Efficient clinical diagnosis of pathogens is important for the management of infectious diseases. Conventional methods have longer turnaround time and, in most cases, lower sensitivity. Nucleic acid based methods for detection of microorganisms are rapid, sensitive, and are generally successful even when the culturing of microorganisms fails. Sequence-based molecular methods such as real-time PCR provide rapid diagnostics and higher sensitivity, allowing differentiation between related strains.
Although numerous technologies are available for the molecular level identification of pathogens, the most common is real-time PCR. This technique has a high accuracy when used with specific primers and probes. Manual design of these primer and probes is tedious and results in lower quality results owing to the inability to simultaneously handle multiple criteria for design. AlleleID® from Premier Biosoft is a new tool that designs real-time PCR assays to identify and detect pathogens.
Oral pathogens such as periodontopathic bacteria are the etiological factors in the development of gum diseases. Quantitative analysis with the identification of periodontopathic bacteria is important for the diagnosis, therapeutic evaluation, and the risk assessment of periodontal diseases. Real-time PCR is often used for this process. Scientists at Premier Biosoft have quantified six—Porphyromonas gingivalis, Tannerella forsythia, Actinobacillus actinomycetemcomitans, Treponema denticola, Prevotella intermedia, and Prevotella nigrescens—using real-time PCR.
In our recent studies, plaque and tongue debris specimens were collected from 10 patients with advanced periodontitis and 10 periodontally healthy individuals. All species, except for P. nigrescens, were detected in diseased samples in significantly greater numbers than in those from healthy patients, which had greater number of P. nigrescens.
Sensitivity of real-time PCR to detect periodontopathic bacteria depends on the ability of the species-specific primers and probes to amplify and detect all possible species circulating in the population. An example of species-specific detection is shown in Figure 1. 16s ribosomal RNA gene sequences from six periodontal bacteria were obtained from GenBank and aligned using AlleleID. The unique regions identified were used for the assay.
Species-specific TaqMan® probes were designed to detect six bacterial species. These primer-probe sets uniquely detect each of them in the sample. The sets using AlleleID gave an efficiency of more than 93.5%.
In cases where the nature of the sequences is such that a unique probe for each strain cannot be designed, a minimal set using fewer probes can be used to detect all the sequences in an aligned set. Such an assay is useful for for major histocompatibility (MHC) proteins. They are the cell-surface antigens present in most eukaryotes that identify a particular tissue type. In humans, MHC typing plays an important role in tissue grafting.
Due to high conservancy, minor differences in the MHC sequences of different species were observed. In many cases, each sequence was identified with a unique probe without cross hybridizing with any other sequence in the alignment. If such a design fails, the minimal probe set design option can be used. Though a single probe can identify more than one sequence, the combination of such probes uniquely identifies a given sequence.