| Autor: |
Ogunremi O; Ontario Animal Health Laboratory, Canadian Food Inspection Agency, Ottawa Laboratory Fallowfield, 3851 Fallowfield road, Ottawa, Ontario KsH 8P9, Canada. dogunremi@inspection.gc.ca, Benjamin J, MacDonald L, Schimpf R |
| Jazyk: |
angličtina |
| Zdroj: |
The Journal of parasitology [J Parasitol] 2008 Dec; Vol. 94 (6), pp. 1402-9. |
| DOI: |
10.1645/GE-1557.1 |
| Abstrakt: |
Newly developed serological tests for diagnosing parelaphostrongylosis in cervids, using the excretory-secretory products (ES) of the infective larvae of Parelaphostrongylus tenuis in enzyme-linked immunosorbent assays (ELISAs), have demonstrable superiority over the traditional method of larval recovery and microscopic identification. To generate a source of ELISA antigen by genetic engineering, we created a complementary DNA (cDNA) expression library by the reverse transcription of mRNA of P. tenuis adult worms, and ligation with the vector lambda-ZAP II. The library was screened using antisera produced in mice by immunization with a somatic antigen preparation of adult worms. Seventeen clones were isolated, sequenced, and checked for similarity to other DNA sequences in GenBank. A previously identified parasite gene encoding an aspartyl protease inhibitor (API) was isolated from the cDNA library, subcloned and expressed using the pET expression vector to produce a glutathione S transferase (GST)-His-S.Tag-P. tenuis API fusion protein (molecular weight = 63 kDa). An enzyme-linked immunosorbent assay utilizing the API fusion protein as the coating antigen was used to serologically diagnose all white-tailed deer (WTD, 10 out of 10) that had been inoculated with 6 - 150 L3 P. tenuis, indicating that the antigen may be a useful serodiagnostic antigen for P. tenuis infection in this cervid species. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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