Jessé Henrique Truppel

The capybara eye: clincial tests, anatomic and biometric features

PURPOSE To carry out a descriptive investigation of the capybara (Hydrochaeris hydrochaeris) eye and to perform selected ophthalmic diagnostic tests with the aim of establishing normal physiological reference values for this species. METHOD A total of 22 healthy, capybaras were used to test most of the parameters in this investigation. Ages varied from 2 to 4 years of age. Selected diagnostic ocular tests were performed including Schirmer tear test, tonometry using an applanation tonometer (Tonopen), central corneal thickness using an ultrasonic pachymeter (Sonomed, Micropach, Model 200P +), axial globe length and culture of the normal conjunctival bacterial flora. RESULTS AND DISCUSSION Capybaras normal ocular features include: dorsal and ventral puncta, vestigial third eyelid, true cilia only at the upper eyelid margins. The bulbar conjunctiva is noticeably densely pigmented with a brown to bronze color. The capybaras pupil is oval in shape and vertical in position No tapetum lucidum is present in this species and the retinal blood vessels are almost absent. Results for selected ocular diagnostic tests investigated were: Intraocular pressure: 18.4 +/- 3.8 mmHg; Schirmer tear test: 14.9 +/- 5.1 mm/min; Central corneal thickness: 0.46 +/- 0.03 mm; Axial globe length: 22.20 +/- 1.71 mm. No statistically significant differences between ages or genders were found for any of the results. Corynebacterium sp., Micrococcus sp., Bacillus sp. and Staphylococcus sp. were isolated from healthy conjunctiva, suggesting they are normal constituents of the conjunctival flora of the capybara eye. The corneal epithelium of the capybara possesses a thin and discrete Bowmans layer. Results and parameters obtained in this investigation exposed unique anatomic features of the capybara eye and will help veterinary ophthalmologists to more accurately diagnose discrete or unusual pathological changes of the capybara eye. Furthermore, corneal thickness and axial length of the capybara are similar to that of human beings, revealing that the worlds largest living rodent might be an excellent biological model for ophthalmic studies.

Biochemical biomarkers of exposure to deltamethrin in freshwater fish, Ancistrus multispinis

ABSTRACT This study aimed to determine the effect of sublethal doses of deltamethrin, using biochemical biomarkers as activities of cholinesterase (ChE), ethoxyresorufin-O-deethylase (EROD) and the Na + K + - ATPase and levels of total cytochrome P450 (CYP450). Fishes received sublethal doses of deltamethrin and were sacrificed after 96 h of exposure. Samples of gills, heart, brain, liver and muscle were collected for enzymatic analyses. Deltamethrin inhibited the activity of the gills and heart Na + K + -ATPase, induced the liver total CYP450, as well as the liver EROD activity. The activity of the ChE was not inhibited by deltamethrin. Deltamethrin altered the hepatic metabolism and the normal ionic flux in Ancistrus multispinis . Key words: deltamethrin, cytochrome P450, fish, Ancistrus multispinis , biomarker * Author for correspondence: helassis@ufpr.br INTRODUCTION Pyrethroids are synthetic derivatives of pyrethrins, which are toxic components contained in the flowers of Chrysanthemum cinerariaefolium . Although synthetic pyrethroids are less persistent and less toxic to mammals and birds (Sayeed et al, 2003), they are highly toxic to a number of non-target organisms such as bees, freshwater fish and other aquatic organisms even at very low concentrations (Oudou et al, 2004). For this reason, these organisms are extremely sensitive to neurotoxic effects of pyrethroids when they reach surface water-courses (Bradbury and Coats 1989, Haya, 1989; Mittal et al, 1994). One of the pyrethroids that has found wide acceptability and is extremely used in agriculture and forestry because of its high activity against a broad spectrum of insect pests (Villarini et al, 1998) is deltamethrin ((S) α-cyano-3-phenoxybenzyl-(1R)-cis-3-(2.2-dibromovinyl)-2,2- dimethyl cyclopropane carboxylate). However, its effects on nervous, respiratory, and hematological systems in fishes have been reported (Ural and Sa glam, 2005, Pimpao et al, 2007). Balint et al (1995) observed 20% decrease in acetylcholinesterase activity of brain, heart, blood, liver and skeletal muscle of carp after the 3 days exposure to deltamethrin. In rats, the main reaction involved in the metabolism of deltamethrin is ester cleavage, by CYP450 and carboxyesterase action. Metabolism in fish is largely oxidative and deficient in esterases metabolization (Demoute, 1989). ATPase has been demonstrated to be one of the targets of pyrethroids. Some authors showed that ATPase including cell membrane-associated

Corneal squamous cell carcinoma in a dog: a case report

PURPOSE To report a case of primary corneal squamous cell carcinoma (SCC) in an English Bulldog. In addition, immunohistochemistry of the corneal tissue mass was performed using a panel of antibodies. A prominent feature of the present case was the clinical history of chronic keratitis due to eyelid abnormalities. RESULTS No papillomavirus antigen was detected in section of normal or neoplastic corneal tissue. The corneal epithelial cells were positive for pancytokeratins AE1/AE3 and MNF116, and E-cadherin. The neoplastic cells in close proximity to the normal epithelial lining were positive for both pancytokeratins and E-cadherin with gradual loss of staining toward the center of the neoplastic mass. Rare neoplastic cells demonstrated positive staining for caspase 3 and a large number was strongly positive for GADD45 and p53. CONCLUSION AND DISCUSSION The observed loss of the various cytokeratins, the strong p53 expression, and low numbers of caspase 3 positive cells were suggestive that a p53 mutation may have caused this primary corneal SCC. Over-expression of the tumor-suppressor gene p53 is likely to be a consequence of ultraviolet radiation exposure. Two factors, however, may have played a role in the formation of this primary corneal SCC: chronic irritation of the corneal surface (microtrauma) and exposure to UV radiation.

Conjunctival changes induced by prostaglandin analogues and timolol maleate: a histomorphometric study

PURPOSE To compare histological changes induced by antiglaucoma medications in the rabbit conjunctiva. METHODS Fifty New Zealand rabbits were divided in 5 groups of 10 animals. The left eyes were treated daily with one drop of bimatoprost 0.03%, travoprost 0.004%, latanoprost 0.005%, timolol maleate 0.5% or artificial tears containing benzalkonium chloride (BAK) for 30 days. The right eyes served as controls. Superior limbic conjunctival biopsies were performed at the 8th and 30th day in 5 rabbits of each group. The conjunctiva was fixed with 10% formaldehyde, followed by HE and PAS staining. Morphohistometric quantitative analyses were performed to evaluate the following parameters: inflammatory infiltrate, epithelial thickness, number of goblet cells, diameter and number of blood vessels. RESULTS At the 8th and 30th posttreatment days, all groups, except one that received artificial tears, exhibited a diffuse inflammatory infiltrate, composed by lymphocytes and neutrophils, which was denser in the timolol group than in the prostaglandin (PG) analogues groups. At the 30th day, the timolol group also showed an increased subepithelial collagen density and a significant increase in epithelial thickness (p=0.0035). The goblet cell density was significantly increased at the 8th day in the group treated with travoprost (p=0.0006), and at the 30th day in those treated with bimatoprost (p=0.0021) and latanoprost (p=0.009). CONCLUSIONS Although a moderate, diffuse inflammatory infiltrate was observed in PG-treated eyes, no changes in conjunctival epithelial thickness or subconjunctival collagen density were observed with these medications, suggesting that these drugs induce fewer changes than timolol maleate in the rabbit conjunctiva.

Detection of Neospora caninum DNA in capybaras and phylogenetic analysis.

The role of rodents in the sylvatic cycle of Neospora sp. and in the neosporosis epidemiology is still uncertain. The aim of the present work was to detect Neospora caninum and to determine its prevalence in capybaras (Hydrochaeris hydrochaeris), to help elucidate the role of this rodent in the life cycle of the parasite. N.caninum DNA was detected by PCR using 4 different sets of primers specific to the Nc5 and ITS1 sequences. The parasite was found in the lymph nodes, heart, liver, and blood of 23% of the twenty-six capybaras studied. Sequencing the amplified DNA revealed 98% of similarity with N. caninum sequences deposited in the Genbank. Our findings provide the first molecular evidence of N. caninum infection in capybaras, supporting the hypothesis that these rodents can act as reservoirs of N. caninum and play a role in the life cycle of this parasite.

Toxoplasma gondii in Capybara ( Hydrochaeris hydrochaeris ) antibodies and DNA detected by IFAT and PCR

Toxoplasmosis is considered nowadays as one of the most important foodborne diseases in the world. One of the emerging risks in acquiring infection with Toxoplasma gondii is the increasing popularity of wild animals and game meat. Capybara (Hydrochaeris hydrochaeris) is the world’s largest extant rodent and is used for human consumption in many areas of South America, and in case it carries T. gondii cysts, it may act as a source of infection. In the present study, we detected infection with T. gondii in capybaras from the south of Brazil. Antibodies to T. gondii were assayed in the serum of capybaras using the indirect fluorescent antibody test (IFAT ≥ 1:16). Blood, liver, heart, lymph nodes, and spleen tissues were collected and tested by polymerase chain reaction (PCR) for B1 gene and ITS1 region. The results showed that 61.5% (16/26) capybaras were seropositive to T. gondii. Titers of specific antibodies to T. gondii ranged from 1:16 to 1:512. Among the feral rodents studied, 7.7% (2/26) were PCR positive for B1 gene assay and 11.5% (3/26) were positive for ITS1 PCR assay; for both test, the prevalence was 15.4%. Liver, heart, and blood tissues were those which tested positive for the apicomplexan. Our findings show a high percentage of infection with T. gondii in asymptomatic capybaras. Based on those data, we hypothesize that the consumption of raw or undercooked capybara meat could be a source of infection for humans.

Can Equids Be a Reservoir of Leishmania braziliensis in Endemic Areas

In this study, we detected Leishmania (Viannia) braziliensis infection in equids living in endemic regions of cutaneous leishmaniasis. To determine the role of these animals in the Leishmania cycle, we used two approaches: serological and molecular methods. Antibodies to the parasite were assayed using the Enzyme Linked Immunosorbent Assay (ELISA). Blood samples were collected and tested by polymerase chain reaction (PCR), and the positive products were sequenced. The results showed that 11.0% (25/227) of the equids were seropositive for Leishmania sp, and 16.3% (37/227) were PCR positive. Antibodies were detected in 20 horses, 3 donkeys, and 2 mules, and the parasite DNA was detected in 30 horses, 5 donkeys, and 2 mules. Sequencing the amplified DNA revealed 100% similarity with sequences for Viannia complex, corroborating the results of PCR for L. braziliensis. Our results show that equids are infected with L. braziliensis, which could be food sources for phlebotomines in the peridomiciliary environment and consequently play a role in the cutaneous leishmaniasis cycle.