Literature DB >> 12695039

Infectivity and pathogenicity of 14-month-cultured embryonated eggs of Toxocara canis in mice.

Chia-Kwung Fan1, Yun-Ho Lin, Wen-Yuan Du, Kua-Eyre Su.   

Abstract

Infectivity and pathogenicity to mice of embryonated eggs of Toxocara canis, that had been maintained in 2% formalin for 14 months at 4 degrees C, were evaluated by immunological and pathological assessment at 1, 4, 8, 12, 16, 20, 24, 28, 42 and 67 weeks post-infection (WPI). On each date, three infected mice and two age-matched uninfected mice were sacrificed for serum collection and histological processing of the liver, lungs, musculature, and brain. Infectivity assessment by enzyme-linked immunosorbent assay (ELISA) revealed that the overall immunological pattern of infected mice tended to be towards the Th2 type response. Serum IgG1 antibody titers in infected mice were significantly higher than that of the uninfected control mice throughout the trial (P<0.05). On the other hand, no significant difference in titers of IgG3 antibody, an indicator for the Th1 type response, was observed between the infected and control mice, except at eight WPI (P<0.05). Pathogenicity was assessed semiquantitatively by comparing the mean number or diameter of inflammatory foci as well as histopathological changes in the liver, musculature, brain, or lungs of the infected mice and the control mice. Each hematoxylin and eosin (H&E) stained tissue section slide was examined under 100x magnification and 15 random fields were counted. Degree of inflammatory injury among the four organs was scored and categorized into four levels: normal (0), mild (1+), moderate (2+), and severe (3+). An index of inflammatory injury (mean score of experimental group/mean score of 10 control groups of 20 uninfected mice) of 2-3 is considered as moderate to severe, 1-2 as mild to moderate, and 0-1 as normal to mild. Histopathological changes were moderate to severe in the liver and lungs, mild to moderate in the musculature, and only normal to mild in the brain throughout the trial. It is noteworthy that apocrine-like change in epithelial cells of the bile duct was observed in most of the infected mice from eight WPI onward. Furthermore, larvae trapped by organized granulomas were found in soft tissue near the musculature at 12, 20, and 28 WPI. Altogether, not only were the infectivity and pathogenicity of the 14-month-cultured T. canis embryonated eggs retained, the hatched larvae were also capable of eliciting some special pathological changes in the murine host.

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Year:  2003        PMID: 12695039     DOI: 10.1016/s0304-4017(03)00046-3

Source DB:  PubMed          Journal:  Vet Parasitol        ISSN: 0304-4017            Impact factor:   2.738


  16 in total

Review 1.  Cerebral Toxocariasis: Silent Progression to Neurodegenerative Disorders?

Authors:  Chia-Kwung Fan; Celia V Holland; Karen Loxton; Ursula Barghouth
Journal:  Clin Microbiol Rev       Date:  2015-07       Impact factor: 26.132

2.  Larval distribution, migratory pattern and histological effects of Toxocara canis in Rattus norvegicus.

Authors:  Kennesa Klariz R Llanes; Cyrelle M Besana; Vachel Gay V Paller
Journal:  J Parasit Dis       Date:  2019-09-04

3.  Toxocara canis larvae reinfecting BALB/c mice exhibit accelerated speed of migration to the host CNS.

Authors:  Petra Kolbeková; David Větvička; Jan Svoboda; Karl Skírnisson; Markéta Leissová; Martin Syrůček; Helena Marečková; Libuše Kolářová
Journal:  Parasitol Res       Date:  2011-05-03       Impact factor: 2.289

4.  Enhanced expression of transforming growth factor-beta1 in inflammatory cells and secretory granules in Paneth cells in the small intestine of mice infected with Toxocara canis.

Authors:  Chia-Kwung Fan; Chien-Ching Hung; Yun-Ho Lin; Ming-Hsien Li; Kua-Eyre Su
Journal:  Parasitol Res       Date:  2004-10-13       Impact factor: 2.289

5.  The hamster (Mesocricetus auratus) as an experimental model of toxocariasis: histopathological, immunohistochemical, and immunoelectron microscopic findings.

Authors:  Ana Maria Gonçalves da Silva; Pedro Paulo Chieffi; Wellington Luiz Ferreira da Silva; Edite Hatsumi Yamashiro Kanashiro; Guita Rubinsky-Elefant; Edécio Cunha-Neto; Eliane Conti Mairena; Thales De Brito
Journal:  Parasitol Res       Date:  2014-12-19       Impact factor: 2.289

6.  Induction of matrix metalloproteinase-9 in mice during Toxocara canis larvae migration.

Authors:  S C Lai; K M Chen; H C Chen; H H Lee
Journal:  Parasitol Res       Date:  2005-01-06       Impact factor: 2.289

7.  Bone marrow mesenchymal stem cell co-adjuvant therapy with albendazole for managing Toxocara vitulorum-rat model.

Authors:  Faten A M Abo-Aziza; Abdel Kader A Zaki; Ahmed I Alajaji; Saleh M Al Barrak
Journal:  Vet World       Date:  2021-02-08

8.  Detection and Evaluation of Antibody Response to a Baylisascaris-Specific Antigen in Rodent Hosts with the Use of Western Blotting and Elisa.

Authors:  Sarah G H Sapp; Sukwan Handali; Sara B Weinstein; Michael J Yabsley
Journal:  J Parasitol       Date:  2018-08-29       Impact factor: 1.276

9.  Meningitis by Toxocara canis after ingestion of raw ostrich liver.

Authors:  Young Noh; Sung-Tae Hong; Ji Young Yun; Hong-Kyun Park; Jung-Hwan Oh; Young Eun Kim; Beom S Jeon
Journal:  J Korean Med Sci       Date:  2012-08-22       Impact factor: 2.153

10.  Inducible nitric oxide synthase inhibition influenced granuloma formation with suppressed collagen expression in myositis caused by Toxocara canis in mice.

Authors:  Su-Mei Lin; Chien-Wei Liao; Yun-Ho Lin; Chin-Cheng Lee; Ting-Chang Kao; Chia-Kwung Fan
Journal:  Parasitol Res       Date:  2007-11-22       Impact factor: 2.289

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