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Original Articles

Flow cytometry as a tool for measuring the kinetics of IgM-positive cells in the gill and spleen of sea bream juveniles after bath immunization against Photobacterium damselae subsp. piscicida (Phdp)

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Pages 56-59 | Received 26 Feb 2015, Accepted 08 Sep 2015, Published online: 08 Dec 2015

Figures & data

Figure 1. (A) Histogram of non-washed spleen leucocytes from commercial group after incubation. We observe two picks of cells. Stained cells (H) and not-stained cells (on the left, not-gated). (B) Histogram of washed spleen leucocytes from commercial group after incubation. We observe two picks of cells. Stained cells (H) and not-stained cells (on the left). No differences between (A) and (B) are observed.

Figure 1. (A) Histogram of non-washed spleen leucocytes from commercial group after incubation. We observe two picks of cells. Stained cells (H) and not-stained cells (on the left, not-gated). (B) Histogram of washed spleen leucocytes from commercial group after incubation. We observe two picks of cells. Stained cells (H) and not-stained cells (on the left). No differences between (A) and (B) are observed.

Figure 2. Percentages of IgM-positive cells in the gill and spleen of vaccinated fish. Values expressed as increment above control.

Figure 2. Percentages of IgM-positive cells in the gill and spleen of vaccinated fish. Values expressed as increment above control.