An experimental model for amoebic abscess production in the cheek pouch of the Syrian golden hamster, Mesocricetus auratus

2004 ◽  
Vol 53 (3) ◽  
pp. 247-254
Author(s):  
M.A Beg ◽  
S Kobayashi ◽  
A.S Hussainy ◽  
A Hamada ◽  
E Okuzawa ◽  
...  
2004 ◽  
Vol 19 (suppl 1) ◽  
pp. 69-78 ◽  
Author(s):  
Bernardo Hochman ◽  
Lydia Masako Ferreira ◽  
Flaviane Cássia Vilas Bôas ◽  
Mario Mariano

Syrian golden hamster (Mesocricetus auratus) has in its cheek pouches sub-epithelium an "Immunologically Privileged Site" which allows the integration of homo- and heterologous graft. This paper describes some anatomical and histological characteristics of that site, as well as analyzes aspects related with its immune properties. It also focuses the advantages of this experimental model over other models which are natural or induced carriers of immunodeficiency. Based on both these advantages and literature, this study aims to establish this model, through the performance of heterologous graft, as another option for the investigation of scar disturbances, as keloids and other diseases which may interest Plastic Surgery, as benign cutaneous lesions, and malignant neoplasias such as skin carcinomas and melanomas. The work also addresses perspectives for using this model, which still is a source scarcely known by Brazilian medical class.


Gene ◽  
2001 ◽  
Vol 278 (1-2) ◽  
pp. 235-243 ◽  
Author(s):  
Peter Muscarella ◽  
Thomas J. Knobloch ◽  
Alexis B. Ulrich ◽  
Bruce C. Casto ◽  
Nicolas Moniaux ◽  
...  

2021 ◽  
Vol 11 ◽  
Author(s):  
Voddu Suresh ◽  
Deepti Parida ◽  
Aliva P. Minz ◽  
Manisha Sethi ◽  
Bhabani S. Sahoo ◽  
...  

The Syrian golden hamster (Mesocricetus auratus) has recently been demonstrated as a clinically relevant animal model for SARS-CoV-2 infection. However, lack of knowledge about the tissue-specific expression pattern of various proteins in these animals and the unavailability of reagents like antibodies against this species hampers these models’ optimal use. The major objective of our current study was to analyze the tissue-specific expression pattern of angiotensin-converting enzyme 2, a proven functional receptor for SARS-CoV-2 in different organs of the hamster. Using two different antibodies (MA5-32307 and AF933), we have conducted immunoblotting, immunohistochemistry, and immunofluorescence analysis to evaluate the ACE2 expression in different tissues of the hamster. Further, at the mRNA level, the expression of Ace2 in tissues was evaluated through RT-qPCR analysis. Both the antibodies detected expression of ACE2 in kidney, small intestine, tongue, and liver. Epithelium of proximal tubules of kidney and surface epithelium of ileum expresses a very high amount of this protein. Surprisingly, analysis of stained tissue sections showed no detectable expression of ACE2 in the lung or tracheal epithelial cells. Similarly, all parts of the large intestine were negative for ACE2 expression. Analysis of tissues from different age groups and sex didn’t show any obvious difference in ACE2 expression pattern or level. Together, our findings corroborate some of the earlier reports related to ACE2 expression patterns in human tissues and contradict others. We believe that this study’s findings have provided evidence that demands further investigation to understand the predominant respiratory pathology of SARS-CoV-2 infection and disease.


Anaerobe ◽  
2018 ◽  
Vol 52 ◽  
pp. 29-42 ◽  
Author(s):  
Jinshan Jin ◽  
Lei Guo ◽  
Linda VonTungeln ◽  
Michelle Vanlandingham ◽  
Carl E. Cerniglia ◽  
...  

2002 ◽  
Vol 49 (2) ◽  
pp. 427-431
Author(s):  
Zuzanna Dobrzańska ◽  
Joanna Wieckiewicz ◽  
Jacek Bigda

In this study we cloned and analysed partial cDNA of tumor necrosis factor (TNF) and p75 TNF-R receptor of Syrian golden hamster (Mesocricetus auratus). We obtained a 382-bp sequence of TNF and a 148-bp sequence coding for p75 TNF-R. The primers used for the cloning were designed on the basis of inter-species homology, thus presumably can be used for cloning and analysis of TNF and p75 TNF-R genes of other mammals.


2003 ◽  
Vol 89 (12) ◽  
pp. 2320-2326 ◽  
Author(s):  
F Borle ◽  
A Radu ◽  
C Fontolliet ◽  
H van den Bergh ◽  
P Monnier ◽  
...  

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