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1.
Annu Rev Anim Biosci ; 7: 221-243, 2019 02 15.
Artículo en Inglés | MEDLINE | ID: mdl-30418803

RESUMEN

Feed protein supplements are one of the most expensive and limiting feed ingredients. This review offers a comprehensive analysis of how the expected expansion of animal production, driven by the rising world population and living standards for more animal-sourced foods, is creating a global shortage of feed protein supply. Because ruminants, chickens, and pigs contribute to 96% of the global supply of animal protein and aquaculture is growing fast, means of meeting the feed protein requirements of these species are elaborated. Geographic variation and interdependence among China, Europe, and North America in the demand and supply of feed protein are compared. The potential and current state of exploration into alternative feed proteins, including microalgae, insects, single-cell proteins, and coproducts, are highlighted. Strategic innovations are proposed to upgrade feed protein processing and assessment, improve protein digestion by exogenous enzymes, and genetically select feed-efficient livestock breeds. An overall successful and sustainable solution in meeting global feed protein demands will lead to a substantial net gain of human-edible animal protein with a minimal environmental footprint.


Asunto(s)
Alimentación Animal , Pollos/crecimiento & desarrollo , Proteínas en la Dieta , Suplementos Dietéticos , Abastecimiento de Alimentos , Rumiantes/crecimiento & desarrollo , Porcinos/crecimiento & desarrollo , Proteínas Dietéticas Animales , Animales , Dieta/veterinaria , Ambiente , Humanos , Ganado
2.
N Engl J Med ; 379(26): 2529-2539, 2018 12 27.
Artículo en Inglés | MEDLINE | ID: mdl-30586509

RESUMEN

BACKGROUND: Plumbing systems are an infrequent but known reservoir for opportunistic microbial pathogens that can infect hospitalized patients. In 2016, a cluster of clinical sphingomonas infections prompted an investigation. METHODS: We performed whole-genome DNA sequencing on clinical isolates of multidrug-resistant Sphingomonas koreensis identified from 2006 through 2016 at the National Institutes of Health (NIH) Clinical Center. We cultured S. koreensis from the sinks in patient rooms and performed both whole-genome and shotgun metagenomic sequencing to identify a reservoir within the infrastructure of the hospital. These isolates were compared with clinical and environmental S. koreensis isolates obtained from other institutions. RESULTS: The investigation showed that two isolates of S. koreensis obtained from the six patients identified in the 2016 cluster were unrelated, but four isolates shared more than 99.92% genetic similarity and were resistant to multiple antibiotic agents. Retrospective analysis of banked clinical isolates of sphingomonas from the NIH Clinical Center revealed the intermittent recovery of a clonal strain over the past decade. Unique single-nucleotide variants identified in strains of S. koreensis elucidated the existence of a reservoir in the hospital plumbing. Clinical S. koreensis isolates from other facilities were genetically distinct from the NIH isolates. Hospital remediation strategies were guided by results of microbiologic culturing and fine-scale genomic analyses. CONCLUSIONS: This genomic and epidemiologic investigation suggests that S. koreensis is an opportunistic human pathogen that both persisted in the NIH Clinical Center infrastructure across time and space and caused health care-associated infections. (Funded by the NIH Intramural Research Programs.).


Asunto(s)
Infección Hospitalaria/microbiología , Reservorios de Enfermedades/microbiología , Infecciones por Bacterias Gramnegativas/microbiología , Ingeniería Sanitaria , Sphingomonas/genética , Antibacterianos/farmacología , Hospitales Federales , Humanos , Metagenómica , Pruebas de Sensibilidad Microbiana , National Institutes of Health (U.S.) , Estudios Retrospectivos , Sphingomonas/efectos de los fármacos , Sphingomonas/aislamiento & purificación , Estados Unidos , Abastecimiento de Agua , Secuenciación Completa del Genoma
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