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Peer-reviewed veterinary case report

Trypanosoma cruzi strains affect nerve damage in Beagle dogs' gut

By Nogueira-Paiva, Nívia Carolina et al.·Published in Memorias do Instituto Oswaldo Cruz·2014·Laborat&#xf3·View original on PubMed

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Original publication title: Myenteric plexus is differentially affected by infection with distinct Trypanosoma cruzi strains in Beagle dogs.

Species:
dog

Plain-English summary

A group of Beagle dogs infected with different strains of the Trypanosoma cruzi parasite showed digestive issues, including problems with their esophagus and colon. During the acute phase of infection, both strains caused inflammation, but only the Be-78 strain led to ongoing digestive problems in the chronic phase. This suggests that while both strains initially affect the digestive system, the Be-78 strain causes more severe and lasting damage. The findings indicate that treatment may need to be tailored based on the specific strain of the parasite involved.

People also search for: Beagle dog digestive problems · Trypanosoma cruzi infection treatment · dog megaesophagus symptoms

Abstract

Chagasic megaoesophagus and megacolon are characterised by motor abnormalities related to enteric nervous system lesions and their development seems to be related to geographic distribution of distinct Trypanosoma cruzi subpopulations. Beagle dogs were infected with Y or Berenice-78 (Be-78) T. cruzi strains and necropsied during the acute or chronic phase of experimental disease for post mortem histopathological evaluation of the oesophagus and colon. Both strains infected the oesophagus and colon and caused an inflammatory response during the acute phase. In the chronic phase, inflammatory process was observed exclusively in the Be-78 infected animals, possibly due to a parasitism persistent only in this group. Myenteric denervation occurred during the acute phase of infection for both strains, but persisted chronically only in Be-78 infected animals. Glial cell involvement occurred earlier in animals infected with the Y strain, while animals infected with the Be-78 strain showed reduced glial fibrillary acidic protein immunoreactive area of enteric glial cells in the chronic phase. These results suggest that although both strains cause lesions in the digestive tract, the Y strain is associated with early control of the lesion, while the Be-78 strain results in progressive gut lesions in this model.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/24271001/