Nutrient inputs in soil cultivated with coffee crop fertigated with domestic sewage

Fertigation with wastewaters is a great option for reuse of effluents in agriculture. Domestic effluent can be reused after primary treatment, reducing treatment costs and pollution, also providing water and nutrients to crops. This work aimed to quantify the nutrients income in coffee crop fertigated with domestic sewage. Five treatments were used. T1 received only clean water, and treatments T2, T3, T4 e T5 received 180, 350, 480 and 638 mm of sewage, respectively, during four months. Monthly soil analyses allowed to quantify nutrient inputs of 67.45 kg ha-1 of N, 81.89 kg ha-1 of P, 33.34 kg ha-1 of K+, 173.24 kg ha-1 of Ca2+, 49.18 kg ha-1 of Mg2+, 161.56 kg ha-1 of Na+ and 116.19 kg ha-1 of S. Even though the treatments promoted reductions in fertilization and liming, it was still necessary to complement fertilization of coffee crop fertigated with domestic sewage

Novel rearrangements between different chromosomes with direct impact on the diagnosis of 5p- syndrome

Objectives: Copy Number Variations (CNVs) in the human genome account for common populational variations but can also be responsible for genetic syndromes depending on the affected region. Although a deletion in 5p is responsible for a syndrome with highly recognizable phenotypical features, other chromosomal abnormalities might overlap phenotypes, especially considering that most studies in 5p use traditional cytogenetic techniques and not molecular techniques. Methods: The authors have investigated 29 patients with clinical suspicion of 5p- syndrome using Chromosomal Microarray (CMA), and have gathered information on previous tests, clinical signs, symptoms, and development of the patients. Results: The results showed 23 pure terminal deletions, one interstitial deletion, one deletion followed by a 3 Mb duplication in 5p, three cases of 5p deletion concomitant to duplications larger than 20 Mb in chromosomes 2, 9, and 18, and one 5p deletion with a chromosome Y deletion. CMA showed relevant CNVs not typically associated with 5p- that may have contributed to the final phenotype in these patients. Conclusions: The authors have identified three novel rearrangements between chromosomes 5 and 2 (Patient 27), 5 and 18 (Patient 11), and 5 and Y (Patient 22), with breakpoints and overlapped phenotypes that were not previously described. The authors also highlight the need for further molecular investigation using CMA, in different chromosomes beyond chromosome 5 (since those cases did not show only the typical deletion expected for the 5p- syndrome) to explain discordant chromosomal features and overlapped phenotypes to unravel the cause of the syndrome in atypical cases

Canagliflozin and renal outcomes in type 2 diabetes and nephropathy

BACKGROUND Type 2 diabetes mellitus is the leading cause of kidney failure worldwide, but few effective long-term treatments are available. In cardiovascular trials of inhibitors of sodium–glucose cotransporter 2 (SGLT2), exploratory results have suggested that such drugs may improve renal outcomes in patients with type 2 diabetes. METHODS In this double-blind, randomized trial, we assigned patients with type 2 diabetes and albuminuric chronic kidney disease to receive canagliflozin, an oral SGLT2 inhibitor, at a dose of 100 mg daily or placebo. All the patients had an estimated glomerular filtration rate (GFR) of 30 to <90 ml per minute per 1.73 m2 of body-surface area and albuminuria (ratio of albumin [mg] to creatinine [g], >300 to 5000) and were treated with renin–angiotensin system blockade. The primary outcome was a composite of end-stage kidney disease (dialysis, transplantation, or a sustained estimated GFR of <15 ml per minute per 1.73 m2), a doubling of the serum creatinine level, or death from renal or cardiovascular causes. Prespecified secondary outcomes were tested hierarchically. RESULTS The trial was stopped early after a planned interim analysis on the recommendation of the data and safety monitoring committee. At that time, 4401 patients had undergone randomization, with a median follow-up of 2.62 years. The relative risk of the primary outcome was 30% lower in the canagliflozin group than in the placebo group, with event rates of 43.2 and 61.2 per 1000 patient-years, respectively (hazard ratio, 0.70; 95% confidence interval [CI], 0.59 to 0.82; P=0.00001). The relative risk of the renal-specific composite of end-stage kidney disease, a doubling of the creatinine level, or death from renal causes was lower by 34% (hazard ratio, 0.66; 95% CI, 0.53 to 0.81; P<0.001), and the relative risk of end-stage kidney disease was lower by 32% (hazard ratio, 0.68; 95% CI, 0.54 to 0.86; P=0.002). The canagliflozin group also had a lower risk of cardiovascular death, myocardial infarction, or stroke (hazard ratio, 0.80; 95% CI, 0.67 to 0.95; P=0.01) and hospitalization for heart failure (hazard ratio, 0.61; 95% CI, 0.47 to 0.80; P<0.001). There were no significant differences in rates of amputation or fracture. CONCLUSIONS In patients with type 2 diabetes and kidney disease, the risk of kidney failure and cardiovascular events was lower in the canagliflozin group than in the placebo group at a median follow-up of 2.62 years

ATLANTIC-PRIMATES: a dataset of communities and occurrences of primates in the Atlantic Forests of South America

Primates play an important role in ecosystem functioning and offer critical insights into human evolution, biology, behavior, and emerging infectious diseases. There are 26 primate species in the Atlantic Forests of South America, 19 of them endemic. We compiled a dataset of 5,472 georeferenced locations of 26 native and 1 introduced primate species, as hybrids in the genera Callithrix and Alouatta. The dataset includes 700 primate communities, 8,121 single species occurrences and 714 estimates of primate population sizes, covering most natural forest types of the tropical and subtropical Atlantic Forest of Brazil, Paraguay and Argentina and some other biomes. On average, primate communities of the Atlantic Forest harbor 2 ± 1 species (range = 1–6). However, about 40% of primate communities contain only one species. Alouatta guariba (N = 2,188 records) and Sapajus nigritus (N = 1,127) were the species with the most records. Callicebus barbarabrownae (N = 35), Leontopithecus caissara (N = 38), and Sapajus libidinosus (N = 41) were the species with the least records. Recorded primate densities varied from 0.004 individuals/km 2 (Alouatta guariba at Fragmento do Bugre, Paraná, Brazil) to 400 individuals/km 2 (Alouatta caraya in Santiago, Rio Grande do Sul, Brazil). Our dataset reflects disparity between the numerous primate census conducted in the Atlantic Forest, in contrast to the scarcity of estimates of population sizes and densities. With these data, researchers can develop different macroecological and regional level studies, focusing on communities, populations, species co-occurrence and distribution patterns. Moreover, the data can also be used to assess the consequences of fragmentation, defaunation, and disease outbreaks on different ecological processes, such as trophic cascades, species invasion or extinction, and community dynamics. There are no copyright restrictions. Please cite this Data Paper when the data are used in publications. We also request that researchers and teachers inform us of how they are using the data. © 2018 by the The Authors. Ecology © 2018 The Ecological Society of Americ

Padronização do critério de exclusão para o vírus HTLV I e II nos bancos de olhos do Brasil

RESUMO Objetivo: Investigar em quais Bancos de olhos do Brasil o HTLV I e II é utilizado como critério de exclusão para córnea. Atualmente a legislação brasileira pela Lei nº 9.434/97 e Portaria 2600/09 determina que a cada doação devem ser realizados, obrigatoriamente, testes laboratoriais de triagem de alta sensibilidade, para detecção de marcadores para doenças infecciosas transmissíveis pelo sangue: Vírus da Imunodeficiência Humana (HIV), Vírus da Hepatite B (HbsAg), Anticorpo do Vírus da Hepatite B (AntiHBs), Anticorpo do Vírus da Hepetite B total (Anti-HBc total) e Vírus da Hepatite C (Anti-HCV), no entanto, o Capítulo VI, art. 47, alínea a exclui o Vírus Linfotrópico das Células T-Humanas (HTLV) como critério de exclusão para doadores de córnea. Métodos: Para a realização da pesquisa, foram analisadas as informações de 35 Bancos de Olhos pela base de dados da Central de Transplante da Paraíba, avaliados através do Teste de Homogeneidade do Qui-Quadrado. Resultados: Constatou-se que a sorologia positiva para HTLV I e II foi considerada critério de exclusão em 18 dos 35 Bancos de Olhos analisados. Quanto à análise geográfica dos Bancos de Olhos do Brasil, os da região Nordeste e Sul foram os que mais consideraram o HTLV como critério de exclusão. Conclusão: Os Bancos de Olhos analisados não apresentaram diferença ou associação significativa entre os que consideram e os que não consideram este critério, mostrando, desta forma, não haver uma padronização entre os Bancos de Olhos do Brasil