Gastric lesions in free-living sea turtles: An underestimated disease that reflects the health of the ecosystem.

Free-living marine turtles are constantly exposed to aggression factors and the gastrointestinal tract is one of the main gateways of entry. The objective of this study was to identify, and describe the anatomopathological alterations in the stomach of free-living marine turtles found dead on the beaches of the Microrregião dos Lagos, Rio de Janeiro, Brazil. Twenty-two sea turtles were necropsied, and stomach fragments were collected, fixed, and processed routinely. The presence of gastritis, parasitism, and adaptative morphological alteration of the cells were evaluated in a microscopic analysis. Descriptive statistics and Fisher's exact test were performed. Of the samples, 59.1% had stomach hyperemia. Microscopically, gastritis was found in 86.4% of cases, parasitism in 72.7%, and adaptive morphological alteration in 59.1%. There was an association between the presence of cellular adaptive morphological alteration and chronic inflammation. This the first report to describe the adaptive morphological changes observed in the stomach cells. The chronicity of the lesions was due to continuous aggressions to the tissue, with parasitism, garbage ingestion, and environmental pollutants as possible causes. The results obtained in this study demonstrate that the chronicity of the stomach lesions is due to continuous aggressions to this tissue, and the irritating factors have environmental origin, such as parasites, garbage, and toxic pollutants, including heavy metals, which are ingested by free-living sea turtles. This article demonstrates that stomach injuries in free-living marine turtles are frequent, severe, and possibly underdiagnosed; these lesions reflect the diseased ecosystem in which those animals live.

Morphometric measurements and zootechnical indices of the Pantanal in race horses of different ages and gender.

The aim of this study was to perform linear measurements and assess morphometric indices of equines of the Pantanal race of different ages in the municipality of Poconé-Mato Grosso. Fifty-seven clinically healthy male and female horses between 1 and 19 years of age were selected and divided into groups by sex: 41 animals males and 17 animals femeles, and age groups: group 1 (nine animals up to 12 months of age), group 2 (eight animals from 12 to 24 months), group 3 (15 animals from 24 to 48 months), and group 4 (27 animals older than 48 months). With the aid of a hypometer, the following linear measures were carried out: height at the withers and croup, and body length. The thoracic circumference and cinnamon were measured with a tape. From these measures, the following zootechnical indices were calculated: estimated weight, relationship between height at the whithers and height at the croup (RHC), dactyl thoracic (DTI), body index (BI), forming index (FI), load index 1 (LI1), load index 2 (LI2), body relative index (BRI), compactness index 1 (COI1), compactness index 2 (COI2), load index in cinnamon (LIC). In general, horses of the Pantanal breed are hipometric and longilinear; only the adult group of animals were mediolinear, with a good relationship between the withers and croup. They can be used with a saddle or take traction, with the ability to move their limbs slowing down with age. An influence of sex and age on the analyzed variables was observed.

ACTN3 gene variants as potential phenotype and performance biomarkers in Brazilian sport horses training for eventing in a tropical climate.

The aim of this study was to look for mutations in the equine ACTN3 gene and to identify sequence variants that might be associated with the phenotype and performance of Brazilian sport horses training for events in a tropical climate. Among 17 such horses direct DNA sequencing and mutation analysis of the exon 15 and the intron-exon boundaries of ACTN3 revealed 2 new sequence variants in the ACTN3 intron 14-15, designated c.1681-86G > A and c.1681-129delA. Wild-type/deletion heterozygotes (A/del) had a lower mean subcutaneous fat layer in the region of the gluteus medius, as measured by ultrasonography, than the del/del homozygotes; the correlation was significant (P = 0.017). This single base-pair deletion in ACTN3 intron 14-15 may have resulted in metabolic changes that led to increased deposition of body fat in the homozygous state. However, neither sequence variant was correlated with the time to fatigue in a test on a high-speed treadmill with an incremental-speed protocol.

Le but de la présente étude était de vérifier pour la présence de mutations dans le gène ACTN3 équin et d'identifier des variants de séquence qui pourraient être associés avec le phénotype et la performance de chevaux de sport brésiliens qui s'entraînent pour des concours dans un climat tropical. Parmi 17 chevaux qui correspondent à ces critères, le séquençage direct de l'ADN et l'analyse de mutation de l'exon 15 et des frontières de l'intron-exon d'ACTN3 a révélé deux nouveaux variants de séquence dans l'intron 14­15 d'ACTN3, désigné c.1681­86G > A et c.1681­129delA. Chez les hétérozygotes type-sauvage/délétion (A/del) la moyenne de l'épaisseur de la couche de gras sous-cutané dans la région du gluteus medius était plus petite, telle que mesurée par échographie, que celle des homozygotes del/del; la corrélation était significative (P = 0,017). Cette délétion unique de paire de bases dans l'intron 14­15 d'ACTN3 pourrait avoir résulté dans des changements métaboliques qui auraient mené à une augmentation du dépôt de gras chez les homozygotes. Toutefois, aucun des variants de séquence n'était corrélé avec le temps de fatigue dans un test sur un tapis-roulant à haute vitesse avec un protocole d'augmentation de vitesse.(Traduit par Docteur Serge Messier).

Effect of selection for eventing on the MSTN gene in Brazilian sport horses.

Polymorphisms in MSTN have previously been associated with equine performance. Therefore, the aim of this study was to identify variants in MSTN intron 1 in 16 Brazilian Sport Horses selected for competition in eventing and their possible effects of selection on performance. Among the nine variants identified, eight had already been reported in previous studies or genomic databases, although they showed differences in frequencies when compared with other horse breeds. Moreover, a new mutation was identified in two horses, both in heterozygous form. Considering the absence of molecular studies in this valuable Brazilian breed, these findings represent an important contribution to the characterization of its genetic profile and may possibly aid in further genotype-phenotype association studies.