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1 berculosis complex, namely M. microti and M. africanum.
2 lineage, the Euro-American X lineage, and M. africanum.
3 . tuberculosis, 6 (1%) were identified as M. africanum, 8 (1%) were identified as M. bovis, and 13 (2
4 and CFP-10, comparing M. tuberculosis to M. africanum and a strain of M. africanum complemented with
5 IFN-alphabeta receptor knockout mice with M. africanum and monitored bacterial growth, lung disease,
6 complex (354 cases of M. tuberculosis, 20 M. africanum and one case of M. bovis) and 69 (15%) were du
7 apparatus member, Rv3879c, is mutated in M. africanum, and individuals infected with M. africanum le
9 rculosis, Mycobacterium bovis, Mycobacterium africanum, and Mycobacterium microti and had a sensitivi
10 However, there is no simple definition of M. africanum, and some authors question the validity of thi
11 y identified as M. bovis were shown to be M. africanum because they had a wild-type pncA sequence wit
12 dentifications for all TBC members except M. africanum, but further characterization resulted in prof
13 isolates from Sierra Leone, identified as M. africanum by biochemical and growth characteristics.
14 strains, although these were enriched in M. africanum cell lysates, suggesting a modest ESX-1 secret
15 erculosis to M. africanum and a strain of M. africanum complemented with M. tuberculosis Rv3879c.
17 Genotypic analyses identified a cluster (M. africanum group A) which included M. africanumT and was
18 These results confirm impaired fitness of M. africanum in vivo and indicate that Rv3879c is not requi
19 FN-alphabeta is pathogenic during chronic M. africanum infection and that the pathogenic effects may
24 etion, specific to the animal-adapted and M. africanum L6 lineages, that restores ESAT-6 secretion by
25 africanum, and individuals infected with M. africanum less frequently demonstrate T-cell responses t
26 ovis and in the closely linked Mycobacterium africanum lineage 6 (L6) that likely account for this di
27 berculosis complex (TBC; M. tuberculosis, M. africanum, M. canettii, M. microti, M. bovis, and M. bov
28 M. tuberculosis, M. bovis, M. bovis BCG, M. africanum, M. microti, and M. canettii was developed.
30 ositive pulmonary tuberculosis exposed to M. africanum progress less frequently to active disease wit
34 ngly, coincident polymorphisms linked one M. africanum subtype I genotype with the dassie bacillus an
36 uberculosis (or M. africanum subtype II), M. africanum subtype I, M. bovis, M. bovis BCG, M. caprae,
37 r as MtbC composed of M. tuberculosis (or M. africanum subtype II), M. africanum subtype I, M. bovis,
38 de Mycobacterium tuberculosis, Mycobacterium africanum (subtypes I and II), Mycobacterium bovis (alon
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