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We used a simple log-transformation for antibody level data.
P-values are obtained by χ-test for antibody prevalence or Wilcoxon Rank-sum test for antibody level.
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Serum and bronchoalveolar lavage fluid (BALF) (collected as described below) were evaluated for antibody levels were by ELISA in plates coated with PspA5.
Test results for antibody levels against Campylobacter spp. and gangliosides (anti-GQ1b IgG) were negative.
Samples were considered as IgG- or IgM-positive for antibody levels ≥0.6 IU/ml and ≥30 IU/ml, respectively.
However, following up individuals who have antibodies would not be an overwhelming procedure as it merely involves taking blood and screening with the arrays for antibody levels- possibly in parallel with mammography screening.
A similar response was also seen for antibody levels against P. papatasi saliva, with a moderate decrease from day 0 to day 30 (P = 0.19), followed by a significant increase after release from a hospital (P = 0.001).
Dogs at the age of 1-2.49 1-2.49at vaccination that were tested for antibodyearsels at day 151-180 had a reduced risk of havaccinationdy thates < 0.5 IU/mL compared to dogs < 6 months, and dogs of ≥ 5 years of age at the time of vaccination, that were tested at day 151-180.
Microneutralization test has been used for determination of antibody levels.
Serum for analysis of antibody levels was taken at indicated time points and at the end of all experiments.
The non-parametric Mann-Whitney U statistical test was used for comparison of antibody levels in the different groups.
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