Abstract

The distribution of Cardicola forsteri eggs in the gills of southern bluefin tuna (Thunnus maccoyii) was analysed. Eggs were confirmed to be C. forsteri using laser-capture microdissection and quantitative polymerase chain reaction (qPCR) analyses. Prevalence of infection was significantly higher in the second gill arch (χ2=6.49, P<0.05) than in the fourth gill arch, and significantly lower in the basal region of the second gill arch (χ2=6.29, d.f.=2, P<0.05). The intensity of infection was not significantly different between the gill arches (F=0.03, d.f.=1, P>0.05). Similarly, there was no significant difference in the intensity of C. forsteri eggs between the gill arches (F=3.43, d.f.=2, P>0.05), or at different depth of sectioning (F=0.08, d.f.=1.12, P>0.05). Results suggest that the presence of C. forsteri eggs in the gills of tuna is more likely to be detected by sampling the second gill arch. Furthermore, targeting the middle region and increasing the sectioning depth may reduce the proportion of false negatives.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call