Prevalence and parasite burden of oocysts in captive and free-living saffron finches, Sicalis flaveola.

The saffron finch, Sicalis flaveola, a passerine bird, can be found in nearly all Brazilian territory and is also raised in captivity. The objective of this work was to determine the prevalence and load of oocysts in captive saffron finches in the municipality of Campos dos Goytacazes, state of Rio de Janeiro and in free-living saffron finches in the municipality of Eugenopolis, state of Minas Gerais. In this analysis, 30 captive and 30 wild birds were assessed. Feces eliminated in a 24-hour period were collected and weighed to determine the number of oocysts per gram of feces (OoPG). Statistical analyses were performed using Microsoft Excel and GraphPad Prism Software. All birds in the present study were positive for one or more species of coccidia. Captive birds had a mean total oocyst count higher than that of wild birds. No significant differences in OoPG counts were observed when comparing males and females or captive and wild birds. We can conclude that due to the fact that birds both eat and defecate in their cages, it is essential to keep them as clean as possible, since captive birds have a higher prevalence of coccidia.

Molecular and phylogenetic characterization of Cryptosporidium species in the saffron finch Sicalis flaveola.

BACKGROUND: Cryptosporidium is the most common protozoan that can infect a wide variety of animals, including mammals and birds. Fecal samples of six saffron finches, Sicalis flaveola, from a commercial establishment were screened for the presence of Cryptosporidium by the modified Ziehl-Neelsen technique and nested PCR of the 18S rRNA gene followed by sequencing of the amplified fragments. RESULTS: The species Cryptosporidium galli was identified in all six saffron fiches, in addition to Cryptosporidium andersoni in one of the birds, indicating a mixed infection. Only two birds had feathers that were ruffled and dirty with feces. Concomitant infection with Isospora spp. was observed in all birds. CONCLUSIONS: Saffron finches are a possible host of C. andersoni and this is the first report of this species in a captive bird and the third report of parasitism by C. galli in Sicalis flaveola.

A New Species of Eimeria Schneider, 1875 from the Saffron Finch, Sicalis flaveola (Aves: Passeriformes) in Brazil.

PURPOSE: The present study describes a new species of Eimeria found in free-living S. flaveola that inhabit the city of Eugenópolis in the state of Minas Gerais, Brazil. METHODS: Fecal samples from all captured birds were filtered through double gauze, mixed with 2.5% potassium dichromate (K2Cr2O7), placed in a Petri dish and incubated at 23-28 °C until 70% of the oocysts were sporulated. RESULTS: Eimeria flaveola n. sp. from the saffron finch, Sicalis flaveola (Aves: Passeriformes), was described in Brazil. Sporulated oocysts are subspherical; 22.67 ± 1.57 (18.47-26.48) × 21.19 ± 1.42 (16.69-24.91) µm; with a shape-index of 1.07 ± 0.05 (1.00-1.25) µm and a smooth, bilayered wall, ~ 1.09 µm. A micropyle and an oocyst residuum are absent, but one polar granule is present. Sporocysts are ovoidal, 14.24 ± 1.71 (9.02-19.33) × 9.98 ± 1.02 (6.80-12.87) µm; with a shape-index of 1.43 ± 0.16 (0.74-2.11). The Stieda body is button-shaped; sub-Stieda body and para-Stieda absent. The sporocyst residuum is formed by a compact rounded mass of granules. The sporozoite is claviform, 11.53 µm in length and 2.84 µm in width, with a refractile body and a nucleus. CONCLUSIONS: Based on its morphological and morphometric characteristics, we consider E. flaveola a newly identified species.

Lesions caused by Sarcocystis spp., parasites of opossums (Didelphis aurita), in acute and chronic infections in birds (Melopsittacus undulatus).

Protozoa of the genus Sarcocystis are obligatory heterogenous parasites with both definitive and intermediate hosts. Opossums (Didelphis aurita) can shed multiple species of Sarcocystis with birds as the intermediate host. The pathologies of Sarcocystis species in birds have not been thoroughly elucidated. Therefore, the aim of the present study to determine the main lesions that can occur in acute and chronic infections in intermediate hosts, when they ingest infective sporocysts that are shed in the opossum's feces, using budgerigars as a model. To this end, 12 budgerigars, Melopsittacus undulatus, were divided into two groups that received an inoculum with 60 and 120 sporocysts. Birds that died or were euthanized were necropsied, and the lung, tongue, liver, brain, heart, and skeletal striated muscles were collected and fixed in 10% formalin for histopathological analysis. The infectivity varied according to the sample and infective dose. Acute histopathological lesions were characterized by evidence of slightly degenerated hepatocyte cords that permeated the region of the blood vessel and hepatic sinusoids. Pulmonary tissue lesions were also observed in the parabronchial region with the presence of inflammatory infiltrates associated with areas of edema and atelectasis. In chronic infections, few mature cysts were observed in the chest, and many mature cysts in the thigh and tongue muscles. Thus, it was possible to conclude that lesions are highly characteristic in acute infection and, in chronic infections, cysts were present but without major lesions. In this case, the preferred organs of parasitism were the thigh and the tongue.

Natural infection by Procyrnea uncinipenis (Nematoda, Habronematidae), a parasite from rheas, an autoctone bird from South America, in emus Dromaius novaehollandiae, a ratite from New Zealand.

The present study reports a natural infection of emus, Dromaius novaehollandiae, by the nematode Procyrnea uncinipenis. Five adult emus from a scientific breeding farm at North Fluminense State University located in the city of Campos dos Goytacazes, Rio de Janeiro state, Brazil were necropsied, and their gastrointestinal tract were collected and examined for the presence of parasites from October 2013 to November 2015. Two of the five (40%) emus necropsied were infected with nematodes, and a portion of the nematodes were processed for light microscopy. In addition, two other nematodes (a male and a female) were prepared for scanning electron microscopy. In a female bird, one nematode was collected in the proventriculus and two nematodes in the gizzard and in the male bird four nematodes were collected in the gizzard. The morphological and morphometric analyzes allowed to identify the nematodes as P. uncinipenis, this being the first report of an infection by P. uncinipenis in emus. Therefore, we infer that these emus were naturally infected by nematodes that were considered specific to rheas.

Correction to: Description of a new species Physaloptera goytaca n. sp. (Nematoda, Physalopteridae) from Cerradomys goytaca Tavares, Pessôa & Gonçalves, 2011 (Rodentia, Cricetidae) from Brazil.

The name of Luanna Castro Oliveira was incorrectly spelled as Luana Castro Oliveira in the original version of this article.

Description of a new species Physaloptera goytaca n. sp. (Nematoda, Physalopteridae) from Cerradomys goytaca Tavares, Pessôa & Gonçalves, 2011 (Rodentia, Cricetidae) from Brazil.

Nematodes of the genus Physaloptera are common in rodents, including in species of the Family Cricetidae. There is no report of nematodes parasitizing Cerradomys goytaca, so this is the first one. For this study, 16 rodents were captured in the city of Quissamã, in the northern of Rio de Janeiro State. The rodents were necropsied, and the digestive tracts were analyzed under a stereomicroscope for the presence of parasites. The nematodes were fixed in hot AFA, clarified in Amann's lactophenol, mounted on slides with coverslip, and observed under an optical microscope. Part of the nematodes was fixed in Karnovisk solution for scanning electron microscopy. Nematodes presented evident sexual dimorphism. Oral openings had two semicircular pseudolabia, with an external lateral tooth and an internal lateral tripartite tooth on each pseudolabium. Males had a ventral spiral curved posterior ends with the presence of a caudal alae with 21 papillae with four pairs of pedunculated papillae arranged laterally, three pre-cloacal sessile papillae arranged rectilinearly and five pairs of post-cloacal sessile papillae. There was also a pair of phasmids located between the fourth and fifth pairs of post-cloacal papillae as well as two spicules that were sub-equal in size but of distinct shapes. The females have five uterine branches. The morphological and morphometrical analyses of the nematodes collected from C. goytaca were compared with other species, and the results indicated that this is a new species of the genus Physaloptera, Physaloptera goytaca n. sp.

Identification of opossums Didelphis aurita (Wied-Neuweid, 1826) as a definitive host of Sarcocystis falcatula-like sporocysts.

This study was conducted to identify the Sarcocystis species that infect the opossum Didelphis aurita in order to determine which sporocysts they are excreating in to the environment and help determine the role of D. aurita in the epidemiology of Sarcocystis. Sporocysts were obtained from intestinal tracts of 8 of 13 D. aurita trapped in Rio de Janeiro state, Brazil, and were orally inoculated into Melopsittacus undulatus and Balb/c nude Mus musculus. Portions of organs and muscles were processed for histology, immunohistochemistry, transmission electron microscopy (TEM), and PCR using primers JNB 33/54, and ITS. Amplification products were subjected to RFLP using DraI and HinfI. Some birds were euthanized 6, 7, 13, 16, and 24 days after inoculation (DAI). All other birds and all mice were euthanized 60 DAI. Schizonts were observed in the lungs using histology and immunostaining in birds examined prior to 60 DAI. Sarcocysts with a ~ 1.5-µm-thick wall were found in the breast, thigh, and tongue of some birds. Sarcocystis asexual stages were isolated in cell cultures inoculated with sporozoites. Parasite DNA isolated from bird tissues and cell cultures demonstrated that S. falcatula-like parasites were present in all samples derived from positive opossums. Asexual stages molecularly characterized as S. lindsayi-like were isolated in cell culture from one opossum with an apparent multiple infection. This study demonstrated that D. aurita is a definitive host for S. falcatula-like parasites and indicates that S. lindsayi-like parasites can be found in coinfections of this opossum species.

Isospora dromaii n. sp. (Apicomplexa, Eimeriidae) isolated from emus, Dromaius novaehollandiae (Casuariiformes, Casuariidae).

A new species of Coccidia (Protozoa: Apicomplexa: Eimeriidae) isolated from emus, Dromaius novaehollandiae, which was observed in Brazil is described and named. Oocysts of Isospora dromaii n. sp. are subspheroidal to ovoid in shape, measure 21.6 × 19.8 µm, and have a double and smooth wall thickness of approximately 1.4 µm. In this species, micropyle, oocyst residuum, and polar granules are absent. The sporocysts are slightly ovoid in shape and measure 13.7 × 10.0 µm. Nipple-like Stieda body and prominent sub-Stieda body are present. The sporocyst residuum is composed of small dispersed granules of varying sizes. The sporozoites are characterized by an oblong refractile body and one centrally located nucleus. This is the first description of isosporid coccidia infecting birds of the family Dromaiidae.