Most cases of chicken salmonellosis are caused by serovar Gallinarum biovars Gallinarum and Pullorum, which lead to a significant morbidity and fatality rate. Although the conventional Kaufmann-White scheme is the reliable method for the serotyping of , it does not distinguish between closely related biotypes like . Pullorum and . Gallinarum. Herein, we conducted a single one-step multiplex PCR assay that can identify and distinguish between . Pullorum and . Gallinarum in an accurate manner. This PCR method was based on three genes, including for . Pullorum identification, for . Gallinarum identification, and as the genus-level reference gene for . By comparing . Pullorum to . Gallinarum and other serovars ... More
Most cases of chicken salmonellosis are caused by serovar Gallinarum biovars Gallinarum and Pullorum, which lead to a significant morbidity and fatality rate. Although the conventional Kaufmann-White scheme is the reliable method for the serotyping of , it does not distinguish between closely related biotypes like . Pullorum and . Gallinarum. Herein, we conducted a single one-step multiplex PCR assay that can identify and distinguish between . Pullorum and . Gallinarum in an accurate manner. This PCR method was based on three genes, including for . Pullorum identification, for . Gallinarum identification, and as the genus-level reference gene for . By comparing . Pullorum to . Gallinarum and other serovars of study revealed that only the former has a deletion of 126 bp-region in the carboxyl terminus of . The gene does not exist in . Gallinarum. However, it is present in all other serotypes. The multiplex PCR approach utilizes unique sets of primers that are intended to specifically target these three different genes. The established PCR method was capable of distinguishing between the biovars Pullorum and Gallinarum from the 29 distinct serotypes as well as the 50 distinct pathogens that are not , showing excellent specificity and exclusivity. The minimal amount of bacterial cells required for PCR detection was 100 CFU, while the lowest level of genomic DNA required was 27.5 pg/μL for both . Pullorum and . Gallinarum. After being implemented on the clinical isolates collected from a poultry farm, the PCR test was capable of distinguishing the two biovars Pullorum and Gallinarum from the other strains. The findings of the PCR assay were in line with those of the traditional serotyping and biochemical identification methods. This new multiplex PCR could be used as a novel tool to reinforce the clinical diagnosis and differentiation of . Pullorum and . Gallinarum, particularly in high-throughput screening situations, providing the opportunity for early screening of infections and, as a result, more effective management of the illness among flocks.
