First report of the genus Retortamonas (Sarcomastigophora: Retortamonadidae) in birds. (9/71)

In studies carried out on the parasites infecting ostriches (Struthio camelus) in Spain, trophozoites of Retortamonas sp. have been found in the intestinal contents of 28 out of 146 slaughtered ostriches. The species infecting ostriches could not be determined from the morphological data available. However, these findings are important as they constitute the first report of the genus Retortamonas in birds.  (+info)

Relationship between seasonal changes in spermatogenesis in the juvenile ostrich (Stuthio camelus) and the presence of the LH receptor and 3beta-hydroxysteroid dehydrogenase. (10/71)

The immunohistochemical localization of the LH receptor and 3beta-hydroxysteroid dehydrogenase (3beta-HSD) was studied in the testis of the juvenile ostrich (Stuthio camelus) throughout a 1 year period. Spermatogenic activity of juvenile birds changed throughout the year, as has been reported previously for sexually mature birds. During the active stage of the testicular cycle, from September to January, spermatogenesis progressed up to the stage of formation of spermatozoa, although spermatozoa could not be detected in the epididymis. Leydig cells stained intensely with antibodies against the LH receptor and 3beta-HSD during the quiescent, recrudescent and active phases of the testicular cycle. During the regressive phase, there was a slight decrease in immunostaining for 3beta-HSD in these cells. These results indicate that Leydig cells in the testis of the juvenile ostrich are able to respond to LH and are capable of steroid synthesis. Furthermore, in juvenile (prepubertal) ostriches, spermatogeneic activity can be observed and, as in mature birds, spermatogenesis undergoes seasonal changes.  (+info)

Turlock-like bunyavirus associated with encephalomyelitis and myocarditis in an ostrich chick. (11/71)

In the fall of 1995, a 20-day-old female ostrich chick, 1 of a group of 20, was presented live with clinical signs of 2 days duration characterized by unsteady gait, circling to the left, and walking backward. Another bird with similar clinical signs had died and another had recovered. The bird was euthanized and examined at necropsy. Twenty-five milliliters of serous fluid was in the abdominal cavity and there was increased pericardial fluid. Histopathology of the brain revealed mild to moderate nonsuppurative encephalitis characterized by mild multifocal malacia, perivascular cuffing by lymphocytes, and gliosis. The heart had multifocal infiltrations of lymphocytes mixed with macrophages and a few plasma cells throughout the myocardium. Cytopathic effects were observed in primary chicken embryo liver cells following inoculation with a tissue homogenate prepared from the brain of the affected ostrich. Virus particles the size and morphology of the family Bunyaviridae were observed in cell culture lysate by negative-stain electron microscopy. Viral characterization demonstrated that the virus isolate is a previously unknown serotypic variant (subtype) of Turlock virus. Twelve of 65 sera collected over a 3-year period from ostriches aged from 1 month to 4 years were positive for neutralizing antibody to both the Turlock prototype strain and the new subtype of Turlock virus described in this report.  (+info)

Large scale sex typing of ostriches using DNA extracted from feathers. (12/71)

BACKGROUND: Ostrich (Struthio camelus) breeds have been gaining increasing significance around the world. The large-scale sex determination of chicks is an important task in the development of these breeds. To date, two PCR-based methods have been established for ostrich sex typing, neither of them intended for large-scale analyses. Here, we report on a protocol adapted to carry out large-scale gender scoring using DNA obtained from chick feathers. RESULTS: The DNA was extracted using a fast and simple alkaline extraction protocol that provided sufficient template for an early diagnosis. Tests with several primer sets enabled us to determine the best internal control primers associated with the sex-specific primers, avoiding spurious bands. Using DNA extracted from a single bulb and the best set of primers, we applied this protocol to simultaneously sex-type 96 individuals accurately. CONCLUSION: We have established a fast, safe, accurate and inexpensive procedure for large-scale sex typing of ostriches using DNA extracted from feathers. This procedure is useful for the gender identification of chicks in the first days of nestling life.  (+info)

Variability in brain and arterial blood temperatures in free-ranging ostriches in their natural habitat. (13/71)

We used implanted miniature data loggers to measure brain (in or near the hypothalamus) and carotid arterial blood temperatures at 5 min intervals in six free-ranging ostriches Struthio camelus in their natural habitat, for a period of up to 14 days. Carotid blood temperature exhibited a large amplitude (3.0-4.6 degrees C) circadian rhythm, and was positively correlated with air temperature. During the day, brain temperature exceeded carotid blood temperature by approx. 0.4 degrees C, but there were episodes when brain temperature was lowered below blood temperature. Selective brain cooling, however, was not present in all ostriches, and was not tightly coupled to the prevailing body temperature. Brain temperature was maintained within narrow daily limits of approx. 2 degrees C, and varied significantly less than blood temperature at short time scales of 5 to 20 min. At night, brain temperature exceeded blood temperature by as much as 3 degrees C. We attribute the elevated brain temperatures to warming of cerebral arterial blood, by reduced heat exchange in the ophthalmic rete or possibly heat gain from cranial structures, before supplying the hypothalamus. Further studies are necessary to elucidate the significance of such variations in brain temperature and the importance of selective brain cooling in free-living birds.  (+info)

Disulfide pairings and secondary structure of porcine beta-microseminoprotein. (14/71)

A sperm motility inhibitor isolated from porcine seminal plasma is identical to porcine beta-microseminoprotein (MSP). Circular dichroism (CD) and nuclear magnetic resonance (NMR) data showed that the native and recombinant porcine MSPs exhibit very similar structure. The five disulfide pairings on porcine MSP were unambiguously assigned based on NMR data and further confirmed using structural calculations. Surprisingly, our derived pairings differ from those recently reported for ostrich MSP based on matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) analysis. Furthermore, the secondary structure was determined to comprise one four-stranded and two double-stranded antiparallel beta-sheets. As we know, this is the first detailed secondary structure reported among several types of MSPs.  (+info)

Expression of a synthetic gene coding for ostrich egg-white lysozyme in Pichia pastoris and its enzymatic activity. (15/71)

To investigate the structure-function relationships of goose-type lysozyme, a gene coding for ostrich egg-white lysozyme (OEL) was designed based on the published amino acid sequence and constructed by assembling 32 chemically synthesized oligonucleotides. To obtain the recombinant OEL (rOEL), the synthetic gene was fused to the alpha-factor signal peptide in the expression vector pPIC9K and expressed in the methylotrophic yeast Pichia pastoris. The secreted protein from the transformed yeast was found to be processed at three different sites, including the correct site. The correctly processed rOEL was purified to homogeneity and shown to be indistinguishable from the authentic form in terms of circular dichroism (CD) spectrum and enzyme activity. Furthermore, the time-course of the reaction catalyzed by OEL was studied using (GlcNAc)(n) (n = 5 and 6) as the substrate and compared to that of goose egg-white lysozyme (GEL) [Honda and Fukamizo (1998) BIOCHIM: Biophys. Acta 1388, 53-65]. OEL hydrolyzed (GlcNAc)(6) in an endo-splitting manner producing mainly (GlcNAc)(2), (GlcNAc)(3), and (GlcNAc)(4), and cleavage to (GlcNAc)(3) + (GlcNAc)(3) predominated over that to (GlcNAc)(2) + (GlcNAc)(4). This indicates that OEL hydrolyzes preferentially the third glycosidic linkage from the nonreducing end of (GlcNAc)(6) as in the case of GEL. The cleavage pattern seen for (GlcNAc)(5) was similar to that seen for (GlcNAc)(6). Theoretical analysis of the reaction time-course for OEL revealed that the binding free energy values for subsites B, E, and G were different between OEL and GEL, although these lysozymes were estimated to have the same type of subsite structure.  (+info)

Ostrich (Struthio camelus) eggshell matrix contains two different C-type lectin-like proteins. Isolation, amino acid sequence, and posttranslational modifications. (16/71)

In contrast to chicken and goose, the ostrich calcified eggshell layer matrix contained two different C-type lectin-like proteins as major components. These proteins, named struthiocalcin-1 (SCA-1) and struthiocalcin-2 (SCA-2), were isolated and their amino acid sequence was determined. SCA-1 clearly was the ortholog of goose eggshell ansocalcin. Its amino acid sequence had the same length as that of ansocalcin (132 aa) and showed 65% sequence identity with the goose eggshell protein compared to 41% with chicken eggshell ovocleidin-17. Furthermore, as ansocalcin and unlike ovocleidin-17, it contained an additional, seventh, cysteine that was, however, located close to the C-terminus of SCA-1 and not in the N-terminal third of the sequence as in ansocalcin. SCA-2 showed features of both ansocalcin and chicken eggshell ovocleidin-17 (OC-17). Its sequence was 46% identical to that of ansocalcin and 36% identical to OC-17. It contained the same stretches of negatively charged amino acids conserved in ansocalcin and SCA-1, which are absent in OC-17. On the other hand, its length of 142 amino acids was identical to that of OC-17 and it contained only the usual set of six cysteines conserved in most C-type lectin-like proteins. The presence of three phosphorylated serines located at exactly the same region of the sequence as the two phosphoserines of OC-17 further stressed the similarity between SCA-2 and OC-17.  (+info)