Evaluation of two cocktails containing ESAT-6, CFP-10 and Rv-3615c in the intradermal test and the interferon-γ assay for diagnosis of bovine tuberculosis

C. Casal, J. Bezos, A. Díez-Guerrier, J. Álvarez, B. Romero, L. de Juan, S. Rodriguez-Campos, M. Vordermeier, A. Whelan, R. G. Hewinson, A. Mateos, L. Domínguez, A. Aranaz

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38 Scopus citations


The intradermal tuberculin tests and the interferon-gamma (IFN-γ) assay are the principal tests used worldwide for the ante-mortem diagnosis of bovine tuberculosis. The conventional reagent currently in use in these tests is purified protein derivative (PPD) tuberculin obtained from Mycobacterium bovis culture. The components of PPD are poorly characterized and difficult to standardize. To overcome this issue, antigens specific to the Mycobacterium tuberculosis complex are being studied. Here we have assessed the biological potency of ESAT-6, CFP-10 and Rv-3615c presented as peptide or recombinant protein cocktails in comparison with the standard bovine PPD used routinely in Spanish eradication campaigns. The study was performed in cattle (n= 23) from a herd with natural M. bovis infection. Animals were simultaneously injected with PPD and the peptide and protein cocktails. The percentages of cattle reacting positively to single intradermal test were 60.9% (bovine PPD), 47.8% (peptide cocktail) and 60.9% (protein cocktail), with no significant difference between the actual skin fold thickness increases (p> 0.05). The IFN-γ assay detected 60.9% of animals when stimulation was performed with bovine PPD, but decreased to 52.2% when stimulation was performed with the peptide cocktail and to 47.8% when stimulation was performed with the protein cocktail. However, no significant differences were found between IFN-γ responder frequencies (p> 0.05). These results show a potential use of these defined reagents for in vivo tuberculosis diagnosis.

Original languageEnglish (US)
Pages (from-to)149-154
Number of pages6
JournalPreventive Veterinary Medicine
Issue number1-2
StatePublished - Jun 1 2012

Bibliographical note

Funding Information:
This study was funded by the EU Project FP7-KBBE-2007-1 “Strategies for the eradication of bovine tuberculosis (TB-STEP)”. C. Casal is recipient of a research contract assigned by Comunidad de Madrid (FINNOVA II Programme). We thank the Mycobacteria and Computer and Communication Units staff for their technical support.


  • Bovine tuberculosis
  • IFN-γ assay
  • Intradermal test
  • Specific antigens


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