A PCR Method to Detect Nocardia seriolae in Fish Samples

N/ACitations
Citations of this article
21Readers
Mendeley users who have this article in their library.

Abstract

Species-specific polymerase chain reaction (PCR) targeting the 16S rRNA gene of Nocardia seriolae was developed. The PCR targeted nucleotide #609 to 1038 (Escherichia coli numbering), which gave a 432 bp-length product. This method could detect N. seriolae type strain (JCM3360) and eight clinical isolates of this species from yellowtail Seriola quinqueradiata and Japanese flounder Paralichthys olivaceus, but not those of other bacterial species including 5 other Nocardia spp. and 4 yellowtail pathogens. The detection limit of the PCR was 102 CFU. Eight diseased yellowtail were employed for detection of the bacterium by the PCR. Positive results were obtained from all fish.

Cite

CITATION STYLE

APA

Miyoshi, Y., & Suzuki, S. (2003). A PCR Method to Detect Nocardia seriolae in Fish Samples. Fish Pathology, 38(3), 93–97. https://doi.org/10.3147/jsfp.38.93

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free