Development of a PCR method for the detection of pathogenic Aeromonas veronii
Pan Xiao
Abstract
Pan Xiao
Abstract
The aim of the study was explore a set of new detective targets in pathogenic Aeromonas veronii which was more specific than others at present,to develop a new duplex PCR method which could effectively detection the pathogenic A.veronii.Comparison analysis of the 16S rRNA gene se-quences of Aeromonas spp.was used to explore A.veronii specific targets,which were then evaluated and used to design specific primers,and select the conservative primers of aerolysin genes in Aeromo-nas spp.to explore pathogenic targets.PCR parameters were optimized,its reaction system was devel-oped,and its sensitivity and specificity were checked.12 Aeromonas stains and 10 non-Aeromonas stains were tested for pathogenic A.veronii by duplex PCR method.The duplex PCR can clearly iden-tify A.veronii from Aeromonas species,and can identify aerolysin-producing stains of A.veronii.The detection limit of genomic DNA by the duplex PCR was 1.35×10-3 mg/L.A novel duplex PCR method was successfully developed in this study,which could effectively detect pathogenic A.veronii with high accuracy and sensitivity.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
The aim of the study was explore a set of new detective targets in pathogenic Aeromonas veronii which was more specific than others at present,to develop a new duplex PCR method which could effectively detection the pathogenic A.veronii.Comparison analysis of the 16S rRNA gene se-quences of Aeromonas spp.was used to explore A.veronii specific targets,which were then evaluated and used to design specific primers,and select the conservative primers of aerolysin genes in Aeromo-nas spp.to explore pathogenic targets.PCR parameters were optimized,its reaction system was devel-oped,and its sensitivity and specificity were checked.12 Aeromonas stains and 10 non-Aeromonas stains were tested for pathogenic A.veronii by duplex PCR method.The duplex PCR can clearly iden-tify A.veronii from Aeromonas species,and can identify aerolysin-producing stains of A.veronii.The detection limit of genomic DNA by the duplex PCR was 1.35×10-3 mg/L.A novel duplex PCR method was successfully developed in this study,which could effectively detect pathogenic A.veronii with high accuracy and sensitivity.
Key concepts: Aerolysin, Aeromonas veronii, Aeromonas, Biology, 16S ribosomal RNA, Microbiology, Pathogenic bacteria, Duplex (building)