Technical advance

Usefulness of real time PCR for the differentiation and quantification of 652 and JP2 Actinobacillus actinomycetemcomitans genotypes in dental plaque and saliva

Germano Orrù¹ , Mario Francesco Marini^1,2 , Maria Laura Ciusa¹ , Daniela Isola¹ , Marina Cotti¹ , Marco Baldoni² , Vincenzo Piras¹ , Elisabetta Pisano¹ and Caterina Montaldo¹

¹  O.B.L. (Oral Biotechnology Laboratory), Dipartimento di Chirurgia e Odontostomatologia Università degli Studi di Cagliari, Cagliari, Italy

²  Universita' degli Studi Milano Bicocca, Dipartimento di Neuroscienze, Dottorato di Ricerca in Parodontologia Sperimentale, Milano, Italy

author email corresponding author email

BMC Infectious Diseases 2006, 6:98doi:10.1186/1471-2334-6-98

Published:	13 June 2006

Abstract

Background

The aim of our study is to describe a fast molecular method, able to distinguish and quantize the two different genotypes (652 and JP2) of an important periodontal pathogen: Actinobacillus actinomycetemcomitans. The two genotypes show differences in the expression of an important pathogenic factor: the leukotoxin (ltx). In order to evidence this, we performed a real time PCR procedure on the ltx operon, able to recognize Aa clinical isolates with different leukotoxic potentials.

Methods

The specificity of the method was confirmed in subgingival plaque and saliva specimens collected from eighty-one Italian (Sardinian) subjects with a mean age of 43.9, fifty five (68 %) of whom had various clinical forms of periodontal disease.

Results

This procedure showed a good sensitivity and a high linear dynamic range of quantization (10⁷-10² cells/ml) for all genotypes and a good correlation factor (R2 = 0.97–0.98). Compared with traditional cultural methods, this real time PCR procedure is more sensitive; in fact in two subgingival plaque and two positive saliva specimens Aa was only detected with the molecular method.

Conclusion

A low number of Sardinian patients was found positive for Aa infections in the oral cavity, (just 10 positive periodontal cases out of 81 and two of these were also saliva positive). The highly leukotoxic JP2 strain was the most representative (60 % of the positive specimens); the samples from periodontal pockets and from saliva showed some ltx genotype for the same patient. Our experience suggests that this approach is suitable for a rapid and complete laboratory diagnosis for Aa infection.