Abdominal angiostrongyliasis: pathologic findings in Swiss mice infected with different doses of Angiostrongylus costaricensis
Abstract
Abdominal angiostrongyliasis is caused by Angiostrongylus costaricensis, the definitive and intermediate hosts of which are wild rodents and terrestrial molluscs, respectively. Humans are accidental hosts and can be infected by ingesting the third-stage (infective) larvae (L3). It remains unclear whether the number of L3 inoculated is related to lesion severity. Our aim was to analyse histopathological alterations in Swiss mice infected with different doses of A. costaricensis. Thirty-two mice were randomly divided into four groups (n = 8/group): uninfected, control mice; mice infected with a low dose (five L3); mice infected with an intermediate dose (15 L3); and mice infected with a high dose (30 L3). The frequency of intestinal thrombi, splenitis, eggs/larvae, hepatic infarction and acute pancreatitis differed among the groups, the last being considered a significant finding. We conclude that different infective doses alter the histopathological aspects of the infection in Swiss mice, those aspects being more pronounced at medium and high doses, with no effect on the development of the disease. This experimental model shows that the parasite life cycle can be maintained in Swiss mice through the inoculation of a low dose (five L3).
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In abdominal angiostrongyliasis, worms can cause lesions after their death inside the blood vessels.
“since the worms can cause lesions after their death inside the blood vessels [131]”
From Albendazole and Mebendazole as Anti-Parasitic and Anti-Cancer Agents: an Update (2021) · cites this paper as [131]
In abdominal angiostrongyliasis due to A. costaricensis, anthelmintics such as albendazole and mebendazole have not proven efficient.
“In abdominal angiostrongyliasis due to infection with Angiostrongylus costaricensis, anthelmintics such as albendazole and mebendazole have not proven to be efficient”
From Albendazole and Mebendazole as Anti-Parasitic and Anti-Cancer Agents: an Update (2021) · cites this paper as [131]
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Albendazole and Mebendazole as Anti-Parasitic and Anti-Cancer Agents: an Update
Chai, J.-Y., Jung, B.-K., & Hong, S.-J. (2021) · The Korean Journal of Parasitology · doi:10.3347/kjp.2021.59.3.189 · Cited by 286 · see citing works
- Authors
- Hermes, C. C., Benvegnú, E., Costa, M. M., Rodriguez, R., & Vieira, M. I. B.
- Affiliations
- Universidade de Passo Fundo (BR)
- Corresponding author
- Vieira, M.I.B.
- Venue
- Journal of Helminthology
- Publisher
- Cambridge University Press (CUP)
- Published
- 2020
- Volume
- 94
- Pages
- e169-e169
- ISSN
- 0022-149X (ISSN-L)
- 1475-2697
- OpenAlex
- W3041347392
- Cited by
- 3
- References
- 0
- Citations by year
- 2024: 1 · 2021: 2
- FWCI
- 0.35
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Helminthology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Insect Science › Mollusks and Parasites Studies
- Life Sciences › Immunology and Microbiology › Parasitology › Parasites and Host Interactions
- Health Sciences › Veterinary › Small Animals › Helminth infection and control
- Keywords
- abdominal angiostrongyliasis, Angiostrongylus costaricensis, infectious dose, third-stage larvae, histopathology, Swiss mice, experimental infection model, splenitis, hepatic infarction, acute pancreatitis, parasite life cycle, rodent hosts
- MeSH terms
- Acute Disease, Angiostrongylus, Animals, Host-Parasite Interactions, Larva, Male, Pancreatitis, Strongylida Infections, Gastrointestinal Tract, Mice, Parasite Load
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