Cardiac thrombosis normally occurs in old Syrian hamsters and according to the research it has a higher incidence rate in females than males. The most frequent site of thrombus formation has been reported to be the left atrium and it usually occurs secondary to degenerative cardiomyopathy and amyloidosis. In this study during a period of 2 years, 22 pet Syrian hamsters aged between 1-3 years-old with signs of cardiovascular disease and referred to the small animal Veterinary Teaching Hospital of University of Tehran were examined in order to evaluate for cardiac diseases as well as atrial thrombosis. During the examinations and observations clinical signs such as lethargy, anorexia, hyperpnoea, reduced daily activity, tachycardia, cyanosis, and vaginal discharge were observed. Based on the clinical sings, the initial diagnosis of cardiac disease was made and for more accurate evaluation of cardiac disease, the cases were referred to the radiology department. For detection of specific signs of cardiac disease echocardiography was performed on all patients. in some cases, sampling of vaginal discharge was taken as well and transferred to the lab for bacterial culture. Cardiac thrombosis and especially atrial thrombosis in all cases were diagnosed by echocardiography so that 9 cases showed pyometra concurrently.

O estabelecimento e a evolução da leptospirose em hamster (Mesocricetus auratus) pela infecção experimental com Leptospira interrogans sorovar Canicola, estirpe LO4, pela exposição cutânea íntegra e escarificada, tendo como controle a via intraperitoneal foram avaliados. Foram utilizados 120 hamsters, fêmeas, distribuídas em dois grupos de acordo com a via de inoculação (pele escarificada e pele íntegra). O inóculo infeccioso foi constituído por uma cultura pura de L. interrogans sorovar Canicola (estirpe LO4), isolada do fígado de um suíno de abatedouro em Londrina, Estado do Paraná e tipificada pela técnica de adsorção de aglutininas com o kit de anticorpos monoclonais no Royal Tropical Institute, Amsterdã, Holanda. Os animais foram observados duas vezes ao dia, durante 21 dias. Os animais que vieram a óbito foram necropsiados e colhidos assepticamente rins, fígado, sistema genital (útero e ovário) e cérebro. Os animais sobreviventes foram eutanasiados após 21 dias. Foram ainda colhidas amostras de soro sanguíneo por punção cardíaca para a pesquisa de aglutininas antileptospiras nos animais sobreviventes, pela técnica de soroaglutinação microscópica (SAM). Para a detecção de leptospiras, foram utilizados microscopia direta a fresco e cultivo microbiológico. A via cutânea escarificada induziu maior letalidade quando comparada com a pele integra, com estabelecimento e evolução da leptospirose. Por outro lado, a via cutânea íntegra induziu mais frequentemente o estado de portador renal e/ou genital para leptospirose. A estirpe LO4 apresentou baixo poder imunogênico, induzindo soroconversão na SAM em apenas um animal. | The establishment and evolution of leptospirosis in hamster (Mesocricetus auratus) by experimental infection with Leptospira interrogans serovar Canicola, LO4 strain, by intact and scratched skin exposures, having as control the intraperitoneal route, were evaluated. Hundred-twenty female hamsters distributed in two groups according to inoculation route (intact and scratched skin) were used. Infectious inoculum was constituted by a pure culture of L. interrogans serovar Canicola (strain LO4), isolated from liver from a slaughtered swine in Londrina, Paraná state and typified by agglutinins adsortion technique with monoclonal antibody kit at the Royal Tropical Institute, Amsterdam, the Netherlands. The animals were observed twice a day during 21 days. Animals that died were necropsied and kidneys, liver, genital tract (uterus and ovaries) and brain were aseptically collected. On the 21st post-inoculation day, surviving animals were euthanized. In these animals, serum samples were also collected by cardiac puncture to antileptospires agglutinins research using microscopic agglutination test (MAT). Fresh direct microscopy and microbiological culture were used for the detection of leptospires. Scratched skin route induced larger lethality when compared to intact skin route, with establishment and evolution of leptospirosis. On the other hand, intact skin route induced renal and/or genital carrier state more frequently. LO4 strain presented low immunogenic power, characterized by soroconversion at the MAT in only one inoculated animal.

Hamsters orally inoculated with ERA and PV strains of rabies virus were sacrificed at 24, 48, 72 hours, 21 and 30 days after inoculation. Brain fragments were examined by Fluorescent Antibody test (FAT) and heminested PCR (hn-PCR). Fragments from stomach, blood, heart, and lung were examined only by hn-PCR. Sera of other hamsters, similarly inoculated, obtained at 30th day after inoculation were submitted to mouse neutralization test. The hamsters were challenged intracerebrally with CVS strain with 10(2.7)mouse LD50/0.03mL, 45 days after inoculation. Brains examined by FAT were negative. The hn-PCR detected the presence of rabies virus RNA in the lung of one animal inoculated with ERA, and in the brain, stomach, blood, and lung of PV-infected animals. The orally inoculated virus was capable to infect and replicate in several organs and tissues; however, none of the challenged hamsters did survive after challenge. | Hamsters inoculados oralmente com as amostras de vírus rábico ERA e PV foram sacrificados após 24, 48 e 72 horas, 21 e 30 dias. Fragmentos do cérebro foram analisados através da imunofluorescência direta (IFD) e heminested-PCR (hn-PCR). Os fragmentos do estômado, sangue, coração e pulmão foram examinados somente com a técnica de hn-PCR. Soros de outros hamsters, inoculados de modo similar e obtidos 30 dias após a inoculação, foram submetidos ao teste de soroneutralização (SNT) em camundongos. No 45º dia pós-inoculação, os hamsters foram desafiados intracerebralmente com a amostra CVS, contendo 10(2,7)DL50 em camundongos/0,03 mL. Os fragmentos do cérebro foram todos negativos ao teste de imunofluorescência. A hn-PCR detectou a presença de RNA do vírus da raiva no pulmão de um animal inoculado com a amostra ERA e, no cérebro, estômago, sangue e pulmão de hamsters inoculados com a amostra PV. As amostras de vírus inoculadas oralmente foram capazes de se replicar em diferentes órgãos, no entanto, todos od hamsters morreram ao desafio, indicando uma resposta imunológica insuficiente.