Development of cattle TB vaccines based on heterologous prime-boosting strategies

AbstractDevelopment of a TB vaccine for cattle is a research priority in Great Britain. Two challenges need to be addressed. Firstly, vaccine strategies enhancing the efficacy of M. bovis bacille Calmette Guérin (BCG), currently the only potentially available TB vaccine, and secondly the development of a diagnostic test to be used alongside vaccination to differentiate vaccinated and infected animals (DIVA test). Significant progress in developing TB vaccines for cattle has been made over the last 7 years. Specifically: (i) DNA, protein, or viral subunit subunit vaccines used in combination with BCG have been shown to give superior protection against experimental challenge in cattle than BCG (heterologous prime-boost), (ii) neonatal BCG vaccination provides protection, (iii) prototype reagents that allow discrimination between vaccinated and infected animals have been developed; and (iv) and correlates of disease severity have been identified that can predict the success or failure of vaccination. The present overview provides details of some of these advances. [Ethiop.J.Health Dev. 2008;22(Special Issue):100-104

Rapid detection of Mycobacterium bovis DNA in cattle lymph nodes with visible lesions using PCR

BACKGROUND: We have evaluated a sensitive screening assay for Mycobacterium tuberculosis (MTB) complex organisms and a specific assay for detecting Mycobacterium bovis DNA in lymph nodes taken from cattle with evidence of bovine tuberculosis. Underlying these series of experiments was the need for a versatile DNA extraction protocol which could handle tissue samples and with the potential for automation. The target for the screening assay was the multi-copy insertion element IS1081, present in 6 copies in the MTB complex. For confirmation of M. bovis we used primers flanking a specific deletion in the genome of M. bovis known as region of difference 4 (RD4). The sensitivity and specificity of these PCRs has been tested on genomic DNA from MTB complex reference strains, mycobacteria other than tuberculosis (MOTT), spiked samples and on clinical material. RESULTS: The minimum detection limits of the IS1081 method was < I genome copy and for the RD4 PCR was 5 genome copies. Both methods can be readily adapted for quantitative PCR with the use of SYBR Green intercalating dye on the RotorGene 3000 platform (Corbett Research). Initial testing of field samples of bovine lymph nodes with visible lesions (VL, n = 109) highlighted two shortfalls of the molecular approach. Firstly, comparison of IS1081 PCR with the "gold standard" of culture showed a sensitivity of approximately 70%. The sensitivity of the RD4 PCR method was 50%. Secondly, the success rate of spoligotyping applied directly to clinical material was 51% compared with cultures. A series of further experiments indicated that the discrepancy between sensitivity of detection found with purified mycobacterial DNA and direct testing of field samples was due to limited mycobacterial DNA recovery from tissue homogenates rather than PCR inhibition. The resilient mycobacterial cell wall, the presence of tissue debris and the paucibacillary nature of some cattle VL tissue may all contribute to this observation. Any of these factors may restrict application of other more discriminant typing methods. A simple means of increasing the efficiency of mycobacterial DNA recovery was assessed using a further pool of 95 cattle VL. Following modification of the extraction protocol, detection rate with the IS1081 and RD4 methods increased to 91% and 59% respectively. CONCLUSION: The IS1081 PCR is a realistic screening method for rapid identification of positive cases but the sensitivity of single copy methods, like RD4 and also of spoligotyping will need to be improved to make these applicable for direct testing of tissue extracts

A comparative study on the epidemiology and immuno-pathology of bovine tuberculosis in Bos indicus and Bos taurus cattle in Ethiopia

AbstractBovine tuberculosis is a disease of dual effect, having public health and economic implications. The present study was conducted on its epidemiology and immuno-pathology in Holstein and Zebu breeds of cattle. Skin test, post mortem examination and pathology scoring, bacteriology, whole blood gamma interferon assay, ELISPOT assay, and lateral flow assay were used. An overall prevalence of 13.5% (n=5,424) was recorded; both prevalence (2 =61.8; P&lt;0.001) and severity of pathology (mean pathology scores + SEM: 6.84±0.79 vs. 5.21±0.30; P=0.018, Mann-Whitney test) were significantly higher in Holstein than in Zebu. Similarly, IFN- responses to avian PPD (0.490.10 vs. 0.390.07), bovine PPD (0.630.11 vs. 0.430.07), or the ESAT6-CFP10 protein cocktail (0.430.01 vs. 0.300.05) were significantly higher (for all antigens: p&lt;0.02) in Holstein than in Zebu cattle. However, both Holstein and Zebu exhibited similar T cell and antibody responses to different mycobacterial antigens i.e. no repertoire difference was observed between the two breeds. Thus, the present study showed increased susceptibility of Holsteins to bovine TB as compared to Zebu, similarity between Holsteins and Zebus in their antigen responses, and a positive correlation between IFN- responses and severity of pathology of bovine TB. [Ethiop.J.Health Dev. 2008;22(Special Issue):132-134