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)

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)

Use of an ultrasound device to determine sex and to perform gonad biopsy in the European eel Anguilla Anguilla / Uso de um dispositivo ultrasonográfico para determinar o sexo e efetuar a biópsia das gônadas da Enguia-Européia Anguilla anguilla

The European eel Anguilla anguilla is a highly important market species which is also increasingly in danger of extinction in Europe. One of the ways of protecting the species in the natural environment, while maintaining its market supply, is its aquaculture, e.g. due to much higher survival rate under controlled conditions than in the wild. However, this can be done only when an effective artificial reproduction biotechnique is developed. The aim of this study was to use an ultrasound device to determine the sex and to perform a biopsy of the gonads, which is a part of complete protocol of eel artificial reproduction. The findings indicate that ultrasonography is highly useful in determining the sex in migrating eel (100% of sureness) and in performing high-precision biopsy of the gonads. The present method gives the possibility to quick determine the maturity of the female gonads. The application of ultrasonography (USG) is totally safe for fish and a portable ultrasound device can be used in both the laboratory and in the field...

A Enguia-Européia Anguilla anguilla é uma espécie de grande importância comercial e que apresenta também grande risco de extinção na Europa. Uma das formas para a proteção das espécies em seu ambiente natural e de manter o seu suprimento no comércio é a aquicultura, por exemplo, devido à taxa de sobrevivência em condições controladas ser muito superior a existente em condições naturais. Contudo isto só pode ser obtido quando é desenvolvida uma biotécnica de reprodução artificial eficiente. O presente trabalho foi delineado para utilizar um dispositivo ultrassonográfico a fim de determinar o sexo e de possibilitar a realização de biópsias das gônadas, o que é parte do protocolo complete de reprodução artificial de enguias. As constatações indicaram que a ultrassonografia é muito útil para a determinação do sexo das enguias (100% de exatidão) e também é capaz de possibilitar a realização de uma biópsia das gônadas de alta precisão. O método descrito oferece possibilidades para a rápida determinação da maturidade das gônadas das fêmeas. A aplicação da ultrassonografia é totalmente segura para peixes e o dispositivo portátil de ultrassonografia pode ser utilizado tanto no laboratório como em condições de campo...

Sensibilidade da PCR na amplificação do DNA bovino em diluição seriada e mistura de amostra macho e fêmea / Sensitivity of PCR to amplify sex-specific bovine DNA in diluted samples

A mixture of bovine DNA from a male and a female Jersey (Bos taurus taurus) bred in different proportions was used to determine the sensitivity of PCR to amplify and discriminate the bovine DNA samples. Samples were obtained from the peripheral blood of a bull and a heifer and DNA was isolated using a commercial kit for extraction and purification of nucleic acids. Two primers sets were designed to flank genomic regions: one autosomal and one Y-specific. DNA samples were diluted in water to a final concentration of 4x10-14 ng. The results showed positive amplification of the samples diluted to a concentration of 4x10-10ng and 4x10-4ng for the autosomal and Y-specific regions, respectively. PCR was able to discriminate the male DNA in a mixture of 99:1 (DNA ♀: DNA ♂) heifer to bull ratio. Therefore, the PCR was successful in amplifying the bovine genome in samples containing low concentrations of DNA. Thus, PCR can be used as a sensitive and efficient tool to determine the sex of the fetus in pregnant cows, helping to promote correct and efficient animal management, sex selection, and breeding in commercial herds.

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.