Correlation of maternal concentrations of plasma testosterone with fetal sex in horses / Correlação das concentrações plasmáticas de testosterona materna com o sexo fetal em equinos

ABSTRACT: The objectives of this study were to evaluate the correlation of fetal sex and plasma testosterone concentrations between the 5th and 8th months of pregnancy in mares and to verify the applicability of this test to predict fetal sex. Blood samples were collected from 21 mares at 30-day intervals of between 150 and 240 days of pregnancy. Plasma testosterone was determined by radioimmunoassay and the sex of the foals confirmed at birth. The levels of maternal testosterone were higher in mares carrying female fetuses at months 5 and 8 (P < 0.05). Limit values were determined by analyzing the receiver operating characteristic (ROC) estimates: 35.5 pg/mL and 40 pg/mL for the 5th and 8th month, respectively. For the mares with plasma testosterone values equal to or above the threshold, gestation of female foals was predicted, and for those with plasma testosterone below the threshold values pregnancy of male foals was predicted. In the 5th month, the predictive values for male and female fetuses were 70% and 88.9%, respectively; the detection rates were 87.5% and 72.7%, and the total accuracy of the examination was 78.9%. In the 8th month, the predictive values for male and female fetuses were 80% and 90%, respectively; the detection rates were 88.9% and 81.8%, and the total accuracy of the examination was 85%. It was concluded that there was a correlation between fetal sex and plasma testosterone concentrations in pregnant mares. Prediction of fetal sex based on plasma concentrations of maternal testosterone can be performed in months 5 and 8 with 78.9% and 85% accuracy, respectively.

RESUMO: Os objetivos do estudo foram avaliar a correlação do sexo fetal com as concentrações plasmáticas de testosterona entre o 5° e o 8º mês de gestação na égua e verificar a aplicabilidade deste exame para a predição do sexo fetal. Amostras de sangue foram coletadas de 21 éguas, com intervalos de 30 dias, entre 150 e 240 dias de gestação. A testosterona plasmática foi determinada por radioimunoensaio e o sexo dos potros foi confirmado ao nascimento. Os valores de testosterona materna foram superiores nas éguas gestando fetos fêmeas aos cinco e oito meses (P< 0.05). Através da análise da curva ROC (receiver operating characteristic) foram determinados valores limites de 35,5 pg/mL e 40 pg/mL para o 5º e o 8° mês, respectivamente. Éguas com testosterona plasmática igual ou acima dos valores limites foram preditas como gestando fêmeas e éguas com testosterona plasmática abaixo dos valores limites foram preditas como gestando machos. Aos cinco meses, os valores preditivos para fetos machos e fêmeas foram 70% e 88,9%, respectivamente; as taxas de detecção foram 87,5% e 72,7% e a acurácia total do exame foi de 78,9%. Aos oito meses, os valores preditivos para fetos machos e fêmeas foram 80% e 90%, respectivamente; as taxas de detecção foram 88,9% e 81,8% e a acurácia total do exame foi de 85%. Conclui-se que houve correlação entre o sexo fetal e as concentrações de testosterona plasmática em éguas prenhes. A predição do sexo fetal baseada nas concentrações plasmáticas de testosterona materna pode ser realizada aos cinco e oito meses de gestação com 78,9% e 85% de acurácia, respectivamente.

Sêmen ovino e caprino imunossexado e diluído em meio de conservação à base de água de coco em pó (ACP101/102c) / Ram and goat semen immunosexed and diluted in powdered coconut water-based preservation medium (ACP101/102c)

Sperm sexing aims to separate sperm populations in carriers of the "X" or "Y" chromosome. Currently, flow cytometry is a technique that allows greater accuracy; however, it causes structural changes in sperm, reduces viability, and has a high cost. As a result, other methods have been researched, including immunosexing, which uses monoclonal antibodies to detect sex-specific surface antigens. Thus, the objective of this study was to evaluate the immunosexing technique using a monoclonal antibody against sex-specific protein (HY) in the conservation of ram and goat semen in ACP101/102c. Ejaculates from five rams and five goats were collected with the aid of an artificial vagina; they were evaluated and submitted to the immunosexing protocol, according to the manufacturer's recommendations, using the Monoclonal Antibody Kit specific for mammalian sperm with "Y" chromosomes (HY; HY Biotechnology, Rio de Janeiro, RJ, Brazil). After sexing, the supernatant was resuspended in the cryopreservation diluent: ACP ram (ACP101/102c + 20% egg yolk + 7% glycerol) and ACP goat (ACP101/102c + 2.5% egg yolk + 7% glycerol), packaged in 0.25 mL straws, refrigerated at 4°C, stabilized for 30 min, frozen in liquid nitrogen vapor (-60°C) for 15 min, immersed in liquid nitrogen, and stored in cryogenic cylinders. The samples were evaluated in natura (T1), after immunosexing (T2) and after thawing (T3) for sperm motility subjectively using conventional microscopy (40x). Plasma membrane integrity (IMP) and sperm cell morphology were evaluated by the smear staining technique using eosin-nigrosine dye, and the percentages of healthy and morphologically defect spermatozoa were determined. In the evaluation of ram semen regarding sperm motility and IMP, no statistically significant differences were observed between treatments after sexing in the evaluation of absolute data (P > 0.05), with the difference being observed only between T1 and T2, and T3 (P < 0.05). Regarding the relative percentage and sperm morphology, no statistically significant differences were observed (P > 0.05). Regarding the evaluation of goat semen samples, the motility parameters were consistent with the technique submitted; however, the IMP data did not appear as expected, requiring further evaluation for a better assessment of the technique for this species. The data obtained from ram semen submitted to the immunosexing protocol, regarding the absolute evaluation of motility and IMP, demonstrated that the non-sexed semen (T1) was superior to the sexed treatments (T2 and T3); however, it is noteworthy that freezing started with approximately 50% of the cells, since the immunosexing technique results in a loss of viability of approximately 50% of the sperm, which corresponds to the ratio of sperm carrying the X chromosome. In addition, when the data in this study were transformed into relative values, no statistical differences were observed, indicating that the immunosexing protocol, as well as the freezing protocol, did not significantly affect the quality of ram sperm cells. In relation to the immunosexing of goat semen, future studies should be conducted in vitro to define a more appropriate protocol for the species and, in addition, in vivo studies should be performed to prove the quality of the technique. It was concluded that the immunosexing process using a monoclonal antibody against sex-specific protein (HY) associated with the use of powdered coconut water diluent (ACP101/102c) in the cryopreservation of semen proved to be efficient in the in vitro evaluation of ovine species.(AU)

Rapid molecular assays for species and sex identification of swamp deer and other coexisting cervids in human-dominated landscapes of the Terai region and upper Gangetic plains, northern India: implications in understanding species distribution and population parameters

Burgeoning pressures of habitat loss is a major cause of herbivore decline across India, forcing them to coexist with humans in non-protected areas. Their conservation in such landscapes is challenging due to paucity of ecological and demographic information. The northern subspecies of swamp deer, Rucervus duvaucelii duvaucelii, is one such herbivore that lives across human dominated landscapes in Terai region and upper Gangetic plains of north India. Here, we describe species-specific molecular markers and a cervid-specific molecular sexing assay for swamp deer and four other coexisting cervids sambar, chital, barking deer and hog deer. Our markers show species-specific band patterns and a high success rate of 88.21% in large number of field collected referencesamples for all species. Faecal pellets from pilot swamp deer survey samples from upper Ganges basin show 93.81% success rate, and only 5.5% misidentification based on morphological characteristics. Our cervid-specific molecular sexing multiplex assay accurately ascertained 81.15% samples to respective sexes. These molecular approaches provide an easy, quick and cheap option to generate critical information on herbivore population parameters and aid their conservation in this mosaic of protected and non-protected grassland habitats.

Identification of sex using SBNO1 gene in the Chinese softshell turtle, Pelodiscus sinensis (Trionychidae)

The Chinese softshell turtle exhibits ZZ/ZW sex determination. To identify the sex of embryos, juvenile and adult individuals, we designed two pairs of polymerase chain reaction primers, SB1-196, which amplifies a fragment of 196 bp in the female and the other, CK1-482, which amplifies the 482-bp fragment in both the sexes. It is validated in 24 adult turtles of known sex, sampled from three different locations. This one-step sexing technique is rapid and easy to perform and is reported for the first time.

Sexagem em tamanduá-bandeira (Myrmecophaga tridactyla) por meio do teste da reação em cadeia da polimerase / Polymerase chain reaction for sexing in giant anteater's (Myrmecophaga tridactyla)

Em tamanduá-bandeira (Myrmecophaga tridactyla) não há dimorfismo sexual, tornando-se necessária a diferenciação entre machos e fêmeas, em especial naqueles indivíduos com finalidade reprodutiva. Entre as diversas técnicas empregadas para a caracterização sexual, a reação em cadeia da polimerase (PCR) é utilizada em mamíferos para identificar uma sequência genética especifica do cromossomo Y (SRY), sendo considerado um meio moderno e eficaz de determinação sexual. O objetivo deste trabalho é padronizar um protocolo para determinação sexual de tamanduá-bandeira por meio da técnica de PCR, utilizando material genético extraído do bulbo capilar desses animais. Mediante esse protocolo, foi possível determinar o sexo de sete animais testados, sendo compatível com o sexo de cada indivíduo. Conclui-se que o protocolo padronizado apresentou total eficácia, sendo possível determinar o sexo de tamanduás-bandeira utilizando material genético extraído do bulbo capilar.(AU)

There is no sexual dimorphism in the giant anteater (Myrmecophaga tridactyla), so the distinction between males and females become necessary, especially in animals with reproductive purpose. The Polymerase Chain Reaction (PCR), among the various techniques used for characterization, is considered a modern and effective means of sex determination and used in mammals to identify the Y chromosome (SRY) specifies genetic sequence. The objective of this work is to standardize a protocol for sex determination of giant anteater by PCR technique, using genetic material extracted from the capillary bulb of these animals. With this protocol was possible the sex determination of seven tested animals, being compatible with the sex of each individual. In conclusion, this protocol showed total effectiveness, being possible to determine the giant anteater sex using genetic material extracted from the capillary bulb.(AU)

Development of an Extraction Protocol for Fetal Sexing from the Fourth Week of Gestation by Real Time PCR

Abstract Low number of fetal cells in maternal blood limited the use of fetal materials in diagnostic and clinical applications. This research developed a technology which allowed the extraction of fetal DNA by a non-invasive method that offers no risk to the mother or fetus. A total of 132 pregnant women participated in this inquiry. The DNA extraction was performed employing an in-house method based on guanidine thiocyanate and magnetic bead. For the amplification it was used the Quantifier Y Kit™. The fetal sexing analysis of the 132 pregnant women were 100% in agreement with the ultrasound. Sensitivity and specificity for detection of Y chromosome sequences was possible using Real-Time Polymerase Chain Reaction since the 4th week of gestation. This non-invasive early determination could be employed in fetal gender and also to be extended to detection of genetic diseases in the shortest possible time avoiding invasive methods that puts the fetus at risk.

Sêmen sexado através de citometria de fluxo e centrifugação por gradiente de concentração / Semen sexed using flow cytometry and concentration gradient centrifugation / Semen sexado a través de citometría de flujo y centrifugación por gradiente de concentración

Resumo O objetivo deste trabalho foi apresentar uma revisão completa e atualizada sobre a origem do sêmen sexuado, os requisitos e as técnicas de sexagem espermáticas. Nas últimas décadas, desenvolveram-se várias tecnologias na área da reprodução animal. O sêmen sexado é uma biotecnologia recente que ainda se encontra em fase de estudo e aperfeiçoamento em diversas etapas, devido a que o processo de sexagem causa estresse ao espermatozoide, e o deixa mais sensível ao processo de armazenamento; isto interfere diretamente na fertilidade. Esta tecnologia, que chegou ao Brasil em 2004, vem ganhando adeptos entre produtores que desejam produzir animais mais homogêneos para o sacrifício ou para a produção de leite. O uso do sêmen sexado tem sido difundido em muitos rebanhos do mundo, já que se apresenta como uma técnica com um direcionamento maior na seleção do sexo. Muitas técnicas têm sido utilizadas com a finalidade de buscar uma maior separação de espermatozoides portadores de cromossomas X e Y, com mínima agressão espermática. Desta forma, a utilização da sexagem espermática tem obtido resultados na aplicação de biotecnologias da reprodução assistida, e com isso tem elevado o lucro no melhoramento genético e tem otimizado a produtividade no sexo escolhido. Entretanto, ainda existem muitas limitações, principalmente referentes al tempo de exposição, o índice de aproveitamento e os resultados de índices de gestação em condições de campo. Por outro lado, a dose de sêmen sexado pode custar de duas a oito vezes o valor de uma convencional; da mesma forma, o seu uso avança no Brasil.

Abstract This study aimed to present a complete and updated review on the origin of sexed semen, as well as on the requirements and techniques of sperm sexing. In the last decades, several technologies were developed in the field of animal reproduction. Sexed semen is a recent biotechnology that is still under study and refinement in various stages, because the sexing process causes stress to the sperm, leaving it more sensitive to the storage process; this directly interferes with fertility. This technology, which arrived in Brazil in 2004, has been gaining support among producers who want to produce more homogeneous animals for slaughter or for dairy production. The use of sexed semen has been disseminated in many herds of the world, since it is a technique with better results in the selection of sex. Many techniques have been used in order to seek a greater separation of sperms carrying X and Y chromosomes, with minimal sperm aggression. In this way, the use of sperm sexing has obtained results in the application of assisted reproductive biotechnologies, which has increased the gain in genetic improvement and has optimized productivity in the chosen sex. In the meantime, there are still many limitations, mainly concerning exposure time, exploitation rate, and the results of pregnancy rates in field conditions. On the other hand, the dose of sexed semen can cost two to eight times the value of conventional semen; nevertheless, its use progresses in Brazil.

Resumen El objetivo de este trabajo fue presentar una revisión completa y actualizada sobre el origen del semen sexado, los requisitos y las técnicas de sexaje espermáticas. En las últimas décadas, se desarrollaron varias tecnologías en el área de la reproducción animal. El semen sexado es una biotecnología reciente que aún se encuentra en fase de estudio y perfeccionamiento en diversas etapas, debido a que el proceso de sexaje causa estrés al espermatozoide, y lo deja más sensible al proceso de almacenamiento; esto interfiere directamente en la fertilidad. Esta tecnología, que llegó a Brasil en 2004, viene ganando adeptos entre productores que desean producir animales más homogéneos para el sacrificio o para la producción lechera. El uso del semen sexado ha sido difundido en muchos rebaños del mundo, ya que se presenta como una técnica con un direccionamiento mayor en la selección del sexo. Muchas técnicas han sido utilizadas con el fin de buscar una mayor separación de espermatozoides portadores de cromosomas X y Y, con mínima agresión espermática. De esta forma, la utilización del sexaje espermático ha obtenido resultados en la aplicación de biotecnologías de la reproducción asistida, y con eso ha elevado la ganancia en el mejoramiento genético y ha optimizado la productividad en el sexo escogido. Entretanto, aún existen muchas limitaciones, principalmente referentes al tiempo de exposición, la taza de aprovechamiento y los resultados de tazas de gesta ción en condiciones de campo. Por otro lado, la dosis de semen sexado puede costar de dos a ocho veces el valor de una convencional; así mismo, su uso avanza en Brasil.

Identificación molecular del sexo en 9 especies de aves del Centro de Investigación en Animales Silvestres de la hidroeléctrica de Itaipu, lado paraguayo / Sex identification by molecular methods in 9 species of birds from the wild animal research center of Itaipu dam on the paraguayan side

La importancia de determinar el sexo en especies monomórficas que viven en cautiverio conlleva a estrategias de apareamiento a fin de poder incentivar la reproducción. Existen métodos no moleculares de reconocimiento pero son factibles en edad adulta y mucho más difícil cuando son polluelos. Mediante la técnica molecular de PCR, se amplificó el gen de la Cromo Helicasa de Unión al ADN empleando los cebadores, 2550F/2718R. Por este método molecular se consiguió determinar el sexo en 19 de 23 especies de las cuales 3 son ejemplares de: Amazona aestiva, 1 de Pipile grayi, 1 de Bubo virginianus, 4 de Ara chloropterus, 6 de Crax fasciolata, 2 de Caracara plancus, 3 de Chauna torquata, 1 de Cariama cristata y 2 de Cairina moschata del Centro de Investigación de Animales Silvestres de ITAIPU binacional, del lado paraguayo. Nuestros resultados sugieren que el par de cebadores 2550F/2718R podría ser de utilidad para determinar el sexo en las especies estudiadas en el país.

In monomorphic species living in captivity, determining the sex is important because it may allow choosing mating strategies to enhance reproduction. Sex can be determined either by non-molecular recognition methods, which are only feasible in adult birds, or by molecular techniques, which may allow sexing monomorphic species at young ages. Thus, in this study, we used molecular techniques such PCR to amplifying the CHD gene by using 2550F/2718R primers. This method allowed us to determine the sex in 19 out of 23 bird specimens from the Centro de Investigación de Animales Silvestres (CIASI) of the ITAIPÚ BINACIONAL at Paraguayan side. The specimens belonged to the following species: Amazona aestiva (3), Pipile grayi (1), Bubo virginianus (1), Ara chloropterus (4), Crax fasciolata (6), Caracara plancus (2), Chauna torquata (3), Cariama cristata (1) and Cairina moschata (2). The 2550F/2718R primers were useful for determine the sex of the studied species.

Citometría de flujo y sexaje de espermatozoides en animales / Flow cytometry and sperm sexing in animals

Actualmente, cientos de crías se han gestado a través de inseminación artificial conespermatozoides sexados en producción animal. Desde 1992 se utiliza la citometría de flujo, técnica que permite diferenciar espermatozoides X e Y según su contenido de ADN. No existe, hasta el momento, ninguna otra técnica práctica para sexar espermatozoides manteniendo la capacidad fecundante. Los objetivos de esta revisión son explicar: (1) por qué los espermatozoides que contienen el cromosoma X o Y son similaresfenotípicamente, pero a la vez mantienen diferencias entre ellos, (2) los principios y procedimientos utiliza-dos para sexar espermatozoides mediante citometría de flujo y sorting (3) la precisión, velocidad y la eficiencia de los procedimientos actuales de sexaje espermático, (4) el daño espermático ocurrido durante el sexaje espermático y consecuentemente los efectos sobre la fecundidad.

Flow cytometry is a useful technology in the sexed sperm, which measures and analyzes simultaneously, multiple physical characteristics of the cell, as they flow in a stream flow, through a lightbeam. The measured properties are the size of a particle, relative internal granularity, relative complexity and relative fluorescence intensity. Currently, hundreds of calves have been gestated through artificial insemination with sexed sperm in animal production. Since 1992, flow cytometry has been used, a technique that allows spermatozoa X and Y differentiation by DNA content. There is no other practical technique forsperm sexing to keep sperm functionality. The objectives of this review are to explain: (1) why the sperm containing the X or Y chromosome are phenotypically similar, but differ among themselves, (2) the principlesand procedures used for sexing sperm by flow cytometry and sorting ( 3) accuracy, speed and efficiency ofcurrent procedure sperm sexing, (4) sperm damage occurred during sperm sexing and consequently the effects on fertility.

Morphological and morphometric analysis of skeletal muscle between male and female young adult Colossoma macropomum (Characiformes: Serrasalmidae)

This study aimed to evaluate muscle organization in tambaqui in order to describe the muscle growth process. We analyzed the morphometric pattern of fibers from white muscle of young-adults (300 days) by smaller diameter. The organization of white muscle exhibited a typical morphological pattern found in other fish species. Heavier animals showed higher frequency of larger diameter fibers (>50 m ) and smaller animals had higher frequency of smaller diameter fibers ( 20 m ) (P =0.005). However, both animals showed the same frequency of intermediate diameter fibers (20-50 m ). Body weight showed a positive correlation with muscle diameter fiber (r=0.45), being 20-50 m the diameters that contributed the most to animal weight (P 0.0001). A weak correlation between fiber diameter and animal sex was observed (r=0.2). Females showed higher frequency of large fiber diameters (>50 m ) than males. However, there was no difference between body weight and sex (P =0.8). Our results suggest that muscle growth is by hypertrophy and hyperplasia due to a mosaic appearance from different diameters fibers, which is characteristic of large size fish species.

O objetivo deste trabalho foi avaliar a organização muscular em tambaqui, a fim de descrever o processo de crescimento muscular. Foi analisado o padrão morfométrico das fibras do músculo branco de animais com 300 dias de idade usando o método de diâmetro menor. O músculo branco apresentou uma organização morfológica padrão encontrado em peixes. Animais de maior peso apresentaram maior frequência de fibras de maior diâmetro (> 50 m ) e os animais de menor peso apresentaram maior frequência de fibras de menor diâmetro ( 20 m ) (P = 0,005). Entretanto, ambos os animais, com maior e menor peso, apresentaram frequências semelhantes de fibras de diâmetro intermediário (20-50 m ). O parâmetro peso corporal mostrou correlação positiva com o diâmetro da fibra muscular (r = 0,45), sendo as fibras de diâmetro intermediários (20-50 m ) que mais contribuíram para o peso do animal (P 0,0001). Fêmeas apresentaram maior frequência de fibras de maior diâmetro (>50 m ) que machos. Observou-se uma fraca correlação entre o diâmetro da fibra e o sexo dos animais (r = 0,2). Apesar de fraca, a correlação estimada é corroborada pela fibras de grandes diâmetros (> 50 m ) serem mais frequente nas fêmeas que nos machos. No entanto, não houve diferença entre o peso corporal dos animais aos 300 dias de idade e sexo (P = 0,8). Os resultados encontrados sugerem que o crescimento muscular ocorre por hipertrofia e hiperplasia, caracterizado pela aparência em mosaico de fibras de diferentes diâmetros, característico de peixes de grande tamanho.

Computer-assisted sperm morphometry fluorescence-based analysis has potential to determine progeny sex / 亚洲男科学杂志(英文版)

This study was designed to determine the ability of computer-assisted sperm morphometry analysis (CASA-Morph) with fluorescence to discriminate between spermatozoa carrying different sex chromosomes from the nuclear morphometrics generated and different statistical procedures in the bovine species. The study was divided into two experiments. The first was to study the morphometric differences between X- and Y-chromosome-bearing spermatozoa (SX and SY, respectively). Spermatozoa from eight bulls were processed to assess simultaneously the sex chromosome by FISH and sperm morphometry by fluorescence-based CASA-Morph. SX cells were larger than SY cells on average (P < 0.001) although with important differences between bulls. A simultaneous evaluation of all the measured features by discriminant analysis revealed that nuclear area and average fluorescence intensity were the variables selected by stepwise discriminant function analysis as the best discriminators between SX and SY. In the second experiment, the sperm nuclear morphometric results from CASA-Morph in nonsexed (mixed SX and SY) and sexed (SX) semen samples from four bulls were compared. FISH allowed a successful classification of spermatozoa according to their sex chromosome content. X-sexed spermatozoa displayed a larger size and fluorescence intensity than nonsexed spermatozoa (P < 0.05). We conclude that the CASA-Morph fluorescence-based method has the potential to find differences between X- and Y-chromosome-bearing spermatozoa in bovine species although more studies are needed to increase the precision of sex determination by this technique.

An Anatomical Study of Adult Sacrum With its Emphasis on its Sexual Dimorphism in South Indian Populition.

Aim: To study the various morphometric parameters of the dry sacra of unknown sex in South Indian population in detail and to determine their demarcating points in order to increase the efficiency of sexing in the given population. Methods: 87 dry adult human sacrum of known sex (42 males and 45 females), belonging to South Indian (Karnataka) region were obtained. Various parameters like Length (L), breadths (B), Transverse diameter of the body of the 1st sacral vertebrae (TS1) & Curved Length of Sacrum (CL) were obtained. From these parameters, Sacral Index (SI), Curvature Index (CI) and Corporo-basal Index (CBI) were calculated & from the obtained values demarking points (D.P) were calculated. The values were stastically analyzed. Results: Among these parameters, the values for the Length (L), Curved Length (CL) and Sacral Index (SI) were stastically significant Conclusion: Length (L), Curved Length (CL) and Sacral Index (SI) were useful parameters and by obtaining their demarking points, it helps in sexing the sacrum with greater accuracy.

Probióticos em dietas para tilápia do Nilo durante a reversão sexual / Probiotics in diets for Nile tilapia during the sex reversal

Objetivou-se avaliar o desempenho produtivo, sexagem fenotípica e microbiologia intestinal de tilápia do Nilo, linhagem GIFT, alimentadas com ração contendo Bacillus cereus var. Toyoi e Bacillus subtilis C-3102, durante a fase de reversão sexual. Os peixes (24,7±0,50mg) foram distribuídos aleatoriamente em 24 aquários, num delineamento inteiramente casualizado, composto por três tratamentos (dois probióticos e ausente de probiótico) e oito repetições. A utilização de B. cereus melhorou os parâmetros de peso final, ganho em peso, ganho em peso médio diário e crescimento específico dos peixes alimentados em relação à B. subtilis. Não houve associação entre a proporção de machos e fêmeas e a inclusão de probióticos. As contagens de bactérias totais e coliformes totais não foram influenciadas pela adição de probióticos nas rações. O probiótico Bacillus subtilis não melhora o desempenho produtivo das tilápias do Nilo. Na decisão entre os dois probióticos estudados, recomenda-se o probiótico contendo Bacillus cereus C-3102 por não afetar negativamente a efetividade sexual e parâmetros zootécnicos.

The objective was to evaluate the productive performance, phenotypic sexing, and intestinal microbiology of Nile tilapia, GIFT strain, fed with diets formulated with Bacillus cereus var. Toyoi and Bacillus subtilis C-3102, during sex reversal. Fish (24.7±0.50mg) were randomly distributed in 24 aquaria in a completely randomized design compound for three treatments (two probiotics and absent) and eight replications. The use of B. cereus and improved the final weight, weight gain, average daily weight gain and specific growth rate fed in relation to B. subtilis. There was no association between the proportion of males and females and inclusion of the probiotics. The counts of total bacteria and total coliforms were not influenced by the addition of probiotics. Bacillus subtilis did not improve the productive performance in Nile tilapia. Bacillus subtilis did not improve the productive performance of Nile tilapia. Among the two studied probiotics is recommended probiotic containing Bacillus cereus C-3102 not adversely affect the sex reversal effectiveness and performance zootechnical.

Morfometria e histologia das gônadas de machos e fêmeas recém-eclodidos de Podocnemis expansa e Podocnemis unifilis (Testudines, Podocnemididae) / Morphometry and histology of the gonads of males and females hatchlings of Podocnemis expansa and Podocnemis. unifilis (Testudines, Podocnemididae)

Considerando a importância da técnica histológica na sexagem de quelônios e os poucos trabalhos direcionados para esta técnica, é proposto neste estudo caracterizar morfometricamente e histologicamente as gônadas de P. expansa e P. unifilis. Todos os espécimes utilizados neste trabalho foram procedentes do rio Javaés, entorno do Parque Nacional do Araguaia, Estado do Tocantins, Brasil. Após estudo sob estereomicroscópio, foram coletadas as gônadas para o procedimento histológico de rotina. Foram analisadas 187 amostras de P. expansa, das quais 81,2% foram identificadas como fêmeas e 18,7% como machos; e 98 de P. unifilis, das quais 31,6% eram fêmeas e 68,4% machos. Não foram verificadas diferenças microscópicas relevantes na sexagem entre estas espécies. Os critérios utilizados no diagnóstico microscópico foram principalmente a morfologia das gônadas, a presença do apêndice no oviduto remanescente, a morfologia do oviduto e as características das células de revestimento dos folículos e túbulos seminíferos. Quando comparadas as medidas biométricas dos ovários e testículos, somente foram observadas diferenças para a largura.

Considering the importance of the histological sexing technique of turtles and the few works directed to this objective, it was proposed in this study to morphometrically and histologically characterize the gonads of P. unifilis and P. expansa. All specimens used in this work originated in the Javaés river, around the Araguaia National Park, Tocantins State, Brazil. Following a study under a stereoscope, the gonads were collected for the routine histological procedure. A total of 187 samples of P. expansa were analyzed, of which 81.2% were identified as female and 18.7% as male; as well as 98 P. unifilis samples, of which 31.6% were female and 68.4% males. No relevant microscopic differences were verified in the sexing between these species. The criteria used in the microscopically diagnosis were primarily gonad morphology, presence of the appendix in the remaining oviduct, oviduct morphology and the characteristics of covering cells of the follicles and somniferous tubules. When the measurements of the ovaries and testicles were compared, only differences in width were observed.

Morfometria e histologia das gônadas de machos e fêmeas recém-eclodidos de Podocnemis expansa e Podocnemis unifilis (Testudines, Podocnemididae) - doi: 10.4025/actascibiolsci.v34i1.7257

Considering the importance of the histological sexing technique of turtles and the few works directed to this objective, it was proposed in this study to morphometrically and histologically characterize the gonads of P. unifilis and P. expansa. All specimens used in this work originated in the Javaés river, around the Araguaia National Park, Tocantins State, Brazil. Following a study under a stereoscope, the gonads were collected for the routine histological procedure. A total of 187 samples of P. expansa were analyzed, of which 81.2% were identified as female and 18.7% as male; as well as 98 P. unifilis samples, of which 31.6% were female and 68.4% males. No relevant microscopic differences were verified in the sexing between these species. The criteria used in the microscopically diagnosis were primarily gonad morphology, presence of the appendix in the remaining oviduct, oviduct morphology and the characteristics of covering cells of the follicles and somniferous tubules. When the measurements of the ovaries and testicles were compared, only differences in width were observed

P. expansa e P. unifilis. Todos os espécimes utilizados neste trabalho foram procedentes do rio Javaés, entorno do Parque Nacional do Araguaia, Estado do Tocantins, Brasil. Após estudo sob estereomicroscópio, foram coletadas as gônadas para o procedimento histológico de rotina. Foram analisadas 187 amostras de P. expansa, das quais 81,2% foram identificadas como fêmeas e 18,7% como machos; e 98 de P. unifilis, das quais 31,6% eram fêmeas e 68,4% machos. Não foram verificadas diferenças microscópicas relevantes na sexagem entre estas espécies. Os critérios utilizados no diagnóstico microscópico foram principalmente a morfologia das gônadas, a presença do apêndice no oviduto remanescente, a morfologia do oviduto e as características das células de revestimento dos folículos e túbulos seminíferos. Quando comparadas as medidas biométricas dos ovários e testículos, somente foram observadas diferenças para a largura

Validação comparativa utilizando PCR quantitativo em tempo real (qPCR) e PCR convencional de sêmen bovino centrifugado em gradiente de densidade contínuo / Comparative validation using quantitative real-time PCR (qPCR) and conventional PCR of bovine semen centrifuged in continuous density gradient

The objective of the present study was to determine the sperm enrichment with X-bearing spermatozoa, after one centrifugation in a Percoll or OptiPrep continuous density gradient, using quantitative real-time polymerase chain reaction (qPCR) of sperm DNA and resultant in vitro-produced bovine embryos by PCR. Frozen/thawed sperm was layered on density gradients and the tubes were centrifuged. Supernatants were gently aspirated and the sperm recovered from the bottom of the tubes. Cleavage and blastocyst rates were determined through in vitro production of embryos and PCR was performed to identify the embryos' genetic sex. A difference in blastocyst rate was found in the Percoll treatment compared to OptiPrep (P<0.05). The percentage of female embryos in the Percoll and OptiPrep groups was 62.0 percent and 47.1 percent, respectively. These results were confirmed by qPCR of spermatozoa DNA and underestimation was seen only in the Percoll group. It was possible to sexing sperm using simple approach.

O objetivo do presente estudo foi determinar o enriquecimento de espermatozoides portadores do cromossomo X após a centrifugação em gradiente de densidade contínuo de Percoll ou OptiPrep, utilizando reação em cadeia da polimerase quantitativa em tempo real (qPCR) do DNA do espermatozoide e dos embriões bovinos produzidos in vitro resultantes pela PCR convencional. Espermatozoides descongelado foram depositados em gradientes de densidade e os tubos foram centrifugados. Os sobrenadantes foram gentilmente aspirados e os espermatozoides recuperados do fundo dos tubos. As taxas de clivagem e de blastocisto foram determinadas pela produção in vitro de embriões e a PCR foi realizada para a identificação genética do sexo dos embriões. Verificou-se diferença na taxa de blastocistos entre os grupos Percoll e OptiPrep (P<0,05). A porcentagem de embriões de fêmeas nos grupos Percoll e OptiPrep foi de 62,0 por cento e 47,1 por cento, respectivamente. Estes resultados foram confirmados pela qPCR do DNA de espermatozoides e uma subestimação foi observada no grupo do gradiente de densidade de Percoll. Foi possível a sexagem de espermatozoides utilizando uma metodologia simples.

Pregnancy diagnosis, fetal quantification and gender estimation by ultra-sonography in ewes / Diagnóstico de gestação, quantificação e sexagem fetal por ultra-sonografia em ovelhas

The objective of this experiment was to evaluate the accuracy of gestation, fetal sexing and quantification diagnoses in ewes. Pregnancy and fetal quantification were diagnosed in 105 ewes at 35 days of pregnancy. For the fetal gender diagnosis sexing diagnose 55 ewes between 49 and 59 days of pregnancy were used. All exams were recorded on DVD for posterior analysis. After birth, lamb sex was recorded to determine fetal sexing precision. Data were analyzed by chisquare ( 2) or Fisher’s test, with a significance of 0.05. One hundred percent of pregnancy ultrasound diagnoses were correct. As for the fetal quantification diagnoses, there was an error of 12%. It was possible to diagnose the fetal sex in 87% of the 69 examined fetuses, and 90% of these were estimated correctly. The realtime ultrasound diagnoses were not different from the recorded DVD image diagnoses. Therefore, pregnancy diagnosis accuracy may reach 100%, differing from fetal gender estimation and quantification, which are dependent upon other variables such as fetal genderand examiner experience.

O objetivo deste experimento foi avaliar a acurácia do diagnóstico de gestação, quantificação e sexagem fetal em ovelhas. Foram realizados o diagnóstico de gestação e a quantificação fetal em 105 ovelhas aos 35 dias de gestação. Para o diagnóstico da sexagem fetal foram utilizadas 55 ovelhas com período de gestação entre 49 e 59 dias. As imagens de todos os exames foram gravadas em DVD para permitir posterior análise. Após o nascimento dos cordeiros, os respectivos sexos foram observados para determinar a precisão do exame de sexagem fetal. Os dados foram analisados pelo teste Qui- quadrado ( 2) ou Teste de Fisher, com nível de significância de 5%. Observou-se 100% de acerto no diagnóstico de gestação pela ultra-sonografia. Quanto ao diagnóstico de quantificação fetal, houve 12% de erro. Foi possível diagnosticar o sexo fetal em 87% dos fetos e destes, 90% estavam corretos. Os diagnósticos em tempo real não foram significativamente diferentes dos diagnósticos feitos após a observação de imagens gravadas em DVD. Portanto, a acurácia do diagnóstico de gestação pode alcançar 100%, diferente da quantificação e sexagem fetal, que dependem de outras variáveis como tipo de gestação e experiência do operador.

Iris colour as an indicator of age feature in female Brazilian tanagers (Passeriformes: Emberizidae) confirmed by a molecular sexing technique

The Brazilian tanager, Ramphocelus bresilius is an endemic species from Brazil that is sexually dimorphic in adult plumage. Young males are similar to adult and young females until their second year. Adults and young females are not distinguishable in plumage. We tested whether iris colour can be used to separate adult females from immature females. We used for the first time the molecular sexing technique based on CHD-genes to confirm the sex of the individuals classified as "female plumage with red iris", and to identify the sex of individuals classified as "female plumage and brown iris". The adult males were used as a positive control. DNA samples from 190 individuals were analysed. The sizes of the PCR products were identified as 350 base pairs (bp) for CHD-Z and 388 bp for CHD-W. We confirmed that adult females have a red iris and the young females a brown iris. We could also separate young males and females which present the same iris colour and plumage. Although there are indications that the iris colour can be used by birds to identify the adults in co-operative breeding species such as the Brazilian tanager, more behavioural data are required to understand the role of iris coloration in this species. Rev. Biol. Trop. 56 (4): 1629-1633. Epub 2008 December 12.

El ave Ramphocelus bresilius es una especie endémica de Brasil con dimorfismo sexual en el plumaje del adulto. Los machos jóvenes son similares a las hembras adultas y jóvenes hasta el segundo año de vida. Adultos y hembras jóvenes son indistinguibles por el plumaje. Evaluamos si el color del iris puede ser utilizado para distinguir hembras adultas de hembras inmaduras. Utilizamos por primera vez la técnica molecular de identificación de sexos basada en los genes CHD para confirmar el género de individuos clasificados como plumaje femenino con iris rojo, y para identificar el sexo de los individuos clasificados como plumaje femenino e iris marrón. Usamos machos adultos como control. Analizamos muestras de DNA de 190 individuos. Los tamaños de los productos del PCR fueron identificados como 350 pares de bases (pb) para CHD-Z y 388 pb para CHD-W. Pudimos confirmar que las hembras adultas presentan iris rojo y las hembras jóvenes iris marrón. También pudimos distinguir machos jóvenes de hembras, que presentan el mismo color de iris y plumaje.

Falha na sexagem por inibição do desenvolvimento de embriões bovinos produzidos in vitro com anticorpos anti H-Y / Failure of sexing by developmental arrest of bovine embryos in vitro produced with H-Y antisera

Embriões bovinos produzidos in vitro, em estádio de mórula, foram cultivados em meio contendo anticorpos anti H-Y de alto título proveniente de ratos por 24h e, após este tempo, classificados em dois grupos: 1) embriões inibidos em estádio de mórula (classificados como machos) e 2) embriões que se desenvolveram e formaram a blastocele (classificados como fêmeas). O sexo de 311 embriões, distribuídos em três grupos de concentração dos anticorpos, 3 por cento, 5 por cento ou 7 por cento, foi identificado pela reação em cadeia da polimerase. Não houve desvio da proporção entre machos e fêmeas (P>0,05) nos grupos em que se utilizaram os anticorpos anti H-Y, quando comparadas ao grupo-controle, sem adição de anticorpos anti H-Y. Diferentemente dos resultados obtidos utilizando-se embriões bovinos produzidos in vivo, a sexagem com anticorpos anti H-Y de alto título em embriões produzidos in vitro não propiciou sucesso.

In vitro produced bovine embryos at morula stage were cultured in medium containing high titer of rat H-Y antisera for 24h. The embryos were classified in two groups: 1) embryos arrested at morula stage (classified as males); and 2) embryos that developed and formed a blastocoele (classified as female). The sex of 311 embryos, divided in three groups of concentration of H-Y antisera, 3 percent, 5 percent or 7 percent, was identified by polimerase chain reaction. The results showed no difference (P>0.05) on sexual deviation in groups in which the H-Y antisera was added, in relation to control group, in which no H-Y antisera was added. In contrast with results obtained with in vivo produced bovine embryos, the sexing of in vitro produced bovine embryos with high H-Y antisera titer did not succed.