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. 2008 Jun 2;76(9):3932–3939. doi: 10.1128/IAI.00150-08

TABLE 2.

Candidate antigensa

M. tuberculosis H37Rv designation M. bovis designation % Amino acid sequence identity to M. tuberculosis H37Rv
High-expression conditionsb Functionc
M. tuberculosis M. bovis M. avium M. bovis BCG Pasteur
Rv1211 Mb1243 100 100 70 100 Mtb CHP
Rv1222 Mb1254 100 100 23 100 Mb CHP
Rv1398c Mb1433c 100 100 100 Mtb+Mb CHP
Rv2081c Mb2107c 100 100 13 74 Mb Possible TP
Rv2876 Mb2901 100 99 6 98 Mb Possible conserved TP
Rv3271c Mb3299c 100 100 100 Mtb Probable conserved IMP
Rv3407 Mb3441 100 100 100 Mtb CHP
Rv3477 Mb3504 100 98 47 99 Mtb+Mb PE family protein (PE31)
Rv3613c Mb3643c 100 100 100 Mtb HP
Rv3614c Mb3644c 100 100 100 Mtb+Mb CHP
Rv3615c Mb3645c 100 100 100 Mtb+Mb CHP
Rv3633 Mb3657 100 100 28 100 Mb CHP
Rv3750c Mb3776c 100 100 100 Mtb Possible excisionase
Rv3866 Mb3896 100 100 13 100 Mb CHP
a

The 14 candidates were screened for stimulation of an IFN-γ response in M. bovis-infected cattle. Both the M. tuberculosis H37Rv and M. bovis AF2122/97 designations are indicated. The levels of amino acid homology of the M. tuberculosis protein to homologues in M. bovis and seven closely related species are indicated.

b

The antigens were expressed in either four M. tuberculosis conditions (Mtb), two M. bovis conditions (Mb), or all six conditions (Mtb+Mb).

c

CHP, conserved hypothetical protein; HP, hypothetical protein; IMP, integral membrane protein; TP, transmembrane protein.