Development and application of DNA probes and PCR tests for Haemophilus paragallinarum

Chen, X., Miflin, J.K., Zhang, P. and Blackall, P.J. (1996) Development and application of DNA probes and PCR tests for Haemophilus paragallinarum. Avian Diseases, 40 2: 398-407.


Author Chen, X.
Miflin, J.K.
Zhang, P.
Blackall, P.J.
Title Development and application of DNA probes and PCR tests for Haemophilus paragallinarum
Journal name Avian Diseases   Check publisher's open access policy
ISSN 0005-2086
1938-4351
Publication date 1996-04
Sub-type Article (original research)
DOI 10.2307/1592238
Volume 40
Issue 2
Start page 398
End page 407
Total pages 10
Place of publication Jacksonville, FL, United States
Publisher American Association of Avian Pathologists
Language eng
Formatted abstract A genomic DNA library of Haemophilus paragallinarum strain Modesto was created. Screening of this library identified four clones that reacted specifically with all 56 isolates of H. paragallinarum tested and failed to react with 24 closely related bacteria from the genera Pasteurella and Actinobacillus. All four clones also failed to react with DNA extracted from one field isolate each of Mycoplasma gallisepticum and Mycoplasma synoviae. The probes based on these four clones were approximately 1.8, 2.3, 3.5, and 5.5 kb in size. The four probes were able to detect between 7.8 and 31.25 ng of purified DNA from homologous strains with no obvious correlation between probe size and sensitivity. The smallest probe, termed P601, was partially sequenced, and primers for two polymerase chain reaction (PCR) tests were designed from these sequence data. Both PCR tests, termed HPG-1 and HPG-2, were shown to be specific, all 41 isolates of H. paragallinarum tested being positive and all 26 non-H. paragallinarum isolates being negative. Both PCR tests were able to detect 1 pg DNA and between 10 2 and 10 3 cells. A method for using the HPG-2 PCR test directly on sinus swabs was developed. Using this method, there was 100% agreement between culture and the direct HPG-2 PCR for the 36 swabs processed. The DNA probes and PCR tests appear to be useful diagnostic tools for the detection of infectious coryza. The tests can be used as confirmatory tests following the isolation of a hemophilic organism. As well, the HPG-2 PCR test appears to be a potential alternative to culture.
Keyword H. paragallinarum
DNA probe
Polymerase chain reaction
Sinus swabs
Q-Index Code C1
Q-Index Status Provisional Code
Institutional Status Non-UQ

Document type: Journal Article
Sub-type: Article (original research)
Collection: Queensland Alliance for Agriculture and Food Innovation
 
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