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Comparison of the biological characteristics of two isolates of Neospora caninum
This study compared the biological and genetic properties of a bovine (NC-SweB1) and a canine (NC-Liverpool) isolate of Neospora caninum. A mouse model for CNS infection demonstrated marked differences in pathogenicity between the isolates. NC-Liverpool induced severe clinical signs of neosporosis i...
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Published in: | Parasitology 1999-04, Vol.118 (4), p.363-370 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | This study compared the biological and genetic properties of a
bovine (NC-SweB1) and a canine (NC-Liverpool) isolate
of Neospora caninum. A mouse model for CNS infection demonstrated
marked differences in pathogenicity between the
isolates. NC-Liverpool induced severe clinical signs of neosporosis in
57/58 mice including discoordinated movement,
hindlimb paralysis and coat ruffling with severe weight loss. In contrast
NC-SweB1 induced similar but less severe
symptoms in a much smaller proportion of mice over the same time-period.
Statistically significant differences were
observed between the isolates in the response (mean weight loss) of mice
through time to the different doses inoculated.
Histopathological effects on brain tissue reflected the isolate-based differences
described above. NC-Liverpool infection
resulted in intense inflammatory infiltrates and highly necrotic lesions
whereas NC-SweB1 induced a milder meningoencephalitis.
Passage in cell-culture over a period of 14 months did not affect the pathogenicity
of NC-Liverpool.
Immunoblots showed that antibodies to N. caninum appeared earlier
in mice inoculated with NC-Liverpool than with
NC-SweB1. Finally, RAPD–PCR analysis of NC-Liverpool DNA generated
profiles distinct from that observed with
DNA from NC-SweB1 or Toxoplasma gondii. In summary this study
provides evidence for significant biological and
genetic differences between 2 isolates of N. caninum. |
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ISSN: | 0031-1820 1469-8161 |
DOI: | 10.1017/S0031182098003898 |