Correção de medida ultrassonográfica de carcaça em coelhos usando modelo linear misto com covariáveis / Correction ultrasonographic measurement of carcass in rabbits using mixed linear Model with covariates

Objetivou-se avaliar a correção da medida ultrassonográfica da área do músculo Longissimus dorsi, em coelhos da raça Nova Zelândia, pela análise de covariância usando modelos mistos. Foram realizadas análises em delineamento em blocos completos ao acaso, com cinco tratamentos (operadores) e seis blocos (animais), considerando na análise: a inexistência de covariáveis; a covariável comprimento de olho de lombo; a covariável profundidade de olho de lombo; e as duas covariáveis juntas. Como os animais são uma amostra aleatória, o efeito de bloco foi considerado como aleatório. Consideraram-se as covariáveis como medidas com efeito fixo sem erro, independentemente do tratamento e do comportamento linear. As estatísticas de critério de decisão CV%, R ² e R ¯ ² evidenciaram relação direta entre si e podem ser consideradas para avaliar a precisão experimental em ensaios com avaliação de carcaças. Os valores das estatísticas AIC, BIC e AICC apresentam coerência com a interpretação dos critérios de decisão e indicam que o modelo com duas covariáveis proporciona resultados acurados. A inclusão das covariáveis complementa o controle de local com melhoria na precisão do experimento. A utilização das medidas ultrassonográficas de profundidade e comprimento corrige a média da área do músculo Longissimus dorsi avaliado por diferentes operadores.(AU)

The objective of this study was to evaluate the correction ultrasonographic measurement of area the Longissimus dorsi muscle in New Zealand rabbits by covariance analysis using mixed linear models. The analyzes were performed in randomized block design with 5 treatments (operators) and 6 blocks (animals), considering in the analysis: absence of covariates; rib eye length as covariate; rib eye depth as covariate; the two covariates together. As the animals are a random sample, the block effect was considered to be random. The covariates were considered as measures of fixed effect without error, independent of treatment and linear comportment. The decision criterion statistics CV%, R², and R ¯ ²showed a direct relationship between them and can be taken into consideration to evaluate the experimental accuracy in tests with carcass evaluation. The AIC, BIC, and AICC statistics are consistent with the interpretation of the decision criteria and indicate that the two covariates in model provides accurate results. The inclusion of covariates complements the local control to improve the accuracy of the experiment. The use of ultrasound measurements of depth and length corrects the mean area of the Longissimus dorsi muscle evaluated by different operators.(AU)

Identification of midgut microvillar proteins from Tenebrio molitor and Spodoptera frugiperda by cDNA library screenings with antibodies.

The objective of this study was to identify midgut microvillar proteins in insects appearing earlier (Coleoptera) and later (Lepidoptera) in evolution. For this, cytoskeleton-free midgut microvillar membrane from Spodoptera frugiperda (Lepidoptera) and Tenebrio molitor (Coleoptera) were used to raise antibodies. These were used for screening midgut cDNA expression libraries. Positive clones were sequenced, assembled and searched for similarities with gene/protein databases. The predicted midgut microvillar proteins from T. molitor were: cockroach allergens (unknown function), peritrophins (peritrophic membrane proteins), digestive enzymes (aminopeptidase, alpha-mannosidase) and unknown proteins. Predicted S. frugiperda midgut proteins may be grouped into six classes: (a) proteins involved in protection of midgut (thioredoxin peroxidase, aldehyde dehydrogenase, serpin and juvenile hormone epoxide hydrolase); (b) digestive enzymes (astacin, transporter-like amylase, aminopeptidase, and carboxypeptidase); (c) peritrophins; (d) proteins associated with microapocrine secretion (gelsolin, annexin); (e) membrane-tightly bound-cytoskeleton proteins (fimbrin, calmodulin) and (f) unidentified proteins. The novel approach is compared with others and microvillar function is discussed in the light of the predicted proteins.