Opportunities involving microfluidics and 3D culture systems to the in vitro embryo production

Traditional methods of gamete handling, fertilization, and embryo culture often face limitations in efficiency, consistency, and the ability to closely mimic in vivo conditions. This review explores the opportunities presented by microfluidic and 3D culture systems in overcoming these challenges and enhancing in vitro embryo production. We discuss the basic principles of microfluidics, emphasizing their inherent advantages such as precise control of fluid flow, reduced reagent consumption, and high-throughput capabilities. Furthermore, we delve into microfluidic devices designed for gamete manipulation, in vitro fertilization, and embryo culture, highlighting innovations such as droplet-based microfluidics and on-chip monitoring. Next, we explore the integration of 3D culture systems, including the use of biomimetic scaffolds and organ-on-a-chip platforms, with a particular focus on the oviduct-on-a-chip. Finally, we discuss the potential of these advanced systems to improve embryo production outcomes and advance our understanding of early embryo development. By leveraging the unique capabilities of microfluidics and 3D culture systems, we foresee significant advancements in the efficiency, effectiveness, and clinical success of in vitro embryo production.(AU)

Bem-estar animal nos procedimentos de produção in vivo de embriões na espécie ovina / Animal welfare in the in vivo production of sheep embryos

A presente revisão tem por objetivo abordar aspectos relacionados ao bem-estar animal na produção in vivo de embriões ovinos. A cobrança da sociedade tem impulsionado o uso de práticas que atendam os preceitos de bem-estar na produção animal. Nesse contexto, destaca-se a necessidade de aprimoramento de procedimentos menos invasivos, como a coleta não cirúrgica de embriões. Avanços recentes nos protocolos de dilatação cervical melhoraram os resultados e tornaram essa técnica uma alternativa viável na espécie ovina. No entanto, a avaliação do estado de bem-estar das doadoras submetidas à coleta transcervical mostra a necessidade de melhor controle da dor durante a sua realização. Assim, acreditamos que a associação dos esforços de diferentes pesquisas pode proporcionar a resolução desses entraves e possibilitar maior aplicabilidade comercial da biotécnica.(AU)

This review aims to address aspects related to animal welfare in the in vivo production of ovine embryos. The use of practices that meet the precepts of welfare in animal production has been driven by demands from society. In this context, there is a need to improve less invasive procedures, such as nonsurgical embryo collection. Recent advances in cervical dilation protocols have improved results and made this technique a viable alternative in sheep. However, the assessment of the state of welfare of donors undergoing transcervical collection shows the need for better pain control during its performance. Thus, the association of different research efforts can provide the resolution of these obstacles and enable greater commercial applicability of the biotechnique.(AU)

Desafios e perspectivas na produção comercial de embriões in vivo e in vitro de raças taurinas e sintéticas / Current challenges and perspectives of in vivo and in vitro commercial embryo production of taurine and synthetic breeds

As biotécnicas de produção in vivo e in vitro de embriões bovinos permitem aumentar significativamente o número de descendentes de fêmeas genética e/ou zootecnicamente importantes. Porém, antes de se optar por um dos métodos, deve-se avaliar suas peculiaridades. A produção in vivo pode ser empregada de forma satisfatória tanto em zebuínos quanto em raças sintéticas e taurinas, permitindo a obtenção de, em média, seis a sete embriões viáveis por coleta, com boa tolerância à criopreservação. Já a produção in vitro é mais eficiente em raças zebuínas e sintéticas, visto que possuem maior número de folículos antrais aspiráveis. Além disso, esta técnica permite a produção de embriões sem estímulos hormonais exógenos, porém com menor criotolerância. Desse modo, a presente revisão discute os desafios atuais e perspectivas futuras na produção de embriões in vivo e in vitro com base nos dados da rotina de uma central de doadoras e laboratório de produção de embriões que desenvolve simultaneamente ambas as técnicas de produção de embriões na região Sul do Brasil.(AU)

Biotechniques for in vivo and in vitro production of bovine embryos allow to significantly increase the number of descendants from cows genetically and/or zootechnically superior. However, before opting for one of the methods, one should evaluate its peculiarities. In vivo production can be used satisfactorily both in zebu cattle and in synthetic and taurine breeds, allowing to obtain, on average, six to seven viable embryos per procedure, with good tolerance to cryopreservation. In vitro production is more efficient in Zebu and synthetic breeds, since they have a greater number of aspirable antral follicles. In addition, this technique allows the production of embryos without exogenous hormonal stimuli, but with lower cryotolerance. This review discusses current challenges and future perspectives in in vivo and in vitro embryo production based on routine data from an embryo production center and a laboratory that develop, simultaneously, the two embryo production techniques in southern Brazil.(AU)

The interaction between the environment and embryo development in assisted reproduction

It can be assumed that the natural processes of selection and developmental condition in the animal provide the best prerequisites for embryogenesis resulting in pregnancy and subsequent birth of a healthy neonate. In contrast, circumventing the natural selection mechanisms and all developmental conditions in a healthy animal harbors the risk of counteracting, preventing or reducing the formation of embryos or substantially restricting their genesis. Considering these facts, it seems to be obvious that assisted reproductive techniques focusing on early embryonic stages serve an expanded and unselected germ cell pool of oocytes and sperm cells, and include the culture of embryos outside their natural habitat during and after fertilization for manipulation and diagnostic purposes, and for storage. A significant influence on the early embryonic development is seen in the extracorporeal culture of bovine embryos (in vitro) or stress on the animal organism (in vivo). The in vitro production per se and metabolic as well as endocrine changes in the natural environment of embryos represent adequate models and serve for a better understanding. The purpose of this review is to give a brief presentation of recent techniques aimed at focusing more on the complex processes in the Fallopian tube to contrast in vivo and in vitro prerequisites and abnormalities in early embryonic development and serve to identify potential new ways to make the use of ARTs more feasible.(AU)

The embryo non-invasive pre-implantation diagnosis era: how far are we?

Advancements in assisted reproduction (AR) methodologies have allowed significant improvements in live birth rates of women who otherwise would not be able to conceive. One of the tools that allowed this improvement is the possibility of embryo selection based on genetic status, performed via preimplantation genetic testing (PGT). Even though the widespread use of PGT from TE biopsy helped to decrease the interval from the beginning of the AR intervention to pregnancy, especially in older patients, in AR, there are still many concerns about the application of this invasive methodology in all cycles. Therefore, recently, researchers started to study the use of cell free DNA (cfDNA) released by the blastocyst in its culture medium to perform PGT, in a method called non-invasive PGT (niPGT). The development of a niPGT would bring the diagnostics power of conventional PGT, but with the advantage of being potentially less harmful to the embryo. Its implementation in clinical practice, however, is under heavy discussion since there are many unknowns about the technique, such as the origin of the cfDNA or if this genetic material is a true representative of the actual ploidy status of the embryo. Available data indicates that there is high correspondence between results observed in TE biopsies and the ones observed from cfDNA, but these results are still contradictory and highly debatable. In the present review, the advantages and disadvantages of niPGT are presented and discussed in relation to tradition TE biopsy-based PGT. Furthermore, there are also presented some other possible non-invasive tools that could be applied in the selection of the best embryo, such as quantification of other molecules as quality biomarkers, or the use artificial intelligence (AI) to identify the best embryos based on morphological and/or morphokitetic parameters.(AU)

Pantoea ananatis in Oryza sativa in Brazil / Pantoea ananatis em Oryza sativa no Brasil

The state of Santa Catarina is the second-largest producer of rice seeds in Brazil. Research on phytopathogenicbacterias in this crop is scarce and the high frequency of panicle diseases leads to the hypothesis that seeds may be infected by bacteria. This research quantified the incidence of bacteria in the seeds, verified the bacteria viability during the storage period and characterized the associated bacteria. Seeds from the 2018/19 and 2019/20 seasons were analyzed. To check the incidence, the seeds were disinfected, plated on a nutrient agar + fungicide culture medium, and incubated for seven days at 27 °C. To assess viability, every 45 days, three cultivars stored in a processing unit were subjected to the same detection methodology. To characterize, prevalent colonies were isolated on semi-selective culture medium Pantoea genus-specific agar (PGSA), where the ones that showed growth were subjected to deoxyribonucleic acid (DNA) extraction and Polymerase Chain Reaction (PCR), DNA sequencing, and sequence comparison on GenBank. The hypersensitivity reaction (HR) in tobacco was performed using a bacterial suspension of each isolate. All seed samples had an average incidence of 83%. During storage, the seeds maintained stable bacterial viability, with an average incidence of 95% at the beginning of storage and 99% at the end of it. All isolates that grew in PGSA culture medium were identified by molecular characterization with 100% identity with two specimens of Pantoeaananatis and one of them induced RH in tobacco.

O estado de Santa Catarina é o segundo maior produtor de sementes de arroz do Brasil. As pesquisas com bactérias fitopatogênicas nesta cultura são escassas e a alta frequência de doenças da panícula leva à hipótese de que sementes podem estar infectadas por bactérias. O objetivo desta pesquisa foi quantificar a incidência de bactérias nas sementes, verificar a viabilidade das bactérias durante o período de armazenamento e caracterizar as bactérias associadas. Foram analisadas sementes das safras 2018/19 e 2019/20. Para verificar a incidência, as sementes foram desinfestadas, plaqueadas em meio de cultura ágar nutriente + fungicida e incubadas por sete dias a 27 °C. Para avaliar a viabilidade, a cada 45 dias, três cultivares armazenadas em uma unidade de beneficiamento foram submetidas à mesma metodologia de detecção. Para caracterizar, colônias prevalentes foram isoladas em meio de cultura semisseletivo Pantoea genus-specific ágar (PGSA), onde as que apresentaram crescimento foram submetidas à extração do ácido desoxirribonucléico (DNA) e Reação em Cadeia da Polimerase (PCR), sequenciamento do DNA e comparação de sequências no GenBank. A reação de hipersensibilidade (HR) em tabaco foi realizada utilizando uma suspensão bacteriana de cada isolado. Todas as amostras de sementes apresentaram incidência média de 83%. Durante o armazenamento, as sementes mantiveram viabilidade bacteriana estável, com incidência média de 95% no início do armazenamento e 99% ao fim. Todos os isolados que cresceram no meio de cultura PGSA, foram identificados por caracterização molecular com 100% de identidade com dois espécimes de Pantoea ananatis e um deles induziu HR em tabaco.

Market and production of agroecological seeds / Mercado e produção de sementes agroecológicas

In recent decades, agriculture has been changing mainly in terms of organic production, consumption and market. This increase is due to people's interest in pesticide-free products that meet all environmental, cultural and social issues, presenting itself as a highly competitive and lucrative market niche. For this reason, this bibliographic review aims to describe the market scenario and the production of agroecological seeds, in addition to characterizing the production of organic seeds and evaluating the potential of this market niche, which is increasingly the target of investments and demand for food., but it is important to have more studies about it, as well as specific legislation for organic seeds.(AU)

Nas últimas décadas, a agricultura vem mudando principalmente em termos de produção orgânica, consumo e mercado. Esse aumento se deve ao interesse das pessoas por produtos livres de agrotóxicos que atendam a todas as questões ambientais, culturais e sociais, apresentando-se como um nicho de mercado altamente competitivo e lucrativo. Por esse motivo, esta revisão bibliográfica tem como objetivo descrever o cenário de mercado e a produção de sementes agroecológicas, além de caracterizar a produção de sementes orgânicas e avaliar o potencial desse nicho de mercado que é cada vezmais alvo de investimentos e demanda por alimentos, porém é importante que se tenha mais estudos a respeito, bem como uma legislação especifica para sementes orgânicas.(AU)

Inheritance of seedlessness and the molecular characterization of the INO gene in Annonaceae / Herança da ausência de sementes e a caracterização molecular do gene INO em Annonaceae

Abstract The inheritance of the seedless fruit characteristic of Annona squamosa has not yet been explained. Molecular techniques may aid breeding programs, mainly in the assisted selection of the target gene. The INO gene may be related to seed development in these fruits. The objective of the present paper was to investigate the inheritance of seedlessness in the 'Brazilian seedless' sugar apple and INO gene conservation in Annona squamosa and Annona cherimola x Annona squamosa genotypes by assessing their homology with the INO database genes. The F1 generation was obtained by crossing the mutant 'Brazilian seedless' (male genitor) (P1) with the wild-type A. squamosa with seeds (M1 and M2, female genitors). The INO gene was studied in mutant and wild-type A. squamosa (P1, M1, M2 and M3) and in the Gefner atemoya (A. cherimola x A. squamosa) (M4) cultivar. The DNA was extracted from young leaves, and four sets of specific primers flanking the INO gene were amplified. The seedless characteristic was identified as stenospermatic in the fruits of parental P1, suggesting monogenic inheritance with complete dominance. High sequence similarity of the INO gene amplifications in the sugar apple accessions (M1, M2, M3) and the atemoya cultivar Gefner (M4) reinforces the hypothesis of their conservation.

Resumo A herança da característica de fruto sem sementes de Annona squamosa ainda não foi esclarecida. Técnicas moleculares podem auxiliar em programas de melhoramento, principalmente na seleção assistida do gene de interesse. O gene INO pode estar relacionado ao desenvolvimento da semente dessas frutas. O objetivo foi investigar a herança da ausência de sementes em Annona squamosa e a conservação do gene INO nos genótipos Annona squamosa e Annona cherimola x Annona squamosa avaliando sua homologia com banco de dados de genes INO. A geração F1 foi obtida pelo cruzamento do mutante 'Brazilian seedless' (genitor masculino) (P1) com o tipo selvagem com sementes (A. squamosa) (M1 e M2, genitores femininos). O gene INO foi estudado em A. squamosa, mutante e selvagem (P1, M1, M2 e M3) e na cultivar Gefner atemoya (A. cherimola x A. squamosa) (M4). O DNA foi extraído de folhas jovens, e quatro conjuntos de primers específicos flanqueando o gene INO foram amplificados. A característica sem sementes foi identificada como estenospermática nos frutos do parental P1, sugerindo herança monogênica com dominância completa. A alta similaridade de sequência das amplificações do gene INO nos acessos de pinha (M1, M2, M3) e na cultivar de atemóia Gefner (M4) reforça a hipótese de sua conservação.

ISOLATION AND AMPLIFICATION OF Anaplasma marginale IN CHICKEN EMBRYO FIBROBLAST CELL CULTURE / ISOLATION AND AMPLIFICATION OF Anaplasma marginale IN CHICKEN EMBRYO FIBROBLAST CELL CULTURE

Anaplasma marginale is an important agent for animal livestock, its presence in herds of cattle, sheep and goats leads to losses for Brazilian agribusiness. The present study aimed to describe an isolation technique for A. marginale, using chicken embryo fibroblast (CEF) cell culture. For this, blood and tick samples were collected from 5 calves, between 2 and 3 months of age, which due to anemia, jaundiced mucous membranes and prostration, were considered supposedly infected with A.marginale. For the diagnosis, DNA extraction and PCR was performed from the blood and tick samples collected. All the tick and blood samples were positive in the PCR test. Additionally, ticks were crushed with the aid of a blender for inoculation in CEF cell culture. After inoculation, the cultures were kept at 37ºC and 5% CO2 for 15 days. The cell supernatant of cell cultures were again analyzed by PCR and by the technique Wrighte stain to confirm A. marginale isolation. Cell cultures were positive in PCR and the presence of the agent was demonstrated by Wrighte stain. Therefore, using CEF cell culture was possible to isolate and amplify the A. marginale in a concentration of 1.3 x 107.2 bodies per ml. The CEF cells are undemanding, easy to maintain and they are an option for isolation and production of A. marginale in the laboratory condition.

Anaplasma marginale (A. marginale) is a worldwide pathogen that infects a variety ofruminants, but mostly cattle. The present study aimed to describe an isolation technique for A. marginale, using chicken embryo Þ broblast (CEF) cell culture. Blood and tick samples were collected from 5 calves from 2 to 3 months old, which were considered to be infected with A.marginale due to anemia, jaundiced mucous membranes, and prostration. DNA extractionand PCR were performed for diagnosis using blood and tick samples. All tick and blood samples tested positive in PCR. Additionally,ticks were crushed with the aid of a blender for inoculation in CEF cell culture. After inoculation, the cultures were kept at 37ºC and 5%CO2 for 15 days. The cell supernatant of cell cultures was again analyzed using PCR and Wright stain method to conÞ rm A. marginaleisolation. Cell cultures tested positive in PCR, and the presence of the agent was demonstrated by Wright stain. Therefore, by using CEFcell culture it was possible to isolate and amplify the A. marginale in a concentration of 1.3x 107.2 bodies per mL. The CEF cells are undemanding and easy to preserve; they are anoption for isolation and production of A. marginale under laboratory conditions.

Manual collapse of blastocoels in not effective in increasing the viability of vitrified equine embryos / Colabamento manual da blastocele não foi efetivo para aumentar a viabilidade de embriões equinos vitrificados

Embryo cryopreservation methods have been used for commercialization and formation of genetic banks. Cryopreservation of equine embryos <300 µm in diameter, collected at days 6-6.5 after ovulation, allows satisfactory pregnancy rates. However, higher embryo collection rates in mares are obtained when uterine flush is performed between days 7 and 8 after ovulation when embryos are >300 µm in diameter, needing blastocoel collapse for satisfactory resistance to cryopreservation by vitrification. To evaluate the viability of simplified blastocoel collapse by embryo puncture with low technology and low-cost equipment, 22 embryos, collected at day 8 post-ovulation (D8), were allocated to the following groups: (1) micropuncture with a 30 G needle, assisted by a mechanical micromanipulator, before vitrification (n=4); (2) manual blade microsection before vitrification (n=6); (3) no manipulation prior to vitrification (n=8); and (4) freshly inovulated embryos (n=4). Despite the high re-expansion rates observed after vitrification, embryos manipulated prior to vitrification (groups MP and MS) did not result in pregnancy 25 days after transfer. On the other hand, embryos from groups NM (non-micromanipulated) and FR (freshly inovulated) resulted in pregnancies at 25 days. Under the conditions of the present study, manual blastocoel collapse was not efficient in increasing cryotolerance to vitrification among large embryos, requiring improvements to obtain pregnancies.(AU)

Métodos de criopreservação de embriões têm sido utilizados com diversos objetivos. Maiores taxas de coleta embrio-nária em éguas com lavagem uterina realizada 7 a 8 dias pós ovulação. A criopreservação de embriões equinos com diâmetro <300 µm (6-6,5 dias após a ovulação) permite a obtenção de taxas de prenhez satisfatórias. Embriões com diâmetro >300 µm (7º dia pós-ovulação) somente são adequadamente criopreservados quando submetidos a colabamento da blastocele. Objetivando avaliar a viabilidade da punção da blastocele com equipamento de baixa sofisticação e custo, 22 embriões coletados no 8º. dia pós-ovulação (D8) foram alocados aos seguintes grupos: (1) micropunção com uma agulha 30 G assistida por micromanipula-dor antes da vitrificação (n=4); (2) microssecção manual por lâmina antes da vitrificação (n=6); (3) sem manipulação anterior à vitrificação (n=8); e (4) transferidos a fresco (n=4). Apesar de altas taxas de reexpansão após a criopreservação, os embriões manipulados previamente a vitrificação não resultaram em prenhez aos 25 dias. Tanto os embriões não micromanipulados, quanto os transferidos a fresco resultaram em prenhezes aos 25 dias. A microssecção manual não se mostrou eficiente como método para aumento da criotolerância de embriões grandes, necessitando um aprimoramento visando a obtenção de prenhezes.(AU)

The effect of adding L-ergothioneine in culture medium on blastocyst development rates

Background: Oocytes and embryos produce energy through mitochondrial oxidative phosphorylation by using oxygen. The membrane structure of the embryo is mostly composed of unsaturated fatty acids, for this reason DNA fragmentation, apoptosis, and abnormal gene expression are shaped as a result of the lipid peroxidation during culture. Oxidative stress (OS) is one of the most important problems affecting the in vitro embryo development. Antioxidant supplementation to the culture medium has been an alternative way to reduce cell damage caused by oxidative stress in in vitro embryo production systems. In this study, it was aimed to determine the effect of L-ergothioneine on blastocyst development when added to the culture medium. Materials, Methods & Results: The material of the study consisted of oocytes aspirated from the ovaries of Holstein cows which were collected from the local slaughterhouse. The ovaries were delivered to the laboratory within 2-3 h in a thermos which provided a constant temperature of 25-30o C with physiological saline (0.9%) containing antibiotics. All follicles in the 3-8 mm range on the ovaries were aspirated using 20 G needle. The collected follicle fluid was filtered through filters with a pore diameter of 70 micrometers. Cells remaining in the filter were washed with OPU medium and transferred to the petri dishes. Fluids were examined under a stereomicroscope. The cumulus-oocyte complexes were classified, and A and B quality oocytes were included to the study (A, B, C, and D quality COC). Oocytes aspirated from the ovaries and collected later on were incubated in IVM medium for 22 h. After maturation, it was taken into IVF medium, semen was added and incubated for 20-22 h. Possible zygotes to be taken to the culture stage were transferred to culture (IVC) drops with (L-ergothioneine 100 µL/mL (n:121) added and without antioxidant (control (n:124)), and kept in the incubator for 6-7 days. Evaluated on the 7th day differences in in vitro embryo production stages were evaluated with the Chi-square test. The study was run in 5 replicates each time, with at least 20 possible zygotes for per group being cultured. It was determined that 262 (87.33%) of a total of 300 oocytes undergoing in vitro maturation were matured. It was determined that 245 of the mature oocytes were fertilized (93.51%). The cleavage rates of the groups were determined as 87.60% and 86.29%, respectively. Eighty-two (33.47%) blastocysts were obtained from 245 zygotes taken into the culture stage, and the blastocyst rates in the groups were found to be 40.50% and 26.61%, respectively. After the study, it was determined that the statistical difference between L-ergothioneine and control in cleavage rates was insignificant (P > 0.05) and blastocyst rates was significant (P < 0.05) Discussion: Oxygen content above normal ratios can increase the formation of reactive oxygen species (ROS), particularly hydrogen peroxide (H2 O2 ), hydroxyl radical (HO·), and peroxyl radicals (ROO·). The increased rate of ROS negatively affects the success of IVP in mammalian embryos. It was observed that L-ergothioneine, which has high antioxidant activity, improved blastocyst development rates, and higher blastocyst rates could be achieved compared to the control group. By investigating the use of L-ergothioneine in different doses, it was thought that the dose with the highest antioxidant activity could be added to the culture medium in in vitro embryo production and more blastocysts could be produced.

In vitro toxicity of Niedenzuella (Tetrapterys) multiglandulosa on bovine embryos / Toxicidade in vitro da Niedenzuella (Tetrapterys) multiglandulosa em embriões bovinos

Niedenzuella (Tetrapterys) multiglandulosa, a vine plant found in Brazil, has been correlated to outbreaks of poisoning in cattle and buffaloes, generating economic losses related to the death due to heart failure, miscarriage, abortion, stillbirth, and neonatal mortality. The aim of this study was to examine the embryotoxic potential of the aqueous plant extract on in vitro bovine embryos. In vitro study was performed in five replicates of bovine embryo culture assigned in two groups: control, in vitro embryo culture medium without the aqueous plant extract; treated group, with addition of 2.7mg/mL of aqueous plant extract (10%) to the embryo culture on the sixth day of culture. Cleavage rate was evaluated at day 2 of the cell culture. Viability, hatchability and underdevelopment of blastocysts on the seventh, eighth, and ninth days (D7, D8, and D9, respectively) of culture were assessed under stereoscopic microscope. On day 7, blastocysts were submitted to TUNEL assay to determine apoptotic index. In vitro exposure of bovine embryos to of N. multiglandulosa resulted in reduced embryo development and survival, evaluated by dark cytoplasm indicating poor morphology and poor quality with marked reduction of hatchability. We observed a significant reduction of blastocyst production/number of cleaved embryos (60.6% vs 41.5%); reduction of blastocysts production/total number of matured bovine oocytes (35.1% vs 21.3%); and embryonic hatching rates (38.0% vs 10.0%). However, no effects were observed on the apoptotic rate. In conclusion, aqueous extract of N. multiglandulosa leaves reduces bovine embryo viability in vitro, suggesting possible detrimental effects on embryo development.(AU)

Niedenzuella (Tetrapterys) multiglandulosa, uma videira encontrada no Brasil, tem sido correlacionada a surtos de intoxicações em bovinos e búfalos, gerando perdas econômicas relacionadas à morte por insuficiência cardíaca, aborto, natimorto e mortalidade neonatal. O objetivo deste estudo foi examinar o potencial embriotóxico do extrato vegetal aquoso em embriões bovinos in vitro. O estudo in vitro foi realizado em cinco repetições de cultura de embriões bovinos distribuídos em dois grupos: controle, meio de cultura de embriões in vitro sem o extrato aquoso da planta; grupo tratado, com adição de 2,7mg / mL de extrato vegetal aquoso (10%) à cultura do embrião no sexto dia de cultivo. A taxa de clivagem foi avaliada no dia 2 da cultura de células. Viabilidade, eclodibilidade e subdesenvolvimento de blastocistos no sétimo, oitavo e nono dia (D7, D8 e D9, respectivamente) de cultura foram avaliados em microscópio estereoscópico. No dia 7, os blastocistos foram submetidos ao ensaio TUNEL para determinar o índice apoptótico. Observamos redução significativa da produção de blastocisto / número de embriões clivados (60,6% vs 41,5%); redução da produção de blastocistos / número total de oócitos bovinos maturados (35,1% vs 21,3%); e taxas de eclosão embrionária (38,0% vs 10,0%). No entanto, nenhum efeito foi observado na taxa de apoptose. Em conclusão, o extrato aquoso das folhas de N. multiglandulosa reduz a viabilidade do embrião bovino in vitro, sugerindo possíveis efeitos prejudiciais no desenvolvimento embrionário.(AU)

The embryo culture media in the era of epigenetics: is it time to go back to nature?

This review is intended to draw attention to the importance of the culture media composition on the health of the embryos, fetuses, newborns, and adults derived from assisted reproductive technologies (ART). Although current research and industry trends are to use chemically defined media because of their suitability for manufacturing, commercialization, and regulatory purposes, compelling evidence indicates that those media fail to adequately account for the biological demands of early embryogenesis. Here, we list the main undesirable consequences of the ART described in the literature and results we and others have obtained over the past decade exploring an alternative and more natural way to support embryo growth in vitro: inclusion of endogenous reproductive fluids as additives in the ART culture media for pigs, cows, and humans. This review systematically assesses the pros and cons of using reproductive fluid additives, as well as the requirements to implement this approach in the future.(AU)

In vitro germination of Abricó-de-Macaco (Couroupita guianensis aubl.)zygotic embryos in different culture media and light spectra / Germinação in vitro de embriões zigóticos de Abricó-de-Macaco (Couroupita guianensis aubl.) em diferentes meios de cultivo e espectros de luz

ABSTRACT: Couroupita guianensis Aubl. is an Amazonian forest species with important medicinal and ornamental value. This study evaluated the effect of different culture media and light spectra on the in vitro germination and development of the zygotic embryos of C. guianensis. The culture media, MS and WPM, were evaluated without the addition of plant growth regulators and were associated with four LED light spectra: white (CW), 70% red + 30% blue (R2B), 100% red (R), and 100% blue (B). One hundred percent of the seeds successfully underwent in vitro germination, and the culture media did not interfere with embryo development. In addition to this, the different light spectra induced in vitro morphogenesis and R2B treatment significantly promoted the production of secondary roots. This effect may aid in the rooting and acclimatization of seedlings of this species.

RESUMO: Couropita guianensis Aubl. é uma espécie florestal de origem amazônica, de importância no uso medicinal e ornamental. O objetivo do presente estudo foi avaliar o efeito de diferentes meios de cultivo e espectros de luz na germinação e desenvolvimento in vitro de embriões zigóticos de Couropita guianensis. Os meios de cultura avaliados foram o MS e o WPM, sem adição de reguladores de crescimento, associados a quatro espectros de luz de LED branca (CW), 70% vermelha + 30% azul (R2B), 100% vermelha (R) e 100% azul (B). Ocorreu 100% de germinação in vitro e os meios de cultivo não interferiram no desenvolvimento dos embriões. Os diferentes espectros de luz induziram a morfogênese in vitro e o tratamento R2B promoveu a produção de raízes secundárias em número significativo. Este efeito poderá auxiliar no processo de enraizamento e aclimatização de mudas dessa espécie.

Use of ozone in the culture medium of zebrafish (Danio rerio) embryos / Uso do ozônio no meio de cultura para embriões de zebrafish (Danio rerio)

In this study, we sought to demonstrate the toxicity of different concentrations of ozonated water in zebrafish embryos up to 120 hours postfertilization (hpf ) and their antimicrobial activity advantages. For the test, we placed 40 embryos per treatment in Petri dishes containing 30 ml of solution to be tested. The ozone concentrations used were calculated from an initial concentration of 72 µg/ml using the O&L 1.5 RM ozone generator (Ozone & Life, Brazil). Five serial dilutions 1:1 was performed in egg water to produce the ozone treatments. We also analyzed a treatment with 30 ml of egg water without ozone, with only the addition of methylene blue, and a treatment with 30 ml of egg water without the addition of any antifungal agent. The plates were incubated at 28 ± 1°C, and the embryos were analyzed daily until 120 hpf. The survival rate, incubation period, and possible deformities were analyzed. In addition, egg water microbiological analyses were performed to detect total coliforms and fungi and yeasts. The data were tested for normality, and analysis of variance was performed within Minitab®version 1.8 software. The results showed that there was no significant difference in embryo survival or hatching rate between treatments with different ozone concentrations (p > 0.05), and no embryonic deformities were found under any of the ozone concentrations evaluated. It can be concluded that ozone within the concentrations analyzed is not toxic to zebrafish embryos and has antifungal and antimicrobial action.(AU)

Neste estudo, procuramos demonstrar a toxicidade de diferentes concentrações de água ozonizada em embriões de zebrafish até 120 horas pós-fertilização (hpf ) e suas vantagens na atividade antimicrobiana. Para o teste, colocamos 40 embri-ões por tratamento em placas de Petri contendo 30 ml da solução a ser testada. As concentrações de ozônio utilizadas foram calculadas a partir de uma concentração inicial de 72 µg/ml usando o gerador de ozônio O&L 1,5 RM (Ozone & Life, Brasil). Foram realizadas cinco diluições seriadas 1:1 em Egg Water. Também analisamos um tratamento com 30 ml de Egg Water sem ozônio, apenas com adição de azul de metileno, e um tratamento com 30 ml de Egg Water sem adição de nenhum agente antifúngico. As placas foram incubadas a 28 ± 1°C e os embriões foram analisados diariamente até 120 hpf. A taxa de sobrevi-vência, período de incubação e possíveis deformidades foram analisados. Além disso, foram realizadas análises microbiológicas da Egg Water para detectar coliformes totais, fungos e leveduras. Os dados foram testados quanto à normalidade e a análise de variância foi realizada no software Minitab® versão 1.8. Os resultados mostraram que não houve diferença significativa na sobrevivência de embriões ou taxa de eclosão entre os tratamentos com diferentes concentrações de ozônio (p > 0,05), e não foram encontradas deformidades embrionárias sob nenhuma das concentrações de ozônio avaliadas. Pode-se concluir que o ozônio dentro das concentrações analisadas não é tóxico para embriões de zebrafish e possui ação antifúngica e antimicrobiana.(AU)

Modified hydroponics and phenolic foam as technological innovations in the production of coffee seedlings from cuttings / Hidroponia modificada e espuma fenólica como inovações tecnológicas na produção de mudas de cafeeiro oriundas de estacas

Brazilian coffee production represents an important activity in the country's agricultural sector and, for this reason, it requires innovative technologies for the production of seedlings, which is one of the most important inputs in crop implantation. Thus, plant cloning by cutting, mineral nutrition via modified hydroponics and the use of alternative substrates appear as technological innovations for seedling production. This study evaluated the production of clonal coffee seedlings in a modified hydroponic system in comparison to the conventional climate-controlled greenhouse system, using vermiculite and phenolic foam as alternative substrates. At the end of the experiment, the seedlings were analyzed for growth (height, stem diameter, number of total leaves, leaf area, root area, shoot and root dry matter) and physiological (chlorophyll content and stomatal conductance) characteristics. For the statistical analysis, a completely randomized design was used in a factorial scheme 2 (types of substrate) x 2 (cultivation systems) with six replications and ten plants per plot. The innovative modified hydroponic system leads to a greater growth of coffee seedlings produced by cuttings in tubes with vermiculite compared to those produced in conventional systems. The substrate phenolic foam can be used alternatively in the air-conditioned greenhouse system. However, in the modified hydroponic system, it is not indicated, as it causes total seedling mortality.(AU)

A cafeicultura brasileira representa uma importante atividade no setor agrícola do país e por isto necessita de tecnologias inovadoras para a produção de mudas, que é um dos insumos de maior importância na implantação das lavouras. Sendo assim a clonagem de plantas por estaquia, a nutrição mineral via hidroponia modificada e o uso de substratos alternativos surgem como inovações tecnológicas para a produção de mudas. Objetivou-se com o presente trabalho avaliar a produção de mudas clonais de cafeeiro em sistema hidropônico modificado em comparação ao sistema convencional de casa de vegetação climatizada, utilizando a vermiculita e espuma fenólica como substratos alternativos. Ao final do experimento as mudas foram analisadas quanto as características de crescimento (altura, diâmetro de caule, número total de folhas, área foliar, área radicular, matéria seca da parte aérea e raiz) e fisiológicas (teores de clorofila e condutância estomática). Para a análise estatística foi utilizado o delineamento inteiramente casualizado no esquema fatorial 2 (tipos de substrato) x 2 (sistemas de cultivo) com seis repetições e dez plantas por parcela. Concluiu-se, portanto que o sistema inovador de hidroponia modificada promove maior crescimento das mudas de cafeeiro produzidas por estaquia em tubetes com vermiculita em relação àquelas produzidas em sistema convencional. O substrato espuma fenólica pode ser utilizado alternativamente no sistema de casa de vegetação climatizada, porém no sistema de hidroponia modificada não é indicado pois promove mortalidade total das mudas.(AU)

In vitro germination of Abricó-de-Macaco (Couroupita guianensis aubl)zygotic embryos in different culture media and light spectra / Germinação in vitro de embriões zigóticos de Abricó-de-Macaco (Couroupita guianensis aubl) em diferentes meios de cultivo e espectros de luz

Couroupita guianensis Aubl. is an Amazonian forest species with important medicinal and ornamental value. This study evaluated the effect of different culture media and light spectra on the in vitro germination and development of the zygotic embryos of C. guianensis. The culture media, MS and WPM, were evaluated without the addition of plant growth regulators and were associated with four LED light spectra: white (CW), 70% red + 30% blue (R2B), 100% red (R), and 100% blue (B). One hundred percent of the seeds successfully underwent in vitro germination, and the culture media did not interfere with embryo development. In addition to this, the different light spectra induced in vitro morphogenesis and R2B treatment significantly promoted the production of secondary roots. This effect may aid in the rooting and acclimatization of seedlings of this species.

Couropita guianensis Aubl. é uma espécie florestal de origem amazônica, de importância no uso medicinal e ornamental. O objetivo do presente estudo foi avaliar o efeito de diferentes meios de cultivo e espectros de luz na germinação e desenvolvimento in vitro de embriões zigóticos de Couropita guianensis. Os meios de cultura avaliados foram o MS e o WPM, sem adição de reguladores de crescimento, associados a quatro espectros de luz de LED branca (CW), 70% vermelha + 30% azul (R2B), 100% vermelha (R) e 100% azul (B). Ocorreu 100% de germinação in vitro e os meios de cultivo não interferiram no desenvolvimento dos embriões. Os diferentes espectros de luz induziram a morfogênese in vitro e o tratamento R2B promoveu a produção de raízes secundárias em número significativo. Este efeito poderá auxiliar no processo de enraizamento e aclimatização de mudas dessa espécie.

In vitro germination of Abricó-de-Macaco (Couroupita guianensis aubl)zygotic embryos in different culture media and light spectra / Germinação in vitro de embriões zigóticos de Abricó-de-Macaco (Couroupita guianensis aubl) em diferentes meios de cultivo e espectros de luz

Couroupita guianensis Aubl. is an Amazonian forest species with important medicinal and ornamental value. This study evaluated the effect of different culture media and light spectra on the in vitro germination and development of the zygotic embryos of C. guianensis. The culture media, MS and WPM, were evaluated without the addition of plant growth regulators and were associated with four LED light spectra: white (CW), 70% red + 30% blue (R2B), 100% red (R), and 100% blue (B). One hundred percent of the seeds successfully underwent in vitro germination, and the culture media did not interfere with embryo development. In addition to this, the different light spectra induced in vitro morphogenesis and R2B treatment significantly promoted the production of secondary roots. This effect may aid in the rooting and acclimatization of seedlings of this species.(AU)

Couropita guianensis Aubl. é uma espécie florestal de origem amazônica, de importância no uso medicinal e ornamental. O objetivo do presente estudo foi avaliar o efeito de diferentes meios de cultivo e espectros de luz na germinação e desenvolvimento in vitro de embriões zigóticos de Couropita guianensis. Os meios de cultura avaliados foram o MS e o WPM, sem adição de reguladores de crescimento, associados a quatro espectros de luz de LED branca (CW), 70% vermelha + 30% azul (R2B), 100% vermelha (R) e 100% azul (B). Ocorreu 100% de germinação in vitro e os meios de cultivo não interferiram no desenvolvimento dos embriões. Os diferentes espectros de luz induziram a morfogênese in vitro e o tratamento R2B promoveu a produção de raízes secundárias em número significativo. Este efeito poderá auxiliar no processo de enraizamento e aclimatização de mudas dessa espécie.(AU)

Isolation and amplification of Anaplasma marginale in chicken embryo fibroblast cell culture / Isolamento e amplificação de Anaplasma marginale em cultivos celulares de fibroblastos de embriões de galinhas

Anaplasma marginale (A. marginale) is a worldwide pathogen that infects a variety of ruminants, but mostly cattle. The present study aimed to describe an isolation technique for A. marginale, using chicken embryo Þ broblast (CEF) cell culture. Blood and tick samples were collected from 5 calves from 2 to 3 months old, which were considered to be infected with A.marginale due to anemia, jaundiced mucous membranes, and prostration. DNA extraction and PCR were performed for diagnosis using blood and tick samples. All tick and blood samples tested positive in PCR. Additionally, ticks were crushed with the aid of a blender for inoculation in CEF cell culture. After inoculation, the cultures were kept at 37ºC and 5% CO2 for 15 days. The cell supernatant of cell cultures was again analyzed using PCR and Wright stain method to conÞ rm A. marginale isolation. Cell cultures tested positive in PCR, and the presence of the agent was demonstrated by Wright stain. Therefore, by using CEF cell culture it was possible to isolate and amplify the A. marginale in a concentration of 1.3 x 107.2 bodies per mL. The CEF cells are undemanding and easy to preserve; they are an option for isolation and production of A. marginale under laboratory conditions.(AU)

Anaplasma marginale (A. marginale) é um patógeno mundial que infecta uma variedade de ruminantes, mas principalmente bovinos. O presente estudo teve como objetivo descrever uma técnica de isolamento para A. marginale, utilizando cultivo celular de Þ broblastos de embriões (CFE) de galinhas. Para isso, foram coletadas amostras de sangue e de carrapatos de 5 bezerros, entre 2 e 3 meses de idade, os quais, devido a anemia, icterícia de mucosas e prostração, foram considerados supostamente infectados com A. marginale. Ethics Approval This study was approved by Credenciamento Institucional para Atividades com Animais em Ensino ou Pesquisa (CIAEP: 02.0420.2021). Consent to participate Not applicable Consent to publish Not applicable Data availability Not applicable Para o diagnóstico, realizaram-se extração de DNA e posterior PCR a partir das amostras de sangue e de carrapatos coletados. Todos os carrapatos e amostras de sangue foram positivas para o teste de PCR. Além disso, os carrapatos foram triturados com o auxílio de um liquidiÞ cador para inoculação em CFE. Após a inoculação, as culturas foram mantidas a 37ºC e a 5% de CO2 durante 15 dias. O sobrenadante celular das culturas foi novamente analisado por PCR e pela técnica de coloração de Wright para conÞ rmar o isolamento de Anaplasma marginale. As culturas celulares foram po sitivas por PCR, e a presença do agente foi comprovada por meio da coloração de Wright. Portanto, utilizando CFE, foi possível isolar e ampliÞ car o A. marginale em uma concentração de 1,3x107,2 bactérias por ml. As células da CEF são pouco exigentes, de fácil manutenção e uma boa opção para isolamento e produção de A. marginale em condição laboratorial.(AU)

Morphology of seeds and seedlings, and substrates in germination of Citrus limetta / Morfologia de sementes, plântulas e substratos na germinação de Citrus limetta

This research studied the morphology of seeds and seedlings, in addition to obtaining information about the type and time of germination of sweet lemon seeds in five substrates (on blotting paper, between blotting paper, on washed sterilized sand, between washed sterilized sand and in paper roll). C. limetta seeds were measured, and external description was performed. Afterwards, sown in the sand and kept at 25 ºC to monitoring germination and morphological description of the resulting seedlings. A second experiment was evaluated for substrate efficiency: paper roll, on and between paper, on and between sand in the germination of C. limetta seeds. Speed index, average time and relative frequency of germination were evaluated. In addition, date of the first and last germination count was established. Treatment averages were compared using the Tukey test at 5% probability. C. limetta seeds are ovoid, slightly wrinkled and polyembryonic. Germination is hypogeal, cryptocotylar or phanerocotylar. The seedlings have leathery eophylls with simple leaves, elliptical shape or close to the elliptical, tending to ovate. It has a pivoting root system that is colored yellow to cream with the presence of secondary roots. The average germination time is between 18 and 22 days. The substrate indicated for seed germination is on paper.

Objetivou-se com o presente trabalho estudar a morfologia de sementes e plântulas, além de se obter informações sobre o tipo e tempo da germinação das sementes de limão-doce em cinco substratos (em papel mata-borrão, entre papel mata-borrão, em areia esterilizada lavada, entre areia esterilizada lavada e em rolo de papel). Sementes de C. limetta foram mensuradas suas dimensões e realizada a descrição externa. Posteriomente, semeadas entre areia e mantidas à 25 ºC para acompanhamento da germinação e descrição morfologica das plântulas resultantes. Um segundo experimento foi avaliado quanto a eficiência dos substratos: rolo de papel, sobre e entre papel, sobre e entre areia na germinação de sementes de C. limetta. Foram avaliados o índice de velocidade, o tempo médio e a frequência relativa da germinação. Além disso, foi estabelecida a data da primeira e última contagem da germinação. As médias dos tratamentos foram comparadas pelo teste de Tukey a 5% de probabilidade. As sementes de C. limetta são ovoides, levemente enrugadas e poliembrionicas. A germinação é hipógea, criptocotiledonar ou fanerocotiledonar. As plântulas apresentam eofilos coriáceos com folhas simples, formato elíptico ou próximo do elíptico, tendendo para ovado. Apresenta sistema radicular pivotante coloração de amarelo a creme com presença de raízes secundárias. O tempo médio de germinação é entre 18 e 22 dias. O substrato indicado para germinação das sementes é sobre papel.