The aim of this research was to describe two fatal cases of Yersinia enterocolitica bioserotype 4/O:3 infection in non-human primates and to characterise the isolates by PCR and PFGE. In July 2004, two marmosets (Callitrix jacchuss) born in captivity in Zagreb Zoo, died following a few days of intermittent diarrhoea in intervals of 2 weeks. The pathomorphological diagnosis of the female (born in 1997) and the male (born in 1995) marmoset, was disseminated miliary necrosis of the liver. Y. enterocolitica 4/O:3 was isolated from both livers showing that monkeys are susceptible to this bioserotype. The ail gene, which is an essential chromosomal virulence factor in pathogenic Y. enterocolitica isolates, was present in the marmoset isolates. Two different PFGE patterns were obtained from the isolates of the male liver with NotI enzyme. One genotype of the male marmoset isolate was indistinguishable from the genotype of the female marmoset isolate when NotI, ApaI and XhoI enzymes were used indicating a common infection source for the marmosets. The genotypes of the marmoset isolates differed only slightly from one human (of seven Croatian isolates) and from one pig isolate (representing a common genotype found among human and porcine isolates in Germany) suggesting that raw pork fed to the marmoset could have been the infection source.
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http://dx.doi.org/10.1016/j.vetmic.2006.12.010 | DOI Listing |
Cell Tissue Res
September 2015
Centre of Reproductive Medicine and Andrology, CeRA, Institute of Reproductive and Regenerative Biology, Albert-Schweizer-Campus 1, Building D11, 48149, Münster, Germany.
The chemokine receptor CXCR7 interacts with the chemokines CXCL11 and CXCL12. During development, this ligand receptor system (C-X-C) provokes cell-type-specific responses in terms of migration, adhesion or ligand sequestration. It is active in zebrafish and rodents but no data are available for its presence or function in primate testes.
View Article and Find Full Text PDFVet Microbiol
April 2007
Institute of Hygiene and Technology of Food of Animal Origin, Ludwig Maximilian University, Munich, Germany.
The aim of this research was to describe two fatal cases of Yersinia enterocolitica bioserotype 4/O:3 infection in non-human primates and to characterise the isolates by PCR and PFGE. In July 2004, two marmosets (Callitrix jacchuss) born in captivity in Zagreb Zoo, died following a few days of intermittent diarrhoea in intervals of 2 weeks. The pathomorphological diagnosis of the female (born in 1997) and the male (born in 1995) marmoset, was disseminated miliary necrosis of the liver.
View Article and Find Full Text PDFEur J Neurosci
November 2004
Faculty of Rehabilitation Medicine, University of Alberta, Edmonton, T6G 2G4, Canada.
Neutralizing the myelin-associated growth inhibitor Nogo-A in adult spinal cord-injured rats can promote regeneration of injured and compensatory sprouting of uninjured axons. Nogo-A is present in humans, making its neutralization a possible novel treatment option for paraplegic patients. In this study we examined the effects of an extensively used anti-Nogo-A antibody (mAb IN-1) on the regenerative capabilities of lesioned corticospinal tract (CST) axons in a primate, the Marmoset monkey.
View Article and Find Full Text PDFCan J Microbiol
July 2002
Departamento de Microbiología, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Specific clonal types of Actinobacillus actinomycetemcomitans, a major human periodontal pathogen, may be responsible for clinical manifestations and the production of leukotoxin virulence factors. Leukotoxicity is associated with genetic polymorphism at the promoter region of the leukotoxin (lItx) gene. Here, we describe the use of arbitrarily primed polymerase chain reaction (AP-PCR) and ltx promoter PCR to molecularly characterise 35 A.
View Article and Find Full Text PDFArzneimittelforschung
October 1988
Department of Biochemistry, Dr. Karl Thomae GmbH, Biberach an der Riss, Fed. Rep. of Germany.
Pharmacokinetics and biodiposition of recombinant human interferon-alpha 2C (IFN-alpha 2C) were studied in rats and marmosets (Callitrix jacchus). After intravenous bolus dose, serum concentrations of IFN-alpha 2C antigen declined triexponentially. After administration of 15 MIU/kg IFN-alpha 2C the mean t1/2 alpha was 3 min (rat) and 10 min (marmoset), t1/2 beta was 0.
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