Bochum, Universiẗat, Diss., 2000.

vii, 261 leaves : photos., ill., tables, graphs ; 30 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / Thesis (Ph.D.)--University of Adelaide, Dept. of Zoology, 1979

Zugl.: Giessen, Univ., Diss., 2006

Thesis (Ph.D.)-- University of Adelaide, Department of Zoology, 1979.

Zugl.: Giessen, Universiẗat, Diss., 2008.

Thesis (M.S.)--University of Missouri--Columbia, 2003. / "December 2003." Typescript. Includes bibliographical references (leaves 62-74). Also issued on the Internet.

O gênero Sarcocystis é constituído por várias espécies que se diferenciam pelas características morfológicas, biológicas e moleculares. Foram relatadas mais de 196 espécies encontradas em mamíferos, aves e répteis e somente 26 dessas espécies possuem o ciclo completo conhecido. Toxoplasma gondii é um parasito intracelular obrigatório, com distribuição geográfica cosmopolita, capaz de infectar uma ampla variedade de mamíferos e aves, inclusive o homem, caracterizando seu potencial zoonótico. Nas últimas décadas, a quantidade de pinguins vindos da Patagônia argentina e chilena, região de nascimento dessas aves, para o litoral brasileiro, onde muitos encalham e são resgatados, tem aumentado significativamente. Pouco se sabe sobre as doenças causadas por protozoários nessas aves. O presente estudo teve como objetivo conhecer aspectos epidemiológicos da infecção por coccídios da família Sarcocystidae em pinguins-de-magalhães (Spheniscus magellanicus), através de análises moleculares e sorológicas. Foram realizadas duas campanhas, uma em 2014 e outra em 2015, com a finalidade de obter amostras de sangue e tecidos dos pinguins que vieram a óbito durante reabilitação no Instituto de Pesquisa e Reabilitação de Animais Marinhos (IPRAM) localizada em Cariacica, Espírito Santo. Foram colhidas 514 amostras de tecidos (músculo=342, coração=86, cérebro=86) de 310 indivíduos. Dos tecidos de 54 pinguins foi realizado o bioensaio em camundongos para o isolamento de T. gondii, mas nenhum isolado foi obtido. Amostras de 310 indivíduos tiveram o DNA extraído para a pesquisa de coccídios da família Sarcocystidae utilizando-se os marcadores 18S rDNA, espaçador interno transcrito 1 (ITS1), codificador de proteínas de superfície (SAG)2, SAG3 e SAG4, subunidade beta da RNA polimerase (RPOB) e citocromo B (CytB). Destas, 16 (3.0%) amostras de músculo peitoral foram positivas para o gênero Sarcocystis spp., quando analisadas pelo marcador 18S, e todas com resultados idênticos. Com o ITS1, RPOB e Ctv. foram confirmadas as espécies de Sarcocystis em 12 amostras, todas idênticas a S. falcatula-like. Com os marcadores SAGs foi possível observar que as sequências não tinham variabilidade genética. Das 145 amostras de soro avaliadas para a presença de anticorpos anti-T. gondii, pelo Teste de Aglutinação Modificado (MAT ≥20), 18 aves foram positivas com títulos de: 20 (7 aves), 40 (9 aves) e 80 (2 aves). Este é o primeiro relato de S. falcatula-like e de anticorpos anti - T. gondii em pinguins-de-magalhães de vida livre. / The genus Sarcocystis is composed of several species that are differentiated by the morphological, biological and molecular characteristics. More than 196 species found in mammals, birds and reptiles have been reported, and only 26 of these species have the complete known cycle. Toxoplasma gondii is an obligate intracellular parasite with cosmopolitan geographic distribution, capable of infecting a wide variety of mammals and birds, including man, characterizing its zoonotic potential. In recent decades, the number of penguins that have come from Argentine and Chilean Patagonia, the region of birth of these birds, to the Brazilian coast, where many of them are stranded and rescued, has increased significantly. Little is known about the diseases caused by protozoa in these birds. The present study had as objective to study epidemiological aspects of coccidia infection of the family Sarcocystidae in Magellanic Penguins (Spheniscus magellanicus), through molecular and serological analyzes. Two campaigns were carried out, one in 2014 and another in 2015, in order to obtain blood and tissue samples from penguins who died during rehabilitation at the Institute of Research and Rehabilitation of Marine Animals (IPRAM) in the municipality of Cariacica, Espírito Santo. Tissue samples (total = 514: muscle = 342, heart = 86, brain = 86) were collected from 310 birds. From the tissues of 54 penguins the mouse bioassay was performed for the isolation of T. gondii, but no isolates were obtained. Samples of 310 individuals had DNA extracted for coccidia from the Sarcocystidae family using the 18S rDNA, Transcribed internal spacer 1(ITS1), surface protein encoder (SAG)2, SAG3, SAG4, beta subunit of RNA polymerase (RPOB) and citocrome B (CytB) markers. Of these, 16 (3.0%) samples, of pectoral muscle, were positive and all were identical to Sarcocystis spp. when analyzed by the 18S marker. With ITS1, RPOB and CytB the Sarcocystis species were confirmed in 12 samples, all identical to S. falcatula-like. With the SAGs it was possible to observe that the sequences had no genetic variability. Of the 145 serum samples evaluated for the presence of anti-T. gondii antibodies by Modified Agglutination Test (MAT ≥20), 18 were positive with titers of: 20 (7 birds), 40 (9 birds) and 80 (2 birds). This is the first report of S. falcatula-like and the presence of antibodies to T. gondii in free-living magellanic penguins.

O gênero Sarcocystis é constituído por várias espécies que se diferenciam pelas características morfológicas, biológicas e moleculares. Foram relatadas mais de 196 espécies encontradas em mamíferos, aves e répteis e somente 26 dessas espécies possuem o ciclo completo conhecido. Toxoplasma gondii é um parasito intracelular obrigatório, com distribuição geográfica cosmopolita, capaz de infectar uma ampla variedade de mamíferos e aves, inclusive o homem, caracterizando seu potencial zoonótico. Nas últimas décadas, a quantidade de pinguins vindos da Patagônia argentina e chilena, região de nascimento dessas aves, para o litoral brasileiro, onde muitos encalham e são resgatados, tem aumentado significativamente. Pouco se sabe sobre as doenças causadas por protozoários nessas aves. O presente estudo teve como objetivo conhecer aspectos epidemiológicos da infecção por coccídios da família Sarcocystidae em pinguins-de-magalhães (Spheniscus magellanicus), através de análises moleculares e sorológicas. Foram realizadas duas campanhas, uma em 2014 e outra em 2015, com a finalidade de obter amostras de sangue e tecidos dos pinguins que vieram a óbito durante reabilitação no Instituto de Pesquisa e Reabilitação de Animais Marinhos (IPRAM) localizada em Cariacica, Espírito Santo. Foram colhidas 514 amostras de tecidos (músculo=342, coração=86, cérebro=86) de 310 indivíduos. Dos tecidos de 54 pinguins foi realizado o bioensaio em camundongos para o isolamento de T. gondii, mas nenhum isolado foi obtido. Amostras de 310 indivíduos tiveram o DNA extraído para a pesquisa de coccídios da família Sarcocystidae utilizando-se os marcadores 18S rDNA, espaçador interno transcrito 1 (ITS1), codificador de proteínas de superfície (SAG)2, SAG3 e SAG4, subunidade beta da RNA polimerase (RPOB) e citocromo B (CytB). Destas, 16 (3.0%) amostras de músculo peitoral foram positivas para o gênero Sarcocystis spp., quando analisadas pelo marcador 18S, e todas com resultados idênticos. Com o ITS1, RPOB e Ctv. foram confirmadas as espécies de Sarcocystis em 12 amostras, todas idênticas a S. falcatula-like. Com os marcadores SAGs foi possível observar que as sequências não tinham variabilidade genética. Das 145 amostras de soro avaliadas para a presença de anticorpos anti-T. gondii, pelo Teste de Aglutinação Modificado (MAT ≥20), 18 aves foram positivas com títulos de: 20 (7 aves), 40 (9 aves) e 80 (2 aves). Este é o primeiro relato de S. falcatula-like e de anticorpos anti - T. gondii em pinguins-de-magalhães de vida livre. / The genus Sarcocystis is composed of several species that are differentiated by the morphological, biological and molecular characteristics. More than 196 species found in mammals, birds and reptiles have been reported, and only 26 of these species have the complete known cycle. Toxoplasma gondii is an obligate intracellular parasite with cosmopolitan geographic distribution, capable of infecting a wide variety of mammals and birds, including man, characterizing its zoonotic potential. In recent decades, the number of penguins that have come from Argentine and Chilean Patagonia, the region of birth of these birds, to the Brazilian coast, where many of them are stranded and rescued, has increased significantly. Little is known about the diseases caused by protozoa in these birds. The present study had as objective to study epidemiological aspects of coccidia infection of the family Sarcocystidae in Magellanic Penguins (Spheniscus magellanicus), through molecular and serological analyzes. Two campaigns were carried out, one in 2014 and another in 2015, in order to obtain blood and tissue samples from penguins who died during rehabilitation at the Institute of Research and Rehabilitation of Marine Animals (IPRAM) in the municipality of Cariacica, Espírito Santo. Tissue samples (total = 514: muscle = 342, heart = 86, brain = 86) were collected from 310 birds. From the tissues of 54 penguins the mouse bioassay was performed for the isolation of T. gondii, but no isolates were obtained. Samples of 310 individuals had DNA extracted for coccidia from the Sarcocystidae family using the 18S rDNA, Transcribed internal spacer 1(ITS1), surface protein encoder (SAG)2, SAG3, SAG4, beta subunit of RNA polymerase (RPOB) and citocrome B (CytB) markers. Of these, 16 (3.0%) samples, of pectoral muscle, were positive and all were identical to Sarcocystis spp. when analyzed by the 18S marker. With ITS1, RPOB and CytB the Sarcocystis species were confirmed in 12 samples, all identical to S. falcatula-like. With the SAGs it was possible to observe that the sequences had no genetic variability. Of the 145 serum samples evaluated for the presence of anti-T. gondii antibodies by Modified Agglutination Test (MAT ≥20), 18 were positive with titers of: 20 (7 birds), 40 (9 birds) and 80 (2 birds). This is the first report of S. falcatula-like and the presence of antibodies to T. gondii in free-living magellanic penguins.

There is little information on the distribution and diversity of Apicomplexan protozoal infections in the tissues of raptors in the United States. Protozoan encephalitis caused by Sarcocystis species and Toxoplasma gondii is being increasingly reported in raptors from various locations in the United States. To better determine the exposure of raptors to these Apicomplexan parasites, we examined breast and heart muscle tissue of raptors from the Carolina Raptor Center for the presence of Sarcocystis species, T. gondii and Neospora caninum via histology, Polymerase Chain Reaction (PCR) and Restriction Fragment Length Polymorphism (RFLP) using DraI and HinfI enzymes (Sarocystis only). Of 187 available HandE stained tissue sections, 33 contained sarcocysts. Nineteen of these slides had a matching DNA sample to compare via PCR. Nine of these 19 were positive for Sarcocystis via ITS PCR. Using ITS PCR, we detected Sarcocystis DNA in 24 of 114 birds (21.1%). Further molecular differentiation using JNB primers showed that 9 of the 24 birds were positive for either S. neurona or S. falcatula. RFLP analysis of these 9 indicated that 4 were S. falcatula samples, and 3 were S. falcatula Arg samples that cut with both enzymes. Our Sarcocystis positive samples were also tested for S. calchasi, S. columbae and Sarcocystis sp. Ex. A. nisus using PCR primers designed for these species. These species are emerging in Europe and have already shown an expansion of their distribution. Two samples (14567 and 15203) suggestive of Sarcocystis sp. Ex. A. nisus were identified, as well as one sample (14567), which suggested the presence of S. columbae. None of these samples were confirmed by sequencing the amplicons and the other 22 samples were all negative for these parasites. Recent reports have demonstrated DNA of S. falcatula in the brain and muscles of great horned owls (Bubo virginianus), golden eagles (Aquila chrysaetos), and bald eagles (Haliaeetus leucocephalus) with encephalitis in rehabilitation centers in Indiana, Minnesota, and Virginia using PCR. DNA of S. calchasi has been found in CNS tissue of several species of birds suffering encephalitis in an aviary in California. Hawks (Accipiter species) are believed to be the source of infection. The prevalence of T. gondii was 18.4% (21 of 114) in these birds by PCR, but none were positive by histopathology. N. caninum prevalence in raptors has been poorly discussed in the literature. This parasite uses canids as the definitive host in its life cycle, and is considered to have a much more restricted host range than T. gondii. Thirty-five of 114 birds (30.7%) were found to be PCR positive for N. caninum, but no tissue cysts of N. caninum were observed in histological sections. Co-infection of 2 or all 3 species was detected in 16 of 114 birds (14%). This study demonstrates that there may be a higher prevalence of S. falcatula in raptors than was previously known, including more, as yet unknown, species of Sarcocystis capable of infecting raptors as intermediate hosts. Our PCR prevalence for T. gondii is similar to the serological prevalence for this parasite in raptors. The high PCR prevalence of N. caninum needs to be confirmed by sequencing the amplicons and the use of additional PCR primers. Information from the present study may help to inform zoos, aviaries and wildlife rehabilitation centers about parasite host diversity and reinforce the importance of preventative measures, such as making sure opossums (S. falcatula and S. falcatula-like), feral cats (T. gondii), and wild raptors (S. calchasi) do not have access to facilities. Insect control should also be emphasized because of their ability to serve as phoretic hosts and carry oocysts/sporocysts into zoos, aviaries, and rehabilitation centers. / Master of Science

Los macroquistes de S. aucheniae producen cuadros de intoxicación alimentaria muy variada en humanos y los conejos son altamente susceptibles cuando se le inyecta extractos proteicos intramuscularmente. Esta susceptibilidad variada por especies filogenéticas distintas podrían deberse a los receptores celulares para las endotoxinas de los macroquistes. En el presente trabajo se buscó determinar el efecto tóxico del extracto proteico de macroquistes de S. aucheniae sobre leucocitos circulantes de conejo (citotoxicidad) in vitro. Se expusieron diversas concentraciones de extracto proteico (0.5, 1, 50, 500, 1000 ng/100μl) a una población de 500 000 leucocitos/ml por 1 y 12 horas mantenidos en un medio de cultivo a un ambiente de 37ºC, midiéndose la viabilidad celular por exclusión con azul de tripán y la degranulación de enzimas leucocitarias (Mieloperoxidasa y Glucosaminidasa) mediante electroforesis en geles de poliacrilamida y transferencia a membranas de nitrocelulosa (Western Blotting). Sobre los tratamientos, el recuento de células a la hora de incubación demostró que existe mortalidad alta entre 57.7% y 58.1% y a las 12 horas fue de 65.2% y 99.4% en todos los grupos de tratamiento (desde 0.5 hasta 1000ng/100μl de antígeno), observándose que no existe diferencia estadística significativa (p>0.05) entre las medias del número de leucocitos que sobreviven a cada tratamiento. La mortalidad en el grupo control de suero fisiológico alcanza 5% y 57% a 1 y 12 horas de incubación respectivamente. Sobre la degranulación de leucocitos, se observa que existe secreción de proteínas diferentes a las observadas en el control inoculado con suero fisiológico en los tratamientos evidenciado por la tinción de bandas en las membranas de transferencia. Se concluye que el extracto proteico de macroquistes de S aucheniae es altamente citotóxico para los leucocitos de conejo y se observa la secreción de proteínas.