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Pathoanatomical studies of diseases that affect wild animals are extremely important as appropriate measures can then be taken for the prevention and control of such diseases. We report here the case of death of a greater rhea ( ) by intestinal intussusception secondary to the ingestion of a large amount of sand. The animal was bred at the Center for Multiplication of Wild Animals of the Federal Rural University of the Semi-Arid. The animal died after presenting clinical signs of apathy, weakness, prostration, and inability to move, drink water, or eat. After death, the carcass was immediately sent for necropsy. During necropsy, intussusception was found involving the jejunum, ileum, and colon. The duodenum contained large amounts of coarse sand. The invaginated intestinal segments were reddish in color, with necrotic spots, and covered by a fibrinous exudate. Histopathological examination of the invaginated segments showed necrosis of the enterocytes, detachment of the intestinal epithelium, and the presence of inflammatory cells. The ingestion of a large amount of sand may have resulted in altered intestinal transit, contributing to the occurrence of intussusception, which resulted in ischemic alterations, intestinal necrosis, and consequent death of the animal.

Diseases of the nasal cavity have a diverse etiology and cause severe disorders in animals. Conidiobolomycosis is a type of zygomycosis caused by the fungus Conidiobolus spp., occurring more frequently in sheep. The objective of this study is to describe the clinical and epidemiological characteristics, as well as microbiological and histopathological findings, of an outbreak of conidiobolomycosis in sheep. A total of 12 animals out of a herd of 70 were affected, representing a morbidity of 17.1%; mortality and lethality were 11.4% (8/70) and 66.6% (8/12), respectively, of which 4 sheep died spontaneously and 4 were euthanized for diagnostic purposes due to the severity of the clinical condition. Necropsy was performed on 4 (33.3%) of the 12 affected animals, and after opening the skull in the sagittal section, a friable mass with coloration ranging from whitish-yellow to gray-green, as well as areas of necrosis, were evident in regions such as the nasal meatus, conchae, nasopharynx, hard palate, cribriform plate, meninges, and frontal lobe of the brain. Conidiobolus lamprauges was isolated from samples collected from 6 animals from nasal discharge, fungal granuloma, and intranasal swab. Reproductive structures consistent as kind of zygospores with C. lamprauges and C. incongruus were also identified. Regarding the clinical form, animals 1, 2, 3, and 4 presented manifestations of the nasopharyngeal form, with the first three progressing to the rhinocerebral form; in animal 5, the clinical form found was rhinofacial. It is concluded that clinical signs may vary with the presentation of the disease as well as the involved agent. Early diagnostic alternatives such as fungal isolation from material collected from intranasal swabs can be useful and employed in affected herds, enabling earlier intervention.

Background Research on cancer in wild animals provides important insights into the mechanisms of carcinogenesis. Histiocytic sarcomas comprise a rare malignant macrophage-dendritic cell lineage neoplasm in wildlife. This study reports a case of histiocytic sarcoma in the small intestine of a collared peccary ( Pecari tajacu ), describing its clinical, anatomopathological, and immunohistochemical aspects. Case presentation A six-year-old male collared peccary maintained in captivity at a facility in Northeastern Brazil presented progressive weight loss, diarrhea, anorexia, dyspnea, lethargy, abdominal distension, bristled fur, and pale mucous membranes. A complete blood count indicated a mild degree of anemia and moderate leukocytosis. Treatment included anti-inflammatories and antibiotics; however, on the 18th day after initial presentation, the animal was found dead in its enclosure. An anatomopathological examination revealed that the animal exhibited poor body condition, scant body fat with a gelatinous appearance, hydrothorax, pulmonary edema, and ascites. Thickening of the duodenal wall was observed, along with the presence of a yellowish-white tumor. Histopathological examination of the affected intestinal segment revealed a neoplastic proliferation of round cells with large, hyperchromatic nuclei, prominent nucleoli, and a high mitotic index (20 mitoses per high-power field). Numerous multinucleated and binucleated giant cells were present. The neoplastic cells extensively infiltrated all layers of the intestinal wall, from the mucosa to the serosa. Immunohistochemical analysis showed strong positivity for macrophage/mononuclear phagocytic lineage markers (CD18, IBA-1, and lysozyme), while negative for T-cell (CD3), B-cell (CD79), and plasma cell (MUM1) markers. The proliferation index assessed by Ki-67 was approximately 60%. Conclusions The histopathological and immunohistochemical findings confirmed the diagnosis of intestinal histiocytic sarcoma in a collared peccary, representing the first documented case of this neoplasm in this species.

The objective was to evaluate the in vitro antioxidant, genotoxic, antigenotoxic, and antineoplastic activities of apitoxin produced by the bee Apis mellifera. The antioxidant activity of the apitoxin solution was evaluated using the DPPH (2,2-diphenyl-1-picrilhydrazyl) method. Genotoxic potential of apitoxin was analyzed by comparing the mean DNA damage indices (idDNA) of L929 strain fibroblasts exposed to hydrogen peroxide (H2O2 - genotoxic substance), distilled water, or apitoxin. The antigenotoxic effect of apitoxin was analyzed by assessing the percentage decrease in H2O2-induced genotoxicity in L929 fibroblasts co-treated with three concentrations of the aqueous apitoxin solution and subjected to comet assay. In vitro antineoplastic activity in human tumor cell lines of prostate adenocarcinoma (PC3), hepatocellular carcinoma (HEPGE2), melanoma (MAD-MB435), and astrocytoma (SNB19), were verified by MTT [3- (4) bromide colorimetric method, 5-dimethylthiazol-2-yl) -2,5-diphenyltetrazolium]. Apitoxin had no genotoxic effect on L929 cells at concentrations of 30, 10, and 5 µg/mL after 24 hours of exposure. This effect was only evident at 50 µg/mL. Apitoxin promoted a significant reduction in DNA damage index (idDNA) at all concentrations tested. At 30 µg/mL, apitoxin attenuated the genotoxic effects induced by H2O2. Apitoxin also demonstrated in vitro antineoplastic potential, since the cytotoxic effect was observed at concentrations of 50 µg/mL and 25 µg/mL, with significant reduction in viability percentage of PC3 tumor cell lines, HEPGE2, MAD-MB435, and SNB19. The high antioxidant activity associated with the absence of genotoxic effect and the genoprotective and antineoplastic effect demonstrated by apitoxin here provide indications of apitoxin’s therapeutic potential. RESUMO: O objetivo deste estudo foi avaliar as atividades antioxidantes, genotóxicas, antigenotóxicas e antineoplásicas in vitro da apitoxina produzida pela abelha Apis mellifera. A atividade antioxidante da solução da apitoxina foi avaliada pelo método DPPH (2,2-difenil-1-picrilhidrazil). O potencial genotóxico da apitoxina foi analisado através dos índices médios de dano ao DNA (idDNA) dos fibroblastos da linhagem L929 expostos à peróxido de hidrogênio (H2O2 - substância genotóxica), água destilada ou apitoxina. O efeito antigenotóxico da apitoxina foi analisado através da avaliação da diminuição percentual na genotoxicidade induzida por H2O2 nos fibroblastos L929 co-tratados com três concentrações da solução aquosa de apitoxina e submetidos ao ensaio cometa. A atividade antineoplásica in vitro em linhagens celulares tumorais humanas de adenocarcinoma da próstata (PC3), carcinoma hepatocelular (HEPGE2), melanoma (MAD-MB435) e astrocitoma (SNB19), foram verificadas pelo método colorimétrico do brometo de MTT [3- (4), 5-dimetiltiazol -2-il) -2,5-difeniltetrazólio]. A apitoxina não teve efeito genotóxico nas células L929 nas concentrações de 30, 10 e 5 µg / mL após 24 horas de exposição. Este efeito foi apenas evidente a 50 µg / mL. A apitoxina promoveu uma redução significativa no índice de danos ao DNA (idDNA) em todas as concentrações testadas. A 30 µg / mL, a apitoxina atenuou os efeitos genotóxicos induzidos por H2O2. A apitoxina também demonstrou potencial antineoplásico in vitro, uma vez que o efeito citotóxico foi observado em concentrações de 50 µg / mL e 25 µg / mL, com redução significativa na porcentagem de viabilidade das linhagens celulares de PC3, HEPGE2, MAD-MB435 e SNB19. A alta atividade antioxidante associada à ausência de efeito genotóxico e o efeito genoprotetor e antineoplásico demonstrado pela apitoxina aqui fornecem indicações do potencial terapêutico da apitoxina.

The present work aimed to investigate the presence of T. vivax DNA in the semen of experimentally infected goats. Twelve male goats native to the Brazilian Northeast, adults, were randomly assigned to two experimental groups: the infected group consisting of six goats infected intravenously with 0.5 mL of blood containing approximately 1.25 × 105 trypomastigotes of T. vivax, and a control group composed of six uninfected goats. After the infection, clinical examinations aiming to evaluate rectal temperature, parasitemia and hematocrit were performed. Semen samples were collected from goats by electroejaculation on the 7th, 14th and 21st days post-infection (dpi). The recombinant DNA-encoding gene encoding the L-like-specific gene for T. vivax. The infection was characterized by increased rectal temperature, high parasitemia and significant reduction of hematocrit values. Results for T. vivax DNA detection using TviCatL-PCR were positive in all semen samples from the infected group collected on 7th, 14th and 21st dpi. The presence of T. vivax DNA in 7th dpi suggests the early invasion of the parasite in the reproductive organs. Also, the finding of T. vivax DNA in all periods analyzed may suggest the continued elimination of the parasite in the semen, which may increase the chances of sexual transmission. Thus, T. vivax DNA is recorded for the first time in the semen of infected goats. Thus, these data are of great importance, since the detection of the T. vivax genetic material in the semen may point to the possibility that the parasite may be transmitted through the sexual pathway.

Gastrointestinal perforation in sea turtles may be associated with the ingestion of solid waste; however, other factors, including the ingestion of marine organisms, may cause intestinal perforation. Herein, we report, presumably, the first case of a death of a loggerhead sea turtle (Caretta caretta) from ingesting a live goldspotted eel (Myrichthys ocellatus) and describe the necropsy findings. The adult female loggerhead sea turtle was registered alive by a team of the Cetáceos da Costa Branca Project of Rio Grande do Norte State University (PCCB-UERN). The animal died in captivity after 8 days of an attempted rehabilitation process, and the carcass was immediately sent for necropsy. After incision, an encapsulated structure in the cranial region of the left lung was identified as a specimen of the ingested eel. The histopathological examination of the lung showed fibrin and numerous leukocytes, mainly macrophages, in the alveolus and bronchioles. The necropsy revealed that the ingestion of a live goldspotted eel (M. ocellatus) caused a gastric perforation in the turtle; this resulted in the displacement of the eel to the celomatic cavity with its cranial portion in the left lung, leading to sepsis and the consequent death of the turtle.

Considering that neem (Azadirachta indica A. Juss.) causes deleterious effects on fertility, the objective was to evaluate the effect of feeding quail (Coturnix coturnix japonica Linnaeus, 1758) of 90 days old with neem seeds on seminal quality, biometric parameters, and testicular morphometrics, as an experimental model. After the 30 day adaptation period to the experimental conditions, birds were randomly distributed in five treatments of neem seeds incorporated into feed, with 10 replicates: T1 (0%), T2 (5%), T3 (10%), T4 (20%) and T5 (40%). After 60 days of receiving experimental rations, their semen was collected to evaluate the sperm quality, the birds were euthanized, and testes were submitted to biometric, histological, and histomorphometric evaluation. The data were evaluated by analysis of variance and later by Tukey test with a significance level of 5%. The mean values of testicle weight, length, and width significantly decreased in T4 and T5, due degeneration of germinal epithelial cells. In these treatments, it occurred a significant increase (P>0.05) in the average values of the tunica albuginea thickness and a significant reduction in the values of the seminiferous tubule diameter and the height of the germinal epithelium. In addition, the mean values of seminal volume, sperm concentration, sperm motility, vigor, and sperm viability were significantly reduced. Thus, the use of neem in bird feeding, as well as the use for therapeutic purposes, is questionable, considering its negative impact on reproduction. RESUMO: Considerando que o neem (Azadirachta indica A. Juss.) causa efeitos deletérios na fertilidade, objetivou-se avaliar o efeito da alimentação com sementes de neem sobre a qualidade seminal, parâmetros biométricos e morfometria testicular com codornas (Coturnix coturnix japonica Linnaeus, 1758) com 90 dias de idade, como modelo experimental. Após o período de adaptação de 30 dias às condições experimentais, as aves foram distribuídas aleatoriamente em cinco tratamentos de sementes de neem incorporadas na ração, com 10 repetições: T1 (0%), T2 (5%), T3 (10%), T4 (20%) e T5 (40%). Após 60 dias de receber rações experimentais, seu sêmen foi coletado para avaliar a qualidade espermática, as aves foram sacrificadas e os testículos foram submetidos à avaliação biométrica, histológica e histomorfométrica. Os dados foram avaliados por análise de variância e mais tarde pelo teste de Tukey com um nível de significância de 5%. Os valores médios do peso, comprimento e largura do testículo diminuíram significativamente em T4 e T5, devido à degeneração de células epiteliais germinativas. Nestes tratamentos, ocorreu um aumento significativo (P>0,05) nos valores médios da espessura da túnica albugínea e uma redução significativa nos valores do diâmetro do túbulo seminífero e a altura do epitélio germinal. Além disso, os valores médios do volume seminal, concentração de esperma, motilidade espermática, vigor e viabilidade espermática foram significativamente reduzidos. Assim, o uso de neem na alimentação de aves, bem como o uso para fins terapêuticos, são questionáveis, considerando seu impacto negativo na reprodução.

This study aimed to evaluate the pathological changes that occur after administering different doses of R. jimi (Stevaux, 2002) parotoid glands secretion to Gallus gallus domesticus chicks. Twenty-three animals were used in this study and were divided into 5 groups that received a toad venom dose of 0, 3.0 mg/kg, 6.0 mg/kg, 10.0 mg/kg, and 25.0 mg/kg. After 48 h, the necropsy and pathological examinations were performed. No clinical signs of toxicity were observed in any group. Macroscopically, hepatomegaly, areas of liver necrosis, splenomegaly, necrotic and hemorrhagic cardiac regions, hydropericardium, dark necrotic lesions of Meckel’s diverticulum, and hemorrhages in the lungs and kidneys were detected. Histopathological changes included diffuse vacuolar degeneration of hepatocytes, severe sinusoidal congestion, focal areas of hemorrhage in the parenchyma, swollen cardiac fibers, necrotic myocardial fibers, moderate to acute diffuse alveolar hemorrhage, vacuolar degeneration of the renal tubular epithelium, necrosis of renal tubules, and extensive hemorrhagic areas below the brain and cerebellar meninges. In conclusion, pathological changes of the R. jimi toxins in chicks were noted in the heart, spleen, liver, Meckel’s diverticulum, lungs, and kidneys. Most of the changes were similar to those observed in humans and animals exposed to toxins from other toad species.

The jandaíra bee ( ) is a species native to northeastern Brazil that produces geopropolis, a mixture of clay and propolis, used in folk medicine. Geopropolis has traditionally been used in folk medicine because of its potential therapeutic properties, including antimicrobial, anti-inflammatory, and wound-healing effects. Recent studies have highlighted the rich composition of bioactive compounds such as flavonoids and phenolic acids, contributing to their pharmacological potential. Despite these findings, the gastroprotective properties of geopropolis and the underlying mechanisms remain underexplored and warrant further investigation. Therefore, we aimed to evaluate the gastroprotective effects of a hydroethanolic extract of geopropolis (HEG) produced by  in Wistar rats, focusing on its antioxidant activity and the role of its bioactive compounds in preventing gastric mucosal damage. The gastroprotective potential was evaluated in Wistar rats pre-treated with HEG (250, 500, and 1 000 mg/kg, orally) for seven days and subjected to acute gastric lesions with ethanol (0.2 ml/animal, orally). One group of rats that received only distilled water served as the negative control, whereas the other group that received only ethanol served as the positive control. The stomachs were evaluated to determine the following parameters: evidence of macroscopic and histological changes, volume of mucus-containing mucin, stomach pH, and index of ulcerative lesions. Kolmogorov-Smirnov and Levene tests were performed, followed by the Tukey test, with values considered significant at  0.05. HEG reduced the severity of the ulcerative lesions at all doses tested. Additionally, there was no significant difference in the pH values of gastric secretions, mucus volume, and mucin content in the stomachs of animals pretreated with HEG compared to the negative control group. These results indicate that HEG has gastroprotective activity, which may be related to the presence of phenolic compounds and its high antioxidant activity.

Este trabalho foi realizado com o intuito de avaliar a produção de geleia real de abelhas africanizadas com a utilização de diferentes concentrações de água de coco no substrato-base das larvas. O experimento foi realizado durante o mês de agosto de 2010 na Fazenda Experimental da UFERSA, Mossoró-RN. Para produção da geleia real foi utilizado o método Doolittle, utilizando-se cúpulas de acrílico de cor laranja. Cada cúpula recebeu 300 µl de solução com geleia real (GR). Foram utilizadas 03 colmeias mini-recria modelo Ribeirão Preto. Os tratamentos testados constaram de solução de GR diluída em água de coco nas seguintes concentrações: 25% de GR; 50% de GR; e 75% de GR. Cada parcela foi composta de 20 cúpulas, sendo contabilizadas apenas as cúpulas com larvas aceitas pelas operárias para o cálculo das variáveis: PA - Percentual de aceitação de larvas; PL - Peso das larvas; PGR - Produção por cúpula de GR; GRT - Produção de Geleia Real total. Os dados foram analisados utilizando-se ANOVA em blocos casualizados com 03 repetições, e os tratamentos também foram comparadas por analise de regressão linear com o auxilio do software R versão 2.13.0. Verificou-se efeito significativo para a aceitação das larvas (P>0,01) e a variável produção de geleia real por tratamento (P>0,05), o peso das larvas, submetidos aos tratamentos, não mostrou efeito significativo. Houve influencia da concentração de substrato ofertado às larvas transferidas na aceitação das mesmas pelas operárias e na produção de geleia real. Conclui-se que o uso do substrato com geleia real influencia no índice de aceitação e sobrevivência das larvas e que o uso da água de coco na diluição da geleia real apresentou resultados satisfatórios.