| Title | Identification of Actinobacillus actinomycetemcomitans Using Species-Specific 16S rDNA Primers |
|---|---|
| Author | Su-Gwan Kim1,3, Soo-Heung Kim1, Mi-Kwang Kim2, Hwa-Sook Kim2, and Joong-Ki Kook2,3,* |
| Address | 1Department of Oral and Maxillofacial Surgery, College of Dentistry, Chosun University. 375 Seo-Suk Dong, Dong-ku, Gwang-ju 501-759, Republic of Korea, 2Department of Oral Biochemistry, College of Dentistry, Chosun University. 375 Seo-Suk Dong, Dong-ku, Gwang-ju 501-759, Republic of Korea, 3Oral Biology Research Institute, College of Dentistry, Chosun University. 375 Seo-Suk Dong, Dong-ku, Gwang-ju 501-759, Republic of Korea |
| Bibliography | Journal of Microbiology, 43(2),209-212, 2005, |
| DOI | |
| Key Words | Actinobacillus actinomycetemcomitans, 16S rDNA, species-specific PCR primer |
| Abstract | The purpose of this study was to develop species-specific PCR primers for use in the identification and detection of Actinobacillus actinomycetemcomitans. These primers target variable regions of the 16S ribosomal RNA coding gene (rDNA). We assessed the specificity of the primers against 9 A. actinomycetemcomitans strains and 11 strains (3 species) of the Haemophilus genus. Primer sensitivity was determined by testing serial dilutions of the purified genomic DNAs of A. actinomycetemcomitans ATCC 33384^T. Our obtained data revealed that we had obtained species-specific amplicons for all of the tested A. actinomycetemcomitans strains, and that none of these amplicons occurred in any of the other species. Our PCR protocol proved able to detect as little as 4 fg of A. actinomycetemcomitans chromosomal DNA. Our findings suggest that these PCR primers are incredibly sensitive, and should prove suitable for application in epidemiological studies, as well as the diagnosis and monitoring of periodontal pathogens after treatment for periodontitis. |
| Download PDF | p.209-212.pdf |