novel Retinal Gene Causes Progressive Rod-Cone Degeneration in Dogs and Retinitis Pigmentosa in Humans

Progressive rod–cone degeneration (prcd) is a late-onset, autosomal recessive photoreceptor degeneration of dogs and a homolog for some forms of human retinitis pigmentosa (RP). Previously, the disease-relevant interval was reduced to a 106-kb region on CFA9, and a common phenotype-specific haplotype was identified in all affected dogs from several different breeds and breed varieties. Screening of a canine retinal EST library identified partial cDNAs for novel candidate genes in the disease-relevant interval. The complete cDNA of one of these, PRCD, was cloned in dog, human, and mouse. The gene codes for a 54-amino-acid (aa) protein in dog and human and a 53-aa protein in the mouse; the first 24 aa, coded for by exon 1, are highly conserved in 14 vertebrate species. A homozygous mutation (TGC → TAC) in the second codon shows complete concordance with the disorder in 18 different dog breeds/breed varieties tested. The same homozygous mutation was identified in a human patient from Bangladesh with autosomal recessive RP. Expression studies support the predominant expression of this gene in the retina, with equal expression in the retinal pigment epithelium, photoreceptor, and ganglion cell layers. This study provides strong evidence that a mutation in the novel gene PRCD is the cause of autosomal recessive retinal degeneration in both dogs and humans

Modeling the Structural Consequences of \u3cem\u3eBEST1\u3c/em\u3e Missense Mutations

Mutations in the bestrophin-1 gene (BEST1) are an important cause of inherited retinal disorders. Hitherto, over 100 unique allelic variants have been linked to the human BEST1 (hBEST1), and associated with disease phenotypes, broadly termed as bestrophinopathies. A spontaneous animal model recapitulating BEST1-related phenotypes, canine multifocal retinopathy (cmr), is caused by mutations in the canine gene ortholog (cBEST1). We have recently characterized molecular consequences of cmr, demonstrating defective protein trafficking as a result of G161D (cmr2) mutation. To further investigate the pathological effects of BEST1 missense mutations, canine and human peptide fragments derived from the protein sequence have been studied in silico as models for early events in the protein folding. The results showed that G161D as well as I201T substitutions cause severe conformational changes in the structure of bestrophin-1, suggesting protein misfolding as an underlying disease mechanism. The comparative modeling studies expand our insights into BEST1 pathogenesis

DNA testing and domestic dogs

There are currently about 80 different DNA tests available for mutations that are associated with inherited disease in the domestic dog, and as the tools available with which to dissect the canine genome become increasingly sophisticated, this number can be expected to rise dramatically over the next few years. With unrelenting media pressure focused firmly on the health of the purebred domestic dog, veterinarians and dog breeders are turning increasingly to DNA tests to ensure the health of their dogs. It is ultimately the responsibility of the scientists who identify disease-associated genetic variants to make sensible choices about which discoveries are appropriate to develop into commercially available DNA tests for the lay dog breeder, who needs to balance the need to improve the genetic health of their breed with the need to maintain genetic diversity. This review discusses some of the factors that should be considered along the route from mutation discovery to DNA test and some representative examples of DNA tests currently available