Dynamics of Lymphocyte Subpopulations in Immune Organs of Chickens Infected with Salmonella enteritidis

Asheg A. A. , M. Levkut , V. Revajová, Z. ·evãíková, L. Kolodzieyski , J . Pis t l : Dynamics of Lymphocyte Subpopulations in Immune Organs of Chickens Infected with Salmonella enteritidis. Acta Vet. Brno 2003, 72: 359-364. To determine the effect of different doses of Salmonella enteritidis on immunocompetent cells, the thymus, bursa of Fabricius, and peripheral blood were examined. One-day-old chickens were orally infected with 2 × 102 CFU/ml (low dose) and 2 × 108 CFU/ml (high dose) of S. enteritidis PT4. Subsets of T lymphocytes (CD3, CD4, and CD8), and BU1b cells using an indirect immunofluorescent method and flow cytometry were analysed on days 7, 10, 14, 21, and 27 postinoculation (dpi). The actual number of lymphocytes in the peripheral blood showed a significant increase in the low dose group (P < 0.05) on day 21 pi, and in the high dose group on day 27 pi (P < 0.001) compared to controls. The increase of CD3+, CD4+, and CD8+ T cells was observed in both infected groups compared to the controls from day 14 pi, significant on day 21 pi (P < 0.05) in the high dose group. The subpopulation of CD8+ was higher also on day 27 pi (P < 0.01) compared with the values of the control group. The subpopulation of BU1b+ B cells in both infected groups showed higher values, but without significant differences from controls. The thymus T lymphocytes showed a significant decline in CD3+ T cells on day 7 pi, whereas CD4+ T cells were significantly (P < 0.05) increased on day 7 pi in both infected groups. The bursal lymphocytes showed a decrease in BU1b+ B cells in both infected groups compared with the control group, significant in the high dose group on day 21 pi (P < 0.05). These results indicate that S. enteritidis infection induced the changes in immunocompetent cells, included cellular and humoral immune response. Salmonella infection accelerated the maturation and differentiation of thymus T cells in the first phase of infection, what was secondarily reflected by increased number of studied T lymphocyte subpopulations in the peripheral blood from day 14 to 27 after infection. Similarly, it appears that the activation of B cells in bursa of Fabricius caused the decrease number of bursal B lymphocytes and increased number of these cells in the peripheral blood from day 14 to 27 pi in both infected groups. Salmonella enteritidis, immune response, flow cytometry, lymphocyte subpopulations, chickens Salmonella enteritidis (S. enteritidis) has become the most important cause of human food poisoning throughout the world in recent years. Current research has attempted to identify the defence mechanism of chickens against S. enteritidis (Arnold and Holt 1995). Salmonella invades the intestinal epithelium and stimulates mucosal immunity. In chickens the cell-mediated immune response has been shown to play an important role in host protection against many intracellular pathogens (Schat 1994; Kaufmann 1995; Lil lehoj and Trout 1996). Sasai et al. (1997) reported that S. enteritidis infection induces changes in the lymphocyte subpopulations in the spleen and thymus that reflect the dynamics of the host’s protective immune response. Although some aspects of cellular immune responses to S. enteritidis have been examined in chickens, the exact protective immune mechanism remains to be determined. In the present study, the percentage of CD3, CD4, CD8 T cells, and BU1b B cells in the thymus, bursa of Fabricius and peripheral blood of one-day-old chickens orally infected with S. enteritidis were investigated. ACTA VET. BRNO 2003, 72: 359–364 Address for correspondence: MVDr. V. Revajová, PhD. Dept. of Pathological Anatomy University of Veterinary Medicine Komenského 73, 041 81 Ko‰ice, Slovakia Phone: + 421 556 338 191 Fax: + 421 556 338 191 E-mail: [email protected] http://www.vfu.cz/acta-vet/actavet.htm Materials and Methods Chickens A total of ninety, one-day-old White Plymouth Rock chickens were randomly divided into three groups, containing 30 birds each. The birds were kept in isolation in floor pens of 1 m2 per group on wood shavings that were not changed during the experiment. The pen was lit continuously. The temperature was maintained at that required for the age of the birds (32 ̊C at first week and was reduced weekly by about 2 ̊C). Water and feed were available ad libitum. Reagents Mouse monoclonal antibodies (Mab) against chicken CD3, CD4, CD8 T lymphocytes (Scandic, Czech Republic), and BU1b (Southern Biotechnology Associates, Inc., Birmingham, USA) expressed on B cells at a dilution of 1:25 were used for flow cytometry. Salmonel la Experimental infection was carried out with S. enteritidis PT4. Bacterial culture and doses were previously described (Asheg et al. 2001a). Experimental design Chickens in the first and second groups were orally inoculated with 2 × 102 CFU/ml (low dose) and 2 × 108 CFU/ml (high dose) of S. enteritidis PT4, respectively. Chickens of the third group were used as control animals and obtained a placebo (1 ml PBS per os). Five birds from each group were venipunctured and then killed by cervical dislocation on days 7, 10, 14, 21, and 27 post-inoculation (dpi). The peripheral blood, the thymus, and bursa of Fabricius were used for flow cytometry analysis. White blood cel l count (WBC) Leukocytes were counted by a routine laboratory method using Fried-Lukáãová solution (475 μl solution plus 25 μl blood). Differential cell counts were made on blood smears after Hemacolor (Merck, Germany) staining by counting 100 cells per slide. Flow cytometry in the per ipheral blood and organs The thymus and bursal lymphocytes were removed by teasing through a 70 μm mash screen (Hel ler and Schat 1987) and then isolated on a density gradient Telebrix (SEVAC, Prague, Czech Republic). Telebrix was also used for the separation of lymphocytes from the peripheral blood. After separation, the lymphocytes were twice washed with phosphate buffer saline (PBS). Fifty l of cellular suspension (1 × 106 lymphocytes in PBS) and 50 l of specific MoAb (Tab. 1) were mixed and incubated at 4 °C for 30 min. After incubation the cells were washed twice in the PBS and pellets were mixed with 25 l of the secondary antibody (FITC-conjugated goat antimouse immunoglobulin; Dakopatts, Germany) in a dilution of 1:50 and incubated in the dark as described above. The cells were washed twice in the PBS and resuspended in 0.5 ml of 1% paraformaldehyde in PBS. Samples were analysed by FACScan flow cytometer (Becton Dickinson, Germany). Data on 1 × 104 viable cells were collected using the Cell Quest program (Becton Dickinson, Germany). For the peripheral blood the absolute lymphocyte counts were computed as follows: WBC count × % of the relative lymphocytes × % lymphocyte subpopulation. 360 Table 1 Primary monoclonal antibodies used in the experiment Specificity MoAbs Isotype Dilution CD3 RTMCA1378 mouse IgG1 1:25 CD4 SRTMCA1473 mouse IgG1 1:25 CD8 SRTMCA1377 mouse IgG1 1:25 BU1b 8370-01 mouse IgG1 1:25 Stat is t ical analysis All data were tested by one-way ANOVA using the Bonferoni test. Differences between the mean values for the groups of chickens were considered significant, when probabilities of less than 0.05 were obtained.