The behavior and pathogenicity ofToxacara canis larvae in mice of different strains (original) (raw)
Abstract
In the present study the behavior and pathogenicity of second-stage larvae of_Toxocara canis_ were examined in different mouse strains with special emphasis on the major histocompatibility complex (MHC). Mice of the inbred strains BALB, C3H, C57BL, and DBA and the outbred strain NMRI were infected orally with 1000 second-stage larvae of_T. canis_. The clinical behavior of the animals: the numbers of larvae detected in the liver, lungs, brain and musculature; the hematological and serological parameters; and histological sections were examined. In mice of the BALB strain, no death occurred during the entire period of the investigation and the pattern of body-weight development of infected and uninfected animals was almost identical. The highest larval counts in the brain of all strains were found in BALB mice. The percentage of eosinophils in the blood of BALB mice increased after the 8th week postinfection, whereas it decreased in the other strains. Histological and pathophysiological changes developed to a lesser extent in this strain than in the other strains. In mice of the strains C3H, C57BL, DBA, and NMRI, deaths occurred from the 4th week postinfection onward. The infected animals lost weight in comparison with the uninfected controls; the numbers of larvae found in the brains of infected mice of the above-mentioned strains were lower than those detected in the BALB strain. There is no evidence that mechanical damage caused by migrating larvae in the brain tissue is mainly responsible for symptoms of central nervous toxocariasis. Likewise, the assumption that the MHC is involved in the allergicinflammatory response in the brain could not be proven: infected mice of the BALB and DBA strains reacted completely differently, although both are equipped with the same MHC haplotype.
Access this article
Subscribe and save
- Starting from 10 chapters or articles per month
- Access and download chapters and articles from more than 300k books and 2,500 journals
- Cancel anytime View plans
Buy Now
Price excludes VAT (USA)
Tax calculation will be finalised during checkout.
Instant access to the full article PDF.
Similar content being viewed by others
References
- Abraham D, Grieve RB (1990) Genetic control of murine responses to larval_Dirofilaria immitis_ J Parasitol 76: 523–528
PubMed Google Scholar - Baermann G (1917) Eine einfache Methode yur Auffindung von Ankylostomum-(Nematoden)/Larven in Erdproben. Tijdschr Diergeneesk 57: 131–137
Google Scholar - Dunsmore JD, Thompson RCA, Bates IA (1983) The accumulation of_Toxocara canis_ larvae in the brains of mice Int J Parasitol 13: 517–521
PubMed Google Scholar - Else K, Wakelin, D (1988) The effects of H-2 and non-H-2 genes on the expulsion of the nematode_Trichuris muris_ from inbred and congenic mice. Parasitology 96: 543–550
PubMed Google Scholar - Else K, Wakelin D (1990) Genetically-determined influences on the ability of poor responder mice to respond to immunization against_Trichuris muris_. Parasitology 100: 479–489
PubMed Google Scholar - Horn G (1983) Verhalten und Pathogenität der Larven von_Toxocara canis_ Werner 1782 (Anisakidae) bei ganzkörperbestrahlten Mäusen. Veterinary medicine dissertation, University of Hannover
- Kayes SG, Oaks JA (1978) Development of the granulomatous response in murine toxocariasis. Initial events. Am J Pathol 93: 277–294
PubMed Google Scholar - Kennedy MW (1990) Resistance to parasitic nematodes—how is the MHC involved. Parasitol Today 6: 374–375
PubMed Google Scholar - Kennedy MW, Gordon AMS, Tomlinson LA, Fureshi F (1987) Genetic (major histocompatibility complex? control of antibody repertoire to the second stage antigens of_Ascaris_. Parasite Immunol 9: 269
PubMed Google Scholar - Kennedy MW, McIntosh AE, Blair AJ, McLaughlin D (1990a) MHC (RT1) restriction of the antibody repertoire to infection with the nematode_Nippostrongylus brasiliensis_ in the rat. Immunology 71: 317–322
PubMed Google Scholar - Kennedy MW, Tomlinson LA, Fraser EM, Christie JF (1990b) The specificity of the antibody response to internal antigens of_Ascaris_: heterogeneity in infected humans, and MHC (H-2) control of the repertoire in mice. Clin Exp Immunol 80: 219–224
PubMed Google Scholar - Kennedy MW, Fraser EM, Christie JF (1991) MHC class II (I-A) region control of the IgE antibody repertoire to the ABA-I allergen of the nematode_Ascaris_ Immunology 72: 577–579
PubMed Google Scholar - Levine HS, Silverman PH (1969) Cultivation of_Ascaris suum_ larvae in supplemented and unsupplemented chemically defined media. J Parasitol 55: 17–21
PubMed Google Scholar - Lohmann K (1989) Verhalten und Pathogenität der Larven von_Toxocara canis_ Verner 1782 (Anisakidae) in der Maus. Zentralbl Veterinarmed [B] 36: 609–618
Google Scholar - Mitruka BM, Rawnsley HM (1981) Clinical biochemical and hematological reference values in normal experimental animals and normal humans, 2nd edn. Masson, New York, p 59
Google Scholar - Peppersack T (1981) Zur Pathogenität der Larven von_Toxocara canis_ Werner 1782 (Anisakidae) bei der Maus. Veterinary medicine dissertation, University of Hannover
- Sonnen P (1981) Zur Wirkung verschiedener Benzimidazolcarbamate auf somatische Larven von_Ancylostoma caninum_ Ercolani 1859 (Ancylostomidae) und_Toxocara canis_ Werner 1782 (Anisakidae). 1. Untersuchungen an der weißen Maus. Zentralbl Veterinarmed [B] 28: 226–240
Google Scholar - Sugane K, Oshima T (1984) Interrelationship of eosinophilia and IgE antibody production to larval ES antigen in_Toxocara canis_ infected mice. Parasite Immunol 6: 409–420
PubMed Google Scholar
Author information
Authors and Affiliations
- Institute of Parasitology, School of Veterinary Medicine Hannover, Bünteweg 17, D-30559, Hannover, Germany
C. Epe, T. Sabel, T. Schnieder & M. Stoye
Authors
- C. Epe
- T. Sabel
- T. Schnieder
- M. Stoye
Rights and permissions
About this article
Cite this article
Epe, C., Sabel, T., Schnieder, T. et al. The behavior and pathogenicity of_Toxacara canis_ larvae in mice of different strains.Parasitol Res 80, 691–695 (1994). https://doi.org/10.1007/BF00932955
- Received: 01 February 1994
- Accepted: 24 June 1994
- Issue date: August 1994
- DOI: https://doi.org/10.1007/BF00932955