Immune response profiles of calves following vaccination with live BCG and inactivated Mycobacterium bovis vaccine candidates
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Date
Authors
Van der Heijden, E.M.D.L. (Elisabeth)
Chileshe, J.
Vernooij, J.C.M.
Gortazar, G.
Juste, R.A.
Sevilla, I.
Crafford, Jan Ernst
Rutten, Victor P.M.G.
Michel, Anita Luise
Journal Title
Journal ISSN
Volume Title
Publisher
Public Library of Science
Abstract
Conventional control and eradication strategies for bovine tuberculosis (BTB) face tremendous
difficulties in developing countries; countries with wildlife reservoirs, a complex wildlifelivestock-
human interface or a lack of veterinary and veterinary public health surveillance.
Vaccination of cattle and other species might in some cases provide the only suitable control
strategy for BTB, while in others it may supplement existing test-and-slaughter schemes.
However, the use of live BCG has several limitations and the global rise of HIV/AIDS infections
has furthermore warranted the exploration of inactivated vaccine preparations. The
aim of this study was to compare the immune response profiles in response to parenteral
vaccination with live BCG and two inactivated vaccine candidates in cattle.
Twenty-four mixed breed calves (Bos taurus) aged 4±6 months, were allocated to one of
four groups and vaccinated sub-cutaneously with live M. bovis BCG (Danish 1331), formalin-
inactivated M. bovis BCG, heat-killed M. bovis or PBS/Montanide™ (control). Interferon-
γ responsiveness and antibody production were measured prior to vaccination and at
weekly intervals thereafter for twelve weeks. At nine weeks post-priming, animals were skin
tested using tuberculins and MTBC specific protein cocktails and subsequently challenged
through intranodular injection of live M. bovis BCG.
The animals in the heat-killed M. bovis group demonstrated strong and sustained cellmediated
and humoral immune responses, significantly higher than the control group in
response to vaccination, which may indicate a protective immune profile. Animals in this
group showed reactivity to the skin test reagents, confirming good vaccine take. Lastly, although not statistically significant, recovery of BCG after challenge was lowest in the heatkilled
M. bovis group.
In conclusion, the parenteral heat-killed M. bovis vaccine proved to be clearly immunogenic
in cattle in the present study, urging further evaluation of the vaccine in challenge studies
using virulent M. bovis and assessment of vaccine efficacy in field conditions.
Description
S1 Fig. Conventional PCR for the detection ofMycobacterium bovis. PCR targeting RD1,
RD4 and RD9 as previously described. PCR products of +- 268bp (RD4 absent), +- 196bp
(RD1 absent) and +- 108bp (RD9 absent) indicate M. bovis BCG. Animals 18, 21 and 31 belong
to group 1 (live M. bovis BCG), animals 2, 6, 7, 16 and 29 belong to group 2 (formalin-inactivated
M. bovis BCG), animals 8, 9, 10, 11 and 26 belong to group 3 (heat-killed M. bovis) and
animals 12 and 15 belong to group 4 (control). R = right prescapular lymph node.
S1 Dataset. Tables containing the raw data of the immunological assays. (A) BOVIGAM assay. OD-values for all stimulations and controls. (B) IDEXX TB ELISA. OD-values for the samples and controls as well as S/P-ratio. (C) Skin test. Skin fold thickness measurements at 0hrs, 72hrs and the difference (Δmm) in mm. Avian = PPD-A; Bovine = PPD-B; PC1 = protein cocktail 1; PC2 = protein cocktail 2. (D) Culture. Weights (g) and bacterial counts (CFU/g of PLN) of left and right PLNs.
S2 Dataset. Tables describing the statistical models and their outcomes. (A) Linear mixed effects models describing PPD-B and the ratios of PPD-B/PPD-A and PPD-B/PPD-F. Outcome = a + b1 time + b2 group + b3 (time group). Data were log transformed in order to meet the model assumptions of normality and homoscedasticity. Back-transformed estimates and 95% confidence intervals are given. Significant results are in bold. (B) Linear mixed effects models describing ESAT-6 and CFP-10. Outcome = a + b1 time + b2 group + b3 (time group). Data were log transformed in order to meet the model assumptions of normality and homoscedasticity. Back-transformed estimates and 95% confidence are given. Significant results are in bold. (C) Linear mixed effects model describing the S/P ratio. Outcome = a + b1 time + b2 group + b3 (time group). Data were log transformed in order to meet the model assumptions of normality and homoscedasticity. Back-transformed estimates and 95% confidence intervals are given. Significant results are in bold. (D) Double generalized linear model describing ΔPPDBÐΔPPDA in the skin test. Outcome = a + b1 group. Estimates and 95% confidence intervals are given. Significant results are in bold. (E) A simple general linear model describing ΔPC1 and ΔPC2. Outcome = a + b1 group. Estimates and 95% confidence intervals are given. Significant results are in bold. (F) Linear mixed effects model describing the PLN weights. Outcome = a + b1 LN side + b2 group + b3 (LN side group) + b4 gender. Data (PLN weights) were log transformed in order to meet the model assumptions of normality and homoscedasticity. Estimates and 95% confidence intervals are given. Significant results are in bold. (G) Negative binomial generalized linear model describing the bacterial counts. Outcome = a + b1 group. Back-transformed estimates and 95% confidence intervals are given. Significant results are in bold.
S1 Dataset. Tables containing the raw data of the immunological assays. (A) BOVIGAM assay. OD-values for all stimulations and controls. (B) IDEXX TB ELISA. OD-values for the samples and controls as well as S/P-ratio. (C) Skin test. Skin fold thickness measurements at 0hrs, 72hrs and the difference (Δmm) in mm. Avian = PPD-A; Bovine = PPD-B; PC1 = protein cocktail 1; PC2 = protein cocktail 2. (D) Culture. Weights (g) and bacterial counts (CFU/g of PLN) of left and right PLNs.
S2 Dataset. Tables describing the statistical models and their outcomes. (A) Linear mixed effects models describing PPD-B and the ratios of PPD-B/PPD-A and PPD-B/PPD-F. Outcome = a + b1 time + b2 group + b3 (time group). Data were log transformed in order to meet the model assumptions of normality and homoscedasticity. Back-transformed estimates and 95% confidence intervals are given. Significant results are in bold. (B) Linear mixed effects models describing ESAT-6 and CFP-10. Outcome = a + b1 time + b2 group + b3 (time group). Data were log transformed in order to meet the model assumptions of normality and homoscedasticity. Back-transformed estimates and 95% confidence are given. Significant results are in bold. (C) Linear mixed effects model describing the S/P ratio. Outcome = a + b1 time + b2 group + b3 (time group). Data were log transformed in order to meet the model assumptions of normality and homoscedasticity. Back-transformed estimates and 95% confidence intervals are given. Significant results are in bold. (D) Double generalized linear model describing ΔPPDBÐΔPPDA in the skin test. Outcome = a + b1 group. Estimates and 95% confidence intervals are given. Significant results are in bold. (E) A simple general linear model describing ΔPC1 and ΔPC2. Outcome = a + b1 group. Estimates and 95% confidence intervals are given. Significant results are in bold. (F) Linear mixed effects model describing the PLN weights. Outcome = a + b1 LN side + b2 group + b3 (LN side group) + b4 gender. Data (PLN weights) were log transformed in order to meet the model assumptions of normality and homoscedasticity. Estimates and 95% confidence intervals are given. Significant results are in bold. (G) Negative binomial generalized linear model describing the bacterial counts. Outcome = a + b1 group. Back-transformed estimates and 95% confidence intervals are given. Significant results are in bold.
Keywords
HIV/AIDS, Infection, Vaccination, Bovine tuberculosis (bTB), Human immunodeficiency virus (HIV), Acquired immune deficiency syndrome (AIDS), Immune response, Calves, Mycobacterium bovis
Sustainable Development Goals
Citation
van der Heijden EMDL, Chileshe J,
Vernooij JCM, Gortazar C, Juste RA, Sevilla I, et al.
(2017) Immune response profiles of calves
following vaccination with live BCG and inactivated
Mycobacterium bovis vaccine candidates. PLoS
ONE 12(11): e0188448. https://DOI.org/10.1371/journal.pone.0188448