Staphylococcus aureus in Some Brazilian Dairy Industries: Changes of Contamination and Diversity

Staphylococcus aureus, a major food-poisoning pathogen, is a common contaminant in dairy industries worldwide, including in Brazil. We determined the occurrence of S. aureus in five dairies in Brazil over 8 months. Of 421 samples, 31 (7.4%) were positive for S. aureus and prevalence varied from 0 to 63.3% between dairies. Sixty-six isolates from the 31 samples were typed by Multi-Locus Sequence Typing to determine if these isolates were persistent or continuously reintroduced. Seven known sequence types (STs), ST1, ST5, ST30, ST97, ST126, ST188 and ST398, and four new ST were identified, ST3531, ST3540, ST3562 and ST3534. Clonal complex (CC) 1 (including the four new ST), known as an epidemic clone, was the dominant CC. However, there were no indications of persistence of particular ST. The resistance toward 11 antibiotic compounds was assessed. Twelve profiles were generated with 75.8% of strains being sensitive to all antibiotic classes and no Methicillin-resistant S. aureus (MRSA) strains were found. The enterotoxin-encoding genes involved in food-poisoning, e.g., sea, sed, see, and seg were targeted by PCR. The two toxin-encoding genes, sed and see, were not detected. Only three strains (4.5%) harbored seg and two of these also harbored sea. Despite the isolates being Methicillin-sensitive S. aureus (MSSA), the presence of CC1 clones in the processing environment, including some harboring enterotoxin encoding genes, is of concern and hygiene must have high priority to reduce contamination

Tecidos vegetais.

Amostragem; Procedimento para coleta de amostras de folhas no campo; Coleta da amostra; Identificacao da amostra; Moagem; Armazenagem; Integridade da amostra; Problemas de contaminacao; Arquivo de amostra

EFEITO DE DIFERENTES DOSES DE CLOPROSTENOL SÓDICO NO PERÍODO PÓS-PARTO DE VACAS DE CORTE

O restabelecimento da atividade reprodutiva pós-parto é dependente de dois processos fisiológicos, a involução uterina e o restabelecimento da atividade luteal cíclica. Problemas ou atrasos na involução uterina podem afetar diretamente a atividade ovariana pós-parto. As prostaglandinas F2a (PGF2a) exercem uma importante função no processo de involução uterina. Entretanto, a utilização dos análogos sintéticos da PGF2a para estimular involução uterina em bovinos tem sido pequena. O objetivo deste estudo foi avaliar o efeito de duas doses de uma mistura racêmica de cloprostenol (D+L-Cloprostenol), aplicadas no pós-parto imediato, sobre o desempenho reprodutivo de vacas mestiças de corte. Vacas de corte com parto normal foram divididas aleatoriamente em três grupos: G1(n=144), grupo controle; G2 (n=145), 0.530mg de D+L-Cloprostenol, aplicados IM de três a cinco dias após o parto, e G3 (n=145), 1.060 mg de D+L-Cloprostenol, no mesmo protocolo de G2. Foram analisados os serviços por concepção (c2), dias do parto à primeira inseminação e período de serviço. Não foram observadas diferenças no número de serviços por concepção nos três grupos (P>0.05). A média de dias do parto à primeira inseminação foi de 88,77 + 23,64ª; 77,59 + 26,95b e 76,22 + 26,28b, e o intervalo parto-concepção foi de 97.34±26.54ª; 86,38 + 28,81b; 85,23 + 30,12b, para os grupos 1, 2 e 3, respectivamente (P<0.05). O tratamento, independente da dose de cloprostenol, antecipou o reinicio da atividade reprodutiva em mais de 10 dias. A aplicação de cloprostenol sódico no pós-parto pode melhorar a eficiência reprodutiva de vacas de corte. Não existem diferenças entre as duas doses comparadas. PALAVRAS-CHAVE: bovino; involução uterina; prostaglandinas

Electrochemical mediated oxidation of phenol using Ti/IrO2 and Ti/Pt-SnO2-Sb2O5 electrodes

The indirect electrochemical oxidation of phenol was studied at Ti/IrO2 and Ti/Pt-SnO2-Sb2O5 electrodes by bulk electrolysis experiments under galvanostatic control. The obtained results clearly shown that the electrode material was an impor­tant para­me­ter for the optimization of such processes determining their mecha­nism and oxidation products. Different current efficiencies were obtained at Ti/IrO2 and Ti/Pt-SnO2-Sb2O5, depending on the applied current density in the range from 10, 20 and 30 mA cm−2. The effect of the amount of dissolved NaCl was studied also. It was observed that the electrochemical processes (direct/indirect) favor specific oxidation pathways depending on electrocatalytic material. Phenol degradation generates several intermediates eventually leading to complete mineralization, as indicated by the results obtained with the High-performance liquid chromatography (HPLC) technique

Aedes fluviatilis cell lines as new tools to study metabolic and immune interactions in mosquito‑Wolbachia symbiosis

In the present work, we established two novel embryonic cell lines from the mosquito Aedes fluviatilis containing or not the naturally occurring symbiont bacteria Wolbachia, which were called wAflu1 and Aflu2, respectively. We also obtained wAflu1 without Wolbachia after tetracycline treatment, named wAflu1.tet. Morphofunctional characterization was performed to help elucidate the symbiont-host interaction in the context of energy metabolism regulation and molecular mechanisms of the immune responses involved. The presence of Wolbachia pipientis improves energy performance in A. fluviatilis cells; it affects the regulation of key energy sources such as lipids, proteins, and carbohydrates, making the distribution of actin more peripheral and with extensions that come into contact with neighboring cells. Additionally, innate immunity mechanisms were activated, showing that the wAflu1 and wAflu1.tet cells are responsive after the stimulus using Gram negative bacteria. Therefore, this work confirms the natural, mutually co-regulating symbiotic relationship between W. pipientis and A. fluviatilis, modulating the host metabolism and immune pathway activation. The results presented here add important resources to the current knowledge of Wolbachia-arthropod interactions

Antibody dynamics and spontaneous viral clearance in patients with acute hepatitis C infection in Rio de Janeiro, Brazil

Submitted by Sandra Infurna ([email protected]) on 2017-01-18T10:31:05Z No. of bitstreams: 1 clara_yoshida_etal_IOC_2011.pdf: 146042 bytes, checksum: 8ec889224534b76d755828a99d0660c2 (MD5)Approved for entry into archive by Sandra Infurna ([email protected]) on 2017-01-18T10:59:52Z (GMT) No. of bitstreams: 1 clara_yoshida_etal_IOC_2011.pdf: 146042 bytes, checksum: 8ec889224534b76d755828a99d0660c2 (MD5)Made available in DSpace on 2017-01-18T10:59:52Z (GMT). No. of bitstreams: 1 clara_yoshida_etal_IOC_2011.pdf: 146042 bytes, checksum: 8ec889224534b76d755828a99d0660c2 (MD5) Previous issue date: 2011Innsbruck Medical University. Department of Medical Statistics, Informatics and Health Economics. Innsbruck, Austria.Harvard Medical School. Boston, MA, USA / Massachussets General Hospital. Division of Infectious Diseases. Boston, MA, USA.Harvard Medical School. Boston, MA, USA / Massachussets General Hospital. Gastrointestinal Unit. Boston, MA, USA.Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Hepatites Virais. Rio de Janeiro, RJ. Brasil.Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Hepatites Virais. Rio de Janeiro, RJ. Brasil.Laboratório Central de Saúde Pública Noel Nutels. Divisão de Hepatites. Rio de Janeiro, RJ, Brasil.Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Hepatites Virais. Rio de Janeiro, RJ. Brasil.Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Hepatites Virais. Rio de Janeiro, RJ. Brasil / Universidade Federal do Estado do Rio de Janeiro. Hospital Universitário Gaffrée Guinle. Unidade de Hepatologia. Rio de Janeiro, RJ, Brasil.Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Desenvolvimento Tecnológico em Virologia. Rio de Janeiro, RJ, Brasil.Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Hepatites Virais. Rio de Janeiro, RJ. Brasil.Universitätsklinikum Eppendorf. Medizinische Klinik I. Hamburg, Germany.Fondation Merieux. Emerging Pathogens Laboratory. Lyon, France.University of Innsbruck. Institute of Statistics. Innsbruck, Austria.National Institute on Aging. Gerontology Research Center. Baltimore, USA.Innsbruck Medical University. Department of Medical Statistics, Informatics and Health Economics. Innsbruck, Austria.Innsbruck Medical University. Department of Medical Statistics, Informatics and Health Economics. Innsbruck, Austria.Innsbruck Medical University. Department of Medical Statistics, Informatics and Health Economics. Innsbruck, Austria.Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Hepatites Virais. Rio de Janeiro, RJ. Brasil.Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Hepatites Virais. Rio de Janeiro, RJ. Brasil.Background: The anti-HCV antibody response has not been well characterized during the early phase of HCV infection and little is known about its relationship to the clinical course during this period. Methods: We analyzed serial anti-HCV antibodies longitudinally obtained from a prospective cohort of 65 patients with acute HCV infection by using a microparticle enzyme immunoassay AxSYM HCV 3.0 (Abbott Diagnostics) during the first 12 months from HCV acquisition in Rio de Janeiro, Brazil. Spontaneous viral clearance (SVC) was defined as undetectable HCV RNA in serum, in the absence of treatment, for three consecutive HCV PCR tests within 12-months of follow-up. Results: Baseline antibody values were similar among patient groups with self-limiting HCV evolution (n = 34) and persistent viremia (n = 31) [median (interquartile range) signal/cut-off ratio (s/co) 78.7 (60.7-93.8) vs. 93.9 (67.8- 111.9), p = 0.26]. During 12-months follow-up, patients with acute spontaneous resolving HCV infection showed significantly lower serial antibody response in comparison to individuals progressing to chronic infection [median (interquartile range) s/co 62.7 (35.2-85.0) vs. 98.4 (70.4-127.4), p < 0.0001]. In addition, patients with self-limiting HCV evolution exhibited an expeditious, sharp decline of serial antibody values after SVC in comparison to those measured before SVC [median (interquartile range) s/co 56.0 (25.4-79.3) vs. 79.4 (66.3-103.0), p < 0.0001]. Conclusion: Our findings indicate a rapid short-term decline of antibody values in patients with acute spontaneous resolving HCV infection

Levantamento sorológico de anticorpos anti-Neospora caninum e anti-Toxoplasma gondii em ovinos no interior de São Paulo, SP: Serological survey of anti-Neospora caninum and anti-Toxoplasma gondii antibodies in sheep in the interior of São Paulo, SP

A ovinocultura no Brasil é uma atividade lucrativa, produzindo no ano de 2019 em torno de 19,7 milhões de cabeças. No entanto, algumas doenças podem trazer prejuízo ao produtor, como por exemplo, a neosporose e a toxoplasmose, que são responsáveis por perdas econômicas significativas especialmente devido ao abortamento. A neosporose é uma importante enfermidade causada pelo protozoário Neospora caninum. A toxoplasmose é uma zoonose de distribuição mundial, causada pelo Toxoplasma gondii, protozoário unicelular. Nesse contexto, o presente estudo teve como objetivo realizar a pesquisa de anticorpos anti-Neospora caninum e anti-Toxoplasma gondii em ovinos da região de Indaiatuba, interior do estado de São Paulo. Para tanto, foram colhidas amostras de sangue de 100 animais de diferentes idade e sexo. Para a detecção de anticorpos foram empregadas a reação de imunofluorescência indireta (RIFI). Para a detecção de IgG anti-Neospora caninum foi utilizado como antígeno taquizoítos da cepa NC-1. Como anticorpo secundário foi utilizado o conjugado comercial anti-ovino IgG (Sigma, USA, F7887) marcado com isotiocianato de fluoresceína. Para a detecção de anticorpos IgG anti-Toxoplasma gondii foi adotado o protocolo preconizado por Camargo (1964), utilizando-se anticorpos anti-IgG-ovino (Sigma®) conjugado ao isotiocianato de fluoresceína, com ponto de corte 64, utilizando-se como antígeno, taquizoítos da cepa RH. Em todas as reações foram incluídos controle positivo e negativo, previamente conhecidos. A RIFI foi realizada no Departamento de Medicina Veterinária (DMV), da Universidade Federal Rural de Pernambuco (UFRPE). Dos 100 animais testados para Neospora caninum, os resultados do teste de sorodiagnóstico indicaram 12% (12/100) de animais positivos, sendo 25% (3/12) filhotes, 25% (3/12) jovens e 50% (6/12) adultos. Em relação ao sexo, 16,70% (2/12) eram machos e 83,30% (10/12) fêmeas. Os resultados para Toxoplasma gondii indicaram 37% (37/100) de animais soropositivos. Em relação a idade, observou-se 16,22% (6/37) filhotes, 2,70% (1/37) jovens e 81,08% (30/37) adultos. Em relação ao sexo verificou-se que dos animais positivos, 27,02% (10/37) eram machos e 72,97% (27/37) fêmeas. Com base nos resultados do presente estudo concluiu-se que a ocorrência de animais com neoporose e toxoplasmose é expressiva na propriedade pesquisada. Novos estudos devem ser conduzidos para verificação dos fatores de riscos a fim de adotarem medidas de prevenção e controle

Scalable production of human mesenchymal stromal cell-derived extracellular vesicles under serum-/xeno-free conditions in a microcarrier-based bioreactor culture system

Copyright © 2020 de Almeida Fuzeta, Bernardes, Oliveira, Costa, Fernandes-Platzgummer, Farinha, Rodrigues, Jung, Tseng, Milligan, Lee, Castanho, Gaspar, Cabral and da Silva. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.Mesenchymal stromal cells (MSC) hold great promise for tissue engineering and cell-based therapies due to their multilineage differentiation potential and intrinsic immunomodulatory and trophic activities. Over the past years, increasing evidence has proposed extracellular vesicles (EVs) as mediators of many of the MSC-associated therapeutic features. EVs have emerged as mediators of intercellular communication, being associated with multiple physiological processes, but also in the pathogenesis of several diseases. EVs are derived from cell membranes, allowing high biocompatibility to target cells, while their small size makes them ideal candidates to cross biological barriers. Despite the promising potential of EVs for therapeutic applications, robust manufacturing processes that would increase the consistency and scalability of EV production are still lacking. In this work, EVs were produced by MSC isolated from different human tissue sources [bone marrow (BM), adipose tissue (AT), and umbilical cord matrix (UCM)]. A serum-/xeno-free microcarrier-based culture system was implemented in a Vertical-WheelTM bioreactor (VWBR), employing a human platelet lysate culture supplement (UltraGROTM-PURE), toward the scalable production of MSC-derived EVs (MSC-EVs). The morphology and structure of the manufactured EVs were assessed by atomic force microscopy, while EV protein markers were successfully identified in EVs by Western blot, and EV surface charge was maintained relatively constant (between −15.5 ± 1.6 mV and −19.4 ± 1.4 mV), as determined by zeta potential measurements. When compared to traditional culture systems under static conditions (T-flasks), the VWBR system allowed the production of EVs at higher concentration (i.e., EV concentration in the conditioned medium) (5.7-fold increase overall) and productivity (i.e., amount of EVs generated per cell) (3-fold increase overall). BM, AT and UCM MSC cultured in the VWBR system yielded an average of 2.8 ± 0.1 × 1011, 3.1 ± 1.3 × 1011, and 4.1 ± 1.7 × 1011 EV particles (n = 3), respectively, in a 60 mL final volume. This bioreactor system also allowed to obtain a more robust MSC-EV production, regarding their purity, compared to static culture. Overall, we demonstrate that this scalable culture system can robustly manufacture EVs from MSC derived from different tissue sources, toward the development of novel therapeutic products.unding received by iBB-Institute for Bioengineering and Biosciences from the Portuguese Foundation for Science and Technology (FCT) (UID/BIO/04565/2020) and through the projects PTDC/EQU-EQU/31651/2017, PTDC/BBB-BQB/1693/2014, and PTDC/BTM-SAL/31057/2017 is acknowledged. Funding received from POR de Lisboa 2020 through the project PRECISE – Accelerating progress toward the new era of precision medicine (Project N. 16394) is also acknowledged. MAF (PD/BD/128328/2017) and FO (PD/BD/135046/2017) acknowledge FCT for the Ph.D. fellowships and DG (SFRH/BPD/109010/2015) for the Post-Doctoral fellowship.info:eu-repo/semantics/publishedVersio