Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8980742 | Journal of Comparative Pathology | 2005 | 4 Pages |
Abstract
Mycoplasma haemosuis DNA was detected in experimentally infected splenectomized pigs by in-situ hybridization (ISH) with a nonradioactive digoxigenin-labelled DNA probe. An 839 base pair DNA probe targeting a 16S rRNA gene was generated by the polymerase chain reaction. Eight 6-week-old pigs were inoculated intraperitoneally with 6Â ml of M. haemosuis-infected pig blood and eight negative control pigs were inoculated intraperitoneally with 6Â ml of M. haemosuis-free blood. Two pigs from each group were killed for examination at 3, 7, 15 and 30 days post-inoculation (dpi). Red blood cells infected with M. haemosuis were first detected by light microscopy at 3 to 7 dpi. No M. haemosuis was observed in negative control pigs. Hybridization signals were evident in blood from the infected pigs at 3 dpi. The ISH method developed in this study was useful for the detection of M. haemosuis DNA in formalin-fixed, paraffin wax-embedded tissues and may be valuable for studying the pathogenesis of M. haemosuis infection.
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Authors
S.-K. Ha, K. Jung, C. Choi, Y. Ha, H.-C. Song, J.-H. Lim, S.-H. Kim, C. Chae,