Aims: The aim of this study was to design a set of primers for speciﬁc detection and identiﬁcation of Streptococcus agalactiae in polymerase chain reaction (PCR) that can detect a diverse range of S. agalactiae isolates from different hosts and that it is capable of discriminating between S. agalactiae and other species that are closely related or potentially present in aquaculture environments, notably Streptococcus iniae. Methods and Results: Primers, based on the groEL2 gene of S. agalactiae, were shown to be epidemiologically sensitive to 97 isolates of S. agalactiae, representing 11 clonal complexes derived from piscine, terrestrial and aquatic mammalian host species. The primers were tested with 10 S. iniae isolates and 22 other comparator species with no cross-reaction observed after optimization of reaction conditions. They have a high analytical sensitivity, detecting as few as 10 copies of S. agalactiae genomic DNA per reaction and are capable of detecting the target in DNA extracted from the brains of infected ﬁsh. Conclusions: The primers proved suitable for the sensitive and speciﬁc detection of S. agalactiae from dairy-, human- and ﬁsh-related origins by PCR. Signiﬁcance and Impact of the Study: Due to the importance of S. agalactiae as a pathogen, many PCR primers have been published for this bacterium, designed largely for its detection in dairy and human samples, but many cross- reacting with S. iniae. The ability to differentiate between S. agalactiae and S. iniae in aquaculture derived samples is important as both infect ﬁsh, causing similar disease symptoms and are phenotypically similar, yet control strategies and zoonotic risk are species speciﬁc.
|Pages (from-to)||666 - 674|
|Number of pages||9|
|Journal||Journal of Applied Microbiology|
|Early online date||22 May 2018|
|Publication status||First published - 22 May 2018|
- Fish (live)