Cooling of porcine semen in an extender supplemented with isoespintanol / Resfriamento de sêmen suíno em um diluente suplementado com isoespintanol

ABSTRACT: Spermatozoa experience oxidative, osmotic, chemical, and thermal stresses when cooled, which degrade the quality and fertilizing capacity of the cells. Adding antioxidants to the sperm extender mitigates these alterations. This study evaluated the effect of isoespintanol (ISO) on boar semen subjected to cooling. Fifteen ejaculates from five boars (Susscrofadomestica) were extended in Beltsville thawing solution (BTS) supplemented with 0 µM (control), 5 µM (ISO5), 10 µM (ISO10), 15 µM (ISO15), 20 µM (ISO20), 25 µM (ISO25), and 30 µM (ISO30) of ISO, which were then cooled for five days at 16 °C. Sperm kinetics, total motility (TM), and progressive motility (PM) were evaluated every 24 h using an IVOS computer-assisted sperm analysis (CASA) system. On day 1 and day 5 of cooling, a hypoosmotic test, spectrofluorometry, and flow cytometry were performed to evaluate the following: membrane functionality, measured as a function of hypoosmotic swelling (HOS); total antioxidant capacity (TAC); reactive oxygen species (ROS); and mitochondrial membrane potential (Δ¥M). Regression analysis and comparison of means using the Duncan test were performed. The ISO added had a slight impact on sperm motility, as evidenced by a reduction in TM at 24 h of cooling (but not prior) with the addition of 20 µM of ISO. Similarly, no effect of the ISO on the kinetics and functional integrity of the sperm membrane was observed at 96 h of cooling; however, the regression coefficients indicated that the ISO lowered the rate of decrease in sperm motility and the proportion of rapid spermatozoa relative to the concentration of ISO used. The ISO did not affect the TAC of the cooled semen; however, different concentrations of ISO lowered ROS production in the semen after 96 h of cooling. ISO also impacted the Δ¥M of the spermatozoa at 0 h of cooling, increasing the proportion of low Δ¥M cells and decreasing the proportion of high Δ¥M cells. In conclusion, ISO can reduce the loss of quality and oxidative stress occurring in boar semen during cooling and can modulate the mitochondrial activity of sperm.

RESUMO: Durante a refrigeração, os espermatozoides sofrem estresse oxidativo, osmótico, químico e térmico, que diminuem sua qualidade e afetam sua capacidade de fertilização. A adição de antioxidantes ao diluente espermático é uma alternativa para mitigar essas alterações. O objetivo desta pesquisa foi avaliar o efeito do isospintanol (ISO) na refrigeração do sêmen suíno. Quinze ejaculados de cinco varrascos (Sus scrofa domestica) foram diluídos em BTS suplementado com ISO a 0 (controle), 5 (ISO5), 10 (ISO10), 15 (ISO15), 20 (ISO20), 25 (ISO25) e 30 (ISO30) µM e foram refrigerados por cinco dias a 16 °C. A motilidade total (MT), motilidade progressiva (MP) e cinética dos espermatozóides foram avaliadas a cada 24 h com um sistema CASA IVOS. Nos dias um e cinco de refrigeração, foram avaliadas a funcionalidade da membrana, a capacidade antioxidante total (CAT), as espécies reativas de oxigênio (ROS) e o potencial de membrana mitocondrial (Δ¥M), através do teste hiposmótico (HOS), espectrofluorimetría e citometria de fluxo. Foram realizadas análises de regressão e comparação de médias, pelo teste de Duncan. A adição de ISO teve pouca influência na motilidade espermática, apresentando apenas redução na MT em 24 h de refrigeração, devido à adição de 20 µM. Da mesma forma, não foi observada influência de ISO na cinética e integridade funcional da membrana em 96 horas de refrigeração; porém, os coeficientes de regressão mostraram que ISO produziu menor taxa de diminuição da motilidade e proporção de espermatozoides rápidos dependendo da concentração utilizada. ISO não influenciou significativamente na CAT do sêmen refrigerado; entretanto, diferentes concentrações de ISO reduziram a produção de EROs a partir do sêmen após de 96 h de refrigeração. ISO também influenciou o Δ¥M dos espermatozóides em 0 h de refrigeração, com aumento das células de baixo Δ¥M e diminuição das células de alto Δ¥M. Em conclusão, o isospintanol pode reduzir a perda da qualidade e o estresse oxidativo do sêmen suíno durante a refrigeração e pode modular a atividade mitocondrial do esperma.

Evaluation of an automated temperature control equipment for lactating sows

The present study aimed to develop and evaluate an automated cooling control system (ATCE) for sows in the farrowing phase. The experiment was conducted at the Swine Production Unit, Federal Institute of Education, Science and Technology, Campus Machado, Machado, state of Minas Gerais. Sixteen sows and their offspring were evaluated, eight treated and eight controls, in a randomized block design, with eight replications. Surface temperature, body temperature and respiratory rate of the animals were evaluated, in addition to floor temperature and performance parameters. The use of ATCE decreased the floor temperature (12h) and neck temperature (12 and 16h) (p < 0.10). In addition, there was a reduction in rectal temperature (12h) and respiratory rate (12 and 16h) in ATCE animals (p < 0.10). No significant differences were detected in the coefficient of variation (CV) of birth weight, but at weaning the CV of piglet weight was 26.3% lower in animals subjected to the ATCE (p = 0.079). Furthermore, the difference in CV between birth and weaning was also lower with the use of ATCE (p = 0.015). It can be concluded that the use of ATCE has a positive influence on the thermal comfort of females, in addition to improving litter uniformity.(AU)

Eficiência de três diluidores inespecíficos na refrigeração do sêmen de coelho (Oryctolagus cuniculus f. domesticus) / Efficiency of three unspecific diluents in refrigeration of rabbit (Oryctolagus cuniculus f. domesticus) semen / Eficiencia de tres diluyentes inespecíficos en la refrigeración de semen de conejo (Oryctolagus cuniculus f. domesticus)

Objetivou-se com este trabalho avaliar a viabilidade seminal de coelhos após refrigeração a 5°C utilizando três diluentes comerciais, indicados para refrigeração de sêmen de outras espécies monogástricas. Foram realizadas dez colheitas de sêmen de cada reprodutor. Os ejaculados de cada coelho eram misturados, obtendo-se um pool de sêmen. Em seguida, o pool heterospérmico foi dividido em três tratamentos, de acordo com o diluente utilizado: BotuDogⓇ (cães); BotuSemen® (equinos); e Beltsville Thawing Solution - BTS (suínos). As amostras foram avaliadas quanto aos parâmetros macroscópicos, microscópicos e funcionais em quatro momentos: sêmen fresco (0 h) e refrigerado (16, 24 e 48 h). Os valores médios de motilidade, vigor e defeitos totais do sêmen fresco foram de 86,0%, 3,05 e 11,5%, respectivamente. Após o início do resfriamento, observou-se comportamento linear decrescente para a motilidade e vigor espermático do sêmen em função do tempo, diferindo (P < 0,05) entre os tratamentos. Destaca-se que o tratamento diluído em BTS apresentou redução na manutenção dos parâmetros avaliados de forma mais pronunciada (P < 0.05) ao longo do tempo, apresentando os menores valores para motilidade e vigor espermático dentro de cada tempo avaliado: 16h [20,6 ± 7,28 e 0,75 (0,375 1,5)], 24h [12,0 ± 6,80 e 0 (0 - 1,0)] e 48h [3,0 ± 2,13 e 0 (0 - 0,125)]. Após 48 h de resfriamento, o BotuDogⓇ foi o que apresentou maior valor para motilidade espermática (71,0 ± 2,08) e, juntamente, com o BotuSemenⓇ apresentaram maior valor para vigor espermático (2,5). De acordo com os dados obtidos os diluentes BotuDogⓇ e BotuSemenⓇ mostraram-se eficientes em manter parâmetros espermáticos adequados, apresentando boa viabilidade espermática em até 48h pós refrigeração a 5°C. Foram obtidos, resultados inéditos quanto a parâmetros espermáticos do sêmen de coelho refrigerado que podem ser utilizados como valores de referência para o manejo reprodutivo e processamento do semen desses animais, visto a inexistênca dessas recomendações técnicas.

The objective of this work was to evaluate the seminal viability of rabbits after refrigeration at 5°C using three commercial diluents, indicated for refrigeration of semen from other monogastric species. Ten semen collections were performed from each breeder. The ejaculates of each rabbit were mixed, obtaining a pool of semen. Then, the heterospermic pool was divided into three treatments, according to the diluent used: BotuDog (dogs); BotuSemenⓇ (horses); and Beltsville Thawing Solution - BTS (pigs). The samples were evaluated for macroscopic, microscopic, and functional parameters in four moments: fresh (0 h) and refrigerated (16, 24, and 48 h) semen. The average values of motility, vigor, and total defects of fresh semen were 86.0%, 3.05 and 11.5%, respectively. After the beginning of cooling, a decreasing linear behavior was observed for motility and sperm vigor of semen as a function of time, differing (P < 0.05) between treatments. It is noteworthy that the treatment diluted in BTS® showed a more pronounced reduction in the maintenance of the evaluated parameters (P < 0.05) over time, with the lowest values for sperm motility and vigor within each evaluated time: 16h [20.6 +7.28 and 0.75 (0.375 - 1.5)], 24h [12.0± 6.80 and 0 (0 - 1.0)] and 48h [3.0±2.13 and 0 (0 - 0.125)]. After 48 h of cooling, BotuDog presented the highest value for sperm motility (71.0 ± 2.08) and, together with BotuSemenⓇ, presented the highest value for sperm vigor (2.5). According to the data obtained, BotuDog and BotuSemenⓇ diluents were efficient in maintaining adequate sperm parameters, showing good sperm viability in up to 48 hours after refrigeration at 5°C. Through this work, unpublished results were obtained regarding spermatic parameters of refrigerated rabbit semen that can be used as reference values for reproductive management and semen processing of these animals, given the lack of these technical recommendations.

El objetivo de este trabajo fue evaluar la viabilidad seminal de conejos después de refrigeración a 5°C utilizando tres diluyentes comerciales, indicados para la refrigeración de semen de otras especies monogástricas. Se realizaron diez colectas de semen de cada reproductora. Se mezclaron los eyaculados de cada conejo, obteniendo un pool de semen. Luego, el pool heterospérmico se dividió en tres tratamientos, según el diluyente utilizado: BotuDogⓇ (perros); BotuSemenⓇ (caballos); y Beltsville Thawing Solution - BTS® (cerdos). Las muestras fueron evaluadas para parámetros macroscópicos, microscópicos y funcionales en cuatro momentos: semen fresco (0 h) y refrigerado (16, 24 y 48 h). Los valores promedio de motilidad, vigor y defectos totales del semen fresco fueron 86,0%, 3,05 y 11,5%, respectivamente. Después del inicio del enfriamiento, se observó un comportamiento lineal decreciente para la motilidad y el vigor espermático del semen en función del tiempo, difiriendo (P < 0.05) entre tratamientos. Cabe destacar que el tratamiento diluido en BTS® mostró una reducción más pronunciada en el mantenimiento de los parámetros evaluados (P<0,05) a lo largo del tiempo, con los valores más bajos de motilidad espermática y vigor dentro de cada tiempo evaluado: 16h [20,6 ± 7,28 y 0,75 (0,375 -1.5)], 24h [12,0 ± 6,80 y 0 (0 - 1,0)] y 48h [3,0±2,13 y 0 (0 - 0,125)]. Después de 48 h de enfriamiento, BotuDogⓇ presentó el valor más alto de motilidad espermática (71,0 +2,08) y, junto con BotuSemenⓇ, presentó el valor más alto de vigor espermático (2,5). De acuerdo con los datos obtenidos, los diluyentes BotuDogⓇ y BotuSemenⓇ fueron eficientes en mantener parámetros espermáticos adecuados, mostrando buena viabilidad espermática hasta 48 horas después de la refrigeración a 5°C. A través de este trabajo se obtuvieron resultados inéditos respecto a parámetros espermáticos de semen de conejo refrigerado que pueden ser utilizados como valores de referencia para el manejo reproductivo y procesamiento de semen de estos animales, dada la falta de estas recomendaciones técnicas.

Effect of heat stress and solar radiation on dry matter intake, biochemical indicators, production, and quality of Holstein and Jersey cows' milk / Efeito do estresse calórico e da insolação sobre consumo, indicadores bioquímicos, produção e qualidade do leite de vacas Holandês e Jersey

The objective of this work was to compare the dry matter intake, milk yield and quality, physiological and biochemical parameters in Holstein (n=10) and Jersey (n=10) cows under heat stress and insolation, in two treatments: CL - cooling by ventilation and sprinkling and HS - heat stress and insolation. Data were submitted to ANOVA. There was an interaction between treatment and breed and day effect for dry matter intake. For consumption in % of body weight, CL and Jersey cows consumed more. CL cows produced more milk and 3.5% fat-corrected milk. Feed efficiency was similar between treatments and breeds. Fat, lactose, total solids, and somatic cell score did not differ. The concentration of milk urea nitrogen was higher for CL cows. Milk from Holstein cows had greater stability to alcohol, and from HT cows had a greater freezing point of milk. HT cows had higher respiratory rates in the morning and surface temperatures in the afternoon. There were no differences in beta-hydroxybutyrate and glucose concentrations. Heat stress, with insulation, reduces intake, especially in Holstein cows, as well as milk production and increases the freezing point of milk, respiratory rate, and surface temperature.

O objetivo deste trabalho foi comparar o consumo de matéria seca, a produção e a qualidade do leite, os parâmetros fisiológicos e bioquímicos em vacas das raças Holandesa (n=10) e Jersey (n=10) sob estresse calórico e insolação, em dois tratamentos: CL - resfriamento por ventilação e aspersão; HS - estresse térmico e insolação. Os dados foram submetidos à análise de variância. Houve interação entre tratamento e raça e efeito de dia para consumo de matéria seca. Para consumo em % de peso vivo, vacas CL e Jersey consumiram mais. Vacas CL produziram mais leite e leite corrigido a 3,5% de gordura. A eficiência alimentar foi similar entre tratamentos e raças. Teores de gordura, lactose, sólidos totais e escore de células somáticas não diferiram. A concentração de nitrogênio ureico do leite foi maior para vacas CL. O leite das vacas Holandesas apresentou maior estabilidade ao álcool, e de vacas HT maior crioscopia. Vacas HT apresentaram maior frequência respiratória de manhã e temperatura superficial à tarde. Não houve diferenças para concentração de beta-hidroxibutirato e glicose. O estresse calórico, com insolação, reduz o consumo, especialmente em vacas Holandesas, bem como a produção de leite, com aumento da crioscopia, elevando a frequência respiratória e a temperatura superficial.

Carcass characteristics and meat quality of lambs fed diets with different roughage: concentrate ratios supplemented with liquid residue of cassava

The objective of this study was to evaluate the effects of lambs fed two roughage: concentrate (R:C) ratios, with or without the liquid residue of cassava (LRC) on carcass traits and meat quantity. Forty lambs (19.5 ± 1.45 kg body weight), non-castrated, crossbred Santa Inês were distributed in a completely randomized 2 × 2 factorial design. There was no effect (p > 0.05) of the inclusion of LRC on the variables. The roughage:concentrate ratio of 40:60 promoted higher values for empty body weight, hot carcass weight, cold carcass weight, subcutaneous thickness fat, cooling loss, Longissimus muscle area, carcass morphometric measurements, and commercial cuts. Higher weight of leg, muscles, fat, bone and other tissues, as well as for the ratio muscle:fat, and muscle:bone was observed in lambs fed 40R:60C. For the meat chemical composition, there was the effect (p < 0.05) only for ether extract (EE) for lambs fed 40R:60C ratio. The redness (a*) of meat was greater (p < 0.05) for lambs fed 80R:20C. The other physicochemical characteristics were not influenced. The roughage:concentrate ratio of 40:60 improves the carcass traits and commercial cuts, but does not promote changes in meat quality, independent of supplementation with liquid residue of cassava.(AU)

Refrigeração de sêmen canino em meio diluente à base de água de coco (Cocos nucifera) natural / Canine semen refrigeration in a natural coconut water (Cocos nucifera)-based extender / Refrigeración de semen canino en un medio diluyente natural a base de agua de coco (Cocos nucifera)

A inseminação artificial em cadelas contribui para o melhoramento genético da espécie, previne algumas doenças sexualmente transmissíveis a partir da cópula e possibilita a reprodução de animais que não poderiam copular de forma natural, seja por motivos anatômicos, geográficos ou comportamentais. Todavia, nem sempre é possível utilizar o sêmen fresco, sendo assim necessário um diluente para resfriar e mantê-lo viável por determinado período. Diante disso, o objetivo com este trabalho foi analisar o sêmen canino diluído em água de coco e refrigerado, à 5 ºC em diferentes tempos. Foram utilizados cinco cães da raça Hounds do Brasil, realizando três colheitas de sêmen de cada animal, com intervalos de sete dias. Os ejaculados foram mantidos a temperatura de 37ºC e realizado análises macroscópicas (volume, cor, aspecto e odor) e microscópicas (motilidade, vigor, concentração e morfologia espermática). Em seguida, os ejaculados foram diluídos em água de coco natural a uma concentração de 200 milhões de espermatozoides/mL, e mantidos à temperatura de 5 °C, por até 72 horas. Nos intervalos de seis, doze, vinte e quatro, trinta e seis, quarenta e oito, e setenta e duas horas, as amostras foram avaliadas quanto a motilidade e vigor espermático. Os ejaculados frescos apresentaram em média volume de 6,2 mL, cor branca, aspecto aquoso a leitoso, odor "sui generis", motilidade espermática de 89,5 %, vigor espermático 4,3, concentração média de 418 x106espermatozoides/mL e 7,3% de alterações patológicas. Após o início do resfriamento à 5 ºC, os valores de motilidade e vigor diminuíram com o passar do tempo, sendo os menores valores encontrados após 48 e 72 horas. O diluente a água de coco in natura mostrou-se eficiente para refrigeração de sêmen canino, à 5 ºC, conservando-o por um período de até 36h após a colheita, conforme preconizado pelo Colégio Brasileiro de Reprodução Animal.(AU)

improvement of the species, prevents some sexually transmitted diseases through copulation and allows the reproduction of animals that could not copulate naturally, either for anatomical, geographic or behavioral reasons. However, it is not always possible to use fresh semen, thus requiring a diluent to cool and keep it viable for a certain period. Therefore, the objective of this work was to analyze canine semen diluted in coconut water and refrigerated at 5 ºC at different times. Five Brazilian Hounds were used, performing three semen collections from each animal, with intervals of seven days. The ejaculates were kept at a temperature of 37 ºC and macroscopic (volume, color, appearance and odor) and microscopic (motility, vigor, concentration and sperm morphology) analyzes were performed. Then, the ejaculates were diluted in natural coconut water at a concentration of 200 million sperm/mL, and kept at a temperature of 5 °C for up to 72 hours. At intervals of six, twelve, twenty-four, thirty-six, forty-eight, and seventy-two hours, samples were evaluated for sperm motility and vigor. Fresh ejaculates had an average volume of 6.2 mL, white color, watery to milky appearance, "sui generis" odor, 89.5% sperm motility, 4.3 sperm vigor, average concentration of 418 x106 spermatozoa/mL and 7.3%pathological changes. After the beginning of cooling at 5 °C, the values of motility and vigor decreased over time, with the lowest values found after 48 and 72 hours. The in natura coconut water extender proved to be efficient for cooling canine semen at5 ºC, keeping it for a period of up to 36 hours after harvest, as recommended by the Brazilian College of Animal Reproduction.(AU)

Artificial insemination in bitches contributes to the genetic La inseminación artificial en perras contribuye a la mejora genética de la especie, previene algunas enfermedades de transmisión sexual a través de la cópula y permite la reproducción de animales que no podrían copular de forma natural, ya sea por razones anatómicas, geográficas o de comportamiento. Sin embargo, no siempre es posible utilizar semen fresco, por lo que se requiere un diluyente para enfriarlo y mantenerlo viable durante un cierto período. Por tanto, el objetivo de este trabajo fue analizar semen canino diluido en agua de coco y refrigerado a 5 ºC en diferentes tiempos. Se utilizaron cinco sabuesos brasileños, realizándose tres colectas de semen de cada animal, con intervalos de siete días. Los eyaculados se mantuvieron a una temperatura de 37 ºC y se realizaron análisis macroscópicos (volumen, color, apariencia y olor) y microscópicos (motilidad, vigor, concentración y morfología espermática). Luego, los eyaculados se diluyeron en agua de coco natural a una concentración de 200 millones de espermatozoides/mL y se mantuvieron a una temperatura de 5 °C hasta por 72 horas. A intervalos de seis, doce, veinticuatro, treinta y seis, cuarenta y ocho y setenta y dos horas, se evaluó la motilidad y el vigor de los espermatozoides en las muestras. Los eyaculados frescos tuvieron un volumen promedio de 6,2 mL, color blanco, apariencia acuosa a lechosa, olor "sui generis", motilidad espermática de 89,5%, vigor espermático de 4,3, concentración promedio de 418 x106 espermatozoides/mL y cambios patológicos de 7,3%. Después del inicio del enfriamiento a 5 °C, los valores de motilidad y vigor disminuyeron con el tiempo, encontrándose los valores más bajos a las 48 y 72 horas. El diluyente de agua de coco in natura demostró ser eficaz para enfriar el semen canino a5 ºC, manteniéndolo por un período de hasta 36 horas después de la cosecha, según lo recomendado por el Colegio Brasileño de Reproducción Animal.(AU)

Kinetic vitrification: concepts and perspectives in animal sperm cryopreservation

Sperm cryopreservation is an important tool for genetic diversity management programs and the conservation of endangered breeds and species. The most widely used method of sperm conservation is slow freezing, however, during the process, sperm cells suffer from cryoinjury, which reduces their viability and fertility rates. One of the alternatives to slow freezing is vitrification, that consist on rapid freezing, in which viable cells undergo glass-like solidification. This technology requires large concentrations of permeable cryoprotectants (P- CPA's) which increase the viscosity of the medium to prevent intracellular ice formation during cooling and warming, obtaining successful results in vitrification of oocytes and embryos. Unfortunately, this technology failed when applied to vitrification of sperm due to its higher sensitivity to increasing concentrations of P-CPAs. Alternatively, a technique termed 'kinetic sperm vitrification' has been used and consists in a technique of permeant cryoprotectant-free cryopreservation by direct plunging of a sperm suspension into liquid nitrogen. Some of the advantages of kinetic vitrification are the speed of execution and no rate-controlled equipment required. This technique has been used successfully and with better results for motility in human (50-70% motility recovery), dog (42%), fish (82%) and donkey (21.7%). However, more studies are required to improve sperm viability after devitrification, especially when it comes to motility recovery. The objective of this review is to present the principles of kinetic vitrification, the main findings in the literature, and the perspectives for the utilization of this technique as a cryopreservation method.(AU)

Expression analysis of transcription factors in sugarcane during cold stress / Análise de expressão de fatores de transcrição em cana-de-açúcar sob estresse por frio

Abstract Transcription factors (TF) are a wide class of genes in plants, and these can regulate the expression of other genes in response to various environmental stresses (biotic and abiotic). In the current study, transcription factor activity in sugarcane was examined during cold stress. Initially, RNA transcript reads of two sugarcane cultivars (ROC22 and GT08-1108) under cold stress were downloaded from SRA NCBI database. The reads were aligned into a reference genome and the differential expression analyses were performed with the R/Bioconductor edgeR package. Based on our analyses in the ROC22 cultivar, 963 TF genes were significantly upregulated under cold stress among a total of 5649 upregulated genes, while 293 TF genes were downregulated among a total of 3,289 downregulated genes. In the GT08-1108 cultivar, 974 TF genes were identified among 5,649 upregulated genes and 283 TF genes were found among 3,289 downregulated genes. Most transcription factors were annotated with GO categories related to protein binding, transcription factor binding, DNA-sequence-specific binding, transcription factor complex, transcription factor activity in RNA polymerase II, the activity of nucleic acid binding transcription factor, transcription corepressor activity, sequence-specific regulatory region, the activity of transcription factor of RNA polymerase II, transcription factor cofactor activity, transcription factor activity from plastid promoter, transcription factor activity from RNA polymerase I promoter, polymerase II and RNA polymerase III. The findings of above results will help to identify differentially expressed transcription factors during cold stress. It also provides a comprehensive analysis of the regulation of the transcription activity of many genes. Therefore, this study provides the molecular basis for improving cold tolerance in sugarcane and other economically important grasses.

Resumo Fatores de transcrição (FT) são uma ampla classe de genes em plantas e podem regular a expressão de outros genes em resposta a vários estresses ambientais (estresses bióticos e abióticos). No presente estudo, a atividade do fator de transcrição na cana-de-açúcar foi examinada durante o estresse pelo frio. Inicialmente, as leituras de transcrição de RNA de duas cultivares de cana-de-açúcar (ROC22 e GT08-1108) sob estresse frio foram baixadas do banco de dados SRA NCBI. As leituras foram alinhadas em um genoma de referência e as análises de expressão diferencial foram realizadas com o pacote R / Bioconductor edgeR. Com base em nossas análises no cultivar ROC22, 963 genes TF foram significativamente regulados positivamente sob estresse pelo frio entre um total de 5.649 genes regulados positivamente, enquanto 293 genes TF foram regulados negativamente entre um total de 3.289 genes regulados negativamente. No cultivar GT08-1108, 974 genes TF foram identificados entre 5.649 genes regulados positivamente e 283 genes TF foram encontrados entre 3.289 genes regulados negativamente. Os fatores de transcrição, em sua maioria, foram anotados com categorias GO relacionadas à ligação de proteína, ligação de fator de transcrição, ligação específica de sequência de DNA, complexo de fator de transcrição, atividade de fator de transcrição em RNA polimerase II, atividade de fator de transcrição de ligação de ácido nucleico, atividade de corepressor de transcrição, sequência específica da região reguladora, atividade do fator de transcrição da RNA polimerase II, atividade do cofator do fator de transcrição, atividade do fator de transcrição do promotor do plastídio, atividade do fator de transcrição do promotor da RNA polimerase I, polimerase II e RNA polimerase III. As descobertas dos resultados acima ajudarão a identificar fatores de transcrição expressos diferencialmente durante o estresse pelo frio. Ele também fornece uma análise abrangente da regulação da atividade de transcrição de muitos genes. Portanto, este estudo fornece base molecular para melhorar a tolerância ao frio em cana-de-açúcar e outras gramíneas economicamente importantes.

Pre-cooling water applied to porous plates of evaporative cooling systems / Efeito do pré-resfriamento da água aplicada em placas porosas de sistemas de resfriamento evaporativo

This study assessed the ways the thermal environment is influenced by pre-cooling the water employed in wetting the porous plates present in the evaporative cooling systems (ECS). The experiment was performed using two physical models constructed on a distorted and reduced scale, which simulated closed agricultural facilities equipped with ECS made up of porous cellulose panels. In one physical model, the plates were made wet using chilled water (ECScw), while in the other they were moistened using natural water, at environment temperature (ECSnw). Both inside the physical models and outside, in the external environment, the air dry-bulb temperature (tdb), black globe temperature (tbg) and air relative humidity (RH) were measured, at 10 sec intervals. Later, the environmental indices, ECSnw cooling effectiveness and ECScw performance factor were assessed. When the porous ECS plates were thoroughly wet using pre-cooled water, lowering of the thermal variables and comfort indices was seen to be greater than when wetting the plates was done using water at room temperature. An empirical equation was proposed to determine the cooling performance factor applied to the ECScw related to water temperature, tdb and air wet-bulb temperature.

Objetivou-se com o presente trabalho avaliar o efeito do pré-resfriamento da água usada no molhamento de placas porosas de sistemas de resfriamento evaporativo (SRE) sobre o ambiente térmico. O experimento foi realizado em dois modelos físicos construídos em escala reduzida e distorcida que simularam instalações agrícolas fechadas, equipadas com SRE composto por painéis porosos de celulose. Em um modelo físico, o molhamento das placas foi realizado por meio de água resfriada (SRAR) e o outro por meio de água natural à temperatura ambiente (SRAN). Mensurou-se a temperatura de bulbo seco do ar (tbs), temperatura de globo negro (tgn) e umidade relativa do ar (UR) no interior dos modelos físicos e no ambiente externo em intervalos de 10s. Posteriormente, foram calculados índices ambientais, a efetividade de resfriamento do SRAN e fator de desempenho do SRAR. O pré-resfriamento da água usada no molhamento de placas porosas de SRE propiciou maior redução nas variáveis térmicas e índices de conforto em relação ao molhamento com água à temperatura ambiente, sendo proposta uma equação empírica para a estimativa do fator de desempenho de resfriamento aplicada ao SRAR em função da temperatura da água, da tbs e da temperatura de bulbo úmido do ar.

Sperm cell capacitation status of ram semen after cooling

Background: The use of conventional artificial insemination (AI) in sheep production is usually associated with lower fertility rates when frozen semen is used. Cooled ram semen has been an alternative over frozen semen due to the higher viability, seminal quality and fertility rates following AI. The semen preservation process promotes sperm cell modifications similar to capacitation (capacitation-like) that causes cell damage affecting viability and seminal quality, but such effects are unclear for cooled semen. The aim of this study was to determine the status of sperm cell capacitation (CA) and acrosome reaction (AR) during ram semen processing and cooling under different extenders, dilution factors, and aerobiosis conditions as a function of storage time at 5o C. Materials, Methods & Results: Two consecutive ejaculates per day per male were collected from 2 adult rams by artificial vagina at 48-72 h intervals, in three replications. After macro- and microscopic evaluations, semen was segregated into groups under 3 extenders (Tris-egg yolk or TY, citrate-egg yolk or CY, skimmed milk or SM), 2 dilution factors (1 x 109 or Bi, 100 x 106 or Mi cells/mL), and 2 aerobiosis conditions (aerobic or A, semi-anaerobic or SA). Diluted semen was cooled to 5ºC and stored for up to 72 h, with evaluations every 24 h. Aliquots of fresh ejaculates and of each cooled diluted subgroup, according to extender, dilution, and aerobiosis, were collected at times T0 and T72 for determination of acrosome status and membrane integrity by the chlortetracycline (CTC) and trypan blue-Giemsa stainings, respectively. No differences were detected in sperm cell motility (M) and motility vigor (V) between fresh and diluted semen. After cooling, a significant decrease in M was observed after 48 h in CY and SM compared with fresh semen and 0 h of cooling, while V started to decrease after 24 h in CY compared with TY. Likewise, M/V from different dilutions and aerobic conditions decreased more significantly after 48 and 24 h of cooling, respectively. The sperm capacitation status did not show differences in the proportion of non-capacitated (NCA), CA and AR sperm cells between TY, CY, and SM extenders (NCA: 75.0%, 71.3%, 74.0%; CA: 15.7%, 17.2%, 15.9%; AR: 9.3%, 11.5%, 10.2%) or between Bi and Mi dilutions (NCA: 74.0%, 72.9%; CA: 15.9%, 16.6%; AR: 10.1%, 10.5%), respectively. However, differences (P < 0.05) were observed between A and SA aerobic conditions, with CA (17.0% vs. 15.5%) and AR (11.9% vs. 8.7%) rates being higher in A than SA, respectively, with no differences in NCA (71.1% vs. 75.8%), irrespective of the storage time. Sperm cell viability decreased after 48 h, especially in CY (P < 0.05). Discussion: Ram sperm cells can suffer irreversible damage due to thermal shock during cooling. Egg yolk-based extenders provide phospholipids and cholesterol to protect the sperm cell membrane during the thermal shock caused by the change in temperature. In this study, sperm cells had irreversible decreases in M/V, with increase in acrosome and plasma membrane damage after cooling to 5ºC. The largest and smallest decreases in M and V over time were observed in the CY and TY extenders, respectively. In addition to the extender type, the semen preservation method and storage time promoted changes in the capacitation status, AR and in sperm cell viability, which per se were associated with a decrease in semen fertility. In fact, the proportions of CA and/or AR sperm cells gradually increased over time after dilution and storage at 5ºC, with a negative correlation between sperm cell viability and M/V over time. In summary, extender and cooling time affected mostly M/V, while aerobiosis condition and dilution factor were more associated with acrosome status and sperm survival, with the extender having less impact on the acrosome status as a function of time.

Effect of glycerol addition time on the cryopreserved Korean native brindle cattle (Chikso) sperm quality

Although cryopreservation is an efficient method for maintaining the biological and genetic resources of sperm, the sperm damage during the cryopreservation process cannot be ignored. It should be possible to obtain the most effective cryopreservation performance by accurately grasping the effects of various factors on the cryopreservation of sperm. The previous study demonstrated that a suitable standard protocol for cryopreservation of Korean native brindled cattle (Chikso) does not exist, based on the methods for semen cryopreservation of Chikso differ in each research center. The most obvious difference between most of protocols is the addition of glycerol before and after cooling during the Chikso cryopreserved semen process. Therefore we focused on the effects of glycerol addition time on the quality of cryopreserved Chikso sperm. In the present study, 27 individual Chikso samples were collected by transrectal massage and divided into two parts: the "cryopreservation method A" group (adding glycerol before cooling) and the "cryopreservation method B" group (adding glycerol after cooling). Meanwhile, the values of various sperm parameters were derived from each group, including sperm motility, kinematics, capacitation status, cell viability, and intracellular ATP levels, which we used to compare and evaluate sperm function. The results of this study indicated that during the semen cryopreservation process of the Chikso, the addition of glycerol after cooling yielded superior results in a variety of sperm parameters, such as sperm motility, progressive motility, rapid motility, VCL, VSL, VAP, ALH, capacitation status, viability, and intracellular ATP level after freezing and thawing. Our study is suggested that the glycerol addition time during the cryopreservation process for Chikso should be considered. In addition, our results may be provided reference to develop suitable the cryopreservation procedure of the Chikso sperm.(AU)

Evaluation of forestripping milk and its effects on milk quality / Avaliação do leite do teste de Tamis e seu efeito sobre a qualidade do leite

Consumers demand for food safety affects dairy industry, restraining the sector to adapt to milk quality parameters established by legislation, such as somatic cell count (SCC) and standard plate count (SPC). Good agricultural practices have positive impact over these parameters, especially Forestripping Milk (FSM), which consists of observing the first milk streams collected in a dark-bottomed mug for identification of clinical mastitis. These first milk streams have high somatic cells count and bacteria. Therefore, the aim of this study was to evaluate the characteristics of milk from FSM, such as SCC and SPC values, and its impacts on milk quality of the cooling tank through simulating contamination. Fourteen dairy farms and one experimental farm were evaluated for SCC and SPC parameters of FSM. It was observed that there was no statistically significant difference for SCC and SPC between milk samples from the cooling tank and cooling tank simulating the inclusion of milk from FSM. Statistically significant difference for somatic cell score (SCS) and SPC was observed when tanks were classified by SCC. In addition, difference in SCS was observed between morning and afternoon milking. The collection of first milk streams can contribute to decrease in SCC and SPC of milk in the cooling tank. FSM must be practiced by all dairy farmers as milking management, to assist in clinical mastitis diagnosis and improve milk quality.(AU)

A exigência dos consumidores por alimentos seguros pressiona a indústria leiteira a se adequar aos parâmetros esta-belecidos pela legislação, como a contagem de células somáticas (CCS) e a contagem padrão em placas (CPP). As boas práticas agropecuárias impactam positivamente sobre esses parâmetros, destacando-se o teste de Tamis ou Forestripping Milk (FSM), que consiste na observação dos primeiros jatos de leite retirados em uma caneca de fundo escuro para a identificação da mastite clínica. Esses primeiros jatos possuem elevada quantidade de células somáticas e bactérias. O objetivo deste estudo foi avaliar as características do leite do FSM quanto aos valores de CCS e CPP, e seus impactos na qualidade do leite do tanque de res-friamento por meio de simulação de contaminação. Foram avaliadas 14 propriedades leiteiras comerciais e uma experimental quanto aos parâmetros de CCS e CPP oriundos do FSM. Observou-se que não houve diferença significante para CCS e CPP entre as amostras de leite do tanque e do tanque simulando a inclusão de leite do FSM. Diferenças estatisticamente significa-tivas para escore de CCS e CPP foram observadas quando os tanques foram classificados por CCS. Além disso, foi observada diferença nas CCS entre as ordenha da manhã e da tarde. A coleta dos primeiros fluxos de leite pode contribuir na redução da CCS e da CPP do leite do tanque de resfriamento. O FSM deve ser praticado por todos os produtores de leite no manejo da ordenha para auxiliar no diagnóstico clínico da mastite e melhorar a qualidade do leite.(AU)

Thermal environment characterization of laying hen-housing systems

This study systematically collected data on variables that influence the thermal environment characteristics in poultry houses. Laying poultry farming is a relevant economic activity in Brazilian agriculture and has been expressively growing mainly regarding genetics and nutrition. Thermal comfort in poultry houses is needed to achieve poultry's maximum productive potential. Therefore, laying aviaries previously naturally ventilated (positive pressure) are starting to be equipped with cage batteries and designed with lateral closures, using negative pressure ventilation and in some cases associated with adiabatic cooling. However, negative pressure ventilation systems' thermal efficiency in tunnel mode and its distribution in different cage levels is still slightly known. Consequently, this system's thermal efficiency needs to be investigated to ensure adequate climate indices recommendations and avoid costs and losses due to inadequate handling and facilities.

Isolation of Escherichia coli and Staphylococcus aureusin raw milk from refrigeration tanks: identification and antimicrobial resistance profiles / Isolamento de Escherichia coli e Staphylococcus aureus em leite cru de tanques de refrigeração: identificação e perfis de resistência antimicrobiana

Escherichia coli and Staphylococcus aureus in milk cooling tank reflects a hygienic deficit in animal management, production environment, and milk obtainment. With implications for public health as agents of infection and food poisoning, and the presence of antimicrobial-resistant strains. Therefore, were investigated in cooling tanks with high counts of somatic cells and total bacteria in milk. Microorganisms, in which a profile of resistance to antimicrobials was investigated, and whether there was a similarity in this profile between the strains of the eight dairy properties.Therefore, eighty-eight samples were obtained, and inoculated on Compact Dry® plates. Of this total, 27.27% (24/88) samples tested positive for E. coli and 56.81% (50/88) for S. aureus. Among 24 E. coli strains subjected to disk-diffusion antibiograms, 70.83% were resistant to rifampicin, 50% to ampicillin and 41.67% to cefoxitin and erythromycin, while of the 51 S. aureus strains, 94.32% expressed resistance to azetroanam, 86.27% to ampicillin and nalidixic acid, 76.47% to rifampicin and 47.06 % to erythromycin and cefoxitin. A criterion of resistance to over three antibiotics was observed for 8.33% (2/24) of the isolated E. coli strains and 17.65% (9/51) of the S. aureus strains, characterizing them as multidrug resistant (MDR) strains. Resistance phenotypes displayed high similarity between properties F5 and F6 for S. aureus, and properties F6 and F8 for E. coli when applying the Jaccard index. The presence of these antibiotic-resistant pathogenic microorganisms indicate flaws in milk production handling and sanitary conditions, representing risk to milk consumers.(AU)

Escherichia coli e Staphylococcus aureus no tanque de resfriamento de leite refletem um déficit higiênico no manejo animal, ambiente de produção e obtenção de leite. Com implicações para a saúde pública como agentes de infecção e intoxica-ção alimentar e presença de cepas resistentes a antimicrobianos. Portanto, foram investigados em tanques de resfriamento com altas contagens de células somáticas e bactérias totais no leite. Microrganismos, nos quais foi investigado o perfil de resistência aos antimicrobianos e se havia semelhança nesse perfil entre as cepas das oito propriedades leiteira. Para tanto, oitenta e oito amostras foram coletadas inoculadas em placas de Compact Dry®, destas 27,27% (24/88) amostras revelaram contaminação com E. coli, e 56,81% (50/88) com S. aureus. Entre 24 cepas de E. coli submetidas a antibiograma por disco-difusão 70,83% foram resistentes a rifampicina, 50% ampicilina, 41,67% cefoxitina e eritromicina, enquanto das 51 cepas de S. aureus 94,32% expressaram resistência a azetroanam, 86,27% a ampicilina e nalidíxico ácido, 76,47 % a rifampicina, e 47,06% a cefoxitina e eritromicina. O critério de resistência a mais de três antibióticos caracterizou 8,33% (2/24) das cepas de E. coli, e 17,65% (9/51) de S. aureus como multidroga resistente (MDR). O fenótipo resistência mostrou elevada similaridade entre as proprie-dades (F5 e F6) para S. aureus, e das propriedades (F6 e F8) para E. coli aplicando-se o índice de Jaccard. Estes microrganis-mos patogênicos resistentes a antibióticos, indicam falhas no manuseio e obtenção higiênica do leite, e que estes representam risco aos consumidores do leite.(AU)

Equine semen cooled with chemically defined extender containing soy lecithin / Sêmen equino refrigerado com diluidor quimicamente definido contendo lecitina de soja

Equine semen has historically been chilled using milk-based media. However, the use of animal-based components presents several potential concerns, such as variability in formulations, microbial contamination and regulatory issues. We aimed to evaluate the potential of including different concentrations of soy lecithin (LS) in chemically defined Biggers, Whitten and Whittingham (BWW) medium for cooling equine semen to 15°C. Ejaculates were diluted as six different experimental groups: 1) BotuSêmen® (control); 2) BWW; 3) BWW + 1% LS; 4) BWW + 2% LS; 5) BWW + 4% LS and 6) BWW + 6% LS. BWW medium, did not preserve motility, velocity, straightness (STR), linearity (LIN), amplitude of lateral sperm head displacement (ALH), cross flagellar beat frequency (BCF), functional and structural integrity of equine spermatozoa during 24 h of refrigeration when compared to BotuSêmen® (P <0.05). The use of BWW for cooling equine semen was only possible with the addition of LS, being the concentrations equal or higher than 2% better, because they preserved total motility, curvilinear velocity (VCL) and LIN with the same potential of BotuSêmen® (P >0.05). Nevertheless, BotuSêmen® showed superiority in preserving the percentage of sperm progressive motility, average path velocity (VAP), linear progressive velocity (VSL) and BCF during cooling compared to the other extenders (P <0.05). The inclusion of soy lecithin, from 2 to 6% in the BWW medium, allowed maintaining the viability of equine semen cooled at 15ºC for up to 24 hours.

O sêmen equino tem sido historicamente refrigerado usando meios à base de leite. No entanto, o uso de componentes de origem animal causa várias preocupações potenciais, como variabilidade nas formulações, contaminação microbiana e questões regulatórias. Objetivou-se avaliar o potencial de inclusão de diferentes concentrações de lecitina de soja (LS) no meio quimicamente definido BWW - Biggers, Whitten e Whittingham para refrigeração de sêmen equino e armazenamento na temperatura de 15°C. Os ejaculados foram diluídos em seis diferentes grupos experimentais: 1) BotuSêmen® (controle); 2) BWW; 3) BWW + 1% lecitina de soja (LS); 4) BWW + 2% LS; 5) BWW + 4% LS e 6) BWW + 6% LS. O meio BWW, não preservou a motilidade, a velocidade, a retilinearidade (STR), a linearidade (LIN), a amplitude do deslocamento lateral da cabeça (ALH), a frequência de batimento flagelar cruzado (BCF), a integridade funcional e estrutural dos espermatozoides equino durante 24 h de refrigeração quando comparado ao BotuSêmen® (P <0,05). O uso de BWW para refrigeração de sêmen equino só foi possível com adição de lecitina de soja, sendo as concentrações igual ou superior a 2% melhores, pois preservaram a motilidade total, a velocidade curvilinear (VCL) e LIN com mesmo potencial do BotuSêmen® (P >0,05). Ainda assim, o diluidor comercial BotuSêmen® apresentou superioridade em preservar o percentual de espermatozoides progressivamente móveis, a velocidade média da trajetória (VAP), a velocidade linear progressiva (VSL) e a frequência do batimento flagelar cruzado (BCF) durante a refrigeração comparado aos demais diluidores (P <0,05). A inclusão de lecitina de soja, de 2 a 6% no meio BWW, permitiu a manutenção da viabilidade do sêmen equino refrigerado a 15ºC por até 24 horas.

Wooden sticks for plaque streaking and microbiological inoculation might be more cost- effective, but is its large scale use feasible? Quality control methods and proof of concept

Abstract The loop is a material classically used in the laboratory for the purpose of plate streaking and handling biological materials. However, metal loops techniques might be time consuming, considering the amount of time spent to guarantee its cooling process through each inoculation. Furthermore, plastic loops may also represent environmental issues during its production and discard process and can also represent higher costs for the laboratory. Thus, in situations of limited resources, even the simplest materials can be restricted due to logistical and budgetary issues, especially in developing countries. Inspired by demands like these, facing an occasional shortage of supply of laboratory plastic handles, we hereby present a quality control for sterilization methods and cost-effectiveness studies towards the use of wooden sticks in a Latin American country and we discuss the possibility of the large-scale use of this technique.

Resumo A alça calibrada é um material usado classicamente em laboratório para fins de inoculação em placas e manuseio de materiais biológicos. No entanto, as técnicas de alças metálicas podem consumir muito tempo, considerando a quantidade de tempo gasto para garantir seu processo de resfriamento a cada inoculação. Além disso, alças de plástico também podem representar questões ambientais durante o processo de produção e descarte e também podem representar custos mais altos para o laboratório. Assim, em situações de recursos limitados, até os materiais mais simples podem ser restringidos devido a questões logísticas e orçamentárias, especialmente nos países em desenvolvimento. Inspirados por demandas como essas, diante de uma escassez ocasional de suprimentos de alças de plástico de laboratório, apresentamos um controle de qualidade para métodos de esterilização e estudos de custo-efetividade para o uso de varas de madeira em um país latino-americano e discutimos a possibilidade de grande uso em escala dessa técnica.

Effective temperature for overcoming dormancy of 'Fuyu' persimmon tree buds

The objective of this study was to evaluate the effective temperature for overcoming the dormancy of 'Fuyu' persimmon tree buds. Stem samples were collected three times between 2013 and 2014. Stems were maintained in a climate incubator chamber at 3, 6, 9, and 12 °C. For each temperature, five numbers of additional chilling hours (CH) (0, 240, 384, 528, and 672 CH) were studied. The experimental design was completely randomized in a 5 × 4 factorial design (chilling hours × temperatures) with four replications with 10 cuttings. The maintenance of branches at cold temperatures from 3 to 12 °C intensified endodormancy of the buds when the plants were at the beginning of endodormancy. The most effective temperatures for overcome dormancy when the buds were in transition from paradormancy to endodormancy were from 3 to 6 °C. When the buds were already in endodormancy, temperatures of 3, 6, 9, and 12 °C were effective for the accumulation of cold and overcoming dormancy. The increase in the number of chilling hours from 3 to 12 °C induced budburst and the temperature of 12 °C was able to slowly induce and overcome bud dormancy.

Preservation of cv. Jubileu peaches in a conventional cold storage system under a dynamic controlled atmosphere / Conservação de pêssegos cv. Jubileu em sistema refrigerado convencional, atmosfera controlada e dinâmica

The peach tree (Prunus persica) has a considerable global economic impact because its fruits are consumed worldwide. As climacteric fruits, peaches ripen after harvest and are also highly perishable postharvest. The aim of this study was to investigate alternatives for extending storage time and preventing a decline in quality in peaches using conventional cold storage (CS) compared with controlled atmosphere (CA) and ultralow oxygen (ULO) systems. A completely randomized design was used, with a 3 x 6 factorial scheme (3 storage systems x 6 storage times), thirteen parameters assessed by analysis of variances and significance by Tukey's test and regression. Total soluble solids (TSS) varied from 12.72 to 16.07ºBrix, titratable acidity (TA) declined during storage and pH varied significantly among the systems used from 40 days of storage onwards. The best TSS/TA ratio was obtained under ULO after 40 days, while firmness and weight loss declined in CA and ULO, contrasting with the brightly colored pulp. Reducing and non-reducing sugars decreased under CA and ULO at 30 and 40 days of storage, whereas phenolic compounds and antioxidant activity remained similar in these systems at 30, 40 and 50 days. Carotenoids remained stable for up to 40 days in ULO.CA and ULO maintained the best physical and chemical quality parameters, both systems being the most recommended. The phytochemical compounds analyzed in this study changed little during storage in the systems analyzed.(AU)

O pessegueiro (Prunus persica) apresenta grande impacto econômico global, por produzirem frutos apreciados em todo o mundo. Seus frutos climatérios amadurecem após a colheita, além disso, possuem alta perecibilidade pós-colheita. O objetivo deste trabalho foi buscar alternativas que ampliem ainda mais o tempo de armazenamento evitando-se o decaimento da qualidade dos pêssegos, utilizando o sistema refrigerado convencional (SAR) em contraponto com a atmosfera controlada (SAC) e dinâmica com ultrabaixo oxigênio (SAUO). O delineamento experimental foi inteiramente casualizado em um esquema fatorial 3 x 6 (3 sistemas x 6 períodos) de armazenamento, e treze parâmetros analisados pelo teste análise de variância, significância pelo teste Tukey e regressão. Os valores de sólidos solúveis variaram de 12,72ºBrix a 16,07ºBrix, a acidez titulável reduziu ao longo do armazenamento, já o pH apresentou variação significativa a partir de 40 dias entre os sistemas utilizados. A relação SS/AT alcançou os melhores índices no SAUO até 40 dias, já a firmeza de polpa e a perda de massa apresentaram redução nos SAC e SAUO, contrastando com elevada coloração da polpa. Açúcares redutores e não redutores apresentaram redução no SAC e SAUO aos 30 e 40 dias de armazenamento, já para os compostos fenólicos e atividade antioxidante, nestes sistemas, com 30, 40 e 50 dias os valores mantiveram-se semelhantes. Os carotenóides foram mantidos até 40 dias no SAUO. O SAC manteve os melhores parâmetros de qualidade físico-químicos analisados, juntamente com SAUO, sendo ambos os mais indicados. Os compostos fitoquímicos analisados neste estudo apresentaram poucas alterações durante os dias de armazenamento nos sistemas analisados.(AU)

Wooden sticks for plaque streaking and microbiological inoculation might be more cost- effective, but is its large scale use feasible? Quality control methods and proof of concept / Métodos de controle de qualidade e prova de conceito para a utilização de palitos de madeira em microbiologia podem ser mais econômicas, mas seu uso em larga escala é viável? Método de controle de qualidade e prova de conceito

The loop is a material classically used in the laboratory for the purpose of plate streaking and handling biological materials. However, metal loops techniques might be time consuming, considering the amount of time spent to guarantee its cooling process through each inoculation. Furthermore, plastic loops may also represent environmental issues during its production and discard process and can also represent higher costs for the laboratory. Thus, in situations of limited resources, even the simplest materials can be restricted due to logistical and budgetary issues, especially in developing countries. Inspired by demands like these, facing an occasional shortage of supply of laboratory plastic handles, we hereby present a quality control for sterilization methods and cost-effectiveness studies towards the use of wooden sticks in a Latin American country and we discuss the possibility of the large-scale use of this technique.

A alça calibrada é um material usado classicamente em laboratório para fins de inoculação em placas e manuseio de materiais biológicos. No entanto, as técnicas de alças metálicas podem consumir muito tempo, considerando a quantidade de tempo gasto para garantir seu processo de resfriamento a cada inoculação. Além disso, alças de plástico também podem representar questões ambientais durante o processo de produção e descarte e também podem representar custos mais altos para o laboratório. Assim, em situações de recursos limitados, até os materiais mais simples podem ser restringidos devido a questões logísticas e orçamentárias, especialmente nos países em desenvolvimento. Inspirados por demandas como essas, diante de uma escassez ocasional de suprimentos de alças de plástico de laboratório, apresentamos um controle de qualidade para métodos de esterilização e estudos de custo-efetividade para o uso de varas de madeira em um país latino-americano e discutimos a possibilidade de grande uso em escala dessa técnica.

Effect of quercetin or butylated hydroxytoluene on cooled or frozen-thawed ram sperm quality / Efeito da inclusão de quercetina ou butil-hidroxitolueno na qualidade do sêmen de carneiro resfriado ou congelado

Cooling and freezing processes cause physical and chemical damage to sperm by cold shock and oxidative stress. This study aimed to evaluate the effect of two antioxidants on sperm parameters of cooled and frozen-thawed ram semen diluted in an egg yolk-based extender. Semen was collected from 30 rams and processed in two consecutive experiments to test the inclusion of different concentrations of quercetin and butylated hydroxytoluene (BHT) in an egg yolk-based semen extender. Dimethyl sulfoxide (DMSO) was added as a solvent to the semen extender in a ratio of 1 mL DMSO for 90 mg of quercetin and 1 mL DMSO for 880 mg of BHT. After collection, semen was diluted at 200 × 106 motile sperm/mL (control) and split into different groups in each experiment. In experiment 1, semen was diluted with the extender containing quercetin (Q5, 5 µg/mL; Q10, 10 µg/mL; Q15, 15 µg/mL) or DMSO alone (DMSO1, 0.055 µL DMSO per mL; DMSO2, 0.165 µL DMSO per mL). In experiment 2, semen was diluted with the extender with BHT (BHT1, 0.5 µg/mL; BHT2, 1 µg/mL; BHT3, 1.5 µg/mL) or DMSO alone (DMSO3, 0.375 µL DMSO per mL; DMSO4, 1.125 µL DMSO per mL). After dilution, the semen was divided into two aliquots. Treated ram sperm samples were also subjected to different storage methods. The first set of samples was cooled at 5 °C for 24 h, whereas the second set of samples was frozen-thawed. Sperm motility parameters and plasma membrane integrity (PMI) were evaluated immediately after dilution (0h) and 24 h after cooling and in the frozen-thawed samples via computer-assisted sperm analysis and epifluorescence microscopy, respectively. The inclusion of quercetin or BHT did not affect sperm motility parameters or PMI of fresh, cooled, or frozen-thawed sperm in this study (P < 0.05). However, further studies are needed to test the effects of these antioxidants on the fertility of cryopreserved ram semen.(AU)

O resfriamento e o congelamento causam danos físicos e químicos aos espermatozoides por choque térmico e estresse oxidativo. Portanto, este estudo teve como objetivo avaliar o efeito da inclusão de dois antioxidantes em um diluente à base de gema de ovo sobre os parâmetros espermáticos do sêmen ovino resfriado e congelado. Trinta carneiros tiveram o sêmen coletado e processado em dois experimentos consecutivos para testar a inclusão de diferentes concentrações de quercetina e hidroxitolueno butilado (BHT) em diluente de sêmen à base de gema de ovo. O DMSO foi adicionado como solvente ao diluente de sêmen em uma proporção de 1 mL de DMSO parra 90 mg de quercetina e 1 Ml de DMSO para 880 mg de BHT. Após a coleta, o sêmen foi diluído a 200 × 106 espermatozoides móveis/mL (Controle) e dividido em diferentes grupos em cada experimento. Experimento 1, Quercetina (Q5, 5 µg / mL; Q10, 10 µg / mL; Q15, 15 µg / mL) ou DMSO (DMSO1, 0,055 µL de DMSO por ml; DMSO2, 0,165 µL de DMSO / mL) foram adicionados ao extensor. Experimento 2, BHT (BHT1, 0,5 µg / mL; BHT2, 1 µg / mL; BHT3, 1,5 µg / mL) ou DMSO (DMSO3, 0,375 µL de DMSO por ml; DMSO4, 1,125 µL de DMSO / mL) foram adicionados à o extensor. Após a diluição, o sêmen foi dividido em duas alíquotas. O primeiro foi resfriado a 5 ° C por 24h, enquanto o segundo foi congelado. Os parâmetros de motilidade espermática e integridade da membrana plasmática (PMI) foram avaliados, imediatamente após a diluição (0h) e 24h após o resfriamento e nas amostras congeladas, pelo CASA e microscopia de epifluorescência, respectivamente. A inclusão de quercetina ou BHT não afetou os parâmetros de motilidade espermática e PMI de espermatozoides frescos, resfriados ou congelados (P < 0,05). Portanto, a inclusão de quercetina e BHT não beneficiou os parâmetros espermáticos do sêmen ovino submetido a armazenamento líquido a 5 ° C por 24h ou protocolo de congelamento no presente estudo. No entanto, mais estudos são necessários para testar o efeito desses antioxidantes na fertilidade do sêmen ovino criopreservado.(AU)